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  • United States  (1,743)
  • Male  (1,584)
  • Adult  (369)
  • American Association for the Advancement of Science (AAAS)  (3,371)
  • American Chemical Society
  • 1995-1999  (1,333)
  • 1985-1989  (1,002)
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  • 1965-1969
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  • American Association for the Advancement of Science (AAAS)  (3,371)
  • American Chemical Society
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Year
  • 101
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1998-03-21
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Korn, D -- New York, N.Y. -- Science. 1998 Feb 20;279(5354):1113.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/9508677" target="_blank"〉PubMed〈/a〉
    Keywords: Biological Products ; *Research ; United States ; *United States Food and Drug Administration/legislation & ; jurisprudence/organization & administration
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 102
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1998-10-17
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Garber, K -- New York, N.Y. -- Science. 1998 Sep 18;281(5384):1788.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/9776678" target="_blank"〉PubMed〈/a〉
    Keywords: Base Sequence ; Chromatography, High Pressure Liquid ; Databases, Factual ; *Genetic Markers ; Genetic Predisposition to Disease ; *Genetic Techniques ; *Genome, Human ; Humans ; National Institutes of Health (U.S.) ; Neoplasms/*genetics ; Point Mutation ; *Polymorphism, Genetic ; United States
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 103
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1998-07-21
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Garber, K -- New York, N.Y. -- Science. 1998 Jun 19;280(5371):1841.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/9669935" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Cats/*genetics ; *Chromosome Mapping ; Crosses, Genetic ; Disease Models, Animal ; Female ; Genetic Diseases, Inborn/genetics ; *Genome ; Humans ; Male ; Microsatellite Repeats
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 104
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1998-08-26
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Gardner, W -- Rosenbaum, J -- New York, N.Y. -- Science. 1998 Aug 7;281(5378):786-7.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Medicine, University of Pittsburgh School of Medicine, Pennsylvania, USA. gardnerwp@msx.upmc.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/9714683" target="_blank"〉PubMed〈/a〉
    Keywords: Copyright ; Databases as Topic/*legislation & jurisprudence ; *Intellectual Property ; Ownership ; United States
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 105
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1998-05-09
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Lawler, A -- New York, N.Y. -- Science. 1998 Apr 24;280(5363):515-6.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/9575093" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; *Nervous System Physiological Phenomena ; Rats ; *Research ; Space Flight ; *Spacecraft ; United States ; United States National Aeronautics and Space Administration ; *Weightlessness
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 106
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1998-04-16
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Lawler, A -- New York, N.Y. -- Science. 1998 Mar 27;279(5359):2035.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/9537911" target="_blank"〉PubMed〈/a〉
    Keywords: Budgets/*legislation & jurisprudence ; Financing, Government ; National Institutes of Health (U.S.)/*economics ; *Research Support as Topic ; United States
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 107
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1998-03-21
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉New York, N.Y. -- Science. 1998 Feb 20;279(5354):1116-7.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/9508681" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Aged ; Chromosomes, Human, Pair 4 ; Female ; France ; Genes, Dominant ; Humans ; Italy ; Male ; Middle Aged ; Mutation ; Nerve Tissue Proteins/*genetics ; Parkinson Disease/*genetics ; Synucleins ; alpha-Synuclein
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 108
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1998-05-09
    Description: Many molecular mechanisms for neural adaptation to stress remain unknown. Expression of alternative splice variants of Slo, a gene encoding calcium- and voltage-activated potassium channels, was measured in rat adrenal chromaffin tissue from normal and hypophysectomized animals. Hypophysectomy triggered an abrupt decrease in the proportion of Slo transcripts containing a "STREX" exon. The decrease was prevented by adrenocorticotropic hormone injections. In Xenopus oocytes, STREX variants produced channels with functional properties associated with enhanced repetitive firing. Thus, the hormonal stress axis is likely to control the excitable properties of epinephrine-secreting cells by regulating alternative splicing of Slo messenger RNA.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Xie, J -- McCobb, D P -- New York, N.Y. -- Science. 1998 Apr 17;280(5362):443-6.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Section of Neurobiology and Behavior, Cornell University, Ithaca, NY 14853, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/9545224" target="_blank"〉PubMed〈/a〉
    Keywords: Adrenal Medulla/*metabolism ; Adrenocorticotropic Hormone/metabolism/*pharmacology ; *Alternative Splicing ; Amino Acid Sequence ; Animals ; Chromaffin Cells/*metabolism ; Corticosterone/blood/*metabolism ; Dexamethasone/pharmacology ; Epinephrine/secretion ; Exons ; Female ; Hypophysectomy ; Large-Conductance Calcium-Activated Potassium Channel alpha Subunits ; Large-Conductance Calcium-Activated Potassium Channels ; Male ; Molecular Sequence Data ; Oocytes ; Phenylethanolamine N-Methyltransferase/genetics ; Polymerase Chain Reaction ; Potassium Channels/*genetics ; *Potassium Channels, Calcium-Activated ; RNA, Messenger/genetics/metabolism ; Rats ; Rats, Sprague-Dawley ; Xenopus
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
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  • 109
    Publication Date: 1998-06-11
    Description: The mouse Clock gene encodes a bHLH-PAS protein that regulates circadian rhythms and is related to transcription factors that act as heterodimers. Potential partners of CLOCK were isolated in a two-hybrid screen, and one, BMAL1, was coexpressed with CLOCK and PER1 at known circadian clock sites in brain and retina. CLOCK-BMAL1 heterodimers activated transcription from E-box elements, a type of transcription factor-binding site, found adjacent to the mouse per1 gene and from an identical E-box known to be important for per gene expression in Drosophila. Mutant CLOCK from the dominant-negative Clock allele and BMAL1 formed heterodimers that bound DNA but failed to activate transcription. Thus, CLOCK-BMAL1 heterodimers appear to drive the positive component of per transcriptional oscillations, which are thought to underlie circadian rhythmicity.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Gekakis, N -- Staknis, D -- Nguyen, H B -- Davis, F C -- Wilsbacher, L D -- King, D P -- Takahashi, J S -- Weitz, C J -- New York, N.Y. -- Science. 1998 Jun 5;280(5369):1564-9.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Neurobiology, Harvard Medical School, Boston MA 02115, USA. 02115, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/9616112" target="_blank"〉PubMed〈/a〉
    Keywords: ARNTL Transcription Factors ; Animals ; Basic Helix-Loop-Helix Transcription Factors ; Biological Clocks ; CLOCK Proteins ; Cell Cycle Proteins ; Circadian Rhythm/genetics/*physiology ; Cloning, Molecular ; Cricetinae ; DNA/metabolism ; Dimerization ; Feedback ; Gene Expression ; Helix-Loop-Helix Motifs ; Male ; Mesocricetus ; Mice ; Mutation ; Nuclear Proteins/*genetics/metabolism ; Period Circadian Proteins ; Promoter Regions, Genetic ; Retina/metabolism ; Suprachiasmatic Nucleus/metabolism ; Trans-Activators/genetics/*metabolism ; Transcription Factors/genetics/*metabolism ; *Transcriptional Activation
    Print ISSN: 0036-8075
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  • 110
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1998-10-10
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Lenfant, C -- New York, N.Y. -- Science. 1998 Sep 25;281(5385):1961.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/9767040" target="_blank"〉PubMed〈/a〉
    Keywords: Blood Pressure ; *Diet, Sodium-Restricted ; Humans ; Hypertension/*etiology ; National Institutes of Health (U.S.) ; *Nutrition Policy ; Sodium, Dietary/*administration & dosage ; United States
    Print ISSN: 0036-8075
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  • 111
    Publication Date: 1998-01-31
    Description: Candidate mammalian odorant receptors were first cloned some 6 years ago. The physiological function of these receptors in initiating transduction in olfactory receptor neurons remains to be established. Here, a recombinant adenovirus was used to drive expression of a particular receptor gene in an increased number of sensory neurons in the rat olfactory epithelium. Electrophysiological recording showed that increased expression of a single gene led to greater sensitivity to a small subset of odorants.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Zhao, H -- Ivic, L -- Otaki, J M -- Hashimoto, M -- Mikoshiba, K -- Firestein, S -- New York, N.Y. -- Science. 1998 Jan 9;279(5348):237-42.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Interdepartmental Neuroscience Program, Yale University, New Haven, CT 06510, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/9422698" target="_blank"〉PubMed〈/a〉
    Keywords: Adenoviridae/genetics/physiology ; Aldehydes/metabolism/*pharmacology ; Animals ; Electrophysiology ; Female ; Gene Expression ; Genetic Vectors ; Green Fluorescent Proteins ; Luminescent Proteins/analysis/genetics ; Male ; *Odors ; Olfactory Receptor Neurons/*physiology/virology ; Patch-Clamp Techniques ; Rats ; Rats, Sprague-Dawley ; Receptors, Odorant/genetics/metabolism/*physiology ; Recombinant Proteins
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 112
    Publication Date: 1998-09-22
    Description: Fertilin, a member of the ADAM family, is found on the plasma membrane of mammalian sperm. Sperm from mice lacking fertilin beta were shown to be deficient in sperm-egg membrane adhesion, sperm-egg fusion, migration from the uterus into the oviduct, and binding to the egg zona pellucida. Egg activation was unaffected. The results are consistent with a direct role of fertilin in sperm-egg plasma membrane interaction. Fertilin could also have a direct role in sperm-zona binding or oviduct migration; alternatively, the effects on these functions could result from the absence of fertilin activity during spermatogenesis.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Cho, C -- Bunch, D O -- Faure, J E -- Goulding, E H -- Eddy, E M -- Primakoff, P -- Myles, D G -- HD16580/HD/NICHD NIH HHS/ -- U54HD29125/HD/NICHD NIH HHS/ -- New York, N.Y. -- Science. 1998 Sep 18;281(5384):1857-9.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Section of Molecular and Cellular Biology, University of California, Davis, CA 95616, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/9743500" target="_blank"〉PubMed〈/a〉
