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  • Mice  (1,035)
  • General Chemistry
  • Cell & Developmental Biology
  • Inorganic Chemistry
  • 2000-2004  (1,413)
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  • 1
    Publication Date: 2004-06-26
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Beckman, Mary -- New York, N.Y. -- Science. 2004 Jun 25;304(5679):1888-9.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15218114" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Animals, Newborn ; Bedding and Linens ; *Behavior, Animal ; Female ; Male ; *Maternal Deprivation ; Mice ; *Mothers ; Mutation ; *Object Attachment ; Odors ; Receptors, Opioid, mu/genetics/*physiology ; Vocalization, Animal
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 2
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-11-30
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Marx, Jean -- New York, N.Y. -- Science. 2004 Nov 26;306(5701):1455-7.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15567822" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Bone Marrow Cells/*cytology ; Bone Marrow Transplantation ; Cell Differentiation ; Cell Fusion ; Disease Progression ; Female ; Gastric Mucosa/chemistry/pathology ; Gastritis/microbiology/*pathology ; Helicobacter Infections/*pathology ; *Helicobacter felis ; Male ; Mice ; Mice, Inbred C57BL ; Stem Cells/*cytology ; Stomach Neoplasms/*pathology
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 3
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-08-18
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Bedalov, Antonio -- Simon, Julian A -- New York, N.Y. -- Science. 2004 Aug 13;305(5686):954-5.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Clinical Research Division and J. A. Simon is in the Clinical Research and Human Biology Divisions, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA. abedalov@fhcrc.org〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15310883" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Axons/*physiology ; Cell Nucleus/metabolism ; Cell Survival ; Cells, Cultured ; Ganglia, Spinal/cytology ; Mice ; Mutation ; NAD/biosynthesis/*metabolism ; Nerve Tissue Proteins/genetics/*metabolism ; Neurodegenerative Diseases/drug therapy/physiopathology ; Neuroprotective Agents/therapeutic use ; Nicotinamide-Nucleotide Adenylyltransferase/metabolism ; RNA, Small Interfering ; Sirtuin 1 ; Sirtuins/metabolism ; Ubiquitin-Protein Ligases/metabolism ; Wallerian Degeneration/metabolism/*physiopathology
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 4
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-11-06
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Marx, Jean -- New York, N.Y. -- Science. 2004 Nov 5;306(5698):966-8.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15528423" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Cyclooxygenase 2 ; Humans ; Inflammation/*complications/immunology ; Isoenzymes/metabolism ; Macrophage Colony-Stimulating Factor/physiology ; Macrophages/immunology ; Membrane Proteins ; Mice ; NF-kappa B/physiology ; Neoplasms/*etiology/immunology ; Prostaglandin-Endoperoxide Synthases/metabolism ; Risk Factors
    Print ISSN: 0036-8075
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    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 5
    Publication Date: 2004-10-02
    Description: The Golgi enzyme beta1,6 N-acetylglucosaminyltransferase V (Mgat5) is up-regulated in carcinomas and promotes the substitution of N-glycan with poly N-acetyllactosamine, the preferred ligand for galectin-3 (Gal-3). Here, we report that expression of Mgat5 sensitized mouse cells to multiple cytokines. Gal-3 cross-linked Mgat5-modified N-glycans on epidermal growth factor and transforming growth factor-beta receptors at the cell surface and delayed their removal by constitutive endocytosis. Mgat5 expression in mammary carcinoma was rate limiting for cytokine signaling and consequently for epithelial-mesenchymal transition, cell motility, and tumor metastasis. Mgat5 also promoted cytokine-mediated leukocyte signaling, phagocytosis, and extravasation in vivo. Thus, conditional regulation of N-glycan processing drives synchronous modification of cytokine receptors, which balances their surface retention against loss via endocytosis.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Partridge, Emily A -- Le Roy, Christine -- Di Guglielmo, Gianni M -- Pawling, Judy -- Cheung, Pam -- Granovsky, Maria -- Nabi, Ivan R -- Wrana, Jeffrey L -- Dennis, James W -- New York, N.Y. -- Science. 2004 Oct 1;306(5693):120-4.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Samuel Lunenfeld Research Institute, Mount Sinai Hospital, 600 University Avenue, Toronto, ON M5G 1X5, Canada.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15459394" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Cell Line, Tumor ; Cell Membrane/metabolism ; Cell Movement ; Cell Transformation, Neoplastic ; *Endocytosis ; Galectin 3/metabolism ; Genetic Vectors ; Glycosylation ; Golgi Apparatus/enzymology ; Growth Substances/metabolism/pharmacology ; Macrophages, Peritoneal/physiology ; Mammary Neoplasms, Animal/metabolism/pathology ; Mice ; Mice, Transgenic ; N-Acetylglucosaminyltransferases/genetics/*metabolism ; Neoplasm Metastasis ; Phagocytosis ; Polysaccharides/*metabolism ; Receptor, Epidermal Growth Factor/*metabolism ; Receptors, Cytokine/*metabolism ; Receptors, Transforming Growth Factor beta/*metabolism ; Signal Transduction
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  • 6
    Publication Date: 2004-01-06
    Description: MDM2 binds the p53 tumor suppressor protein with high affinity and negatively modulates its transcriptional activity and stability. Overexpression of MDM2, found in many human tumors, effectively impairs p53 function. Inhibition of MDM2-p53 interaction can stabilize p53 and may offer a novel strategy for cancer therapy. Here, we identify potent and selective small-molecule antagonists of MDM2 and confirm their mode of action through the crystal structures of complexes. These compounds bind MDM2 in the p53-binding pocket and activate the p53 pathway in cancer cells, leading to cell cycle arrest, apoptosis, and growth inhibition of human tumor xenografts in nude mice.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Vassilev, Lyubomir T -- Vu, Binh T -- Graves, Bradford -- Carvajal, Daisy -- Podlaski, Frank -- Filipovic, Zoran -- Kong, Norman -- Kammlott, Ursula -- Lukacs, Christine -- Klein, Christian -- Fotouhi, Nader -- Liu, Emily A -- New York, N.Y. -- Science. 2004 Feb 6;303(5659):844-8. Epub 2004 Jan 2.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Discovery Oncology, Roche Research Center, Hoffmann-La Roche, Inc., Nutley, NJ 07110, USA. lyubomir.vassilev@roche.com〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/14704432" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Apoptosis/*drug effects ; Binding Sites ; Cell Cycle/drug effects ; Cell Division/*drug effects ; Cell Line ; Cell Line, Tumor ; Cell Survival/drug effects ; Crystallization ; Crystallography, X-Ray ; Cyclin-Dependent Kinase Inhibitor p21 ; Cyclins/metabolism ; Dose-Response Relationship, Drug ; Gene Expression ; Genes, p53 ; Humans ; Hydrophobic and Hydrophilic Interactions ; Imidazoles/chemistry/metabolism/*pharmacology ; Mice ; Mice, Nude ; Models, Molecular ; Molecular Weight ; NIH 3T3 Cells ; Neoplasm Transplantation ; Neoplasms, Experimental/drug therapy/metabolism/*pathology ; *Nuclear Proteins ; Phosphorylation ; Piperazines/chemistry/metabolism/*pharmacology ; Protein Conformation ; Proto-Oncogene Proteins/*antagonists & inhibitors/chemistry/metabolism ; Proto-Oncogene Proteins c-mdm2 ; Stereoisomerism ; Transplantation, Heterologous ; Tumor Suppressor Protein p53/*metabolism
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  • 7
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-12-18
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Beutler, Ernest -- New York, N.Y. -- Science. 2004 Dec 17;306(5704):2051-3.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Molecular and Experimental Medicine, Scripps Research Institute, La Jolla, CA 92037, USA. beutler@scripps.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15604397" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Antimicrobial Cationic Peptides/*metabolism ; Biological Transport ; Cation Transport Proteins/genetics/*metabolism ; Enterocytes/metabolism ; Erythropoiesis ; Erythropoietin/genetics/metabolism ; Gene Expression Regulation ; Hemochromatosis/genetics ; Hepatocytes/metabolism ; Hepcidins ; Histocompatibility Antigens Class I/genetics ; Homeostasis ; Iron/*metabolism ; Iron Regulatory Protein 1/*metabolism ; Iron Regulatory Protein 2/*metabolism ; Membrane Proteins/genetics ; Mice ; Models, Biological ; Mutation ; Nitric Oxide/metabolism ; Oxygen/physiology ; Response Elements ; Signal Transduction ; Transcription, Genetic
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  • 8
    Publication Date: 2004-09-11
    Description: The turnover of Jun proteins, like that of other transcription factors, is regulated through ubiquitin-dependent proteolysis. Usually, such processes are regulated by extracellular stimuli through phosphorylation of the target protein, which allows recognition by F box-containing E3 ubiquitin ligases. In the case of c-Jun and JunB, we found that extracellular stimuli also modulate protein turnover by regulating the activity of an E3 ligase by means of its phosphorylation. Activation of the Jun amino-terminal kinase (JNK) mitogen-activated protein kinase cascade after T cell stimulation accelerated degradation of c-Jun and JunB through phosphorylation-dependent activation of the E3 ligase Itch. This pathway modulates cytokine production by effector T cells.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Gao, Min -- Labuda, Tord -- Xia, Ying -- Gallagher, Ewen -- Fang, Deyu -- Liu, Yun-Cai -- Karin, Michael -- AI43477/AI/NIAID NIH HHS/ -- ES04151/ES/NIEHS NIH HHS/ -- ES06376/ES/NIEHS NIH HHS/ -- R21AI48542/AI/NIAID NIH HHS/ -- New York, N.Y. -- Science. 2004 Oct 8;306(5694):271-5. Epub 2004 Sep 9.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Laboratory of Gene Regulation and Signal Transduction, Department of Pharmacology, School of Medicine, University of California, San Diego, 9500 Gilman Drive, La Jolla, CA 92093-0723, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15358865" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Antigens, CD28/immunology ; CD4-Positive T-Lymphocytes/immunology/*metabolism ; Interferon-gamma/metabolism ; Interleukins/metabolism ; Lymphocyte Activation ; *MAP Kinase Kinase Kinase 1 ; MAP Kinase Kinase Kinases/genetics/metabolism ; Mice ; Mitogen-Activated Protein Kinase 8 ; Mitogen-Activated Protein Kinase 9 ; Mitogen-Activated Protein Kinases/*metabolism ; Phosphorylation ; Proto-Oncogene Proteins c-jun/genetics/*metabolism ; RNA, Messenger/genetics/metabolism ; Receptors, Antigen, T-Cell/immunology ; Recombinant Fusion Proteins/metabolism ; T-Lymphocytes/immunology/*metabolism ; Th2 Cells/cytology/immunology/metabolism ; Ubiquitin/metabolism ; Ubiquitin-Protein Ligases/*metabolism
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  • 9
    Publication Date: 2004-12-14
    Description: Mammalian oocytes are held in prophase arrest by an unknown signal from the surrounding somatic cells. Here we show that the orphan Gs-linked receptor GPR3, which is localized in the oocyte, maintains this arrest. Oocytes from Gpr3 knockout mice resume meiosis within antral follicles, independently of an increase in luteinizing hormone, and this phenotype can be reversed by injection of Gpr3 RNA into the oocytes. Thus, the GPR3 receptor is a link in communication between the somatic cells and oocyte of the ovarian follicle and is crucial for the regulation of meiosis.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Mehlmann, Lisa M -- Saeki, Yoshinaga -- Tanaka, Shigeru -- Brennan, Thomas J -- Evsikov, Alexei V -- Pendola, Frank L -- Knowles, Barbara B -- Eppig, John J -- Jaffe, Laurinda A -- New York, N.Y. -- Science. 2004 Dec 10;306(5703):1947-50.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Cell Biology, University of Connecticut Health Center (UCHC), Farmington, CT 06032, USA. lmehlmann@neuron.uchc.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15591206" target="_blank"〉PubMed〈/a〉
    Keywords: Adenylyl Cyclases/metabolism ; Animals ; Chondroitin Sulfate Proteoglycans/genetics/metabolism ; Expressed Sequence Tags ; Female ; Granulosa Cells/physiology ; Heterotrimeric GTP-Binding Proteins/*metabolism ; In Situ Hybridization ; Lectins, C-Type ; Ligands ; Luteinizing Hormone/metabolism ; *Meiosis ; Metaphase ; Mice ; Mice, Inbred C57BL ; Mice, Knockout ; Mitosis ; Oocytes/*physiology ; Ovarian Follicle/*physiology ; RNA/genetics/metabolism ; Receptors, G-Protein-Coupled/genetics/*physiology ; Versicans
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  • 10
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-08-18
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Couzin, Jennifer -- New York, N.Y. -- Science. 2004 Aug 13;305(5686):929.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15310869" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Blast Crisis/*pathology ; Cell Differentiation ; Cell Division ; Cells, Cultured ; Cytoskeletal Proteins/metabolism ; Granulocytes/cytology ; Humans ; Leukemia, Myelogenous, Chronic, BCR-ABL Positive/blood/*pathology ; Macrophages/cytology ; Mice ; Myeloid Progenitor Cells/pathology/*physiology ; Stem Cells/physiology ; Trans-Activators/metabolism ; beta Catenin
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  • 11
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-11-06
    Description: One of the important roles of microRNA (miRNA) is to direct the cleavage of messenger RNA (mRNA). However, the mechanisms of decay of the cleaved mRNA products is not well understood. We show that miRNA-directed cleavage products in organisms as diverse as Arabidopsis, mouse, and Epstein-Barr virus have at their 3' ends a stretch (1 to 24 nucleotides) of oligouridine posttranscriptionally added downstream of the cleavage site. This 3' uridine addition, as shown for Arabidopsis, is correlated with decapping and 5' shortening of the cleaved products, suggesting a mechanistic step in the miRNA-directed mRNA decay mechanism.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Shen, Binzhang -- Goodman, Howard M -- New York, N.Y. -- Science. 2004 Nov 5;306(5698):997.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Genetics, Harvard Medical School, and Department of Molecular Biology, Massachusetts General Hospital, 50 Blossom Street, Boston, MA 02114, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15528436" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Arabidopsis ; Cells, Cultured ; Cloning, Molecular ; Herpesvirus 4, Human/metabolism ; Humans ; Mice ; MicroRNAs/*metabolism ; Poly U/metabolism ; RNA, Messenger/metabolism ; Reverse Transcriptase Polymerase Chain Reaction ; Uridine/*metabolism
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  • 12
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-04-24
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Vogel, Gretchen -- New York, N.Y. -- Science. 2004 Apr 23;304(5670):501-3.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15105467" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Animals, Newborn ; *Embryonic and Fetal Development ; Female ; Gene Expression Regulation, Developmental ; *Genomic Imprinting ; Insulin-Like Growth Factor II/genetics/physiology ; Japan ; Mice ; Mutation ; Oocytes/*physiology ; *Parthenogenesis ; RNA, Long Noncoding ; RNA, Untranslated/genetics/physiology
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  • 13
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-08-03
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Couzin, Jennifer -- New York, N.Y. -- Science. 2004 Jul 30;305(5684):589.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15286333" target="_blank"〉PubMed〈/a〉
    Keywords: Amyloid/chemistry/metabolism ; Animals ; Brain Chemistry ; Escherichia coli/genetics/metabolism ; Mice ; Mice, Transgenic ; Prion Diseases/*etiology ; Prions/administration & dosage/biosynthesis/chemistry/*pathogenicity ; Protein Folding ; Recombinant Proteins/administration & dosage/chemistry ; Time Factors
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  • 14
    Publication Date: 2004-03-27
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Bidoia, C -- Misgeld, T -- Weinzierl, E -- Buffelli, M -- Feng, G -- Cangiano, A -- Lichtman, J W -- Sanes, J R -- New York, N.Y. -- Science. 2004 Mar 26;303(5666):1977; author reply 1977.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Dipartimento di Scienze Neurologiche e della Visione, Universita' di Verona, Strada Le Grazie 8, Verona, Italy.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15044788" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Axons/physiology/ultrastructure ; Cell Adhesion Molecules, Neuronal/genetics/*physiology ; Crosses, Genetic ; Diaphragm/innervation ; Extracellular Matrix Proteins/genetics/*physiology ; Mice ; Mice, Neurologic Mutants ; Mice, Transgenic ; Motor Endplate/ultrastructure ; Muscle, Skeletal/innervation ; Mutation ; Nerve Tissue Proteins ; Neuromuscular Junction/*growth & development/physiology/ultrastructure ; Phenotype ; Serine Endopeptidases ; Synapses/*physiology/ultrastructure
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  • 15
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-08-07
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Couzin, Jennifer -- New York, N.Y. -- Science. 2004 Aug 6;305(5685):772-3.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15297645" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Antirheumatic Agents/therapeutic use ; Arthritis, Juvenile/drug therapy/genetics/immunology ; Autoimmunity ; Cell Movement ; Child ; Dendritic Cells/*immunology/physiology ; Humans ; *Immune Tolerance ; Interleukin 1 Receptor Antagonist Protein ; Interleukin-1/genetics/physiology ; Lymph Nodes/immunology ; Mice ; Sialoglycoproteins/therapeutic use ; T-Lymphocytes/immunology ; Up-Regulation
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  • 16
    Publication Date: 2004-02-21
    Description: Feline immunodeficiency virus (FIV) induces a disease similar to acquired immunodeficiency syndrome (AIDS) in cats, yet in contrast to human immunodeficiency virus (HIV), CD4 is not the viral receptor. We identified a primary receptor for FIV as CD134 (OX40), a T cell activation antigen and costimulatory molecule. CD134 expression promotes viral binding and renders cells permissive for viral entry, productive infection, and syncytium formation. Infection is CXCR4-dependent, analogous to infection with X4 strains of HIV. Thus, despite the evolutionary divergence of the feline and human lentiviruses, both viruses use receptors that target the virus to a subset of cells that are pivotal to the acquired immune response.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Shimojima, Masayuki -- Miyazawa, Takayuki -- Ikeda, Yasuhiro -- McMonagle, Elizabeth L -- Haining, Hayley -- Akashi, Hiroomi -- Takeuchi, Yasuhiro -- Hosie, Margaret J -- Willett, Brian J -- R01 AI49765-01A1/AI/NIAID NIH HHS/ -- New York, N.Y. -- Science. 2004 Feb 20;303(5661):1192-5.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Veterinary Microbiology, Graduate School of Agricultural and Life Sciences, University of Tokyo, 1-1-1 Yayoi, Bunkyo-ku, Tokyo 113-8657, Japan.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/14976315" target="_blank"〉PubMed〈/a〉
    Keywords: Amino Acid Sequence ; Animals ; CD4-Positive T-Lymphocytes/immunology/metabolism/virology ; Cats ; Cell Line ; Cell Line, Tumor ; DNA, Complementary ; Gene Library ; HIV/metabolism ; HeLa Cells ; Heterocyclic Compounds/pharmacology ; Humans ; Immunodeficiency Virus, Feline/*metabolism/pathogenicity ; Mice ; Molecular Sequence Data ; NIH 3T3 Cells ; Receptors, CXCR4/antagonists & inhibitors/metabolism ; Receptors, OX40 ; Receptors, Tumor Necrosis Factor/chemistry/genetics/immunology/*metabolism ; Receptors, Virus/chemistry/genetics/immunology/*metabolism ; Species Specificity ; Transduction, Genetic ; Transfection
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  • 17
    Publication Date: 2004-02-07
