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  • Humans  (3,501)
  • 2000-2004  (3,501)
  • 1930-1934
  • 101
    Publication Date: 2004-04-17
    Description: Calmodulin (CaM) interactions with Ca2+ channels mediate both Ca2+ regulation of channels and local Ca2+ triggering of transcription factors implicated in neuronal memory. Crucial to these functions are the number of CaM molecules (CaMs) regulating each channel, and the number of CaMs privy to the local Ca2+ signal from each channel. To resolve these parameters, we fused L-type Ca2+ channels to single CaM molecules. These chimeric molecules revealed that a single CaM directs L-type channel regulation. Similar fusion molecules were used to estimate the local CaM concentration near Ca2+ channels. This estimate indicates marked enrichment of local CaM, as if a "school" of nearby CaMs were poised to enhance the transduction of local Ca2+ entry into diverse signaling pathways.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Mori, Masayuki X -- Erickson, Michael G -- Yue, David T -- New York, N.Y. -- Science. 2004 Apr 16;304(5669):432-5.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Ca2+ Signals Laboratory, Department of Biomedical Engineering , Johns Hopkins University School of Medicine, 720 Rutland Avenue, Baltimore, MD 21205, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15087548" target="_blank"〉PubMed〈/a〉
    Keywords: Calcium/*metabolism ; Calcium Channels, L-Type/chemistry/*metabolism ; Calcium Signaling ; Calmodulin/chemistry/genetics/*metabolism ; Cell Line ; Cell Nucleus/metabolism ; Cyclic AMP Response Element-Binding Protein/metabolism ; Fluorescence Resonance Energy Transfer ; Humans ; Mathematics ; Mutation ; Patch-Clamp Techniques ; Peptides/chemistry/genetics ; Protein Structure, Tertiary ; Recombinant Fusion Proteins/chemistry/metabolism ; Transfection
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    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 102
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-09-09
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Dennis, Phillip A -- New York, N.Y. -- Science. 2004 Sep 3;305(5689):1401-2.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15353780" target="_blank"〉PubMed〈/a〉
    Keywords: Biomedical Research/*economics ; Breast Neoplasms/mortality ; Female ; Humans ; *Lung Neoplasms/mortality ; Male ; Prostatic Neoplasms/mortality ; *Research Support as Topic ; Tobacco
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  • 103
    Publication Date: 2004-03-27
    Description: Heterosexual transmission accounts for the majority of human immunodeficiency virus-1 (HIV-1) infections worldwide, yet the viral properties that determine transmission fitness or outgrowth have not been elucidated. Here we show, for eight heterosexual transmission pairs, that recipient viruses were monophyletic, encoding compact, glycan-restricted envelope glycoproteins. These viruses were also uniquely sensitive to neutralization by antibody from the transmitting partner. Thus, the exposure of neutralizing epitopes, which are lost in chronic infection because of immune escape, appears to be favored in the newly infected host. This reveals characteristics of the envelope glycoprotein that influence HIV-1 transmission and may have implications for vaccine design.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Derdeyn, Cynthia A -- Decker, Julie M -- Bibollet-Ruche, Frederic -- Mokili, John L -- Muldoon, Mark -- Denham, Scott A -- Heil, Marintha L -- Kasolo, Francis -- Musonda, Rosemary -- Hahn, Beatrice H -- Shaw, George M -- Korber, Bette T -- Allen, Susan -- Hunter, Eric -- AI-40951/AI/NIAID NIH HHS/ -- AI-51231/AI/NIAID NIH HHS/ -- N01-85338/PHS HHS/ -- U01-AI-41530/AI/NIAID NIH HHS/ -- New York, N.Y. -- Science. 2004 Mar 26;303(5666):2019-22.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Microbiology, University of Alabama at Birmingham, Birmingham, AL 35294 USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15044802" target="_blank"〉PubMed〈/a〉
    Keywords: AIDS Vaccines ; Amino Acid Sequence ; Cohort Studies ; Epitopes/immunology ; Female ; Genes, env ; Glycosylation ; HIV Antibodies/*immunology ; HIV Envelope Protein gp120/chemistry/genetics/*immunology ; HIV Infections/*immunology/*transmission/virology ; HIV-1/genetics/*immunology/physiology ; Heterosexuality ; Humans ; Likelihood Functions ; Male ; Molecular Sequence Data ; Neutralization Tests ; Prospective Studies ; Viral Load ; Zambia
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  • 104
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-04-27
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Kane, Gordon -- New York, N.Y. -- Science. 2004 Apr 23;304(5670):516-8; author reply 516-8.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15108367" target="_blank"〉PubMed〈/a〉
    Keywords: Humans ; *Intelligence ; *Language ; *Mathematics ; Physical Phenomena ; *Physics
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  • 105
    Publication Date: 2004-02-07
    Description: The 1918 "Spanish" influenza pandemic represents the largest recorded outbreak of any infectious disease. The crystal structure of the uncleaved precursor of the major surface antigen of the extinct 1918 virus was determined at 3.0 angstrom resolution after reassembly of the hemagglutinin gene from viral RNA fragments preserved in 1918 formalin-fixed lung tissues. A narrow avian-like receptor-binding site, two previously unobserved histidine patches, and a less exposed surface loop at the cleavage site that activates viral membrane fusion reveal structural features primarily found in avian viruses, which may have contributed to the extraordinarily high infectivity and mortality rates observed during 1918.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Stevens, James -- Corper, Adam L -- Basler, Christopher F -- Taubenberger, Jeffery K -- Palese, Peter -- Wilson, Ian A -- AI058113/AI/NIAID NIH HHS/ -- AI42266/AI/NIAID NIH HHS/ -- AI50619/AI/NIAID NIH HHS/ -- CA55896/CA/NCI NIH HHS/ -- P50-GM 62411/GM/NIGMS NIH HHS/ -- New York, N.Y. -- Science. 2004 Mar 19;303(5665):1866-70. Epub 2004 Feb 5.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Molecular Biology, The 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/14764887" target="_blank"〉PubMed〈/a〉
    Keywords: Amino Acid Sequence ; Binding Sites ; Carbohydrate Conformation ; Cloning, Molecular ; Crystallography, X-Ray ; Glycosylation ; Hemagglutinin Glycoproteins, Influenza Virus/*chemistry/metabolism ; Histidine/chemistry/metabolism ; History, 20th Century ; Humans ; Hydrogen Bonding ; Influenza A virus/classification/*immunology/pathogenicity ; Influenza, Human/epidemiology/history/virology ; Molecular Sequence Data ; Protein Conformation ; Protein Structure, Quaternary ; Protein Structure, Secondary ; Protein Structure, Tertiary ; Receptors, Virus/metabolism ; Sialic Acids/metabolism
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  • 106
    Publication Date: 2004-09-09
    Description: We describe the synthesis and properties of a small molecule mimic of Smac, a pro-apoptotic protein that functions by relieving inhibitor-of-apoptosis protein (IAP)-mediated suppression of caspase activity. The compound binds to X chromosome- encoded IAP (XIAP), cellular IAP 1 (cIAP-1), and cellular IAP 2 (cIAP-2) and synergizes with both tumor necrosis factor alpha (TNFalpha) and TNF-related apoptosis-inducing ligand (TRAIL) to potently induce caspase activation and apoptosis in human cancer cells. The molecule has allowed a temporal, unbiased evaluation of the roles that IAP proteins play during signaling from TRAIL and TNF receptors. The compound is also a lead structure for the development of IAP antagonists potentially useful as therapy for cancer and inflammatory diseases.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Li, Lin -- Thomas, Ranny Mathew -- Suzuki, Hidetaka -- De Brabander, Jef K -- Wang, Xiaodong -- Harran, Patrick G -- P01 CA95471/CA/NCI NIH HHS/ -- New York, N.Y. -- Science. 2004 Sep 3;305(5689):1471-4.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Biochemistry, University of Texas Southwestern Medical Center at Dallas, 5323 Harry Hines Boulevard, Dallas, TX 75390-9038, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15353805" target="_blank"〉PubMed〈/a〉
    Keywords: Alkynes/chemical synthesis/chemistry/metabolism/*pharmacology ; *Apoptosis ; Apoptosis Regulatory Proteins ; Biotinylation ; *Carrier Proteins/chemistry/metabolism ; Caspase Inhibitors ; Caspases/metabolism ; Cell Line, Tumor ; Computer Simulation ; Dimerization ; Dipeptides/chemical synthesis/chemistry/metabolism/*pharmacology ; Diynes ; Glioblastoma ; Humans ; Inhibitor of Apoptosis Proteins ; Intracellular Signaling Peptides and Proteins ; Membrane Glycoproteins/metabolism/*pharmacology ; *Mitochondrial Proteins/chemistry/metabolism ; *Molecular Mimicry ; NF-kappa B/metabolism ; Poly(ADP-ribose) Polymerases/metabolism ; Protein Binding ; Protein Conformation ; Protein Engineering ; Proteins/metabolism ; Signal Transduction ; TNF-Related Apoptosis-Inducing Ligand ; Tetrazoles/chemical synthesis/chemistry/metabolism/*pharmacology ; Tumor Necrosis Factor-alpha/metabolism/*pharmacology ; X-Linked Inhibitor of Apoptosis Protein
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  • 107
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-04-17
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Willis, K J -- Gillson, L -- Brncic, T M -- New York, N.Y. -- Science. 2004 Apr 16;304(5669):402-3.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Oxford Long-term Ecology Laboratory, Biodiversity Research Group, School of Geography and the Environment, University of Oxford, Oxford OX1 3TB, UK. kathy.willis@geog.ox.ac.uk〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15087539" target="_blank"〉PubMed〈/a〉
    Keywords: Africa ; Agriculture ; Animals ; Archaeology ; Asia, Southeastern ; *Biodiversity ; Conservation of Natural Resources ; *Ecosystem ; Forestry ; Human Activities ; Humans ; Population Dynamics ; South America ; Time Factors ; *Trees ; *Tropical Climate
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    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 108
    Publication Date: 2004-11-30