    Keywords: ADAM Proteins ; Animals ; Calcium/metabolism ; Cell Adhesion ; Cell Membrane/physiology ; Fallopian Tubes ; Female ; Male ; Membrane Fusion ; Membrane Glycoproteins/genetics/metabolism/*physiology ; Metalloendopeptidases/genetics/metabolism/*physiology ; Mice ; Mice, Inbred C57BL ; Mice, Knockout ; Ovum/physiology ; Sperm Capacitation ; *Sperm-Ovum Interactions ; Spermatogenesis ; Spermatozoa/chemistry/*physiology ; Zona Pellucida/physiology
    Print ISSN: 0036-8075
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  • 113
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1998-10-24
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Agnew, B -- New York, N.Y. -- Science. 1998 Oct 2;282(5386):18-9.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/9786788" target="_blank"〉PubMed〈/a〉
    Keywords: National Institutes of Health (U.S.)/*economics ; Public Opinion ; *Public Policy ; *Research Support as Topic ; United States
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  • 114
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1998-06-27
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Agnew, B -- New York, N.Y. -- Science. 1998 Jun 5;280(5369):1516-8.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/9644013" target="_blank"〉PubMed〈/a〉
    Keywords: *Biomedical Engineering ; *Biotechnology ; *Computational Biology ; *National Institutes of Health (U.S.)/organization & administration ; Research Support as Topic ; United States
    Print ISSN: 0036-8075
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  • 115
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1998-10-10
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Lanphear, B P -- New York, N.Y. -- Science. 1998 Sep 11;281(5383):1617-8.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Children's Hospital Medical Center, University of Cincinnati, Cincinnati, OH 45229-3039, USA. bruce.lanphear@chmcc.org〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/9767027" target="_blank"〉PubMed〈/a〉
    Keywords: Child ; Costs and Cost Analysis ; Dust/analysis ; *Environmental Exposure ; *Housing/standards ; Humans ; Lead/analysis/*blood ; Lead Poisoning/economics/*prevention & control ; Mass Screening ; Maximum Allowable Concentration ; Paint ; United States ; United States Environmental Protection Agency
    Print ISSN: 0036-8075
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  • 116
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1998-12-29
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Lasagna, L -- Kaitin, K I -- New York, N.Y. -- Science. 1998 Nov 13;282(5392):1263.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/9867628" target="_blank"〉PubMed〈/a〉
    Keywords: Advertising as Topic ; *Drug Approval ; Humans ; Pediatrics ; Phytotherapy ; Publishing ; United States ; *United States Food and Drug Administration/organization & administration
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 117
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1998-10-10
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉New York, N.Y. -- Science. 1998 Sep 25;281(5385):1939-40.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/9767035" target="_blank"〉PubMed〈/a〉
    Keywords: Allergy and Immunology/history ; Cell Physiological Phenomena ; History, 20th Century ; Switzerland ; United States
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  • 118
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1998-08-26
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉New York, N.Y. -- Science. 1998 Jul 31;281(5377):651-2.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/9714673" target="_blank"〉PubMed〈/a〉
    Keywords: Data Collection ; Disclosure ; Embryo Transfer ; Federal Government ; Female ; *Government Regulation ; Humans ; Information Dissemination ; Informed Consent ; Licensure ; Male ; Practice Guidelines as Topic ; Records as Topic ; Reproductive Techniques/adverse effects/*legislation & jurisprudence/*standards ; United States
    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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  • 119
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1998-10-10
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Pennisi, E -- New York, N.Y. -- Science. 1998 Sep 25;281(5385):1984-5.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/9767051" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Arabidopsis/embryology/genetics ; *Biological Evolution ; Embryonic and Fetal Development/*genetics ; Female ; Genes, Plant ; *Genomic Imprinting ; Humans ; Insects/*genetics ; Male ; Peromyscus ; Seeds/*growth & development
    Print ISSN: 0036-8075
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  • 120
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1998-07-11
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉New York, N.Y. -- Science. 1998 Jun 12;280(5370):1697.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/9660708" target="_blank"〉PubMed〈/a〉
    Keywords: *AIDS Vaccines/therapeutic use ; Acquired Immunodeficiency Syndrome/immunology/*prevention & control ; *Controlled Clinical Trials as Topic ; HIV/immunology/physiology ; HIV Envelope Protein gp120/immunology ; HIV Infections/prevention & control/therapy/virology ; Humans ; Male ; Thailand ; United States ; Viral Load
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  • 121
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1998-06-20
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Lawler, A -- New York, N.Y. -- Science. 1998 May 29;280(5368):1338.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/9634407" target="_blank"〉PubMed〈/a〉
    Keywords: Academies and Institutes/economics/*organization & administration ; Administrative Personnel ; Biological Science Disciplines/organization & administration ; Europe ; Exobiology/economics/*organization & administration ; Financing, Government ; Origin of Life ; Research Support as Topic ; United States ; United States National Aeronautics and Space ; Administration/economics/*organization & administration ; Universities/economics
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  • 122
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1998-07-21
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Pennisi, E -- New York, N.Y. -- Science. 1998 Jun 19;280(5371):1837-8.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/9669933" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Anura/*genetics/physiology ; Diptera/*genetics/physiology ; Eye/anatomy & histology ; Female ; *Genes ; Male ; Sex Ratio ; *Sexual Behavior, Animal ; Vocalization, Animal
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  • 123
    Publication Date: 1998-10-23
    Description: The Human Genome Project has successfully completed all the major goals in its current 5-year plan, covering the period 1993-98. A new plan, for 1998-2003, is presented, in which human DNA sequencing will be the major emphasis. An ambitious schedule has been set to complete the full sequence by the end of 2003, 2 years ahead of previous projections. In the course of completing the sequence, a "working draft" of the human sequence will be produced by the end of 2001. The plan also includes goals for sequencing technology development; for studying human genome sequence variation; for developing technology for functional genomics; for completing the sequence of Caenorhabditis elegans and Drosophila melanogaster and starting the mouse genome; for studying the ethical, legal, and social implications of genome research; for bioinformatics and computational studies; and for training of genome scientists.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Collins, F S -- Patrinos, A -- Jordan, E -- Chakravarti, A -- Gesteland, R -- Walters, L -- New York, N.Y. -- Science. 1998 Oct 23;282(5389):682-9.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉National Human Genome Research Institute, National Institutes of Health, Bethesda, MD 20892, USA. fc23a@nih.gov〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/9784121" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Bioethics ; Computational Biology ; Databases, Factual ; Databases, Nucleic Acid ; Federal Government ; Genetic Research ; Genetic Variation ; Genome ; Genome, Human ; *Human Genome Project/economics/organization & administration ; Humans ; Information Dissemination ; International Cooperation ; Internationality ; Molecular Biology/education ; Point Mutation ; Polymorphism, Genetic ; Sequence Analysis, DNA/economics/methods ; Sociology ; Species Specificity ; Time Factors ; United States
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  • 124
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1998-06-20
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Littman, R A -- New York, N.Y. -- Science. 1998 May 22;280(5367):1174; author reply 1176-7.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/9634391" target="_blank"〉PubMed〈/a〉
    Keywords: History, 20th Century ; Humans ; Infant ; *Language ; Learning ; Male ; *Memory ; Time Factors
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  • 125
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1998-05-23
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Pennisi, E -- New York, N.Y. -- Science. 1998 May 8;280(5365):814-7.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/9599151" target="_blank"〉PubMed〈/a〉
    Keywords: Automation ; Costs and Cost Analysis ; Government Agencies ; *Human Genome Project/economics/organization & administration ; Humans ; National Institutes of Health (U.S.) ; Pilot Projects ; Research Personnel ; Research Support as Topic ; Robotics ; *Sequence Analysis, DNA/methods ; United States
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  • 126
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1998-06-20
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Pennisi, E -- New York, N.Y. -- Science. 1998 May 22;280(5367):1185.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/9634394" target="_blank"〉PubMed〈/a〉
    Keywords: *Biotechnology ; Human Genome Project/*economics ; Humans ; International Cooperation ; National Institutes of Health (U.S.)/economics ; Patents as Topic ; *Research Support as Topic ; *Sequence Analysis, DNA/instrumentation/methods ; United States
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  • 127
    Publication Date: 1999-04-17
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Lanza, R P -- Arrow, K J -- Axelrod, J -- Baltimore, D -- Benacerraf, B -- Bloch, K E -- Bloembergen, N -- Brown, H C -- Brown, M S -- Cibelli, J B -- Cohen, S -- Cooper, L N -- Corey, E J -- Dulbecco, R -- Fischer, E H -- Fitch, V L -- Friedmen, M -- Friedman, M -- Furchgott, R F -- Gell-Mann, M -- Glaser, D A -- Glashow, S L -- Gilbert, W -- Goldstein, J L -- Wilson, R W -- New York, N.Y. -- Science. 1999 Mar 19;283(5409):1849-50.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10206888" target="_blank"〉PubMed〈/a〉
    Keywords: *Bioethics ; Biomedical Research ; *Embryo Research ; Embryo, Mammalian/*cytology ; Federal Government ; Government Regulation ; Humans ; Politics ; Research/*legislation & jurisprudence ; Research Support as Topic/legislation & jurisprudence ; *Risk Assessment ; *Stem Cells ; United States ; United States Dept. of Health and Human Services
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  • 128
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1999-08-14