    Description: Stromal cells can have a significant impact on the carcinogenic process in adjacent epithelia. The role of transforming growth factor-beta (TGF-beta) signaling in such epithelial-mesenchymal interactions was determined by conditional inactivation of the TGF-beta type II receptor gene in mouse fibroblasts (Tgfbr2fspKO). The loss of TGF-beta responsiveness in fibroblasts resulted in intraepithelial neoplasia in prostate and invasive squamous cell carcinoma of the forestomach, both associated with an increased abundance of stromal cells. Activation of paracrine hepatocyte growth factor (HGF) signaling was identified as one possible mechanism for stimulation of epithelial proliferation. Thus, TGF-beta signaling in fibroblasts modulates the growth and oncogenic potential of adjacent epithelia in selected tissues.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Bhowmick, Neil A -- Chytil, Anna -- Plieth, David -- Gorska, Agnieszka E -- Dumont, Nancy -- Shappell, Scott -- Washington, M Kay -- Neilson, Eric G -- Moses, Harold L -- AR41943/AR/NIAMS NIH HHS/ -- CA102162/CA/NCI NIH HHS/ -- CA68485/CA/NCI NIH HHS/ -- CA85492/CA/NCI NIH HHS/ -- DK46282/DK/NIDDK NIH HHS/ -- New York, N.Y. -- Science. 2004 Feb 6;303(5659):848-51.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Cancer Biology, Vanderbilt University School of Medicine, Nashville, TN 37232, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/14764882" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Carcinoma, Squamous Cell/etiology/metabolism/pathology ; Cell Division ; *Cell Transformation, Neoplastic ; Cells, Cultured ; Epithelial Cells/*physiology ; Female ; Fibroblasts/*physiology ; Hepatocyte Growth Factor/metabolism ; Male ; Mice ; Mice, Inbred C57BL ; Mice, Knockout ; Mice, Transgenic ; Neoplasms, Glandular and Epithelial/*etiology/metabolism/pathology ; Prostate/cytology/metabolism/pathology ; Prostatic Intraepithelial Neoplasia/etiology/metabolism/pathology ; Protein-Serine-Threonine Kinases ; Proto-Oncogene Proteins c-met/metabolism ; Receptors, Transforming Growth Factor beta/genetics/metabolism ; Recombination, Genetic ; *Signal Transduction ; Stomach/cytology/metabolism/pathology ; Stomach Neoplasms/etiology/metabolism/pathology ; Stromal Cells/*physiology ; Transforming Growth Factor beta/*physiology
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  • 18
    Publication Date: 2004-05-15
    Description: In higher metazoans, phagocytosis is essential in host defense against microbial pathogens and in clearance of apoptotic cells. Both microbial and apoptotic cells are delivered on a common route from phagosomes to lysosomes for degradation. Here, we found that activation of the Toll-like receptor (TLR) signaling pathway by bacteria, but not apoptotic cells, regulated phagocytosis at multiple steps including internalization and phagosome maturation. Phagocytosis of bacteria was impaired in the absence of TLR signaling. Two modes of phagosome maturation were observed, constitutive and inducible; their differential engagement depended on the ability of the cargo to trigger TLR signaling.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Blander, J Magarian -- Medzhitov, Ruslan -- AI46688/AI/NIAID NIH HHS/ -- New York, N.Y. -- Science. 2004 May 14;304(5673):1014-8.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Howard Hughes Medical Institute, Section of Immunobiology, Yale University School of Medicine, New Haven, Connecticut 06520, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15143282" target="_blank"〉PubMed〈/a〉
    Keywords: Adaptor Proteins, Signal Transducing ; Animals ; Antigens, Differentiation/metabolism ; Apoptosis ; Bacteria/*immunology/metabolism ; Enzyme Activation ; Enzyme Inhibitors/pharmacology ; Escherichia coli/immunology/physiology ; Lysosomes/ultrastructure ; Macrophages/*immunology/metabolism/microbiology/ultrastructure ; Membrane Glycoproteins/genetics/*metabolism ; Mice ; Microscopy, Immunoelectron ; Mitogen-Activated Protein Kinases/antagonists & inhibitors/metabolism ; Myeloid Differentiation Factor 88 ; *Phagocytosis ; Phagosomes/microbiology/*physiology/ultrastructure ; Receptors, Cell Surface/genetics/*metabolism ; Receptors, Immunologic/metabolism ; Recombinant Proteins/metabolism ; Salmonella typhimurium/immunology/physiology ; *Signal Transduction ; Staphylococcus aureus/immunology/physiology ; Toll-Like Receptors ; p38 Mitogen-Activated Protein Kinases
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    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 19
    Publication Date: 2004-12-04
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Godfrey, Dale I -- Pellicci, Daniel G -- Smyth, Mark J -- New York, N.Y. -- Science. 2004 Dec 3;306(5702):1687-9.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Microbiology and Immunology, University of Melbourne, Melbourne, Victoria, Australia. godfrey@unimelb.edu.au〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15576595" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Antigens, CD1/immunology ; Antigens, CD1d ; Carbohydrate Conformation ; Galactosyltransferases/genetics/metabolism ; Globosides/*immunology/metabolism ; Humans ; Immune Tolerance ; Killer Cells, Natural/*immunology ; Ligands ; Lymphocyte Activation ; Lysosomes/metabolism ; Mice ; T-Lymphocyte Subsets/*immunology ; Thymus Gland/immunology ; beta-N-Acetylhexosaminidases/metabolism
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  • 20
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-05-15
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Watts, Colin -- New York, N.Y. -- Science. 2004 May 14;304(5673):976-7.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Wellcome Trust Biocentre, School of Life Sciences, University of Dundee, Dundee DD1 5EH, UK. c.watts@dundee.ac.uk〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15143270" target="_blank"〉PubMed〈/a〉
    Keywords: Adaptor Proteins, Signal Transducing ; Animals ; Antigens, Differentiation/metabolism ; Apoptosis ; Bacteria/*immunology/metabolism ; Enzyme Activation ; Guanine Nucleotide Dissociation Inhibitors/metabolism ; Lysosomes/physiology ; Macrophages/*immunology/metabolism/microbiology ; Membrane Fusion ; Membrane Glycoproteins/*metabolism ; Mice ; Mitogen-Activated Protein Kinases/metabolism ; Mycobacterium tuberculosis/immunology/metabolism ; Myeloid Differentiation Factor 88 ; *Phagocytosis ; Phagosomes/microbiology/*physiology ; Receptors, Cell Surface/*metabolism ; Receptors, Immunologic/metabolism ; *Signal Transduction ; Toll-Like Receptors ; p38 Mitogen-Activated Protein Kinases
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  • 21
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-05-29
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Ploegh, Hidde L -- New York, N.Y. -- Science. 2004 May 28;304(5675):1262-3.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Pathology, Harvard Medical School, Boston, MA 02115, USA. ploegh@hms.harvard.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15166355" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; *Antigen Presentation ; Antigen-Presenting Cells/immunology ; Antigens/*immunology ; Antigens, Viral/immunology ; CD8-Positive T-Lymphocytes/*immunology ; *Cross-Priming ; Cysteine Endopeptidases/metabolism ; Endoplasmic Reticulum/metabolism ; Epitopes, T-Lymphocyte/immunology/metabolism ; Histocompatibility Antigens Class I/immunology ; Immune Tolerance ; Lymphocyte Activation ; Mice ; Multienzyme Complexes/metabolism ; Peptides/immunology/metabolism ; Phagocytosis ; Phagosomes/immunology/metabolism ; Proteasome Endopeptidase Complex ; Receptors, Antigen, T-Cell/immunology ; Vaccines/immunology
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  • 22
    Publication Date: 2004-01-31
    Description: Neuronal death is a prominent, but poorly understood, pathological hallmark of prion disease. Notably, in the absence of the cellular prion protein (PrPC), the disease-associated isoform, PrPSc, appears not to be intrinsically neurotoxic, suggesting that PrPC itself may participate directly in the prion neurodegenerative cascade. Here, cross-linking PrPC in vivo with specific monoclonal antibodies was found to trigger rapid and extensive apoptosis in hippocampal and cerebellar neurons. These findings suggest that PrPC functions in the control of neuronal survival and provides a model to explore whether cross-linking of PrPC by oligomeric PrPSc can promote neuronal loss during prion infection.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Solforosi, Laura -- Criado, Jose R -- McGavern, Dorian B -- Wirz, Sebastian -- Sanchez-Alavez, Manuel -- Sugama, Shuei -- DeGiorgio, Lorraine A -- Volpe, Bruce T -- Wiseman, Erika -- Abalos, Gil -- Masliah, Eliezer -- Gilden, Donald -- Oldstone, Michael B -- Conti, Bruno -- Williamson, R Anthony -- AG00080/AG/NIA NIH HHS/ -- AG04342/AG/NIA NIH HHS/ -- AI09484/AI/NIAID NIH HHS/ -- HL63817/HL/NHLBI NIH HHS/ -- New York, N.Y. -- Science. 2004 Mar 5;303(5663):1514-6. Epub 2004 Jan 29.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Immunology, The Scripps Research Institute, La Jolla, CA 92037, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/14752167" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Antibodies, Monoclonal/immunology/*metabolism ; *Apoptosis ; Cell Survival ; Cerebellum/*cytology ; Complement Activation ; Dimerization ; Hippocampus/*cytology ; Immunoglobulin Fab Fragments/immunology/metabolism ; Immunoglobulin G/immunology/metabolism ; In Situ Nick-End Labeling ; Mice ; Mice, Inbred C57BL ; Neural Cell Adhesion Molecules/immunology/metabolism ; Neurons/*physiology ; PrPC Proteins/chemistry/immunology/*metabolism ; Recombinant Proteins/metabolism ; Signal Transduction
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  • 23
    Publication Date: 2004-06-12
    Description: During embryogenesis, differentiation of skeletal muscle is regulated by transcription factors that include members of the Msx homeoprotein family. By investigating Msx1 function in repression of myogenic gene expression, we identified a physical interaction between Msx1 and H1b, a specific isoform of mouse histone H1. We found that Msx1 and H1b bind to a key regulatory element of MyoD, a central regulator of skeletal muscle differentiation, where they induce repressed chromatin. Moreover, Msx1 and H1b cooperate to inhibit muscle differentiation in cell culture and in Xenopus animal caps. Our findings define a previously unknown function for "linker" histones in gene-specific transcriptional regulation.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Lee, Hansol -- Habas, Raymond -- Abate-Shen, Cory -- HD29446/HD/NICHD NIH HHS/ -- New York, N.Y. -- Science. 2004 Jun 11;304(5677):1675-8.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Center for Advanced Biotechnology and Medicine, University of Medicine and Dentistry of New Jersey (UMDNJ)-Robert Wood Johnson Medical School, Piscataway, NJ 08854, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15192231" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Cell Differentiation ; Cell Line ; Embryo, Nonmammalian/cytology/metabolism ; Enhancer Elements, Genetic ; *Gene Expression Regulation, Developmental ; Histones/genetics/*metabolism ; Homeodomain Proteins/chemistry/genetics/*metabolism ; MSX1 Transcription Factor ; Mice ; Models, Genetic ; *Muscle Development ; Muscle, Skeletal/*cytology/metabolism ; Mutation ; MyoD Protein/genetics ; Myoblasts/*cytology/metabolism ; Precipitin Tests ; Protein Binding ; RNA Interference ; Recombinant Proteins/metabolism ; Regulatory Sequences, Nucleic Acid ; Transcription Factors/chemistry/genetics/*metabolism ; *Transcription, Genetic ; Xenopus/embryology/metabolism ; Xenopus Proteins
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  • 24
    Publication Date: 2004-07-13
    Description: Erythropoietin (EPO) is both hematopoietic and tissue protective, putatively through interaction with different receptors. We generated receptor subtype-selective ligands allowing the separation of EPO's bioactivities at the cellular level and in animals. Carbamylated EPO (CEPO) or certain EPO mutants did not bind to the classical EPO receptor (EPOR) and did not show any hematopoietic activity in human cell signaling assays or upon chronic dosing in different animal species. Nevertheless, CEPO and various nonhematopoietic mutants were cytoprotective in vitro and conferred neuroprotection against stroke, spinal cord compression, diabetic neuropathy, and experimental autoimmune encephalomyelitis at a potency and efficacy comparable to EPO.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Leist, Marcel -- Ghezzi, Pietro -- Grasso, Giovanni -- Bianchi, Roberto -- Villa, Pia -- Fratelli, Maddalena -- Savino, Costanza -- Bianchi, Marina -- Nielsen, Jacob -- Gerwien, Jens -- Kallunki, Pekka -- Larsen, Anna Kirstine -- Helboe, Lone -- Christensen, Soren -- Pedersen, Lars O -- Nielsen, Mette -- Torup, Lars -- Sager, Thomas -- Sfacteria, Alessandra -- Erbayraktar, Serhat -- Erbayraktar, Zubeyde -- Gokmen, Necati -- Yilmaz, Osman -- Cerami-Hand, Carla -- Xie, Qiao-Wen -- Coleman, Thomas -- Cerami, Anthony -- Brines, Michael -- New York, N.Y. -- Science. 2004 Jul 9;305(5681):239-42.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉H. Lundbeck A/S, 2500 Valby, Denmark.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15247477" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Apoptosis ; Binding Sites ; Cells, Cultured ; Diabetic Neuropathies/drug therapy ; Drug Design ; Encephalomyelitis, Autoimmune, Experimental/drug therapy ; Erythropoiesis ; Erythropoietin/*analogs & ; derivatives/chemistry/genetics/metabolism/pharmacology/*therapeutic use ; Female ; Hematocrit ; Humans ; Ligands ; Mice ; Mice, Inbred C3H ; Mutagenesis ; Nervous System Diseases/*drug therapy ; Neurons/metabolism ; Neuroprotective Agents/chemistry/metabolism/pharmacology/*therapeutic use ; Rats ; Rats, Sprague-Dawley ; Receptors, Erythropoietin/metabolism ; Recombinant Proteins ; Signal Transduction ; Spinal Cord Compression/drug therapy ; Stroke/drug therapy ; Structure-Activity Relationship
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  • 25
    Publication Date: 2004-06-26
    Description: Endogenous opioid binding to micro receptors is hypothesized to mediate natural rewards and has been proposed to be the basis of infant attachment behavior. Here, we report that micro-opioid receptor knockout mouse pups emit fewer ultrasonic vocalizations when removed from their mothers but not when exposed to cold or male mice odors. Moreover these knockout pups do not show a preference toward their mothers' cues and do not show ultrasonic calls potentiation after brief maternal exposure. Results from this study may indicate a molecular mechanism for diseases characterized by deficits in attachment behavior, such as autism or reactive attachment disorder.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Moles, Anna -- Kieffer, Brigitte L -- D'Amato, Francesca R -- New York, N.Y. -- Science. 2004 Jun 25;304(5679):1983-6.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Consiglio Nazionale delle Ricerche Institute of Neuroscience, Psychobiology and Psychopharmacology, Viale Marx 43, 00137 Roma, Italy.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15218152" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Animals, Newborn ; Bedding and Linens ; *Behavior, Animal ; Cold Temperature ; Cues ; Female ; Genotype ; Male ; Maternal Behavior ; *Maternal Deprivation ; Mice ; Mice, Knockout ; *Mothers ; Mutation ; *Object Attachment ; Odors ; Receptors, Opioid, mu/genetics/*physiology ; Reward ; Vocalization, Animal
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  • 26
    Publication Date: 2004-12-25
    Description: In the developing brain, transcription factors (TFs) direct the formation of a diverse array of neurons and glia. We identifed 1445 putative TFs in the mouse genome. We used in situ hybridization to map the expression of over 1000 of these TFs and TF-coregulator genes in the brains of developing mice. We found that 349 of these genes showed restricted expression patterns that were adequate to describe the anatomical organization of the brain. We provide a comprehensive inventory of murine TFs and their expression patterns in a searchable brain atlas database.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Gray, Paul A -- Fu, Hui -- Luo, Ping -- Zhao, Qing -- Yu, Jing -- Ferrari, Annette -- Tenzen, Toyoaki -- Yuk, Dong-In -- Tsung, Eric F -- Cai, Zhaohui -- Alberta, John A -- Cheng, Le-Ping -- Liu, Yang -- Stenman, Jan M -- Valerius, M Todd -- Billings, Nathan -- Kim, Haesun A -- Greenberg, Michael E -- McMahon, Andrew P -- Rowitch, David H -- Stiles, Charles D -- Ma, Qiufu -- New York, N.Y. -- Science. 2004 Dec 24;306(5705):2255-7.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Neurobiology, Harvard Medical School, Boston, MA 02115, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15618518" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Animals, Newborn ; Brain/anatomy & histology/embryology/*growth & development/*metabolism ; Cloning, Molecular ; Corpus Striatum/anatomy & histology/embryology/growth & development/metabolism ; DNA Primers ; Databases, Factual ; *Gene Expression Profiling ; *Genome ; Hypothalamus/anatomy & histology/embryology/growth & development/metabolism ; In Situ Hybridization ; Mesencephalon/anatomy & histology/embryology/growth & development/metabolism ; Mice ; Neocortex/anatomy & histology/embryology/growth & development/metabolism ; Polymerase Chain Reaction ; Rhombencephalon/anatomy & histology/embryology/growth & development/metabolism ; Spinal Cord/anatomy & histology/embryology/growth & development/metabolism ; Thalamus/anatomy & histology/embryology/growth & development/metabolism ; Transcription Factors/*genetics/*metabolism
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  • 27
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-01-06
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Levitt, Pat -- New York, N.Y. -- Science. 2004 Jan 2;303(5654):48-9.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Vanderbilt Kennedy Center for Research on Human Development and Department of Pharmacology, Vanderbilt University, Nashville, TN 37203, USA. pat.levitt@vanderbilt.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/14704417" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Cell Differentiation ; Cell Lineage ; Cerebral Cortex/*cytology/embryology ; DNA-Binding Proteins/*genetics/*metabolism ; Down-Regulation ; Forkhead Transcription Factors ; Gene Expression Regulation, Developmental ; Mice ; Nerve Tissue Proteins/*genetics/*metabolism ; Neurons/*cytology/*physiology ; Stem Cells/cytology/*physiology ; Time Factors ; Transcription Factors/genetics/*metabolism
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  • 28
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-10-16
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Grimm, David -- New York, N.Y. -- Science. 2004 Oct 15;306(5695):389.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15486263" target="_blank"〉PubMed〈/a〉
    Keywords: *Aneuploidy ; Animals ; Cell Cycle Proteins ; Child ; *Chromosomal Instability ; *DNA Repair ; *Genetic Predisposition to Disease ; Genomic Instability ; Humans ; Mice ; Mosaicism ; Mutation ; Neoplasms/*genetics ; Protein Kinases/genetics ; Protein-Serine-Threonine Kinases
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  • 29
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-09-18
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Wills-Karp, Marsha -- Karp, Christopher L -- New York, N.Y. -- Science. 2004 Sep 17;305(5691):1726-9.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Division of Immunobiology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH 45229, USA. wildc7@cchmc.org〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15375256" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Asthma/immunology/*pathology/*physiopathology ; Cytokines/physiology/secretion ; DNA-Binding Proteins/genetics ; Eosinophil Peroxidase ; Eosinophils/*physiology ; Erythroid-Specific DNA-Binding Factors ; Gene Targeting ; Humans ; Immunoglobulin E/blood ; Lung/immunology/*pathology/*physiopathology ; Mice ; Mice, Inbred BALB C ; Mice, Transgenic ; Mucus/secretion ; Peroxidases/genetics ; Promoter Regions, Genetic ; Respiratory Hypersensitivity/immunology/*pathology/physiopathology ; Th2 Cells/immunology ; Transcription Factors/genetics
