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  • American Association for the Advancement of Science (AAAS)  (24.137)
  • 1990-1994  (13.320)
  • 1980-1984  (10.817)
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  • 101
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 1990-08-03
    Beschreibung: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉New York, N.Y. -- Science. 1990 Aug 3;249(4968):475.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17735276" target="_blank"〉PubMed〈/a〉
    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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  • 102
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 1990-02-09
    Beschreibung: The control of cellular senescence by specific human chromosomes was examined in interspecies cell hybrids between diploid human fibroblasts and an immortal, Syrian hamster cell line. Most such hybrids exhibited a limited life span comparable to that of the human fibroblasts, indicating that cellular senescence is dominant in these hybrids. Karyotypic analyses of the hybrid clones that did not senesce revealed that all these clones had lost both copies of human chromosome 1, whereas all other human chromosomes were observed in at least some of the immortal hybrids. The application of selective pressure for retention of human chromosome 1 to the cell hybrids resulted in an increased percentage of hybrids that senesced. Further, the introduction of a single copy of human chromosome 1 to the hamster cells by microcell fusion caused typical signs of cellular senescence. Transfer of chromosome 11 had no effect on the growth of the cells. These findings indicate that human chromosome 1 may participate in the control of cellular senescence and further support a genetic basis for cellular senescence.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Sugawara, O -- Oshimura, M -- Koi, M -- Annab, L A -- Barrett, J C -- New York, N.Y. -- Science. 1990 Feb 9;247(4943):707-10.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉National Institute of Environmental Health Sciences, National Institutes of Health, Research Triangle Park, NC 27709.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/2300822" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): Animals ; Cell Line ; Cell Survival/*genetics ; Chromosome Mapping ; *Chromosomes, Human, Pair 1 ; Clone Cells ; Cricetinae ; Diploidy ; Fibroblasts/*cytology ; Humans ; Hybrid Cells/*cytology ; Hypoxanthine Phosphoribosyltransferase/genetics ; Karyotyping ; Mice ; Ploidies ; Transfection ; Translocation, Genetic ; X Chromosome
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    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
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  • 103
    Publikationsdatum: 1990-10-05
    Beschreibung: The functional competence of extrageniculate visual pathways in hemianopic humans was demonstrated by showing that distractor signals in the blind half of the visual field could inhibit saccades toward targets in the intact visual field. This inhibitory effect of unseen distractors in patients occurred only when distractors were presented in the temporal half of the visual field, was specific to oculomotor responses, and did not occur in normal subjects. These results show that a peripheral visual signal activates retinotectal pathways to prime the oculomotor system and that these pathways can mediate orienting behavior in hemianopic humans.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Rafal, R -- Smith, J -- Krantz, J -- Cohen, A -- Brennan, C -- MH 41544/MH/NIMH NIH HHS/ -- New York, N.Y. -- Science. 1990 Oct 5;250(4977):118-21.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Clinical Neurosciences, Brown University, Providence, RI 02908.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/2218503" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): Analysis of Variance ; Brain/anatomy & histology/*physiopathology/radiography ; Hemianopsia/*physiopathology/radiography ; Humans ; Reference Values ; *Saccades ; Scotoma/physiopathology ; Tomography, X-Ray Computed ; *Vision, Ocular ; *Visual Fields
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    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
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  • 104
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 1990-09-28
    Beschreibung: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Dusheck, J -- New York, N.Y. -- Science. 1990 Sep 28;249(4976):1494-5.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/2218487" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): *Biological Evolution ; Congresses as Topic ; Female ; Humans ; Male ; Men ; United States ; *Women
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    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
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  • 105
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 1990-06-15
    Beschreibung: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Kuliopulos, H -- New York, N.Y. -- Science. 1990 Jun 15;248(4961):1305.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17747513" target="_blank"〉PubMed〈/a〉
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    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
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  • 106
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 1990-08-03
    Beschreibung: Eukaryotic cells respond to elevated temperatures by rapidly activating the expression of heat shock genes. Central to this activation is heat shock-inducible binding of the transcriptional activator, termed heat shock factor (HSF), to common regulatory elements, which are located upstream of all heat shock genes. The DNA binding activity of the inactive form of Drosophila HSF was induced in vitro by treatment with polyclonal antibodies to the purified, in vivo-activated factor. This finding, together with observations that high temperature and low pH activate HSF binding in vitro, suggests that the inactive form of HSF can directly recognize and transduce the heat shock signal without undergoing a covalent modification of protein structure.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Zimarino, V -- Wilson, S -- Wu, C -- New York, N.Y. -- Science. 1990 Aug 3;249(4968):546-9.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Laboratory of Biochemistry, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/2200124" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): Animals ; Antibodies ; Drosophila/*genetics ; *Gene Expression Regulation ; HeLa Cells/metabolism ; Heat-Shock Proteins/*genetics/immunology/isolation & purification/metabolism ; Humans ; Saccharomyces cerevisiae/genetics ; Transcription Factors/*metabolism ; *Transcription, Genetic
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    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
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  • 107
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 1990-06-01
    Beschreibung: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉H, C -- New York, N.Y. -- Science. 1990 Jun 1;248(4959):1069.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17733356" target="_blank"〉PubMed〈/a〉
    Print ISSN: 0036-8075
    Digitale ISSN: 1095-9203
    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
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  • 108
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 1990-08-17
    Beschreibung: The map accompanying the article "Amazon biodiversity" (News & Comment, 15 June, p. 1305) should have been credited to Conservation International.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉New York, N.Y. -- Science. 1990 Aug 17;249(4970):724.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17756773" target="_blank"〉PubMed〈/a〉
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    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
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  • 109
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 1990-06-15
    Beschreibung: The specificity of mature CD8+ and CD4+ T lymphocytes is controlled by major histocompatibility complex (MHC) class I and class II molecules, respectively. The MHC class specificity of T cells is stringent in many assays, but is less evident when cells are supplemented with exogenous lymphokines. The repertoire of T cells is shaped through contact with MHC molecules in the thymus and involves a complex process of positive selection and negative selection (tolerance). Tolerance of immature T cells to MHC molecules can reflect either clonal deletion or anergy and results from intrathymic contact with several cell types, including epithelial cells and cells with antigen-presenting function. Unlike immature T cells, mature T cells are relatively resistant to tolerance induction. In certain situations partial unresponsiveness of mature T cells can be achieved by exposing T cells to foreign MHC molecules expressed on atypical antigen-presenting cells. Tolerance is rarely complete, however, and the precise requirements for tolerizing mature T cells are still unclear.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Sprent, J -- Gao, E K -- Webb, S R -- AI21487/AI/NIAID NIH HHS/ -- CA25803/CA/NCI NIH HHS/ -- CA38355/CA/NCI NIH HHS/ -- New York, N.Y. -- Science. 1990 Jun 15;248(4961):1357-63.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Immunology, Research Institute of Scripps Clinic, La Jolla, CA 92037.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/1694041" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): Animals ; Antigen-Presenting Cells/immunology ; Bone Marrow/immunology ; CD4-Positive T-Lymphocytes/immunology ; Clone Cells/immunology ; Epitopes/immunology ; Histocompatibility Antigens/*immunology ; Histocompatibility Antigens Class II/immunology ; *Immune Tolerance ; *Immunity ; Interleukin-2/physiology ; Mice ; Mice, Transgenic ; Receptors, Antigen, T-Cell/immunology ; T-Lymphocytes/*immunology ; T-Lymphocytes, Regulatory/immunology ; Thymus Gland/immunology
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    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
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  • 110
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 1990-07-06
    Beschreibung: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Koshland, D E Jr -- New York, N.Y. -- Science. 1990 Jul 6;249(4964):13.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17787609" target="_blank"〉PubMed〈/a〉
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    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