    Description: The circadian clock consists of a feedback loop in which clock genes are rhythmically expressed, giving rise to cycling levels of RNA and proteins. Four of the five circadian genes identified to date influence responsiveness to freebase cocaine in the fruit fly, Drosophila melanogaster. Sensitization to repeated cocaine exposures, a phenomenon also seen in humans and animal models and associated with enhanced drug craving, is eliminated in flies mutant for period, clock, cycle, and doubletime, but not in flies lacking the gene timeless. Flies that do not sensitize owing to lack of these genes do not show the induction of tyrosine decarboxylase normally seen after cocaine exposure. These findings indicate unexpected roles for these genes in regulating cocaine sensitization and indicate that they function as regulators of tyrosine decarboxylase.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Andretic, R -- Chaney, S -- Hirsh, J -- DA05942/DA/NIDA NIH HHS/ -- GM/DA 27318/GM/NIGMS NIH HHS/ -- New York, N.Y. -- Science. 1999 Aug 13;285(5430):1066-8.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Biology, Gilmer Hall, University of Virginia, Charlottesville, VA 22903, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10446052" target="_blank"〉PubMed〈/a〉
    Keywords: ARNTL Transcription Factors ; Animals ; Basic Helix-Loop-Helix Transcription Factors ; Behavior, Animal/drug effects ; Biological Clocks/genetics ; CLOCK Proteins ; *Casein Kinase Iepsilon ; Circadian Rhythm/*genetics ; Cocaine/*pharmacology ; Dopamine Agonists/pharmacology ; *Drosophila Proteins ; Drosophila melanogaster/*drug effects/genetics/physiology ; *Genes, Insect ; Insect Proteins/genetics/physiology ; Male ; Motor Activity/drug effects ; Mutation ; Nuclear Proteins/*genetics/physiology ; Period Circadian Proteins ; Protein Kinases/genetics/physiology ; Quinpirole/pharmacology ; Receptors, Dopamine D2/agonists/physiology ; Trans-Activators/genetics/physiology ; Transcription Factors/genetics ; Tyramine/metabolism/pharmacology ; Tyrosine Decarboxylase/metabolism
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  • 129
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1999-06-05
    Description: Strains of mice that show characteristic patterns of behavior are critical for research in neurobehavioral genetics. Possible confounding influences of the laboratory environment were studied in several inbred strains and one null mutant by simultaneous testing in three laboratories on a battery of six behaviors. Apparatus, test protocols, and many environmental variables were rigorously equated. Strains differed markedly in all behaviors, and despite standardization, there were systematic differences in behavior across labs. For some tests, the magnitude of genetic differences depended upon the specific testing lab. Thus, experiments characterizing mutants may yield results that are idiosyncratic to a particular laboratory.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Crabbe, J C -- Wahlsten, D -- Dudek, B C -- AA00170/AA/NIAAA NIH HHS/ -- AA10760/AA/NIAAA NIH HHS/ -- DA10731/DA/NIDA NIH HHS/ -- New York, N.Y. -- Science. 1999 Jun 4;284(5420):1670-2.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Portland Alcohol Research Center, Department of Veterans Affairs Medical Center, Portland, OR 97201, USA. crabbe@ohsu.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10356397" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Animals, Laboratory/genetics ; Anxiety ; *Behavior, Animal ; Confounding Factors (Epidemiology) ; Drinking Behavior ; *Environment ; Female ; Genetics, Behavioral/*methods ; Genotype ; Male ; Mice ; Mice, Inbred Strains/genetics ; Mice, Mutant Strains/genetics ; Motor Activity ; Psychological Tests ; Reproducibility of Results
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  • 130
    Publication Date: 1999-08-28
    Description: The gene expression profile of the aging process was analyzed in skeletal muscle of mice. Use of high-density oligonucleotide arrays representing 6347 genes revealed that aging resulted in a differential gene expression pattern indicative of a marked stress response and lower expression of metabolic and biosynthetic genes. Most alterations were either completely or partially prevented by caloric restriction, the only intervention known to retard aging in mammals. Transcriptional patterns of calorie-restricted animals suggest that caloric restriction retards the aging process by causing a metabolic shift toward increased protein turnover and decreased macromolecular damage.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Lee, C K -- Klopp, R G -- Weindruch, R -- Prolla, T A -- P01 AG11915/AG/NIA NIH HHS/ -- R01 CA78723/CA/NCI NIH HHS/ -- New York, N.Y. -- Science. 1999 Aug 27;285(5432):1390-3.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Environmental Toxicology Center, Institute on Aging, Department of Genetics, University of Wisconsin, Madison, WI 53706, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10464095" target="_blank"〉PubMed〈/a〉
    Keywords: Aging/*genetics ; Animals ; DNA Damage/genetics ; DNA Repair/genetics ; *Diet ; *Energy Intake ; Energy Metabolism/genetics ; *Gene Expression Regulation ; Male ; Mice ; Mice, Inbred C57BL ; Mitochondria, Muscle/metabolism ; Muscle, Skeletal/innervation/*metabolism ; Oligonucleotide Array Sequence Analysis ; Oxidative Stress/genetics ; Proteins/metabolism ; RNA, Messenger/genetics/metabolism
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  • 131
    Publication Date: 1998-05-23
    Description: The neural basis of navigation by humans was investigated with functional neuroimaging of brain activity during navigation in a familiar, yet complex virtual reality town. Activation of the right hippocampus was strongly associated with knowing accurately where places were located and navigating accurately between them. Getting to those places quickly was strongly associated with activation of the right caudate nucleus. These two right-side brain structures function in the context of associated activity in right inferior parietal and bilateral medial parietal regions that support egocentric movement through the virtual town, and activity in other left-side regions (hippocampus, frontal cortex) probably involved in nonspatial aspects of navigation. These findings outline a network of brain areas that support navigation in humans and link the functions of these regions to physiological observations in other mammals.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Maguire, E A -- Burgess, N -- Donnett, J G -- Frackowiak, R S -- Frith, C D -- O'Keefe, J -- Wellcome Trust/United Kingdom -- New York, N.Y. -- Science. 1998 May 8;280(5365):921-4.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Wellcome Department of Cognitive Neurology, Institute of Neurology, University College London, 12 Queen Square, London WC1N 3BG, UK. e.maguire@fil.ion.ucl.ac.uk〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/9572740" target="_blank"〉PubMed〈/a〉
    Keywords: Brain Mapping ; Caudate Nucleus/blood supply/*physiology/radionuclide imaging ; Cues ; Frontal Lobe/blood supply/*physiology/radionuclide imaging ; Hippocampus/blood supply/*physiology/radionuclide imaging ; Humans ; Male ; Memory ; Neural Pathways ; *Orientation ; Parietal Lobe/blood supply/*physiology/radionuclide imaging ; Psychomotor Performance ; Regional Blood Flow ; *Space Perception ; Tomography, Emission-Computed
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  • 132
    Publication Date: 1999-07-20
    Description: Intervertebral disc disease is one of the most common musculoskeletal disorders. A number of environmental and anthropometric risk factors may contribute to it, and recent reports have suggested the importance of genetic factors as well. The COL9A2 gene, which codes for one of the polypeptide chains of collagen IX that is expressed in the intervertebral disc, was screened for sequence variations in individuals with intervertebral disc disease. The analysis identified a putative disease-causing sequence variation that converted a codon for glutamine to one for tryptophan in six out of the 157 individuals but in none of 174 controls. The tryptophan allele cosegregated with the disease phenotype in the four families studied, giving a lod score (logarithm of odds ratio) for linkage of 4.5, and subsequent linkage disequilibrium analysis conditional on linkage gave an additional lod score of 7.1.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Annunen, S -- Paassilta, P -- Lohiniva, J -- Perala, M -- Pihlajamaa, T -- Karppinen, J -- Tervonen, O -- Kroger, H -- Lahde, S -- Vanharanta, H -- Ryhanen, L -- Goring, H H -- Ott, J -- Prockop, D J -- Ala-Kokko, L -- AR39740/AR/NIAMS NIH HHS/ -- HG00008/HG/NHGRI NIH HHS/ -- New York, N.Y. -- Science. 1999 Jul 16;285(5426):409-12.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Collagen Research Unit, Biocenter and Department of Medical Biochemistry, University of Oulu, 90220 Oulu, Finland.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10411504" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Aged ; Alleles ; Amino Acid Substitution ; Case-Control Studies ; Codon ; Collagen/chemistry/*genetics ; *Collagen Type IX ; Female ; Genetic Linkage ; *Genetic Predisposition to Disease ; Humans ; Intervertebral Disc Displacement/*genetics ; Linkage Disequilibrium ; Male ; Middle Aged ; Mutation ; Penetrance ; Polymorphism, Genetic ; Sciatica/*genetics ; Tryptophan/genetics
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  • 133
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1999-05-18
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Wickelgren, I -- New York, N.Y. -- Science. 1999 Apr 23;284(5414):571.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10328731" target="_blank"〉PubMed〈/a〉
    Keywords: *Genetic Linkage ; Homosexuality, Male/*genetics ; Humans ; Male ; *Microsatellite Repeats ; Nuclear Family ; Research Design ; X Chromosome/*genetics
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  • 134
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1999-10-16
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Lasley, E N -- New York, N.Y. -- Science. 1999 Sep 10;285(5434):1649-50.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10523176" target="_blank"〉PubMed〈/a〉
    Keywords: *Animal Experimentation ; *Animal Welfare ; Animals ; *Animals, Laboratory ; Federal Government ; Government Regulation ; National Institutes of Health (U.S.) ; New Mexico ; *Pan troglodytes ; Research ; United States ; United States Department of Agriculture
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  • 135
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1999-04-30
    Description: Morphological analysis was performed on multilegged deformed frogs representing five species from 12 different localities in California, Oregon, Arizona, and New York. The pattern of duplicated limbs was consistent with mechanical perturbation by trematode infestation but not with the effects of retinoids.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Sessions, S K -- Franssen, R A -- Horner, V L -- New York, N.Y. -- Science. 1999 Apr 30;284(5415):800-2.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Biology, Hartwick College, Oneonta, NY 13820, USA. sessionss@hartwick.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10221911" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Anura/*abnormalities/*parasitology ; Forelimb/*abnormalities ; Gene Expression Regulation, Developmental/drug effects ; Hindlimb/*abnormalities/parasitology ; Limb Buds/drug effects/metabolism ; Ranidae/abnormalities/parasitology ; Trematode Infections/parasitology/*veterinary ; Tretinoin/*toxicity ; United States
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  • 136
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1999-05-08
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Malakoff, D -- New York, N.Y. -- Science. 1999 Apr 9;284(5412):230.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10232965" target="_blank"〉PubMed〈/a〉
    Keywords: *Animal Experimentation ; *Animal Rights ; *Animal Testing Alternatives ; Animals ; Animals, Laboratory/immunology ; Antibodies, Monoclonal/*biosynthesis ; Ascites ; Culture Techniques ; Federal Government ; Government Regulation ; Hybridomas ; Internationality ; *Mice/immunology ; *National Institutes of Health (U.S.)/legislation & jurisprudence ; United States
