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  • Animals  (4,137)
  • Inorganic Chemistry
  • 2000-2004  (4,137)
  • 101
    Publication Date: 2004-05-15
    Description: Although the ability of engrafted stem cells to regenerate tissue has received much attention, the molecular mechanisms controlling regeneration are poorly understood. In the Drosophila male germline, local activation of the Janus kinase-signal transducer and activator of transcription (Jak-STAT) pathway maintains stem cells; germline stem cells lacking Jak-STAT signaling differentiate into spermatogonia without self-renewal. By conditionally manipulating Jak-STAT signaling, we find that spermatogonia that have initiated differentiation and are undergoing limited mitotic (transit-amplifying) divisions can repopulate the niche and revert to stem cell identity. Thus, in the appropriate microenvironment, transit-amplifying cells dedifferentiate, becoming functional stem cells during tissue regeneration.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Brawley, Crista -- Matunis, Erika -- R01HD40307/HD/NICHD NIH HHS/ -- New York, N.Y. -- Science. 2004 May 28;304(5675):1331-4. Epub 2004 May 13.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Cell Biology, 725 North Wolfe Street, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15143218" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Cell Differentiation ; Cell Division ; DNA-Binding Proteins/metabolism ; Drosophila/*physiology ; *Drosophila Proteins ; Germ Cells/cytology/*physiology ; Male ; Mitosis ; Protein-Tyrosine Kinases/metabolism ; *Regeneration ; STAT Transcription Factors ; Signal Transduction ; Spermatocytes/physiology ; Spermatogonia/*cytology/*physiology ; Stem Cells/cytology/*physiology ; Testis/cytology ; Trans-Activators/metabolism
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  • 102
    Publication Date: 2004-12-25
    Description: In the developing brain, transcription factors (TFs) direct the formation of a diverse array of neurons and glia. We identifed 1445 putative TFs in the mouse genome. We used in situ hybridization to map the expression of over 1000 of these TFs and TF-coregulator genes in the brains of developing mice. We found that 349 of these genes showed restricted expression patterns that were adequate to describe the anatomical organization of the brain. We provide a comprehensive inventory of murine TFs and their expression patterns in a searchable brain atlas database.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Gray, Paul A -- Fu, Hui -- Luo, Ping -- Zhao, Qing -- Yu, Jing -- Ferrari, Annette -- Tenzen, Toyoaki -- Yuk, Dong-In -- Tsung, Eric F -- Cai, Zhaohui -- Alberta, John A -- Cheng, Le-Ping -- Liu, Yang -- Stenman, Jan M -- Valerius, M Todd -- Billings, Nathan -- Kim, Haesun A -- Greenberg, Michael E -- McMahon, Andrew P -- Rowitch, David H -- Stiles, Charles D -- Ma, Qiufu -- New York, N.Y. -- Science. 2004 Dec 24;306(5705):2255-7.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Neurobiology, Harvard Medical School, Boston, MA 02115, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15618518" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Animals, Newborn ; Brain/anatomy & histology/embryology/*growth & development/*metabolism ; Cloning, Molecular ; Corpus Striatum/anatomy & histology/embryology/growth & development/metabolism ; DNA Primers ; Databases, Factual ; *Gene Expression Profiling ; *Genome ; Hypothalamus/anatomy & histology/embryology/growth & development/metabolism ; In Situ Hybridization ; Mesencephalon/anatomy & histology/embryology/growth & development/metabolism ; Mice ; Neocortex/anatomy & histology/embryology/growth & development/metabolism ; Polymerase Chain Reaction ; Rhombencephalon/anatomy & histology/embryology/growth & development/metabolism ; Spinal Cord/anatomy & histology/embryology/growth & development/metabolism ; Thalamus/anatomy & histology/embryology/growth & development/metabolism ; Transcription Factors/*genetics/*metabolism
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  • 103
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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〉Wickelgren, Ingrid -- New York, N.Y. -- Science. 2004 Jul 9;305(5681):162-3.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15247444" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Arm/physiology ; Cues ; Goals ; Haplorhini ; *Intention ; Motivation ; *Movement ; Neurons/*physiology ; Paralysis/physiopathology/psychology ; Parietal Lobe/*physiology ; Prostheses and Implants ; Reward ; Software
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  • 104
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-01-06
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Levitt, Pat -- New York, N.Y. -- Science. 2004 Jan 2;303(5654):48-9.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Vanderbilt Kennedy Center for Research on Human Development and Department of Pharmacology, Vanderbilt University, Nashville, TN 37203, USA. pat.levitt@vanderbilt.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/14704417" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Cell Differentiation ; Cell Lineage ; Cerebral Cortex/*cytology/embryology ; DNA-Binding Proteins/*genetics/*metabolism ; Down-Regulation ; Forkhead Transcription Factors ; Gene Expression Regulation, Developmental ; Mice ; Nerve Tissue Proteins/*genetics/*metabolism ; Neurons/*cytology/*physiology ; Stem Cells/cytology/*physiology ; Time Factors ; Transcription Factors/genetics/*metabolism
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  • 105
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-07-13
    Description: The field of immunotherapy holds clear promise not only for the development of new approaches to cancer and other diseases, but also for providing fundamental insight into the human immune response. In order for this promise to be realized, however, the scientific community must overcome an array of challenges. These challenges reflect not only the difficulties inherent in conducting investigations in human patients, but also difficulties created by the culture and practice of our own institutions, reward structure, and funding mechanisms. We suggest steps to be taken to reinvigorate basic research in human subjects as part of the mainstream of science.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Steinman, Ralph M -- Mellman, Ira -- New York, N.Y. -- Science. 2004 Jul 9;305(5681):197-200.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Laboratory of Cellular Physiology and Immunology, Rockefeller University, New York, NY 10021-6399, USA. steinma@mail.rockefeller.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15247468" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; *Biomedical Research ; Cancer Vaccines/therapeutic use ; Clinical Trials as Topic ; Dendritic Cells/immunology ; Human Experimentation ; Humans ; Immune System/physiology ; Immune Tolerance ; *Immunotherapy ; Neoplasms/immunology/*therapy ; Peer Review, Research ; Publishing ; Research Support as Topic
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    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 106
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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〉Stern, Alan H -- New York, N.Y. -- Science. 2004 Feb 6;303(5659):763-6; author reply 763-6.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/14764851" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Cysteine/*analogs & derivatives/analysis/toxicity ; *Fishes ; *Food Contamination ; Humans ; Mercury/analysis ; Methylmercury Compounds/*analysis/toxicity ; *Public Health ; Seafood/*analysis
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  • 107
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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〉Wickelgren, Ingrid -- New York, N.Y. -- Science. 2004 Jan 2;303(5654):28-9.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/14704404" target="_blank"〉PubMed〈/a〉
    Keywords: Amino Acid Sequence ; Animals ; Aplysia/physiology ; Memory/*physiology ; Neurons/*physiology ; Prions/chemistry/metabolism/*physiology ; Protein Biosynthesis ; Protein Conformation ; RNA, Messenger/genetics/metabolism ; Solubility ; Transcription Factors/chemistry/genetics/*metabolism ; Yeasts/genetics/metabolism ; mRNA Cleavage and Polyadenylation Factors/chemistry/genetics/*metabolism
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  • 108
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-10-09
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Proffitt, Fiona -- Bagla, Pallava -- New York, N.Y. -- Science. 2004 Oct 8;306(5694):223.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15472057" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Animals, Domestic ; Anti-Inflammatory Agents, Non-Steroidal/poisoning/therapeutic use ; Bird Diseases/*chemically induced/epidemiology/mortality ; Conservation of Natural Resources ; Diclofenac/*poisoning/therapeutic use ; Drug Residues/poisoning ; Gout/chemically induced/epidemiology/mortality/veterinary ; India/epidemiology ; Nepal/epidemiology ; Pakistan/epidemiology ; Population Dynamics ; *Raptors ; Uric Acid ; Veterinary Drugs/poisoning/therapeutic use
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  • 109
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-08-03
    Description: In the mitochondrial pathway of apoptosis, caspase activation is closely linked to mitochondrial outer membrane permeabilization (MOMP). Numerous pro-apoptotic signal-transducing molecules and pathological stimuli converge on mitochondria to induce MOMP. The local regulation and execution of MOMP involve proteins from the Bcl-2 family, mitochondrial lipids, proteins that regulate bioenergetic metabolite flux, and putative components of the permeability transition pore. MOMP is lethal because it results in the release of caspase-activating molecules and caspase-independent death effectors, metabolic failure in the mitochondria, or both. Drugs designed to suppress excessive MOMP may avoid pathological cell death, and the therapeutic induction of MOMP may restore apoptosis in cancer cells in which it is disabled. The general rules governing the pathophysiology of MOMP and controversial issues regarding its regulation are discussed.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Green, Douglas R -- Kroemer, Guido -- New York, N.Y. -- Science. 2004 Jul 30;305(5684):626-9.〈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. doug@liai.org〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15286356" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; *Apoptosis ; Disease/*etiology ; Humans ; Intracellular Membranes/*physiology ; Mitochondria/*physiology ; Models, Biological ; Neoplasms/physiopathology ; Permeability ; Proteins/*metabolism ; Proto-Oncogene Proteins c-bcl-2/metabolism ; Signal Transduction ; Viral Proteins/metabolism ; Virus Physiological Phenomena