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  • 30
    Publication Date: 2004-10-23
    Description: Computational tools can markedly accelerate the rate at which murine genetic models can be analyzed. We developed a computational method for mapping phenotypic traits that vary among inbred strains onto haplotypic blocks. This method correctly predicted the genetic basis for strain-specific differences in several biologically important traits. It was also used to identify an allele-specific functional genomic element regulating H2-Ealpha gene expression. This functional element, which contained the binding sites for YY1 and a second transcription factor that is probably serum response factor, is located within the first intron of the H2-Ealpha gene. This computational method will greatly improve our ability to identify the genetic basis for a variety of phenotypic traits, ranging from qualitative trait information to quantitative gene expression data, which vary among inbred mouse strains.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Liao, Guochun -- Wang, Jianmei -- Guo, Jingshu -- Allard, John -- Cheng, Janet -- Ng, Anh -- Shafer, Steve -- Puech, Anne -- McPherson, John D -- Foernzler, Dorothee -- Peltz, Gary -- Usuka, Jonathan -- 1 R01 HG02322-01/HG/NHGRI NIH HHS/ -- New York, N.Y. -- Science. 2004 Oct 22;306(5696):690-5.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Genetics and Genomics, Roche Palo Alto, 3431 Hillview Avenue, Palo Alto, CA 94304-1397, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15499019" target="_blank"〉PubMed〈/a〉
    Keywords: Alleles ; Animals ; Binding Sites ; *Computational Biology ; Electrophoretic Mobility Shift Assay ; Gene Expression Profiling ; *Gene Expression Regulation ; Genes, MHC Class II ; Genetic Variation ; H-2 Antigens/*genetics ; Haplotypes ; Hydrocarbons, Aromatic/pharmacology ; Introns ; Liver/metabolism ; Lung/metabolism ; Major Histocompatibility Complex ; Mice ; Mice, Inbred Strains ; Oligodeoxyribonucleotides/metabolism ; Oligonucleotide Array Sequence Analysis ; Phenotype ; Polymorphism, Single Nucleotide ; Receptors, Aryl Hydrocarbon/chemistry/genetics/metabolism ; Regulatory Sequences, Nucleic Acid ; Serum Response Factor/metabolism ; Transcription Factors/metabolism
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  • 31
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-07-13
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Guy-Grand, Delphine -- Vassalli, Pierre -- New York, N.Y. -- Science. 2004 Jul 9;305(5681):185-7.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Unite de Recherche et d'Expertise Antivirale, INSERM U277, Institut Pasteur, 75724 Paris Cedex 15, France. guygrand@pasteur.fr〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15247461" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; CD4-Positive T-Lymphocytes/immunology ; CD8-Positive T-Lymphocytes/immunology ; Cell Lineage ; DNA-Binding Proteins/metabolism ; Female ; Hematopoietic Stem Cells/immunology/physiology ; Immunity, Innate ; Immunity, Mucosal ; Interleukins/biosynthesis ; Intestinal Mucosa/cytology/*immunology ; Killer Cells, Natural/immunology ; Ligands ; Lymphoid Tissue/embryology/immunology ; Lymphotoxin-alpha/analysis ; Male ; Mice ; Mice, Nude ; Mice, Transgenic ; Models, Immunological ; Mutation ; Nuclear Receptor Subfamily 1, Group F, Member 3 ; Receptors, Antigen, T-Cell, alpha-beta/analysis/genetics ; Receptors, Antigen, T-Cell, gamma-delta/analysis ; Receptors, Retinoic Acid/genetics/metabolism ; Receptors, Thyroid Hormone/genetics/metabolism ; T-Lymphocyte Subsets/immunology ; T-Lymphocytes/*immunology ; Thymus Gland/cytology/*immunology
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    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 32
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-10-16
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Muoio, Deborah M -- Newgard, Christopher B -- New York, N.Y. -- Science. 2004 Oct 15;306(5695):425-6.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Sarah W. Stedman Nutrition and Metabolism Center, Duke University Medical Center, Durham, NC 27710, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15486283" target="_blank"〉PubMed〈/a〉
    Keywords: Adipose Tissue/metabolism ; Animals ; Cells, Cultured ; DNA-Binding Proteins/genetics/metabolism ; Endoplasmic Reticulum/*metabolism ; Endoribonucleases ; Enzyme Activation ; Homeostasis ; Humans ; Insulin/*metabolism ; Insulin Receptor Substrate Proteins ; Insulin Resistance/*physiology ; Islets of Langerhans/metabolism ; Liver/metabolism ; Membrane Proteins/metabolism ; Mice ; Mitogen-Activated Protein Kinase 8 ; Mitogen-Activated Protein Kinases/*metabolism ; Muscle, Skeletal/metabolism ; Nuclear Proteins/genetics/metabolism ; Obesity/*metabolism ; Phosphoproteins/metabolism ; Phosphorylation ; Protein-Serine-Threonine Kinases/metabolism ; Signal Transduction ; Transcription Factors ; eIF-2 Kinase/metabolism
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    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 33
    Publication Date: 2004-09-14
    Description: Signaling proteins are tightly regulated spatially and temporally to perform multiple functions. For Cdc42 and other guanosine triphosphatases, the subcellular location of activation is a critical determinant of cell behavior. However, current approaches are limited in their ability to examine the dynamics of Cdc42 activity in living cells. We report the development of a biosensor capable of visualizing the changing activation of endogenous, unlabeled Cdc42 in living cells. With the use of a dye that reports protein interactions, the biosensor revealed localized activation in the trans-Golgi apparatus, microtubule-dependent Cdc42 activation at the cell periphery, and activation kinetics precisely coordinated with cell extension and retraction.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Nalbant, Perihan -- Hodgson, Louis -- Kraynov, Vadim -- Toutchkine, Alexei -- Hahn, Klaus M -- GM57464/GM/NIGMS NIH HHS/ -- GM64346/GM/NIGMS NIH HHS/ -- R01 GM057464/GM/NIGMS NIH HHS/ -- New York, N.Y. -- Science. 2004 Sep 10;305(5690):1615-9.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Pharmacology, University of North Carolina School of Medicine, Chapel Hill, NC 27599-7365, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15361624" target="_blank"〉PubMed〈/a〉
    Keywords: Actins/metabolism ; Algorithms ; Animals ; *Biosensing Techniques ; Cell Adhesion ; Cell Line ; Cell Membrane/*metabolism ; Cell Polarity ; Cell Surface Extensions/metabolism/ultrastructure ; Endothelial Cells/metabolism/ultrastructure ; Fibroblasts ; Fluorescence ; Fluorescent Dyes/chemistry/metabolism ; Green Fluorescent Proteins ; Humans ; Luminescent Proteins ; Mice ; Microtubules/metabolism ; Neutrophil Activation ; Neutrophils/*metabolism ; Proteins/chemistry/metabolism ; Pseudopodia/metabolism ; Pyrimidinones/metabolism ; Sensitivity and Specificity ; Wiskott-Aldrich Syndrome Protein ; cdc42 GTP-Binding Protein/*metabolism ; rho GTP-Binding Proteins/metabolism ; trans-Golgi Network/*metabolism/ultrastructure
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  • 34
    Publication Date: 2004-01-24
    Description: Jun N-terminal kinases (JNKs) are essential for neuronal microtubule assembly and apoptosis. Phosphorylation of the activating protein 1 (AP1) transcription factor c-Jun, at multiple sites within its transactivation domain, is required for JNK-induced neurotoxicity. We report that in neurons the stability of c-Jun is regulated by the E3 ligase SCF(Fbw7), which ubiquitinates phosphorylated c-Jun and facilitates c-Jun degradation. Fbw7 depletion resulted in accumulation of phosphorylated c-Jun, stimulation of AP1 activity, and neuronal apoptosis. SCF(Fbw7) therefore antagonizes the apoptotic c-Jun-dependent effector arm of JNK signaling, allowing neurons to tolerate potentially neurotoxic JNK activity.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Nateri, Abdolrahman S -- Riera-Sans, Lluis -- Da Costa, Clive -- Behrens, Axel -- New York, N.Y. -- Science. 2004 Feb 27;303(5662):1374-8. Epub 2004 Jan 22.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Mammalian Genetics Laboratory, Cancer Research UK, London Research Institute, Lincoln's Inn Fields Laboratories, 44 Lincoln's Inn Fields, London WC2A 3PX, UK.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/14739463" target="_blank"〉PubMed〈/a〉
    Keywords: Amino Acid Sequence ; Animals ; *Apoptosis ; Base Sequence ; Cell Cycle Proteins/genetics/*metabolism ; Cell Line ; F-Box Proteins/genetics/*metabolism ; Humans ; JNK Mitogen-Activated Protein Kinases ; MAP Kinase Signaling System ; Mice ; Mitogen-Activated Protein Kinases/*metabolism ; Molecular Sequence Data ; Neurons/*physiology ; PC12 Cells ; Phosphorylation ; Proto-Oncogene Proteins c-jun/*metabolism ; RNA, Small Interfering/metabolism ; Rats ; Transcription Factor AP-1/metabolism ; Transfection ; Ubiquitin/metabolism ; Ubiquitin-Protein Ligases/genetics/*metabolism
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  • 35
    Publication Date: 2004-02-07
    Description: The bacterium Listeria monocytogenes can cause a life-threatening systemic illness in humans. Despite decades of progress in animal models of listeriosis, much remains unknown about the processes of infection and colonization. Here, we report that L. monocytogenes can replicate in the murine gall bladder and provide evidence that its replication there is extracellular and intraluminal. In vivo bioluminescence imaging was employed to determine the location of the infection over time in live animals, revealing strong signals from the gall bladder over a period of several days, in diseased as well as asymptomatic animals. The data suggest that L. monocytogenes may be carried in the human gall bladder.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Hardy, Jonathan -- Francis, Kevin P -- DeBoer, Monica -- Chu, Pauline -- Gibbs, Karine -- Contag, Christopher H -- R01HD37543/HD/NICHD NIH HHS/ -- New York, N.Y. -- Science. 2004 Feb 6;303(5659):851-3.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Pediatrics, Stanford University School of Medicine, Stanford, CA 94305, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/14764883" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Colony Count, Microbial ; Female ; Gallbladder/*microbiology ; Gallbladder Diseases/*microbiology ; Listeria monocytogenes/genetics/*growth & development/isolation & ; purification/pathogenicity ; Listeriosis/*microbiology ; Liver/microbiology ; Luminescence ; Mice ; Mice, Inbred BALB C ; Mutation ; Spleen/microbiology ; Time Factors ; Virulence
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  • 36
    Publication Date: 2004-06-26
    Description: The nuclear factor-kappa B (NF-kappaB) family of transcription factors plays a seminal role in inflammation, apoptosis, development, and cancer. Modulation of NF-kappaB-mediated gene expression in response to diverse signals is coordinated by the IkappaB kinase (IKK) complex. We identified ELKS, an essential regulatory subunit of the IKK complex. Silencing ELKS expression by RNA interference blocked induced expression of NF-kappaB target genes, including the NF-kappaB inhibitor IkappaBalpha and proinflammatory genes such as cyclo-oxygenase 2 and interleukin 8. These cells were also not protected from apoptosis in response to cytokines. ELKS likely functions by recruiting IkappaBalpha to the IKK complex and thus serves a regulatory function for IKK activation.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Ducut Sigala, Jeanette L -- Bottero, Virginie -- Young, David B -- Shevchenko, Andrej -- Mercurio, Frank -- Verma, Inder M -- New York, N.Y. -- Science. 2004 Jun 25;304(5679):1963-7.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Salk Institute for Biological Sciences, 10010 North Torrey Pines Road, La Jolla, CA 92037, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15218148" target="_blank"〉PubMed〈/a〉
    Keywords: Adaptor Proteins, Signal Transducing ; Animals ; Apoptosis ; Carrier Proteins/genetics/*metabolism ; Cell Line ; Cyclooxygenase 2 ; Gene Expression ; Genes, Reporter ; HeLa Cells ; Humans ; I-kappa B Kinase ; I-kappa B Proteins/genetics/metabolism ; Interleukin-1/pharmacology ; Interleukin-8/genetics ; Isoenzymes/genetics ; Membrane Proteins ; Mice ; Mice, Knockout ; Mitogen-Activated Protein Kinases/metabolism ; Mutation ; NF-kappa B/*metabolism ; Nerve Tissue Proteins/genetics/*metabolism ; Phosphorylation ; Precipitin Tests ; Prostaglandin-Endoperoxide Synthases/genetics ; Protein-Serine-Threonine Kinases/*metabolism ; RNA Interference ; Tumor Necrosis Factor-alpha/pharmacology
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  • 37
    Publication Date: 2004-01-31
    Description: Protein tyrosine kinases and phosphatases cooperate to regulate normal immune cell function. We examined the role of PEST domain-enriched tyrosine phosphatase (PEP) in regulating T cell antigen-receptor function during thymocyte development and peripheral T cell differentiation. Although normal naive T cell functions were retained in pep-deficient mice, effector/memory T cells demonstrated enhanced activation of Lck. In turn, this resulted in increased expansion and function of the effector/memory T cell pool, which was also associated with spontaneous development of germinal centers and elevated serum antibody levels. These results revealed a central role for PEP in negatively regulating specific aspects of T cell development and function.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Hasegawa, Kiminori -- Martin, Flavius -- Huang, Guangming -- Tumas, Dan -- Diehl, Lauri -- Chan, Andrew C -- New York, N.Y. -- Science. 2004 Jan 30;303(5658):685-9.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Immunology, Genentech, Inc., One DNA Way, South San Francisco, CA 94080, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/14752163" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Autoimmunity ; B-Lymphocytes/physiology ; CD4-Positive T-Lymphocytes/immunology/physiology ; CD8-Positive T-Lymphocytes/immunology/physiology ; Cell Cycle ; Gene Targeting ; Germinal Center/physiology ; Hydrogen-Ion Concentration ; Immunoglobulins/blood ; *Immunologic Memory ; Lymphocyte Activation ; Lymphocyte Count ; Lymphocyte Specific Protein Tyrosine Kinase p56(lck)/metabolism ; Mice ; Mice, Inbred BALB C ; Mice, Transgenic ; Phosphorylation ; Protein Tyrosine Phosphatase, Non-Receptor Type 12 ; Protein Tyrosine Phosphatases/genetics/*metabolism ; Receptors, Antigen, T-Cell/genetics/immunology ; Signal Transduction ; T-Lymphocyte Subsets/immunology ; T-Lymphocytes/*immunology/physiology
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  • 38
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-02-07
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Hartwell, Lee -- New York, N.Y. -- Science. 2004 Feb 6;303(5659):774-5.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Genetics, University of Washington, Seattle, WA 98195, USA. lhartwel@fhcrc.org〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/14764857" target="_blank"〉PubMed〈/a〉
    Keywords: Alleles ; Animals ; Computational Biology ; Gene Deletion ; Genes, Essential ; *Genes, Fungal ; Genetic Variation ; Genotype ; Humans ; Mice ; Mutation ; Phenotype ; Quantitative Trait, Heritable ; Saccharomyces cerevisiae/*genetics/*metabolism ; Saccharomyces cerevisiae Proteins/genetics/*metabolism ; Selection, Genetic
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  • 39
    Publication Date: 2004-05-08
    Description: Prostaglandin E2 (PGE2) is a crucial mediator of inflammatory pain sensitization. Here, we demonstrate that inhibition of a specific glycine receptor subtype (GlyR alpha3) by PGE2-induced receptor phosphorylation underlies central inflammatory pain sensitization. We show that GlyR alpha3 is distinctly expressed in superficial layers of the spinal cord dorsal horn. Mice deficient in GlyR alpha3 not only lack the inhibition of glycinergic neurotransmission by PGE2 seen in wild-type mice but also show a reduction in pain sensitization induced by spinal PGE2 injection or peripheral inflammation. Thus, GlyR alpha3 may provide a previously unrecognized molecular target in pain therapy.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Harvey, Robert J -- Depner, Ulrike B -- Wassle, Heinz -- Ahmadi, Seifollah -- Heindl, Cornelia -- Reinold, Heiko -- Smart, Trevor G -- Harvey, Kirsten -- Schutz, Burkhard -- Abo-Salem, Osama M -- Zimmer, Andreas -- Poisbeau, Pierrick -- Welzl, Hans -- Wolfer, David P -- Betz, Heinrich -- Zeilhofer, Hanns Ulrich -- Muller, Ulrike -- New York, N.Y. -- Science. 2004 May 7;304(5672):884-7.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Pharmacology, The School of Pharmacy, London WC1N 1AX, UK.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15131310" target="_blank"〉PubMed〈/a〉
    Keywords: Amino Acid Sequence ; Animals ; Cell Line ; Cyclic AMP-Dependent Protein Kinases/metabolism ; Dinoprostone/administration & dosage/*metabolism/pharmacology ; Female ; Freund's Adjuvant ; Glycine/metabolism ; Humans ; Inflammation/metabolism/*physiopathology ; Male ; Mice ; Mice, Knockout ; Molecular Sequence Data ; Neurons/metabolism ; Pain/*physiopathology ; Patch-Clamp Techniques ; Phosphorylation ; Posterior Horn Cells/*metabolism ; Receptors, Glycine/chemistry/genetics/*metabolism ; Signal Transduction ; Spinal Cord/*metabolism ; Synaptic Transmission ; Transfection ; Zymosan
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  • 40
    Publication Date: 2004-03-06
    Description: The central amygdala (CeA) plays a role in the relationship among stress, corticotropin-releasing factor (CRF), and alcohol abuse. In whole-cell recordings, both CRF and ethanol enhanced gamma-aminobutyric acid-mediated (GABAergic) neurotransmission in CeA neurons from wild-type and CRF2 receptor knockout mice, but not CRF1 receptor knockout mice. CRF1 (but not CRF2) receptor antagonists blocked both CRF and ethanol effects in wild-type mice. These data indicate that CRF1 receptors mediate ethanol enhancement of GABAergic synaptic transmission in the CeA, and they suggest a cellular mechanism underlying involvement of CRF in ethanol's behavioral and motivational effects.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Nie, Zhiguo -- Schweitzer, Paul -- Roberts, Amanda J -- Madamba, Samuel G -- Moore, Scott D -- Siggins, George Robert -- AA06420/AA/NIAAA NIH HHS/ -- AA10994/AA/NIAAA NIH HHS/ -- DA03665/DA/NIDA NIH HHS/ -- DA13658/DA/NIDA NIH HHS/ -- New York, N.Y. -- Science. 2004 Mar 5;303(5663):1512-4.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Neuropharmacology and Alcohol Research Center, Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, CA 92037, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15001778" target="_blank"〉PubMed〈/a〉
    Keywords: Alcohol Drinking ; Amygdala/drug effects/*physiology ; Animals ; Corticotropin-Releasing Hormone/pharmacology ; Dose-Response Relationship, Drug ; Ethanol/*pharmacology ; Evoked Potentials/drug effects ; Mice ; Mice, Inbred C57BL ; Mice, Knockout ; Neurons/drug effects/*physiology ; Patch-Clamp Techniques ; Receptors, Corticotropin-Releasing Hormone/antagonists & ; inhibitors/genetics/*metabolism ; Receptors, GABA-A/metabolism ; Stress, Psychological/physiopathology ; Synaptic Transmission/*drug effects ; gamma-Aminobutyric Acid/*metabolism
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  • 41
    Publication Date: 2004-04-17