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  • 137
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1999-06-26
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Enserink, M -- New York, N.Y. -- Science. 1999 May 28;284(5419):1445.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10383318" target="_blank"〉PubMed〈/a〉
    Keywords: Financing, Government ; Intellectual Property ; *National Institutes of Health (U.S.) ; Publishing ; Research Support as Topic ; *Technology Transfer ; United States
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  • 138
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1999-05-18
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Perpich, J G -- New York, N.Y. -- Science. 1999 Apr 23;284(5414):591-2.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10328741" target="_blank"〉PubMed〈/a〉
    Keywords: *Academies and Institutes ; *Education, Graduate ; Education, Medical, Graduate ; Fellowships and Scholarships ; *Physicians ; *Research ; *Research Personnel ; Research Support as Topic ; United States
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  • 139
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1999-11-30
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Peters, R -- Sikorsky, R -- New York, N.Y. -- Science. 1999 Oct 15;286(5439):434.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10577206" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Binding Sites, Antibody ; Biological Availability ; Half-Life ; Immunoglobulin Fab Fragments/*immunology/*metabolism ; Male ; Polyethylene Glycols/*metabolism ; Rats ; Rats, Wistar
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  • 140
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1999-11-30
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Marshall, E -- New York, N.Y. -- Science. 1999 Oct 22;286(5440):655-6.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10577213" target="_blank"〉PubMed〈/a〉
    Keywords: *Internet ; National Institutes of Health (U.S.) ; *Peer Review, Research ; Periodicals as Topic ; *Publishing ; United States
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  • 141
    Publication Date: 1999-05-21
    Description: Mutations of the breast cancer susceptibility gene BRCA1 confer increased risk for breast, ovarian, and prostatic cancers, but it is not clear why the mutations are associated with these particular tumor types. In transient transfection assays, BRCA1 was found to inhibit signaling by the ligand-activated estrogen receptor (ER-alpha) through the estrogen-responsive enhancer element and to block the transcriptional activation function AF-2 of ER-alpha. These results raise the possibility that wild-type BRCA1 suppresses estrogen-dependent transcriptional pathways related to mammary epithelial cell proliferation and that loss of this ability contributes to tumorigenesis.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Fan, S -- Wang, J -- Yuan, R -- Ma, Y -- Meng, Q -- Erdos, M R -- Pestell, R G -- Yuan, F -- Auborn, K J -- Goldberg, I D -- Rosen, E M -- R01-CA75503/CA/NCI NIH HHS/ -- R01-ES09169/ES/NIEHS NIH HHS/ -- New York, N.Y. -- Science. 1999 May 21;284(5418):1354-6.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Radiation Oncology, Long Island Jewish Medical Center, The Long Island Campus for the Albert Einstein College of Medicine, 270-05 76th Avenue, New Hyde Park, NY 11040, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10334989" target="_blank"〉PubMed〈/a〉
    Keywords: BRCA1 Protein/*physiology ; Breast/cytology ; Breast Neoplasms/etiology ; Cell Division ; Enhancer Elements, Genetic ; Epithelial Cells/cytology ; Estradiol/metabolism ; Estrogen Receptor alpha ; Female ; Genes, BRCA1 ; Genes, Reporter ; Humans ; Ligands ; Male ; Receptors, Estrogen/*metabolism ; *Signal Transduction ; Transcription Factors/metabolism ; *Transcriptional Activation ; Transfection ; Tumor Cells, Cultured
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  • 142
    Publication Date: 1999-04-30
    Description: Solid tumors depend on angiogenesis for their growth. In a transgenic mouse model of pancreatic islet cell carcinogenesis (RIP1-Tag2), an angiogenic switch occurs in premalignant lesions, and angiogenesis persists during progression to expansive solid tumors and invasive carcinomas. RIP1-Tag2 mice were treated so as to compare the effects of four angiogenesis inhibitors at three distinct stages of disease progression. AGM-1470, angiostatin, BB-94, and endostatin each produced distinct efficacy profiles in trials aimed at preventing the angiogenic switch in premalignant lesions, intervening in the rapid expansion of small tumors, or inducing the regression of large end-stage cancers. Thus, anti-angiogenic drugs may prove most efficacious when they are targeted to specific stages of cancer.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Bergers, G -- Javaherian, K -- Lo, K M -- Folkman, J -- Hanahan, D -- New York, N.Y. -- Science. 1999 Apr 30;284(5415):808-12.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Biochemistry and Biophysics and Hormone Research Institute, University of California, San Francisco, 513 Parnassus Ave, San Francisco, CA 94143-0534, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10221914" target="_blank"〉PubMed〈/a〉
    Keywords: Angiostatins ; Animals ; Anticarcinogenic Agents/pharmacology ; Antineoplastic Agents/*pharmacology ; Apoptosis ; Carcinoma, Islet Cell/blood supply/*drug therapy/pathology/prevention & control ; Collagen/pharmacology ; Cyclohexanes ; Disease Progression ; Drug Evaluation, Preclinical ; Endostatins ; Female ; Male ; Mice ; Mice, Inbred C57BL ; Mice, Transgenic ; Neoplasm Staging ; Neovascularization, Pathologic/*prevention & control ; Pancreatic Neoplasms/blood supply/*drug therapy/pathology/prevention & control ; Peptide Fragments/pharmacology ; Phenylalanine/analogs & derivatives/pharmacology ; Plasminogen/pharmacology ; Sesquiterpenes/pharmacology ; Thiophenes/pharmacology
    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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  • 143
    Publication Date: 1999-12-11
    Description: In vitro PA28 binds and activates proteasomes. It is shown here that mice with a disrupted PA28b gene lack PA28a and PA28b polypeptides, demonstrating that PA28 functions as a hetero-oligomer in vivo. Processing of antigenic epitopes derived from exogenous or endogenous antigens is altered in PA28-/- mice. Cytotoxic T lymphocyte responses are impaired, and assembly of immunoproteasomes is greatly inhibited in mice lacking PA28. These results show that PA28 is necessary for immunoproteasome assembly and is required for efficient antigen processing, thus demonstrating the importance of PA28-mediated proteasome function in immune responses.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Preckel, T -- Fung-Leung, W P -- Cai, Z -- Vitiello, A -- Salter-Cid, L -- Winqvist, O -- Wolfe, T G -- Von Herrath, M -- Angulo, A -- Ghazal, P -- Lee, J D -- Fourie, A M -- Wu, Y -- Pang, J -- Ngo, K -- Peterson, P A -- Fruh, K -- Yang, Y -- New York, N.Y. -- Science. 1999 Dec 10;286(5447):2162-5.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉The R. W. Johnson Pharmaceutical Research Institute, 3210 Merryfield Row, San Diego, CA 92121, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10591649" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; *Antigen Presentation ; Autoantigens ; Cysteine Endopeptidases/chemistry/*metabolism ; Enzyme Activators/*metabolism ; Epitopes, T-Lymphocyte/immunology ; Female ; H-Y Antigen/immunology ; Herpesviridae Infections/immunology ; Histocompatibility Antigens Class I/immunology/metabolism ; Interferons/pharmacology ; Lymphocytic Choriomeningitis/immunology ; Lymphocytic choriomeningitis virus/immunology ; Male ; Mice ; Multienzyme Complexes/chemistry/*metabolism ; Muromegalovirus/immunology ; Ovalbumin/immunology ; Peptide Fragments/immunology ; Proteasome Endopeptidase Complex ; Proteins/genetics/*metabolism ; T-Lymphocytes, Cytotoxic/*immunology
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  • 144
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1999-04-17
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Strauss, E -- New York, N.Y. -- Science. 1999 Mar 5;283(5407):1435, 1437-8.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10206868" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; DNA, Mitochondrial/*genetics ; *Evolution, Molecular ; Female ; Fossils ; Humans ; Male ; Mutation ; Ovum ; *Paleontology ; Recombination, Genetic ; Spermatozoa ; Statistics as Topic
    Print ISSN: 0036-8075
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  • 145
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1999-08-14
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Marshall, E -- New York, N.Y. -- Science. 1999 Jul 23;285(5427):519.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10447481" target="_blank"〉PubMed〈/a〉
    Keywords: China ; *International Cooperation ; Lobbying ; *National Institutes of Health (U.S.) ; *Research ; Research Support as Topic ; United States
    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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  • 146
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1999-11-30
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Bloom, F E -- New York, N.Y. -- Science. 1999 Oct 22;286(5440):679.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10577220" target="_blank"〉PubMed〈/a〉
    Keywords: Databases, Factual ; *Internet ; Medline ; National Library of Medicine (U.S.) ; *Online Systems ; *Periodicals as Topic ; *Publishing ; Signal Transduction ; United States
    Print ISSN: 0036-8075
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  • 147
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1999-09-15
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Bloom, F E -- New York, N.Y. -- Science. 1999 Aug 20;285(5431):1207.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10484728" target="_blank"〉PubMed〈/a〉
    Keywords: *Periodicals as Topic ; Publishing/*organization & administration ; *Societies, Medical ; *Societies, Scientific ; United States
    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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  • 148
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1999-06-26
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Marshall, E -- New York, N.Y. -- Science. 1999 May 21;284(5418):1246.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10383299" target="_blank"〉PubMed〈/a〉
    Keywords: Academic Medical Centers/*standards ; Bioethics ; Clinical Trials as Topic/*standards ; Ethics Committees, Research ; Federal Government ; *Government Regulation ; Humans ; Informed Consent ; National Institutes of Health (U.S.) ; North Carolina ; Professional Staff Committees ; Research/*standards ; Research Support as Topic ; United States
    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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  • 149
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1999-12-28
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Ferber, D -- New York, N.Y. -- Science. 1999 Nov 26;286(5445):1662-6.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10610557" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Bacterial Proteins/genetics/toxicity ; *Bacterial Toxins ; *Biotechnology ; Butterflies/physiology ; Crops, Agricultural/adverse effects/*genetics ; Drug Resistance, Microbial/genetics ; Endotoxins/genetics/toxicity ; Food Hypersensitivity ; *Genetic Engineering ; Hemolysin Proteins ; Humans ; *Plants, Genetically Modified/adverse effects ; Pollen/genetics ; Public Opinion ; Risk Assessment ; United States ; United States Department of Agriculture ; United States Environmental Protection Agency ; United States Food and Drug Administration