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  • 110
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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〉Proffitt, Fiona -- New York, N.Y. -- Science. 2004 Mar 26;303(5666):1955-6.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15044773" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Azerbaijan ; *Conservation of Natural Resources ; *Fisheries ; *Fishes ; Iran ; Kazakhstan ; Population Density ; Russia ; Turkmenistan ; *United Nations
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  • 111
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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〉Przyborski, Jude -- Lanzer, Michael -- New York, N.Y. -- Science. 2004 Dec 10;306(5703):1897-8.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Parasitology, Universitatsklinikum Heidelberg, Im Neuenheimer Feld 324, 69120 Heidelberg, Germany.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15591189" target="_blank"〉PubMed〈/a〉
    Keywords: Amino Acid Motifs ; Animals ; Cytoplasm/metabolism ; Erythrocyte Membrane/metabolism ; Erythrocytes/parasitology ; Humans ; Plasmodium/chemistry/genetics/metabolism ; Plasmodium falciparum/chemistry/genetics/*metabolism/pathogenicity ; *Protein Sorting Signals ; Protein Transport ; Protozoan Proteins/chemistry/genetics/*metabolism ; Vacuoles/metabolism/parasitology
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  • 112
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-07-27
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Staley, Kevin -- New York, N.Y. -- Science. 2004 Jul 23;305(5683):482-3.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Neurology and Pediatrics, University of Colorado Health Sciences Center, Denver, CO 80262, USA. kevin.staley@uchsc.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15273382" target="_blank"〉PubMed〈/a〉
    Keywords: Action Potentials ; Animals ; Axons/physiology ; Dendrites/*physiology ; Epilepsy, Temporal Lobe/*physiopathology ; Feedback, Physiological ; Hippocampus/cytology/*physiopathology ; Humans ; Nerve Net/physiology ; Neural Inhibition ; Neurons/*physiology ; Pilocarpine/administration & dosage ; Potassium/*metabolism ; Potassium Channels/*physiology ; Rats ; Synapses/physiology ; Synaptic Transmission
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  • 113
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-06-12
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉White, Alice -- New York, N.Y. -- Science. 2004 Jun 11;304(5677):1595.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15192200" target="_blank"〉PubMed〈/a〉
    Keywords: Air Microbiology ; *Animal Husbandry ; Animals ; Drug Resistance, Bacterial ; Politics ; Public Policy ; *Science ; *Swine ; United States
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  • 114
    Publication Date: 2004-10-02
    Description: Like most vertebrates, humans die within minutes when deprived of molecular oxygen (anoxia), in part because of cardiac failure. In contrast, some freshwater turtles can survive anoxia for months at low temperatures, but to do so, they drastically suppress cardiac activity and autonomic cardiovascular control. Although Carassius carassius, the crucian carp, shares this anoxia tolerance, we show that it has a unique ability among vertebrates to retain normal cardiac performance and autonomic cardiovascular regulation for at least 5 days of anoxia. These responses point to an unusual tolerance of a vertebrate heart and autonomic nervous system to prolonged anoxia.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Stecyk, Jonathan A W -- Stenslokken, Kare-Olav -- Farrell, Anthony P -- Nilsson, Goran E -- New York, N.Y. -- Science. 2004 Oct 1;306(5693):77.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Biological Sciences, Simon Fraser University, 8888 University Drive, Burnaby V5A 1S6, Canada. jstecyk@interchange.ubc.ca〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15459381" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Anoxia/*physiopathology ; Autonomic Nervous System/*physiology ; Blood Pressure ; Cardiac Output ; Carps/*physiology ; Ethanol/metabolism ; Heart/*physiology ; Heart Rate ; *Hemodynamics ; Respiration ; Stroke Volume ; Vascular Resistance
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  • 115
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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〉Moore, Leroy -- New York, N.Y. -- Science. 2004 Nov 5;306(5698):975; author reply 975.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15528425" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Colorado ; Ecosystem ; *Environmental Pollution/legislation & jurisprudence ; Humans ; *Plutonium ; Public Policy ; *Radioactive Pollutants ; Risk Assessment ; United States Government Agencies
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  • 116
    Publication Date: 2004-04-06
    Description: Huntington's disease (HD) is characterized by the accumulation of a pathogenic protein, Huntingtin (Htt), that contains an abnormal polyglutamine expansion. Here, we report that a pathogenic fragment of Htt (Httex1p) can be modified either by small ubiquitin-like modifier (SUMO)-1 or by ubiquitin on identical lysine residues. In cultured cells, SUMOylation stabilizes Httex1p, reduces its ability to form aggregates, and promotes its capacity to repress transcription. In a Drosophila model of HD, SUMOylation of Httex1p exacerbates neurodegeneration, whereas ubiquitination of Httex1p abrogates neurodegeneration. Lysine mutations that prevent both SUMOylation and ubiquitination of Httex1p reduce HD pathology, indicating that the contribution of SUMOylation to HD pathology extends beyond preventing Htt ubiquitination and degradation.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Steffan, Joan S -- Agrawal, Namita -- Pallos, Judit -- Rockabrand, Erica -- Trotman, Lloyd C -- Slepko, Natalia -- Illes, Katalin -- Lukacsovich, Tamas -- Zhu, Ya-Zhen -- Cattaneo, Elena -- Pandolfi, Pier Paolo -- Thompson, Leslie Michels -- Marsh, J Lawrence -- CA-62203/CA/NCI NIH HHS/ -- HD36049/HD/NICHD NIH HHS/ -- HD36081/HD/NICHD NIH HHS/ -- New York, N.Y. -- Science. 2004 Apr 2;304(5667):100-4.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Psychiatry and Human Behavior, Gillespie 2121, University of California, Irvine, CA 92697, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15064418" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Animals, Genetically Modified ; Cell Line ; Cell Nucleus/metabolism ; Corpus Striatum/cytology ; Cytoplasm/metabolism ; Drosophila ; Genes, MDR ; HeLa Cells ; Humans ; Huntington Disease/metabolism/*pathology ; Lysine/genetics/metabolism ; Mutation ; Nerve Degeneration ; Nerve Tissue Proteins/chemistry/genetics/*metabolism ; Neurons/metabolism ; Nuclear Proteins/chemistry/genetics/*metabolism ; Proline/genetics/metabolism ; Promoter Regions, Genetic ; Rats ; Recombinant Fusion Proteins/metabolism ; SUMO-1 Protein/genetics/*metabolism ; Transcription, Genetic ; Transfection ; Ubiquitin/metabolism
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  • 117
    Publication Date: 2004-03-06
    Description: Neutrophils engulf and kill bacteria when their antimicrobial granules fuse with the phagosome. Here, we describe that, upon activation, neutrophils release granule proteins and chromatin that together form extracellular fibers that bind Gram-positive and -negative bacteria. These neutrophil extracellular traps (NETs) degrade virulence factors and kill bacteria. NETs are abundant in vivo in experimental dysentery and spontaneous human appendicitis, two examples of acute inflammation. NETs appear to be a form of innate response that binds microorganisms, prevents them from spreading, and ensures a high local concentration of antimicrobial agents to degrade virulence factors and kill bacteria.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Brinkmann, Volker -- Reichard, Ulrike -- Goosmann, Christian -- Fauler, Beatrix -- Uhlemann, Yvonne -- Weiss, David S -- Weinrauch, Yvette -- Zychlinsky, Arturo -- AI037720/AI/NIAID NIH HHS/ -- New York, N.Y. -- Science. 2004 Mar 5;303(5663):1532-5.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Microscopy Core Facility, Max Planck Institute for Infection Biology, Schumannstrasse 21/22, 10117 Berlin, Germany.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15001782" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Appendicitis/immunology ; Bacterial Proteins/metabolism ; Blood Bactericidal Activity ; Cytochalasin D/pharmacology ; Cytoplasmic Granules/metabolism ; DNA/analysis/metabolism ; Dysentery, Bacillary/immunology ; Endopeptidases/metabolism ; Histones/analysis/metabolism ; Humans ; *Immunity, Innate ; Leukocyte Elastase/analysis/metabolism ; Microscopy, Electron ; *Neutrophil Activation ; Neutrophils/chemistry/*immunology/physiology/ultrastructure ; Phagocytosis ; Rabbits ; Salmonella typhimurium/immunology/*physiology ; Shigella flexneri/immunology/*physiology ; Staphylococcus aureus/immunology/*physiology ; Virulence Factors/metabolism
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  • 118
    Publication Date: 2004-01-17
    Description: Several human and animal Ebola outbreaks have occurred over the past 4 years in Gabon and the Republic of Congo. The human outbreaks consisted of multiple simultaneous epidemics caused by different viral strains, and each epidemic resulted from the handling of a distinct gorilla, chimpanzee, or duiker carcass. These animal populations declined markedly during human Ebola outbreaks, apparently as a result of Ebola infection. Recovered carcasses were infected by a variety of Ebola strains, suggesting that Ebola outbreaks in great apes result from multiple virus introductions from the natural host. Surveillance of animal mortality may help to predict and prevent human Ebola outbreaks.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Leroy, Eric M -- Rouquet, Pierre -- Formenty, Pierre -- Souquiere, Sandrine -- Kilbourne, Annelisa -- Froment, Jean-Marc -- Bermejo, Magdalena -- Smit, Sheilag -- Karesh, William -- Swanepoel, Robert -- Zaki, Sherif R -- Rollin, Pierre E -- New York, N.Y. -- Science. 2004 Jan 16;303(5656):387-90.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Institut de Recherche pour le Developpement, UR034, Centre International de Recherches Medicales de Franceville, BP 769 Franceville, Gabon. Eric.Leroy@ird.fr〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/14726594" target="_blank"〉PubMed〈/a〉
    Keywords: Africa, Central/epidemiology ; Animals ; Animals, Wild/*virology ; Ape Diseases/*epidemiology/virology ; Base Sequence ; *Disease Outbreaks/veterinary ; Disease Reservoirs ; Ebolavirus/classification/*genetics/isolation & purification ; Gabon/epidemiology ; Genes, Viral ; Gorilla gorilla/virology ; Hemorrhagic Fever, Ebola/*epidemiology/transmission/*veterinary/virology ; Humans ; Molecular Sequence Data ; Pan troglodytes/virology ; Population Density ; Population Surveillance ; Ruminants/virology ; Viral Envelope Proteins/genetics
