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  • Humans  (549)
  • Earth model, also for more shallow analyses !
  • 2000-2004  (561)
  • 1980-1984
  • 1925-1929  (5)
  • 2000  (561)
  • 1926  (5)
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  • 2000-2004  (561)
  • 1980-1984
  • 1925-1929  (5)
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  • 1
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    Unbekannt
    In:  Eos, Trans., Am. Geophys. Un., Jena, Physica-Verlag, vol. 81, no. 19, pp. 210, pp. 2096, (ISSN: 1340-4202)
    Publikationsdatum: 2000
    Schlagwort(e): Earth model, also for more shallow analyses ! ; Seismology ; Velocity depth profile ; double-prime
    Standort Signatur Erwartet Verfügbarkeit
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  • 2
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    In:  Phys. Earth Plan. Int., Stuttgart, Schweizerbart'sche Verlagsbuchhandlung, vol. 119, no. 1-2, pp. 3-23, pp. 2271, (ISSN 0016-8548, ISBN 3-510-50045-8)
    Publikationsdatum: 2000
    Schlagwort(e): Seismology ; Review article ; Project report/description ; Synthetic seismograms ; Clevede ; PEPI ; Earth model, also for more shallow analyses !
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  • 3
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    In:  Eos, Trans., Am. Geophys. Un., Berlin, Ges. f. Geowissenschaften e.V., vol. 81, no. 19, pp. 210, pp. L02309, (ISSN 0343-5164)
    Publikationsdatum: 2000
    Schlagwort(e): Earth model, also for more shallow analyses ! ; Seismology ; Velocity depth profile ; double-prime
    Standort Signatur Erwartet Verfügbarkeit
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  • 4
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    Unbekannt
    In:  Tectonophysics, Tokyo, Conseil de l'Europe, vol. 320, no. 3-4, pp. 175-194, pp. L01306, (ISSN: 1340-4202)
    Publikationsdatum: 2000
    Schlagwort(e): Dynamic ; Tectonics ; Reflection seismics ; Refraction seismics ; EUROPROBE (Geol. and Geophys. in eastern Europe) ; Rheology ; Earth model, also for more shallow analyses ! ; Velocity depth profile ; Inelastic
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  • 5
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    In:  Eos, Trans., Am. Geophys. Un., Warszawa, Conseil de l'Europe, vol. 81, no. 19, pp. 210, pp. L19608, (ISBN: 0-12-018847-3)
    Publikationsdatum: 2000
    Schlagwort(e): Earth model, also for more shallow analyses ! ; Seismology ; Velocity depth profile ; double-prime
    Standort Signatur Erwartet Verfügbarkeit
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  • 6
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    Unbekannt
    In:  Zeitschrift für Geophysik, Jena, Gustav Fischer, vol. 2, no. 3, pp. 24-29, pp. L24306, (ISBN: 0534351875, 2nd edition)
    Publikationsdatum: 1926
    Schlagwort(e): Earth model, also for more shallow analyses ! ; Seismology
    Standort Signatur Erwartet Verfügbarkeit
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  • 7
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    Unbekannt
    In:  Meteorologische Zeitschrift, Jena, Gustav Fischer, vol. 43, no. 3, pp. 427-430, pp. L24306, (ISBN: 0534351875, 2nd edition)
    Publikationsdatum: 1926
    Schlagwort(e): Earth model, also for more shallow analyses ! ; Meteorology
    Standort Signatur Erwartet Verfügbarkeit
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  • 8
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    In:  Terra Nova, Oslo, Wiley, vol. 12, no. 3, pp. 102-108, pp. B08303, (ISSN: 1340-4202)
    Publikationsdatum: 2000
    Schlagwort(e): Plate tectonics ; China ; Geol. aspects ; Volcanology ; Subduction zone ; Earth model, also for more shallow analyses ! ; Schaerer ; Scharer
    Standort Signatur Erwartet Verfügbarkeit
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  • 9
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    In:  Geophys. J. Int., Veldhoven, Kluwer, vol. 142, no. 2, pp. 351-360, pp. 2502, (ISSN: 1340-4202)
    Publikationsdatum: 2000
    Schlagwort(e): Modelling ; Gravimetry, Gravitation ; Inelastic ; Rheology ; Earth model, also for more shallow analyses ! ; isostasy ; GJI
    Standort Signatur Erwartet Verfügbarkeit
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  • 10
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    Unbekannt
    Bornträger
    In:  Professional Paper, Lehrbuch der Geophysik, Berlin, 6 + 1017 pp., Bornträger, vol. 3, no. VIIa, pp. 434-499, (ISBN: 3-540-23712-7)
    Publikationsdatum: 1926
    Schlagwort(e): Seismology ; Earth model, also for more shallow analyses !
    Standort Signatur Erwartet Verfügbarkeit
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  • 11
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    Unbekannt
    In:  Natur und Museum, Jena, Gustav Fischer, vol. 56, no. 3, pp. 33-41, pp. L24306, (ISBN: 0534351875, 2nd edition)
    Publikationsdatum: 1926
    Schlagwort(e): Handbook of geophysics ; Earth model, also for more shallow analyses !
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  • 12
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    Unbekannt
    In:  Die Umschau, Jena, Gustav Fischer, vol. 30, no. 3, pp. 265-268, pp. L24306, (ISBN: 0534351875, 2nd edition)
    Publikationsdatum: 1926
    Schlagwort(e): Earth model, also for more shallow analyses ! ; Velocity depth profile
    Standort Signatur Erwartet Verfügbarkeit
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  • 13
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    Unbekannt
    In:  Geophys. J. Int., Darmstadt, Wissenschaftliche Buchgesellschaft, vol. 142, no. 3, pp. 948-969, pp. B09404, (ISSN: 1340-4202)
    Publikationsdatum: 2000
    Schlagwort(e): Earth model, also for more shallow analyses ! ; CRUST ; Anisotropy ; Electromagnetic methods/phenomena ; magneto-tellurics ; GJI
    Standort Signatur Erwartet Verfügbarkeit
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  • 14
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    Unbekannt
    In:  Phys. Earth Plan. Int., Washington, D.C., AGU, vol. 119, no. 1-2, pp. 25-36, pp. 8011, (ISSN: 1340-4202)
    Publikationsdatum: 2000
    Schlagwort(e): Modelling ; Synthetic seismograms ; Three dimensional ; Inhomogeneity ; PEPI ; Earth model, also for more shallow analyses ! ; Seismology
    Standort Signatur Erwartet Verfügbarkeit
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  • 15
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    Unbekannt
    In:  Geophys. J. Int., Tokyo, Lawrence Livermore National Laboratory, vol. 141, no. 3, pp. F7-F11, pp. L18610, (ISSN: 1340-4202)
    Publikationsdatum: 2000
    Schlagwort(e): Crustal deformation (cf. Earthquake precursor: deformation or strain) ; Inelastic ; Rheology ; Earthquake ; Earth model, also for more shallow analyses ! ; Modelling
    Standort Signatur Erwartet Verfügbarkeit
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  • 16
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    In:  J. Geophys. Res., Kunming, China, 3-4, vol. 105, no. B2, pp. 2969-2980, pp. B05308, (ISSN: 1340-4202)
    Publikationsdatum: 2000
    Schlagwort(e): Seismology ; Modelling ; Velocity depth profile ; Teleseismic events ; Earth model, also for more shallow analyses ! ; Plate tectonics ; Tectonics ; 7205 ; Seismology ; Continental ; crust ; (1242) ; 7260 ; Theory ; and ; modeling ; 8105 ; Tectonophysics ; Continental ; margins ; JGR ; sedimentary ; basins ; 8150 ; Plate ; boundary--general ; (3040)
    Standort Signatur Erwartet Verfügbarkeit
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  • 17
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    In:  Rev. Geophys., Luxembourg, Conseil de l'Europe, vol. 38, no. 1, pp. 141-158, pp. 1484, (ISSN 0343-5164)
    Publikationsdatum: 2000
    Schlagwort(e): Earth model, also for more shallow analyses ! ; Seismology ; 410 ; 660 ; earth mantle ; Subduction zone ; Waves ; Wave propagation ; 3630 ; Mineralogy ; petrology ; rock ; chemistry ; Experimental ; mineralogy ; and ; petrology ; 3939 ; Mineral ; physics ; Physical ; thermodynamics ; 7203 ; Seismology ; Body ; wave ; propagation ; 8124 ; Tectonophysics ; Earth's ; interior--composition ; and ; state ; (old ; 8105)
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  • 18
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 2000-01-05
    Beschreibung: The assumption that human mitochondrial DNA is inherited from one parent only and therefore does not recombine is questionable. Linkage disequilibrium in human and chimpanzee mitochondrial DNA declines as a function of the distance between sites. This pattern can be attributed to one mechanism only: recombination.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Awadalla, P -- Eyre-Walker, A -- Smith, J M -- New York, N.Y. -- Science. 1999 Dec 24;286(5449):2524-5.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Institute of Cell, Animal and Population Biology, University of Edinburgh, Edinburgh EH9 1JT, UK.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10617471" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): Animals ; DNA, Mitochondrial/*genetics ; Evolution, Molecular ; Fathers ; Female ; Hominidae/*genetics ; Humans ; *Linkage Disequilibrium ; Male ; NADH Dehydrogenase/genetics ; Pan troglodytes/*genetics ; Polymorphism, Restriction Fragment Length ; *Recombination, Genetic
    Print ISSN: 0036-8075
    Digitale ISSN: 1095-9203
    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
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  • 19
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 2000-01-05
    Beschreibung: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Cyster, J G -- New York, N.Y. -- Science. 1999 Dec 10;286(5447):2098-102.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Microbiology and Immunology, University of California San Francisco, San Francisco, CA 94143, USA. cyster@itsa.ucsf.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10617422" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): Animals ; B-Lymphocytes/*immunology ; Cell Movement ; Chemokines/*immunology ; *Chemotaxis, Leukocyte ; Dendritic Cells/immunology ; Humans ; Immunologic Memory ; Ligands ; Lymphocyte Activation ; Lymphoid Tissue/*immunology ; T-Lymphocytes/*immunology
    Print ISSN: 0036-8075
    Digitale ISSN: 1095-9203
    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
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  • 20
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 2000-01-15
    Beschreibung: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Hathcock, J N -- New York, N.Y. -- Science. 1999 Dec 17;286(5448):2269; author reply 2270-1.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10636785" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): Consumer Advocacy ; Consumer Product Safety/legislation & jurisprudence ; *Dietary Supplements ; Humans ; *Legislation, Drug ; *Legislation, Food ; Lobbying ; United States ; United States Food and Drug Administration
    Print ISSN: 0036-8075
    Digitale ISSN: 1095-9203
    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
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  • 21
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 2000-01-05
    Beschreibung: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Wuethrich, B -- New York, N.Y. -- Science. 1999 Dec 10;286(5447):2054-6.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10617414" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): Anthropology ; DNA, Mitochondrial/*genetics ; Genetic Variation ; *Genetics, Population ; Humans ; Language ; Melanesia ; Polynesia ; *Sequence Deletion
    Print ISSN: 0036-8075
    Digitale ISSN: 1095-9203
    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
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  • 22
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 2000-01-15
    Beschreibung: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Henry, S H -- Bosch, F X -- Troxell, T C -- Bolger, P M -- New York, N.Y. -- Science. 1999 Dec 24;286(5449):2453-4.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Center for Food Safety and Applied Nutrition, U.S. Food and Drug Administration, Washington, DC 20204, USA. SHenry@bangate.fda.gov〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10636808" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): Aflatoxins/*analysis/toxicity ; Animals ; Developing Countries ; Food/*standards ; Food Analysis ; Food Contamination/*prevention & control ; *Global Health ; Hepatitis B Vaccines ; Humans ; Immunization Programs ; *Legislation, Food ; Liver Neoplasms/epidemiology/etiology/*prevention & control ; Prevalence ; Public Health ; Public Policy ; Risk Assessment ; United Nations
    Print ISSN: 0036-8075
    Digitale ISSN: 1095-9203
    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
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  • 23
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 2000-09-30
    Beschreibung: Researchers have deciphered how a promising cancer drug acts like a smart bomb, homing in on only a very narrow range of its potential targets in the cell. The compound, known as STI-571, has shown remarkable success in early clinical trials on patients with chronic myelogenous leukemia. Now, in work reported on page 1938, scientists reveal just how the compound works--information that could aid in the design of similar cancer therapies.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Marx, J -- New York, N.Y. -- Science. 2000 Sep 15;289(5486):1857-9.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/11012350" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): Antineoplastic Agents/chemistry/*therapeutic use ; Benzamides ; Catalytic Domain/drug effects ; Clinical Trials as Topic ; Enzyme Activation/drug effects ; Enzyme Inhibitors/therapeutic use ; Humans ; Imatinib Mesylate ; Leukemia, Myelogenous, Chronic, BCR-ABL Positive/*drug therapy/enzymology ; *Piperazines ; Protein Conformation ; Protein-Tyrosine Kinases/antagonists & inhibitors/chemistry ; Proto-Oncogene Proteins c-abl/*antagonists & inhibitors ; Pyrimidines/chemistry/*therapeutic use
    Print ISSN: 0036-8075
    Digitale ISSN: 1095-9203
    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
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  • 24