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Gura, Trisha -- New York, N.Y. -- Science. 2004 Nov 26;306(5701):1453-4.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15567820" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Appetite/*drug effects ; Appetite Depressants/administration & dosage/*pharmacology ; Body Weight/drug effects ; Dose-Response Relationship, Drug ; Gastric Emptying/drug effects ; Humans ; Macaca mulatta ; Peptide Fragments ; Peptide YY/administration & dosage/metabolism/*pharmacology ; Rats
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  • 109
    Publication Date: 2004-12-25
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Stohr, Klaus -- Esveld, Marja -- New York, N.Y. -- Science. 2004 Dec 24;306(5705):2195-6.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉World Health Organization Influenza Programme, Geneva, Switzerland.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15618505" target="_blank"〉PubMed〈/a〉
    Keywords: Clinical Trials as Topic ; *Disease Outbreaks ; Drug Industry ; Humans ; Influenza A virus/immunology/pathogenicity ; Influenza Vaccines/administration & dosage/economics/*supply & distribution ; Influenza, Human/*epidemiology/*prevention & control/virology ; International Cooperation ; Population Surveillance ; Public Policy ; World Health Organization
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  • 110
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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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  • 111
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-04-10
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Wilson, Chris -- New York, N.Y. -- Science. 2004 Apr 9;304(5668):207-9.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15073356" target="_blank"〉PubMed〈/a〉
    Keywords: Developed Countries ; Developing Countries ; Female ; *Fertility ; Humans ; *Population Density ; Population Growth
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  • 112
    Publication Date: 2004-08-18
    Description: Helicobacter pylori infects the stomachs of nearly a half the human population, yet most infected individuals remain asymptomatic, which suggests that there is a host defense against this bacterium. Because H. pylori is rarely found in deeper portions of the gastric mucosa, where O-glycans are expressed that have terminal alpha1,4-linked N-acetylglucosamine, we tested whether these O-glycans might affect H. pylori growth. Here, we report that these O-glycans have antimicrobial activity against H. pylori, inhibiting its biosynthesis of cholesteryl-alpha-D-glucopyranoside, a major cell wall component. Thus, the unique O-glycans in gastric mucin appeared to function as a natural antibiotic, protecting the host from H. pylori infection.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Kawakubo, Masatomo -- Ito, Yuki -- Okimura, Yukie -- Kobayashi, Motohiro -- Sakura, Kyoko -- Kasama, Susumu -- Fukuda, Michiko N -- Fukuda, Minoru -- Katsuyama, Tsutomu -- Nakayama, Jun -- CA 33000/CA/NCI NIH HHS/ -- CA 71932/CA/NCI NIH HHS/ -- New York, N.Y. -- Science. 2004 Aug 13;305(5686):1003-6.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Pathology, Shinshu University School of Medicine, Asahi 3-1-1, Matsumoto 390-8621, Japan.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15310903" target="_blank"〉PubMed〈/a〉
    Keywords: Acetylglucosamine/pharmacology/*physiology ; Animals ; *Anti-Bacterial Agents/chemistry/pharmacology ; Antigens, CD/chemistry/pharmacology ; Antigens, CD43 ; Bacterial Adhesion ; CHO Cells ; Carbohydrate Conformation ; Cell Line, Tumor ; Cell Wall/metabolism ; Cholesterol/analogs & derivatives/biosynthesis/metabolism ; Cricetinae ; Gastric Mucins/chemistry/pharmacology/*physiology ; Gastric Mucosa/microbiology ; Glucosyltransferases/antagonists & inhibitors/metabolism ; Helicobacter pylori/cytology/drug effects/*growth & development/physiology ; Humans ; Polysaccharides/chemistry/pharmacology/*physiology ; Recombinant Proteins ; Sialoglycoproteins/chemistry/pharmacology ; Solubility
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  • 113
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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〉New York, N.Y. -- Science. 2004 Dec 17;306(5704):2014.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15604369" target="_blank"〉PubMed〈/a〉
    Keywords: Anti-Obesity Agents/therapeutic use ; Autophagy ; Europe ; Haplotypes ; Humans ; Nanotechnology/standards ; Nuclear Warfare ; Research ; Saturn ; *Science
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  • 114
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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〉Stokstad, Erik -- New York, N.Y. -- Science. 2004 Oct 22;306(5696):603.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15498990" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Bird Diseases/epidemiology/*prevention & control ; Birds ; Culicidae/virology ; Hawaii ; Humans ; Insect Vectors/virology ; Population Surveillance ; Public Health Practice ; United States/epidemiology ; West Nile Fever/epidemiology/*prevention & control/transmission/*veterinary ; *West Nile virus/isolation & purification
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  • 115
    Publication Date: 2004-10-23
    Description: Hypertension and dyslipidemia are risk factors for atherosclerosis and occur together more often than expected by chance. Although this clustering suggests shared causation, unifying factors remain unknown. We describe a large kindred with a syndrome including hypertension, hypercholesterolemia, and hypomagnesemia. Each phenotype is transmitted on the maternal lineage with a pattern indicating mitochondrial inheritance. Analysis of the mitochondrial genome of the maternal lineage identified a homoplasmic mutation substituting cytidine for uridine immediately 5' to the mitochondrial transfer RNA(Ile) anticodon. Uridine at this position is nearly invariate among transfer RNAs because of its role in stabilizing the anticodon loop. Given the known loss of mitochondrial function with aging, these findings may have implications for the common clustering of these metabolic disorders.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3033655/" 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/PMC3033655/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Wilson, Frederick H -- Hariri, Ali -- Farhi, Anita -- Zhao, Hongyu -- Petersen, Kitt Falk -- Toka, Hakan R -- Nelson-Williams, Carol -- Raja, Khalid M -- Kashgarian, Michael -- Shulman, Gerald I -- Scheinman, Steven J -- Lifton, Richard P -- MO1 RR-00125/RR/NCRR NIH HHS/ -- P50 HL-55007/HL/NHLBI NIH HHS/ -- R01 AG023686/AG/NIA NIH HHS/ -- R01 AG023686-01A1/AG/NIA NIH HHS/ -- R01 AG023686-02/AG/NIA NIH HHS/ -- R01 AG023686-03/AG/NIA NIH HHS/ -- R01 AG023686-04/AG/NIA NIH HHS/ -- R01 DK-49230/DK/NIDDK NIH HHS/ -- R01 DK049230/DK/NIDDK NIH HHS/ -- New York, N.Y. -- Science. 2004 Nov 12;306(5699):1190-4. Epub 2004 Oct 21.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Howard Hughes Medical Institute, 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/15498972" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Aging ; Anticodon ; Body Mass Index ; Cluster Analysis ; Cytidine ; *Extrachromosomal Inheritance ; Female ; Humans ; Hypercholesterolemia/*genetics/physiopathology ; Hypertension/*genetics/physiopathology ; Magnesium/*blood/urine ; Male ; Metabolic Syndrome X/genetics ; Middle Aged ; Mitochondria/*genetics/metabolism ; Mitochondria, Muscle/metabolism/pathology ; Muscle Fibers, Skeletal/pathology ; *Mutation ; Pedigree ; Phenotype ; RNA/genetics ; RNA, Transfer, Ile/*genetics ; Syndrome ; Thymidine ; Uridine
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  • 116
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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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  • 117
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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〉Lin, Zhen -- Owen, Art B -- Altman, Russ B -- LM007033/LM/NLM NIH HHS/ -- U01-GM61374/GM/NIGMS NIH HHS/ -- New York, N.Y. -- Science. 2004 Jul 9;305(5681):183.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Genetics, Stanford University School of Medicine, CA 94305-5120, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15247459" target="_blank"〉PubMed〈/a〉
    Keywords: *Databases, Genetic/legislation & jurisprudence ; *Genetic Privacy/legislation & jurisprudence ; *Genetic Research/legislation & jurisprudence ; *Genomics/legislation & jurisprudence ; Genotype ; Humans ; Informed Consent ; Pharmacogenetics ; Phenotype ; *Polymorphism, Single Nucleotide ; Public Policy ; United States
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    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 118
    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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  • 119
    Publication Date: 2004-09-28
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Stokstad, Erik -- New York, N.Y. -- Science. 2004 Sep 24;305(5692):1889.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15448235" target="_blank"〉PubMed〈/a〉
    Keywords: Agriculture ; *Environment ; *Geography ; Humans ; Polynesia ; Trees
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  • 120
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-01-31
    Description: Sixty-one SARS coronavirus genomic sequences derived from the early, middle, and late phases of the severe acute respiratory syndrome (SARS) epidemic were analyzed together with two viral sequences from palm civets. Genotypes characteristic of each phase were discovered, and the earliest genotypes were similar to the animal SARS-like coronaviruses. Major deletions were observed in the Orf8 region of the genome, both at the start and the end of the epidemic. The neutral mutation rate of the viral genome was constant but the amino acid substitution rate of the coding sequences slowed during the course of the epidemic. The spike protein showed the strongest initial responses to positive selection pressures, followed by subsequent purifying selection and eventual stabilization.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Chinese SARS Molecular Epidemiology Consortium -- New York, N.Y. -- Science. 2004 Mar 12;303(5664):1666-9. Epub 2004 Jan 29.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/14752165" target="_blank"〉PubMed〈/a〉