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    Publication Date: 2004-10-16
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Grimm, David -- New York, N.Y. -- Science. 2004 Oct 15;306(5695):389.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15486263" target="_blank"〉PubMed〈/a〉
    Keywords: *Aneuploidy ; Animals ; Cell Cycle Proteins ; Child ; *Chromosomal Instability ; *DNA Repair ; *Genetic Predisposition to Disease ; Genomic Instability ; Humans ; Mice ; Mosaicism ; Mutation ; Neoplasms/*genetics ; Protein Kinases/genetics ; Protein-Serine-Threonine Kinases
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  • 120
    Publication Date: 2004-10-30
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Wickelgren, Ingrid -- New York, N.Y. -- Science. 2004 Oct 29;306(5697):791-2.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15514121" target="_blank"〉PubMed〈/a〉
    Keywords: Amyloid beta-Peptides/*chemistry/metabolism/toxicity ; Animals ; Cell Death/drug effects ; Cells, Cultured ; Congo Red/*analogs & derivatives/*chemical ; synthesis/chemistry/*metabolism/*pharmacology ; Ligands ; Neurons/cytology/*drug effects ; Piperidines/*chemical synthesis/chemistry/metabolism/*pharmacology ; Protein Conformation ; Rats ; Tacrolimus Binding Proteins/*metabolism/pharmacology
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  • 121
    Publication Date: 2004-01-24
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Racki, Grzegorz -- Koeberl, Christian -- New York, N.Y. -- Science. 2004 Jan 23;303(5657):471; author reply 471.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Earth Sciences, University of Silesia, PL-41-200, Sosnowiec, Poland. racki@us.edu.pl〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/14739442" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; *Ecosystem ; *Geologic Sediments ; Magnetics ; *Meteoroids ; Seawater ; Time
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  • 122
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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〉Kaiser, Jocelyn -- New York, N.Y. -- Science. 2004 Jan 2;303(5654):25-6.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/14704401" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Dinoflagellida/growth & development/metabolism/*pathogenicity ; Fish Diseases/parasitology ; Fishes ; Humans ; Life Cycle Stages ; Pfiesteria piscicida/growth & development/metabolism/*pathogenicity ; Protozoan Infections, Animal/parasitology ; Toxins, Biological/*biosynthesis
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  • 123
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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〉Grimm, David -- New York, N.Y. -- Science. 2004 Sep 24;305(5692):1907.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15448250" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; *Awards and Prizes ; Chiroptera/*physiology ; *Echolocation ; History, 21st Century ; *Multimedia ; United States
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  • 124
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-12-25
    Description: Diving mosasaurs, plesiosaurs, and humans develop dysbaric osteonecrosis from end-artery nitrogen embolism ("the bends") in certain bones. Sixteen sperm whales from calves to large adults showed a size-related development of osteonecrosis in chevron and rib bone articulations, deltoid crests, and nasal bones. Occurrence in animals from the Pacific and Atlantic oceans over 111 years made a pathophysiological diagnosis of dysbarism most likely. Decompression avoidance therefore may constrain diving behavior. This suggests why some deep-diving mammals show periodic shallow-depth activity and why gas emboli are found in animals driven to surface precipitously by acoustic stressors such as mid-frequency sonar systems.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Moore, Michael J -- Early, Greg A -- New York, N.Y. -- Science. 2004 Dec 24;306(5705):2215.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Biology, Woods Hole Oceanographic Institution, Woods Hole, MA 02543, USA. mmoore@whoi.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15618509" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Atlantic Ocean ; Body Size ; Bone Density ; Bone Remodeling ; Bone and Bones/*pathology ; Decompression Sickness/complications/pathology/*veterinary ; *Diving ; Female ; Male ; Osteonecrosis/etiology/pathology/*veterinary ; Pacific Ocean ; *Whales/anatomy & histology/physiology
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  • 125
    Publication Date: 2004-08-18
    Description: Colonies of the Caribbean coral Montastraea cavernosa exhibit a solar-stimulated orange-red fluorescence that is spectrally similar to a variety of fluorescent proteins expressed by corals. The source of this fluorescence is phycoerythrin in unicellular, nonheterocystis, symbiotic cyanobacteria within the host cells of the coral. The cyanobacteria coexist with the symbiotic dinoflagellates (zooxanthellae) of the coral and express the nitrogen-fixing enzyme nitrogenase. The presence of this prokaryotic symbiont in a nitrogen-limited zooxanthellate coral suggests that nitrogen fixation may be an important source of this limiting element for the symbiotic association.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Lesser, Michael P -- Mazel, Charles H -- Gorbunov, Maxim Y -- Falkowski, Paul G -- New York, N.Y. -- Science. 2004 Aug 13;305(5686):997-1000.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Zoology and Center for Marine Biology, University of New Hampshire, Durham, NH 03824, USA. mpl@cisunix.unh.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15310901" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Anthozoa/*microbiology/physiology ; Cyanobacteria/genetics/isolation & purification/*physiology/ultrastructure ; Dinoflagellida/isolation & purification/physiology ; Fluorescence ; Microscopy, Fluorescence ; Molecular Sequence Data ; *Nitrogen Fixation ; Nitrogenase/genetics/metabolism ; Organelles/ultrastructure ; Phycoerythrin/metabolism ; *Symbiosis ; Thylakoids/ultrastructure
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  • 126
    Publication Date: 2004-07-24
    Description: The hippocampus has differentiated into an extensively connected recurrent stage (CA3) followed by a feed-forward stage (CA1). We examined the function of this structural differentiation by determining how cell ensembles in rat CA3 and CA1 generate representations of rooms with common spatial elements. In CA3, distinct subsets of pyramidal cells were activated in each room, regardless of the similarity of the testing enclosure. In CA1, the activated populations overlapped, and the overlap increased in similar enclosures. After exposure to a novel room, ensemble activity developed slower in CA3 than CA1, suggesting that the representations emerged independently.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Leutgeb, Stefan -- Leutgeb, Jill K -- Treves, Alessandro -- Moser, May-Britt -- Moser, Edvard I -- New York, N.Y. -- Science. 2004 Aug 27;305(5688):1295-8. Epub 2004 Jul 22.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Centre for the Biology of Memory, Medical-Technical Research Centre, Norwegian University of Science and Technology, 7489 Trondheim, Norway.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15272123" target="_blank"〉PubMed〈/a〉
    Keywords: Action Potentials ; Animals ; Brain Mapping ; Cues ; Electrodes, Implanted ; Entorhinal Cortex/physiology ; Hippocampus/cytology/*physiology ; Male ; *Memory ; Nerve Net/*physiology ; Neurons/*physiology ; Pyramidal Cells/*physiology ; Rats ; Rats, Long-Evans ; *Space Perception
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  • 127
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-06-12
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Kaiser, Michel J -- New York, N.Y. -- Science. 2004 Jun 11;304(5677):1595.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15192198" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; *Anthozoa ; *Conservation of Natural Resources ; *Ecosystem ; Environment ; *Fishes ; Seawater ; United States
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  • 128
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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〉Morell, Virginia -- New York, N.Y. -- Science. 2004 Apr 16;304(5669):372.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15087514" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Color ; Decision Making ; Female ; Male ; Pigmentation ; *Sexual Behavior, Animal ; *Songbirds/anatomy & histology ; Vocalization, Animal
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  • 129
    Publication Date: 2004-02-21
    Description: PTEN is a tumor suppressor protein that dephosphorylates phosphatidylinositol 3,4,5 trisphosphate and antagonizes the phosphatidylinositol-3 kinase signaling pathway. We show here that PTEN can also inhibit cell migration through its C2 domain, independent of its lipid phosphatase activity. This activity depends on the protein phosphatase activity of PTEN and on dephosphorylation at a single residue, threonine(383). The ability of PTEN to control cell migration through its C2 domain is likely to be an important feature of its tumor suppressor activity.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Raftopoulou, Myrto -- Etienne-Manneville, Sandrine -- Self, Annette -- Nicholls, Sarah -- Hall, Alan -- New York, N.Y. -- Science. 2004 Feb 20;303(5661):1179-81.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Medical Research Council Laboratory for Molecular Cell Biology and Cell Biology Unit, Cancer Research UK Oncogene and Signal Transduction Group, University College London, Gower Street, London WC1E 6BT, UK.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/14976311" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; COS Cells ; Catalysis ; Catalytic Domain ; Cell Line, Tumor ; Cell Movement/*physiology ; Cercopithecus aethiops ; Glioma ; Humans ; Mutation ; PTEN Phosphohydrolase ; Phosphoprotein Phosphatases/chemistry/metabolism ; Phosphoric Monoester Hydrolases/*chemistry/genetics/metabolism/*physiology ; Phosphorylation ; Phosphothreonine/metabolism ; Precipitin Tests ; Protein Structure, Tertiary ; Recombinant Proteins/pharmacology ; Sequence Deletion ; Transfection ; Tumor Suppressor Proteins/*chemistry/genetics/metabolism/*physiology
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-08-31
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Grimm, David -- New York, N.Y. -- Science. 2004 Aug 27;305(5688):1235.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15333821" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Biodiversity ; *Ecosystem ; Fisheries ; *Fishes ; Humans ; Population Density ; *Recreation ; United States