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 2000-09-23
    Beschreibung: The use of microarrays--slides or chips systematically dotted with DNA from thousands of genes--to determine gene expression patterns is providing a wealth of new information that should aid in cancer diagnosis and ultimately in therapy. In the past several months, researchers in several labs have used microarray technology to identify specific subtypes of a variety of cancers, including leukemias and lymphomas, the dangerous skin cancer melanoma, and breast cancer. In some cases, they can determine which cancers are likely to respond to current therapies and which aren't. In addition, the studies are giving researchers a fix on which genes are important for the development, maintenance, and spread of the various cancers, and are thus possible drug targets.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Marx, J -- New York, N.Y. -- Science. 2000 Sep 8;289(5485):1670-2.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/11001727" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): Disease Progression ; *Gene Expression Profiling ; Gene Expression Regulation, Neoplastic ; Genes, Tumor Suppressor ; Humans ; Neoplasm Invasiveness ; Neoplasm Metastasis/genetics ; Neoplasms/*classification/diagnosis/*genetics/therapy ; *Oligonucleotide Array Sequence Analysis ; Oncogenes ; Prognosis
    Print ISSN: 0036-8075
    Digitale ISSN: 1095-9203
    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
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  • 25
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 2000-07-15
    Beschreibung: Mutation at the mouse progressive ankylosis (ank) locus causes a generalized, progressive form of arthritis accompanied by mineral deposition, formation of bony outgrowths, and joint destruction. Here, we show that the ank locus encodes a multipass transmembrane protein (ANK) that is expressed in joints and other tissues and controls pyrophosphate levels in cultured cells. A highly conserved gene is present in humans and other vertebrates. These results identify ANK-mediated control of pyrophosphate levels as a possible mechanism regulating tissue calcification and susceptibility to arthritis in higher animals.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Ho, A M -- Johnson, M D -- Kingsley, D M -- 5T32GM07365/GM/NIGMS NIH HHS/ -- New York, N.Y. -- Science. 2000 Jul 14;289(5477):265-70.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Developmental Biology and Howard Hughes Medical Institute, Beckman Center B300, Stanford University School of Medicine, Stanford, CA 94305-5327, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10894769" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): Animals ; Arthritis/*genetics/metabolism/pathology ; Base Sequence ; Biological Transport ; COS Cells ; Calcinosis/*genetics ; Chromosome Mapping ; Cloning, Molecular ; Dna ; Diphosphates/*metabolism ; Durapatite/metabolism ; Gene Expression ; Genetic Complementation Test ; Humans ; Membrane Proteins/*genetics/metabolism/*physiology ; Mice ; Mice, Transgenic ; Molecular Sequence Data ; Mutation ; Phenotype ; Phosphate Transport Proteins ; Physical Chromosome Mapping ; Sequence Homology, Nucleic Acid ; Tissue Distribution
    Print ISSN: 0036-8075
    Digitale ISSN: 1095-9203
    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
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  • 26
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 2000-09-02
    Beschreibung: Although for the last 50 years, ethicists dealing with human experimentation have focused primarily on the need to protect individual research subjects and vulnerable groups, biomedical research, especially in genetics, now requires the establishment of standards for the protection of communities. We have developed such a strategy, based on five steps. (i) Identification of community characteristics relevant to the biomedical research setting, (ii) delineation of a typology of different types of communities using these characteristics, (iii) determination of the range of possible community protections, (iv) creation of connections between particular protections and one or more community characteristics necessary for its implementation, and (v) synthesis of community characteristics and possible protections to define protections appropriate for each type of community. Depending on the particular community, consent and consultation, consultation alone, or no added protections may be required for research.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Weijer, C -- Emanuel, E J -- New York, N.Y. -- Science. 2000 Aug 18;289(5482):1142-4.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Bioethics, Dalhousie University, Halifax, Nova Scotia, B3H 4H7, Canada. charles.weijer@dal.ca〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10970227" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): *Bioethics ; *Culture ; Guidelines as Topic ; *Human Experimentation ; Humans ; Informed Consent ; Research/*standards ; *Residence Characteristics ; Truth Disclosure ; Vulnerable Populations
    Print ISSN: 0036-8075
    Digitale ISSN: 1095-9203
    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
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  • 27
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 2000-06-17
    Beschreibung: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Enserink, M -- New York, N.Y. -- Science. 2000 Jun 2;288(5471):1562-3.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10858127" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): Budgets ; Developing Countries ; Drug Industry/economics ; Financing, Government ; Humans ; Immunization Programs ; National Institutes of Health (U.S.)/economics ; *Research Support as Topic ; United States ; *Vaccines
    Print ISSN: 0036-8075
    Digitale ISSN: 1095-9203
    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
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  • 28
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 2000-09-30
    Beschreibung: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Sinclair, A R -- Ludwig, D -- Clark, C W -- New York, N.Y. -- Science. 2000 Sep 15;289(5486):1875.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/11012354" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): Animals ; *Conservation of Natural Resources/methods ; *Ecosystem ; Humans ; Residence Characteristics
    Print ISSN: 0036-8075
    Digitale ISSN: 1095-9203
    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
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  • 29
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 2000-02-26
    Beschreibung: Stem cells are the natural units of embryonic generation, and also adult regeneration, of a variety of tissues. Recently, the list of tissues that use the model of differentiation from stem to progenitor to mature cell has increased from blood to include a variety of tissues, including both central and peripheral nervous systems and skeletal muscle; it is also possible that all organs and tissues are derived from, and still contain, stem cells. Because the number and activities of stem cells and their progeny are homeostatically regulated, clinical stem cell transplantation could greatly add to the physician's armamentarium against degenerative diseases.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Weissman, I L -- New York, N.Y. -- Science. 2000 Feb 25;287(5457):1442-6.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Departments of Pathology and Developmental Biology, Stanford University School of Medicine, Stanford, CA 94302-5323, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10688785" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): Animals ; Autoimmune Diseases/therapy ; Bone Marrow Transplantation ; Cell Differentiation ; Cell Division ; *Hematopoietic Stem Cell Transplantation ; Hematopoietic Stem Cells/cytology/*physiology ; Humans ; Immune Tolerance ; Neoplasms/therapy ; Nervous System Diseases/therapy ; Regeneration ; *Stem Cell Transplantation ; Stem Cells/cytology/*physiology ; Transplantation, Homologous
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  • 30
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 2000-03-24
    Beschreibung: The 120-megabase euchromatic portion of the Drosophila melanogaster genome has been sequenced. Because the genome is compact and many genetic tools are available, and because fly cell biology and development have much in common with mammals, this sequence may be the Rosetta stone for deciphering the human genome.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Kornberg, T B -- Krasnow, M A -- New York, N.Y. -- Science. 2000 Mar 24;287(5461):2218-20.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Biochemistry and Biophysics, University of California at San Francisco, San Francisco, CA 94143, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10731136" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): Animals ; *Biology ; Cloning, Molecular ; DNA Transposable Elements ; Drosophila melanogaster/*genetics/physiology ; Genes, Insect ; *Genetics, Medical ; *Genome ; *Genome, Human ; Humans ; Mutation ; Physical Chromosome Mapping ; *Sequence Analysis, DNA
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  • 31
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 2000-10-29
    Beschreibung: The central nervous system functions primarily to convert patterns of activity in sensory receptors into patterns of muscle activity that constitute appropriate behavior. At the anatomical level this requires two complementary processes: a set of genetically encoded rules for building the basic network of connections, and a mechanism for subsequently fine tuning these connections on the basis of experience. Identifying the locus and mechanism of these structural changes has long been among neurobiology's major objectives. Evidence has accumulated implicating a particular class of contacts, excitatory synapses made onto dendritic spines, as the sites where connective plasticity occurs. New developments in light microscopy allow changes in spine morphology to be directly visualized in living neurons and suggest that a common mechanism, based on dynamic actin filaments, is involved in both the formation of dendritic spines during development and their structural plasticity at mature synapses.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Matus, A -- New York, N.Y. -- Science. 2000 Oct 27;290(5492):754-8.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Friedrich Miescher Institute, Maulbeerstrasse 66, 4058 Basel, Switzerland. matus@fmi.ch〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/11052932" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): Actin Cytoskeleton/*physiology ; Actins/*physiology ; Animals ; Brain/embryology/growth & development/physiology ; Calcium/metabolism ; Dendrites/*physiology/ultrastructure ; Humans ; Learning ; Long-Term Potentiation ; Neural Pathways ; *Neuronal Plasticity ; Receptors, Glutamate/metabolism ; Synapses/*physiology
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  • 32
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 2000-02-26
    Beschreibung: Most, if not all, epithelial tissues contain stem cells. They are responsible for normal tissue renewal or for regeneration following damage. Our present knowledge of their properties is limited and is mainly derived from studies of cell kinetics and from clonal analysis.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Slack, J M -- New York, N.Y. -- Science. 2000 Feb 25;287(5457):1431-3.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Developmental Biology Programme, Department of Biology and Biochemistry, University of Bath, Bath BA2 7AY, UK. j.m.w.slack@bath.ac.uk.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10688782" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): Animals ; *Cell Differentiation ; *Cell Division ; Clone Cells/cytology/physiology ; Embryo, Mammalian/cytology ; Epithelial Cells/*cytology/pathology/physiology ; Humans ; Metaplasia ; Regeneration ; Stem Cells/*cytology/physiology
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  • 33
    Publikationsdatum: 2000-03-17
    Beschreibung: Allergic asthma is caused by the aberrant expansion in the lung of T helper cells that produce type 2 (TH2) cytokines and is characterized by infiltration of eosinophils and bronchial hyperreactivity. This disease is often triggered by mast cells activated by immunoglobulin E (IgE)-mediated allergic challenge. Activated mast cells release various chemical mediators, including prostaglandin D2 (PGD2), whose role in allergic asthma has now been investigated by the generation of mice deficient in the PGD receptor (DP). Sensitization and aerosol challenge of the homozygous mutant (DP-/-) mice with ovalbumin (OVA) induced increases in the serum concentration of IgE similar to those in wild-type mice subjected to this model of asthma. However, the concentrations of TH2 cytokines and the extent of lymphocyte accumulation in the lung of OVA-challenged DP-/- mice were greatly reduced compared with those in wild-type animals. Moreover, DP-/- mice showed only marginal infiltration of eosinophils and failed to develop airway hyperreactivity. Thus, PGD2 functions as a mast cell-derived mediator to trigger asthmatic responses.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Matsuoka, T -- Hirata, M -- Tanaka, H -- Takahashi, Y -- Murata, T -- Kabashima, K -- Sugimoto, Y -- Kobayashi, T -- Ushikubi, F -- Aze, Y -- Eguchi, N -- Urade, Y -- Yoshida, N -- Kimura, K -- Mizoguchi, A -- Honda, Y -- Nagai, H -- Narumiya, S -- New York, N.Y. -- Science. 2000 Mar 17;287(5460):2013-7.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Pharmacology, Kyoto University Faculty of Medicine, Kyoto 606-8501, Japan.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10720327" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): Allergens/immunology ; Animals ; Asthma/immunology/metabolism/pathology/*physiopathology ; Bronchial Hyperreactivity ; Bronchoalveolar Lavage Fluid/cytology/immunology ; Crosses, Genetic ; Female ; Gene Targeting ; Humans ; Immunoglobulin E/blood ; Interferon-gamma/metabolism ; Interleukins/metabolism ; Lung/immunology/metabolism/pathology ; Lymphocytes/immunology ; Male ; Mast Cells/metabolism ; Mice ; Mice, Inbred C57BL ; Mucus/secretion ; Ovalbumin/immunology ; Prostaglandin D2/metabolism/*physiology ; *Receptors, Immunologic ; Receptors, Prostaglandin/genetics/metabolism/*physiology ; Respiratory Mucosa/secretion