    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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  • 150
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1999-07-17
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Marshall, E -- New York, N.Y. -- Science. 1999 Jun 25;284(5423):2067, 2069.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10409058" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; *Chimera ; *Embryo, Mammalian ; Humans ; Pan troglodytes ; *Patents as Topic ; United States
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  • 151
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1999-06-05
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Fairchild, A L -- Bayer, R -- New York, N.Y. -- Science. 1999 May 7;284(5416):919-21.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Program in the History of Public Health and Medicine, Division of Sociomedical Sciences, The Joseph L. Mailman School of Public Health, Columbia University, New York, NY 10032-2625, USA. alf4@columbia.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10357678" target="_blank"〉PubMed〈/a〉
    Keywords: African Americans/history ; Alabama ; Anonymous Testing ; Anti-HIV Agents/*therapeutic use ; Clinical Trials as Topic ; Developing Countries ; Disclosure ; Ethics, Medical ; Female ; HIV Infections/prevention & control/*transmission ; *HIV Seroprevalence ; History, 20th Century ; *Human Experimentation/history ; Humans ; Infectious Disease Transmission, Vertical/*prevention & control ; Informed Consent/history ; Male ; *Needle-Exchange Programs ; *Persons ; Pregnant Women ; Syphilis/history ; *Trust ; United States ; *Vulnerable Populations ; Withholding Treatment
    Print ISSN: 0036-8075
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  • 152
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1999-07-17
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Marshall, E -- New York, N.Y. -- Science. 1999 Jun 25;284(5423):2062-3.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10409054" target="_blank"〉PubMed〈/a〉
    Keywords: Costs and Cost Analysis ; Europe ; Financing, Government ; History, 20th Century ; *Internet ; National Institutes of Health (U.S.) ; Peer Review, Research ; *Periodicals as Topic ; *Publishing/economics ; Societies, Scientific ; United States
    Print ISSN: 0036-8075
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  • 153
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1999-05-08
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Fears, R -- Poste, G -- New York, N.Y. -- Science. 1999 Apr 9;284(5412):267-8.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉SmithKline Beecham, New Frontiers Science Park, Harlow, Essex CM19 5AW, UK. robin_b_fears@sbphrd.com〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10232974" target="_blank"〉PubMed〈/a〉
    Keywords: Bioethics ; Confidentiality ; Databases, Factual ; *Databases, Nucleic Acid ; *Delivery of Health Care ; *Genetic Privacy ; *Genetic Research ; *Genetics, Medical ; *Genetics, Population ; Great Britain ; Humans ; Informed Consent ; Medical Informatics ; Medical Records Systems, Computerized ; Private Sector ; Public Sector ; *Research ; Research Subjects ; *Resource Allocation ; Social Control, Formal ; *State Medicine/organization & administration ; United States
    Print ISSN: 0036-8075
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  • 154
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1999-05-08
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Marshall, E -- New York, N.Y. -- Science. 1999 Apr 16;284(5413):406-7.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10232976" target="_blank"〉PubMed〈/a〉
    Keywords: Chromosome Mapping ; *Databases, Factual ; *Drug Industry ; Genetic Predisposition to Disease ; *Genome, Human ; Humans ; *Information Dissemination ; *Mutation ; National Institutes of Health (U.S.) ; *Polymorphism, Genetic ; Private Sector ; Public Sector ; Sequence Analysis, DNA ; United States
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  • 155
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1999-03-20
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Marshall, E -- New York, N.Y. -- Science. 1999 Feb 26;283(5406):1234-5.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10084920" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Anthrax/prevention & control/therapy ; *Biological Warfare/prevention & control ; *Financing, Government ; Government Agencies/economics ; Humans ; Military Medicine/economics ; *Public Health/economics ; Research Support as Topic ; Smallpox/prevention & control/therapy ; United States ; United States Public Health Service/economics ; *Violence/prevention & control
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  • 156
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1999-10-16
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Martin, J B -- New York, N.Y. -- Science. 1999 Sep 10;285(5434):1671.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10523179" target="_blank"〉PubMed〈/a〉
    Keywords: Academic Medical Centers/*economics ; Budgets ; Hospitals, Teaching/economics ; Managed Care Programs ; Medical Indigency ; National Institutes of Health (U.S.) ; *Research ; *Research Support as Topic ; United States
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  • 157
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1999-10-09
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Zeisel, S H -- New York, N.Y. -- Science. 1999 Sep 17;285(5435):1853-5.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉School of Public Health, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599-7400, USA. stevenvzeisel@unc.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10515789" target="_blank"〉PubMed〈/a〉
    Keywords: Consumer Product Safety ; *Dietary Supplements/economics ; Food ; Humans ; *Legislation, Drug ; *Legislation, Food ; National Institutes of Health (U.S.) ; United States ; United States Food and Drug Administration
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  • 158
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1999-05-08
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Marshall, E -- New York, N.Y. -- Science. 1999 Apr 16;284(5413):413, 415.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10232981" target="_blank"〉PubMed〈/a〉
    Keywords: Aborted Fetus ; Advisory Committees ; *Bioethics ; *Embryo Research ; Embryo, Mammalian/*cytology ; Federal Government ; Fetal Research ; Financing, Government ; *Government Regulation ; Guidelines as Topic ; Humans ; Informed Consent ; *National Institutes of Health (U.S.) ; Public Policy ; *Research ; Research Support as Topic ; *Stem Cells ; United States
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  • 159
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1999-04-03
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Marshall, E -- New York, N.Y. -- Science. 1999 Mar 12;283(5408):1610-1.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10189309" target="_blank"〉PubMed〈/a〉
    Keywords: *Internet ; *National Institutes of Health (U.S.) ; Peer Review, Research ; *Publishing ; Societies, Scientific ; United States
    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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  • 160
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1999-03-13
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Marshall, E -- New York, N.Y. -- Science. 1999 Feb 12;283(5404):913-4.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10075554" target="_blank"〉PubMed〈/a〉
    Keywords: Biomedical Research ; Federal Government ; Government Regulation ; Scientific Misconduct/*legislation & jurisprudence ; Texas ; United States ; United States Dept. of Health and Human Services ; Universities
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  • 161
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1999-02-13
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Marshall, E -- New York, N.Y. -- Science. 1999 Jan 22;283(5401):465, 467.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/9988645" target="_blank"〉PubMed〈/a〉
    Keywords: Advisory Committees ; Bioethics ; Cell Line ; *Embryo Research ; Embryo, Mammalian/*cytology ; Federal Government ; *Government Regulation ; Humans ; National Institutes of Health (U.S.)/economics/*legislation & jurisprudence ; Research ; Research Support as Topic/*legislation & jurisprudence ; *Stem Cells ; United States
    Print ISSN: 0036-8075
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  • 162
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1999-08-24
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Fiske, M R -- New York, N.Y. -- Science. 1999 Aug 6;285(5429):837-8.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10454934" target="_blank"〉PubMed〈/a〉
    Keywords: *Crystallization ; Proteins/*chemistry ; Societies, Scientific ; Space Flight ; United States ; *United States National Aeronautics and Space Administration ; *Weightlessness
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  • 163
    Publication Date: 1999-11-27
    Description: Apoptosis can be triggered by members of the Bcl-2 protein family, such as Bim, that share only the BH3 domain with this family. Gene targeting in mice revealed important physiological roles for Bim. Lymphoid and myeloid cells accumulated, T cell development was perturbed, and most older mice accumulated plasma cells and succumbed to autoimmune kidney disease. Lymphocytes were refractory to apoptotic stimuli such as cytokine deprivation, calcium ion flux, and microtubule perturbation but not to others. Thus, Bim is required for hematopoietic homeostasis and as a barrier to autoimmunity. Moreover, particular death stimuli appear to activate apoptosis through distinct BH3-only proteins.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Bouillet, P -- Metcalf, D -- Huang, D C -- Tarlinton, D M -- Kay, T W -- Kontgen, F -- Adams, J M -- Strasser, A -- CA43540/CA/NCI NIH HHS/ -- CA80188/CA/NCI NIH HHS/ -- New York, N.Y. -- Science. 1999 Nov 26;286(5445):1735-8.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉The Walter and Eliza Hall Institute of Medical Research, Melbourne, Victoria 3050, Australia.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10576740" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; *Apoptosis ; Apoptosis Regulatory Proteins ; Autoimmune Diseases/etiology ; *Autoimmunity ; B-Lymphocytes/physiology ; Carrier Proteins/*physiology ; Cells, Cultured ; Crosses, Genetic ; Female ; Gene Targeting ; Glomerulonephritis/etiology ; Hematopoietic Stem Cells/physiology ; Homeostasis ; Leukocyte Count ; Leukocytes/*physiology ; Male ; *Membrane Proteins ; Mice ; Mice, Transgenic ; *Proto-Oncogene Proteins ; Proto-Oncogene Proteins c-bcl-2/physiology ; Signal Transduction ; T-Lymphocyte Subsets/physiology
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1999-09-18
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Barinaga, M -- New York, N.Y. -- Science. 1999 Aug 27;285(5432):1337-8.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10490403" target="_blank"〉PubMed〈/a〉
    Keywords: Adolescent ; California ; Clinical Trials as Topic/legislation & jurisprudence/*standards ; Conduct Disorder/*drug therapy ; Ethics Committees, Research ; Government Regulation ; Human Experimentation/legislation & jurisprudence ; Humans ; Male ; Nontherapeutic Human Experimentation ; Placebos ; *Prisoners/legislation & jurisprudence ; Therapeutic Human Experimentation ; Valproic Acid/*administration & dosage/therapeutic use ; Violence
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  • 165