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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〉Sternberg, Paul W -- New York, N.Y. -- Science. 2004 Jan 30;303(5658):637-8.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Howard Hughes Medical Institute and Division of Biology 156-29, California Institute of Technology, Pasadena, CA 91125, USA. pws@caltech.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/14752152" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Caenorhabditis elegans/cytology/genetics/*growth & development/metabolism ; Caenorhabditis elegans Proteins/genetics/*metabolism ; Epidermal Growth Factor/metabolism ; Female ; Gene Expression Regulation, Developmental ; Genes, Helminth ; Intercellular Signaling Peptides and Proteins/genetics/metabolism ; Ligands ; Membrane Proteins/*metabolism ; Morphogenesis ; Receptor, Epidermal Growth Factor/*metabolism ; Receptors, Notch ; *Signal Transduction ; Stem Cells/physiology ; Vulva/cytology/growth & development/metabolism
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  • 132
    Publication Date: 2004-06-05
    Description: Episodes of coral bleaching (loss of the symbiotic dinoflagellates) and coral mortality have occurred with increasing frequency over the past two decades. Although some corals recover from bleaching events, the source of the repopulating symbionts is unknown. Here we show that after bleaching, the adult octocoral Briareum sp. acquire dinoflagellate symbionts (Symbiodinium sp.) from the environment. Uptake of exogenous symbionts provides a mechanism for response to changes in the environment and resilience in the symbiosis.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Lewis, Cynthia L -- Coffroth, Mary Alice -- New York, N.Y. -- Science. 2004 Jun 4;304(5676):1490-2.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Biological Sciences, State University of New York at Buffalo, Buffalo, NY 14260, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15178798" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Anthozoa/*physiology ; Dinoflagellida/genetics/*physiology ; Ecosystem ; Eukaryota ; Genotype ; *Symbiosis
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  • 133
    Publication Date: 2004-06-12
    Description: During speech acquisition, children form quick and rough hypotheses about the meaning of a new word after only a single exposure-a process dubbed "fast mapping." Here we provide evidence that a border collie, Rico, is able to fast map. Rico knew the labels of over 200 different items. He inferred the names of novel items by exclusion learning and correctly retrieved those items right away as well as 4 weeks after the initial exposure. Fast mapping thus appears to be mediated by general learning and memory mechanisms also found in other animals and not by a language acquisition device that is special to humans.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Kaminski, Juliane -- Call, Josep -- Fischer, Julia -- New York, N.Y. -- Science. 2004 Jun 11;304(5677):1682-3.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Developmental and Comparative Psychology, Max-Planck Institute for Evolutionary Anthropology, Deutscher Platz 6, 04103 Leipzig, Germany.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15192233" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; *Dogs ; *Learning ; Male ; *Memory ; Random Allocation ; *Vocabulary
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  • 134
    Publication Date: 2004-11-20
    Description: We describe a partial skeleton with facial cranium of Pierolapithecus catalaunicus gen. et sp. nov., a new Middle Miocene (12.5 to 13 million years ago) ape from Barranc de Can Vila 1 (Barcelona, Spain). It is the first known individual of this age that combines well-preserved cranial, dental, and postcranial material. The thorax, lumbar region, and wrist provide evidence of modern ape-like orthograde body design, and the facial morphology includes the basic derived great ape features. The new skeleton reveals that early great apes retained primitive monkeylike characters associated with a derived body structure that permits upright postures of the trunk. Pierolapithecus, hence, does not fit the theoretical model that predicts that all characters shared by extant great apes were present in their last common ancestor, but instead points to a large amount of homoplasy in ape evolution. The overall pattern suggests that Pierolapithecus is probably close to the last common ancestor of great apes and humans.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Moya-Sola, Salvador -- Kohler, Meike -- Alba, David M -- Casanovas-Vilar, Isaac -- Galindo, Jordi -- New York, N.Y. -- Science. 2004 Nov 19;306(5700):1339-44.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Institut de Paleontologia M. Crusafont, Escola Industrial 23, Sabadell, Barcelona 08201, Spain. moyass@diba.es〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15550663" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Biological Evolution ; Face/anatomy & histology ; Facial Bones/anatomy & histology ; *Fossils ; *Hominidae/anatomy & histology/classification ; Locomotion ; Phylogeny ; Posture ; Ribs/anatomy & histology ; Skeleton ; Skull/anatomy & histology ; Spain ; Spine/anatomy & histology ; Thorax/anatomy & histology ; Wrist/anatomy & histology
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  • 135
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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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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-04-10
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Muller, Ulrike K -- Kranenbarg, Sander -- New York, N.Y. -- Science. 2004 Apr 9;304(5668):217-9.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Experimental Zoology Group, Wageningen University, 6709 PG Wageningen, Netherlands. ulrike.muller@wur.nl〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15073361" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Biomechanical Phenomena ; Cartilage/anatomy & histology/physiology ; Collagen/physiology ; Lizards/anatomy & histology/*physiology ; Muscle Contraction ; Muscle, Skeletal/anatomy & histology/physiology ; Tongue/anatomy & histology/*physiology
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  • 137
    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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  • 138
    Publication Date: 2004-07-13
    Description: Numerous degenerative disorders are associated with elevated levels of prooxidants and declines in mitochondrial aconitase activity. Deficiency in the mitochondrial iron-binding protein frataxin results in diminished activity of various mitochondrial iron-sulfur proteins including aconitase. We found that aconitase can undergo reversible citrate-dependent modulation in activity in response to pro-oxidants. Frataxin interacted with aconitase in a citrate-dependent fashion, reduced the level of oxidant-induced inactivation, and converted inactive [3Fe-4S]1+ enzyme to the active [4Fe-4S]2+ form of the protein. Thus, frataxin is an iron chaperone protein that protects the aconitase [4Fe-4S]2+ cluster from disassembly and promotes enzyme reactivation.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Bulteau, Anne-Laure -- O'Neill, Heather A -- Kennedy, Mary Claire -- Ikeda-Saito, Masao -- Isaya, Grazia -- Szweda, Luke I -- AG-15709/AG/NIA NIH HHS/ -- AG-16339/AG/NIA NIH HHS/ -- NRSA 44748/NR/NINR NIH HHS/ -- New York, N.Y. -- Science. 2004 Jul 9;305(5681):242-5.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Physiology and Biophysics, Case Western Reserve University, Cleveland, OH, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15247478" target="_blank"〉PubMed〈/a〉
    Keywords: Aconitate Hydratase/antagonists & inhibitors/*metabolism ; Animals ; Citric Acid/metabolism/pharmacology ; Dithiothreitol/metabolism ; Electron Spin Resonance Spectroscopy ; Enzyme Activation ; Ferrous Compounds/metabolism ; Hydrogen Peroxide/pharmacology ; Iron/*metabolism ; Iron-Binding Proteins/*metabolism ; Male ; Mitochondria/*metabolism ; Mitochondria, Heart/*metabolism ; Molecular Chaperones/*metabolism ; Oxidation-Reduction ; Oxidative Stress ; Oxygen Consumption ; Rats ; Rats, Sprague-Dawley ; Saccharomyces cerevisiae/*metabolism ; Saccharomyces cerevisiae Proteins/metabolism
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    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 139
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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〉Muller, Ulrike K -- Lentink, David -- New York, N.Y. -- Science. 2004 Dec 10;306(5703):1899-900.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Experimental Zoology, Wageningen University, the Netherlands. ulrike.muller@wur.nl〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15591191" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Biomechanical Phenomena ; Birds/anatomy & histology/*physiology ; *Flight, Animal ; Models, Anatomic ; Wings, Animal/anatomy & histology/*physiology
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  • 140
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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
    Print ISSN: 0036-8075
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  • 141
    Publication Date: 2004-10-23
    Description: Computational tools can markedly accelerate the rate at which murine genetic models can be analyzed. We developed a computational method for mapping phenotypic traits that vary among inbred strains onto haplotypic blocks. This method correctly predicted the genetic basis for strain-specific differences in several biologically important traits. It was also used to identify an allele-specific functional genomic element regulating H2-Ealpha gene expression. This functional element, which contained the binding sites for YY1 and a second transcription factor that is probably serum response factor, is located within the first intron of the H2-Ealpha gene. This computational method will greatly improve our ability to identify the genetic basis for a variety of phenotypic traits, ranging from qualitative trait information to quantitative gene expression data, which vary among inbred mouse strains.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Liao, Guochun -- Wang, Jianmei -- Guo, Jingshu -- Allard, John -- Cheng, Janet -- Ng, Anh -- Shafer, Steve -- Puech, Anne -- McPherson, John D -- Foernzler, Dorothee -- Peltz, Gary -- Usuka, Jonathan -- 1 R01 HG02322-01/HG/NHGRI NIH HHS/ -- New York, N.Y. -- Science. 2004 Oct 22;306(5696):690-5.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Genetics and Genomics, Roche Palo Alto, 3431 Hillview Avenue, Palo Alto, CA 94304-1397, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15499019" target="_blank"〉PubMed〈/a〉