    Keywords: Adaptation, Physiological ; Amino Acid Substitution ; Animals ; Base Sequence ; Carnivora/virology ; China/epidemiology ; Cluster Analysis ; Coronavirus/genetics/isolation & purification ; *Disease Outbreaks ; *Evolution, Molecular ; *Genome, Viral ; Genotype ; Humans ; Membrane Glycoproteins/genetics ; Molecular Sequence Data ; Mutation ; Nucleic Acid Conformation ; Open Reading Frames ; Phylogeny ; Point Mutation ; RNA, Viral/genetics ; SARS Virus/*genetics/isolation & purification/physiology ; Selection, Genetic ; Sequence Deletion ; Severe Acute Respiratory Syndrome/*epidemiology/*virology ; Spike Glycoprotein, Coronavirus ; Viral Envelope Proteins/genetics ; Viral Matrix Proteins/chemistry/genetics
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  • 121
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-03-03
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Wolf, Hans -- New York, N.Y. -- Science. 2004 Feb 27;303(5662):1294-7; author reply 1294-7.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/14991961" target="_blank"〉PubMed〈/a〉
    Keywords: *AIDS Vaccines ; Academies and Institutes/economics/organization & administration ; Biotechnology ; Clinical Trials as Topic ; *Global Health ; HIV Infections/*prevention & control ; Humans ; *International Cooperation ; Multicenter Studies as Topic ; Research Support as Topic
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  • 122
    Publication Date: 2004-01-13
    Description: During genetic recombination and the recombinational repair of chromosome breaks, DNA molecules become linked at points of strand exchange. Branch migration and resolution of these crossovers, or Holliday junctions (HJs), complete the recombination process. Here, we show that extracts from cells carrying mutations in the recombination/repair genes RAD51C or XRCC3 have reduced levels of HJ resolvase activity. Moreover, depletion of RAD51C from fractionated human extracts caused a loss of branch migration and resolution activity, but these functions were restored by complementation with a variety of RAD51 paralog complexes containing RAD51C. We conclude that the RAD51 paralogs are involved in HJ processing in human cells.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Liu, Yilun -- Masson, Jean-Yves -- Shah, Rajvee -- O'Regan, Paul -- West, Stephen C -- New York, N.Y. -- Science. 2004 Jan 9;303(5655):243-6.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Cancer Research UK, London Research Institute, Clare Hall Laboratories, South Mimms, Hertfordshire EN6 3LD, UK.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/14716019" target="_blank"〉PubMed〈/a〉
    Keywords: Amino Acid Substitution ; Animals ; CHO Cells ; Cell Line ; Cricetinae ; DNA Repair ; DNA, Cruciform/chemistry/*metabolism ; DNA-Binding Proteins/chemistry/genetics/isolation & purification/*metabolism ; Electrophoresis, Polyacrylamide Gel ; Female ; HeLa Cells ; Holliday Junction Resolvases/*metabolism ; Humans ; Mutation ; Protein Structure, Tertiary ; Recombinant Proteins/metabolism ; Recombination, Genetic
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  • 123
    Publication Date: 2004-12-14
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Renner, Rebecca -- New York, N.Y. -- Science. 2004 Dec 10;306(5703):1887.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15591183" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Arctic Regions ; Canada ; Caprylates/analysis/chemistry ; Drug Combinations ; Environmental Pollutants/*analysis/toxicity ; Fluorocarbons/*analysis/chemistry/toxicity ; Humans ; Surface-Active Agents/*analysis/chemistry/toxicity ; Trichloroethanes/analysis/chemistry ; United States ; United States Environmental Protection Agency ; Volatilization
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  • 124
    Publication Date: 2004-10-23
    Description: Signaling by the transcription factor nuclear factor kappa B (NF-kappaB) involves its release from inhibitor kappa B (IkappaB) in the cytosol, followed by translocation into the nucleus. NF-kappaB regulation of IkappaBalpha transcription represents a delayed negative feedback loop that drives oscillations in NF-kappaB translocation. Single-cell time-lapse imaging and computational modeling of NF-kappaB (RelA) localization showed asynchronous oscillations following cell stimulation that decreased in frequency with increased IkappaBalpha transcription. Transcription of target genes depended on oscillation persistence, involving cycles of RelA phosphorylation and dephosphorylation. The functional consequences of NF-kappaB signaling may thus depend on number, period, and amplitude of oscillations.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Nelson, D E -- Ihekwaba, A E C -- Elliott, M -- Johnson, J R -- Gibney, C A -- Foreman, B E -- Nelson, G -- See, V -- Horton, C A -- Spiller, D G -- Edwards, S W -- McDowell, H P -- Unitt, J F -- Sullivan, E -- Grimley, R -- Benson, N -- Broomhead, D -- Kell, D B -- White, M R H -- New York, N.Y. -- Science. 2004 Oct 22;306(5696):704-8.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Centre for Cell Imaging, School of Biological Sciences, Bioscience Research Building, Crown Street, Liverpool, L69 7ZB, UK.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15499023" target="_blank"〉PubMed〈/a〉
    Keywords: Active Transport, Cell Nucleus ; Cell Line, Tumor ; Cell Nucleus/metabolism ; Computer Simulation ; Cytoplasm/metabolism ; Etoposide/pharmacology ; Feedback, Physiological ; *Gene Expression Regulation ; HeLa Cells ; Humans ; I-kappa B Proteins/genetics/metabolism ; Models, Biological ; NF-kappa B/*metabolism ; Phosphorylation ; Recombinant Fusion Proteins/metabolism ; *Signal Transduction ; Transcription Factor RelA ; Transcription, Genetic ; Transfection ; Tumor Necrosis Factor-alpha/pharmacology
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  • 125
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-01-13
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Hannon, Bruce -- New York, N.Y. -- Science. 2004 Jan 9;303(5655):169.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/14715992" target="_blank"〉PubMed〈/a〉
    Keywords: *Contraception ; *Global Health ; Health Policy ; Humans ; *Population Control ; *Public Health
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  • 126
    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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  • 127
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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〉Stokstad, Erik -- New York, N.Y. -- Science. 2004 May 28;304(5675):1229.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15166339" target="_blank"〉PubMed〈/a〉
    Keywords: Air Pollution, Indoor ; Asthma/etiology ; Child ; *Fungi ; *Housing ; Humans ; *Humidity ; *Public Health ; Respiratory Tract Diseases/*etiology
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  • 128
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-06-26
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Dove, Alan W -- New York, N.Y. -- Science. 2004 Jun 25;304(5679):1903.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15218124" target="_blank"〉PubMed〈/a〉
    Keywords: Child ; Developing Countries ; Disease Outbreaks ; Humans ; *Immunization Programs ; Poliomyelitis/epidemiology/*prevention & control ; Poliovirus Vaccine, Oral ; *Poliovirus Vaccines ; Vaccination ; World Health Organization
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  • 129
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-07-17
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Kennedy, Donald -- New York, N.Y. -- Science. 2004 Jul 16;305(5682):309.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15256641" target="_blank"〉PubMed〈/a〉
    Keywords: Computers ; *Epidemiologic Studies ; Humans ; Industry/*legislation & jurisprudence ; *Jurisprudence ; Neoplasms/*mortality ; Occupational Exposure/*adverse effects ; *Publishing ; United States
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  • 130
    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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  • 131
    Publication Date: 2004-07-27
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Lund, Eiliv -- Engeset, Dagrun -- Alsaker, Elin -- Skeie, Gun -- Hjartaker, Anette -- Lundebye, Anne-Katrine -- Niebor, Evert -- New York, N.Y. -- Science. 2004 Jul 23;305(5683):477-8; author reply 477-8.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15273378" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Cardiovascular Diseases/prevention & control ; *Diet ; Environmental Pollutants/analysis/toxicity ; Female ; *Fisheries ; *Food Contamination ; Humans ; Neoplasms/chemically induced/*epidemiology ; Norway ; Risk Assessment ; *Salmon
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  • 132
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-12-14
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Ahmed, Serge H -- New York, N.Y. -- Science. 2004 Dec 10;306(5703):1901-2.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉CNRS UMR 5541, Universite Victor-Segalen Bordeaux 2, Bordeaux, France. sahmed@lnpb.u-bordeaux2.fr〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15591193" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; *Choice Behavior ; Cocaine-Related Disorders/*physiopathology/psychology ; Computer Simulation ; Cues ; Dopamine/physiology ; Humans ; Impulsive Behavior ; Learning ; *Models, Neurological ; Models, Psychological ; Neurons/physiology ; *Reinforcement (Psychology) ; *Reward
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  • 133
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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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  • 134
    Publication Date: 2004-08-07
    Description: The cascade of events that leads to vaccinia-induced actin polymerization requires Src-dependent tyrosine phosphorylation of the viral membrane protein A36R. We found that a localized outside-in signaling cascade induced by the viral membrane protein B5R is required to potently activate Src and induce A36R phosphorylation at the plasma membrane. In addition, Src-mediated phosphorylation of A36R regulated the ability of virus particles to recruit and release conventional kinesin. Thus, Src activity regulates the transition between cytoplasmic microtubule transport and actin-based motility at the plasma membrane.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Newsome, Timothy P -- Scaplehorn, Niki -- Way, Michael -- New York, N.Y. -- Science. 2004 Oct 1;306(5693):124-9. Epub 2004 Aug 5.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Cell Motility Laboratory, Room 529, 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/15297625" target="_blank"〉PubMed〈/a〉