    Description: Mitochondrial dysfunction is a hallmark of beta-amyloid (Abeta)-induced neuronal toxicity in Alzheimer's disease (AD). Here, we demonstrate that Abeta-binding alcohol dehydrogenase (ABAD) is a direct molecular link from Abeta to mitochondrial toxicity. Abeta interacts with ABAD in the mitochondria of AD patients and transgenic mice. The crystal structure of Abeta-bound ABAD shows substantial deformation of the active site that prevents nicotinamide adenine dinucleotide (NAD) binding. An ABAD peptide specifically inhibits ABAD-Abeta interaction and suppresses Abeta-induced apoptosis and free-radical generation in neurons. Transgenic mice overexpressing ABAD in an Abeta-rich environment manifest exaggerated neuronal oxidative stress and impaired memory. These data suggest that the ABAD-Abeta interaction may be a therapeutic target in AD.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Lustbader, Joyce W -- Cirilli, Maurizio -- Lin, Chang -- Xu, Hong Wei -- Takuma, Kazuhiro -- Wang, Ning -- Caspersen, Casper -- Chen, Xi -- Pollak, Susan -- Chaney, Michael -- Trinchese, Fabrizio -- Liu, Shumin -- Gunn-Moore, Frank -- Lue, Lih-Fen -- Walker, Douglas G -- Kuppusamy, Periannan -- Zewier, Zay L -- Arancio, Ottavio -- Stern, David -- Yan, Shirley ShiDu -- Wu, Hao -- 1K07AG00959/AG/NIA NIH HHS/ -- AG16736/AG/NIA NIH HHS/ -- AG17490/AG/NIA NIH HHS/ -- NS42855/NS/NINDS NIH HHS/ -- P50AG08702/AG/NIA NIH HHS/ -- New York, N.Y. -- Science. 2004 Apr 16;304(5669):448-52.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Center for Reproductive Sciences and Department of Obstetrics and Gynecology, College of Physicians and Surgeons, Columbia University, 630 West 168th Street, New York, NY 10032, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15087549" target="_blank"〉PubMed〈/a〉
    Keywords: 3-Hydroxyacyl CoA Dehydrogenases/chemistry/*metabolism ; Aged ; Aged, 80 and over ; Alzheimer Disease/*metabolism ; Amino Acid Sequence ; Amyloid beta-Peptides/chemistry/genetics/*metabolism ; Animals ; Binding Sites ; Brain/*metabolism ; Brain Chemistry ; Carrier Proteins/chemistry/*metabolism ; Cells, Cultured ; Cerebral Cortex/chemistry/metabolism ; Crystallization ; DNA Fragmentation ; Hippocampus/physiology ; Humans ; Learning ; Memory ; Mice ; Mice, Transgenic ; Microscopy, Confocal ; Microscopy, Immunoelectron ; Mitochondria/chemistry/*metabolism ; Models, Molecular ; Molecular Sequence Data ; Mutation ; NAD/metabolism ; Neurons/metabolism ; Protein Binding ; Protein Conformation ; Reactive Oxygen Species/metabolism
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  • 42
    Publication Date: 2004-02-21
    Description: Adult stem cells offer the potential to treat many diseases through a combination of ex vivo genetic manipulation and autologous transplantation. Mesenchymal stem cells (MSCs, also referred to as marrow stromal cells) are adult stem cells that can be isolated as proliferating, adherent cells from bones. MSCs can differentiate into multiple cell types present in several tissues, including bone, fat, cartilage, and muscle, making them ideal candidates for a variety of cell-based therapies. Here, we have used adeno-associated virus vectors to disrupt dominant-negative mutant COL1A1 collagen genes in MSCs from individuals with the brittle bone disorder osteogenesis imperfecta, demonstrating successful gene targeting in adult human stem cells.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Chamberlain, Joel R -- Schwarze, Ulrike -- Wang, Pei-Rong -- Hirata, Roli K -- Hankenson, Kurt D -- Pace, James M -- Underwood, Robert A -- Song, Kit M -- Sussman, Michael -- Byers, Peter H -- Russell, David W -- New York, N.Y. -- Science. 2004 Feb 20;303(5661):1198-201.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Medicine, University of Washington, Seattle, WA 98195-7720, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/14976317" target="_blank"〉PubMed〈/a〉
    Keywords: Alleles ; Animals ; Bone Marrow Cells/physiology ; Cell Differentiation ; Cells, Cultured ; Collagen Type I/chemistry/*genetics/metabolism ; Dependovirus/genetics ; *Gene Targeting ; Genetic Therapy ; Genetic Vectors ; Humans ; Kanamycin Kinase/genetics ; Male ; Mesenchymal Stromal Cells/*physiology ; Mice ; Osteogenesis ; Osteogenesis Imperfecta/*genetics/*therapy ; Point Mutation ; Recombination, Genetic ; Stem Cell Transplantation
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  • 43
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-04-24
    Description: MicroRNAs (miRNAs) are endogenous approximately 22-nucleotide RNAs, some of which are known to play important regulatory roles in animals by targeting the messages of protein-coding genes for translational repression. We find that miR-196, a miRNA encoded at three paralogous locations in the A, B, and C mammalian HOX clusters, has extensive, evolutionarily conserved complementarity to messages of HOXB8, HOXC8, and HOXD8. RNA fragments diagnostic of miR-196-directed cleavage of HOXB8 were detected in mouse embryos. Cell culture experiments demonstrated down-regulation of HOXB8, HOXC8, HOXD8, and HOXA7 and supported the cleavage mechanism for miR-196-directed repression of HOXB8. These results point to a miRNA-mediated mechanism for the posttranscriptional restriction of HOX gene expression during vertebrate development and demonstrate that metazoan miRNAs can repress expression of their natural targets through mRNA cleavage in addition to inhibiting productive translation.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Yekta, Soraya -- Shih, I-Hung -- Bartel, David P -- New York, N.Y. -- Science. 2004 Apr 23;304(5670):594-6.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Whitehead Institute for Biomedical Research, Nine Cambridge Center, Cambridge, MA 02142, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15105502" target="_blank"〉PubMed〈/a〉
    Keywords: 3' Untranslated Regions ; Animals ; Base Sequence ; Down-Regulation ; *Genes, Homeobox ; Genes, Reporter ; HeLa Cells ; Homeodomain Proteins/*genetics ; Humans ; Mice ; MicroRNAs/chemistry/genetics/*metabolism ; Molecular Sequence Data ; Neoplasm Proteins/genetics ; RNA, Messenger/chemistry/*genetics/*metabolism ; Sequence Alignment ; Transcription Factors/genetics ; Transfection
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  • 44
    Publication Date: 2004-07-13
    Description: Intestinal intraepithelial T lymphocytes (IELs) are likely to play a key role in host mucosal immunity and, unlike other T cells, have been proposed to differentiate from local precursors rather than from thymocytes. We show here that IELs expressing the alphabeta T cell receptor are derived from precursors that express RORgammat, an orphan nuclear hormone receptor detected only in immature CD4+CD8+ thymocytes, fetal lymphoid tissue-inducer (LTi) cells, and LTi-like cells in cryptopatches within the adult intestinal lamina propria. Using cell fate mapping, we found that all intestinal alphabeta T cells are progeny of CD4+CD8+ thymocytes, indicating that the adult intestine is not a significant site for alphabeta T cell development. Our results suggest that intestinal RORgammat+ cells are local organizers of mucosal lymphoid tissue.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Eberl, Gerard -- Littman, Dan R -- New York, N.Y. -- Science. 2004 Jul 9;305(5681):248-51.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Molecular Pathogenesis Program, Skirball Institute of Biomolecular Medicine, New York University School of Medicine, New York, NY 10016, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15247480" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Antigens, CD4/analysis ; Antigens, CD8/analysis ; Cell Lineage ; DNA-Binding Proteins/metabolism ; Hematopoietic Stem Cells/immunology/physiology ; Immunity, Mucosal ; Intestinal Mucosa/cytology/*immunology ; Lymphoid Tissue/embryology/immunology ; Mice ; Mice, Transgenic ; Nuclear Receptor Subfamily 1, Group F, Member 3 ; Receptors, Antigen, T-Cell, alpha-beta/*analysis/genetics ; Receptors, Antigen, T-Cell, gamma-delta/analysis/genetics ; Receptors, Retinoic Acid/genetics/*metabolism ; Receptors, Thyroid Hormone/genetics/*metabolism ; T-Lymphocyte Subsets/cytology/*immunology ; T-Lymphocytes/cytology/*immunology ; Thymus Gland/cytology/*immunology
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    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 45
    Publication Date: 2004-02-21
    Description: Double-stranded ribonucleic acid (dsRNA) serves as a danger signal associated with viral infection and leads to stimulation of innate immune cells. In contrast, the immunostimulatory potential of single-stranded RNA (ssRNA) is poorly understood and innate immune receptors for ssRNA are unknown. We report that guanosine (G)- and uridine (U)-rich ssRNA oligonucleotides derived from human immunodeficiency virus-1 (HIV-1) stimulate dendritic cells (DC) and macrophages to secrete interferon-alpha and proinflammatory, as well as regulatory, cytokines. By using Toll-like receptor (TLR)-deficient mice and genetic complementation, we show that murine TLR7 and human TLR8 mediate species-specific recognition of GU-rich ssRNA. These data suggest that ssRNA represents a physiological ligand for TLR7 and TLR8.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Heil, Florian -- Hemmi, Hiroaki -- Hochrein, Hubertus -- Ampenberger, Franziska -- Kirschning, Carsten -- Akira, Shizuo -- Lipford, Grayson -- Wagner, Hermann -- Bauer, Stefan -- New York, N.Y. -- Science. 2004 Mar 5;303(5663):1526-9. Epub 2004 Feb 19.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Institute of Medical Microbiology, Immunology and Hygiene, Technische Universitat Munchen, Trogerstr. 9, D - 81675 Munich, Germany.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/14976262" target="_blank"〉PubMed〈/a〉
    Keywords: Adaptor Proteins, Signal Transducing ; Animals ; Antigens, Differentiation/metabolism ; Base Sequence ; Cytokines/biosynthesis ; Dendritic Cells/*immunology ; Fatty Acids, Monounsaturated ; Genetic Complementation Test ; Guanosine/analysis ; HIV-1/genetics/*immunology ; Humans ; Interferon-alpha/biosynthesis ; Leukocytes, Mononuclear/immunology ; Macrophages/*immunology ; Membrane Glycoproteins/genetics/*metabolism ; Mice ; Mice, Inbred C57BL ; Myeloid Differentiation Factor 88 ; Oligoribonucleotides/chemistry/*immunology ; Quaternary Ammonium Compounds ; RNA, Viral/chemistry/*immunology/metabolism ; Receptors, Cell Surface/genetics/*metabolism ; Receptors, Immunologic/metabolism ; Species Specificity ; Thionucleotides/chemistry/immunology ; Toll-Like Receptor 7 ; Toll-Like Receptor 8 ; Toll-Like Receptors ; Transfection ; Uridine/analysis
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  • 46
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-09-28
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Anderson, Daniel G -- Burdick, Jason A -- Langer, Robert -- New York, N.Y. -- Science. 2004 Sep 24;305(5692):1923-4.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Chemical Engineering, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15448260" target="_blank"〉PubMed〈/a〉
    Keywords: Amino Acid Motifs ; Animals ; *Biocompatible Materials ; Cell Differentiation ; Humans ; Laminin/chemistry ; Mice ; Peptide Fragments/chemistry ; Stem Cells/cytology ; Surface Properties
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  • 47
    Publication Date: 2004-06-05
    Description: Strategies for inhibiting phagolysosome fusion are essential for the intracellular survival and replication of many pathogens. We found that the lysosomal synaptotagmin Syt VII is required for a mechanism that promotes phagolysosomal fusion and limits the intracellular growth of pathogenic bacteria. Syt VII was required for a form of Ca2+-dependent phagolysosome fusion that is analogous to Ca2+-regulated exocytosis of lysosomes, which can be triggered by membrane injury. Bacterial type III secretion systems, which permeabilize membranes and cause Ca2+ influx in mammalian cells, promote lysosomal exocytosis and inhibit intracellular survival in Syt VII +/+ but not -/- cells. Thus, the lysosomal repair response can also protect cells against pathogens that trigger membrane permeabilization.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Roy, Deepannita -- Liston, David R -- Idone, Vincent J -- Di, Anke -- Nelson, Deborah J -- Pujol, Celine -- Bliska, James B -- Chakrabarti, Sabyasachi -- Andrews, Norma W -- AI34867/AI/NIAID NIH HHS/ -- AI43389/AI/NIAID NIH HHS/ -- AI48507/AI/NIAID NIH HHS/ -- GM64625/GM/NIGMS NIH HHS/ -- New York, N.Y. -- Science. 2004 Jun 4;304(5676):1515-8.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Section of Microbial Pathogenesis and Department of Cell Biology, Yale University School of Medicine, New Haven, CT 06510, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15178804" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Bacteria/*growth & development/metabolism ; Bacterial Proteins/genetics/metabolism ; CHO Cells ; Calcium/metabolism ; *Calcium-Binding Proteins ; Cell Membrane/*physiology ; Cells, Cultured ; Cricetinae ; Endocytosis ; Exocytosis ; Listeria monocytogenes/growth & development ; Lysosomes/microbiology/physiology ; Macrophages/microbiology ; Membrane Glycoproteins/genetics/*physiology ; Mice ; Mutation ; Nerve Tissue Proteins/genetics/*physiology ; Permeability ; Phagosomes/microbiology/physiology ; Salmonella typhimurium/*growth & development/metabolism ; Synaptotagmins ; Vacuoles/microbiology ; Yersinia pseudotuberculosis/genetics/growth & development
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  • 48
    Publication Date: 2004-01-24
    Description: Mammalian sex chromosomes have undergone profound changes since evolving from ancestral autosomes. By examining retroposed genes in the human and mouse genomes, we demonstrate that, during evolution, the mammalian X chromosome has generated and recruited a disproportionately high number of functional retroposed genes, whereas the autosomes experienced lower gene turnover. Most autosomal copies originating from X-linked genes exhibited testis-biased expression. Such export is incompatible with mutational bias and is likely driven by natural selection to attain male germline function. However, the excess recruitment is consistent with a combination of both natural selection and mutational bias.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Emerson, J J -- Kaessmann, Henrik -- Betran, Esther -- Long, Manyuan -- GM-065429-01A1/GM/NIGMS NIH HHS/ -- New York, N.Y. -- Science. 2004 Jan 23;303(5657):537-40.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Ecology and Evolution, University of Chicago, Chicago, IL 60637, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/14739461" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; *Biological Evolution ; Chromosomes, Human/genetics ; Chromosomes, Human, X/*genetics ; Chromosomes, Mammalian/genetics ; Computational Biology ; Dosage Compensation, Genetic ; Female ; Gene Expression Profiling ; Genes, Duplicate ; Genetic Linkage ; Genome ; Genome, Human ; Humans ; Introns ; Male ; Mice ; Monte Carlo Method ; Mutation ; Oligonucleotide Array Sequence Analysis ; Ovary/metabolism ; Pseudogenes/*genetics ; *Recombination, Genetic ; Retroelements/*genetics ; Selection, Genetic ; Sex Characteristics ; Testis/metabolism ; X Chromosome/*genetics
    Print ISSN: 0036-8075
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  • 49
    Publication Date: 2004-06-12
    Description: Anterior-to-posterior patterning, the process whereby our digits are differently shaped, is a key aspect of limb development. It depends on the localized expression in posterior limb bud of Sonic hedgehog (Shh) and the morphogenetic potential of its diffusing product. By using an inversion of and a large deficiency in the mouse HoxD cluster, we found that a perturbation in the early collinear expression of Hoxd11, Hoxd12, and Hoxd13 in limb buds led to a loss of asymmetry. Ectopic Hox gene expression triggered abnormal Shh transcription, which in turn induced symmetrical expression of Hox genes in digits, thereby generating double posterior limbs. We conclude that early posterior restriction of Hox gene products sets up an anterior-posterior prepattern, which determines the localized activation of Shh. This signal is subsequently translated into digit morphological asymmetry by promoting the late expression of Hoxd genes, two collinear processes relying on opposite genomic topographies, upstream and downstream Shh signaling.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Zakany, Jozsef -- Kmita, Marie -- Duboule, Denis -- New York, N.Y. -- Science. 2004 Jun 11;304(5677):1669-72.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Zoology and Animal Biology and National Program Frontiers in Genetics, University of Geneva, Sciences III, Quai Ernest Ansermet 30, 1211 Geneva 4, Switzerland.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15192229" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Basic Helix-Loop-Helix Transcription Factors ; *Body Patterning ; Chromosome Inversion ; DNA-Binding Proteins/genetics/metabolism ; Forelimb/abnormalities/*embryology ; *Gene Expression Regulation, Developmental ; Gene Targeting ; *Genes, Homeobox ; Hedgehog Proteins ; Heterozygote ; Hindlimb/abnormalities/embryology ; Homeodomain Proteins/genetics/metabolism ; Homozygote ; Kruppel-Like Transcription Factors ; Limb Buds/*embryology/metabolism ; Mice ; Morphogenesis ; *Nerve Tissue Proteins ; Recombination, Genetic ; Signal Transduction ; Toes/abnormalities/embryology ; Trans-Activators/genetics/*metabolism ; Transcription Factors/genetics/metabolism ; Transcription, Genetic ; Zebrafish Proteins
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  • 50
    Publication Date: 2004-02-14
    Description: The tumor suppressor p53 exerts its anti-neoplastic activity primarily through the induction of apoptosis. We found that cytosolic localization of endogenous wild-type or trans-activation-deficient p53 was necessary and sufficient for apoptosis. p53 directly activated the proapoptotic Bcl-2 protein Bax in the absence of other proteins to permeabilize mitochondria and engage the apoptotic program. p53 also released both proapoptotic multidomain proteins and BH3-only proteins [Proapoptotic Bcl-2 family proteins that share only the third Bcl-2 homology domain (BH3)] that were sequestered by Bcl-xL. The transcription-independent activation of Bax by p53 occurred with similar kinetics and concentrations to those produced by activated Bid. We propose that when p53 accumulates in the cytosol, it can function analogously to the BH3-only subset of proapoptotic Bcl-2 proteins to activate Bax and trigger apoptosis.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Chipuk, Jerry E -- Kuwana, Tomomi -- Bouchier-Hayes, Lisa -- Droin, Nathalie M -- Newmeyer, Donald D -- Schuler, Martin -- Green, Douglas R -- AI40646/AI/NIAID NIH HHS/ -- AI47891/AI/NIAID NIH HHS/ -- GM52735/GM/NIGMS NIH HHS/ -- New York, N.Y. -- Science. 2004 Feb 13;303(5660):1010-4.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Division of Cellular Immunology, La Jolla Institute for Allergy and Immunology, 10355 Science Center Drive, San Diego, CA 92121, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/14963330" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; *Apoptosis ; BH3 Interacting Domain Death Agonist Protein ; Carrier Proteins/metabolism ; Cell Line, Transformed ; Cell Nucleus/metabolism ; Cells, Cultured ; Cytochromes c/metabolism ; Cytosol/metabolism ; Gene Expression Regulation ; Genes, p53 ; HeLa Cells ; Humans ; Intracellular Membranes/*physiology ; Liposomes/metabolism ; Mice ; Mitochondria/*physiology ; Mutation ; Permeability ; Protein Conformation ; Proto-Oncogene Proteins/chemistry/genetics/*metabolism ; Proto-Oncogene Proteins c-bcl-2/metabolism ; Recombinant Fusion Proteins/metabolism ; Tumor Suppressor Protein p53/chemistry/*metabolism ; Ultraviolet Rays ; Wheat Germ Agglutinins/pharmacology ; bcl-2-Associated X Protein ; bcl-X Protein
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  • 51
    Publication Date: 2004-12-18
    Description: The inositol pyrophosphates IP7 and IP8 contain highly energetic pyrophosphate bonds. Although implicated in various biologic functions, their molecular sites of action have not been clarified. Using radiolabeled IP7, we detected phosphorylation of multiple eukaryotic proteins. We also observed phosphorylation of endogenous proteins by endogenous IP7 in yeast. Phosphorylation by IP7 is nonenzymatic and may represent a novel intracellular signaling mechanism.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Saiardi, Adolfo -- Bhandari, Rashna -- Resnick, Adam C -- Snowman, Adele M -- Snyder, Solomon H -- DA00074/DA/NIDA NIH HHS/ -- MH068830-02/MH/NIMH NIH HHS/ -- MH18501/MH/NIMH NIH HHS/ -- New York, N.Y. -- Science. 2004 Dec 17;306(5704):2101-5.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Neuroscience, Johns Hopkins University, School of Medicine, 725 North Wolfe Street, Baltimore, MD 21205, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15604408" target="_blank"〉PubMed〈/a〉