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  • 34
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 2000-08-05
    Beschreibung: Reproductive cells that are destined to become sperm or egg undergo meiotic division during which the chromosome number is halved. As Sluder and McCollum explain in their Perspective, new findings (Shonn et al.) in yeast show that there is a spindle checkpoint that operates during meiosis to ensure that an equal number of replicated chromosomes arrives at each pole of the cell. One of the components of this meiotic spindle checkpoint turns out to be Mad2, which gives the signal to halt meiosis if it looks like unequal chromosome segregation is taking place.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Sluder, G -- McCollum, D -- New York, N.Y. -- Science. 2000 Jul 14;289(5477):254-5.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Cell Biology, University of Massachusetts Medical School, Worcester, MA 01655, USA. greenfield.sluder@umassmed.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10917849" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): Calcium-Binding Proteins/physiology ; *Carrier Proteins ; Cell Cycle Proteins ; Chromosome Aberrations ; Chromosome Disorders ; Chromosome Segregation ; Fungal Proteins/physiology ; Humans ; Meiosis/*physiology ; Nuclear Proteins ; Saccharomycetales/genetics/physiology ; Signal Transduction
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  • 35
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 2000-03-25
    Beschreibung: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Enserink, M -- New York, N.Y. -- Science. 2000 Mar 3;287(5458):1571.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10733414" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): *Anti-Infective Agents ; *Developing Countries ; *Drug Industry/economics ; European Union ; Financing, Government ; *Global Health ; Humans ; Immunization Programs ; Japan ; Technology, Pharmaceutical ; United States ; *Vaccines
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    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
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  • 36
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 2000-02-26
    Beschreibung: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Enserink, M -- New York, N.Y. -- Science. 2000 Feb 11;287(5455):951.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10691565" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): *Biotechnology ; *Databases, Factual ; *Databases, Nucleic Acid ; *Genetic Research ; *Genetics, Medical ; Humans ; Iceland ; Medical Records Systems, Computerized
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  • 37
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 2000-07-06
    Beschreibung: A human cytomegalovirus gene array was used to identify a previously unidentified class of viral transcripts. These transcripts, termed virion RNAs, were packaged within infectious virions and were delivered to the host cell on infection. This mechanism of herpesvirus gene expression allows for viral genes to be expressed within an infected cell immediately after virus entry and in the absence of transcription from the viral genome.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Bresnahan, W A -- Shenk, T -- CA85786/CA/NCI NIH HHS/ -- F32 AI010448/AI/NIAID NIH HHS/ -- New York, N.Y. -- Science. 2000 Jun 30;288(5475):2373-6.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Molecular Biology, Princeton University, Princeton, NJ 08544, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10875924" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): Cell Nucleus/metabolism ; Cells, Cultured ; Cytomegalovirus/*genetics/*physiology ; Dactinomycin/pharmacology ; Gene Expression ; Genes, Viral ; Genome, Viral ; Golgi Apparatus/metabolism ; Humans ; Nucleic Acid Hybridization ; Nucleic Acid Synthesis Inhibitors/pharmacology ; Oligonucleotide Array Sequence Analysis ; RNA, Messenger/*genetics/isolation & purification/metabolism ; RNA, Viral/*genetics/isolation & purification/metabolism ; Recombinant Fusion Proteins/metabolism ; Transcription, Genetic ; Viral Proteins/genetics/metabolism ; Virion/*genetics/physiology ; Virus Assembly
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  • 38
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 2000-06-08
    Beschreibung: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Persaud, R -- New York, N.Y. -- Science. 2000 May 12;288(5468):975.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10841715" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): Canada/epidemiology ; Depression/*epidemiology/etiology ; Depressive Disorder/*epidemiology/etiology ; Female ; Humans ; Male
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    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
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  • 39
    Publikationsdatum: 2000-09-01
    Beschreibung: Activation of the transcription factor nuclear factor (NF)-kappaB by proinflammatory stimuli leads to increased expression of genes involved in inflammation. Activation of NF-kappaB requires the activity of an inhibitor of kappaB (IkappaB)-kinase (IKK) complex containing two kinases (IKKalpha and IKKbeta) and the regulatory protein NEMO (NF-kappaB essential modifier). An amino-terminal alpha-helical region of NEMO associated with a carboxyl-terminal segment of IKKalpha and IKKbeta that we term the NEMO-binding domain (NBD). A cell-permeable NBD peptide blocked association of NEMO with the IKK complex and inhibited cytokine-induced NF-kappaB activation and NF-kappaB-dependent gene expression. The peptide also ameliorated inflammatory responses in two experimental mouse models of acute inflammation. The NBD provides a target for the development of drugs that would block proinflammatory activation of the IKK complex without inhibiting basal NF-kappaB activity.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉May, M J -- D'Acquisto, F -- Madge, L A -- Glockner, J -- Pober, J S -- Ghosh, S -- AI 33443/AI/NIAID NIH HHS/ -- New York, N.Y. -- Science. 2000 Sep 1;289(5484):1550-4.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Section of Immunobiology and Department of Molecular Biophysics and Biochemistry, Howard Hughes Medical Institute, Yale University School of Medicine, New Haven, CT 06510, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10968790" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): Amino Acid Sequence ; Animals ; Anti-Inflammatory Agents, Non-Steroidal/chemistry/pharmacology ; COS Cells ; Cells, Cultured ; E-Selectin/biosynthesis/genetics ; Endothelium, Vascular/metabolism ; Gene Expression Regulation ; HeLa Cells ; Humans ; I-kappa B Kinase ; Inflammation/drug therapy ; Mice ; Mice, Inbred C57BL ; Molecular Sequence Data ; Mutation ; NF-kappa B/*metabolism ; Peptides/chemistry/*pharmacology ; Point Mutation ; Protein Structure, Tertiary ; Protein-Serine-Threonine Kinases/chemistry/genetics/*metabolism ; Recombinant Fusion Proteins/metabolism
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  • 40
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 2000-01-22
    Beschreibung: VDJ recombination is developmentally regulated in vivo by enhancer-dependent changes in the accessibility of chromosomal recombination signal sequences to the recombinase, but the molecular nature of these changes is unknown. Here histone H3 acetylation was measured along versions of a transgenic VDJ recombination reporter and the endogenous T cell receptor alpha/delta locus. Enhancer activity was shown to impart long-range, developmentally regulated changes in H3 acetylation, and H3 acetylation status was tightly linked to VDJ recombination. H3 hyperacetylation is proposed as a molecular mechanism coupling enhancer activity to accessibility for VDJ recombination.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉McMurry, M T -- Krangel, M S -- GM 41052/GM/NIGMS NIH HHS/ -- New York, N.Y. -- Science. 2000 Jan 21;287(5452):495-8.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Immunology, Post Office Box 3010, Duke University Medical Center, Durham NC 27710, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10642553" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): Acetylation ; Animals ; Chromatin/metabolism ; DNA Nucleotidyltransferases/metabolism ; DNA-Binding Proteins/metabolism ; Enhancer Elements, Genetic ; *Gene Rearrangement, T-Lymphocyte ; *Genes, T-Cell Receptor alpha ; Genes, T-Cell Receptor beta ; *Genes, T-Cell Receptor delta ; Histones/*metabolism ; Homeodomain Proteins/metabolism ; Humans ; Mice ; Mice, Transgenic ; Nuclear Proteins ; Protein Sorting Signals ; *Recombination, Genetic ; T-Lymphocytes/*metabolism ; Transgenes ; VDJ Recombinases
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  • 41
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 2000-07-06
    Beschreibung: In this month's essay, Anne McLaren traces the winding and pitted pathways that connect the early days of the cell theory of biology in the 1830s to the new and unfolding era of cloning science and technology that came to worldwide attention in 1997 with the announcement of the birth of Dolly, the Scottish cloned sheep. The possibilities, including the potential for new medical treatments and perhaps even human cloning, are fantastic ... and ethically charged.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉McLaren, A -- New York, N.Y. -- Science. 2000 Jun 9;288(5472):1775-80.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Wellcome/CRC Institute, Cambridge, UK.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10877698" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): Animals ; Animals, Domestic/embryology/genetics ; Bioethics ; Cell Differentiation ; Cell Line ; Cell Nucleus/physiology ; *Cloning, Organism/history/trends ; Cytoplasm/physiology ; Embryo, Mammalian/cytology ; Embryo, Nonmammalian/cytology ; History, 19th Century ; History, 20th Century ; Humans ; Nuclear Transfer Techniques ; Stem Cells/cytology/physiology ; Therapeutics
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    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
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  • 42
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 2000-09-23
    Beschreibung: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Starck, W -- New York, N.Y. -- Science. 2000 Sep 8;289(5485):1691.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/11001734" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): Animals ; Australia ; *Cnidaria ; Conservation of Natural Resources ; *Disasters ; *Ecosystem ; Humans
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    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
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  • 43
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 2000-06-10
    Beschreibung: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Phillips, M -- New York, N.Y. -- Science. 2000 May 26;288(5470):1345; author reply 1346-7.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10847844" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): *Bioethics ; Humans ; *Life Expectancy ; *Longevity
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    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
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  • 44
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 2000-03-11
    Beschreibung: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Winn, O H -- New York, N.Y. -- Science. 2000 Feb 18;287(5456):1204.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10712152" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): Humans ; *Science
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    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
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  • 45
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 2000-08-12
    Beschreibung: On page 628, neuroscientists report that painful stimuli delivered to rats shortly after birth permanently rewire the spinal cord circuits that respond to pain. Not only do the circuits contain more axons, but the axons extend to more areas of the spinal cord than they normally would. The results should help convince skeptics of the importance of managing pain in human infants.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Helmuth, L -- New York, N.Y. -- Science. 2000 Jul 28;289(5479):521-2.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10939955" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): Afferent Pathways ; Aging ; Animals ; Animals, Newborn ; Axons/*physiology ; Hindlimb/innervation ; Humans ; Infant, Newborn ; Inflammation/physiopathology ; *Pain ; Pain Threshold ; Rats ; Sciatic Nerve/*anatomy & histology/physiology ; Spinal Cord/*cytology
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    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
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  • 46
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 2000-08-12
    Beschreibung: Experts in the young field of violence epidemiology blame guns and crack cocaine for America's deadly crime surge in the early 1990s. Explaining the subsequent decline in violent crime rates has been more difficult, however. Some of the factors that seem to have helped squelch crime could be temporary, such as low unemployment rates. But others, including a growing intolerance for violence as a means of settling interpersonal disputes, seem to have become cultural norms.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Helmuth, L -- New York, N.Y. -- Science. 2000 Jul 28;289(5479):582-5.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10939973" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): Abortion, Legal ; Crack Cocaine ; Domestic Violence/statistics & numerical data ; Female ; Firearms ; Homicide/*statistics & numerical data ; Humans ; Male ; Police ; Prisons ; Street Drugs ; United States ; Violence/*statistics & numerical data