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  • 111
    Publikationsdatum: 1990-08-24
    Beschreibung: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Morlan, R E -- New York, N.Y. -- Science. 1990 Aug 24;249(4971):937-8.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17773106" target="_blank"〉PubMed〈/a〉
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    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
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  • 112
    Publikationsdatum: 1990-03-09
    Beschreibung: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Sun, M -- New York, N.Y. -- Science. 1990 Mar 9;247(4947):1174-6.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17809259" target="_blank"〉PubMed〈/a〉
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    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
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  • 113
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 1990-02-09
    Beschreibung: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉New York, N.Y. -- Science. 1990 Feb 9;247(4943):632.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17771870" target="_blank"〉PubMed〈/a〉
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    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
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  • 114
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 1990-02-09
    Beschreibung: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉New York, N.Y. -- Science. 1990 Feb 9;247(4943):632.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17771869" target="_blank"〉PubMed〈/a〉
    Print ISSN: 0036-8075
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    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
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  • 115
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 1990-11-23
    Beschreibung: In Aplysia sensory and motor neurons in culture, the contributions of the major classes of calcium current can be selectively examined while transmitter release and its modulation are examined. A slowly inactivating, dihydropyridine-sensitive calcium current does not contribute either to normal synaptic transmission or to any of three different forms of plasticity: presynaptic inhibition, homosynaptic depression, and presynaptic facilitation. This current does contribute, however, to a fourth form of plasticity--modulation of transmitter release by tonic depolarization of the sensory neuron. By contrast, a second calcium current, which is rapidly inactivating and dihydropyridine-insensitive, contributes to release elicited by the transient depolarization of an action potential and to the other three forms of plasticity.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Edmonds, B -- Klein, M -- Dale, N -- Kandel, E R -- New York, N.Y. -- Science. 1990 Nov 23;250(4984):1142-7.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Pharmacology, University College of London, United Kingdom.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/2174573" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): Action Potentials ; Animals ; Aplysia/*physiology ; Cadmium/pharmacology ; Calcium Channels/drug effects/*physiology ; Cells, Cultured ; Dihydropyridines/antagonists & inhibitors/pharmacology ; Electric Conductivity ; FMRFamide ; Motor Neurons/physiology ; Neuronal Plasticity/*physiology ; Neurons, Afferent/physiology ; Neuropeptides/pharmacology ; Nifedipine/pharmacology ; Serotonin/pharmacology ; Synapses/*physiology ; Synaptic Transmission/*physiology
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    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
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  • 116
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 1990-01-05
    Beschreibung: The high degree of tubulin heterogeneity in neurons is controlled mainly at the posttranslational level. Several variants of alpha-tubulin can be posttranslationally labeled after incubation of cells with [3H]acetate or [3H]glutamate. Peptides carrying the radioactive moiety were purified by high-performance liquid chromatography. Amino acid analysis, Edman degradation sequencing, and mass spectrometric analysis of these peptides led to the characterization of a posttranslational modification consisting of the successive addition of glutamyl units on the gamma-carboxyl group of a glutamate residue (Glu445). This modification, localized within a region of alpha-tubulin that is important in the interactions of tubulin with microtubule-associated proteins and calcium, could play a role in regulating microtubule dynamics.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Edde, B -- Rossier, J -- Le Caer, J P -- Desbruyeres, E -- Gros, F -- Denoulet, P -- New York, N.Y. -- Science. 1990 Jan 5;247(4938):83-5.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Laboratoire de Biochimie Cellulaire, College de France, Paris.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/1967194" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): Amino Acids/analysis ; Animals ; Brain/*metabolism ; Chromatography, High Pressure Liquid ; Glutamates/*metabolism ; Glutamic Acid ; Mass Spectrometry ; Mice ; Neurons/*metabolism ; Peptide Fragments/analysis ; *Protein Processing, Post-Translational ; Tubulin/*metabolism
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    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
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  • 117
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 1990-11-09
    Beschreibung: Experimental manipulations of fish in a Northern California river during summer base flow reveal that they have large effects on predators, herbivores, and plants in river food webs. California roach and juvenile steelhead consume predatory insects and fish fry, which feed on algivorous chironomid larvae. In the presence of fish, filamentous green algae are reduced to low, prostrate webs, infested with chironomids. When the absence of large fish releases smaller predators that suppress chironomids, algal biomass is higher, and tall upright algal turfs become covered with diatoms and cyanobacteria. These manipulations provide evidence that the Hairston, Smith, Slobodkin-Fretwell theory of trophic control, which predicts that plants will be alternately limited by resources or herbivores in food webs with odd and even numbers of trophic levels, has application to river communitics.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Power, M E -- New York, N.Y. -- Science. 1990 Nov 9;250(4982):811-4.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17759974" target="_blank"〉PubMed〈/a〉
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    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
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  • 118
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 1990-06-15
    Beschreibung: During development in the thymus, T cells are rendered tolerant to self antigens. It is now apparent that thymocytes bearing self-reactive T cell receptors can be tolerized by processes that result in physical elimination (clonal deletion) or functional inactivation (clonal anergy). As these mechanisms have important clinical implications for transplantation and autoimmunity, current investigations are focused on understanding the cellular and molecular interactions that generate these forms of tolerance.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Ramsdell, F -- Fowlkes, B J -- New York, N.Y. -- Science. 1990 Jun 15;248(4961):1342-8.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Laboratory of Cellular and Molecular Immunology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD 20892.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/1972593" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): Animals ; Antigens, Surface/immunology ; Autoantigens/immunology ; Autoimmunity/immunology ; Bone Marrow/immunology ; CD4-Positive T-Lymphocytes/immunology ; Chickens ; Chimera ; Clone Cells/*immunology ; H-2 Antigens/immunology ; Histocompatibility Antigens/immunology ; Histocompatibility Antigens Class II/immunology ; *Immune Tolerance ; Mice ; Mice, Transgenic ; Minor Lymphocyte Stimulatory Antigens ; Receptors, Antigen, T-Cell/*immunology ; T-Lymphocytes/*immunology ; T-Lymphocytes, Regulatory/immunology ; Thymus Gland/*immunology ; Xenopus
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    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
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  • 119
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 1990-06-01
    Beschreibung: Conjugate eye movements are executed through the concurrent activation of several muscles in both eyes. The neural mechanisms that underlie such synergistic muscle activations have been a matter of considerable experimentation and debate. In order to investigate this issue, the projections of a class of primate premotoneuronal cells were studied, namely, the vertical medium-lead burst neurons (VMLBs), which drive vertical rapid eye movements. Axons of upward VMLBs ramify bilaterally within motoneuron pools that supply the superior rectus and inferior oblique muscles of both eyes. Axons of downward VMLBs ramify ipsilaterally in the inferior rectus portion of the oculomotor nucleus and in the trochlear nucleus. Thus, VMLBs can drive vertical motoneuron pools of both eyes during conjugate vertical rapid eye movements; these data support Hering's law.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Moschovakis, A K -- Scudder, C A -- Highstein, S M -- EY-05433/EY/NEI NIH HHS/ -- EY-05954/EY/NEI NIH HHS/ -- NS-17763/NS/NINDS NIH HHS/ -- New York, N.Y. -- Science. 1990 Jun 1;248(4959):1118-9.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Laboratory of Neural Control, National Institute of Neurological Diseases and Stroke, Bethesda, MD 20892.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/2343316" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): Action Potentials ; Animals ; Axons/ultrastructure ; Eye Movements/*physiology ; *Models, Neurological ; Motor Neurons/cytology/*physiology/ultrastructure ; Neural Pathways/anatomy & histology/cytology ; Oculomotor Muscles/*innervation ; Saimiri
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    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
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  • 120
    Publikationsdatum: 1990-07-27