    Keywords: Adenosine Triphosphate/metabolism ; Amino Acid Sequence ; Amino Acid Substitution ; Animals ; Drosophila Proteins/metabolism ; Drosophila melanogaster ; Escherichia coli Proteins/metabolism ; Humans ; Inositol Phosphates/*metabolism ; Kinetics ; Magnesium/metabolism ; Mice ; Molecular Sequence Data ; Mutation ; Nuclear Proteins/chemistry/*metabolism ; Phosphates/metabolism ; Phosphorylation ; Phosphotransferases (Phosphate Group Acceptor)/metabolism ; Protein Kinases/genetics/metabolism ; Proteins/*metabolism ; RNA-Binding Proteins/chemistry/*metabolism ; Saccharomyces cerevisiae/metabolism ; Saccharomyces cerevisiae Proteins/chemistry/*metabolism ; Serine/metabolism ; Signal Transduction ; Temperature
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  • 52
    Publication Date: 2004-05-15
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Samet, Jonathan M -- DeMarini, David M -- Malling, Heinrich V -- New York, N.Y. -- Science. 2004 May 14;304(5673):971-2.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Epidemiology, Johns Hopkins University, Bloomberg School of Public Health, Baltimore, MD 21205, USA. jsamet@jhsph.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15143266" target="_blank"〉PubMed〈/a〉
    Keywords: Air Pollutants/*toxicity ; Air Pollution/*adverse effects ; Animals ; DNA Damage ; Female ; Filtration/instrumentation ; *Germ-Line Mutation ; Humans ; Industry ; Male ; Mice ; Mutagens/*toxicity ; Ontario ; Particle Size ; Polycyclic Hydrocarbons, Aromatic/toxicity ; Pregnancy ; Spermatogonia/drug effects/physiology ; Stem Cells/drug effects/physiology ; Tandem Repeat Sequences
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  • 53
    Publication Date: 2004-08-31
    Description: Group A streptococci, a common human pathogen, secrete streptokinase, which activates the host's blood clot-dissolving protein, plasminogen. Streptokinase is highly specific for human plasminogen, exhibiting little or no activity against other mammalian species, including mouse. Here, a transgene expressing human plasminogen markedly increased mortality in mice infected with streptococci, and this susceptibility was dependent on bacterial streptokinase expression. Thus, streptokinase is a key pathogenicity factor and the primary determinant of host species specificity for group A streptococcal infection. In addition, local fibrin clot formation may be implicated in host defense against microbial pathogens.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Sun, Hongmin -- Ringdahl, Ulrika -- Homeister, Jonathon W -- Fay, William P -- Engleberg, N Cary -- Yang, Angela Y -- Rozek, Laura S -- Wang, Xixi -- Sjobring, Ulf -- Ginsburg, David -- P01HL057346/HL/NHLBI NIH HHS/ -- New York, N.Y. -- Science. 2004 Aug 27;305(5688):1283-6.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Internal Medicine, University of Michigan, Ann Arbor, MI 48109, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15333838" target="_blank"〉PubMed〈/a〉
    Keywords: Ancrod/pharmacology ; Animals ; Anticoagulants/pharmacology ; Bacterial Proteins/metabolism ; Carrier Proteins/metabolism ; Colony Count, Microbial ; Disease Susceptibility ; Fibrin/metabolism ; Fibrinolysin/metabolism ; Fibrinolysis ; Gene Deletion ; Humans ; Immunity, Innate ; Mice ; Mice, Inbred C57BL ; Plasminogen/genetics/*metabolism ; Skin/blood supply/microbiology ; Species Specificity ; Spleen/microbiology ; Streptococcal Infections/*microbiology ; Streptococcus pyogenes/*enzymology/growth & development/*pathogenicity ; Streptokinase/genetics/*metabolism ; Transgenes ; Virulence
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  • 54
    Publication Date: 2004-12-18
    Description: Olig1 and Olig2 are closely related basic helix-loop-helix (bHLH) transcription factors that are expressed in myelinating oligodendrocytes and their progenitor cells in the developing central nervous system (CNS). Olig2 is necessary for the specification of oligodendrocytes, but the biological functions of Olig1 during oligodendrocyte lineage development are poorly understood. We show here that Olig1 function in mice is required not to develop the brain but to repair it. Specifically, we demonstrate a genetic requirement for Olig1 in repairing the types of lesions that occur in patients with multiple sclerosis.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Arnett, Heather A -- Fancy, Stephen P J -- Alberta, John A -- Zhao, Chao -- Plant, Sheila R -- Kaing, Sovann -- Raine, Cedric S -- Rowitch, David H -- Franklin, Robin J M -- Stiles, Charles D -- 689/Multiple Sclerosis Society/United Kingdom -- NS08952/NS/NINDS NIH HHS/ -- NS11920/NS/NINDS NIH HHS/ -- NS4051/NS/NINDS NIH HHS/ -- New York, N.Y. -- Science. 2004 Dec 17;306(5704):2111-5.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA 02115, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15604411" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Animals, Newborn ; Basic Helix-Loop-Helix Transcription Factors ; Brain/growth & development/*physiology ; Cell Nucleus/metabolism ; Cuprizone/pharmacology ; Cytoplasm/metabolism ; DNA-Binding Proteins/genetics/*metabolism ; Demyelinating Diseases/*physiopathology ; Ethidium/pharmacology ; Humans ; Lysophosphatidylcholines/pharmacology ; Mice ; Mice, Inbred C57BL ; Multiple Sclerosis/physiopathology ; Myelin Sheath/*physiology ; Nerve Tissue Proteins/genetics/*metabolism/physiology ; Oligodendroglia/*physiology ; Rats ; Rats, Sprague-Dawley ; Spinal Cord/growth & development/*physiology ; Stem Cells/physiology ; Transcription Factors/genetics/*metabolism
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  • 55
    Publication Date: 2004-06-19
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Enserink, Martin -- Kaiser, Jocelyn -- New York, N.Y. -- Science. 2004 Jun 18;304(5678):1726-7.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15205495" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Anthrax ; Anthrax Vaccines ; *Bacillus anthracis ; *Containment of Biohazards ; Humans ; Laboratory Infection ; Mice ; *Safety Management ; United States
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  • 56
    Publication Date: 2004-07-17
    Description: Vertebrate limb outgrowth is driven by a positive feedback loop involving Sonic Hedgehog (Shh), Gremlin, and Fgf4. By overexpressing individual components of the loop at a time after these genes are normally down-regulated in chicken embryos, we found that Shh no longer maintains Gremlin in the posterior limb. Shh-expressing cells and their descendants cannot express Gremlin. The proliferation of these descendants forms a barrier separating the Shh signal from Gremlin-expressing cells, which breaks down the Shh-Fgf4 loop and thereby affects limb size and provides a mechanism explaining regulative properties of the limb bud.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Scherz, Paul J -- Harfe, Brian D -- McMahon, Andrew P -- Tabin, Clifford J -- 5T32GM0719T6/GM/NIGMS NIH HHS/ -- HD32443/HD/NICHD NIH HHS/ -- NS33642/NS/NINDS NIH HHS/ -- New York, N.Y. -- Science. 2004 Jul 16;305(5682):396-9.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Genetics, Harvard Medical School, 77 Avenue Louis Pasteur, Boston, MA 02115, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15256670" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Cell Division ; Chick Embryo ; Down-Regulation ; Feedback, Physiological ; Fibroblast Growth Factor 4 ; Fibroblast Growth Factor 8 ; Fibroblast Growth Factor 9 ; Fibroblast Growth Factors/genetics/*metabolism ; Gene Expression Regulation, Developmental ; Hedgehog Proteins ; Intercellular Signaling Peptides and Proteins/genetics/*metabolism ; Limb Buds/cytology/*embryology/metabolism ; Mesoderm/*cytology/metabolism ; Mice ; Models, Biological ; Proto-Oncogene Proteins/genetics/*metabolism ; Signal Transduction ; Trans-Activators/*metabolism ; Up-Regulation
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  • 57
    Publication Date: 2004-11-20
    Description: Mobilization of fatty acids from triglyceride stores in adipose tissue requires lipolytic enzymes. Dysfunctional lipolysis affects energy homeostasis and may contribute to the pathogenesis of obesity and insulin resistance. Until now, hormone-sensitive lipase (HSL) was the only enzyme known to hydrolyze triglycerides in mammalian adipose tissue. Here, we report that a second enzyme, adipose triglyceride lipase (ATGL), catalyzes the initial step in triglyceride hydrolysis. It is interesting that ATGL contains a "patatin domain" common to plant acyl-hydrolases. ATGL is highly expressed in adipose tissue of mice and humans. It exhibits high substrate specificity for triacylglycerol and is associated with lipid droplets. Inhibition of ATGL markedly decreases total adipose acyl-hydrolase activity. Thus, ATGL and HSL coordinately catabolize stored triglycerides in adipose tissue of mammals.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Zimmermann, Robert -- Strauss, Juliane G -- Haemmerle, Guenter -- Schoiswohl, Gabriele -- Birner-Gruenberger, Ruth -- Riederer, Monika -- Lass, Achim -- Neuberger, Georg -- Eisenhaber, Frank -- Hermetter, Albin -- Zechner, Rudolf -- New York, N.Y. -- Science. 2004 Nov 19;306(5700):1383-6.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Institute of Molecular Biosciences, University of Graz, Graz, Austria.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15550674" target="_blank"〉PubMed〈/a〉
    Keywords: 3T3-L1 Cells ; Adipocytes/enzymology/*metabolism ; Adipose Tissue/enzymology/*metabolism ; Adipose Tissue, Brown/enzymology/metabolism ; Amino Acid Sequence ; Animals ; COS Cells ; Cyclic AMP-Dependent Protein Kinases/metabolism ; Cytoplasm/enzymology ; DNA, Complementary ; Diglycerides/metabolism ; Fatty Acids/metabolism ; Gene Silencing ; Glycerol/metabolism ; Humans ; Isoproterenol/pharmacology ; *Lipid Mobilization ; Lipolysis ; Lipoprotein Lipase/chemistry/genetics/immunology/*metabolism ; Mice ; Molecular Sequence Data ; Phosphorylation ; Protein Structure, Tertiary ; RNA, Messenger/genetics/metabolism ; Sterol Esterase/genetics/*metabolism ; Substrate Specificity ; Transfection ; Triglycerides/metabolism
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  • 58
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-06-19
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Schuske, Kim -- Jorgensen, Erik M -- New York, N.Y. -- Science. 2004 Jun 18;304(5678):1750-2.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Biology, University of Utah, 257 South 1400 East, Salt Lake City, UT 84112-0840, USA. jorgensen@biology.utah.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15205517" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Animals, Newborn ; Brain/metabolism ; Carrier Proteins/genetics/*metabolism ; Cell Membrane/physiology ; Cells, Cultured ; Excitatory Postsynaptic Potentials ; Glutamic Acid/metabolism ; Hippocampus/cytology/metabolism ; Membrane Fusion ; *Membrane Transport Proteins ; Mice ; Mice, Knockout ; Models, Neurological ; Mutation ; Neurons/*metabolism ; *Synaptic Transmission ; Synaptic Vesicles/*metabolism/physiology ; Vesicular Glutamate Transport Protein 1 ; Vesicular Glutamate Transport Protein 2 ; *Vesicular Transport Proteins
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  • 59
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-09-18
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Testa, Giuseppe -- Harris, John -- New York, N.Y. -- Science. 2004 Sep 17;305(5691):1719.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Genomics, BIOTEC, Dresden University of Technology, Dresden, Germany. testa@mpi-cbg.de〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15375251" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Bioethical Issues ; Cloning, Organism/*ethics ; Embryo Research/ethics ; Embryo, Mammalian/*cytology ; Female ; Fertilization in Vitro ; Genomic Imprinting ; *Germ Cells ; Humans ; Infertility ; Male ; Mice ; Parents ; Reproductive Techniques, Assisted/*ethics ; *Stem Cells
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    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 60
    Publication Date: 2004-09-09
    Description: Human genetic diseases that resemble accelerated aging provide useful models for gerontologists. They combine known single-gene mutations with deficits in selected tissues that are reminiscent of changes seen during normal aging. Here, we describe recent progress toward linking molecular and cellular changes with the phenotype seen in two of these disorders. One in particular, Werner syndrome, provides evidence to support the hypothesis that the senescence of somatic cells may be a causal agent of normal aging.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Kipling, David -- Davis, Terence -- Ostler, Elizabeth L -- Faragher, Richard G A -- New York, N.Y. -- Science. 2004 Sep 3;305(5689):1426-31.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Pathology, School of Medicine, Cardiff University, Heath Park, Cardiff CF14 4XN, UK.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15353794" target="_blank"〉PubMed〈/a〉
    Keywords: *Aging ; Animals ; Cell Aging ; Cell Division ; DNA Helicases/genetics/physiology ; Exodeoxyribonucleases ; Female ; Gene Expression ; Humans ; Male ; Mice ; Models, Animal ; Mutation ; Phenotype ; RecQ Helicases ; Telomere/metabolism ; *Werner Syndrome/genetics/pathology/physiopathology
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  • 61
    Publication Date: 2004-02-21
    Description: 〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1237009/" target="_blank"〉〈img src="https://static.pubmed.gov/portal/portal3rc.fcgi/4089621/img/3977009" border="0"〉〈/a〉   〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1237009/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Klett, Eric L -- Patel, Shailesh B -- R01 HL060613/HL/NHLBI NIH HHS/ -- New York, N.Y. -- Science. 2004 Feb 20;303(5661):1149-50.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Division of Endocrinology, Diabetes and Medical Genetics, Medical University of South Carolina, Charleston, SC 29403, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/14976303" target="_blank"〉PubMed〈/a〉
    Keywords: ATP-Binding Cassette Transporters/genetics/metabolism ; Animals ; Anticholesteremic Agents/pharmacology ; Azetidines/pharmacology ; Cholesterol, Dietary/*metabolism ; Enterocytes/*metabolism ; Ezetimibe ; Humans ; *Intestinal Absorption/drug effects ; Intestine, Small/metabolism ; Lipoproteins/genetics/metabolism ; Liver/metabolism ; Membrane Proteins/genetics/*metabolism ; Membrane Transport Proteins/genetics/*metabolism ; Mice ; Models, Biological ; Proteins/genetics/*metabolism ; Sitosterols/blood
    Print ISSN: 0036-8075
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  • 62
    Publication Date: 2004-04-06
    Description: Because ethical restrictions limit in vivo studies of the human hemato-lymphoid system, substitute human to small animal xenotransplantation models have been employed. Existing models, however, sustain only limited development and maintenance of human lymphoid cells and rarely produce immune responses. Here we show that intrahepatic injection of CD34+ human cord blood cells into conditioned newborn Rag2-/-gammac-/- mice leads to de novo development of B, T, and dendritic cells; formation of structured primary and secondary lymphoid organs; and production of functional immune responses. This provides a valuable model to study development and function of the human adaptive immune system in vivo.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Traggiai, Elisabetta -- Chicha, Laurie -- Mazzucchelli, Luca -- Bronz, Lucio -- Piffaretti, Jean-Claude -- Lanzavecchia, Antonio -- Manz, Markus G -- New York, N.Y. -- Science. 2004 Apr 2;304(5667):104-7.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Institute for Research in Biomedicine (IRB), Via Vela 6, 6500 Bellinzona, Switzerland.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15064419" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Animals, Newborn ; Antigens, CD34/analysis ; B-Lymphocytes/cytology/*immunology ; Bone Marrow Cells/immunology ; Dendritic Cells/cytology/*immunology ; Dendritic Cells, Follicular/cytology/immunology ; Epstein-Barr Virus Infections/immunology ; Fetal Blood/*cytology ; Gene Rearrangement, T-Lymphocyte ; *Hematopoietic Stem Cell Transplantation ; Humans ; Immune System/*physiology ; Immunoglobulins/analysis ; Infant, Newborn ; Lymph Nodes/cytology/immunology ; Lymphocyte Activation ; Major Histocompatibility Complex ; Mice ; Mice, Inbred BALB C ; Mice, Mutant Strains ; Spleen/cytology/immunology ; T-Lymphocytes/cytology/*immunology ; Tetanus Toxoid/immunology ; Thymus Gland/cytology/immunology ; Transplantation, Heterologous
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  • 63
    Publication Date: 2004-07-13
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Seeman, Philip -- New York, N.Y. -- Science. 2004 Jul 9;305(5681):180; author reply 180.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Departments of Pharmacology, and Psychiatry, 1 King's College Circle, University of Toronto, Toronto, Ontario, Canada M5S 1A8. philip.seeman@utoronto.ca〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15247457" target="_blank"〉PubMed〈/a〉
    Keywords: Amphetamines/metabolism/pharmacology ; Animals ; Behavior, Animal/drug effects ; Brain/drug effects/*metabolism ; Central Nervous System Agents/metabolism/*pharmacology ; Dopamine/metabolism ; Dopamine Agonists/metabolism/pharmacology ; Dopamine and cAMP-Regulated Phosphoprotein 32 ; Mice ; Mice, Knockout ; *Nerve Tissue Proteins ; Phosphoproteins/genetics/*metabolism ; Psychotic Disorders/etiology/metabolism ; Receptors, Dopamine D2/agonists/*metabolism ; *Signal Transduction ; Synaptic Transmission
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  • 64
    Publication Date: 2004-01-13
    Description: The development of osteoporosis involves the interaction of multiple environmental and genetic factors. Through combined genetic and genomic approaches, we identified the lipoxygenase gene Alox15 as a negative regulator of peak bone mineral density in mice. Crossbreeding experiments with Alox15 knockout mice confirmed that 12/15-lipoxygenase plays a role in skeletal development. Pharmacologic inhibitors of this enzyme improved bone density and strength in two rodent models of osteoporosis. These results suggest that drugs targeting the 12/15-lipoxygenase pathway merit investigation as a therapy for osteoporosis.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Klein, Robert F -- Allard, John -- Avnur, Zafrira -- Nikolcheva, Tania -- Rotstein, David -- Carlos, Amy S -- Shea, Marie -- Waters, Ruth V -- Belknap, John K -- Peltz, Gary -- Orwoll, Eric S -- AR44659/AR/NIAMS NIH HHS/ -- HG02322/HG/NHGRI NIH HHS/ -- R01 AR044659/AR/NIAMS NIH HHS/ -- R01 AR044659-08/AR/NIAMS NIH HHS/ -- New York, N.Y. -- Science. 2004 Jan 9;303(5655):229-32.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Bone and Mineral Research Unit, Department of Medicine, School of Medicine, Oregon Health and Science University, 3181 Southwest Sam Jackson Park Road, Portland, OR 97239, USA. kleinro@ohsu.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/14716014" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Arachidonate 12-Lipoxygenase/*genetics/*metabolism ; Arachidonate 15-Lipoxygenase/*genetics/*metabolism ; Bone Density/drug effects/*genetics ; Bone Marrow Cells/metabolism ; Cell Differentiation ; Cells, Cultured ; Crosses, Genetic ; Enzyme Inhibitors/pharmacology ; Female ; Fluorenes/pharmacology ; Gene Expression Profiling ; Genetic Linkage ; Kidney/metabolism ; Lipoxygenase Inhibitors ; Male ; Mice ; Mice, Inbred C57BL ; Mice, Inbred Strains ; Mice, Knockout ; Mice, Transgenic ; Oligonucleotide Array Sequence Analysis ; Osteoblasts/cytology/metabolism/physiology ; Osteogenesis ; Osteoporosis/enzymology ; Polymorphism, Genetic ; Quantitative Trait Loci ; Rats ; Receptors, Cytoplasmic and Nuclear/metabolism ; Stromal Cells/metabolism ; Transcription Factors/metabolism
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  • 65
    Publication Date: 2004-01-13