    Publication Date: 1999-06-18
    Description: In contrast with the prevailing view that most tumors and metastases begin as avascular masses, evidence is presented here that a subset of tumors instead initially grows by coopting existing host vessels. This coopted host vasculature does not immediately undergo angiogenesis to support the tumor but instead regresses, leading to a secondarily avascular tumor and massive tumor cell loss. Ultimately, however, the remaining tumor is rescued by robust angiogenesis at the tumor margin. The expression patterns of the angiogenic antagonist angiopoietin-2 and of pro-angiogenic vascular endothelial growth factor (VEGF) suggest that these proteins may be critical regulators of this balance between vascular regression and growth.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Holash, J -- Maisonpierre, P C -- Compton, D -- Boland, P -- Alexander, C R -- Zagzag, D -- Yancopoulos, G D -- Wiegand, S J -- New York, N.Y. -- Science. 1999 Jun 18;284(5422):1994-8.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Regeneron Pharmaceuticals, 777 Old Saw Mill River Road, Tarrytown, NY 10591, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10373119" target="_blank"〉PubMed〈/a〉
    Keywords: Adenocarcinoma/blood supply/pathology ; Angiopoietin-1 ; Angiopoietin-2 ; Animals ; Apoptosis ; Blood Vessels/pathology ; Endothelial Growth Factors/genetics/*physiology ; Endothelium, Vascular/pathology/physiology ; Glioblastoma/blood supply/pathology ; Glioma/blood supply/pathology ; In Situ Hybridization ; Lymphokines/genetics/*physiology ; Male ; Membrane Glycoproteins/genetics/*physiology ; Mice ; Mice, Inbred C57BL ; Muscle, Smooth, Vascular/pathology/physiology ; Neoplasm Transplantation ; Neoplasms, Experimental/*blood supply/*pathology ; *Neovascularization, Pathologic ; Proteins/genetics/*physiology ; Rats ; Rats, Sprague-Dawley ; Up-Regulation ; Vascular Endothelial Growth Factor A ; Vascular Endothelial Growth Factors
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  • 166
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1999-10-09
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Doniach, S -- New York, N.Y. -- Science. 1999 Sep 17;285(5435):1850.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10515787" target="_blank"〉PubMed〈/a〉
    Keywords: National Institutes of Health (U.S.)/*organization & administration ; *Peer Review, Research ; Research Support as Topic ; United States
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  • 167
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1999-12-28
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Sorenson, S B -- New York, N.Y. -- Science. 1999 Nov 19;286(5444):1481-2.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉School of Public Health, University of California, Los Angeles, Los Angeles, CA 90095-1772, USA. sorenson@ucla.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10610547" target="_blank"〉PubMed〈/a〉
    Keywords: *Consumer Product Safety/legislation & jurisprudence ; Firearms/legislation & jurisprudence/*standards ; Public Opinion ; Public Policy ; Safety ; United States
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  • 168
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1999-09-04
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Dovichi, N -- New York, N.Y. -- Science. 1999 Aug 13;285(5430):1016.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10475843" target="_blank"〉PubMed〈/a〉
    Keywords: Canada ; Financing, Government ; Human Genome Project ; Research Support as Topic ; Sequence Analysis, DNA/*instrumentation ; United States
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  • 169
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1999-05-08
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Soule, H R -- New York, N.Y. -- Science. 1999 Apr 9;284(5412):261.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10232971" target="_blank"〉PubMed〈/a〉
    Keywords: Commerce ; *Foundations ; Humans ; Male ; Prostatic Neoplasms/*therapy ; *Research
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  • 170
    Publication Date: 1999-08-24
    Description: Large (more than 16-fold) differences in susceptibility to disruption of juvenile male reproductive development by 17beta-estradiol (E2) were detected between strains of mice. Effects of strain, E2 dose, and the interaction of strain and E2 dose on testes weight and spermatogenesis were all highly significant (P 〈 0.0001). Spermatid maturation was eliminated by low doses of E2 in strains such as C57BL/6J and C17/Jls. In contrast, mice of the widely used CD-1 line, which has been selected for large litter size, showed little or no inhibition of spermatid maturation even in response to 16 times as much E2. Product safety bioassays conducted with animals selected for fecundity may greatly underestimate disruption of male reproductive development by estradiol and environmental estrogenic compounds.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Spearow, J L -- Doemeny, P -- Sera, R -- Leffler, R -- Barkley, M -- New York, N.Y. -- Science. 1999 Aug 20;285(5431):1259-61.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Section of Neurobiology, Physiology and Behavior, University of California at Davis, Davis, CA 95616, USA. jlspearow@ucdavis.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10455051" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Body Weight/drug effects ; Dose-Response Relationship, Drug ; Estradiol/*pharmacology/toxicity ; *Genetic Variation ; Litter Size ; Male ; Mice ; Mice, Inbred Strains ; Organ Size/drug effects ; Species Specificity ; Spermatids/drug effects ; Spermatogenesis/*drug effects ; Testis/anatomy & histology/*drug effects ; Toxicity Tests
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  • 171
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1999-05-18
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Duke, J A -- New York, N.Y. -- Science. 1999 Apr 23;284(5414):589.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10328736" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; *Biological Evolution ; Brain ; Cooking ; Estrogens, Non-Steroidal/*analysis ; Female ; *Hominidae ; Humans ; *Isoflavones ; Male ; Phytoestrogens ; Plant Preparations ; *Vegetables/chemistry
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  • 172
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1999-09-15
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Holden, C -- New York, N.Y. -- Science. 1999 Aug 20;285(5431):1186-7.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10484724" target="_blank"〉PubMed〈/a〉
    Keywords: *Biological Evolution ; Curriculum ; Kansas ; Religion and Science ; Science/*education ; United States
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  • 173
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1999-12-28
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Malakoff, D -- New York, N.Y. -- Science. 1999 Dec 3;286(5446):1836.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10610571" target="_blank"〉PubMed〈/a〉
    Keywords: *Budgets ; Government Agencies/economics ; National Institutes of Health (U.S.)/*economics ; Research/*economics ; *Research Support as Topic ; United States
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  • 174
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1999-07-31
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Pennisi, E -- New York, N.Y. -- Science. 1999 Jul 9;285(5425):192-3.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10428714" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; *Biological Evolution ; Female ; Genes, Recessive ; Genetic Variation ; Inbreeding ; Male ; Moths/genetics/physiology ; Plants/genetics ; Songbirds/genetics/physiology
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  • 175
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1999-12-28
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Trull, F L -- New York, N.Y. -- Science. 1999 Nov 19;286(5444):1477.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10610546" target="_blank"〉PubMed〈/a〉
    Keywords: *Animal Rights ; Animals ; Animals, Laboratory ; *Organizations ; *Research Personnel ; United States ; *Violence
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  • 176
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1999-11-30
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Kaiser, J -- New York, N.Y. -- Science. 1999 Oct 29;286(5441):883.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10577232" target="_blank"〉PubMed〈/a〉
    Keywords: *Government Regulation ; *Scientific Misconduct ; United States ; United States Office of Research Integrity/*organization & administration
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  • 177
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1999-12-28
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Kaiser, J -- New York, N.Y. -- Science. 1999 Nov 5;286(5442):1059.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10610514" target="_blank"〉PubMed〈/a〉
    Keywords: *Animal Rights ; Animals ; Animals, Laboratory ; *Primates ; *Research Personnel ; United States ; *Violence
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  • 178
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1999-02-27
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Brinkley, W R -- New York, N.Y. -- Science. 1999 Feb 5;283(5403):791.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10049119" target="_blank"〉PubMed〈/a〉
    Keywords: *Career Choice ; *Education, Medical, Graduate ; Humans ; National Institutes of Health (U.S.) ; *Physicians/statistics & numerical data ; Research/*manpower ; *Research Personnel/education/statistics & numerical data ; Research Support as Topic ; Societies, Scientific ; Training Support ; United States
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  • 179
    Publication Date: 1999-01-15
    Description: Phosphoinositide 3-kinase (PI3K) activation has been implicated in many cellular responses, including fibroblast growth, transformation, survival, and chemotaxis. Although PI3K is activated by several agents that stimulate T and B cells, the role of PI3K in lymphocyte function is not clear. The mouse gene encoding the PI3K adapter subunit p85alpha and its splice variants p55alpha and p50alpha was disrupted. Most p85alpha-p55alpha-p50alpha-/- mice die within days after birth. Lymphocyte development and function was studied with the use of the RAG2-deficient blastocyst complementation system. Chimeric mice had reduced numbers of peripheral mature B cells and decreased serum immunoglobulin. The B cells that developed had diminished proliferative responses to antibody to immunoglobulin M, antibody to CD40, and lipopolysaccharide stimulation and decreased survival after incubation with interleukin-4. In contrast, T cell development and proliferation was normal. This phenotype is similar to defects observed in mice lacking the tyrosine kinase Btk.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Fruman, D A -- Snapper, S B -- Yballe, C M -- Davidson, L -- Yu, J Y -- Alt, F W -- Cantley, L C -- R01 GM041890/GM/NIGMS NIH HHS/ -- New York, N.Y. -- Science. 1999 Jan 15;283(5400):393-7.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Division of Signal Transduction, Beth Israel Deaconess Medical Center, Boston, MA 02215, USA. dfruman@bidmc.harvard.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/9888855" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Antigens, CD45/analysis ; Apoptosis ; B-Lymphocytes/cytology/enzymology/*immunology ; Catalytic Domain ; Cell Cycle ; Chimera ; Chromones/pharmacology ; Enzyme Inhibitors/pharmacology ; Female ; Gene Targeting ; Immunoglobulins/*blood ; *Lymphocyte Activation ; Lymphocyte Count ; Male ; Mice ; Mice, Inbred C57BL ; Morpholines/pharmacology ; Phosphatidylinositol 3-Kinases/antagonists & inhibitors/genetics/*metabolism ; Protein-Tyrosine Kinases/genetics/metabolism ; Spleen/immunology ; T-Lymphocytes/cytology/enzymology/immunology