    Beschreibung: The study of magnetic phase transitions in insulating molecular solids provides new insights into mechanisms of magnetic coupling in the solid state and into critical phenomena associated with these transitions. Only a few such materials are known to display cooperative magnetic properties. The use of high-spin molecular components would enhance intermolecular spin-spin interactions and thus a series of chargetransfer (CT) salts have been synthesized that utilize the spin S = 1 molecular cation, [Mn(C(5)(CH(3))(5))(2)](+) (decamethylmanganocenium). The structure and cooperative magnetic behavior of [Mn(C(5)(CH(3))(5))(2)](+)[TCNQ(-) (decamethylmanganocenium 7,7,8,8-tetracyano-p-quinodimethanide) are reported. This salt is a bulk molecular ferromagnet with the highest critical (Curie) temperature (T(c) = 6.2 K) and coercive field (3.6 x 10(3) gauss), yet reported for such a material.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Broderick, W E -- Thompson, J A -- Day, E P -- Hoffman, B M -- New York, N.Y. -- Science. 1990 Jul 27;249(4967):401-3.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17755945" target="_blank"〉PubMed〈/a〉
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    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
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  • 121
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 1990-07-13
    Beschreibung: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Hamilton, D P -- New York, N.Y. -- Science. 1990 Jul 13;249(4965):116.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17836958" target="_blank"〉PubMed〈/a〉
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    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
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  • 122
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 1990-05-18
    Beschreibung: Most proteins destined for export from Escherichia coli are made as precursors containing amino-terminal leader sequences that are essential for export and that are removed during the process. The initial step in export of a subset of proteins, which includes maltose-binding protein, is binding of the precursor by the molecular chaperone SecB. This work shows directly that SecB binds with high affinity to unfolded maltose-binding protein but does not specifically recognize and bind the leader. Rather, the leader modulates folding to expose elements in the remainder of the polypeptide that are recognized by SecB.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Randall, L L -- Topping, T B -- Hardy, S J -- GM 29798/GM/NIGMS NIH HHS/ -- New York, N.Y. -- Science. 1990 May 18;248(4957):860-3.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Biochemistry/Biophysics Program, Washington State University, Pullman 99164-4660.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/2188362" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): *ATP-Binding Cassette Transporters ; Bacterial Proteins/*metabolism ; Binding Sites ; Biological Transport ; Carrier Proteins/*metabolism ; Cytosol/metabolism ; Escherichia coli/*metabolism ; *Escherichia coli Proteins ; Maltose-Binding Proteins ; Molecular Weight ; *Monosaccharide Transport Proteins ; Protein Conformation ; Protein Precursors/*metabolism ; Protein Sorting Signals/*metabolism
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    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
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  • 123
    Publikationsdatum: 1990-07-20
    Beschreibung: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Swalen, J D -- New York, N.Y. -- Science. 1990 Jul 20;249(4966):305-6.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17750113" target="_blank"〉PubMed〈/a〉
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  • 124
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 1990-08-10
    Beschreibung: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Raphals, P -- New York, N.Y. -- Science. 1990 Aug 10;249(4969):619.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/2166338" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): Centers for Disease Control and Prevention (U.S.) ; Eosinophilia/chemically induced/epidemiology/*etiology ; Humans ; Muscular Diseases/chemically induced/epidemiology/*etiology ; New Mexico ; Pain/physiopathology ; Syndrome ; Tryptophan/*adverse effects ; United States
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  • 125
    Publikationsdatum: 1990-08-17
    Beschreibung: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉L, K -- New York, N.Y. -- Science. 1990 Aug 17;249(4970):809.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17756795" target="_blank"〉PubMed〈/a〉
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    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
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  • 126
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 1990-08-10
    Beschreibung: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉New York, N.Y. -- Science. 1990 Aug 10;249(4969):623.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17831951" target="_blank"〉PubMed〈/a〉
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    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
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  • 127
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 1990-03-16
    Beschreibung: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Brown, A -- New York, N.Y. -- Science. 1990 Mar 16;247(4948):1281.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17843777" target="_blank"〉PubMed〈/a〉
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    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
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  • 128
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 1990-05-18
    Beschreibung: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Hamilton, D P -- New York, N.Y. -- Science. 1990 May 18;248(4957):807-8.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17811819" target="_blank"〉PubMed〈/a〉
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    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
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  • 129
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 1990-02-02
    Beschreibung: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉New York, N.Y. -- Science. 1990 Feb 2;247(4942):579.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17743994" target="_blank"〉PubMed〈/a〉
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    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
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  • 130
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 1990-03-23
    Beschreibung: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Swan, H T -- New York, N.Y. -- Science. 1990 Mar 23;247(4949 Pt 1):1387-8.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/2181661" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): Anti-Bacterial Agents/*history ; Great Britain ; History, 20th Century ; Penicillins/history ; United States
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  • 131
    Publikationsdatum: 1990-06-29
    Beschreibung: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉L, K -- New York, N.Y. -- Science. 1990 Jun 29;248(4963):1670.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17746508" target="_blank"〉PubMed〈/a〉
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    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
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  • 132
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 1990-07-27
    Beschreibung: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉New York, N.Y. -- Science. 1990 Jul 27;249(4967):358.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17755933" target="_blank"〉PubMed〈/a〉
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    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
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  • 133
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 1990-10-05
    Beschreibung: Developed for the oil industry, well logging instrumentation based on electrical, acoustic, and nuclear measurements has been providing information about the localization and evaluation of hydrocarbon-bearing strata for petroleum geologists and engineers since 1927. This method of exploring properties of the earth's crust without taking physical samples is attracting a growing audience of geologists and geophysicists because of recent developments that permit nondestructive measurements of subsurface geochemistry. A combination of nuclear measurement techniques, which use gamma ray and neutron sources, can provide detailed information on rock composition of interest to both industry and academia.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Ellis, D V -- New York, N.Y. -- Science. 1990 Oct 5;250(4977):82-7.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17808238" target="_blank"〉PubMed〈/a〉
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    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
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  • 134
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 1990-05-25
    Beschreibung: The present understanding of the atmosphere and surface conditions on Saturn's largest moon, Titan, including the stability of methane, and an application of thermodynamics leads to a strong prediction of liquid hydrocarbons in an ethane-methane mixture on the surface. Such a surface would have nearly unique microwave reflection properties due to the low dielectric constant. Attempts were made to obtain reflections at a wavelength of 3.5 centimeters by means of a 70-meter antenna in California as the transmitter and the Very Large Array in New Mexico as the receiving instrument. Statistically significant echoes were obtained that show Titan is not covered with a deep, global ocean of ethane, as previously thought. The experiment yielded radar cross sections normalized by the Titan disk of 0.38 +/- 0.15, 0.78 +/- 0.15, and 0.25 +/- 0.15 on three consecutive nights during which the sub-Earth longitude on Titan moved 50 degrees. The result for the combined data for the entire experiment is 0.35 +/- 0.08. The cross sections are very high, most consistent with those of the Galilean satellites; no evidence of the putative liquid ethane was seen in the reflection data. A global ocean as shallow as about 200 meters would have exhibited reflectivities smaller by an order of magnitude, and below the detection limit of the experiment. The measured emissivity at similar wavelengths of about 0.9 is somewhat inconsistent with the high reflectivity.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Muhleman, D O -- Grossman, A W -- Butler, B J -- Slade, M A -- New York, N.Y. -- Science. 1990 May 25;248(4958):975-80.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17745402" target="_blank"〉PubMed〈/a〉