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    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
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  • 47
    Publikationsdatum: 2000-03-04
    Beschreibung: To determine the ability of antibodies to provide protection from Ebola viruses, monoclonal antibodies (mAbs) to the Ebola glycoprotein were generated and evaluated for efficacy. We identified several protective mAbs directed toward five unique epitopes on Ebola glycoprotein. One of the epitopes is conserved among all Ebola viruses that are known to be pathogenic for humans. Some protective mAbs were also effective therapeutically when administered to mice 2 days after exposure to lethal Ebola virus. The identification of protective mAbs has important implications for developing vaccines and therapies for Ebola virus.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Wilson, J A -- Hevey, M -- Bakken, R -- Guest, S -- Bray, M -- Schmaljohn, A L -- Hart, M K -- New York, N.Y. -- Science. 2000 Mar 3;287(5458):1664-6.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Virology Division, U.S. Army Medical Research Institute of Infectious Diseases, 1425 Porter Street, Fort Detrick, Frederick, MD 21702-5011, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10698744" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): Animals ; Antibodies, Monoclonal/*immunology ; Antibodies, Viral/*immunology ; Antibody Affinity ; Antigens, Viral/immunology ; Binding, Competitive ; Complement System Proteins/immunology ; Ebolavirus/*immunology/physiology ; Epitopes/immunology ; Female ; Hemorrhagic Fever, Ebola/*prevention & control/therapy ; Humans ; Immunoglobulin G/immunology ; Mice ; Mice, Inbred BALB C ; Mice, Inbred C57BL ; Neutralization Tests ; Specific Pathogen-Free Organisms ; Viral Envelope Proteins/*immunology ; Viral Plaque Assay
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    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
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  • 48
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 2000-09-09
    Beschreibung: Researchers are uncovering disturbing evidence that scientists and tourists are infecting wild primates with human pathogens. In response, ape specialists, including the American Society of Primatologists, are now calling for stricter health standards for researchers and tourists. They are also urging researchers to learn how to diagnose disease in their study animals.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Ferber, D -- New York, N.Y. -- Science. 2000 Aug 25;289(5483):1277-8.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10979848" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): Africa/epidemiology ; Animals ; Ape Diseases/epidemiology/*transmission ; Communicable Diseases/epidemiology/transmission/*veterinary ; *Gorilla gorilla ; Humans ; Parasitic Diseases, Animal/epidemiology/*transmission ; Primate Diseases/epidemiology/*transmission ; Primates ; Research Personnel ; Travel
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    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
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  • 49
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 2000-08-12
    Beschreibung: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Sodha, N -- Williams, R -- Mangion, J -- Bullock, S L -- Yuille, M R -- Eeles, R A -- New York, N.Y. -- Science. 2000 Jul 21;289(5478):359.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Royal Marsden NHS Trust, Sutton, Surrey SM2 5PT, UK.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10939935" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): Checkpoint Kinase 2 ; Chromosomes, Human, Pair 15/genetics ; DNA Mutational Analysis ; Exons ; Gene Duplication ; Genetic Variation ; Humans ; Li-Fraumeni Syndrome/*genetics ; Mutation ; Polymerase Chain Reaction ; Polymorphism, Genetic ; Protein Kinases/*genetics ; *Protein-Serine-Threonine Kinases ; Sequence Homology, Nucleic Acid
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    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
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  • 50
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 2000-01-15
    Beschreibung: The memory consolidation hypothesis proposed 100 years ago by Muller and Pilzecker continues to guide memory research. The hypothesis that new memories consolidate slowly over time has stimulated studies revealing the hormonal and neural influences regulating memory consolidation, as well as molecular and cellular mechanisms. This review examines the progress made over the century in understanding the time-dependent processes that create our lasting memories.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉McGaugh, J L -- MH12526/MH/NIMH NIH HHS/ -- New York, N.Y. -- Science. 2000 Jan 14;287(5451):248-51.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉the Center for the Neurobiology of Learning and Memory and the Department of Neurobiology and Behavior, University of California Irvine, Irvine, CA 92697, USA. jlmcgaug@uci.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10634773" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): Amnesia, Retrograde/physiopathology ; Amygdala/*physiology ; Animals ; Brain/*physiology ; Emotions ; Hippocampus/physiology ; Humans ; Long-Term Potentiation ; Memory/*physiology ; Memory, Short-Term/physiology ; Protein Kinases/metabolism ; Receptors, Adrenergic, beta/physiology
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    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
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  • 51
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 2000-04-01
    Beschreibung: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Marshall, E -- New York, N.Y. -- Science. 2000 Mar 24;287(5461):2127.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10744525" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): Biotechnology/*economics ; Computational Biology ; Databases, Factual ; Genetics, Medical/economics ; *Genome, Human ; Great Britain ; Humans ; International Cooperation ; *Investments ; Molecular Biology/*economics ; Patents as Topic ; Public Policy ; *Sequence Analysis, DNA ; United States
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    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
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  • 52
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 2000-09-09
    Beschreibung: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Pennisi, E -- New York, N.Y. -- Science. 2000 Aug 25;289(5483):1267-9.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10979842" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): Animals ; Financing, Government ; *Genome ; Human Genome Project ; Humans ; Mice/genetics ; National Institutes of Health (U.S.)/economics ; Rats/*genetics ; Research Support as Topic ; *Sequence Analysis, DNA ; United States
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    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
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  • 53
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 2000-07-15
    Beschreibung: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Campbell, P N -- New York, N.Y. -- Science. 2000 Jun 23;288(5474):2131.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10896581" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): Armenia ; *Delivery of Health Care ; Humans ; Moldova
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    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
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  • 54
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 2000-06-08
    Beschreibung: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Campbell, S -- New York, N.Y. -- Science. 2000 May 19;288(5469):1174-5.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10841737" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): Animals ; Biological Clocks/*physiology ; Body Temperature ; Circadian Rhythm/*physiology ; Darkness ; Humans
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    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
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  • 55
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 2000-03-18
    Beschreibung: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Marshall, E -- New York, N.Y. -- Science. 2000 Feb 25;287(5457):1375, 1377.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10722375" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): Anti-HIV Agents ; Biotechnology/economics/*legislation & jurisprudence ; Drug Design ; *Genes ; Humans ; *Patents as Topic ; Receptors, CCR5/*genetics/physiology ; United States
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    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
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  • 56
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 2000-08-12
    Beschreibung: Some 110 scientists from a range of disciplines gathered in the overcast British midlands for the 5th International Ancient DNA Conference, held here from 12 to 14 July. Among the attractions were new insights into the diets of early Americans gleaned from ancient human coprolites and intriguing reports of nuclear DNA and ancient viral sequences extracted from mammoth bones.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Stokstad, E -- New York, N.Y. -- Science. 2000 Jul 28;289(5479):530-1.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10939960" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): Animals ; Bone and Bones/virology ; DNA/*analysis/history ; DNA, Viral/analysis/*history ; Diet/*history ; Elephants/*genetics/virology ; Feces/*chemistry ; Female ; Fossils ; History, Ancient ; Humans ; Male ; Texas
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    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
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  • 57
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 2000-09-29
    Beschreibung: A fundamental question in aging research is whether humans and other species possess an immutable life-span limit. We examined the maximum age at death in Sweden, which rose from about 101 years during the 1860s to about 108 years during the 1990s. The pace of increase was 0.44 years per decade before 1969 but accelerated to 1. 11 years per decade after that date. More than 70 percent of the rise in the maximum age at death from 1861 to 1999 is attributable to reductions in death rates above age 70. The rest are due to increased numbers of survivors to old age (both larger birth cohorts and increased survivorship from infancy to age 70). The more rapid rise in the maximum age since 1969 is due to the faster pace of old-age mortality decline during recent decades.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Wilmoth, J R -- Deegan, L J -- Lundstrom, H -- Horiuchi, S -- K02-AG00778/AG/NIA NIH HHS/ -- R01-AG11552/AG/NIA NIH HHS/ -- R01-AG14698/AG/NIA NIH HHS/ -- New York, N.Y. -- Science. 2000 Sep 29;289(5488):2366-8.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Demography, University of California, Berkeley, CA 94720-2120, USA. jrw@demog.berkeley.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/11009426" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): Aged ; Aged, 80 and over ; Cohort Studies ; Female ; Humans ; Life Expectancy/trends ; Life Tables ; *Longevity ; Male ; Mortality/trends ; Probability ; Sweden
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    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
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  • 58
    Publikationsdatum: 2000-05-29
    Beschreibung: Pathogenic mycobacteria, including the agent of tuberculosis, Mycobacterium tuberculosis, must replicate in macrophages for long-term persistence within their niche during chronic infection: organized collections of macrophages and lymphocytes called granulomas. We identified several genes preferentially expressed when Mycobacterium marinum, the cause of fish and amphibian tuberculosis, resides in host granulomas and/or macrophages. Two were homologs of M. tuberculosis PE/PE-PGRS genes, a family encoding numerous repetitive glycine-rich proteins of unknown function. Mutation of two PE-PGRS genes produced M. marinum strains incapable of replication in macrophages and with decreased persistence in granulomas. Our results establish a direct role in virulence for some PE-PGRS proteins.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Ramakrishnan, L -- Federspiel, N A -- Falkow, S -- AI 32396/AI/NIAID NIH HHS/ -- K08 AI 01400/AI/NIAID NIH HHS/ -- New York, N.Y. -- Science. 2000 May 26;288(5470):1436-9.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Microbiology and Immunology, Stanford University School of Medicine, Stanford, CA 94305, USA. lalitar@cmgm.stanford.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10827956" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): Animals ; Bacterial Proteins/chemistry/*genetics ; Cells, Cultured ; Disease Models, Animal ; Gene Expression Profiling ; Gene Expression Regulation, Bacterial ; Genes, Bacterial ; Glycine/analysis ; Granuloma/*microbiology/pathology ; Humans ; Macrophages/*microbiology ; Mutation ; Mycobacterium Infections, Nontuberculous/*microbiology/pathology ; Mycobacterium marinum/*genetics/growth & development/*pathogenicity ; Mycobacterium tuberculosis/genetics/pathogenicity ; Promoter Regions, Genetic ; Rana pipiens ; Tuberculosis/microbiology ; Virulence
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    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
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  • 59
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 2000-04-01
    Beschreibung: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Stokstad, E -- New York, N.Y. -- Science. 2000 Mar 24;287(5461):2131-2.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10744527" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): Animals ; *Biological Evolution ; Bone and Bones/anatomy & histology ; Forearm/anatomy & histology ; Gorilla gorilla/anatomy & histology/physiology ; Hominidae/*anatomy & histology/physiology ; Humans ; Pan troglodytes/anatomy & histology/physiology ; *Walking ; Wrist Joint/*anatomy & histology