    Description: The imprinted regulation of H19 and Insulin-like growth factor 2 expression involves binding of the vertebrate insulator protein, CCCTC binding factor (CTCF), to the maternally hypomethylated differentially methylated domain (DMD). How this hypomethylated state is maintained during oogenesis and the role of CTCF, if any, in this process are not understood. With the use of a transgenic RNA interference (RNAi)-based approach to generate oocytes with reduced amounts of CTCF protein, we found increased methylation of the H19 DMD and decreased developmental competence of CTCF-deficient oocytes. Our results suggest that CTCF protects the H19 DMD from de novo methylation during oocyte growth and is required for normal preimplantation development.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Fedoriw, Andrew M -- Stein, Paula -- Svoboda, Petr -- Schultz, Richard M -- Bartolomei, Marisa S -- HD-42026/HD/NICHD NIH HHS/ -- T32 HD-07516/HD/NICHD NIH HHS/ -- New York, N.Y. -- Science. 2004 Jan 9;303(5655):238-40.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Howard Hughes Medical Institute, University of Pennsylvania, Philadelphia, PA 19104, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/14716017" target="_blank"〉PubMed〈/a〉
    Keywords: Actins/genetics ; Animals ; DNA Methylation ; DNA-Binding Proteins/genetics/*metabolism ; Embryonic and Fetal Development ; Female ; Fertilization in Vitro ; Gene Targeting ; *Genomic Imprinting ; Litter Size ; Mice ; Mice, Transgenic ; Nuclear Proteins/genetics ; Oocytes/*metabolism ; *RNA Interference ; RNA, Long Noncoding ; RNA, Messenger/genetics/metabolism ; RNA, Untranslated/*genetics ; Repressor Proteins/genetics/*metabolism ; Zygote/physiology
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  • 66
    Publication Date: 2004-02-07
    Description: Microtubule (MT) stabilization is regulated by the small guanosine triphosphate (GTP)-binding protein Rho and its effector, mammalian homolog of Diaphanous (mDia), in migrating cells, but factors responsible for localized stabilization at the leading edge are unknown. We report that integrin-mediated activation of focal adhesion kinase (FAK) at the leading edge is required for MT stabilization by the Rho-mDia signaling pathway in mouse fibroblasts. MT stabilization also involved FAK-regulated localization of a lipid raft marker, ganglioside GM1, to the leading edge. The integrin-FAK signaling pathway may facilitate Rho-mDia signaling through GM1, or through a specialized membrane domain containing GM1, to stabilize MTs in the leading edge of migrating cells.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Palazzo, Alexander F -- Eng, Christina H -- Schlaepfer, David D -- Marcantonio, Eugene E -- Gundersen, Gregg G -- CA87038/CA/NCI NIH HHS/ -- GM 44585/GM/NIGMS NIH HHS/ -- GM 62939/GM/NIGMS NIH HHS/ -- GM 68695/GM/NIGMS NIH HHS/ -- New York, N.Y. -- Science. 2004 Feb 6;303(5659):836-9.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Anatomy and Cell Biology, Columbia University, New York, NY 10032, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/14764879" target="_blank"〉PubMed〈/a〉
    Keywords: Acetylation ; Animals ; Carrier Proteins/metabolism ; Cell Adhesion ; Cell Line ; Cell Membrane/*metabolism ; Cholesterol/metabolism ; Fibronectins/metabolism/pharmacology ; Focal Adhesion Kinase 1 ; Focal Adhesion Protein-Tyrosine Kinases ; G(M1) Ganglioside/metabolism ; Glycosylphosphatidylinositols/metabolism ; Integrins/*metabolism ; Membrane Microdomains/*metabolism ; Mice ; Mice, Knockout ; Microtubules/*metabolism/ultrastructure ; NIH 3T3 Cells ; Phosphorylation ; Protein-Tyrosine Kinases/genetics/*metabolism ; Recombinant Fusion Proteins/metabolism ; Signal Transduction ; Tubulin/metabolism ; rho GTP-Binding Proteins/*metabolism ; rhoA GTP-Binding Protein/genetics/metabolism
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  • 67
    Publication Date: 2004-11-30
    Description: Epithelial cancers are believed to originate from transformation of tissue stem cells. However, bone marrow-derived cells (BMDCs), which are frequently recruited to sites of tissue injury and inflammation, might also represent a potential source of malignancy. We show that although acute injury, acute inflammation, or transient parietal cell loss within the stomach do not lead to BMDC recruitment, chronic infection of C57BL/6 mice with Helicobacter, a known carcinogen, induces repopulation of the stomach with BMDCs. Subsequently, these cells progress through metaplasia and dysplasia to intraepithelial cancer. These findings suggest that epithelial cancers can originate from marrow-derived sources and thus have broad implications for the multistep model of cancer progression.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Houghton, Jeanmarie -- Stoicov, Calin -- Nomura, Sachiyo -- Rogers, Arlin B -- Carlson, Jane -- Li, Hanchen -- Cai, Xun -- Fox, James G -- Goldenring, James R -- Wang, Timothy C -- CA95103/CA/NCI NIH HHS/ -- K22 CA90518/CA/NCI NIH HHS/ -- R01 CA87958/CA/NCI NIH HHS/ -- R01 DK58/DK/NIDDK NIH HHS/ -- New York, N.Y. -- Science. 2004 Nov 26;306(5701):1568-71.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Medicine and Cancer Biology, University of Massachusetts Medical School, Worcester, MA 01605, USA. jeanmarie.houghton@umassmed.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15567866" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Apoptosis ; Bone Marrow Cells/*cytology ; Bone Marrow Transplantation ; Carcinoma in Situ/pathology ; Cell Differentiation ; Cell Fusion ; Disease Progression ; Female ; Gastric Mucosa/chemistry/pathology ; Gastritis/*pathology ; Helicobacter Infections/*pathology ; *Helicobacter felis ; Keratins/analysis ; Male ; Mesenchymal Stromal Cells/physiology ; Metaplasia ; Mice ; Mice, Inbred C57BL ; Mice, Transgenic ; Mucins/analysis ; Muscle Proteins/analysis ; Parietal Cells, Gastric/physiology ; Peptides/analysis ; Phenotype ; Stem Cells/*physiology ; Stomach Neoplasms/*pathology
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  • 68
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-03-16
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Ferster, David -- New York, N.Y. -- Science. 2004 Mar 12;303(5664):1619-21.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Neurobiology and Physiology, Northwestern University, Evanston, IL 60208-3520, USA. ferster@northwestern.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15016985" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Carbolines/pharmacology ; Cats ; Cues ; Diazepam/pharmacology ; Dominance, Ocular/*physiology ; Interneurons/physiology ; Mice ; Models, Neurological ; Mutation ; Neural Inhibition ; *Neuronal Plasticity ; Neurons/*physiology ; Protein Subunits ; Receptors, GABA-A/genetics/*physiology ; Synaptic Transmission ; Thalamus/growth & development/physiology ; Vision, Ocular ; Visual Cortex/anatomy & histology/*growth & development/*physiology ; Visual Pathways ; gamma-Aminobutyric Acid/physiology
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  • 69
    Publication Date: 2004-09-18
    Description: Features of chronic asthma include airway hyperresponsiveness, inflammatory infiltrates, and structural changes in the airways, termed remodeling. The contribution of eosinophils, cells associated with asthma and allergy, remains to be established. We show that in mice with a total ablation of the eosinophil lineage, increases in airway hyperresponsiveness and mucus secretion were similar to those observed in wild-type mice, but eosinophil-deficient mice were significantly protected from peribronchiolar collagen deposition and increases in airway smooth muscle. These data suggest that eosinophils contribute substantially to airway remodeling but are not obligatory for allergen-induced lung dysfunction, and support an important role for eosinophil-targeted therapies in chronic asthma.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Humbles, Alison A -- Lloyd, Clare M -- McMillan, Sarah J -- Friend, Daniel S -- Xanthou, Georgina -- McKenna, Erin E -- Ghiran, Sorina -- Gerard, Norma P -- Yu, Channing -- Orkin, Stuart H -- Gerard, Craig -- 087618/Wellcome Trust/United Kingdom -- AI39759/AI/NIAID NIH HHS/ -- HL10463/HL/NHLBI NIH HHS/ -- New York, N.Y. -- Science. 2004 Sep 17;305(5691):1776-9.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Pediatrics, Children's Hospital, Harvard Medical School, Boston, MA 02115, USA. alison.humbles@childrens.harvard.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15375268" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Asthma/immunology/*pathology/physiopathology ; Bronchi/pathology ; Cell Division ; Collagen/analysis ; Eosinophils/*physiology ; Interleukins/analysis ; Leukocyte Count ; Lung/immunology/*pathology/physiopathology ; Mice ; Mice, Inbred BALB C ; Mucus/secretion ; Muscle, Smooth/pathology ; Respiratory Function Tests ; Respiratory Hypersensitivity/immunology/pathology/physiopathology ; Th2 Cells/immunology ; Transforming Growth Factor beta/metabolism ; Transforming Growth Factor beta1
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  • 70
    Publication Date: 2004-10-23
    Description: Despite evidence that protein kinases are regulators of apoptosis, a specific role for phosphatases in regulating cell survival has not been established. Here we show that alpha4, a noncatalytic subunit of protein phosphatase 2A (PP2A), is required to repress apoptosis in murine cells. alpha4 is a nonredundant regulator of the dephosphorylation of the transcription factors c-Jun and p53. As a result of alpha4 deletion, multiple proapoptotic genes were transcribed. Either inhibition of new protein synthesis or Bcl-xL overexpression suppressed apoptosis initiated by alpha4 deletion. Thus, mammalian cell viability depends on repression of transcription-initiated apoptosis mediated by a component of PP2A.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Kong, Mei -- Fox, Casey J -- Mu, James -- Solt, Laura -- Xu, Anne -- Cinalli, Ryan M -- Birnbaum, Morris J -- Lindsten, Tullia -- Thompson, Craig B -- New York, N.Y. -- Science. 2004 Oct 22;306(5696):695-8.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Abramson Family Cancer Research Institute, University of Pennsylvania, Philadelphia, PA 19104, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15499020" target="_blank"〉PubMed〈/a〉
    Keywords: Adipocytes/cytology ; Animals ; *Apoptosis ; Cell Differentiation ; Cell Line ; Cell Survival ; Cells, Cultured ; Cycloheximide/pharmacology ; Gene Deletion ; Gene Expression Profiling ; Liver/cytology/metabolism ; Mice ; Mice, Transgenic ; Oligonucleotide Array Sequence Analysis ; PPAR gamma/metabolism ; Phosphoprotein Phosphatases/*metabolism ; Phosphoproteins/*metabolism ; Phosphorylation ; Protein Phosphatase 2 ; Protein Synthesis Inhibitors/pharmacology ; Proto-Oncogene Proteins c-bcl-2/metabolism ; Proto-Oncogene Proteins c-jun/metabolism ; Transcription, Genetic ; Tumor Suppressor Protein p53/metabolism ; bcl-X Protein
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  • 71
    Publication Date: 2004-02-14
    Description: Somatic cell nuclear transfer (SCNT) technology has recently been used to generate animals with a common genetic composition. In this study, we report the derivation of a pluripotent embryonic stem (ES) cell line (SCNT-hES-1) from a cloned human blastocyst. The SCNT-hES-1 cells displayed typical ES cell morphology and cell surface markers and were capable of differentiating into embryoid bodies in vitro and of forming teratomas in vivo containing cell derivatives from all three embryonic germ layers in severe combined immunodeficient mice. After continuous proliferation for more than 70 passages, SCNT-hES-1 cells maintained normal karyotypes and were genetically identical to the somatic nuclear donor cells. Although we cannot completely exclude the possibility that the cells had a parthenogenetic origin, imprinting analyses support a SCNT origin of the derived human ES cells.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Hwang, Woo Suk -- Ryu, Young June -- Park, Jong Hyuk -- Park, Eul Soon -- Lee, Eu Gene -- Koo, Ja Min -- Jeon, Hyun Yong -- Lee, Byeong Chun -- Kang, Sung Keun -- Kim, Sun Jong -- Ahn, Curie -- Hwang, Jung Hye -- Park, Ky Young -- Cibelli, Jose B -- Moon, Shin Yong -- New York, N.Y. -- Science. 2004 Mar 12;303(5664):1669-74. Epub 2004 Feb 12.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉College of Veterinary Medicine, Seoul National University, Seoul 151-742, Korea. hwangws@snu.ac.kr〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/14963337" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Biomarkers/analysis ; Blastocyst/*cytology ; Cell Differentiation ; *Cell Line ; *Cloning, Organism ; Culture Media ; Culture Techniques ; DNA Fingerprinting ; Embryo, Mammalian/*cytology ; Female ; Genomic Imprinting ; Humans ; Karyotyping ; Male ; Mice ; Mice, SCID ; Nuclear Transfer Techniques ; Oocyte Donation ; Ovarian Follicle/cytology ; Parthenogenesis ; Pluripotent Stem Cells/chemistry/*cytology ; Reverse Transcriptase Polymerase Chain Reaction ; Tandem Repeat Sequences ; Teratoma/etiology/pathology ; Testicular Neoplasms/etiology/pathology
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  • 72
    Publication Date: 2004-11-20
    Description: The development of a patterned vasculature is essential for normal organogenesis. We found that signaling by semaphorin 3E (Sema3E) and its receptor plexin-D1 controls endothelial cell positioning and the patterning of the developing vasculature in the mouse. Sema3E is highly expressed in developing somites, where it acts as a repulsive cue for plexin-D1-expressing endothelial cells of adjacent intersomitic vessels. Sema3E-plexin-D1 signaling did not require neuropilins, which were previously presumed to be obligate Sema3 coreceptors. Moreover, genetic ablation of Sema3E or plexin-D1 but not neuropilin-mediated Sema3 signaling disrupted vascular patterning. These findings reveal an unexpected semaphorin signaling pathway and define a mechanism for controlling vascular patterning.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Gu, Chenghua -- Yoshida, Yutaka -- Livet, Jean -- Reimert, Dorothy V -- Mann, Fanny -- Merte, Janna -- Henderson, Christopher E -- Jessell, Thomas M -- Kolodkin, Alex L -- Ginty, David D -- CA23767-24/CA/NCI NIH HHS/ -- MH59199-06/MH/NIMH NIH HHS/ -- New York, N.Y. -- Science. 2005 Jan 14;307(5707):265-8. Epub 2004 Nov 18.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, MD 21205-2185, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15550623" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Binding Sites ; Blood Vessels/*embryology/metabolism ; Body Patterning ; COS Cells ; Cercopithecus aethiops ; Chick Embryo ; Endothelial Cells/cytology/physiology ; Endothelium, Vascular/cytology/embryology ; Glycoproteins/*metabolism ; In Situ Hybridization ; Ligands ; Membrane Glycoproteins/*metabolism ; Membrane Proteins/*metabolism ; Mice ; Morphogenesis ; Mutation ; Nerve Tissue Proteins/*metabolism ; Neuropilin-1/metabolism ; Neuropilin-2/metabolism ; Phenotype ; Protein Binding ; Recombinant Fusion Proteins/metabolism ; Signal Transduction ; Somites/*metabolism ; Transfection
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    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 73
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-12-18
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Hug, Christopher -- Lodish, Harvey F -- New York, N.Y. -- Science. 2005 Jan 21;307(5708):366-7. Epub 2004 Dec 16.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Whitehead Institute for Biomedical Research, Cambridge, MA 02142, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15604359" target="_blank"〉PubMed〈/a〉
    Keywords: Adipocytes/metabolism ; Adipose Tissue/*metabolism ; Animals ; Blood Glucose/analysis ; Cytokines/blood/genetics/*metabolism ; Diabetes Mellitus, Experimental/metabolism ; Diabetes Mellitus, Type 2/metabolism ; Female ; Gene Targeting ; Glucose/metabolism ; Hepatocytes/metabolism ; Humans ; Insulin/blood/metabolism ; Mice ; Mice, Obese ; Molecular Mimicry ; Muscle Cells/metabolism ; Nicotinamide Phosphoribosyltransferase ; Receptor, Insulin/metabolism ; Recombinant Proteins/metabolism ; Subcutaneous Tissue ; Viscera
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  • 74
    Publication Date: 2004-12-04
    Description: The degradation of undesirable cellular components or organelles, including invading microbes, by autophagy is crucial for cell survival. Here, Shigella, an invasive bacteria, was found to be able to escape autophagy by secreting IcsB by means of the type III secretion system. Mutant bacteria lacking IcsB were trapped by autophagy during multiplication within the host cells. IcsB did not directly inhibit autophagy. Rather, Shigella VirG, a protein required for intracellular actin-based motility, induced autophagy by binding to the autophagy protein, Atg5. In nonmutant Shigella, this binding is competitively inhibited by IcsB binding to VirG.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Ogawa, Michinaga -- Yoshimori, Tamotsu -- Suzuki, Toshihiko -- Sagara, Hiroshi -- Mizushima, Noboru -- Sasakawa, Chihiro -- New York, N.Y. -- Science. 2005 Feb 4;307(5710):727-31. Epub 2004 Dec 2.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Microbiology and Immunology, Institute of Medical Science, University of Tokyo, 4-6-1, Shirokanedai, Minato-ku, Tokyo 108-8639, Japan.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15576571" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; *Autophagy ; Bacterial Proteins/genetics/*metabolism ; Cell Line ; DNA-Binding Proteins/*metabolism ; Humans ; Mice ; Mice, Knockout ; Microscopy, Electron ; Microtubule-Associated Proteins/metabolism ; Phagosomes/metabolism/*microbiology/ultrastructure ; Protein Binding ; Recombinant Fusion Proteins/metabolism ; Shigella flexneri/genetics/growth & development/metabolism/*pathogenicity ; Transcription Factors/*metabolism
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  • 75
    Publication Date: 2004-04-24
    Description: How can neural activity propagate through cortical networks built with weak, stochastic synapses? We find precise repetitions of spontaneous patterns of synaptic inputs in neocortical neurons in vivo and in vitro. These patterns repeat after minutes, maintaining millisecond accuracy. Calcium imaging of slices reveals reactivation of sequences of cells during the occurrence of repeated intracellular synaptic patterns. The spontaneous activity drifts with time, engaging different cells. Sequences of active neurons have distinct spatial structures and are repeated in the same order over tens of seconds, revealing modular temporal dynamics. Higher order sequences are replayed with compressed timing.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Ikegaya, Yuji -- Aaron, Gloster -- Cossart, Rosa -- Aronov, Dmitriy -- Lampl, Ilan -- Ferster, David -- Yuste, Rafael -- New York, N.Y. -- Science. 2004 Apr 23;304(5670):559-64.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Biological Sciences, Columbia University, New York, NY 10027, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15105494" target="_blank"〉PubMed〈/a〉
    Keywords: 2,3,4,5-Tetrahydro-7,8-dihydroxy-1-phenyl-1H-3-benzazepine/pharmacology ; 2-Amino-5-phosphonovalerate/pharmacology ; Action Potentials ; Animals ; Benzazepines/pharmacology ; Calcium/metabolism ; Cats ; Excitatory Postsynaptic Potentials ; In Vitro Techniques ; Mice ; Mice, Inbred C57BL ; Microscopy, Confocal ; Nerve Net/physiology ; Neurons/*physiology ; Patch-Clamp Techniques ; Prefrontal Cortex/cytology/*physiology ; Pyramidal Cells/physiology ; Receptors, Dopamine D1/physiology ; Receptors, N-Methyl-D-Aspartate/physiology ; Synapses/physiology ; *Synaptic Transmission ; Time Factors ; Visual Cortex/cytology/*physiology
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  • 76
    Publication Date: 2004-08-07
    Description: Vesicle fusion involves vesicle tethering, docking, and membrane merger. We show that mitofusin, an integral mitochondrial membrane protein, is required on adjacent mitochondria to mediate fusion, which indicates that mitofusin complexes act in trans (that is, between adjacent mitochondria). A heptad repeat region (HR2) mediates mitofusin oligomerization by assembling a dimeric, antiparallel coiled coil. The transmembrane segments are located at opposite ends of the 95 angstrom coiled coil and provide a mechanism for organelle tethering. Consistent with this proposal, truncated mitofusin, in an HR2-dependent manner, causes mitochondria to become apposed with a uniform gap. Our results suggest that HR2 functions as a mitochondrial tether before fusion.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Koshiba, Takumi -- Detmer, Scott A -- Kaiser, Jens T -- Chen, Hsiuchen -- McCaffery, J Michael -- Chan, David C -- R01 GM62967/GM/NIGMS NIH HHS/ -- S10 RR019409-01/RR/NCRR NIH HHS/ -- New York, N.Y. -- Science. 2004 Aug 6;305(5685):858-62.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Division of Biology, California Institute of Technology, 1200 East California Boulevard, MC114-96, Pasadena, CA 91125, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15297672" target="_blank"〉PubMed〈/a〉