    Keywords: Alleles ; Animals ; Binding Sites ; *Computational Biology ; Electrophoretic Mobility Shift Assay ; Gene Expression Profiling ; *Gene Expression Regulation ; Genes, MHC Class II ; Genetic Variation ; H-2 Antigens/*genetics ; Haplotypes ; Hydrocarbons, Aromatic/pharmacology ; Introns ; Liver/metabolism ; Lung/metabolism ; Major Histocompatibility Complex ; Mice ; Mice, Inbred Strains ; Oligodeoxyribonucleotides/metabolism ; Oligonucleotide Array Sequence Analysis ; Phenotype ; Polymorphism, Single Nucleotide ; Receptors, Aryl Hydrocarbon/chemistry/genetics/metabolism ; Regulatory Sequences, Nucleic Acid ; Serum Response Factor/metabolism ; Transcription Factors/metabolism
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  • 142
    Publication Date: 2004-09-18
    Description: The age and timing of the Permian-Triassic mass extinction have been difficult to determine because zircon populations from the type sections are typically affected by pervasive lead loss and contamination by indistinguishable older xenocrysts. Zircons from nine ash beds within the Shangsi and Meishan sections (China), pretreated by annealing followed by partial attack with hydrofluoric acid, result in suites of consistent and concordant uranium/lead (U/Pb) ages, eliminating the effects of lead loss. The U/Pb age of the main pulse of the extinction is 252.6 +/- 0.2 million years, synchronous with the Siberian flood volcanism, and it occurred within the quoted uncertainty.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Mundil, Roland -- Ludwig, Kenneth R -- Metcalfe, Ian -- Renne, Paul R -- New York, N.Y. -- Science. 2004 Sep 17;305(5691):1760-3.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Berkeley Geochronology Center, 2455 Ridge Road, Berkeley, CA 94709, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15375264" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; China ; Fossils ; Geologic Sediments ; Geology/*methods ; Lead/*analysis ; *Population Density ; Population Dynamics ; Silicates/*chemistry ; Time ; Uranium/*analysis ; *Volcanic Eruptions ; Zirconium/*chemistry
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    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 143
    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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  • 144
    Publication Date: 2004-03-20
    Description: A key question in evolutionary genetics is whether shared genetic mechanisms underlie the independent evolution of similar phenotypes across phylogenetically divergent lineages. Here we show that in two classic examples of melanic plumage polymorphisms in birds, lesser snow geese (Anser c. caerulescens) and arctic skuas (Stercorarius parasiticus), melanism is perfectly associated with variation in the melanocortin-1 receptor (MC1R) gene. In both species, the degree of melanism correlates with the number of copies of variant MC1R alleles. Phylogenetic reconstructions of variant MC1R alleles in geese and skuas show that melanism is a derived trait that evolved in the Pleistocene.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Mundy, Nicholas I -- Badcock, Nichola S -- Hart, Tom -- Scribner, Kim -- Janssen, Kirstin -- Nadeau, Nicola J -- New York, N.Y. -- Science. 2004 Mar 19;303(5665):1870-3.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Zoology, University of Cambridge, Cambridge CB2 3EJ, UK. nim21@cam.ac.uk〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15031505" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Arctic Regions ; Biological Evolution ; Birds/anatomy & histology/*genetics/physiology ; Color ; *Feathers ; Female ; Geese/anatomy & histology/genetics/physiology ; Gene Frequency ; Haplotypes ; Male ; Melanins/*analysis ; Melanocytes/metabolism ; Phenotype ; Phylogeny ; Pigmentation/*genetics ; *Quantitative Trait, Heritable ; Receptor, Melanocortin, Type 1/chemistry/*genetics ; *Sexual Behavior, Animal
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  • 145
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-11-30
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Stokstad, Erik -- New York, N.Y. -- Science. 2004 Nov 26;306(5701):1467.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15567834" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; *Birds/anatomy & histology ; *Fishes ; Flight, Animal ; *Fossils
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    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 146
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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
    Print ISSN: 0036-8075
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    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 147
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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〉Dicke, Marcel -- van Loon, Joop J A -- de Jong, Peter W -- New York, N.Y. -- Science. 2004 Jul 30;305(5684):618-9.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Laboratory of Entomology, Wageningen University, Post Office Box 8031, NL-6700 EH Wageningen, Netherlands. marcel.dicke@wur.nl〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15286351" target="_blank"〉PubMed〈/a〉
    Keywords: Adaptation, Physiological ; Aldehyde-Lyases/genetics/metabolism ; Animals ; Biological Evolution ; Cytochrome P-450 Enzyme System/genetics/metabolism ; *Ecology ; *Ecosystem ; Gene Expression Regulation, Plant ; Gene Silencing ; *Genomics ; Genotype ; Insects/*physiology ; Intramolecular Oxidoreductases/genetics/metabolism ; Lipoxygenase/genetics/metabolism ; Phenotype ; Plants/genetics ; Signal Transduction ; Tobacco/genetics/*physiology
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  • 148
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-07-13
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Guy-Grand, Delphine -- Vassalli, Pierre -- New York, N.Y. -- Science. 2004 Jul 9;305(5681):185-7.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Unite de Recherche et d'Expertise Antivirale, INSERM U277, Institut Pasteur, 75724 Paris Cedex 15, France. guygrand@pasteur.fr〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15247461" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; CD4-Positive T-Lymphocytes/immunology ; CD8-Positive T-Lymphocytes/immunology ; Cell Lineage ; DNA-Binding Proteins/metabolism ; Female ; Hematopoietic Stem Cells/immunology/physiology ; Immunity, Innate ; Immunity, Mucosal ; Interleukins/biosynthesis ; Intestinal Mucosa/cytology/*immunology ; Killer Cells, Natural/immunology ; Ligands ; Lymphoid Tissue/embryology/immunology ; Lymphotoxin-alpha/analysis ; Male ; Mice ; Mice, Nude ; Mice, Transgenic ; Models, Immunological ; Mutation ; Nuclear Receptor Subfamily 1, Group F, Member 3 ; Receptors, Antigen, T-Cell, alpha-beta/analysis/genetics ; Receptors, Antigen, T-Cell, gamma-delta/analysis ; Receptors, Retinoic Acid/genetics/metabolism ; Receptors, Thyroid Hormone/genetics/metabolism ; T-Lymphocyte Subsets/immunology ; T-Lymphocytes/*immunology ; Thymus Gland/cytology/*immunology
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  • 149
    Publication Date: 2004-11-30
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Stokstad, Erik -- New York, N.Y. -- Science. 2004 Nov 26;306(5701):1467.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15567833" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; *Biological Evolution ; Extremities/anatomy & histology ; Feeding Behavior ; *Fossils ; *Horses/anatomy & histology ; Paleodontology ; *Poaceae ; Time ; Tooth/*anatomy & histology ; Trees
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  • 150
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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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  • 151
    Publication Date: 2004-02-28
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Lindenmayer, D B -- Foster, D R -- Franklin, J F -- Hunter, M L -- Noss, R F -- Schmiegelow, F A -- Perry, D -- New York, N.Y. -- Science. 2004 Feb 27;303(5662):1303.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Centre for Resource and Environmental Studies, Australian National University, Canberra, ACT, 0200, Australia.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/14988539" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Biodiversity ; *Disasters ; *Ecosystem ; *Fires ; *Forestry ; *Trees
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    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 152
    Publication Date: 2004-11-30
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Stokstad, Erik -- New York, N.Y. -- Science. 2004 Nov 26;306(5701):1466.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15567831" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Biomechanical Phenomena ; Dinosaurs/*anatomy & histology/*physiology ; Head ; Locomotion ; *Posture ; Semicircular Canals/*anatomy & histology
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  • 153
    Publication Date: 2004-11-30
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Stokstad, Erik -- New York, N.Y. -- Science. 2004 Nov 26;306(5701):1466-7.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15567832" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Bone and Bones/chemistry ; *Diet ; *Falconiformes ; *Feeding Behavior ; *Fossils ; Isotopes/analysis ; Population Dynamics
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  • 154
    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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  • 155
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-07-17
    Description: Newly discovered, exceptionally preserved, soft-bodied fossils near Spaniard's Bay in eastern Newfoundland exhibit features not previously described from Ediacaran (terminal Neoproterozoic) fossils. All of the Spaniard's Bay taxa were composed of similar architectural elements-centimeter-scale frondlets exhibiting three orders of fracticality in branching. Frondlets were combined as modules atop semi-rigid organic skeletons to form a wide array of larger constructions, including frondose and plumose structures. This architecture and construction define the "rangeomorphs," a biological clade that dominated the Mistaken Point assemblage (575 to 560 million years ago) but does not appear to be ancestral to any Phanerozoic or modern organisms.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Narbonne, Guy M -- New York, N.Y. -- Science. 2004 Aug 20;305(5687):1141-4. Epub 2004 Jul 15.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Geological Sciences and Geological Engineering, Queen's University, Kingston, Ontario K7L 3N6, Canada. narbonne@geol.queensu.ca〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15256615" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Ecosystem ; *Fossils ; Geologic Sediments ; *Invertebrates/anatomy & histology/classification ; Newfoundland and Labrador ; Paleontology