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    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
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  • 60
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 2000-04-15
    Beschreibung: Humans, but no other animal, make meaningful use of spoken language. What is unclear, however, is whether this capacity depends on a unique constellation of perceptual and neurobiological mechanisms or whether a subset of such mechanisms is shared with other organisms. To explore this problem, parallel experiments were conducted on human newborns and cotton-top tamarin monkeys to assess their ability to discriminate unfamiliar languages. A habituation-dishabituation procedure was used to show that human newborns and tamarins can discriminate sentences from Dutch and Japanese but not if the sentences are played backward. Moreover, the cues for discrimination are not present in backward speech. This suggests that the human newborns' tuning to certain properties of speech relies on general processes of the primate auditory system.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Ramus, F -- Hauser, M D -- Miller, C -- Morris, D -- Mehler, J -- P51RR00168-37/RR/NCRR NIH HHS/ -- New York, N.Y. -- Science. 2000 Apr 14;288(5464):349-51.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Laboratoire de Sciences Cognitives et Psycholinguistique, l'Ecole des Hautes Etudes en Sciences Sociales/Centre National de la Recherche Scientifique, 54 Boulevard Raspail, 75006 Paris, France. f.ramus@ucl.ac.uk〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10764650" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): Animals ; Cues ; Habituation, Psychophysiologic ; Humans ; Infant, Newborn ; *Language Development ; Saguinus ; *Speech Perception
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    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
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  • 61
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 2000-08-12
    Beschreibung: In the United States, about 150 police officers die every year in the line of duty, and government figures suggest that some 350 suspected criminals are justifiably killed in confrontations with police. Seeking lessons behind these gruesome statistics and other disturbing trends in violent behavior nationwide (see main text) are researchers at the Federal Bureau of Investigation.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Stokstad, E -- New York, N.Y. -- Science. 2000 Jul 28;289(5479):584.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10939974" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): *Crime ; Criminology ; Humans ; *Personality ; *Police/education ; United States
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    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
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  • 62
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 2000-02-26
    Beschreibung: Repetition priming has been characterized neurophysiologically as a decreased response following stimulus repetition. The present study used event-related functional magnetic resonance imaging to investigate whether this repetition-related response is sensitive to stimulus familiarity. A right fusiform region exhibited an attenuated response to the repetition of familiar stimuli, both faces and symbols, but exhibited an enhanced response to the repetition of unfamiliar stimuli. Moreover, both repetition effects were modulated by lag between successive presentations. Further experiments replicated the interactions between repetition, familiarity, and lag and demonstrated the persistence of these effects over multiple repetitions. Priming-related responses are therefore not unitary but depend on the presence or absence of preexisting stimulus representations.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Henson, R -- Shallice, T -- Dolan, R -- New York, N.Y. -- Science. 2000 Feb 18;287(5456):1269-72.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Wellcome Department of Cognitive Neurology, Institute of Neurology, Institute of Cognitive Neuroscience and Department of Psychology, University College London, London WC1E 6BT, UK. r.henson@ucl.ac.uk〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10678834" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): Adult ; Brain Mapping ; Face ; Female ; Humans ; Magnetic Resonance Imaging ; Male ; Memory/*physiology ; *Pattern Recognition, Visual ; Regression Analysis ; Temporal Lobe/*physiology ; Time Factors
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  • 63
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 2000-09-19
    Beschreibung: Clinicians may soon be able to mount a multipronged attack against cholesterol, the artery-clogging lipid whose buildup in the body is a major contributor to heart attacks and other cardiovascular diseases. In work reported on page 1524, a team has pinpointed a biological master switch in mice that controls three pathways that work together to both rid the body of excess cholesterol and prevent its absorption from the intestine. The work suggests a new mechanism for reducing cholesterol, for example, with drugs that turn up the activity of the master switch, a protein known as the retinoid X receptor.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Ferber, D -- New York, N.Y. -- Science. 2000 Sep 1;289(5484):1446-7.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10991725" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): ATP Binding Cassette Transporter 1 ; ATP-Binding Cassette Transporters/*metabolism ; Animals ; Bile Acids and Salts ; Biological Transport/drug effects ; Cholesterol/*metabolism ; Cholesterol, Dietary/administration & dosage ; DNA-Binding Proteins/metabolism ; Glycoproteins/*metabolism ; Humans ; Intestinal Absorption/drug effects ; Intestines/drug effects/*metabolism ; Liver/metabolism ; Macrophages/metabolism ; Mice ; Orphan Nuclear Receptors ; *Receptors, Cytoplasmic and Nuclear ; Receptors, Retinoic Acid/*metabolism ; Receptors, Thyroid Hormone/metabolism ; Retinoid X Receptors ; Transcription Factors/*metabolism
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    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
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  • 64
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 2000-03-11
    Beschreibung: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Sieber, S M -- Galson, S K -- New York, N.Y. -- Science. 2000 Feb 18;287(5456):1205-6.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10712154" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): Child ; Humans ; *National Institutes of Health (U.S.) ; Neoplasms/epidemiology/*etiology ; United States ; *United States Environmental Protection Agency
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    Digitale ISSN: 1095-9203
    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
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  • 65
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    Unbekannt
    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 2000-02-26
    Beschreibung: Stem cells are currently in the news for two reasons: the successful cultivation of human embryonic stem cell lines and reports that adult stem cells can differentiate into developmentally unrelated cell types, such as nerve cells into blood cells. Both intrinsic and extrinsic signals regulate stem cell fate and some of these signals have now been identified. Certain aspects of the stem cell microenvironment, or niche, are conserved between tissues, and this can be exploited in the application of stem cells to tissue replacement therapy.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Watt, F M -- Hogan, B L -- New York, N.Y. -- Science. 2000 Feb 25;287(5457):1427-30.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Keratinocyte Laboratory, Imperial Cancer Research Fund, 44 Lincoln's Inn Fields, London WC2A 3PX, UK.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10688781" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): Animals ; Cell Communication ; *Cell Differentiation ; *Cell Division ; Cell Lineage ; Extracellular Matrix/physiology ; Homeostasis ; Humans ; Integrins/physiology ; Proteins/physiology ; *Stem Cells/cytology/physiology ; Transcription Factors/physiology
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    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
    Standort Signatur Erwartet Verfügbarkeit
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  • 66
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    Unbekannt
    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 2000-10-21
    Beschreibung: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Stone, R -- New York, N.Y. -- Science. 2000 Sep 29;289(5488):2253-4.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/11041782" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): DNA, Mitochondrial/genetics ; Europe ; History, Ancient ; Humans ; Ice ; Italy ; Male ; *Mummies ; Paleodontology ; Paleopathology
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    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
    Standort Signatur Erwartet Verfügbarkeit
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  • 67
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 2000-08-12
    Beschreibung: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉LeClerc, J E -- Cebula, T A -- New York, N.Y. -- Science. 2000 Jul 21;289(5478):391-2.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10939947" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): *Adenosine Triphosphatases ; Bacterial Proteins/genetics ; Base Pair Mismatch ; Chronic Disease ; Cystic Fibrosis/complications/*microbiology ; DNA Repair ; *DNA-Binding Proteins ; *Escherichia coli Proteins ; Humans ; Lung/*microbiology ; MutS DNA Mismatch-Binding Protein ; *Mutation ; Phenotype ; Pseudomonas Infections/complications/*microbiology ; Pseudomonas aeruginosa/*genetics ; *Recombination, Genetic ; Selection, Genetic
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    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
    Standort Signatur Erwartet Verfügbarkeit
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  • 68
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    Unbekannt
    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 2000-03-25
    Beschreibung: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Freeman, L G -- New York, N.Y. -- Science. 2000 Mar 3;287(5458):1592.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10733424" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): Animals ; *Continental Population Groups ; *Hominidae ; Humans ; Multivariate Analysis ; Sample Size
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    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
    Standort Signatur Erwartet Verfügbarkeit
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  • 69
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    Unbekannt
    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 2000-09-30
    Beschreibung: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Yan, H -- Kinzler, K W -- Vogelstein, B -- New York, N.Y. -- Science. 2000 Sep 15;289(5486):1890-2.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Howard Hughes Medical Institute and the Johns Hopkins Oncology Center, Baltimore, MD 21231, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/11012364" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): Genetic Techniques ; *Genetic Testing/methods ; *Genetics, Medical/trends ; Humans ; Mutation ; Sociology
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    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
    Standort Signatur Erwartet Verfügbarkeit
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  • 70
    Publikationsdatum: 2000-07-06
    Beschreibung: A conserved domain in the extracellular region of the 60- and 80-kilodalton tumor necrosis factor receptors (TNFRs) was identified that mediates specific ligand-independent assembly of receptor trimers. This pre-ligand-binding assembly domain (PLAD) is physically distinct from the domain that forms the major contacts with ligand, but is necessary and sufficient for the assembly of TNFR complexes that bind TNF-alpha and mediate signaling. Other members of the TNFR superfamily, including TRAIL receptor 1 and CD40, show similar homotypic association. Thus, TNFRs and related receptors appear to function as preformed complexes rather than as individual receptor subunits that oligomerize after ligand binding.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Chan, F K -- Chun, H J -- Zheng, L -- Siegel, R M -- Bui, K L -- Lenardo, M J -- New York, N.Y. -- Science. 2000 Jun 30;288(5475):2351-4.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Laboratory of Immunology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD 20892, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10875917" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): Amino Acid Substitution ; Antigens, CD/chemistry/metabolism ; Apoptosis ; Binding Sites ; Cross-Linking Reagents ; Dimerization ; Energy Transfer ; Fluorescence ; Humans ; Ligands ; Macromolecular Substances ; Mutation ; Protein Conformation ; Protein Structure, Tertiary ; Receptors, Tumor Necrosis Factor/*chemistry/*metabolism ; Receptors, Tumor Necrosis Factor, Type I ; Receptors, Tumor Necrosis Factor, Type II ; Recombinant Fusion Proteins/chemistry/metabolism ; *Signal Transduction ; Succinimides ; Tumor Cells, Cultured ; Tumor Necrosis Factor-alpha/*metabolism
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    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
    Standort Signatur Erwartet Verfügbarkeit
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  • 71
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    Unbekannt
    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 2000-04-01