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  • 180
    Publication Date: 1999-08-28
    Description: The selenoprotein phospholipid hydroperoxide glutathione peroxidase (PHGPx) changes its physical characteristics and biological functions during sperm maturation. PHGPx exists as a soluble peroxidase in spermatids but persists in mature spermatozoa as an enzymatically inactive, oxidatively cross-linked, insoluble protein. In the midpiece of mature spermatozoa, PHGPx protein represents at least 50 percent of the capsule material that embeds the helix of mitochondria. The role of PHGPx as a structural protein may explain the mechanical instability of the mitochondrial midpiece that is observed in selenium deficiency.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Ursini, F -- Heim, S -- Kiess, M -- Maiorino, M -- Roveri, A -- Wissing, J -- Flohe, L -- New York, N.Y. -- Science. 1999 Aug 27;285(5432):1393-6.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Dipartmento di Chimica Biologica, Universita di Padova, Viale G. Colombo 3, I-35121 Padova, Italy.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10464096" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Electrophoresis, Gel, Two-Dimensional ; Electrophoresis, Polyacrylamide Gel ; Glutathione Peroxidase/chemistry/isolation & purification/*physiology ; Infertility, Male/metabolism ; Male ; Mitochondria/chemistry/enzymology ; Oxidation-Reduction ; Proteins/chemistry/isolation & purification/*physiology ; Rats ; Rats, Wistar ; Selenium/deficiency/*physiology ; Selenoproteins ; Solubility ; Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization ; Spermatids/chemistry/enzymology ; *Spermatogenesis ; Spermatozoa/chemistry/enzymology/*physiology
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  • 181
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1999-11-05
    Description: The eyes of strepsipteran insects are very unusual among living insects. In their anatomical organization they may form a modern counterpart to the structural plan proposed for the eyes of some trilobites. Externally they differ from the usual "insect plan" by presenting far fewer but much larger lenses. Beneath each lens is its own independent retina. Anatomical and optical measurements indicate that each of these units is image-forming, so that the visual field is subdivided into and represented by "chunks," unlike the conventional insect compound eye that decomposes the visual image in a pointwise manner. This results in profound changes in the neural centers for vision and implies major evolutionary changes.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Buschbeck, E -- Ehmer, B -- Hoy, R -- New York, N.Y. -- Science. 1999 Nov 5;286(5442):1178-80.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Neurobiology and Behavior, Mudd Hall, Cornell University, Ithaca, NY 14853, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10550059" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Biological Evolution ; Eye/anatomy & histology ; Insects/*anatomy & histology/physiology ; Lens, Crystalline/*anatomy & histology/physiology ; Male ; Optic Chiasm/anatomy & histology/physiology ; Photoreceptor Cells, Invertebrate/*anatomy & histology/physiology ; Vision, Ocular/*physiology
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  • 182
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1999-01-23
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Kaiser, J -- New York, N.Y. -- Science. 1999 Jan 1;283(5398):18-9.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/9917257" target="_blank"〉PubMed〈/a〉
    Keywords: Advisory Committees ; *Bioethics ; Federal Government ; *Human Experimentation ; No-Observed-Adverse-Effect Level ; *Nontherapeutic Human Experimentation ; Pesticides/*toxicity ; *Toxicity Tests/standards ; United States ; *United States Environmental Protection Agency
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  • 183
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1999-10-16
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Varmus, H -- New York, N.Y. -- Science. 1999 Sep 10;285(5434):1654-6.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10523178" target="_blank"〉PubMed〈/a〉
    Keywords: Acquired Immunodeficiency Syndrome ; Budgets ; Computational Biology ; Embryo, Mammalian/cytology ; Humans ; Internet ; *National Institutes of Health (U.S.)/economics/organization & administration ; Peer Review, Research ; Public Policy ; Publishing ; Research ; Stem Cells ; United States
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1999-01-30
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Rosenberg, L -- New York, N.Y. -- Science. 1999 Jan 15;283(5400):331-2.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Molecular Biology, Princeton University, NJ 08544, USA. lrosenberg@molbiol.princeton.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/9925491" target="_blank"〉PubMed〈/a〉
    Keywords: Academic Medical Centers ; *Career Choice ; Drug Industry ; *Education, Medical, Graduate ; Fellowships and Scholarships ; Financing, Government ; Foundations ; Health Care Sector ; National Institutes of Health (U.S.) ; *Physicians/statistics & numerical data/trends ; Public Policy ; Research/*manpower ; *Research Personnel ; Research Support as Topic ; United States
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  • 185
    Publication Date: 1999-10-26
    Description: Progressive damage to mitochondrial DNA (mtDNA) during life is thought to contribute to aging processes. However, this idea has been difficult to reconcile with the small fraction of mtDNA so far found to be altered. Here, examination of mtDNA revealed high copy point mutations at specific positions in the control region for replication of human fibroblast mtDNA from normal old, but not young, individuals. Furthermore, in longitudinal studies, one or more mutations appeared in an individual only at an advanced age. Some mutations appeared in more than one individual. Most strikingly, a T414G transversion was found, in a generally high proportion (up to 50 percent) of mtDNA molecules, in 8 of 14 individuals above 65 years of age (57 percent) but was absent in 13 younger individuals.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Michikawa, Y -- Mazzucchelli, F -- Bresolin, N -- Scarlato, G -- Attardi, G -- AG-12117-03/AG/NIA NIH HHS/ -- New York, N.Y. -- Science. 1999 Oct 22;286(5440):774-9.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Division of Biology, California Institute of Technology, Pasadena, CA 91125, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10531063" target="_blank"〉PubMed〈/a〉
    Keywords: Adolescent ; Adult ; Aged ; Aged, 80 and over ; Aging/*genetics ; Cell Line ; Child ; Child, Preschool ; DNA Damage ; DNA Repair ; DNA Replication/*genetics ; DNA, Mitochondrial/biosynthesis/chemistry/*genetics ; Fetus ; Fibroblasts ; Humans ; Infant ; Infant, Newborn ; Longitudinal Studies ; Middle Aged ; Mitochondria/*genetics ; Nucleic Acid Conformation ; Nucleic Acid Heteroduplexes ; *Point Mutation ; Polymerase Chain Reaction ; Pseudogenes
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  • 186
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1999-10-16
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Merrill, S A -- McGeary, M -- New York, N.Y. -- Science. 1999 Sep 10;285(5434):1679-80.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉National Research Council's Board on Science, Technology, and Economic Policy (STEP), Washington, DC 20418, USA. smerrill@nas.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10523184" target="_blank"〉PubMed〈/a〉
    Keywords: Budgets ; Government Agencies/economics ; National Institutes of Health (U.S.)/economics ; *Research ; *Research Support as Topic ; United States
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  • 187
    Publication Date: 1999-03-12
    Description: Segregation Distorter (SD) in Drosophila melanogaster is a naturally occurring meiotic drive system in which the SD chromosome is transmitted from SD/SD+ males in vast excess over its homolog owing to the induced dysfunction of SD+-bearing spermatids. The Sd locus is the key distorting gene responsible for this phenotype. A genomic fragment from the Sd region conferred full distorting activity when introduced into the appropriate genetic background by germline transformation. The only functional product encoded by this fragment is a truncated version of the RanGAP nuclear transport protein. These results demonstrate that this mutant RanGAP is the functional Sd product.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Merrill, C -- Bayraktaroglu, L -- Kusano, A -- Ganetzky, B -- New York, N.Y. -- Science. 1999 Mar 12;283(5408):1742-5.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Laboratory of Genetics, 445 Henry Mall, University of Wisconsin, Madison, WI 53706, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10073941" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Carrier Proteins/chemistry/*genetics/physiology ; Cell Nucleus/metabolism ; Crosses, Genetic ; DNA, Complementary ; *Drosophila Proteins ; Drosophila melanogaster/*genetics/physiology ; Female ; *GTPase-Activating Proteins ; Gene Duplication ; Gene Expression ; *Genes, Insect ; Male ; *Meiosis ; Nuclear Proteins/chemistry/*genetics/physiology ; RNA, Messenger/genetics ; Spermatids/physiology ; Sulfotransferases/chemistry/genetics ; Transcription, Genetic ; Transformation, Genetic
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  • 188
    Publication Date: 1999-12-28
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Velculescu, V E -- New York, N.Y. -- Science. 1999 Nov 19;286(5444):1491-2.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Johns Hopkins Oncology Center, Baltimore, MD 21231, USA. velculescu@jhmi.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10610550" target="_blank"〉PubMed〈/a〉
    Keywords: *Awards and Prizes ; Gene Expression ; *Gene Expression Profiling ; Gene Expression Regulation, Neoplastic ; Genes, ras ; *Genome ; History, 20th Century ; Humans ; Neoplasms/genetics ; RNA, Messenger/*genetics ; Saccharomyces cerevisiae/genetics ; United States
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  • 189
    Publication Date: 1999-10-09
    Description: Many human diseases are associated with the overproduction of oxygen free radicals that inflict cell damage. A manganese(II) complex with a bis(cyclohexylpyridine)-substituted macrocyclic ligand (M40403) was designed to be a functional mimic of the superoxide dismutase (SOD) enzymes that normally remove these radicals. M40403 had high catalytic SOD activity and was chemically and biologically stable in vivo. Injection of M40403 into rat models of inflammation and ischemia-reperfusion injury protected the animals against tissue damage. Such mimics may result in better clinical therapies for diseases mediated by superoxide radicals.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Salvemini, D -- Wang, Z Q -- Zweier, J L -- Samouilov, A -- Macarthur, H -- Misko, T P -- Currie, M G -- Cuzzocrea, S -- Sikorski, J A -- Riley, D P -- New York, N.Y. -- Science. 1999 Oct 8;286(5438):304-6.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉MetaPhore Pharmaceuticals, 1910 Innerbelt Business Center Drive, St. Louis, MO 63114, USA. dsalvemini@metaphore.com〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10514375" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Anti-Inflammatory Agents, Non-Steroidal/chemical ; synthesis/chemistry/metabolism/*therapeutic use ; Cytoprotection ; Dinoprostone/metabolism ; Dose-Response Relationship, Drug ; Drug Design ; Drug Stability ; Inflammation/*drug therapy ; Interleukin-1/metabolism ; L-Lactate Dehydrogenase/metabolism ; Male ; Manganese ; Molecular Mimicry ; Neutrophils/drug effects ; Organometallic Compounds/chemical synthesis/chemistry/metabolism/*toxicity ; Rats ; Rats, Sprague-Dawley ; Reperfusion Injury/*drug therapy ; Splanchnic Circulation ; *Superoxide Dismutase/metabolism ; Superoxides/*metabolism ; Time Factors ; Tumor Necrosis Factor-alpha/metabolism