    Keywords: Amino Acid Sequence ; Amino Acid Substitution ; Animals ; Cell Line ; Crystallography, X-Ray ; Dimerization ; GTP Phosphohydrolases/*chemistry/*metabolism ; Humans ; Hybrid Cells ; Hydrophobic and Hydrophilic Interactions ; Intracellular Membranes/physiology/ultrastructure ; Membrane Fusion ; Mice ; Mitochondria/*metabolism/ultrastructure ; Models, Molecular ; Molecular Sequence Data ; Mutation ; Protein Structure, Secondary ; Protein Structure, Tertiary
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  • 77
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-01-06
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Marx, Jean -- New York, N.Y. -- Science. 2004 Jan 2;303(5654):23-5.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/14704399" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Antineoplastic Agents/metabolism/*pharmacology/therapeutic use ; Crystallography, X-Ray ; Drug Design ; Genes, p53 ; Humans ; Imidazoles/metabolism/*pharmacology/therapeutic use ; Mice ; Neoplasms, Experimental/*drug therapy/pathology ; *Nuclear Proteins ; Piperazines/metabolism/*pharmacology/therapeutic use ; Protein Binding ; Proto-Oncogene Proteins/chemistry/*metabolism ; Proto-Oncogene Proteins c-mdm2 ; Tumor Suppressor Protein p53/chemistry/*metabolism
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    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 78
    Publication Date: 2004-09-14
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Service, Robert F -- New York, N.Y. -- Science. 2004 Sep 10;305(5690):1559.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15361603" target="_blank"〉PubMed〈/a〉
    Keywords: Alzheimer Disease/pathology ; Animals ; *Blood-Brain Barrier ; Brain/*anatomy & histology/metabolism/pathology ; Humans ; Magnetic Resonance Imaging/*methods ; Mice ; Stilbenes/*metabolism
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  • 79
    Publication Date: 2004-10-09
    Description: We report that Id knockout mouse embryos display multiple cardiac defects, but mid-gestation lethality is rescued by the injection of 15 wild-type embryonic stem (ES) cells into mutant blastocysts. Myocardial markers altered in Id mutant cells are restored to normal throughout the chimeric myocardium. Intraperitoneal injection of ES cells into female mice before conception also partially rescues the cardiac phenotype with no incorporation of ES cells. Insulin-like growth factor 1, a long-range secreted factor, in combination with WNT5a, a locally secreted factor, likely account for complete reversion of the cardiac phenotype. Thus, ES cells have the potential to reverse congenital defects through Id-dependent local and long-range effects in a mammalian embryo.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1351017/" target="_blank"〉〈img src="https://static.pubmed.gov/portal/portal3rc.fcgi/4089621/img/3977009" border="0"〉〈/a〉   〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1351017/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Fraidenraich, Diego -- Stillwell, Elizabeth -- Romero, Elizabeth -- Wilkes, David -- Manova, Katia -- Basson, Craig T -- Benezra, Robert -- K01 HL076568/HL/NHLBI NIH HHS/ -- KO1HL076568/HL/NHLBI NIH HHS/ -- R01 CA107429/CA/NCI NIH HHS/ -- R01CA107429/CA/NCI NIH HHS/ -- New York, N.Y. -- Science. 2004 Oct 8;306(5694):247-52.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Cancer Biology and Genetics Program, Department of Medicine, Weill Medical College of Cornell University, New York, NY 10021, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15472070" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Blastocyst ; Cell Division ; Cells, Cultured ; DNA-Binding Proteins/genetics ; Embryo Loss ; Embryo, Mammalian/*cytology ; Female ; Gene Expression Profiling ; Gene Expression Regulation, Developmental ; Heart/*embryology ; Heart Defects, Congenital/embryology/*therapy ; Inhibitor of Differentiation Protein 1 ; Inhibitor of Differentiation Protein 2 ; Insulin-Like Growth Factor I/genetics/physiology ; Maternal-Fetal Exchange ; Mice ; Mice, Knockout ; Myocardium/cytology/metabolism ; Myocytes, Cardiac/cytology ; Oligonucleotide Array Sequence Analysis ; Pericardium/embryology/metabolism ; Pregnancy ; Proto-Oncogene Proteins/genetics/physiology ; Repressor Proteins/genetics ; *Stem Cell Transplantation ; Stem Cells/*physiology ; Transcription Factors/genetics ; Wnt Proteins
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  • 80
    Publication Date: 2004-05-01
    Description: Vesicular glutamate transporters (VGLUTs) 1 and 2 show a mutually exclusive distribution in the adult brain that suggests specialization for synapses with different properties of release. Consistent with this distribution, inactivation of the VGLUT1 gene silenced a subset of excitatory neurons in the adult. However, the same cell populations exhibited VGLUT1-independent transmission early in life. Developing hippocampal neurons transiently coexpressed VGLUT2 and VGLUT1 at distinct synaptic sites with different short-term plasticity. The loss of VGLUT1 also reduced the reserve pool of synaptic vesicles. Thus, VGLUT1 plays an unanticipated role in membrane trafficking at the nerve terminal.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Fremeau, Robert T Jr -- Kam, Kaiwen -- Qureshi, Tayyaba -- Johnson, Juliette -- Copenhagen, David R -- Storm-Mathisen, Jon -- Chaudhry, Farrukh A -- Nicoll, Roger A -- Edwards, Robert H -- R01 EY001869/EY/NEI NIH HHS/ -- New York, N.Y. -- Science. 2004 Jun 18;304(5678):1815-9. Epub 2004 Apr 29.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Neurology, Graduate Programs in Neuroscience and Cell Biology, University of California San Francisco School of Medicine, CA 94143, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15118123" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Animals, Newborn ; Brain/cytology/*metabolism ; Carrier Proteins/genetics/*metabolism ; Cell Membrane/physiology ; Cells, Cultured ; Cerebellum/metabolism/ultrastructure ; Excitatory Postsynaptic Potentials ; Glutamic Acid/metabolism ; Hippocampus/cytology/metabolism/ultrastructure ; In Situ Hybridization ; *Membrane Transport Proteins ; Mice ; Mice, Knockout ; Nerve Tissue Proteins/metabolism ; Neurons/*metabolism/physiology ; Patch-Clamp Techniques ; Purkinje Cells/physiology ; Pyramidal Cells/metabolism ; Synapses/*metabolism/ultrastructure ; *Synaptic Transmission ; Synaptic Vesicles/*metabolism/physiology ; Vesicular Glutamate Transport Protein 1 ; Vesicular Glutamate Transport Protein 2 ; *Vesicular Transport Proteins
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  • 81
    Publication Date: 2004-07-03
    Description: The hippocampus is crucial for spatial memory formation, yet it does not store long-lasting memories. By combining functional brain imaging and region-specific neuronal inactivation in mice, we identified prefrontal and anterior cingulate cortices as critical for storage and retrieval of remote spatial memories [correction]. Imaging of activity-dependent genes also revealed an involvement of parietal and retrosplenial cortices during consolidation of remote memory. Long-term memory storage within some of these neocortical regions was accompanied by structural changes including synaptogenesis and laminar reorganization, concomitant with a functional disengagement of the hippocampus and posterior cingulate cortex [correction]. Thus, consolidation of spatial memory requires a time-dependent hippocampal-cortical dialogue, ultimately enabling widespread cortical networks to mediate effortful recall and use of cortically stored remote memories independently.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Maviel, Thibault -- Durkin, Thomas P -- Menzaghi, Frederique -- Bontempi, Bruno -- New York, N.Y. -- Science. 2004 Jul 2;305(5680):96-9.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Laboratoire de Neurosciences Cognitives, CNRS UMR 5106, Universite de Bordeaux 1, Avenue des Facultes, 33405 Talence, France.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15232109" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Brain Mapping ; GAP-43 Protein/metabolism ; Gene Expression Regulation ; Genes, Immediate-Early ; Gyrus Cinguli/*physiology ; Immediate-Early Proteins/metabolism ; Lidocaine/pharmacology ; Male ; Memory/drug effects/*physiology ; Mental Recall ; Mice ; Mice, Inbred C57BL ; Neocortex/*physiology ; Nerve Net/physiology ; Neuronal Plasticity ; Neurons/physiology ; Parietal Lobe/physiology ; Prefrontal Cortex/*physiology ; Synapses/physiology ; Time Factors
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  • 82
    Publication Date: 2004-11-13
    Description: Elucidating the transcribed regions of the genome constitutes a fundamental aspect of human biology, yet this remains an outstanding problem. To comprehensively identify coding sequences, we constructed a series of high-density oligonucleotide tiling arrays representing sense and antisense strands of the entire nonrepetitive sequence of the human genome. Transcribed sequences were located across the genome via hybridization to complementary DNA samples, reverse-transcribed from polyadenylated RNA obtained from human liver tissue. In addition to identifying many known and predicted genes, we found 10,595 transcribed sequences not detected by other methods. A large fraction of these are located in intergenic regions distal from previously annotated genes and exhibit significant homology to other mammalian proteins.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Bertone, Paul -- Stolc, Viktor -- Royce, Thomas E -- Rozowsky, Joel S -- Urban, Alexander E -- Zhu, Xiaowei -- Rinn, John L -- Tongprasit, Waraporn -- Samanta, Manoj -- Weissman, Sherman -- Gerstein, Mark -- Snyder, Michael -- P50 HG02357/HG/NHGRI NIH HHS/ -- New York, N.Y. -- Science. 2004 Dec 24;306(5705):2242-6. Epub 2004 Nov 11.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Molecular, Cellular, and Developmental Biology, Yale University, New Haven, CT 06520-8103, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15539566" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Base Sequence ; Computational Biology ; Conserved Sequence ; CpG Islands ; DNA, Complementary ; DNA, Intergenic ; Databases, Genetic ; Exons ; *Genome, Human ; Humans ; Introns ; Mice ; Nucleic Acid Hybridization ; Oligonucleotide Array Sequence Analysis/*methods ; Oligonucleotide Probes ; Proteins/chemistry/genetics ; RNA, Messenger/genetics ; Reproducibility of Results ; Reverse Transcriptase Polymerase Chain Reaction ; Sequence Homology, Nucleic Acid ; *Transcription, Genetic
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  • 83
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-04-10
    Description: Invasive bacteria actively induce their own uptake by phagocytosis in normally nonphagocytic cells and then either establish a protected niche within which they survive and replicate, or disseminate from cell to cell by means of an actin-based motility process. The mechanisms underlying bacterial entry, phagosome maturation, and dissemination reveal common strategies as well as unique tactics evolved by individual species to establish infection.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Cossart, Pascale -- Sansonetti, Philippe J -- New York, N.Y. -- Science. 2004 Apr 9;304(5668):242-8.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Unite des Interactions Bacteries-Cellules, INSERM Unite 604, Departement de Biologie Cellulaire et Infection, Institut Pasteur, 28 Rue du Docteur Roux, Paris 75015, France. pcossart@pasteur.fr〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15073367" target="_blank"〉PubMed〈/a〉
    Keywords: Actins/physiology ; Animals ; Bacteria/growth & development/*pathogenicity ; Bacterial Adhesion ; *Bacterial Physiological Phenomena ; Bacterial Proteins/metabolism ; Cytosol/microbiology ; Enterobacteriaceae/*pathogenicity/physiology ; Epithelial Cells/*microbiology/physiology ; Humans ; Intestinal Mucosa/*microbiology/physiology ; Listeria monocytogenes/*pathogenicity/physiology ; Mice ; Models, Biological ; Movement ; Phagocytosis ; Phagosomes/microbiology/physiology ; Vacuoles/microbiology
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  • 84
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-06-12
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Pennisi, Elizabeth -- New York, N.Y. -- Science. 2004 Jun 11;304(5677):1590-1.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15192196" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; *Conserved Sequence ; DNA, Intergenic/*physiology ; Embryo, Mammalian/cytology ; Embryo, Nonmammalian ; Fishes/genetics ; Humans ; Mice ; Mice, Transgenic ; Regulatory Sequences, Nucleic Acid ; Stem Cells
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  • 85
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-11-20
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Couzin, Jennifer -- New York, N.Y. -- Science. 2004 Nov 19;306(5700):1277.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15550635" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Arteriosclerosis/*etiology/prevention & control ; Cyclooxygenase 2 ; Cyclooxygenase 2 Inhibitors ; Cyclooxygenase Inhibitors/adverse effects/therapeutic use ; Disease Susceptibility ; Epoprostenol/biosynthesis ; Estrogens/administration & dosage/*pharmacology/*physiology ; Female ; Humans ; Isoenzymes/*metabolism ; Male ; Membrane Proteins ; Mice ; Oxidative Stress/drug effects ; Prostaglandin-Endoperoxide Synthases/*metabolism ; Receptors, Epoprostenol/genetics/metabolism ; *Sex Characteristics
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    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 86
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-07-03
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Vogel, Gretchen -- New York, N.Y. -- Science. 2004 Jul 2;305(5680):27.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15232079" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Bone Marrow Cells/*physiology ; *Bone Marrow Transplantation ; Cell Differentiation ; Cell Fusion ; Epithelial Cells/*cytology/metabolism ; Female ; Green Fluorescent Proteins ; Luminescent Proteins/analysis ; Male ; Mice ; Recombinases/metabolism ; Stem Cells/cytology/*physiology ; Y Chromosome
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  • 87
    Publication Date: 2004-04-03
    Description: Neural stem cells are reported to lie in a vascular niche, but there is no direct evidence for a functional relationship between the stem cells and blood vessel component cells. We show that endothelial cells but not vascular smooth muscle cells release soluble factors that stimulate the self-renewal of neural stem cells, inhibit their differentiation, and enhance their neuron production. Both embryonic and adult neural stem cells respond, allowing extensive production of both projection neuron and interneuron types in vitro. Endothelial coculture stimulates neuroepithelial cell contact, activating Notch and Hes 1 to promote self-renewal. These findings identify endothelial cells as a critical component of the neural stem cell niche.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Shen, Qin -- Goderie, Susan K -- Jin, Li -- Karanth, Nithin -- Sun, Yu -- Abramova, Natalia -- Vincent, Peter -- Pumiglia, Kevin -- Temple, Sally -- R01 CA081419/CA/NCI NIH HHS/ -- New York, N.Y. -- Science. 2004 May 28;304(5675):1338-40. Epub 2004 Apr 1.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Center for Neuropharmacology and Neuroscience, Albany Medical College, Albany, NY 12208, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15060285" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Astrocytes/cytology/physiology ; Cattle ; Cell Adhesion ; *Cell Communication ; Cell Differentiation ; Cell Division ; Cell Line ; Cell Lineage ; Cells, Cultured ; Cerebral Cortex/embryology ; Clone Cells/physiology ; Coculture Techniques ; Embryo, Mammalian/cytology ; Endothelial Cells/cytology/*physiology ; Endothelium, Vascular/cytology ; Fibroblast Growth Factor 2/pharmacology ; Mice ; Muscle, Smooth, Vascular/cytology/physiology ; Myocytes, Smooth Muscle/cytology/physiology ; Neurons/cytology/*physiology ; Oligodendroglia/cytology/physiology ; Signal Transduction ; Stem Cells/cytology/*physiology
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  • 88
    Publication Date: 2004-06-19
    Description: Exposure of naive B cells to the cytokine interleukin-4 (IL-4) and/or antigen leads to a state of "priming," in which subsequent aggregation of major histocompatibility complex class II molecules induces the mobilization of calcium ions and cell proliferation. However, it is not clear how critical this priming is for immune responses or how it is normally induced in vivo. Injection of mice with the commonly used adjuvant alum led to priming of splenic B cells and to the accumulation in the spleen of a previously unknown population of IL-4-producing, Gr1+ cells. These cells and IL-4 were both required for in vivo priming and expansion of antigen-specific B cells, as well as for optimal production of antibody. These studies reveal a key role for a previously unknown accessory myeloid cell population in the generation of humoral immune responses.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Jordan, Michael B -- Mills, David M -- Kappler, John -- Marrack, Philippa -- Cambier, John C -- AI-17134/AI/NIAID NIH HHS/ -- AI-18785/AI/NIAID NIH HHS/ -- AI-20519/AI/NIAID NIH HHS/ -- AI-22295/AI/NIAID NIH HHS/ -- AI-50802/AI/NIAID NIH HHS/ -- AI-52225/AI/NIAID NIH HHS/ -- New York, N.Y. -- Science. 2004 Jun 18;304(5678):1808-10.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Integrated Department of Immunology, National Jewish Medical and Research Center, University of Colorado Health Sciences Center, 1400 Jackson Street, Denver, CO 80206, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15205534" target="_blank"〉PubMed〈/a〉
    Keywords: *Adjuvants, Immunologic ; Adoptive Transfer ; *Alum Compounds/administration & dosage ; Animals ; B-Lymphocytes/*immunology ; Calcium/metabolism ; Cell Separation ; Cells, Cultured ; Coculture Techniques ; Eosinophils/cytology/immunology ; Freund's Adjuvant ; Granulocyte-Macrophage Colony-Stimulating Factor/pharmacology ; Histocompatibility Antigens Class II/immunology ; Immunization ; Interleukin-4/immunology/metabolism ; Lymphocyte Activation ; Mice ; Mice, Inbred C57BL ; Myeloid Cells/*immunology ; Nitrophenols/immunology ; Serum Albumin, Bovine/immunology ; Signal Transduction ; Spleen/cytology/immunology
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  • 89
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-05-08
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Couzin, Jennifer -- New York, N.Y. -- Science. 2004 May 7;304(5672):816-7.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15131283" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Blueberry Plant ; *Clinical Trials as Topic ; Creatine/administration & dosage/therapeutic use ; Cysteamine/administration & dosage/therapeutic use ; Drug Therapy, Combination ; Drug Therapy, Computer-Assisted ; Fatty Acids, Omega-3/administration & dosage/therapeutic use ; Humans ; Huntington Disease/*drug therapy ; Mice ; Patient Selection ; Phytotherapy ; Plant Extracts/administration & dosage/therapeutic use ; Software ; Trehalose/administration & dosage/therapeutic use ; Ubiquinone/administration & dosage/therapeutic use
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  • 90
    Publication Date: 2004-11-13