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  • 156
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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〉Djerassi, Carl -- New York, N.Y. -- Science. 2004 Jul 30;305(5684):609.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15286347" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Asia ; *Authorship ; Drosophila/genetics ; Europe ; *Internationality ; Publishing ; United States
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    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 157
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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〉Withgott, Jay -- New York, N.Y. -- Science. 2004 Feb 20;303(5661):1123.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/14976289" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; *Conservation of Natural Resources ; Ecosystem ; *Environment ; Fishes ; Oceans and Seas ; *Public Policy ; Research Support as Topic ; *Seawater ; United States
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  • 158
    Publication Date: 2004-01-13
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Witt, Christopher C -- Brumfield, Robb T -- New York, N.Y. -- Science. 2004 Jan 9;303(5655):173; author reply 173.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Biological Sciences and, Museum of Natural Science, Louisiana State University, Baton Rouge, LA 70803, USA. cwitt@lsu.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/14715994" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; *Biological Evolution ; *Evolution, Molecular ; Genes ; Genetics, Population ; Mathematics ; Models, Statistical ; *Phylogeny ; Plants/classification/genetics ; Sampling Studies ; Selection Bias
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  • 159
    Publication Date: 2004-01-31
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Dietsch, Thomas V -- Philpott, Stacy M -- Rice, Robert A -- Greenberg, Russell -- Bichier, Peter -- New York, N.Y. -- Science. 2004 Jan 30;303(5658):625-6; author reply 625-6.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/14752143" target="_blank"〉PubMed〈/a〉
    Keywords: Agriculture ; Animals ; Coffea/*growth & development ; *Coffee/economics ; Commerce ; *Conservation of Natural Resources ; *Crops, Agricultural/economics ; *Ecosystem ; *Public Policy ; Trees ; United States
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  • 160
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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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    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 161
    Publication Date: 2004-09-14
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Stokstad, Erik -- New York, N.Y. -- Science. 2004 Sep 10;305(5690):1554.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15361598" target="_blank"〉PubMed〈/a〉
    Keywords: *Agriculture ; *Ambystoma ; Animals ; California ; *Conservation of Natural Resources ; *Ecosystem ; Environment ; Population Density
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    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 162
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-09-14
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Hambler, Clive -- Speight, Martin R -- New York, N.Y. -- Science. 2004 Sep 10;305(5690):1563-5; author reply 1563-5.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15361605" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Birds ; *Butterflies ; Great Britain ; Plants ; Population Density ; Population Dynamics
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  • 163
    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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  • 164
    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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  • 165
    Publication Date: 2004-09-09
    Description: Beak shape is a classic example of evolutionary diversification. Beak development in chicken and duck was used to examine morphological variations among avian species. There is only one proliferative zone in the frontonasal mass of chickens, but two in ducks. These growth zones are associated with bone morphogenetic protein 4 (BMP4) activity. By "tinkering" with BMP4 in beak prominences, the shapes of the chicken beak can be modulated.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4380220/" 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/PMC4380220/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Wu, Ping -- Jiang, Ting-Xin -- Suksaweang, Sanong -- Widelitz, Randall Bruce -- Chuong, Cheng-Ming -- AR42177/AR/NIAMS NIH HHS/ -- AR47364/AR/NIAMS NIH HHS/ -- CA83716/CA/NCI NIH HHS/ -- R01 AR042177/AR/NIAMS NIH HHS/ -- R01 AR042177-07/AR/NIAMS NIH HHS/ -- R01 AR042177-07S1/AR/NIAMS NIH HHS/ -- R01 AR042177-08/AR/NIAMS NIH HHS/ -- R01 AR042177-08S1/AR/NIAMS NIH HHS/ -- R01 AR042177-09/AR/NIAMS NIH HHS/ -- R01 AR042177-10/AR/NIAMS NIH HHS/ -- R01 AR047364/AR/NIAMS NIH HHS/ -- R01 AR047364-01A2/AR/NIAMS NIH HHS/ -- R01 AR047364-02/AR/NIAMS NIH HHS/ -- R01 AR047364-03/AR/NIAMS NIH HHS/ -- New York, N.Y. -- Science. 2004 Sep 3;305(5689):1465-6.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Pathology, Keck School of Medicine, University of Southern California, Los Angeles, CA 90033, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15353803" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Beak/*embryology ; Bone Morphogenetic Protein 4 ; Bone Morphogenetic Proteins/genetics/*metabolism ; Carrier Proteins ; Cell Division ; *Chick Embryo ; Chickens/genetics/metabolism ; Ducks/*embryology/genetics/metabolism ; Gene Transfer Techniques ; Genetic Vectors ; Mesoderm/metabolism ; Morphogenesis ; Proteins/genetics/physiology ; RNA, Messenger/genetics/metabolism ; Recombinant Proteins/metabolism ; Reverse Transcriptase Polymerase Chain Reaction ; Species Specificity
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  • 166
    Publication Date: 2004-09-09
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Stokstad, Erik -- New York, N.Y. -- Science. 2004 Sep 3;305(5689):1386.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15353767" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; *Biological Evolution ; Echinodermata/*physiology ; Fishes ; *Fossils ; *Predatory Behavior ; *Regeneration
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  • 167
    Publication Date: 2004-06-12
    Description: Cells regulate the biophysical properties of their membranes by coordinated synthesis of different classes of lipids. Here, we identified a highly dynamic feedback mechanism by which the budding yeast Saccharomyces cerevisiae can regulate phospholipid biosynthesis. Phosphatidic acid on the endoplasmic reticulum directly bound to the soluble transcriptional repressor Opi1p to maintain it as inactive outside the nucleus. After the addition of the lipid precursor inositol, this phosphatidic acid was rapidly consumed, releasing Opi1p from the endoplasmic reticulum and allowing its nuclear translocation and repression of target genes. Thus, phosphatidic acid appears to be both an essential ubiquitous metabolic intermediate and a signaling lipid.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Loewen, C J R -- Gaspar, M L -- Jesch, S A -- Delon, C -- Ktistakis, N T -- Henry, S A -- Levine, T P -- BBS/E/B/0000F969/Biotechnology and Biological Sciences Research Council/United Kingdom -- GM-19629/GM/NIGMS NIH HHS/ -- New York, N.Y. -- Science. 2004 Jun 11;304(5677):1644-7.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Division of Cell Biology, Institute of Ophthalmology, Bath Street, London EC1V 9EL, UK.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15192221" target="_blank"〉PubMed〈/a〉
    Keywords: Active Transport, Cell Nucleus ; Animals ; Binding Sites ; COS Cells ; Cell Membrane/metabolism ; Cell Nucleus/metabolism ; Cercopithecus aethiops ; Cytidine Diphosphate Diglycerides/metabolism ; Endoplasmic Reticulum/metabolism ; Inositol/*metabolism ; Liposomes/metabolism ; Mutation ; Nuclear Envelope/metabolism ; Phosphatidic Acids/*metabolism ; Phosphatidylinositols/metabolism ; Phospholipids/biosynthesis/*metabolism ; Recombinant Fusion Proteins/metabolism ; Repressor Proteins/chemistry/genetics/*metabolism ; Saccharomyces cerevisiae/genetics/*metabolism ; Saccharomyces cerevisiae Proteins/chemistry/genetics/*metabolism ; Signal Transduction
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  • 168
    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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  • 169
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-10-09
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Agosta, Salvatore J -- Dunham, Arthur E -- New York, N.Y. -- Science. 2004 Oct 8;306(5694):230; author reply 230.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Biology, University of Pennsylvania, Philadelphia, PA 19104, USA. agosta@sas.upenn.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15472061" target="_blank"〉PubMed〈/a〉
    Keywords: *Adaptation, Biological ; Animals ; Lizards/*anatomy & histology ; Phylogeny ; *Predatory Behavior ; Selection, Genetic ; *Songbirds
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  • 170
    Publication Date: 2004-02-07
    Description: The bacterium Listeria monocytogenes can cause a life-threatening systemic illness in humans. Despite decades of progress in animal models of listeriosis, much remains unknown about the processes of infection and colonization. Here, we report that L. monocytogenes can replicate in the murine gall bladder and provide evidence that its replication there is extracellular and intraluminal. In vivo bioluminescence imaging was employed to determine the location of the infection over time in live animals, revealing strong signals from the gall bladder over a period of several days, in diseased as well as asymptomatic animals. The data suggest that L. monocytogenes may be carried in the human gall bladder.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Hardy, Jonathan -- Francis, Kevin P -- DeBoer, Monica -- Chu, Pauline -- Gibbs, Karine -- Contag, Christopher H -- R01HD37543/HD/NICHD NIH HHS/ -- New York, N.Y. -- Science. 2004 Feb 6;303(5659):851-3.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Pediatrics, Stanford University School of Medicine, Stanford, CA 94305, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/14764883" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Colony Count, Microbial ; Female ; Gallbladder/*microbiology ; Gallbladder Diseases/*microbiology ; Listeria monocytogenes/genetics/*growth & development/isolation & ; purification/pathogenicity ; Listeriosis/*microbiology ; Liver/microbiology ; Luminescence ; Mice ; Mice, Inbred BALB C ; Mutation ; Spleen/microbiology ; Time Factors ; Virulence
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  • 171
    Publication Date: 2004-02-14