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  • 135
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 1990-07-27
    Beschreibung: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉New York, N.Y. -- Science. 1990 Jul 27;249(4967):358.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17755932" target="_blank"〉PubMed〈/a〉
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    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
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  • 136
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 1990-08-31
    Beschreibung: The protein encoded by the wild-type p53 proto-oncogene has been shown to suppress transformation, whereas certain mutations that alter p53 become transformation competent. Fusion proteins between p53 and the GAL4 DNA binding domain were made to anchor p53 to a DNA target sequence and to allow measurement of transcriptional activation of a reporter plasmid. The wild-type p53 stimulated transcription in this assay, but two transforming mutations in p53 were unable to act as transcriptional activators. Therefore, p53 can activate transcription, and transformation-activating mutations result in a loss of function of the p53 protein. The inability of the p53 mutant proteins to activate transcription may enable them to be transformation competent.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2935288/" target="_blank"〉〈img src="https://static.pubmed.gov/portal/portal3rc.fcgi/4089621/img/3977009" border="0"〉〈/a〉   〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2935288/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Raycroft, L -- Wu, H Y -- Lozano, G -- CA16672/CA/NCI NIH HHS/ -- CA47296/CA/NCI NIH HHS/ -- R01 CA047296/CA/NCI NIH HHS/ -- R01 CA047296-12/CA/NCI NIH HHS/ -- New York, N.Y. -- Science. 1990 Aug 31;249(4972):1049-51.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉University of Texas, M. D. Anderson Cancer Center, Department of Molecular Genetics, Houston 77030.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/2144364" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): Base Sequence ; *Cell Transformation, Neoplastic ; *Gene Expression Regulation ; HeLa Cells/metabolism ; Humans ; Molecular Sequence Data ; *Mutation ; Nuclear Proteins/genetics ; Oligonucleotide Probes ; Oncogene Proteins/*genetics ; Phosphoproteins/*genetics ; *Proto-Oncogenes ; RNA, Messenger/genetics ; Suppression, Genetic ; Transcription Factors/*genetics ; *Transcription, Genetic ; Tumor Suppressor Protein p53
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  • 137
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 1990-11-16
    Beschreibung: Molecular chaperones are a family of unrelated proteins found in all types of cell. They mediate the correct assembly of other polypeptides, but are not components of the mature assembled structures. Chaperones function by binding specifically to interactive protein surfaces that are exposed transiently during many cellular processes and so prevent them from undergoing incorrect interactions that might produce nonfunctional structures. The concept of molecular chaperones originated largely from studies of the chloroplast enzyme rubisco, which fixes carbon dioxide in plant photosynthesis; the function of chaperones forces a rethinking of the principle of protein self-assembly.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Ellis, R J -- New York, N.Y. -- Science. 1990 Nov 16;250(4983):954-9.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17746919" target="_blank"〉PubMed〈/a〉
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  • 138
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 1990-08-31
    Beschreibung: Fire scar and tree growth chronologies (1700 to 1905) and fire statistics (since 1905) from Arizona and New Mexico show that small areas burn after wet springs associated with the low phase of the Southern Oscillation (SO), whereas large areas burn after dry springs associated with the high phase of the SO. Through its synergistic influence on spring weather and fuel conditions, climatic variability in the tropical Pacific significantly influences vegetation dynamics in the southwestern United States. Synchrony of fire-free and severe fire years across diverse southwestern forests implies that climate forces fire regimes on a subcontinental scale; it also underscores the importance of exogenous factors in ecosystem dynamics.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Swetnam, T W -- Betancourt, J L -- New York, N.Y. -- Science. 1990 Aug 31;249(4972):1017-20.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17789609" target="_blank"〉PubMed〈/a〉
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  • 139
    Publikationsdatum: 1990-04-20
    Beschreibung: The attenuation of upper crustal seismic waves that are refracted with a velocity of about 6 kilometers per second varies greatly among profiles in the area of the New Madrid seismic zone in the central Mississippi Valley. The waves that have the strongest attenuation pass through the seismic trend along the axis of the Reelfoot rift in the area of the Blytheville arch. Defocusing of the waves in a low-velocity zone and/or seismic scattering and absorption could cause the attenuation; these effects are most likely associated with the highly deformed rocks along the arch. Consequently, strong seismic-wave attenuation may be a useful criterion for identifying seismogenic fault zones.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Hamilton, R M -- Mooney, W D -- New York, N.Y. -- Science. 1990 Apr 20;248(4953):351-4.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17784489" target="_blank"〉PubMed〈/a〉
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  • 140
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 1990-11-02
    Beschreibung: The evolution of biramous appendages in crustaceans is central to the debate on the origin of the arthropods. It is proposed that the biramous limb evolved through the basal fusion of adjacent pairs of ancestrally uniramous appendages. As a result, the existing system of homology, in which uniramous and biramous appendages are considered equivalent, may be invalid. Similarly, the homology of individual body segments between uniramians, such as insects and myriapods, and arthropod groups with biramous limbs is also called into question. Two uniramian segments, or a diplosegment, may be homologous to a single body segment in biramous groups.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Emerson, M J -- Schram, F R -- New York, N.Y. -- Science. 1990 Nov 2;250(4981):667-9.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17810869" target="_blank"〉PubMed〈/a〉
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  • 141
    Publikationsdatum: 1990-05-04
    Beschreibung: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Hamilton, W B -- New York, N.Y. -- Science. 1990 May 4;248(4955):615-6.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17791477" target="_blank"〉PubMed〈/a〉
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  • 142
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 1990-08-17
    Beschreibung: Climate control of nutricline depth in the equatorial Atlantic can be monitored by variations in the abundance of the phytoplankton species Florisphaera profunda. A conceptual model, based on in situ evidence, associates high abundances of F. profunda with a deep nutricline and low abundances with a shallow nutricline. A 200,000-year record of F. profunda relative abundances, obtained from a deep-sea core sited beneath the region of maximum equatorial divergence at 10 degrees W, has 52 percent of its variance centered on the 23,000-year precessional band. Cross-spectral analysis between the signals of F. profunda and sea-surface temperature, independently derived from zooplankton species, shows their 23,000-year cycles to be coherent and nearly in phase. Abundance minima of F. profunda coincide with times of December perihelion, whereas abundance maxima coincide with June perihelion. These relations indicate that nutricline dynamics in the divergence region of the equatorial Atlantic are controlled by variations in the tropical easterlies, forced by the precessional component of orbital insolation, on time scales greater than 10,000 years.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Molfino, B -- McIntyre, A -- New York, N.Y. -- Science. 1990 Aug 17;249(4970):766-9.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17756790" target="_blank"〉PubMed〈/a〉
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  • 143
    Publikationsdatum: 1990-05-18
    Beschreibung: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Zurek, W H -- New York, N.Y. -- Science. 1990 May 18;248(4957):880-1.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17811844" target="_blank"〉PubMed〈/a〉
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  • 144
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 1990-10-12
    Beschreibung: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Dill, K A -- New York, N.Y. -- Science. 1990 Oct 12;250(4978):297-8.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Pharmaceutical Chemistry, School of Pharmacy, University of California, San Francisco 94143.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/2218535" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): Energy Transfer ; Physical Phenomena ; Physics ; *Protein Conformation ; Proteins/*chemistry ; Solutions
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    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
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  • 145
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    Unbekannt
    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 1990-09-07
    Beschreibung: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Emmert, R E -- New York, N.Y. -- Science. 1990 Sep 7;249(4973):1094.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17831969" target="_blank"〉PubMed〈/a〉
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    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
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  • 146
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 1990-01-05