    Keywords: Actins/*metabolism ; Animals ; Cell Line ; Cell Membrane/metabolism/virology ; Chickens ; Consensus Sequence ; Enzyme Activation ; HeLa Cells ; Humans ; Kinesin/metabolism ; Membrane Glycoproteins/chemistry/metabolism ; Microtubules/*metabolism ; Phosphorylation ; Phosphotyrosine/metabolism ; Recombinant Fusion Proteins/metabolism ; Vaccinia virus/genetics/*metabolism/physiology ; Viral Envelope Proteins/chemistry/metabolism ; Viral Structural Proteins/*metabolism ; Virion/metabolism ; src-Family Kinases/*metabolism
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  • 135
    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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  • 136
    Publication Date: 2004-03-16
    Description: To what extent do all brains work alike during natural conditions? We explored this question by letting five subjects freely view half an hour of a popular movie while undergoing functional brain imaging. Applying an unbiased analysis in which spatiotemporal activity patterns in one brain were used to "model" activity in another brain, we found a striking level of voxel-by-voxel synchronization between individuals, not only in primary and secondary visual and auditory areas but also in association cortices. The results reveal a surprising tendency of individual brains to "tick collectively" during natural vision. The intersubject synchronization consisted of a widespread cortical activation pattern correlated with emotionally arousing scenes and regionally selective components. The characteristics of these activations were revealed with the use of an open-ended "reverse-correlation" approach, which inverts the conventional analysis by letting the brain signals themselves "pick up" the optimal stimuli for each specialized cortical area.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Hasson, Uri -- Nir, Yuval -- Levy, Ifat -- Fuhrmann, Galit -- Malach, Rafael -- New York, N.Y. -- Science. 2004 Mar 12;303(5664):1634-40.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Neurobiology, Weizmann Institute of Science, Rehovot 76100, Israel.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15016991" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; *Attention ; Auditory Cortex/physiology ; Brain Mapping ; Cerebral Cortex/*physiology ; Emotions ; Face ; Female ; Humans ; Magnetic Resonance Imaging ; Male ; Middle Aged ; *Motion Pictures as Topic ; Occipital Lobe/physiology ; Photic Stimulation ; Temporal Lobe/physiology ; Vision, Ocular ; Visual Cortex/*physiology ; *Visual Perception
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  • 137
    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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  • 138
    Publication Date: 2004-10-09
    Description: Nitric oxide (NO) is extremely toxic to Clostridium botulinum, but its molecular targets are unknown. Here, we identify a heme protein sensor (SONO) that displays femtomolar affinity for NO. The crystal structure of the SONO heme domain reveals a previously undescribed fold and a strategically placed tyrosine residue that modulates heme-nitrosyl coordination. Furthermore, the domain architecture of a SONO ortholog cloned from Chlamydomonas reinhardtii indicates that NO signaling through cyclic guanosine monophosphate arose before the origin of multicellular eukaryotes. Our findings have broad implications for understanding bacterial responses to NO, as well as for the activation of mammalian NO-sensitive guanylyl cyclase.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Nioche, Pierre -- Berka, Vladimir -- Vipond, Julia -- Minton, Nigel -- Tsai, Ah-Lim -- Raman, C S -- AY343540/PHS HHS/ -- R01 AI054444/AI/NIAID NIH HHS/ -- R01 AI054444-05/AI/NIAID NIH HHS/ -- New York, N.Y. -- Science. 2004 Nov 26;306(5701):1550-3. Epub 2004 Oct 7.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Structural Biology Research Center and Department of Biochemistry and Molecular Biology, University of Texas Medical School, Houston, TX 77030, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15472039" target="_blank"〉PubMed〈/a〉
    Keywords: Aerobiosis ; Amino Acid Sequence ; Amino Acid Substitution ; Animals ; Bacterial Proteins/chemistry/metabolism ; Biological Evolution ; Carrier Proteins/*chemistry/genetics/*metabolism ; Chemotaxis ; Chlamydomonas reinhardtii/chemistry/genetics/metabolism ; Cloning, Molecular ; Clostridium botulinum/*chemistry/genetics/*metabolism ; Crystallography, X-Ray ; Electron Spin Resonance Spectroscopy ; Escherichia coli/genetics/growth & development ; Guanylate Cyclase ; Heme/chemistry/metabolism ; Hemeproteins/*chemistry/genetics/*metabolism ; Humans ; Hydrogen Bonding ; Ligands ; Models, Molecular ; Molecular Sequence Data ; Nitric Oxide/*metabolism ; Protein Folding ; Protein Structure, Secondary ; Protein Structure, Tertiary ; Protoporphyrins/analysis/metabolism ; Receptors, Cytoplasmic and Nuclear/chemistry/metabolism ; Sequence Alignment ; Signal Transduction ; Static Electricity ; Thermoanaerobacter/chemistry
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  • 139
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-03-27
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Roberts, Leslie -- New York, N.Y. -- Science. 2004 Mar 26;303(5666):1960-8.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15044779" target="_blank"〉PubMed〈/a〉
    Keywords: Child ; Child, Preschool ; Developed Countries ; Developing Countries ; Disease Outbreaks/prevention & control ; Endemic Diseases ; *Global Health ; Humans ; *Immunization Programs ; Infant ; Mutation ; Nigeria/epidemiology ; Poliomyelitis/*epidemiology/*prevention & control/transmission/virology ; Poliovirus/genetics/pathogenicity ; Poliovirus Vaccine, Inactivated ; *Poliovirus Vaccine, Oral/administration & dosage/adverse effects/genetics ; Vaccination ; World Health Organization
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  • 140
    Publication Date: 2004-02-14
    Description: Conflict monitoring by the anterior cingulate cortex (ACC) has been posited to signal a need for greater cognitive control, producing neural and behavioral adjustments. However, the very occurrence of behavioral adjustments after conflict has been questioned, along with suggestions that there is no direct evidence of ACC conflict-related activity predicting subsequent neural or behavioral adjustments in control. Using the Stroop color-naming task and controlling for repetition effects, we demonstrate that ACC conflict-related activity predicts both greater prefrontal cortex activity and adjustments in behavior, supporting a role of ACC conflict monitoring in the engagement of cognitive control.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Kerns, John G -- Cohen, Jonathan D -- MacDonald, Angus W 3rd -- Cho, Raymond Y -- Stenger, V Andrew -- Carter, Cameron S -- New York, N.Y. -- Science. 2004 Feb 13;303(5660):1023-6.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Psychological Sciences, University of Missouri-Columbia, Columbia, MO 65211, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/14963333" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Brain Mapping ; *Cognition ; *Conflict (Psychology) ; Cues ; Female ; Frontal Lobe/*physiology ; Gyrus Cinguli/*physiology ; Humans ; Magnetic Resonance Imaging ; Male ; Neuropsychological Tests ; Prefrontal Cortex/*physiology ; Reaction Time
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  • 141
    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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  • 142
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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〉Stokstad, Erik -- New York, N.Y. -- Science. 2004 Jan 2;303(5654):34.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/14704409" target="_blank"〉PubMed〈/a〉
    Keywords: *Air Pollutants/analysis/toxicity ; Animals ; Birds ; Fishes ; Food Chain ; Government Regulation ; Humans ; Maximum Allowable Concentration ; *Mercury/analysis/metabolism/toxicity ; Power Plants/*standards ; United States ; *United States Environmental Protection Agency
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  • 143
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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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  • 144
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-02-21
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Eagleman, David M -- New York, N.Y. -- Science. 2004 Feb 20;303(5661):1144-6.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Laboratory for Perception and Action, Department of Neurobiology and Anatomy, University of Texas, Houston Medical School, Houston, TX 77030, USA. david.eagleman@uth.tmc.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/14976300" target="_blank"〉PubMed〈/a〉
    Keywords: *Attention ; Brain/*physiology ; Brain Mapping ; Humans ; *Intention ; Magnetic Resonance Imaging ; *Motor Activity ; Motor Cortex/blood supply/*physiology ; Parietal Lobe/blood supply/physiology ; Prefrontal Cortex/blood supply/physiology ; Regional Blood Flow ; Time Factors
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  • 145
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-06-26
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Stone, Richard -- New York, N.Y. -- Science. 2004 Jun 25;304(5679):1889-91.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15218116" target="_blank"〉PubMed〈/a〉
    Keywords: *Archaeology ; Dental Enamel/chemistry ; England ; Humans ; Male ; Oxygen Isotopes/analysis ; *Paleodontology ; Strontium/analysis ; Wales
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  • 146
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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〉Normile, Dennis -- New York, N.Y. -- Science. 2004 Nov 5;306(5698):953.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15528412" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Asia ; Chickens ; *Ducks ; Humans ; *Influenza A virus/pathogenicity/physiology ; Influenza in Birds/prevention & control/*virology ; Influenza, Human/prevention & control/*transmission/virology ; Poultry Diseases/prevention & control/virology ; Virus Replication ; Virus Shedding ; World Health Organization