    Beschreibung: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Friedmann, T -- New York, N.Y. -- Science. 2000 Mar 24;287(5461):2163-5.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Program in Human Gene Therapy, University of California at San Diego School of Medicine, La Jolla, CA 92093-0634, USA. tfriedmann@ucsd.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10744537" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): Advisory Committees ; Clinical Trials as Topic/*standards ; Conflict of Interest ; Disclosure ; *Ethics, Medical ; Federal Government ; *Genetic Therapy/adverse effects ; *Government Regulation ; Human Experimentation ; Humans ; Informed Consent ; Nontherapeutic Human Experimentation ; Patient Selection ; Public Policy ; Research Subjects ; Risk Assessment ; Therapeutic Human Experimentation ; United States ; United States Food and Drug Administration
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    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
    Standort Signatur Erwartet Verfügbarkeit
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  • 72
    Publikationsdatum: 2000-10-20
    Beschreibung: Ectodysplasin, a member of the tumor necrosis factor family, is encoded by the anhidrotic ectodermal dysplasia (EDA) gene. Mutations in EDA give rise to a clinical syndrome characterized by loss of hair, sweat glands, and teeth. EDA-A1 and EDA-A2 are two isoforms of ectodysplasin that differ only by an insertion of two amino acids. This insertion functions to determine receptor binding specificity, such that EDA-A1 binds only the receptor EDAR, whereas EDA-A2 binds only the related, but distinct, X-linked ectodysplasin-A2 receptor (XEDAR). In situ binding and organ culture studies indicate that EDA-A1 and EDA-A2 are differentially expressed and play a role in epidermal morphogenesis.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Yan, M -- Wang, L C -- Hymowitz, S G -- Schilbach, S -- Lee, J -- Goddard, A -- de Vos, A M -- Gao, W Q -- Dixit, V M -- New York, N.Y. -- Science. 2000 Oct 20;290(5491):523-7.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Molecular Oncology, Genentech, 1 DNA Way, South San Francisco, CA 94080, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/11039935" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): Amino Acid Sequence ; Amino Acid Substitution ; Animals ; Binding Sites ; Cell Line ; DNA-Binding Proteins/metabolism ; Ectodermal Dysplasia/genetics ; Ectodysplasins ; Epidermis/embryology/*metabolism ; Humans ; *I-kappa B Proteins ; In Situ Hybridization ; Ligands ; Membrane Proteins/*chemistry/*metabolism ; Mice ; Models, Molecular ; Molecular Sequence Data ; Morphogenesis ; NF-kappa B/metabolism ; Phosphorylation ; Point Mutation ; Protein Conformation ; Proteins/metabolism ; Receptors, Cell Surface/chemistry/genetics/*metabolism ; Recombinant Fusion Proteins/metabolism ; Signal Transduction ; TNF Receptor-Associated Factor 6 ; Transfection
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    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
    Standort Signatur Erwartet Verfügbarkeit
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  • 73
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 2000-09-01
    Beschreibung: Osteoporosis, a disease endemic in Western society, typically reflects an imbalance in skeletal turnover so that bone resorption exceeds bone formation. Bone resorption is the unique function of the osteoclast, and anti-osteoporosis therapy to date has targeted this cell. The osteoclast is a specialized macrophage polykaryon whose differentiation is principally regulated by macrophage colony-stimulating factor, RANK ligand, and osteoprotegerin. Reflecting integrin-mediated signals, the osteoclast develops a specialized cytoskeleton that permits it to establish an isolated microenvironment between itself and bone, wherein matrix degradation occurs by a process involving proton transport. Osteopetrotic mutants have provided a wealth of information about the genes that regulate the differentiation of osteoclasts and their capacity to resorb bone.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Teitelbaum, S L -- New York, N.Y. -- Science. 2000 Sep 1;289(5484):1504-8.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Pathology, Washington University School of Medicine, Barnes-Jewish Hospital North, Mailstop 90-31-649, 216 South Kingshighway, St. Louis, MO 63110, USA. teitelbs@medicine wustl.edu.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10968780" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): Animals ; *Bone Resorption ; Carrier Proteins/metabolism ; Cell Differentiation ; Cell Membrane/physiology/ultrastructure ; Glycoproteins/metabolism ; Humans ; Integrins/physiology ; Macrophage Colony-Stimulating Factor/metabolism ; Macrophages/cytology/physiology ; Membrane Glycoproteins/metabolism ; Osteoclasts/cytology/*physiology/ultrastructure ; Osteopetrosis/genetics/metabolism ; Osteoprotegerin ; RANK Ligand ; Receptor Activator of Nuclear Factor-kappa B ; *Receptors, Cytoplasmic and Nuclear ; Receptors, Tumor Necrosis Factor/metabolism ; Stromal Cells/metabolism
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    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
    Standort Signatur Erwartet Verfügbarkeit
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  • 74
    Publikationsdatum: 2000-01-22
    Beschreibung: Stunned myocardium is a syndrome of reversible contractile failure that frequently complicates coronary artery disease. Cardiac excitation is uncoupled from contraction at the level of the myofilaments. Selective proteolysis of the thin filament protein troponin I has been correlated with stunned myocardium. Here, transgenic mice expressing the major degradation product of troponin I (TnI1-193) in the heart were found to develop ventricular dilatation, diminished contractility, and reduced myofilament calcium responsiveness, recapitulating the phenotype of stunned myocardium. Proteolysis of troponin I also occurs in ischemic human cardiac muscle. Thus, troponin I proteolysis underlies the pathogenesis of a common acquired form of heart failure.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Murphy, A M -- Kogler, H -- Georgakopoulos, D -- McDonough, J L -- Kass, D A -- Van Eyk, J E -- Marban, E -- HL 44065/HL/NHLBI NIH HHS/ -- HL 63038/HL/NHLBI NIH HHS/ -- New York, N.Y. -- Science. 2000 Jan 21;287(5452):488-91.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Pediatrics, Johns Hopkins University School of Medicine, Ross Building 1144, 720 Rutland Avenue, Baltimore, MD 21205, USA. murphy@jhmi.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10642551" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): Actin Cytoskeleton/metabolism ; Adrenergic beta-Agonists/pharmacology ; Animals ; Calcium/metabolism ; Cardiomegaly/pathology ; Dilatation, Pathologic ; *Disease Models, Animal ; Heart Rate ; Heart Ventricles/pathology ; Humans ; Isoproterenol/pharmacology ; Mice ; Mice, Inbred C57BL ; *Mice, Transgenic ; Myocardial Contraction ; Myocardial Stunning/*metabolism/pathology/physiopathology ; Myocardium/*metabolism/pathology ; Myofibrils/metabolism ; Troponin I/genetics/*metabolism ; Ventricular Function, Left
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    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
    Standort Signatur Erwartet Verfügbarkeit
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  • 75
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    Unbekannt
    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 2000-06-08
    Beschreibung: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Arstila, T P -- Casrouge, A -- Baron, V -- Even, J -- Kanellopoulos, J -- Kourilsky, P -- New York, N.Y. -- Science. 2000 May 19;288(5469):1135.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10841721" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): Binding Sites/genetics ; *Gene Rearrangement, alpha-Chain T-Cell Antigen Receptor ; *Gene Rearrangement, beta-Chain T-Cell Antigen Receptor ; Humans ; Receptors, Antigen, T-Cell, alpha-beta/biosynthesis/*genetics ; T-Lymphocytes/metabolism
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    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
    Standort Signatur Erwartet Verfügbarkeit
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  • 76
    facet.materialart.
    Unbekannt
    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 2000-08-05
    Beschreibung: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Murphy, K -- New York, N.Y. -- Science. 2000 Jun 30;288(5475):2319.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10917828" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): Animals ; Base Sequence ; Binding Sites ; Consensus Sequence ; Conserved Sequence ; DNA-Binding Proteins/*metabolism ; *Databases, Factual ; GATA3 Transcription Factor ; Gene Expression Regulation ; Humans ; Interleukins/*genetics ; NFATC Transcription Factors ; *Nuclear Proteins ; Trans-Activators/*metabolism ; Transcription Factors/*metabolism
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    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
    Standort Signatur Erwartet Verfügbarkeit
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  • 77
    Publikationsdatum: 2000-09-01
    Beschreibung: Epithelia of the vertebrate intestinal tract characteristically maintain an inflammatory hyporesponsiveness toward the lumenal prokaryotic microflora. We report the identification of enteric organisms (nonvirulent Salmonella strains) whose direct interaction with model human epithelia attenuate synthesis of inflammatory effector molecules elicited by diverse proinflammatory stimuli. This immunosuppressive effect involves inhibition of the inhibitor kappaB/nuclear factor kappaB (IkappaB/NF-kappaB) pathway by blockade of IkappaB-alpha degradation, which prevents subsequent nuclear translocation of active NF-kappaB dimer. Although phosphorylation of IkappaB-alpha occurs, subsequent polyubiquitination necessary for regulated IkappaB-alpha degradation is completely abrogated. These data suggest that prokaryotic determinants could be responsible for the unique tolerance of the gastrointestinal mucosa to proinflammatory stimuli.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Neish, A S -- Gewirtz, A T -- Zeng, H -- Young, A N -- Hobert, M E -- Karmali, V -- Rao, A S -- Madara, J L -- DK-35932/DK/NIDDK NIH HHS/ -- DK-47662/DK/NIDDK NIH HHS/ -- DK09800/DK/NIDDK NIH HHS/ -- etc. -- New York, N.Y. -- Science. 2000 Sep 1;289(5484):1560-3.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Epithelial Pathobiology Unit, Department of Pathology and Laboratory Medicine, Emory University School of Medicine, Atlanta, GA 30322, USA. aneish@emory.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10968793" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): Cell Nucleus/metabolism ; Cysteine Proteinase Inhibitors/pharmacology ; Cytoskeletal Proteins/metabolism ; DNA-Binding Proteins/*metabolism ; Dimerization ; Humans ; *I-kappa B Proteins ; Inflammation Mediators/pharmacology ; Interleukin-8/genetics/metabolism ; Intestinal Mucosa/*metabolism/*microbiology ; Leupeptins/pharmacology ; Ligases/metabolism ; NF-kappa B/genetics/*metabolism ; Phosphorylation ; Salmonella/pathogenicity/*physiology ; Salmonella typhimurium/pathogenicity/physiology ; *Trans-Activators ; Transcription Factor RelA ; Tumor Cells, Cultured ; Tumor Necrosis Factor-alpha/pharmacology ; Ubiquitin-Protein Ligases ; Ubiquitins/metabolism ; beta Catenin
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    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
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  • 78
    Publikationsdatum: 2000-11-25
    Beschreibung: We generated a mutant of the red fluorescent protein drFP583. The mutant (E5) changes its fluorescence from green to red over time. The rate of color conversion is independent of protein concentration and therefore can be used to trace time-dependent expression. We used in vivo labeling with E5 to measure expression from the heat shock-dependent promoter in Caenorhabditis elegans and from the Otx-2 promoter in developing Xenopus embryos. Thus, E5 is a "fluorescent timer" that can be used to monitor both activation and down-regulation of target promoters on the whole-organism scale.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Terskikh, A -- Fradkov, A -- Ermakova, G -- Zaraisky, A -- Tan, P -- Kajava, A V -- Zhao, X -- Lukyanov, S -- Matz, M -- Kim, S -- Weissman, I -- Siebert, P -- 1 RO3 TW01362-01/TW/FIC NIH HHS/ -- New York, N.Y. -- Science. 2000 Nov 24;290(5496):1585-8.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉School of Medicine, Stanford University, Stanford, CA 94305, USA. Alexey.Terskikh@Stanford.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/11090358" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): Animals ; Brain/embryology/metabolism ; Caenorhabditis elegans/embryology/genetics ; Cell Line ; Color ; Fluorescence ; Gene Expression Profiling/*methods ; *Gene Expression Regulation ; Gene Expression Regulation, Developmental ; Heat-Shock Proteins/genetics ; *Homeodomain Proteins ; Humans ; Luminescent Proteins/*chemistry/*genetics/metabolism ; Mutation ; Nerve Tissue Proteins/genetics ; Otx Transcription Factors ; *Promoter Regions, Genetic ; Temperature ; Time Factors ; Trans-Activators/genetics ; Xenopus laevis/embryology
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    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
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  • 79
    facet.materialart.
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 2000-02-05
    Beschreibung: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Gibbons, R D -- Meltzer, D -- Duan, N -- New York, N.Y. -- Science. 2000 Jan 14;287(5451):237-8.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉University of Illinois at Chicago, Chicago, IL 60612, USA. rdgib@uic.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10660422" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): *Government Regulation ; Health Policy ; Humans ; Institute of Medicine (U.S.) ; *Liver Transplantation/mortality ; *Organ Transplantation/mortality ; *Patient Selection ; *Resource Allocation ; Time Factors ; *Tissue and Organ Procurement/legislation & jurisprudence/standards ; United States
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    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
    Standort Signatur Erwartet Verfügbarkeit
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  • 80
    facet.materialart.