    Beschreibung: A nonlysosomal pathway exists for the degradation of newly synthesized proteins retained within the endoplasmic reticulum (ER). This pathway is extremely selective: whereas some proteins are rapidly degraded, others survive for long periods in the ER. The question of whether this selectivity is due to the presence within the sensitive proteins of definable peptide sequences that are sufficient to target them for degradation has been addressed. Deletion of a carboxyl-terminal sequence, comprising the transmembrane domain and short cytoplasmic tail of the alpha chain of the T cell antigen receptor (TCR-alpha), prevented the rapid degradation of this polypeptide. Fusion of this carboxyl-terminal sequence to the extracellular domain of the Tac antigen, a protein that is normally transported to the cell surface where it survives long-term, resulted in the retention and rapid degradation of the chimeric protein in the ER. Additional mutagenesis revealed that the transmembrane domain of TCR-alpha alone was sufficient to cause degradation within the ER. This degradation was not a direct consequence of retention in the ER, as blocking transport of newly synthesized proteins out of the ER with brefeldin A did not lead to degradation of the normal Tac antigen. It is proposed that a 23-amino acid sequence, comprising the transmembrane domain of TCR-alpha, contains information that determines targeting for degradation within the ER system.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Bonifacino, J S -- Suzuki, C K -- Klausner, R D -- New York, N.Y. -- Science. 1990 Jan 5;247(4938):79-82.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Cell Biology and Metabolism Branch, National Institute of Child Health and Human Development, Bethesda, MD 20892.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/2294595" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): Amino Acid Sequence ; Endoplasmic Reticulum/*metabolism ; Humans ; Molecular Sequence Data ; Peptide Fragments/*metabolism ; Proteins/*metabolism ; Receptors, Antigen, T-Cell/metabolism ; Receptors, Interleukin-2/metabolism
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  • 147
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 1990-05-25
    Beschreibung: Geophysical discontinuities in Earth's upper mantle and experimental data predict the structural transformation of pyroxene to garnet and the solid-state dissolution of pyroxene into garnet with increasing depth. These predictions are indirectly verified by omphacitic pyroxene exsolution in pyropic garnet-bearing xenoliths from a diamondiferous kimberlite. Conditions for silicon in octahedral sites in the original garnets are met at pressures greater than 130 kilobars, placing the origin of these xenoliths at depths of 300 to 400 kilometers. These ultradeep xenoliths support the theory that the 400-km seismic discontinuity is marked by a transition from peridotite to eclogite.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Haggerty, S E -- Sautter, V -- New York, N.Y. -- Science. 1990 May 25;248(4958):993-6.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17745405" target="_blank"〉PubMed〈/a〉
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  • 148
    Publikationsdatum: 1990-04-20
    Beschreibung: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Zwally, H J -- Brenner, A C -- Major, J A -- Bindschadler, R A -- Marsh, J G -- New York, N.Y. -- Science. 1990 Apr 20;248(4953):288-9.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17784469" target="_blank"〉PubMed〈/a〉
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  • 149
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 1990-02-23
    Beschreibung: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉New York, N.Y. -- Science. 1990 Feb 23;247(4945):918.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17776444" target="_blank"〉PubMed〈/a〉
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  • 150
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 1990-08-10
    Beschreibung: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉New York, N.Y. -- Science. 1990 Aug 10;249(4969):623.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17831949" target="_blank"〉PubMed〈/a〉
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  • 151
    Publikationsdatum: 1990-02-16
    Beschreibung: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Price, C A -- New York, N.Y. -- Science. 1990 Feb 16;247(4944):866-7.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17746082" target="_blank"〉PubMed〈/a〉
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    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
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  • 152
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 1990-04-06
    Beschreibung: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Koshland, D E Jr -- New York, N.Y. -- Science. 1990 Apr 6;248(4951):9.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/2321029" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): Health Planning/*economics ; National Health Insurance, United States/*economics ; United States
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    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
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  • 153
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 1990-08-10
    Beschreibung: Heterokaryon studies suggest that senescent and quiescent human diploid fibroblasts (HDF) contain a common inhibitor of entry into S phase. DNA synthesis can be induced in senescent and quiescent HDF by fusing them with cells containing DNA viral oncogenes such as SV40 T antigen, adenovirus E1A, or human papillomavirus E7. Both senescent and quiescent HDF contained the unphosphorylated form (p110Rb) of the retinoblastoma protein, a putative inhibitor of proliferation. After serum stimulation, senescent HDF did not phosphorylate p110Rb and did not enter S phase, whereas quiescent HDF phosphorylated p110Rb and entered S phase. These findings, combined with the observations that T antigen, E1A, and E7 form complexes with, and presumably inactivate, unphosphorylated p110Rb, suggest that failure to phosphorylate p110Rb may be an immediate cause of failure to enter S phase in senescent HDF.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Stein, G H -- Beeson, M -- Gordon, L -- AG 00947/AG/NIA NIH HHS/ -- New York, N.Y. -- Science. 1990 Aug 10;249(4969):666-9.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Molecular, Cellular, and Developmental Biology, University of Colorado, Boulder 80309-0347.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/2166342" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): Adenovirus Early Proteins ; Antigens, Polyomavirus Transforming/genetics ; Cell Division ; Cell Line ; Fibroblasts/cytology/metabolism ; Humans ; Interphase ; Molecular Weight ; Nuclear Proteins/*metabolism ; Oncogene Proteins, Viral/metabolism ; Oncogenes ; Papillomaviridae/genetics ; Phosphoproteins/isolation & purification/*metabolism ; Phosphorylation ; Retinoblastoma Protein ; Simian virus 40/genetics/immunology
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    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
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  • 154
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 1990-06-15
    Beschreibung: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Price, D R -- Challoner, D R -- New York, N.Y. -- Science. 1990 Jun 15;248(4961):1280.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17747507" target="_blank"〉PubMed〈/a〉
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    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
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  • 155
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 1990-11-02
    Beschreibung: Some protein kinases and phosphatases are myristoylated on their amino terminus, which perhaps contributes to subcellular localization or regulation. Glycoprotein CD45, a hematopoietic tyrosine phosphatase, was examined for fatty acid content. The CD45 protein incorporated [3H]myristate, but little [3H]palmitate. The label was not metabolized and reincorporated into amino acids or saccharides, as revealed by peptide maps of CD45 labeled with [3H]myristate, 14C-labeled amino acids, [35S]methionine, or 125I, and glycosidase treatments, respectively. The myristate label was resistant to mild alkaline methanolysis and was found in fatty acid and sphingosine, indicating an unusual form of lipid attachment to CD45.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Takeda, A -- Maizel, A L -- CA 45148/CA/NCI NIH HHS/ -- New York, N.Y. -- Science. 1990 Nov 2;250(4981):676-9.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Pathology, Roger Williams General Hospital, Brown University, Providence, RI 02908.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/2146743" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): Antigens, CD45 ; Antigens, Differentiation/*analysis/metabolism ; Chromatography, Thin Layer ; Fatty Acids/*analysis ; Histocompatibility Antigens/*analysis/metabolism ; Myristic Acid ; Myristic Acids/metabolism ; Palmitic Acid ; Palmitic Acids/metabolism ; Peptide Mapping ; Sphingolipids/metabolism
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  • 156
    Publikationsdatum: 1990-12-07
    Beschreibung: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Erickson, P A -- New York, N.Y. -- Science. 1990 Dec 7;250(4986):1456.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17754993" target="_blank"〉PubMed〈/a〉
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  • 157
    Publikationsdatum: 1990-01-12
    Beschreibung: The murine white spotting locus (W) is allelic with the proto-oncogene c-kit, which encodes a transmembrane tyrosine protein kinase receptor for an unknown ligand. Mutations at the W locus affect various aspects of hematopoiesis and the proliferation and migration of primordial germ cells and melanoblasts during development to varying degrees of severity. The W42 mutation has a particularly severe effect in both the homozygous and the heterozygous states. The molecular basis of the W42 mutation was determined. The c-kit protein products in homozygous mutant mast cells were expressed normally but displayed a defective tyrosine kinase activity in vitro. Nucleotide sequence analysis of mutant complementary DNAs revealed a missense mutation that replaces aspartic acid with asparagine at position 790 in the c-kit protein product. Aspartic acid-790 is a conserved residue in all protein kinases. These results provide an explanation for the dominant nature of the W42 mutation and provide insight into the mechanism of c-kit-mediated signal transduction.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Tan, J C -- Nocka, K -- Ray, P -- Traktman, P -- Besmer, P -- P01-CA-16599/CA/NCI NIH HHS/ -- R01-CA-32926/CA/NCI NIH HHS/ -- New York, N.Y. -- Science. 1990 Jan 12;247(4939):209-12.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Molecular Biology Program, Sloan Kettering Institute, New York, NY 10021.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/1688471" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): Amino Acid Sequence ; Animals ; Base Sequence ; Cells, Cultured ; DNA/genetics ; Gene Expression ; Homozygote ; Liver/analysis/cytology/embryology ; Mast Cells/metabolism ; Mice ; Molecular Sequence Data ; *Mutation ; *Phenotype ; Polymerase Chain Reaction ; Protein-Tyrosine Kinases/*genetics ; Proto-Oncogene Proteins/*genetics ; Proto-Oncogene Proteins c-kit ; RNA/analysis ; Receptors, Cell Surface/genetics ; Signal Transduction