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  • 147
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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〉Stone, Richard -- New York, N.Y. -- Science. 2004 Sep 17;305(5691):1696-703.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15375241" target="_blank"〉PubMed〈/a〉
    Keywords: Agriculture ; Animals ; Biomedical Research ; *Biotechnology ; Cloning, Organism ; Humans ; *International Cooperation ; Korea ; Public Health ; *Research ; *Science ; United States ; Universities ; World Health Organization
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  • 148
    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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  • 149
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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〉Mackenzie, Dana -- New York, N.Y. -- Science. 2004 Feb 6;303(5659):786-7.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/14764864" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; *Computer Simulation ; *Electric Countershock ; Electrodes ; Electrophysiology ; Heart/*physiology/physiopathology ; Heart Conduction System/*physiology ; Humans ; Mathematics ; Models, Anatomic ; *Models, Cardiovascular ; Ventricular Fibrillation/*physiopathology/therapy
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  • 150
    Publication Date: 2004-09-09
    Description: Progress in gerontological research has been promoted through the use of numerous animal models, which have helped identify possible mechanisms of aging and age-related chronic diseases and evaluate possible interventions with potential relevance to human aging and disease. Further development of nonhuman primate models, particularly rhesus monkeys, could accelerate this progress, because their closer genetic relationship to humans produces a highly similar aging phenotype. Because the relatively long lives of primates increase the administrative and economic demands on research involving them, new emphasis has emerged on increasing the efficient use of these valuable resources through cooperative, interdisciplinary research.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Roth, George S -- Mattison, Julie A -- Ottinger, Mary Ann -- Chachich, Mark E -- Lane, Mark A -- Ingram, Donald K -- New York, N.Y. -- Science. 2004 Sep 3;305(5689):1423-6.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Laboratory of Experimental Gerontology, Intramural Research Program, Gerontology Research Center, National Institute on Aging, National Institutes of Health, 5600 Nathan Shock Drive, Baltimore, MD 21224, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15353793" target="_blank"〉PubMed〈/a〉
    Keywords: *Aging ; Animals ; Biomarkers ; Caloric Restriction ; Chronic Disease ; Cross-Sectional Studies ; Disease Models, Animal ; Female ; Heart Diseases/physiopathology/therapy ; Humans ; Longitudinal Studies ; Macaca mulatta/*physiology ; Male ; *Models, Animal ; Neoplasms/physiopathology/therapy
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  • 151
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-11-06
    Description: Syntaxin, synaptosome-associated protein of 25 kD (SNAP25), and vesicle-associated membrane protein/synaptobrevin are collectively called SNAP receptor (SNARE) proteins, and they catalyze neuronal exocytosis by forming a "core complex." The steps in core complex formation are unknown. Here, we monitored SNARE complex formation in vivo with the use of a fluorescent version of SNAP25. In PC12 cells, we found evidence for a syntaxin-SNAP25 complex that formed with high affinity, required only the amino-terminal SNARE motif of SNAP25, tolerated a mutation that blocks formation of other syntaxin-SNAP25 complexes, and assembled reversibly when Ca2+ entered cells during depolarization. The complex may represent a precursor to the core complex formed during a Ca2+-dependent priming step of exocytosis.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉An, Seong J -- Almers, Wolfhard -- MH60600/MH/NIMH NIH HHS/ -- New York, N.Y. -- Science. 2004 Nov 5;306(5698):1042-6.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Vollum Institute L-474, Oregon Health Sciences University, 3181 Southwest Sam Jackson Park Road, Portland, OR 97201, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15528447" target="_blank"〉PubMed〈/a〉
    Keywords: Adrenal Medulla/cytology ; Animals ; Bacterial Proteins ; Cell Line ; Fluorescence Resonance Energy Transfer ; Green Fluorescent Proteins ; Humans ; Luminescent Proteins ; Membrane Proteins/genetics/physiology ; Nerve Tissue Proteins/genetics/physiology ; PC12 Cells ; Qa-SNARE Proteins ; Rats ; Recombinant Fusion Proteins ; SNARE Proteins ; Synaptosomal-Associated Protein 25 ; Vesicular Transport Proteins/*physiology
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  • 152
    Publication Date: 2004-07-03
    Description: When we look at our hands, we immediately know that they are part of our own body. This feeling of ownership of our limbs is a fundamental aspect of self-consciousness. We have studied the neuronal counterparts of this experience. A perceptual illusion was used to manipulate feelings of ownership of a rubber hand presented in front of healthy subjects while brain activity was measured by functional magnetic resonance imaging. The neural activity in the premotor cortex reflected the feeling of ownership of the hand. This suggests that multisensory integration in the premotor cortex provides a mechanism for bodily self-attribution.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Ehrsson, H Henrik -- Spence, Charles -- Passingham, Richard E -- New York, N.Y. -- Science. 2004 Aug 6;305(5685):875-7. Epub 2004 Jul 1.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Wellcome Department of Imaging Neuroscience, Institute of Neurology, 12 Queen Square, London WC1N 3BG, UK. h.ehrsson@fil.ion.ucl.ac.uk〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15232072" target="_blank"〉PubMed〈/a〉
    Keywords: *Body Image ; Brain/physiology ; Brain Mapping ; Cerebellum/physiology ; Female ; Hand ; Humans ; Magnetic Resonance Imaging ; Male ; Motor Cortex/*physiology ; Neurons/*physiology ; Parietal Lobe/physiology ; Proprioception ; Time Factors ; Touch ; Vision, Ocular
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  • 153
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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〉Mahmoud, Adel -- New York, N.Y. -- Science. 2004 Jul 9;305(5681):147.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15247440" target="_blank"〉PubMed〈/a〉
    Keywords: *Communicable Disease Control ; Developing Countries ; *Global Health ; Humans ; *Immunization Programs ; International Cooperation ; Politics ; *Vaccination
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  • 154
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-03-27
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Hemingway, Janet -- Craig, Alister -- New York, N.Y. -- Science. 2004 Mar 26;303(5666):1984-5.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Liverpool School of Tropical Medicine, Liverpool L3 5QA, UK. hemingway@liverpool.ac.uk〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15044794" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Anopheles/*genetics/immunology/*parasitology ; Digestive System/parasitology ; Gene Silencing ; Genes, Insect ; Humans ; Insect Proteins/genetics/*physiology ; Insect Vectors/*genetics/immunology/parasitology ; Lectins, C-Type/genetics/*physiology ; Malaria/parasitology/*prevention & control/transmission ; Plasmodium berghei/*growth & development/immunology ; RNA Interference ; RNA, Double-Stranded
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  • 155
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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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  • 156
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-12-14
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Rubin, Vera -- New York, N.Y. -- Science. 2004 Dec 10;306(5703):1891.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15591185" target="_blank"〉PubMed〈/a〉
    Keywords: *Awards and Prizes ; Female ; Humans ; Male ; Men ; *Prejudice ; *Science ; *Women
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  • 157
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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〉Normile, Dennis -- New York, N.Y. -- Science. 2004 May 14;304(5673):945.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15143251" target="_blank"〉PubMed〈/a〉
    Keywords: Authorship ; Cell Line ; Cloning, Organism/*ethics/legislation & jurisprudence ; *Embryo Research ; Embryo, Mammalian/*cytology ; Ethics Committees, Research ; *Ethics, Research ; Female ; Humans ; Korea ; Research Support as Topic ; *Stem Cells ; Tissue Donors
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  • 158
    Publication Date: 2004-01-13
    Description: Over a century ago, Freud proposed that unwanted memories can be excluded from awareness, a process called repression. It is unknown, however, how repression occurs in the brain. We used functional magnetic resonance imaging to identify the neural systems involved in keeping unwanted memories out of awareness. Controlling unwanted memories was associated with increased dorsolateral prefrontal activation, reduced hippocampal activation, and impaired retention of those memories. Both prefrontal cortical and right hippocampal activations predicted the magnitude of forgetting. These results confirm the existence of an active forgetting process and establish a neurobiological model for guiding inquiry into motivated forgetting.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Anderson, Michael C -- Ochsner, Kevin N -- Kuhl, Brice -- Cooper, Jeffrey -- Robertson, Elaine -- Gabrieli, Susan W -- Glover, Gary H -- Gabrieli, John D E -- MH59940/MH/NIMH NIH HHS/ -- MH62126/MH/NIMH NIH HHS/ -- New York, N.Y. -- Science. 2004 Jan 9;303(5655):232-5.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Psychology, University of Oregon, Eugene, OR 97403, USA. mcanders@darkwing.uoregon.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/14716015" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Brain Mapping ; Cues ; Female ; Gyrus Cinguli/physiology ; Hippocampus/*physiology ; Humans ; Magnetic Resonance Imaging ; *Memory ; Mental Recall ; Prefrontal Cortex/*physiology ; *Repression, Psychology ; Retention (Psychology) ; Temporal Lobe/physiology