    Unbekannt
    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 2000-06-10
    Beschreibung: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Kaiser, J -- New York, N.Y. -- Science. 2000 May 26;288(5470):1313-4.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10847834" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): Animals ; Body Burden ; *Carcinogens ; Dioxins/*adverse effects/analysis/pharmacokinetics/toxicity ; Environmental Exposure/adverse effects ; Half-Life ; Humans ; Neoplasms/*chemically induced ; Occupational Exposure/adverse effects ; United States ; United States Environmental Protection Agency
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    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
    Standort Signatur Erwartet Verfügbarkeit
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  • 81
    facet.materialart.
    Unbekannt
    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 2000-03-17
    Beschreibung: Cancer as a disease in the human population is becoming a larger health problem, and the medicines used as treatments have clear limitations. In the past 20 years, there has been a tremendous increase in our knowledge of the molecular mechanisms and pathophysiology of human cancer. Many of these mechanisms have been exploited as new targets for drug development in the hope that they will have greater antitumor activity with less toxicity to the patient than is seen with currently used medicines. The fruition of these efforts in the clinic is just now being realized with a few encouraging results.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Gibbs, J B -- New York, N.Y. -- Science. 2000 Mar 17;287(5460):1969-73.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Cancer Research, Merck Research Laboratories, West Point, PA 19486, USA. jay_gibbs@merck.com〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10720316" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): *Antineoplastic Agents/adverse effects/chemical ; synthesis/pharmacology/therapeutic use ; Breast Neoplasms/drug therapy/metabolism ; *Chemistry, Pharmaceutical ; Clinical Trials as Topic ; *Drug Design ; Drug Screening Assays, Antitumor ; Enzyme Inhibitors/chemical synthesis/pharmacology/therapeutic use ; Genetic Therapy ; Humans ; Neoplasms/*drug therapy/genetics/metabolism/pathology ; Neoplasms, Hormone-Dependent/drug therapy/metabolism
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    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
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  • 82
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 2000-08-12
    Beschreibung: According to researchers who gathered here at a high-powered summit this month, toxicology may be on the verge of changing the way it collects raw data--adopting a process that could reduce animal use and improve test results. The new approach, called "toxicogenomics," uses DNA arrays to profile gene expression in cells exposed to test compounds. But some leaders in the field warn against rushing too quickly to embrace DNA tests, which are still difficult to interpret.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Lovett, R A -- New York, N.Y. -- Science. 2000 Jul 28;289(5479):536-7.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10939962" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): Animal Testing Alternatives ; Animals ; *Gene Expression Profiling ; Humans ; *Oligonucleotide Array Sequence Analysis ; Peroxisome Proliferators/toxicity ; Toxicity Tests/*methods
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    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
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  • 83
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 2000-07-15
    Beschreibung: In December 1996, Omu Anzala returned to Kenya after completing his Ph.D. work in Canada on HIV's interactions with the immune system to work with a collaborative AIDS research project started by researchers from his university and the University of Manitoba. Now the International AIDS Vaccine Initiative has funded Anzala and his collaborators to fashion an AIDS vaccine based on a strain of HIV circulating in Kenya.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Cohen, J -- New York, N.Y. -- Science. 2000 Jun 23;288(5474):2166.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10896605" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): *AIDS Vaccines ; Canada ; History, 20th Century ; Humans ; International Cooperation ; Kenya ; Research
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    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
    Standort Signatur Erwartet Verfügbarkeit
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  • 84
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 2000-05-08
    Beschreibung: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Kaiser, J -- New York, N.Y. -- Science. 2000 Apr 21;288(5465):424-5.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10798974" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): Air Pollutants/*adverse effects ; Animals ; Carbon/*adverse effects ; Heart Diseases/etiology ; Humans ; Immune System/*drug effects ; Immunosuppressive Agents/adverse effects ; Infant ; Polychlorinated Biphenyls/*adverse effects/blood ; Respiratory Tract Diseases/etiology ; United States ; United States Environmental Protection Agency
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    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
    Standort Signatur Erwartet Verfügbarkeit
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  • 85
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 2000-07-15
    Beschreibung: Efforts have recently heated up in several African countries to tailor-make preparations that many believe offer the best hope yet for stopping HIV cold. But all are at the earliest stages, which means it will take years before a vaccine might prove its worth.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Cohen, J -- New York, N.Y. -- Science. 2000 Jun 23;288(5474):2165-7.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10896604" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): *AIDS Vaccines/economics ; Africa South of the Sahara ; *Clinical Trials as Topic/standards ; Developed Countries ; Developing Countries ; Ethics, Medical ; HIV/immunology ; HIV Antibodies/blood/immunology ; HIV Infections/immunology/prevention & control ; Humans ; Immunity, Innate ; Informed Consent ; International Cooperation ; *Research
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    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
    Standort Signatur Erwartet Verfügbarkeit
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  • 86
    Publikationsdatum: 2000-03-10
    Beschreibung: The 2,272,351-base pair genome of Neisseria meningitidis strain MC58 (serogroup B), a causative agent of meningitis and septicemia, contains 2158 predicted coding regions, 1158 (53.7%) of which were assigned a biological role. Three major islands of horizontal DNA transfer were identified; two of these contain genes encoding proteins involved in pathogenicity, and the third island contains coding sequences only for hypothetical proteins. Insights into the commensal and virulence behavior of N. meningitidis can be gleaned from the genome, in which sequences for structural proteins of the pilus are clustered and several coding regions unique to serogroup B capsular polysaccharide synthesis can be identified. Finally, N. meningitidis contains more genes that undergo phase variation than any pathogen studied to date, a mechanism that controls their expression and contributes to the evasion of the host immune system.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Tettelin, H -- Saunders, N J -- Heidelberg, J -- Jeffries, A C -- Nelson, K E -- Eisen, J A -- Ketchum, K A -- Hood, D W -- Peden, J F -- Dodson, R J -- Nelson, W C -- Gwinn, M L -- DeBoy, R -- Peterson, J D -- Hickey, E K -- Haft, D H -- Salzberg, S L -- White, O -- Fleischmann, R D -- Dougherty, B A -- Mason, T -- Ciecko, A -- Parksey, D S -- Blair, E -- Cittone, H -- Clark, E B -- Cotton, M D -- Utterback, T R -- Khouri, H -- Qin, H -- Vamathevan, J -- Gill, J -- Scarlato, V -- Masignani, V -- Pizza, M -- Grandi, G -- Sun, L -- Smith, H O -- Fraser, C M -- Moxon, E R -- Rappuoli, R -- Venter, J C -- New York, N.Y. -- Science. 2000 Mar 10;287(5459):1809-15.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉The Institute for Genomic Research (TIGR), 9712 Medical Center Drive, Rockville, MD 20850, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10710307" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): Antigenic Variation ; Antigens, Bacterial/immunology ; Bacteremia/microbiology ; Bacterial Capsules/genetics ; Bacterial Proteins/genetics/physiology ; DNA Transposable Elements ; Evolution, Molecular ; Fimbriae, Bacterial/genetics ; *Genome, Bacterial ; Humans ; Meningitis, Meningococcal/microbiology ; Meningococcal Infections/microbiology ; Molecular Sequence Data ; Mutation ; Neisseria meningitidis/classification/*genetics/*pathogenicity/physiology ; Open Reading Frames ; Operon ; Phylogeny ; Recombination, Genetic ; *Sequence Analysis, DNA ; Serotyping ; Transformation, Bacterial ; Virulence/genetics
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    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
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  • 87
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 2000-07-15
    Beschreibung: Many South Africans long dreamed of the day when the oppressive apartheid system would end. That day has come, but now the country faces a new disaster: one of the world's worst HIV epidemics--and most confusing government responses.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Cohen, J -- New York, N.Y. -- Science. 2000 Jun 23;288(5474):2168-70.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10896606" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): *Acquired Immunodeficiency Syndrome/epidemiology ; Anti-HIV Agents/therapeutic use ; Disease Outbreaks ; Female ; Government ; HIV Infections/drug therapy/epidemiology ; Humans ; Male ; Pregnancy ; Pregnancy Complications, Infectious/drug therapy ; Public Policy ; *Research ; South Africa/epidemiology
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    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
    Standort Signatur Erwartet Verfügbarkeit
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  • 88
    Publikationsdatum: 2000-03-04
    Beschreibung: The coupling mechanism between endoplasmic reticulum (ER) calcium ion (Ca2+) stores and plasma membrane (PM) store-operated channels (SOCs) is crucial to Ca2+ signaling but has eluded detection. SOCs may be functionally related to the TRP family of receptor-operated channels. Direct comparison of endogenous SOCs with stably expressed TRP3 channels in human embryonic kidney (HEK293) cells revealed that TRP3 channels differ in being store independent. However, condensed cortical F-actin prevented activation of both SOC and TRP3 channels, which suggests that ER-PM interactions underlie coupling of both channels. A cell-permeant inhibitor of inositol trisphosphate receptor (InsP3R) function, 2-aminoethoxydiphenyl borate, prevented both receptor-induced TRP3 activation and store-induced SOC activation. It is concluded that InsP3Rs mediate both SOC and TRP channel opening and that the InsP3R is essential for maintaining coupling between store emptying and physiological activation of SOCs.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Ma, H T -- Patterson, R L -- van Rossum, D B -- Birnbaumer, L -- Mikoshiba, K -- Gill, D L -- AR07592/AR/NIAMS NIH HHS/ -- HL55426/HL/NHLBI NIH HHS/ -- New York, N.Y. -- Science. 2000 Mar 3;287(5458):1647-51.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Biochemistry and Molecular Biology, University of Maryland, School of Medicine, Baltimore, MD 21201, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10698739" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): Actins/metabolism ; Boron Compounds/pharmacology ; Calcium/*metabolism ; Calcium Channels/chemistry/*metabolism ; *Calcium Signaling ; Carbachol/pharmacology ; Cell Line ; Cell Membrane/metabolism ; Diglycerides/metabolism/pharmacology ; Endoplasmic Reticulum/*metabolism ; Enzyme Inhibitors/pharmacology ; Humans ; Inositol 1,4,5-Trisphosphate Receptors ; Ionomycin/pharmacology ; Macrocyclic Compounds ; Oxazoles/pharmacology ; Phosphoprotein Phosphatases/antagonists & inhibitors ; Receptors, Cytoplasmic and Nuclear/chemistry/*metabolism ; Strontium/metabolism ; TRPC Cation Channels ; Thapsigargin/pharmacology ; Transfection ; Type C Phospholipases/metabolism
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  • 89
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 2000-08-12
    Beschreibung: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Zimmer, C -- New York, N.Y. -- Science. 2000 Jul 28;289(5479):525-7.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10939959" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): Animals ; *Behavior, Animal ; Biological Evolution ; *Fear ; Female ; Humans ; Male ; *Personality ; Rats ; Toxoplasma/*physiology ; Toxoplasmosis, Animal/parasitology/*psychology ; Toxoplasmosis, Cerebral/parasitology/*psychology
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    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
    Standort Signatur Erwartet Verfügbarkeit
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  • 90
    Publikationsdatum: 2000-06-10