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    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
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  • 158
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 1990-07-06
    Beschreibung: The structure of the complex formed between the intercalating agent proflavine and fibrous native DNA was studied by one- and two-dimensional high-resolution solid-state nuclear magnetic resonance (NMR). Carbon-13-labeled proflavine was used to show that the drug is stacked with the aromatic ring plane perpendicular to the fiber axis and that it is essentially immobile. Natural abundance carbon-13 NMR of the DNA itself shows that proflavine binding does not change the puckering of the deoxyribose ring. However, phosphorus-31 NMR spectra show profound changes in the orientation of the phosphodiester grouping on proflavine binding, with some of the phosphodiesters tilting almost parallel to the helix axis, and a second set almost perpendicular. The first group to the phosphodiesters probably spans the intercalation sites, whereas the tilting of the second set likely compensates for the unwinding of the DNA by the intercalator.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Tang, P -- Juang, C L -- Harbison, G S -- GM-39071/GM/NIGMS NIH HHS/ -- New York, N.Y. -- Science. 1990 Jul 6;249(4964):70-2.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Chemistry, State University of New York, Stony Brook 11794-3400.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/2367853" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): Acridines/*analysis ; DNA/*analysis ; Intercalating Agents/*analysis ; Magnetic Resonance Spectroscopy ; Molecular Structure ; Nucleic Acid Conformation ; Proflavine/*analysis
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  • 159
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 1990-01-26
    Beschreibung: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉New York, N.Y. -- Science. 1990 Jan 26;247(4941):407.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17788601" target="_blank"〉PubMed〈/a〉
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    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
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  • 160
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 1990-07-20
    Beschreibung: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉New York, N.Y. -- Science. 1990 Jul 20;249(4966):244.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17750103" target="_blank"〉PubMed〈/a〉
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  • 161
    Publikationsdatum: 1990-10-12
    Beschreibung: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Reiner, A -- New York, N.Y. -- Science. 1990 Oct 12;250(4978):303-5.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17797318" target="_blank"〉PubMed〈/a〉
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    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
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  • 162
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 1990-10-26
    Beschreibung: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Tanner, P -- New York, N.Y. -- Science. 1990 Oct 26;250(4980):493.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17751467" target="_blank"〉PubMed〈/a〉
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    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
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  • 163
    Publikationsdatum: 1990-02-09
    Beschreibung: Simulations of carbon storage suggest that conversion of old-growth forests to young fast-growing forests will not decrease atmospheric carbon dioxide (CO(2)) in general, as has been suggested recently. During simulated timber harvest, on-site carbon storage is reduced considerably and does not approach old-growth storage capacity for at least 200 years. Even when sequestration of carbon in wooden buildings is included in the models, timber harvest results in a net flux of CO(2) to the atmosphere. To offset this effect, the production of lumber and other long-term wood products, as well as the life-span of buildings, would have to increase markedly. Mass balance calculations indicate that the conversion of 5 x 10(9) to 1.8 x 10(9) megagrams of carbon to the atmosphere.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Harmon, M E -- Ferrell, W K -- Franklin, J F -- New York, N.Y. -- Science. 1990 Feb 9;247(4943):699-702.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17771887" target="_blank"〉PubMed〈/a〉
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  • 164
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 1990-07-20
    Beschreibung: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉New York, N.Y. -- Science. 1990 Jul 20;249(4966):244.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17750102" target="_blank"〉PubMed〈/a〉
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  • 165
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 1990-01-26
    Beschreibung: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉New York, N.Y. -- Science. 1990 Jan 26;247(4941):406.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17788599" target="_blank"〉PubMed〈/a〉
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  • 166
    Publikationsdatum: 1990-06-22
    Beschreibung: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Harrison, L G -- New York, N.Y. -- Science. 1990 Jun 22;248(4962):1562-3.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17818317" target="_blank"〉PubMed〈/a〉
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  • 167
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 1990-06-01
    Beschreibung: In many organisms, interactions between cells play a critical role in the specification of cell fates. In the sea urchin embryo, primary mesenchyme cells (PMCs) regulate the developmental program of a subpopulation of secondary mesenchyme cells (SMCs). The timing of this cell interaction was analyzed by means of a fluorescence photoablation technique, which was used to specifically ablate PMCs at various stages of development. In addition, the PMCs were microinjected into PMC-depleted recipient embryos at different developmental stages and their effect on SMC fate was examined. The critical interaction between PMCs and SMCs was brief and took place late in gastrulation. Before that time, SMCs were insensitive to the suppressive signals transmitted by the PMCs.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Ettensohn, C A -- HD24690/HD/NICHD NIH HHS/ -- New York, N.Y. -- Science. 1990 Jun 1;248(4959):1115-8.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Biological Sciences, Carnegie Mellon University, Pittsburgh, PA 15213.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/2188366" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): Animals ; Cell Communication/*physiology ; Cell Survival/radiation effects ; Fluorescent Antibody Technique ; Fluorescent Dyes ; Light ; Mesoderm/*cytology/radiation effects ; Microinjections ; Rhodamines ; Sea Urchins/embryology
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  • 168
    Publikationsdatum: 1990-07-27
    Beschreibung: There is currently a need for vaccine development to improve the immunogenicity of protective epitopes, which themselves are often poorly immunogenic. Although the immunogenicity of these epitopes can be enhanced by linking them to highly immunogenic carriers, such carriers derived from current vaccines have not proven to be generally effective. One reason may be related to epitope-specific suppression, in which prior vaccination with a protein can inhibit the antibody response to new epitopes linked to the protein. To circumvent such inhibition, a peptide from tetanus toxoid was identified that, when linked to a B cell epitope and injected into tetanus toxoid-primed recipients, retained sequences for carrier but not suppressor function. The antibody response to the B cell epitope was enhanced. This may be a general method for taking advantage of previous vaccinations in the development of new vaccines.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Etlinger, H M -- Gillessen, D -- Lahm, H W -- Matile, H -- Schonfeld, H J -- Trzeciak, A -- New York, N.Y. -- Science. 1990 Jul 27;249(4967):423-5.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Central Research Unit F. Hoffmann-La Roche, Basel, Switzerland.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/1696030" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): Amino Acid Sequence ; Animals ; Antigens, Protozoan/*immunology ; B-Lymphocytes/immunology ; Epitopes/*immunology ; Humans ; Mice ; Mice, Inbred BALB C ; Molecular Sequence Data ; Peptide Fragments/immunology ; Plasmodium falciparum/*immunology ; T-Lymphocytes/immunology ; T-Lymphocytes, Helper-Inducer/immunology ; T-Lymphocytes, Regulatory/immunology ; Tetanus Toxoid/*immunology ; *Vaccination ; Vaccines/*immunology
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  • 169
    Publikationsdatum: 1990-03-30
    Beschreibung: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉L, K -- New York, N.Y. -- Science. 1990 Mar 30;247(4950):1594.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17782817" target="_blank"〉PubMed〈/a〉
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  • 170
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 1990-06-01
    Beschreibung: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Reilly, W K -- New York, N.Y. -- Science. 1990 Jun 1;248(4959):1064-5.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17733354" target="_blank"〉PubMed〈/a〉
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  • 171
    Publikationsdatum: 1990-02-16