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Duda, Thomas F Jr -- Bingham, Jon-Paul -- Livett, Bruce G -- Kohn, Alan J -- Massilia, Gabriella Raybaudi -- Schultz, Joseph R -- Down, John -- Sandall, David -- Sweedler, Jonathan V -- New York, N.Y. -- Science. 2004 Feb 13;303(5660):955-7; author reply 955-7.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/14963310" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; *Biomedical Research ; Conotoxins ; *Conservation of Natural Resources ; *Ecosystem ; Environment ; *Snails
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  • 172
    Publication Date: 2004-09-14
    Description: It is now widely accepted that global warming is occurring, yet its effects on the world's largest ecosystem, the marine pelagic realm, are largely unknown. We show that sea surface warming in the Northeast Atlantic is accompanied by increasing phytoplankton abundance in cooler regions and decreasing phytoplankton abundance in warmer regions. This impact propagates up the food web (bottom-up control) through copepod herbivores to zooplankton carnivores because of tight trophic coupling. Future warming is therefore likely to alter the spatial distribution of primary and secondary pelagic production, affecting ecosystem services and placing additional stress on already-depleted fish and mammal populations.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Richardson, Anthony J -- Schoeman, David S -- New York, N.Y. -- Science. 2004 Sep 10;305(5690):1609-12.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Sir Alister Hardy Foundation for Ocean Science, The Laboratory, Citadel Hill, Plymouth, PL1 2PB, UK. anr@sahfos.ac.uk〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15361622" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Atlantic Ocean ; *Climate ; Copepoda/*growth & development ; *Ecosystem ; Fisheries ; Fishes ; *Food Chain ; Greenhouse Effect ; Meta-Analysis as Topic ; Phytoplankton/*growth & development ; Population Dynamics ; Seawater ; Temperature ; Zooplankton/*growth & development
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    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 173
    Publication Date: 2004-08-07
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Dratch, Peter -- Coonan, Tim -- Graber, David -- New York, N.Y. -- Science. 2004 Aug 6;305(5685):777-8; author reply 777-8.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15297648" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Animals, Wild ; Biodiversity ; California ; Conservation of Natural Resources/*methods ; *Eagles ; *Ecosystem ; *Foxes ; Geography ; Models, Biological ; Population Density ; Predatory Behavior ; *Sus scrofa
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  • 174
    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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  • 175
    Publication Date: 2004-11-13
    Description: We assess the phylogenetic potential of approximately 300,000 protein sequences sampled from Swiss-Prot and GenBank. Although only a small subset of these data was potentially phylogenetically informative, this subset retained a substantial fraction of the original taxonomic diversity. Sampling biases in the databases necessitate building phylogenetic data sets that have large numbers of missing entries. However, an analysis of two "supermatrices" suggests that even data sets with as much as 92% missing data can provide insights into broad sections of the tree of life.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Driskell, Amy C -- Ane, Cecile -- Burleigh, J Gordon -- McMahon, Michelle M -- O'meara, Brian C -- Sanderson, Michael J -- New York, N.Y. -- Science. 2004 Nov 12;306(5699):1172-4.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Section of Evolution and Ecology, University of California, One Shields Avenue, Davis, CA 95616, USA. acdriskell@ucdavis.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15539599" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Anopheles/classification/genetics ; Biodiversity ; *Biological Evolution ; Classification ; Computational Biology ; *Databases, Nucleic Acid ; *Databases, Protein ; Multigene Family ; *Phylogeny ; Plant Proteins/genetics ; Plants/classification/genetics ; Spodoptera/classification/genetics
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  • 176
    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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  • 177
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-06-19
    Description: The Hedgehog (Hh) signaling pathway is intimately linked to cell growth and differentiation, with normal roles in embryonic pattern formation and adult tissue homeostasis and pathological roles in tumor initiation and growth. Recent advances in our understanding of Hh response have resulted from the identification of new pathway components and new mechanisms of action for old pathway components. The most striking new finding is that signal transmission from membrane to cytoplasm proceeds through recruitment, by the seven-transmembrane protein Smoothened, of an atypical kinesin, which routes pathway activation by interaction with other components of a complex that includes the latent zinc finger transcription factor, Ci.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Lum, Lawrence -- Beachy, Philip A -- New York, N.Y. -- Science. 2004 Jun 18;304(5678):1755-9.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Molecular Biology and Genetics, Howard Hughes Medical Institute, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15205520" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Cell Nucleus/metabolism ; Cytoplasm/metabolism ; DNA-Binding Proteins/metabolism ; Drosophila/metabolism ; Drosophila Proteins/*metabolism ; Gene Expression Regulation ; Hedgehog Proteins ; Kinesin/metabolism ; Mammals/metabolism ; Membrane Proteins/metabolism ; Models, Biological ; Phosphorylation ; Protein Transport ; Receptors, Cell Surface ; Receptors, G-Protein-Coupled/metabolism ; *Signal Transduction ; Trans-Activators/metabolism ; Transcription Factors
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  • 178
    Publication Date: 2004-06-05
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Stokstad, Erik -- New York, N.Y. -- Science. 2004 Jun 4;304(5676):1425.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15178772" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; *Body Patterning ; China ; *Fossils ; Geologic Sediments
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  • 179
    Publication Date: 2004-01-31
    Description: Protein tyrosine kinases and phosphatases cooperate to regulate normal immune cell function. We examined the role of PEST domain-enriched tyrosine phosphatase (PEP) in regulating T cell antigen-receptor function during thymocyte development and peripheral T cell differentiation. Although normal naive T cell functions were retained in pep-deficient mice, effector/memory T cells demonstrated enhanced activation of Lck. In turn, this resulted in increased expansion and function of the effector/memory T cell pool, which was also associated with spontaneous development of germinal centers and elevated serum antibody levels. These results revealed a central role for PEP in negatively regulating specific aspects of T cell development and function.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Hasegawa, Kiminori -- Martin, Flavius -- Huang, Guangming -- Tumas, Dan -- Diehl, Lauri -- Chan, Andrew C -- New York, N.Y. -- Science. 2004 Jan 30;303(5658):685-9.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Immunology, Genentech, Inc., One DNA Way, South San Francisco, CA 94080, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/14752163" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Autoimmunity ; B-Lymphocytes/physiology ; CD4-Positive T-Lymphocytes/immunology/physiology ; CD8-Positive T-Lymphocytes/immunology/physiology ; Cell Cycle ; Gene Targeting ; Germinal Center/physiology ; Hydrogen-Ion Concentration ; Immunoglobulins/blood ; *Immunologic Memory ; Lymphocyte Activation ; Lymphocyte Count ; Lymphocyte Specific Protein Tyrosine Kinase p56(lck)/metabolism ; Mice ; Mice, Inbred BALB C ; Mice, Transgenic ; Phosphorylation ; Protein Tyrosine Phosphatase, Non-Receptor Type 12 ; Protein Tyrosine Phosphatases/genetics/*metabolism ; Receptors, Antigen, T-Cell/genetics/immunology ; Signal Transduction ; T-Lymphocyte Subsets/immunology ; T-Lymphocytes/*immunology/physiology
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  • 180
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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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  • 181
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    Unknown
    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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  • 182
    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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  • 183
    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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  • 184
    Publication Date: 2004-03-06
    Description: The central amygdala (CeA) plays a role in the relationship among stress, corticotropin-releasing factor (CRF), and alcohol abuse. In whole-cell recordings, both CRF and ethanol enhanced gamma-aminobutyric acid-mediated (GABAergic) neurotransmission in CeA neurons from wild-type and CRF2 receptor knockout mice, but not CRF1 receptor knockout mice. CRF1 (but not CRF2) receptor antagonists blocked both CRF and ethanol effects in wild-type mice. These data indicate that CRF1 receptors mediate ethanol enhancement of GABAergic synaptic transmission in the CeA, and they suggest a cellular mechanism underlying involvement of CRF in ethanol's behavioral and motivational effects.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Nie, Zhiguo -- Schweitzer, Paul -- Roberts, Amanda J -- Madamba, Samuel G -- Moore, Scott D -- Siggins, George Robert -- AA06420/AA/NIAAA NIH HHS/ -- AA10994/AA/NIAAA NIH HHS/ -- DA03665/DA/NIDA NIH HHS/ -- DA13658/DA/NIDA NIH HHS/ -- New York, N.Y. -- Science. 2004 Mar 5;303(5663):1512-4.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Neuropharmacology and Alcohol Research Center, Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, CA 92037, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15001778" target="_blank"〉PubMed〈/a〉
    Keywords: Alcohol Drinking ; Amygdala/drug effects/*physiology ; Animals ; Corticotropin-Releasing Hormone/pharmacology ; Dose-Response Relationship, Drug ; Ethanol/*pharmacology ; Evoked Potentials/drug effects ; Mice ; Mice, Inbred C57BL ; Mice, Knockout ; Neurons/drug effects/*physiology ; Patch-Clamp Techniques ; Receptors, Corticotropin-Releasing Hormone/antagonists & ; inhibitors/genetics/*metabolism ; Receptors, GABA-A/metabolism ; Stress, Psychological/physiopathology ; Synaptic Transmission/*drug effects ; gamma-Aminobutyric Acid/*metabolism