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  • 159
    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
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  • 160
    Publication Date: 2004-05-01
    Description: Uganda provides the clearest example that human immunodeficiency virus (HIV) is preventable if populations are mobilized to avoid risk. Despite limited resources, Uganda has shown a 70% decline in HIV prevalence since the early 1990s, linked to a 60% reduction in casual sex. The response in Uganda appears to be distinctively associated with communication about acquired immunodeficiency syndrome (AIDS) through social networks. Despite substantial condom use and promotion of biomedical approaches, other African countries have shown neither similar behavioral responses nor HIV prevalence declines of the same scale. The Ugandan success is equivalent to a vaccine of 80% effectiveness. Its replication will require changes in global HIV/AIDS intervention policies and their evaluation.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Stoneburner, Rand L -- Low-Beer, Daniel -- New York, N.Y. -- Science. 2004 Apr 30;304(5671):714-8.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Population Health Evaluation Unit, Cambridge University, Cambridge, UK. randstoneburner@netzero.net〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15118157" target="_blank"〉PubMed〈/a〉
    Keywords: Adolescent ; Adult ; Age Distribution ; Condoms ; Disease Outbreaks ; Female ; HIV Infections/*epidemiology/*prevention & control ; Health Education ; Health Knowledge, Attitudes, Practice ; Humans ; Incidence ; Information Dissemination ; Male ; Middle Aged ; Pregnancy ; Pregnancy Complications, Infectious/*epidemiology/*prevention & control ; Prevalence ; *Risk Reduction Behavior ; Sexual Abstinence ; *Sexual Behavior ; Social Support ; Uganda/epidemiology
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  • 161
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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〉Herz, Barbara -- New York, N.Y. -- Science. 2004 Sep 24;305(5692):1910-1.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15448252" target="_blank"〉PubMed〈/a〉
    Keywords: Child ; Developing Countries ; *Education ; Family ; Female ; Humans ; Male ; Population Growth ; *Women
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  • 162
    Publication Date: 2004-04-10
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Andrews, Lori B -- Buenger, Nancy -- Bridge, Jennifer -- Rosenow, Laurie -- Stoney, David -- Gaensslen, R E -- Karamanski, Theodore -- Lewis, Russell -- Paradise, Jordan -- Inlander, Amy -- Gonen, David -- New York, N.Y. -- Science. 2004 Apr 9;304(5668):215-6.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Institute for Science, Law, and Technology, Illinois Institute of Technology, Chicago, IL 60661, USA. landrews@kentlaw.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15073360" target="_blank"〉PubMed〈/a〉
    Keywords: Bioethical Issues ; *Codes of Ethics ; Ethics, Professional ; Ethics, Research ; Family ; *Famous Persons ; *Guidelines as Topic ; *History of Medicine ; Humans ; Informed Consent
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  • 163
    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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  • 164
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-02-28
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Normile, Dennis -- New York, N.Y. -- Science. 2004 Feb 27;303(5662):1285.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/14988534" target="_blank"〉PubMed〈/a〉
    Keywords: Amyloid/*analysis ; Animals ; Brain/*pathology ; *Brain Chemistry ; Cattle ; Creutzfeldt-Jakob Syndrome/metabolism/pathology ; Encephalopathy, Bovine Spongiform/diagnosis/*etiology/metabolism/pathology ; Humans ; Prions/*analysis/chemistry
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  • 165
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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〉Enserink, Martin -- New York, N.Y. -- Science. 2004 Dec 17;306(5704):2025.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15604380" target="_blank"〉PubMed〈/a〉
    Keywords: Centers for Disease Control and Prevention (U.S.) ; Disease Outbreaks/*statistics & numerical data ; Forecasting ; *Global Health ; Humans ; Influenza Vaccines ; Influenza, Human/*mortality/transmission/virology ; Orthomyxoviridae/pathogenicity ; United States ; Virulence ; *World Health Organization
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  • 166
    Publication Date: 2004-10-02
    Description: We show that activated collagenase (MMP-1) moves processively on the collagen fibril. The mechanism of movement is a biased diffusion with the bias component dependent on the proteolysis of its substrate, not adenosine triphosphate (ATP) hydrolysis. Inactivation of the enzyme by a single amino acid residue substitution in the active center eliminates the bias without noticeable effect on rate of diffusion. Monte Carlo simulations using a model similar to a "burnt bridge" Brownian ratchet accurately describe our experimental results and previous observations on kinetics of collagen digestion. The biological implications of MMP-1 acting as a molecular ratchet tethered to the cell surface suggest new mechanisms for its role in tissue remodeling and cell-matrix interaction.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Saffarian, Saveez -- Collier, Ivan E -- Marmer, Barry L -- Elson, Elliot L -- Goldberg, Gregory -- AR39472/AR/NIAMS NIH HHS/ -- AR40618/AR/NIAMS NIH HHS/ -- GM-38838/GM/NIGMS NIH HHS/ -- New York, N.Y. -- Science. 2004 Oct 1;306(5693):108-11.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Biochemistry and Molecular Biophysics, Washington University School of Medicine, St. Louis, MO 63110, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15459390" target="_blank"〉PubMed〈/a〉
    Keywords: Adenosine Triphosphate/metabolism ; Amino Acid Substitution ; Animals ; Collagen/*metabolism ; Computer Simulation ; Diffusion ; Fluorescence ; Humans ; Hydrolysis ; Mathematics ; Matrix Metalloproteinase 1/chemistry/genetics/*metabolism ; Microscopy, Fluorescence ; Models, Chemical ; Molecular Motor Proteins/chemistry/metabolism ; Monte Carlo Method ; Point Mutation ; Protein Transport ; Rats ; Recombinant Proteins/chemistry/metabolism
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  • 167
    Publication Date: 2004-01-13
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Normile, Dennis -- New York, N.Y. -- Science. 2004 Jan 9;303(5655):156-7.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/14715985" target="_blank"〉PubMed〈/a〉
    Keywords: Abattoirs ; Animal Feed ; Animals ; Cattle ; Cost-Benefit Analysis ; Creutzfeldt-Jakob Syndrome/epidemiology/transmission ; Encephalopathy, Bovine Spongiform/*diagnosis/epidemiology/*prevention & ; control/transmission ; Enzyme-Linked Immunosorbent Assay ; Europe/epidemiology ; Humans ; Immunohistochemistry ; *Immunologic Tests ; Japan ; Mass Screening/*veterinary ; United States/epidemiology ; United States Department of Agriculture
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  • 168
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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〉Enserink, Martin -- New York, N.Y. -- Science. 2004 Oct 15;306(5695):392-4.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15486266" target="_blank"〉PubMed〈/a〉
    Keywords: Cost of Illness ; *Disease Outbreaks ; *Global Health ; Humans ; Influenza A virus/pathogenicity/physiology ; Influenza Vaccines/administration & dosage/supply & distribution ; Influenza, Human/*epidemiology/transmission/virology ; Models, Biological ; Orthomyxoviridae/pathogenicity/physiology ; Public Health ; Reassortant Viruses
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  • 169
    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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  • 170
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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〉Enserink, Martin -- New York, N.Y. -- Science. 2004 Oct 15;306(5695):385.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15486259" target="_blank"〉PubMed〈/a〉
    Keywords: *Drug Contamination ; *Drug Industry ; Great Britain ; Humans ; Immunization Programs ; Influenza Vaccines/*supply & distribution ; Influenza, Human/prevention & control ; Licensure ; Serratia marcescens ; United States
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  • 171
    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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  • 172
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-01-31
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Normile, Dennis -- New York, N.Y. -- Science. 2004 Jan 30;303(5658):609.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/14752135" target="_blank"〉PubMed〈/a〉
    Keywords: Cloning, Molecular ; Hemagglutinins, Viral/genetics/immunology ; Humans ; Influenza A virus/genetics/*immunology ; *Influenza Vaccines ; Influenza, Human/*prevention & control/transmission/virology ; Neuraminidase/genetics/immunology ; Patents as Topic ; Vaccines, Synthetic ; *World Health Organization
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  • 173
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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〉Malakoff, David -- New York, N.Y. -- Science. 2004 Aug 6;305(5685):760.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15297633" target="_blank"〉PubMed〈/a〉
    Keywords: Bioethical Issues ; *Embryo Research/ethics ; Embryo, Mammalian/*cytology ; Financing, Government ; Humans ; *Politics ; Public Opinion ; Research Support as Topic ; *Stem Cells
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  • 174
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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〉Enserink, Martin -- New York, N.Y. -- Science. 2004 Oct 22;306(5696):590.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15498980" target="_blank"〉PubMed〈/a〉