    Beschreibung: The complex formed in solution by native and chemically modified cytochrome c with cytochrome b5 has been studied by 1H and 13C nuclear magnetic resonance spectroscopy (NMR). Contrary to predictions of recent theoretical analysis, 1H NMR spectroscopy indicates that there is no major movement of cytochrome c residue Phe82 on binding to cytochrome b5. The greater resolution provided by 13C NMR spectroscopy permits detection of small perturbations in the environments of cytochrome c residues Ile75 and Ile85 on binding with cytochrome b5, a result that is in agreement with earlier model-building experiments. As individual cytochrome c lysyl residues are resolved in the 1H NMR spectrum of N-acetimidylated cytochrome c, the interaction of this modified protein with cytochrome b5 has been studied to evaluate the number of cytochrome c lysyl residues involved in binding to cytochrome b5. The results of this experiment indicate that at least six lysyl residues are involved, two more than predicted by static model building, which indicates that cytochrome c and cytochrome b5 form two or more structurally similar 1:1 complexes in solution.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Burch, A M -- Rigby, S E -- Funk, W D -- MacGillivray, R T -- Mauk, M R -- Mauk, A G -- Moore, G R -- GM-28834/GM/NIGMS NIH HHS/ -- New York, N.Y. -- Science. 1990 Feb 16;247(4944):831-3.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉School of Chemical Sciences, University of East Anglia, Norwich, United Kingdom.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/2154849" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): Carbon Isotopes ; Cytochrome c Group/*metabolism ; Cytochromes b5/*metabolism ; Hydrogen ; Magnetic Resonance Spectroscopy/methods ; Protein Binding ; Protein Conformation ; Surface Properties
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  • 172
    Publikationsdatum: 1990-06-01
    Beschreibung: The amyloid beta peptide (A beta P) is a small fragment of the much larger, broadly distributed amyloid precursor protein (APP). Abundant A beta P deposition in the brains of patients with Alzheimer's disease suggests that altered APP processing may represent a key pathogenic event. Direct protein structural analyses showed that constitutive processing in human embryonic kidney 293 cells cleaves APP in the interior of the A beta P, thus preventing A beta P deposition. A deficiency of this processing event may ultimately prove to be the etiological event in Alzheimer's disease that gives rise to senile plaque formation.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Esch, F S -- Keim, P S -- Beattie, E C -- Blacher, R W -- Culwell, A R -- Oltersdorf, T -- McClure, D -- Ward, P J -- New York, N.Y. -- Science. 1990 Jun 1;248(4959):1122-4.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Athena Neurosciences, Incorporated, South San Francisco, CA 94080.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/2111583" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): Amino Acid Sequence ; Amyloid/isolation & purification/*metabolism ; Amyloid beta-Protein Precursor ; Humans ; Molecular Sequence Data ; Peptide Fragments/isolation & purification ; Protein Precursors/isolation & purification/*metabolism ; Protein Processing, Post-Translational/*physiology ; Transfection
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  • 173
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 1990-08-10
    Beschreibung: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉New York, N.Y. -- Science. 1990 Aug 10;249(4969):622.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17831947" target="_blank"〉PubMed〈/a〉
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  • 174
    Publikationsdatum: 1990-09-28
    Beschreibung: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Proffitt, D R -- New York, N.Y. -- Science. 1990 Sep 28;249(4976):1590-1.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17748728" target="_blank"〉PubMed〈/a〉
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  • 175
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 1990-08-10
    Beschreibung: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉New York, N.Y. -- Science. 1990 Aug 10;249(4969):622.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17831946" target="_blank"〉PubMed〈/a〉
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  • 176
    Publikationsdatum: 1990-04-27
    Beschreibung: Molecular dynamics simulations and atomic force microscopy are used to investigate the atomistic mechanisms of adhesion, contact formation, nanoindentation, separation, and fracture that occur when a nickel tip interacts with a gold surface. The theoretically predicted and experimentally measured hysteresis in the force versus tip-to-sample distance relationship, found upon approach and subsequent separation of the tip from the sample, is related to inelastic deformation of the sample surface characterized by adhesion of gold atoms to the nickel tip and formation of a connective neck of atoms. At small tipsample distances, mechanical instability causes the tip and surface to jump-to-contact, which in turn leads to adhesion-induced wetting of the nickel tip by gold atoms. Subsequent indentation of the substrate results in the onset of plastic deformation of the gold surface. The atomic-scale mechanisms underlying the formation and elongation of a connective neck, which forms upon separation, consist of structural transformations involving elastic and yielding stages.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Landman, U -- Luedtke, W D -- Burnham, N A -- Colton, R J -- New York, N.Y. -- Science. 1990 Apr 27;248(4954):454-61.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17815594" target="_blank"〉PubMed〈/a〉
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  • 177
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 1990-09-21
    Beschreibung: Nonobese diabetic (NOD) mice develop an autoimmune form of diabetes, becoming hyperglycemic after 3 months of age. This process was accelerated by injecting young NOD mice with CD4+ islet-specific T cell clones derived from NOD mice. Overt diabetes developed in 10 of 19 experimental animals by 7 weeks of age, with the remaining mice showing marked signs of the disease in progress. Control mice did not become diabetic and had no significant pancreatic infiltration. This work demonstrates that a CD4 T cell clone is sufficient to initiate the disease process in the diabetes-prone NOD mouse.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Haskins, K -- McDuffie, M -- P01 DK40144/DK/NIDDK NIH HHS/ -- New York, N.Y. -- Science. 1990 Sep 21;249(4975):1433-6.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Barbara Davis Center for Childhood Diabetes, University of Colorado Health Sciences Center, Denver 80262.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/2205920" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): Animals ; Antigens, CD4/analysis/*immunology ; Clone Cells ; Diabetes Mellitus, Experimental/*immunology/pathology ; Female ; Islets of Langerhans/*immunology/pathology ; Male ; Mice ; Mice, Inbred Strains ; Mice, Mutant Strains ; T-Lymphocytes/*immunology/transplantation
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  • 178
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 1990-02-16
    Beschreibung: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Koshland, D E Jr -- New York, N.Y. -- Science. 1990 Feb 16;247(4944):777.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/2305247" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): Environmental Pollution/legislation & jurisprudence/*prevention & control ; United States ; United States Environmental Protection Agency
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  • 179
    Publikationsdatum: 1990-10-05
    Beschreibung: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Burke, K -- New York, N.Y. -- Science. 1990 Oct 5;250(4977):145.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17808249" target="_blank"〉PubMed〈/a〉
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  • 180
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 1990-03-16
    Beschreibung: The role of troponin-I (the inhibitory subunit of troponin) in the regulation by Ca2+ of skeletal muscle contraction was investigated with resonance energy transfer and photo cross-linking techniques. The effect of Ca2+ on the proximity of troponin-I to actin in reconstituted rabbit skeletal thin filaments was determined. The distance between the cysteine residue at position 133 (Cys133) of troponin-I and Cys374 of actin increases by approximately 15 angstroms on binding of Ca2+ to troponin-C. Also, troponin-I labeled at Cys133 with benzophenone-4-maleimide could be photo cross-linked to actin in the absence of Ca2+, but not in its presence. These results suggest that troponin-I is attached to actin in the Ca2(+)-free or relaxed state of muscle, and that it detaches from actin on Ca2+ activation of contraction. Thus, troponin-I may function as a Ca2(+)-dependent molecular switch in regulation of skeletal muscle contraction.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Tao, T -- Gong, B J -- Leavis, P C -- AR21673/AR/NIAMS NIH HHS/ -- HL20464/HL/NHLBI NIH HHS/ -- New York, N.Y. -- Science. 1990 Mar 16;247(4948):1339-41.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Muscle Research, Boston Biomedical Research Institute, MA 02114.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/2138356" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): Actins/*physiology ; Ca(2+) Mg(2+)-ATPase/metabolism ; Calcium/*physiology ; Cysteine ; In Vitro Techniques ; *Muscle Contraction ; Muscles/*physiology ; Myosins/metabolism ; Spectrometry, Fluorescence ; Troponin/*physiology ; Troponin I
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  • 181
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 1990-04-27