    Beschreibung: Theories of the regulation of cognition suggest a system with two necessary components: one to implement control and another to monitor performance and signal when adjustments in control are needed. Event-related functional magnetic resonance imaging and a task-switching version of the Stroop task were used to examine whether these components of cognitive control have distinct neural bases in the human brain. A double dissociation was found. During task preparation, the left dorsolateral prefrontal cortex (Brodmann's area 9) was more active for color naming than for word reading, consistent with a role in the implementation of control. In contrast, the anterior cingulate cortex (Brodmann's areas 24 and 32) was more active when responding to incongruent stimuli, consistent with a role in performance monitoring.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉MacDonald, A W 3rd -- Cohen, J D -- Stenger, V A -- Carter, C S -- New York, N.Y. -- Science. 2000 Jun 9;288(5472):1835-8.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Psychology, University of Pittsburgh, Pittsburgh, PA 15260, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10846167" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): Adolescent ; Adult ; Brain Mapping ; Cerebral Cortex/*physiology ; Cognition/*physiology ; Color ; Female ; Humans ; Magnetic Resonance Imaging ; Male ; Prefrontal Cortex/*physiology ; Reading
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  • 91
    Publikationsdatum: 2000-10-20
    Beschreibung: Pseudomonas aeruginosa causes severe infections, particularly of the lung, that are life threatening. Here, we show that P. aeruginosa infection induces apoptosis of lung epithelial cells by activation of the endogenous CD95/CD95 ligand system. Deficiency of CD95 or CD95 ligand on epithelial cells prevented apoptosis of lung epithelial cells in vivo as well as in vitro. The importance of CD95/CD95 ligand-mediated lung epithelial cell apoptosis was demonstrated by the rapid development of sepsis in CD95- or CD95 ligand-deficient mice, but not in normal mice, after P. aeruginosa infection.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Grassme, H -- Kirschnek, S -- Riethmueller, J -- Riehle, A -- von Kurthy, G -- Lang, F -- Weller, M -- Gulbins, E -- New York, N.Y. -- Science. 2000 Oct 20;290(5491):527-30.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Physiology, University of Tuebingen, Gmelinstrasse 5, 72076 Tuebingen, Germany.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/11039936" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): Animals ; Antigens, CD95/genetics/*metabolism ; *Apoptosis ; Bone Marrow Transplantation ; Cell Line ; Epithelial Cells/*immunology/microbiology/pathology ; Fas Ligand Protein ; Humans ; In Situ Nick-End Labeling ; Lung/*immunology/microbiology/pathology ; Lung Diseases/*immunology/microbiology/pathology ; Membrane Glycoproteins/genetics/*metabolism ; Mice ; Mice, Inbred C3H ; Pseudomonas Infections/*immunology/microbiology/pathology ; Pseudomonas aeruginosa/immunology/*pathogenicity ; Sepsis/microbiology ; Spleen/microbiology
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    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
    Standort Signatur Erwartet Verfügbarkeit
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  • 92
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 2000-08-29
    Beschreibung: Experts on brain-riddling spongiform diseases have grown steadily more uneasy over signs that so-called mad cow disease or bovine spongiform encephalopathy (BSE), which is linked to a lethal human illness, may be lurking in sheep. A study in the 10 August issue of Nature now offers evidence that BSE is not rampant in sheep after all, although scientists are far from ready to let their guard down.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Balter, M -- New York, N.Y. -- Science. 2000 Aug 11;289(5481):849.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10960311" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): Animals ; Cattle ; Creutzfeldt-Jakob Syndrome/epidemiology ; Diagnosis, Differential ; Disease Outbreaks ; Encephalopathy, Bovine Spongiform/diagnosis/*epidemiology ; Great Britain/epidemiology ; Humans ; Incidence ; Scrapie/diagnosis/*epidemiology ; Sheep ; Sheep Diseases/diagnosis/*epidemiology
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    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
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  • 93
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 2000-08-06
    Beschreibung: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Balter, M -- New York, N.Y. -- Science. 2000 Jul 7;289(5476):28.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10928924" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): *Acquired Immunodeficiency Syndrome ; *Budgets ; Financing, Government ; Humans ; Italy ; *Research Support as Topic
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    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
    Standort Signatur Erwartet Verfügbarkeit
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  • 94
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 2000-09-19
    Beschreibung: A task force here has been studying cases of variant Creutzfeldt-Jakob disease (vCJD), an incurable malady of the brain and nervous system that has been linked to eating beef or other products from cattle infected with bovine spongiform encephalopathy or "mad cow disease." The team's goal is to find out just how the patients got infected and how many of them there may ultimately be. The number of confirmed or probable vCJD cases in the United Kingdom is still relatively small--a total of 80 as Science went to press--and recent estimates of the number of potential cases are lower than was once feared. Yet the task force's own recent results show that the incidence of vCJD is rising, and researchers remain determined to try to solve the riddles posed by vCJD.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Balter, M -- New York, N.Y. -- Science. 2000 Sep 1;289(5484):1452-4.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10991726" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): Animals ; Bias (Epidemiology) ; Cattle ; Cluster Analysis ; Creutzfeldt-Jakob Syndrome/*epidemiology/transmission ; Disease Outbreaks ; Encephalopathy, Bovine Spongiform/epidemiology/transmission ; Female ; *Food ; Great Britain/epidemiology ; Humans ; Incidence ; Male ; Meat ; Surveys and Questionnaires
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    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
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  • 95
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 2000-09-23
    Beschreibung: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Balter, M -- New York, N.Y. -- Science. 2000 Sep 8;289(5485):1663-6.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/11001722" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): Animals ; *Animals, Domestic ; Carrier State/*veterinary ; Cattle ; Creutzfeldt-Jakob Syndrome/epidemiology/prevention & control/*transmission ; Cricetinae ; Encephalopathy, Bovine Spongiform/epidemiology/prevention & control/*transmission ; Great Britain/epidemiology ; Humans ; Mice ; Prion Diseases/*transmission ; Species Specificity
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    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
    Standort Signatur Erwartet Verfügbarkeit
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  • 96
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 2000-07-15
    Beschreibung: Certain genes are only expressed at one allele, a phenomenon called imprinting. Although it is well established that one allele of certain imprinted genes is silenced through methylation, this does not appear to be the case for all imprinted genes. In a thoughtful Perspective, Thorvaldsen and Bartolomei discuss new findings showing that insertion of insulator elements (boundary regions) between the promoter of a gene and its enhancer (a sequence that boosts gene expression) may be another way in which genes are silenced during imprinting.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Thorvaldsen, J L -- Bartolomei, M S -- New York, N.Y. -- Science. 2000 Jun 23;288(5474):2145-6.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Howard Hughes Medical Institute and Department of Cell and Developmental Biology, University of Pennsylvania School of Medicine, Philadelphia, PA 19104, USA. thorvald@mail.med.upenn.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10896590" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): Alleles ; Animals ; *DNA Methylation ; DNA-Binding Proteins/metabolism ; Dinucleoside Phosphates ; Enhancer Elements, Genetic ; Fathers ; Female ; *Gene Silencing ; *Genomic Imprinting ; Humans ; Insulin-Like Growth Factor II/genetics ; Male ; Models, Genetic ; Mothers ; Muscle Proteins/genetics ; Ovum/metabolism ; Promoter Regions, Genetic ; RNA, Long Noncoding ; *RNA, Untranslated ; Regulatory Sequences, Nucleic Acid ; *Repressor Proteins ; Spermatozoa/metabolism ; Transcription Factors/metabolism ; Zinc Fingers
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    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
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  • 97
    facet.materialart.
    Unbekannt
    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 2000-09-02
    Beschreibung: What are all of those retrotransposons doing buzzing about in our genome? According to Kazazian, in his Perspective this week, these mobile pieces of DNA are busy reshaping our genome, making it more diverse and enabling us to survive and thrive through the vagaries of evolution. And just how do they do this?...zip to page 1152 to find out.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Kazazian, H H Jr -- New York, N.Y. -- Science. 2000 Aug 18;289(5482):1152-3.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Genetics, University of Pennsylvania School of Medicine, Philadelphia, PA 19104, USA. kazazian@mail.med.upenn.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10970230" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): Alu Elements ; Animals ; Dosage Compensation, Genetic ; *Genome ; *Genome, Human ; Humans ; *Long Interspersed Nucleotide Elements ; Mammals/*genetics ; Mutagenesis, Insertional ; Pseudogenes ; RNA, Messenger/genetics/metabolism ; *Retroelements ; Telomerase/chemistry/genetics ; Terminal Repeat Sequences
    Print ISSN: 0036-8075
    Digitale ISSN: 1095-9203
    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
    Standort Signatur Erwartet Verfügbarkeit
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  • 98
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 2000-04-25
    Beschreibung: This study shows that a corpus of proto-word forms shares four sequential sound patterns with words of modern languages and the first words of infants. Three of the patterns involve intrasyllabic consonant-vowel (CV) co-occurrence: labial (lip) consonants with central vowels, coronal (tongue front) consonants with front vowels, and dorsal (tongue back) consonants with back vowels. The fourth pattern is an intersyllabic preference for initiating words with a labial consonant-vowel-coronal consonant sequence (LC). The CV effects may be primarily biomechanically motivated. The LC effect may be self-organizational, with multivariate causality. The findings support the hypothesis that these four patterns were basic to the origin of words.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉MacNeilage, P F -- Davis, B L -- R01 HD 27733-07/HD/NICHD NIH HHS/ -- New York, N.Y. -- Science. 2000 Apr 21;288(5465):527-31.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Psychology, Department of Communication Sciences and Disorders, University of Texas, Austin, TX 78712, USA. macneilage@psy.utexas.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10775113" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): Biomechanical Phenomena ; Humans ; Infant ; *Language Development ; Lip/physiology ; Mandible/physiology ; Movement ; *Phonetics ; *Speech ; Tongue/physiology
    Print ISSN: 0036-8075
    Digitale ISSN: 1095-9203
    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
    Standort Signatur Erwartet Verfügbarkeit
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  • 99
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    Unbekannt
    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 2000-07-15
    Beschreibung: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Balter, M -- New York, N.Y. -- Science. 2000 Jun 23;288(5474):2115.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10896574" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): Base Sequence ; Bioethics ; DNA/genetics ; European Union ; France ; *Genes ; Humans ; Patents as Topic/*legislation & jurisprudence
    Print ISSN: 0036-8075
    Digitale ISSN: 1095-9203
    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
    Standort Signatur Erwartet Verfügbarkeit
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  • 100
    facet.materialart.
    Unbekannt
    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 2000-10-21
    Beschreibung: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Tisdale, M J -- New York, N.Y. -- Science. 2000 Sep 29;289(5488):2293-4.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Pharmaceutical Sciences Research Institute, Aston University, Birmingham B4 7ET, UK.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/11041796" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): Animals ; Blood Proteins/metabolism ; Cachexia/drug therapy/etiology/*metabolism/pathology ; Cell Differentiation ; Cysteine Endopeptidases/genetics/metabolism ; Cytokines/pharmacology ; Homeostasis ; Humans ; Interferon-gamma/pharmacology ; Mice ; Multienzyme Complexes/genetics/metabolism ; Muscle Proteins/*metabolism ; Muscle, Skeletal/cytology/*metabolism/pathology ; MyoD Protein/genetics/metabolism ; Myosins/genetics/metabolism ; NF-kappa B/*metabolism ; Neoplasms/*complications ; Promoter Regions, Genetic ; Proteasome Endopeptidase Complex ; Proteoglycans ; Transcription, Genetic ; Tumor Necrosis Factor-alpha/pharmacology ; Ubiquitins/metabolism
    Print ISSN: 0036-8075
    Digitale ISSN: 1095-9203
    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
    Standort Signatur Erwartet Verfügbarkeit
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