    Keywords: Agricultural Workers' Diseases/epidemiology/virology ; Animals ; Antibodies, Viral/*blood ; Conjunctivitis, Viral/epidemiology/*virology ; Disease Outbreaks/veterinary ; Hemagglutination Inhibition Tests ; Humans ; Influenza A virus/*immunology ; Influenza in Birds/epidemiology ; Netherlands/epidemiology ; Occupational Diseases/*epidemiology/virology ; Orthomyxoviridae Infections/*epidemiology/transmission/virology ; Poultry ; Zoonoses
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  • 175
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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〉Normile, Dennis -- New York, N.Y. -- Science. 2004 Jan 2;303(5654):26.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/14704402" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; *Containment of Biohazards ; Guidelines as Topic ; Humans ; Laboratory Infection/prevention & control/*transmission ; Male ; *Medical Laboratory Personnel ; *SARS Virus ; Severe Acute Respiratory Syndrome/prevention & control/*transmission ; Taiwan ; World Health Organization
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  • 176
    Publication Date: 2004-12-14
    Description: Malaria parasites secrete proteins across the vacuolar membrane into the erythrocyte, inducing modifications linked to disease and parasite survival. We identified an 11-amino acid signal required for the secretion of proteins from the Plasmodium falciparum vacuole to the human erythrocyte. Bioinformatics predicted a secretome of 〉320 proteins and conservation of the signal across parasite species. Functional studies indicated the predictive value of the signal and its role in targeting virulence proteins to the erythrocyte and implicated its recognition by a receptor/transporter. Erythrocyte modification by the parasite may involve plasmodial heat shock proteins and be vastly more complex than hitherto realized.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Hiller, N Luisa -- Bhattacharjee, Souvik -- van Ooij, Christiaan -- Liolios, Konstantinos -- Harrison, Travis -- Lopez-Estrano, Carlos -- Haldar, Kasturi -- AI39071/AI/NIAID NIH HHS/ -- HL69630/HL/NHLBI NIH HHS/ -- New York, N.Y. -- Science. 2004 Dec 10;306(5703):1934-7.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Departments of Pathology and Microbiology-Immunology, Feinberg School of Medicine, Northwestern University, 303 East Chicago Avenue, Chicago, IL 60611, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15591203" target="_blank"〉PubMed〈/a〉
    Keywords: *Amino Acid Motifs ; Amino Acid Sequence ; Animals ; Computational Biology ; Cytosol/metabolism ; Erythrocytes/*metabolism/parasitology ; Genes, Protozoan ; Humans ; Malaria, Falciparum/parasitology ; Membrane Proteins/chemistry/metabolism ; Molecular Sequence Data ; Plasmodium falciparum/genetics/growth & development/*metabolism/*pathogenicity ; *Protein Sorting Signals ; Protein Structure, Tertiary ; Protein Transport ; Protozoan Proteins/chemistry/genetics/*metabolism ; Recombinant Fusion Proteins/chemistry/metabolism ; Transgenes ; Vacuoles/metabolism/parasitology ; Virulence Factors/chemistry/genetics/*metabolism
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  • 177
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-10-02
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Cho, Adrian -- New York, N.Y. -- Science. 2004 Oct 1;306(5693):42-3.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15459363" target="_blank"〉PubMed〈/a〉
    Keywords: Arm/*physiology ; *Biomechanical Phenomena ; Humans ; Movement ; Software
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  • 178
    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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  • 179
    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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  • 180
    Publication Date: 2004-10-16
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Hofreiter, Michael -- Loreille, Odile -- Ferriola, Deborah -- Parsons, Thomas J -- New York, N.Y. -- Science. 2004 Oct 15;306(5695):407-10.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15486274" target="_blank"〉PubMed〈/a〉
    Keywords: Bone and Bones/chemistry ; DNA/analysis/genetics/history ; *DNA Fingerprinting ; DNA, Mitochondrial/chemistry/genetics ; *Famous Persons ; *Forensic Anthropology ; History, 20th Century ; Humans ; Polymerase Chain Reaction ; Russia ; Tissue Preservation
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  • 181
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-04-10
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Enserink, Martin -- New York, N.Y. -- Science. 2004 Apr 9;304(5668):199.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15073353" target="_blank"〉PubMed〈/a〉
    Keywords: Antitubercular Agents/*administration & dosage/therapeutic use ; *Directly Observed Therapy ; Drug Therapy, Combination ; Education, Professional ; European Union ; Health Facilities ; Humans ; Latvia ; Patient Compliance ; Tuberculosis, Multidrug-Resistant/*drug therapy/epidemiology/prevention & control
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  • 182
    Publication Date: 2004-08-07
    Description: Plexins are cell surface receptors for semaphorin molecules, and their interaction governs cell adhesion and migration in a variety of tissues. We report that the Semaphorin 4D (Sema4D) receptor Plexin-B1 directly stimulates the intrinsic guanosine triphosphatase (GTPase) activity of R-Ras, a member of the Ras superfamily of small GTP-binding proteins that has been implicated in promoting cell adhesion and neurite outgrowth. This activity required the interaction of Plexin-B1 with Rnd1, a small GTP-binding protein of the Rho family. Down-regulation of R-Ras activity by the Plexin-B1-Rnd1 complex was essential for the Sema4D-induced growth cone collapse in hippocampal neurons. Thus, Plexin-B1 mediates Sema4D-induced repulsive axon guidance signaling by acting as a GTPase activating protein for R-Ras.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Oinuma, Izumi -- Ishikawa, Yukio -- Katoh, Hironori -- Negishi, Manabu -- New York, N.Y. -- Science. 2004 Aug 6;305(5685):862-5.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Laboratory of Molecular Neurobiology, Graduate School of Biostudies, Kyoto University, Sakyo-ku, Kyoto 606-8502, Japan.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15297673" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; *Antigens, CD ; Axons/physiology ; COS Cells ; Cells, Cultured ; Down-Regulation ; GTP Phosphohydrolases/*metabolism ; GTPase-Activating Proteins/chemistry/genetics/*metabolism ; Guanosine Triphosphate/metabolism ; Hippocampus/cytology ; Humans ; Membrane Glycoproteins/*metabolism/pharmacology ; Neurites/physiology ; Neurons/*metabolism ; PC12 Cells ; Protein Structure, Tertiary ; RNA, Small Interfering ; Rats ; Receptors, Cell Surface/chemistry/genetics/*metabolism ; Recombinant Fusion Proteins/metabolism ; *Semaphorins ; Signal Transduction ; Transfection ; ras Proteins/*metabolism ; rho GTP-Binding Proteins/genetics/metabolism ; rhoA GTP-Binding Protein/metabolism
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  • 183
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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〉Schaitberger, Harold A -- New York, N.Y. -- Science. 2004 Jul 30;305(5684):607.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15286344" target="_blank"〉PubMed〈/a〉
    Keywords: *Fires ; Humans ; *National Institute for Occupational Safety and Health (U.S.)/organization & ; administration ; Occupational Health ; United States
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  • 184
    Publication Date: 2004-05-25
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Enserink, Martin -- New York, N.Y. -- Science. 2004 May 21;304(5674):1097.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15155925" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Antiviral Agents/pharmacology/therapeutic use ; Carnivora/virology ; Clinical Trials as Topic ; Disease Outbreaks ; Genome, Viral ; Humans ; Laboratory Infection/epidemiology ; Rats/virology ; *SARS Virus/drug effects/genetics/immunology/isolation & purification ; *Severe Acute Respiratory Syndrome/drug therapy/epidemiology/prevention & ; control/virology ; Viral Vaccines/adverse effects
    Print ISSN: 0036-8075
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  • 185
    Publication Date: 2004-04-17
    Description: Instrumental conditioning studies how animals and humans choose actions appropriate to the affective structure of an environment. According to recent reinforcement learning models, two distinct components are involved: a "critic," which learns to predict future reward, and an "actor," which maintains information about the rewarding outcomes of actions to enable better ones to be chosen more frequently. We scanned human participants with functional magnetic resonance imaging while they engaged in instrumental conditioning. Our results suggest partly dissociable contributions of the ventral and dorsal striatum, with the former corresponding to the critic and the latter corresponding to the actor.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉O'Doherty, John -- Dayan, Peter -- Schultz, Johannes -- Deichmann, Ralf -- Friston, Karl -- Dolan, Raymond J -- New York, N.Y. -- Science. 2004 Apr 16;304(5669):452-4.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Wellcome Department of Imaging Neuroscience, Institute of Neurology, University College London, London WC1N 3BG, UK. j.odoherty@fil.ion.ucl.ac.uk〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15087550" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Basal Ganglia/*physiology ; Caudate Nucleus/*physiology ; Conditioning, Classical ; *Conditioning, Operant ; Female ; Humans ; Learning ; Magnetic Resonance Imaging ; Male ; Middle Aged ; Nucleus Accumbens/*physiology ; Probability ; Putamen/*physiology ; Reinforcement (Psychology) ; Reward
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-12-21
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Okeke, Iruka N -- New York, N.Y. -- Science. 2004 Dec 17;306(5704):2039-40; author reply 2039-40.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15609423" target="_blank"〉PubMed〈/a〉
    Keywords: Africa ; Animals ; Antimalarials/*pharmacology/therapeutic use ; Asia ; Communicable Disease Control/*methods ; Drug Resistance ; Humans ; Malaria, Falciparum/*parasitology/*prevention & control/transmission ; Mass Screening ; Plasmodium falciparum/*drug effects ; Pyrimethamine/pharmacology/therapeutic use ; Travel