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    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 190
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1999-06-26
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Miller, H I -- New York, N.Y. -- Science. 1999 May 28;284(5419):1471-2.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Hoover Institution, Stanford University, Stanford, CA 94305, USA. miller@hoover.stanford.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10383324" target="_blank"〉PubMed〈/a〉
    Keywords: *Biotechnology/legislation & jurisprudence ; Consumer Product Safety/legislation & jurisprudence ; Costs and Cost Analysis ; *Crops, Agricultural ; Crosses, Genetic ; *Food Labeling/economics/legislation & jurisprudence ; Food Technology/legislation & jurisprudence ; Genetic Engineering ; *Plants, Genetically Modified ; Risk Factors ; United States ; *United States Food and Drug Administration
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    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 191
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1999-11-30
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Cassman, M -- Norvell, J C -- New York, N.Y. -- Science. 1999 Oct 8;286(5438):239-40.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10577190" target="_blank"〉PubMed〈/a〉
    Keywords: Computational Biology ; *Crystallography, X-Ray ; *National Institutes of Health (U.S.)/economics ; Proteins/*chemistry/genetics ; *Research Support as Topic ; *Synchrotrons/economics ; United States
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  • 192
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1999-10-26
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Vogel, G -- New York, N.Y. -- Science. 1999 Oct 1;286(5437):23.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10532882" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Dihydrotestosterone/metabolism ; Egg Yolk/metabolism ; Female ; Genes ; Male ; Ovum/*metabolism ; *Sexual Behavior, Animal ; Songbirds/genetics/*physiology ; Testosterone/*metabolism
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  • 193
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1999-10-26
    Description: The vomeronasal organ (VNO) is a chemoreceptor organ enclosed in a cartilaginous capsule and separated from the main olfactory epithelium. The vomeronasal neurons have two distinct types of receptor that differ from each other and from the large family of odorant receptors. The VNO receptors are seven-transmembrane receptors coupled to GTP-binding protein, but appear to activate inositol 1,4,5-trisphosphate signaling as opposed to cyclic adenosine monophosphate. The nature of stimulus access suggests that the VNO responds to nonvolatile cues, leading to activation of the hypothalamus by way of the accessory olfactory bulb and amygdala. The areas of hypothalamus innervated regulate reproductive, defensive, and ingestive behavior as well as neuroendocrine secretion.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Keverne, E B -- New York, N.Y. -- Science. 1999 Oct 22;286(5440):716-20.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Sub-Department of Animal Behaviour, University of Cambridge, Madingley, Cambridge CB3 8AA, UK. ebk10@cus.cam.ac.uk〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10531049" target="_blank"〉PubMed〈/a〉
    Keywords: Action Potentials ; Afferent Pathways ; Animals ; Behavior, Animal ; Chemoreceptor Cells/chemistry/*physiology ; Female ; GTP-Binding Proteins/metabolism ; Humans ; Hypothalamus/physiology ; Male ; Neurons, Afferent/*physiology ; Olfactory Bulb/physiology ; Pheromones/physiology ; Receptors, Cell Surface/chemistry/genetics/*physiology ; Signal Transduction ; Vomeronasal Organ/anatomy & histology/innervation/*physiology
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  • 194
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1999-07-03
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Goodenough, U W -- New York, N.Y. -- Science. 1999 Jun 11;284(5421):1774.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10391794" target="_blank"〉PubMed〈/a〉
    Keywords: *Foundations ; *Religion and Science ; United States
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  • 195
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1999-09-25
    Description: Cell proliferation requires cell growth; that is, cells only divide after they reach a critical size. However, the mechanisms by which cells grow and maintain their appropriate size have remained elusive. Drosophila deficient in the S6 kinase gene (dS6K) exhibited an extreme delay in development and a severe reduction in body size. These flies had smaller cells rather than fewer cells. The effect was cell-autonomous, displayed throughout larval development, and distinct from that of ribosomal protein mutants (Minutes). Thus, the dS6K gene product regulates cell size in a cell-autonomous manner without impinging on cell number.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Montagne, J -- Stewart, M J -- Stocker, H -- Hafen, E -- Kozma, S C -- Thomas, G -- F32 GM15926/GM/NIGMS NIH HHS/ -- New York, N.Y. -- Science. 1999 Sep 24;285(5436):2126-9.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Friedrich Miescher Institute, Maulbeerstrasse 66, 4058 Basel, Switzerland.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10497130" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Base Sequence ; Body Constitution ; Cell Count ; Cell Division ; Cell Size ; Drosophila melanogaster/cytology/*enzymology/genetics/*growth & development ; Epithelial Cells/cytology ; Female ; Genes, Insect ; Larva/cytology/growth & development ; Male ; Metamorphosis, Biological ; Molecular Sequence Data ; Mutation ; Ribosomal Protein S6 Kinases/genetics/*metabolism ; Wings, Animal/*cytology/growth & development
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  • 196
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1999-10-16
    Description: In primates, prefrontal, inferior temporal, and posterior parietal cortex are important for cognitive function. It is shown that in adult macaques, new neurons are added to these three neocortical association areas, but not to a primary sensory area (striate cortex). The new neurons appeared to originate in the subventricular zone and to migrate through the white matter to the neocortex, where they extended axons. These new neurons, which are continually added in adulthood, may play a role in the functions of association neocortex.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Gould, E -- Reeves, A J -- Graziano, M S -- Gross, C G -- EY11347-29/EY/NEI NIH HHS/ -- MH52423-05/MH/NIMH NIH HHS/ -- New York, N.Y. -- Science. 1999 Oct 15;286(5439):548-52.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Psychology, Princeton University, Princeton, NJ 08544, USA. goulde@princeton.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10521353" target="_blank"〉PubMed〈/a〉
    Keywords: Aging ; Animals ; Astrocytes/cytology ; Axons/ultrastructure ; Bromodeoxyuridine ; Cell Differentiation ; Cell Division ; Cell Movement ; Cell Survival ; Female ; Lateral Ventricles/cytology ; Macaca fascicularis ; Male ; Microscopy, Confocal ; Neocortex/*cytology/physiology ; Neurons/*cytology/physiology ; Parietal Lobe/*cytology/physiology ; Prefrontal Cortex/*cytology/physiology ; Temporal Lobe/*cytology/physiology ; Visual Cortex/cytology/physiology
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  • 197
    Publication Date: 1999-12-11
    Description: Neurofibromatosis type 1 (NF1) is a prevalent familial cancer syndrome resulting from germ line mutations in the NF1 tumor suppressor gene. Hallmark features of the disease are the development of benign peripheral nerve sheath tumors (neurofibromas), which can progress to malignancy. Unlike humans, mice that are heterozygous for a mutation in Nf1 do not develop neurofibromas. However, as described here, chimeric mice composed in part of Nf1-/- cells do, which demonstrates that loss of the wild-type Nf1 allele is rate-limiting in tumor formation. In addition, mice that carry linked germ line mutations in Nf1 and p53 develop malignant peripheral nerve sheath tumors (MPNSTs), which supports a cooperative and causal role for p53 mutations in MPNST development. These two mouse models provide the means to address fundamental aspects of disease development and to test therapeutic strategies.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Cichowski, K -- Shih, T S -- Schmitt, E -- Santiago, S -- Reilly, K -- McLaughlin, M E -- Bronson, R T -- Jacks, T -- New York, N.Y. -- Science. 1999 Dec 10;286(5447):2172-6.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Biology and Center for Cancer Research and Howard Hughes Medical Institute, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10591652" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Cell Line ; Chimera ; *Disease Models, Animal ; Female ; *Genes, Neurofibromatosis 1 ; Genes, p53 ; Germ-Line Mutation ; Humans ; Loss of Heterozygosity ; Male ; Mice ; Mice, Inbred C57BL ; Mice, Transgenic ; Mutation ; Nerve Sheath Neoplasms/*genetics/*pathology ; Nerve Tissue Proteins/analysis/physiology ; Neurofibromatosis 1/*genetics/*pathology ; Neurofibromin 1 ; Proteins/analysis/physiology ; S100 Proteins/analysis ; Schwann Cells/chemistry/ultrastructure ; Stem Cells
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  • 198
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1999-05-18
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Schiff, H -- New York, N.Y. -- Science. 1999 Apr 23;284(5414):589, 591.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10328739" target="_blank"〉PubMed〈/a〉
    Keywords: *Consumer Participation ; *National Institutes of Health (U.S.) ; *Patient Advocacy ; *Peer Review, Research ; *Research Support as Topic ; United States
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  • 199
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1999-12-28
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉New York, N.Y. -- Science. 1999 Nov 12;286(5443):1263.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10610526" target="_blank"〉PubMed〈/a〉
    Keywords: History, 20th Century ; *Periodicals as Topic/history ; Publishing/history ; *Science ; United States
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  • 200
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1999-02-27
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Schneider, E L -- New York, N.Y. -- Science. 1999 Feb 5;283(5403):796-7.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Leonard Davis School of Gerontology, Ethel Percy Andrus Gerontology Center, University of Southern California, Los Angeles, CA 90089-0191, USA. eschneid@usc.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10049123" target="_blank"〉PubMed〈/a〉
    Keywords: Aged ; Aged, 80 and over ; *Aging ; Chronic Disease/economics ; Economics ; *Health Status ; Housing for the Elderly ; Humans ; Medicare ; *Preventive Medicine ; *Research ; Social Security ; Transportation ; United States
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    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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