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  • 185
    Publication Date: 2004-08-25
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Causey, Douglas -- Janzen, Daniel H -- Peterson, A Townsend -- Vieglais, David -- Krishtalka, Leonard -- Beach, James H -- Wiley, Edward O -- New York, N.Y. -- Science. 2004 Aug 20;305(5687):1106-7.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15326336" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Biological Specimen Banks ; *Classification ; Computational Biology ; Databases, Factual ; Ecosystem ; Information Dissemination ; *Museums ; Publishing
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  • 186
    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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  • 187
    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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  • 188
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-11-30
    Description: Resource pulses are occasional events of ephemeral resource superabundance that occur in many ecosystems. Aboveground consumers in diverse communities often respond strongly to resource pulses, but few studies have investigated the belowground consequences of resource pulses in natural ecosystems. This study shows that resource pulses of 17-year periodical cicadas (Magicicada spp.) directly increase microbial biomass and nitrogen availability in forest soils, with indirect effects on growth and reproduction in forest plants. These findings suggest that pulses of periodical cicadas create "bottom-up cascades," resulting in strong and reciprocal links between the aboveground and belowground components of a North American forest ecosystem.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Yang, Louie H -- New York, N.Y. -- Science. 2004 Nov 26;306(5701):1565-7.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Center for Population Biology, Section of Evolution and Ecology, University of California, One Shields Avenue, Davis, CA 95616, USA. lhyang@ucdavis.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15567865" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Bacteria/growth & development ; Biomass ; Campanulaceae/chemistry/*growth & development ; *Ecosystem ; Fatty Acids/analysis ; Fungi/growth & development ; Hemiptera/growth & development/*physiology ; Life Cycle Stages ; Nitrates/analysis ; Nitrogen Isotopes/analysis ; Quaternary Ammonium Compounds/analysis ; Seeds/growth & development ; Soil/analysis ; Soil Microbiology ; Time Factors ; *Trees/growth & development ; United States
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  • 189
    Publication Date: 2004-05-01
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Dushoff, Jonathan -- New York, N.Y. -- Science. 2004 Apr 30;304(5671):684; author reply 684.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Ecology and, Evolutionary Biology, Princeton University, Princeton, NJ 08540, USA. dushoff@eno.princeton.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15118146" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; *Ecosystem ; *Environment ; Population Dynamics ; Probability ; Time Factors
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  • 190
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-01-24
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Stokstad, Erik -- New York, N.Y. -- Science. 2004 Jan 23;303(5657):449.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/14739429" target="_blank"〉PubMed〈/a〉
    Keywords: *Advisory Committees ; Animals ; *Animals, Genetically Modified ; Arthropods/*genetics ; Crops, Agricultural/*genetics ; Genetics, Population ; Government Regulation ; National Academy of Sciences (U.S.) ; *Plants, Genetically Modified ; United States
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  • 191
    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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  • 192
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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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  • 193
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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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  • 194
    Publication Date: 2004-04-10
    Description: In several areas of the macaque brain, neurons fire during delayed-response tasks at a rate determined by the value of the reward expected at the end of the trial. The activity of these neurons might be related to the value of the expected reward or to the degree of motivation induced by expectation of the reward. We describe results indicating that the nature of reward-dependent activity varies across areas. Neuronal activity in orbitofrontal cortex represents the value of the expected reward, whereas neuronal activity in premotor cortex reflects the degree of motivation.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Roesch, Matthew R -- Olson, Carl R -- EY08098/EY/NEI NIH HHS/ -- EY11831/EY/NEI NIH HHS/ -- MH45156/MH/NIMH NIH HHS/ -- P41RR03631/RR/NCRR NIH HHS/ -- New York, N.Y. -- Science. 2004 Apr 9;304(5668):307-10.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Center for the Neural Basis of Cognition, Mellon Institute, Room 115, 4400 Fifth Avenue, Pittsburgh, PA 15213, USA. roesch@cnbc.cmu.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15073380" target="_blank"〉PubMed〈/a〉
    Keywords: Action Potentials ; Animals ; Cues ; Electrodes ; Frontal Lobe/*physiology ; Macaca mulatta ; Magnetic Resonance Imaging ; Male ; *Motivation ; Motor Cortex/physiology ; Neurons/*physiology ; Psychomotor Performance ; *Reward ; Saccades
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  • 195
    Publication Date: 2004-07-13
    Description: Intestinal intraepithelial T lymphocytes (IELs) are likely to play a key role in host mucosal immunity and, unlike other T cells, have been proposed to differentiate from local precursors rather than from thymocytes. We show here that IELs expressing the alphabeta T cell receptor are derived from precursors that express RORgammat, an orphan nuclear hormone receptor detected only in immature CD4+CD8+ thymocytes, fetal lymphoid tissue-inducer (LTi) cells, and LTi-like cells in cryptopatches within the adult intestinal lamina propria. Using cell fate mapping, we found that all intestinal alphabeta T cells are progeny of CD4+CD8+ thymocytes, indicating that the adult intestine is not a significant site for alphabeta T cell development. Our results suggest that intestinal RORgammat+ cells are local organizers of mucosal lymphoid tissue.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Eberl, Gerard -- Littman, Dan R -- New York, N.Y. -- Science. 2004 Jul 9;305(5681):248-51.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Molecular Pathogenesis Program, Skirball Institute of Biomolecular Medicine, New York University School of Medicine, New York, NY 10016, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15247480" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Antigens, CD4/analysis ; Antigens, CD8/analysis ; Cell Lineage ; DNA-Binding Proteins/metabolism ; Hematopoietic Stem Cells/immunology/physiology ; Immunity, Mucosal ; Intestinal Mucosa/cytology/*immunology ; Lymphoid Tissue/embryology/immunology ; Mice ; Mice, Transgenic ; Nuclear Receptor Subfamily 1, Group F, Member 3 ; Receptors, Antigen, T-Cell, alpha-beta/*analysis/genetics ; Receptors, Antigen, T-Cell, gamma-delta/analysis/genetics ; Receptors, Retinoic Acid/genetics/*metabolism ; Receptors, Thyroid Hormone/genetics/*metabolism ; T-Lymphocyte Subsets/cytology/*immunology ; T-Lymphocytes/cytology/*immunology ; Thymus Gland/cytology/*immunology
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  • 196
    Publication Date: 2004-06-05
    Description: Ten phosphatized specimens of a small (〈180 micrometers) animal displaying clear bilaterian features have been recovered from the Doushantuo Formation, China, dating from 40 to 55 million years before the Cambrian. Seen in sections, this animal (Vernanimalcula guizhouena gen. et sp. nov.) had paired coeloms extending the length of the gut; paired external pits that could be sense organs; bilateral, anterior-posterior organization; a ventrally directed anterior mouth with thick walled pharynx; and a triploblastic structure. The structural complexity is that of an adult rather than a larval form. These fossils provide the first evidence confirming the phylogenetic inference that Bilateria arose well before the Cambrian.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Chen, Jun-Yuan -- Bottjer, David J -- Oliveri, Paola -- Dornbos, Stephen Q -- Gao, Feng -- Ruffins, Seth -- Chi, Huimei -- Li, Chia-Wei -- Davidson, Eric H -- New York, N.Y. -- Science. 2004 Jul 9;305(5681):218-22. Epub 2004 Jun 3.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Nanjing Institute of Geology and Paleontology, Nanjing 210008, China. chenjunyuan@163.net〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15178752" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Biological Evolution ; China ; Digestive System/anatomy & histology ; Endoderm ; *Fossils ; *Invertebrates/anatomy & histology/classification ; Mesoderm ; Phylogeny ; Time
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  • 197
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2004-08-10
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Helgen, Kristofer M -- New York, N.Y. -- Science. 2004 Aug 6;305(5685):777-8; author reply 777-8.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15300924" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Animals, Wild ; California ; Eagles ; *Ecosystem ; Foxes ; Polynesia ; Population Density ; Predatory Behavior ; *Sus scrofa
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  • 198
    Publication Date: 2004-10-16
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Normile, Dennis -- New York, N.Y. -- Science. 2004 Oct 15;306(5695):398-9.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15486269" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Asia/epidemiology ; Chickens ; Disease Outbreaks/prevention & control/*veterinary ; Immunization Programs ; Influenza A virus/*immunology ; *Influenza Vaccines/immunology ; Influenza in Birds/epidemiology/*prevention & control/transmission ; Orthomyxoviridae Infections/prevention & control/transmission/virology ; *Poultry ; Risk Assessment ; Vaccination/*veterinary
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  • 199
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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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  • 200
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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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