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  • 187
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-09-09
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Enserink, Martin -- Kaiser, Jocelyn -- New York, N.Y. -- Science. 2004 Sep 3;305(5689):1385.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15353766" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Birds ; Carnivora/*virology ; Cat Diseases/transmission/*virology ; Cats ; Genes, Viral ; Humans ; Influenza A virus/genetics/*pathogenicity ; Influenza in Birds/transmission/virology ; Influenza, Human/transmission/*veterinary/virology ; Poultry ; Swine ; Swine Diseases/virology
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  • 188
    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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  • 189
    Publication Date: 2004-03-16
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Enserink, Martin -- New York, N.Y. -- Science. 2004 Mar 12;303(5664):1605.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15016977" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Centers for Disease Control and Prevention (U.S.) ; Communicable Disease Control ; Communicable Diseases, Emerging/*epidemiology/prevention & control ; *Disease Outbreaks/prevention & control ; Humans ; Population Surveillance ; United States ; *World Health Organization/organization & administration
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  • 190
    Publication Date: 2004-07-13
    Description: Therapeutic vaccines aim to prevent severe complications of a chronic infection by reinforcing host defenses when some immune control, albeit insufficient, can already be demonstrated and when a conventional antimicrobial therapy either is not available or has limited efficacy. We focus on the rationale and challenges behind this still controversial strategy and provide examples from three major chronic infectious diseases- human immunodeficiency virus, hepatitis B virus, and human papillomavirus-for which the efficacy of therapeutic vaccines is currently being evaluated.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Autran, Brigitte -- Carcelain, Guislaine -- Combadiere, Behazine -- Debre, Patrice -- New York, N.Y. -- Science. 2004 Jul 9;305(5681):205-8.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Laboratoire d'Immunologie Cellulaire and INSERM Unit 543, Centre Hospitalier Universitaire Pitie-Salpetriere, Universite Pierre et Marie Curie, 75013 Paris, France. brigitte.autran@psl.ap-hop-paris.fr〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15247470" target="_blank"〉PubMed〈/a〉
    Keywords: AIDS Vaccines/immunology/*therapeutic use ; Adjuvants, Immunologic ; Anti-HIV Agents/therapeutic use ; Chronic Disease ; Clinical Trials as Topic ; Combined Modality Therapy ; HIV Infections/drug therapy/immunology/*therapy ; Hepatitis B/immunology/*therapy ; Hepatitis B Vaccines/immunology/*therapeutic use ; Humans ; Papillomaviridae/*immunology ; Papillomavirus Infections/immunology/*therapy ; T-Lymphocytes/immunology ; Vaccines, DNA/immunology/therapeutic use ; Vaccines, Synthetic/immunology/therapeutic use ; Viral Vaccines/*therapeutic use
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  • 191
    Publication Date: 2004-12-25
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Avery, Mary Ellen -- New York, N.Y. -- Science. 2004 Dec 24;306(5705):2212-3.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15618508" target="_blank"〉PubMed〈/a〉
    Keywords: Child ; Child Welfare ; Forecasting ; Global Health ; Humans ; *Imagination ; Knowledge ; Population Growth ; Public Health ; *Research ; *Science ; United Nations
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    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 192
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-02-21
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Enserink, Martin -- New York, N.Y. -- Science. 2004 Feb 20;303(5661):1121.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/14976284" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Bangladesh/epidemiology ; Communicable Diseases, Emerging/*epidemiology ; *Disease Outbreaks ; *Henipavirus ; Henipavirus Infections/*epidemiology/transmission/veterinary/virology ; Humans ; *Nipah Virus/immunology ; Viral Vaccines
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    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 193
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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〉Enserink, Martin -- Du, Lei -- New York, N.Y. -- Science. 2004 Jul 9;305(5681):163.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15247446" target="_blank"〉PubMed〈/a〉
    Keywords: China/epidemiology ; *Containment of Biohazards ; Disease Outbreaks ; Government Agencies/*organization & administration ; Humans ; Laboratory Infection/*epidemiology ; *SARS Virus ; Severe Acute Respiratory Syndrome/*epidemiology ; Virus Inactivation
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    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 194
    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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  • 195
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-04-03
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Tobena, Adolf -- New York, N.Y. -- Science. 2004 Apr 2;304(5667):47-9; author reply 47-9.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15060306" target="_blank"〉PubMed〈/a〉
    Keywords: *Behavior ; Female ; Humans ; Islam ; Male ; *Personality ; Religion ; *Suicide ; Temperament ; *Terrorism
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    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 196
    Publication Date: 2004-11-30
    Description: Signaling pathways that are activated by epidermal growth factor (EGF) or fibroblast growth factor (FGF) receptors have been identified and compared (detailed Connections Maps are available at Science's Signal Transduction Knowledge Environment). Both receptors stimulate a similar complement of intracellular signaling pathways. However, whereas activated EGF receptors (EGFRs) function as the main platform for recruitment of signaling proteins, signaling through the FGF receptors (FGFRs) is mediated primarily by assembly of a multidocking protein complex. Moreover, FGFR signaling is subject to additional intracellular and extracellular control mechanisms that do not affect EGFR signaling. The differential circuitry of the intracellular networks that are activated by EGFR and FGFR may affect signal specificity and physiological responses.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Schlessinger, Joseph -- R01-AR051448-01/AR/NIAMS NIH HHS/ -- New York, N.Y. -- Science. 2004 Nov 26;306(5701):1506-7.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Pharmacology, Yale University School of Medicine, New Haven, CT 06520, USA. joseph.schlessinger@yale.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15567848" target="_blank"〉PubMed〈/a〉
    Keywords: Adaptor Proteins, Signal Transducing/metabolism ; Binding Sites ; Dimerization ; Epidermal Growth Factor/metabolism ; Fibroblast Growth Factors/metabolism ; Heparan Sulfate Proteoglycans/metabolism ; Humans ; Ligands ; Phosphorylation ; Receptor, Epidermal Growth Factor/chemistry/*metabolism ; Receptors, Fibroblast Growth Factor/chemistry/*metabolism ; Second Messenger Systems ; *Signal Transduction ; Tyrosine/metabolism
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  • 197
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-12-04
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Holden, Constance -- New York, N.Y. -- Science. 2004 Dec 3;306(5702):1666.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15576579" target="_blank"〉PubMed〈/a〉
    Keywords: Aging ; Body Mass Index ; Cell Aging ; Child ; Chronic Disease ; Humans ; Leukocytes/physiology ; *Mothers ; *Oxidative Stress ; *Parenting ; *Stress, Psychological ; Telomerase/*metabolism ; Telomere/*ultrastructure
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    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 198
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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〉Holden, Constance -- New York, N.Y. -- Science. 2004 Jul 30;305(5684):639-40.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15286362" target="_blank"〉PubMed〈/a〉
    Keywords: Anaerobic Threshold ; Body Constitution ; Doping in Sports ; Female ; Heart/physiology ; Humans ; Male ; Muscle, Skeletal/anatomy & histology/physiology ; Oxygen Consumption ; Physical Endurance ; Pulmonary Ventilation ; *Running ; *Sex Characteristics ; Testosterone/metabolism
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    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 199
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-09-09
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Olson, Steve -- New York, N.Y. -- Science. 2004 Sep 3;305(5689):1390-2.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15353772" target="_blank"〉PubMed〈/a〉
    Keywords: Anti-Bacterial Agents/therapeutic use ; Antipsychotic Agents/therapeutic use ; Attention Deficit Disorder with Hyperactivity ; Basal Ganglia/*physiopathology ; Behavior Therapy ; Comorbidity ; Electric Stimulation Therapy ; Humans ; Obsessive-Compulsive Disorder ; Phenotype ; Streptococcal Infections/complications ; Tics ; *Tourette Syndrome/etiology/physiopathology/psychology/therapy
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    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 200
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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〉Holden, Constance -- New York, N.Y. -- Science. 2004 Jul 30;305(5684):637-9.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15286361" target="_blank"〉PubMed〈/a〉
    Keywords: Africa, Eastern ; Africa, Western ; *African Continental Ancestry Group/genetics ; Body Composition ; Body Constitution ; Energy Metabolism ; Female ; Humans ; Kenya ; Lactates/metabolism ; Leg/anatomy & histology ; Male ; Muscle Fibers, Fast-Twitch/physiology ; Muscle Fibers, Slow-Twitch/physiology ; Muscle, Skeletal/anatomy & histology/enzymology/*physiology ; Oxygen Consumption ; Physical Endurance ; Physical Fitness ; *Running/physiology
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    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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