    Description: Variant Creutzfeldt-Jakob disease (vCJD) is a unique and highly distinctive clinicopathological and molecular phenotype of human prion disease associated with infection with bovine spongiform encephalopathy (BSE)-like prions. Here, we found that generation of this phenotype in transgenic mice required expression of human prion protein (PrP) with methionine 129. Expression of human PrP with valine 129 resulted in a distinct phenotype and, remarkably, persistence of a barrier to transmission of BSE-derived prions on subpassage. Polymorphic residue 129 of human PrP dictated propagation of distinct prion strains after BSE prion infection. Thus, primary and secondary human infection with BSE-derived prions may result in sporadic CJD-like or novel phenotypes in addition to vCJD, depending on the genotype of the prion source and the recipient.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Wadsworth, Jonathan D F -- Asante, Emmanuel A -- Desbruslais, Melanie -- Linehan, Jacqueline M -- Joiner, Susan -- Gowland, Ian -- Welch, Julie -- Stone, Lisa -- Lloyd, Sarah E -- Hill, Andrew F -- Brandner, Sebastian -- Collinge, John -- New York, N.Y. -- Science. 2004 Dec 3;306(5702):1793-6. Epub 2004 Nov 11.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Medical Research Council (MRC) Prion Unit and Department of Neurodegenerative Disease, Institute of Neurology, University College London, Queen Square, London WC1N 3BG, UK.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15539564" target="_blank"〉PubMed〈/a〉
    Keywords: Amyloid/genetics ; Animals ; Brain/pathology ; Cattle ; Creutzfeldt-Jakob Syndrome/genetics/*metabolism/*pathology/transmission ; Encephalopathy, Bovine Spongiform/pathology/transmission ; Humans ; Methionine ; Mice ; Mice, Transgenic ; Phenotype ; Polymorphism, Genetic ; PrPC Proteins/chemistry/*genetics/metabolism ; PrPSc Proteins/metabolism/*pathogenicity ; Prions ; Protein Conformation ; Protein Precursors/genetics ; *Valine
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  • 91
    Publication Date: 2004-01-24
    Description: Neural progenitor cells were encapsulated in vitro within a three-dimensional network of nanofibers formed by self-assembly of peptide amphiphile molecules. The self-assembly is triggered by mixing cell suspensions in media with dilute aqueous solutions of the molecules, and cells survive the growth of the nanofibers around them. These nanofibers were designed to present to cells the neurite-promoting laminin epitope IKVAV at nearly van der Waals density. Relative to laminin or soluble peptide, the artificial nanofiber scaffold induced very rapid differentiation of cells into neurons, while discouraging the development of astrocytes. This rapid selective differentiation is linked to the amplification of bioactive epitope presentation to cells by the nanofibers.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Silva, Gabriel A -- Czeisler, Catherine -- Niece, Krista L -- Beniash, Elia -- Harrington, Daniel A -- Kessler, John A -- Stupp, Samuel I -- NS20013/NS/NINDS NIH HHS/ -- NS20778/NS/NINDS NIH HHS/ -- NS34758/NS/NINDS NIH HHS/ -- New York, N.Y. -- Science. 2004 Feb 27;303(5662):1352-5. Epub 2004 Jan 22.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Institute for Bioengineering and Nanoscience in Advanced Medicine, Northwestern University, Chicago, IL 60611, USA. gsilva@ucsd.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/14739465" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Astrocytes/cytology ; *Cell Differentiation ; Cell Movement ; Cell Survival ; Cells, Cultured ; Diffusion ; Epitopes ; Glial Fibrillary Acidic Protein/analysis ; Hydrogen Bonding ; Hydrophobic and Hydrophilic Interactions ; Laminin/administration & dosage/chemistry/immunology/*metabolism ; Mice ; *Nanotechnology ; Neurites/physiology/ultrastructure ; Neurons/*cytology/physiology ; Peptide Fragments/administration & dosage/chemistry/*metabolism ; Rats ; Spinal Cord ; Stem Cells/*cytology/physiology ; Tubulin/analysis
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  • 92
    Publication Date: 2004-05-25
    Description: Pathogenic mycobacteria resist lysosomal delivery after uptake into macrophages, allowing them to survive intracellularly. We found that the eukaryotic-like serine/threonine protein kinase G from pathogenic mycobacteria was secreted within macrophage phagosomes, inhibiting phagosome-lysosome fusion and mediating intracellular survival of mycobacteria. Inactivation of protein kinase G by gene disruption or chemical inhibition resulted in lysosomal localization and mycobacterial cell death in infected macrophages. Besides identifying a target for the control of mycobacterial infections, these findings suggest that pathogenic mycobacteria have evolved eukaryotic-like signal transduction mechanisms capable of modulating host cell trafficking pathways.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Walburger, Anne -- Koul, Anil -- Ferrari, Giorgio -- Nguyen, Liem -- Prescianotto-Baschong, Cristina -- Huygen, Kris -- Klebl, Bert -- Thompson, Charles -- Bacher, Gerald -- Pieters, Jean -- New York, N.Y. -- Science. 2004 Jun 18;304(5678):1800-4. Epub 2004 May 20.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Biozentrum, University of Basel, Klingelbergstr. 50/70, CH-4056 Basel, Switzerland.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15155913" target="_blank"〉PubMed〈/a〉
    Keywords: Amides/pharmacology ; Animals ; Cell Line ; Cyclic GMP-Dependent Protein Kinases/antagonists & ; inhibitors/genetics/*metabolism ; Enzyme Inhibitors/pharmacology ; Gene Deletion ; Lysosomes/microbiology/physiology ; Macrophages/drug effects/*microbiology/ultrastructure ; Mice ; Mycobacterium bovis/drug effects/*enzymology/*growth & development/pathogenicity ; Mycobacterium smegmatis/enzymology/genetics/pathogenicity/physiology ; Mycobacterium tuberculosis/drug effects/enzymology/growth & ; development/pathogenicity ; Phagosomes/enzymology/*microbiology/physiology ; Signal Transduction ; Thiophenes/pharmacology ; Vacuoles/microbiology
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  • 93
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-10-23
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Kaiser, Jocelyn -- New York, N.Y. -- Science. 2004 Oct 22;306(5696):591.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15498981" target="_blank"〉PubMed〈/a〉
    Keywords: Acetamides/therapeutic use ; Animals ; Antiviral Agents/therapeutic use ; *Containment of Biohazards ; Genetic Engineering ; Guidelines as Topic ; Humans ; Influenza A virus/genetics/*pathogenicity ; Influenza Vaccines ; Influenza, Human/prevention & control/virology ; Mice ; Oseltamivir ; United States
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  • 94
    Publication Date: 2004-03-27
    Description: The mammalian cerebral cortex is characterized by complex patterns of anatomical and functional areas that differ markedly between species, but the molecular basis for this functional subdivision is largely unknown. Here, we show that mutations in GPR56, which encodes an orphan G protein-coupled receptor (GPCR) with a large extracellular domain, cause a human brain cortical malformation called bilateral frontoparietal polymicrogyria (BFPP). BFPP is characterized by disorganized cortical lamination that is most severe in frontal cortex. Our data suggest that GPCR signaling plays an essential role in regional development of human cerebral cortex.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Piao, Xianhua -- Hill, R Sean -- Bodell, Adria -- Chang, Bernard S -- Basel-Vanagaite, Lina -- Straussberg, Rachel -- Dobyns, William B -- Qasrawi, Bassam -- Winter, Robin M -- Innes, A Micheil -- Voit, Thomas -- Ross, M Elizabeth -- Michaud, Jacques L -- Descarie, Jean-Claude -- Barkovich, A James -- Walsh, Christopher A -- HD07466/HD/NICHD NIH HHS/ -- K08 NS045762-01A1/NS/NINDS NIH HHS/ -- R37 NS35129/NS/NINDS NIH HHS/ -- New York, N.Y. -- Science. 2004 Mar 26;303(5666):2033-6.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Howard Hughes Medical Institute, Beth Israel Deaconess Medical Center, and Department of Neurology, Harvard Medical School, Boston, MA 02115, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15044805" target="_blank"〉PubMed〈/a〉
    Keywords: Amino Acid Substitution ; Animals ; Antisense Elements (Genetics) ; Biological Evolution ; Body Patterning ; Cerebral Cortex/*abnormalities/embryology ; Cerebral Ventricles/cytology/embryology ; Female ; Frameshift Mutation ; Frontal Lobe/*abnormalities/embryology ; Gene Order ; Humans ; Ligands ; Male ; Mice ; Mutation, Missense ; Neurons/physiology ; Parietal Lobe/abnormalities/embryology ; Receptors, G-Protein-Coupled/chemistry/*genetics/metabolism/*physiology ; Sequence Deletion ; Sequence Homology, Amino Acid ; Signal Transduction ; Stem Cells/physiology
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  • 95
    Publication Date: 2004-09-14
    Description: Although bacteria use different iron compounds in vitGro, the possibility that microbes distinguish between these iron sources during infection has hitherto not been examined. We applied stable isotope labeling to detect source-specific iron by mass spectrometry and show that Staphylococcus aureus preferentially imports heme iron over transferrin iron. By combining this approach with computational genome analysis, we identified hts (heme transport system), a gene cluster that promotes preferred heme iron import by S. aureus. Heme iron scavenging by means of hts is required for staphylococcal pathogenesis in animal hosts, indicating that heme iron is the preferred iron source during the initiation of infection.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Skaar, Eric P -- Humayun, Munir -- Bae, Taeok -- DeBord, Kristin L -- Schneewind, Olaf -- AI52474/AI/NIAID NIH HHS/ -- New York, N.Y. -- Science. 2004 Sep 10;305(5690):1626-8.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Committee on Microbiology, 920 East 58th Street, University of Chicago, Chicago, IL 60637, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15361626" target="_blank"〉PubMed〈/a〉
    Keywords: ATP-Binding Cassette Transporters/genetics/*metabolism ; Abscess/microbiology ; Animals ; Bacterial Proteins/genetics/metabolism ; Biological Transport ; Caenorhabditis elegans/microbiology ; Carrier Proteins/genetics/metabolism ; Cell Membrane/metabolism ; Computational Biology ; Cytoplasm/metabolism ; Genes, Bacterial ; Genome, Bacterial ; Heme/*metabolism ; Hemin/metabolism ; Humans ; Iron/*metabolism ; Iron Isotopes ; Kidney/microbiology ; Liver/microbiology ; Mass Spectrometry ; Mice ; Mice, Inbred BALB C ; Mutagenesis, Insertional ; Operon ; Staphylococcal Infections/*microbiology ; Staphylococcus aureus/genetics/growth & development/*metabolism/pathogenicity ; Transferrin/metabolism
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  • 96
    Publication Date: 2004-06-26
    Description: Arrestin regulates almost all G protein-coupled receptor (GPCR)-mediated signaling and trafficking. We report that the multidomain protein, spinophilin, antagonizes these multiple arrestin functions. Through blocking G protein receptor kinase 2 (GRK2) association with receptor-Gbetagamma complexes, spinophilin reduces arrestin-stabilized receptor phosphorylation, receptor endocytosis, and the acceleration of mitogen-activated protein kinase (MAPK) activity following endocytosis. Spinophilin knockout mice were more sensitive than wild-type mice to sedation elicited by stimulation of alpha2 adrenergic receptors, whereas arrestin 3 knockout mice were more resistant, indicating that the signal-promoting, rather than the signal-terminating, roles of arrestin are more important for certain response pathways. The reciprocal interactions of GPCRs with spinophilin and arrestin represent a regulatory mechanism for fine-tuning complex receptor-orchestrated cell signaling and responses.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Wang, Qin -- Zhao, Jiali -- Brady, Ashley E -- Feng, Jian -- Allen, Patrick B -- Lefkowitz, Robert J -- Greengard, Paul -- Limbird, Lee E -- DA10044/DA/NIDA NIH HHS/ -- DK43879/DK/NIDDK NIH HHS/ -- HL16037/HL/NHLBI NIH HHS/ -- HL42671/HL/NHLBI NIH HHS/ -- MH40899/MH/NIMH NIH HHS/ -- New York, N.Y. -- Science. 2004 Jun 25;304(5679):1940-4.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Pharmacology and Center of Molecular Neuroscience, Vanderbilt University Medical Center, Nashville, TN 37232, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15218143" target="_blank"〉PubMed〈/a〉
    Keywords: Adenosine/*analogs & derivatives/pharmacology ; Adrenergic alpha-Agonists/pharmacology ; Animals ; Arrestin/*antagonists & inhibitors/*metabolism ; Arrestins/genetics/metabolism ; Cell Line ; Cyclic AMP-Dependent Protein Kinases/metabolism ; Endocytosis ; Enzyme Activation ; Epinephrine/pharmacology ; G-Protein-Coupled Receptor Kinase 3 ; GTP-Binding Proteins/*metabolism ; Humans ; MAP Kinase Signaling System ; Mice ; Mice, Inbred C57BL ; Mice, Knockout ; Microfilament Proteins/genetics/*metabolism ; Mitogen-Activated Protein Kinases/metabolism ; Motor Activity ; Nerve Tissue Proteins/genetics/*metabolism ; Phosphorylation ; Receptors, Adrenergic, alpha-2/*metabolism ; Rotarod Performance Test ; Signal Transduction ; Transfection ; beta-Adrenergic Receptor Kinases
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  • 97
    Publication Date: 2004-03-27
    Description: In the nervous system of vertebrates, myelination is essential for rapid and accurate impulse conduction. Myelin thickness depends on axon fiber size. We use mutant and transgenic mouse lines to show that axonal Neuregulin-1 (Nrg1) signals information about axon size to Schwann cells. Reduced Nrg1 expression causes hypomyelination and reduced nerve conduction velocity. Neuronal overexpression of Nrg1 induces hypermyelination and demonstrates that Nrg1 type III is the responsible isoform. We suggest a model by which myelin-forming Schwann cells integrate axonal Nrg1 signals as a biochemical measure of axon size.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Michailov, Galin V -- Sereda, Michael W -- Brinkmann, Bastian G -- Fischer, Tobias M -- Haug, Bernhard -- Birchmeier, Carmen -- Role, Lorna -- Lai, Cary -- Schwab, Markus H -- Nave, Klaus-Armin -- New York, N.Y. -- Science. 2004 Apr 30;304(5671):700-3. Epub 2004 Mar 25.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Neurogenetics, Max Planck Institute of Experimental Medicine, 37075 Gottingen, Germany.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15044753" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Axons/*physiology/*ultrastructure ; Ganglia, Spinal/chemistry ; Gene Targeting ; Genes, erbB ; Genes, erbB-2 ; Heterozygote ; Mice ; Mice, Knockout ; Mice, Transgenic ; Models, Neurological ; Myelin Sheath/*physiology/*ultrastructure ; Neural Conduction ; Neuregulin-1/genetics/*physiology ; Protein Isoforms/physiology ; Receptor, Epidermal Growth Factor/analysis/physiology ; Receptor, ErbB-2/analysis/physiology ; Receptor, ErbB-3/analysis/physiology ; Schwann Cells/physiology ; Sciatic Nerve/chemistry ; Signal Transduction
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  • 98
    Publication Date: 2004-01-13
    Description: Wnt signaling has recently emerged as a key factor in controlling stem cell expansion. In contrast, we show here that Wnt/beta-catenin signal activation in emigrating neural crest stem cells (NCSCs) has little effect on the population size and instead regulates fate decisions. Sustained beta-catenin activity in neural crest cells promotes the formation of sensory neural cells in vivo at the expense of virtually all other neural crest derivatives. Moreover, Wnt1 is able to instruct early NCSCs (eNCSCs) to adopt a sensory neuronal fate in a beta-catenin-dependent manner. Thus, the role of Wnt/beta-catenin in stem cells is cell-type dependent.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Lee, Hye-Youn -- Kleber, Maurice -- Hari, Lisette -- Brault, Veronique -- Suter, Ueli -- Taketo, Makoto M -- Kemler, Rolf -- Sommer, Lukas -- New York, N.Y. -- Science. 2004 Feb 13;303(5660):1020-3. Epub 2004 Jan 8.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Institute of Cell Biology, Department of Biology, Swiss Federal Institute of Technology, ETH-Honggerberg, CH-8093 Zurich, Switzerland.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/14716020" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Basic Helix-Loop-Helix Transcription Factors ; Cadherins/metabolism ; Cell Differentiation ; Cell Division ; Cell Lineage ; Cell Movement ; Cells, Cultured ; Central Nervous System/embryology ; Cytoskeletal Proteins/*metabolism ; DNA-Binding Proteins/metabolism ; Mice ; Models, Neurological ; Multipotent Stem Cells/*physiology ; Mutation ; Nerve Tissue Proteins/metabolism ; Neural Crest/*cytology/embryology/physiology ; Neurons, Afferent/*cytology/physiology ; Proto-Oncogene Proteins/*metabolism ; *Signal Transduction ; Trans-Activators/*metabolism ; Transcription Factor Brn-3 ; Transcription Factors/metabolism ; Wnt Proteins ; Wnt1 Protein ; *Zebrafish Proteins ; beta Catenin
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  • 99
    Publication Date: 2004-09-09
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Sontheimer, Erik J -- Carthew, Richard W -- R01 GM068743/GM/NIGMS NIH HHS/ -- R01 GM077581/GM/NIGMS NIH HHS/ -- New York, N.Y. -- Science. 2004 Sep 3;305(5689):1409-10.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Biochemistry, Molecular Biology, and Cell Biology, Northwestern University, Evanston, IL 60208, USA. erik@northwestern.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15353786" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Archaeal Proteins/*chemistry ; Argonaute Proteins ; Catalytic Domain ; Crystallography, X-Ray ; Embryonic and Fetal Development ; Eukaryotic Initiation Factor-2 ; Humans ; Mice ; MicroRNAs/metabolism ; Peptide Initiation Factors/chemistry/genetics/*metabolism ; Point Mutation ; Protein Structure, Tertiary ; Pyrococcus furiosus/chemistry ; *RNA Interference ; RNA, Double-Stranded/metabolism ; RNA, Messenger/metabolism ; RNA, Small Interfering/metabolism ; RNA-Induced Silencing Complex/*metabolism
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 100
    Publication Date: 2004-04-06
    Description: In adult mammals, the adipocyte-derived hormone leptin acts on the brain to reduce food intake by regulating the activity of neurons in the arcuate nucleus of the hypothalamus (ARH). Here, we report that neural projection pathways from the ARH are permanently disrupted in leptin-deficient (Lepob/Lepob) mice and leptin treatment in adulthood does not reverse these neuroanatomical defects. However, treatment of Lepob/Lepob neonates with exogenous leptin rescues the development of ARH projections, and leptin promotes neurite outgrowth from ARH neurons in vitro. These results suggest that leptin plays a neurotrophic role during the development of the hypothalamus and that this activity is restricted to a neonatal critical period that precedes leptin's acute regulation of food intake in adults.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Bouret, Sebastien G -- Draper, Shin J -- Simerly, Richard B -- DK55819/DK/NIDDK NIH HHS/ -- DK65900/DK/NIDDK NIH HHS/ -- NS37952/NS/NINDS NIH HHS/ -- RR00163/RR/NCRR NIH HHS/ -- New York, N.Y. -- Science. 2004 Apr 2;304(5667):108-10.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Division of Neuroscience, Oregon National Primate Research Center and Oregon Health and Science University, Beaverton, OR 97006, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15064420" target="_blank"〉PubMed〈/a〉
    Keywords: Agouti-Related Protein ; Animals ; Animals, Newborn ; Arcuate Nucleus of Hypothalamus/cytology/growth & development/*physiology ; Axons/*physiology ; Carbocyanines ; Culture Techniques ; Dorsomedial Hypothalamic Nucleus/cytology/growth & development/physiology ; Eating ; *Feeding Behavior ; Hypothalamic Area, Lateral/cytology/growth & development/physiology ; Hypothalamus/cytology/*growth & development/physiology ; Intercellular Signaling Peptides and Proteins ; Leptin/deficiency/genetics/pharmacology/*physiology ; Mice ; Mice, Inbred C57BL ; Mice, Obese ; Nerve Fibers/physiology ; Neurites/physiology ; Neurons/*physiology ; Paraventricular Hypothalamic Nucleus/cytology/growth & development/physiology ; Proteins/analysis ; Recombinant Proteins/pharmacology ; Signal Transduction ; alpha-MSH/analysis
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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