    Beschreibung: Light-dependent expression of rbcS, the gene encoding the small subunit of ribulose-1,5-bisphosphate carboxylase, which is the key enzyme involved in carbon fixation in higher plants, is regulated at the transcriptional level. Sequence analysis of the gene has uncovered a conserved GT motif in the -150 to -100 region of many rbcS promoters. This motif serves as the binding site of a nuclear factor, designated GT-1. Analysis of site-specific mutants of pea rbcS-3A promoter demonstrated that GT-1 binding in vitro is correlated with light-responsive expression of the rbcS promoter in transgenic plants. However, it is not known whether factors other than GT-1 might also be required for activation of transcription by light. A synthetic tetramer of box II (TGTGTGGTTAATATG), the GT-1 binding site located between -152 to -138 of the rbcS-3A promoter, inserted upstream of a truncated cauliflower mosaic virus 35S promoter is sufficient to confer expression in leaves of transgenic tobacco. This expression occurs principally in chloroplast-containing cells, is induced by light, and is correlated with the ability of box II to bind GT-1 in vitro. The data show that the binding site for GT-1 is likely to be a part of the molecular light switch for rbcS activation.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Lam, E -- Chua, N H -- New York, N.Y. -- Science. 1990 Apr 27;248(4954):471-4.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Laboratory of Plant Molecular Biology, Rockefeller University, New York, NY 10021.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/2330508" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): Base Sequence ; Binding Sites ; Chloramphenicol O-Acetyltransferase/genetics ; Cloning, Molecular ; DNA-Binding Proteins/*metabolism ; Gene Expression Regulation/*physiology ; Genetic Vectors ; *Light ; Molecular Sequence Data ; Mutation ; Nuclear Proteins/*metabolism ; Plant Proteins/*metabolism ; *Plants, Toxic ; Promoter Regions, Genetic/genetics ; Ribulose-Bisphosphate Carboxylase/*genetics ; Tobacco/enzymology/*genetics ; Transcription, Genetic/radiation effects ; Transformation, Genetic
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  • 182
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 1990-08-10
    Beschreibung: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉New York, N.Y. -- Science. 1990 Aug 10;249(4969):622.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17831945" target="_blank"〉PubMed〈/a〉
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  • 183
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 1990-12-14
    Beschreibung: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Bouchard, T J -- Lykken, D T -- McGue, M -- Segal, N -- Tellegen, A -- New York, N.Y. -- Science. 1990 Dec 14;250(4987):1498.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/2274774" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): *Genetic Variation ; Genotype ; Humans ; *Intelligence ; Intelligence Tests ; Twins, Monozygotic/*genetics
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    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
    Standort Signatur Erwartet Verfügbarkeit
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  • 184
    Publikationsdatum: 1990-06-22
    Beschreibung: Human platelet-derived growth factor (PDGF) is a connective tissue cell mitogen comprised of two related chains encoded by distinct genes. The B chain is the homolog of the v-sis oncogene product. Properties that distinguish these ligands include greater transforming potency of the B chain and more efficient secretion of the A chain. By a strategy involving the generation of PDGF A and B chimeras, these properties were mapped to distinct domains of the respective molecules. Increased transforming efficiency segregated with the ability to activate both alpha and beta PDGF receptors. These findings genetically map PDGF B residues 105 to 144 as responsible for conformational alterations critical to beta PDGF receptor interaction and provide a mechanistic basis for the greater transforming potency of the PDGF B chain.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉LaRochelle, W J -- Giese, N -- May-Siroff, M -- Robbins, K C -- Aaronson, S A -- New York, N.Y. -- Science. 1990 Jun 22;248(4962):1541-4.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Laboratory of Cellular and Molecular Biology, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/2163109" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): Cell Line, Transformed ; *Cell Transformation, Neoplastic ; Chimera ; Genetic Vectors ; Humans ; Ligands ; Platelet-Derived Growth Factor/*genetics/physiology/secretion ; Precipitin Tests ; Proto-Oncogene Proteins/*genetics/physiology ; Proto-Oncogene Proteins c-sis ; Receptors, Cell Surface/genetics ; Receptors, Platelet-Derived Growth Factor ; Transfection
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    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
    Standort Signatur Erwartet Verfügbarkeit
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  • 185
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 1990-07-13
    Beschreibung: Some animals have larger brains than others, but it is not yet known why. Species differences in life-style, including dietary habits and patterns of development of the young, are associated with variation in brain weight, independently of the effects of body weight and evolutionary history. Taken together with behavioral and neuroanatomical analyses, these studies begin to suggest the evolutionary pressures that favor different sized brains and brain components.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Harvey, P H -- Krebs, J R -- New York, N.Y. -- Science. 1990 Jul 13;249(4965):140-6.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Zoology, University of Oxford, United Kingdom.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/2196673" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): Animals ; *Biological Evolution ; Body Weight ; Brain/*anatomy & histology ; Humans ; Organ Size
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    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
    Standort Signatur Erwartet Verfügbarkeit
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  • 186
    facet.materialart.
    Unbekannt
    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 1990-08-03
    Beschreibung: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Taubes, G -- New York, N.Y. -- Science. 1990 Aug 3;249(4968):464-5.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17735269" target="_blank"〉PubMed〈/a〉
    Print ISSN: 0036-8075
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    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
    Standort Signatur Erwartet Verfügbarkeit
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  • 187
    Publikationsdatum: 1990-06-29
    Beschreibung: The human immunodeficiency virus (HIV) tat protein (Tat) is a positive regulator of virus gene expression and replication. Biotinylated Tat was used as a probe to screen a lambda gt11 fusion protein library, and a complementary DNA encoding a protein that interacts with Tat was cloned. Expression of this protein, designated TBP-1 (for Tat binding protein-1), was observed in a variety of cell lines, with expression being highest in human cells. TBP-1 was localized predominantly in the nucleus, which is consistent with the nuclear localization of Tat. In cotransfection experiments, expression of TBP-1 was able to specifically suppress Tat-mediated transactivation. The strategy described may be useful for direct identification and cloning of genes encoding proteins that associate with other proteins to modulate their activity in a positive or negative fashion.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Nelbock, P -- Dillon, P J -- Perkins, A -- Rosen, C A -- New York, N.Y. -- Science. 1990 Jun 29;248(4963):1650-3.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Molecular Oncology and Virology, Roche Institute of Molecular Biology, Hoffmann-La Roche Inc., Nutley, NJ 07110.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/2194290" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): Amino Acid Sequence ; Animals ; Cell Line ; Cloning, Molecular ; DNA, Neoplasm/genetics ; DNA-Binding Proteins/*genetics/metabolism ; Escherichia coli/genetics ; Gene Expression ; Gene Library ; Gene Products, tat/*metabolism ; HIV/genetics ; Humans ; Molecular Sequence Data ; Plasmids ; Polymerase Chain Reaction ; *Proteasome Endopeptidase Complex ; Recombinant Fusion Proteins/metabolism ; Trans-Activators/*metabolism ; Transcriptional Activation ; Transfection ; tat Gene Products, Human Immunodeficiency Virus
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    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
    Standort Signatur Erwartet Verfügbarkeit
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  • 188
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 1990-01-26
    Beschreibung: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉New York, N.Y. -- Science. 1990 Jan 26;247(4941):405.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17788595" target="_blank"〉PubMed〈/a〉
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    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
    Standort Signatur Erwartet Verfügbarkeit
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  • 189
    Publikationsdatum: 1990-06-29
    Beschreibung: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Nelson, K -- New York, N.Y. -- Science. 1990 Jun 29;248(4963):1669-70.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17746506" target="_blank"〉PubMed〈/a〉
    Print ISSN: 0036-8075
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    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
    Standort Signatur Erwartet Verfügbarkeit
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  • 190
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    Unbekannt
    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 1990-06-22
    Beschreibung: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉C, B J -- New York, N.Y. -- Science. 1990 Jun 22;248(4962):1498.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17818309" target="_blank"〉PubMed〈/a〉
    Print ISSN: 0036-8075
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    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
    Standort Signatur Erwartet Verfügbarkeit
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  • 191
    Publikationsdatum: 1990-03-02
    Beschreibung: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Temple, S A -- New York, N.Y. -- Science. 1990 Mar 2;247(4946):1128.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17800079" target="_blank"〉PubMed〈/a〉
    Print ISSN: 0036-8075
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    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
    Standort Signatur Erwartet Verfügbarkeit
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  • 192
    facet.materialart.
    Unbekannt
    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 1990-08-10
    Beschreibung: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Newton, C R -- New York, N.Y. -- Science. 1990 Aug 10;249(4969):681-3.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17831960" target="_blank"〉PubMed〈/a〉
    Print ISSN: 0036-8075
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    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
    Standort Signatur Erwartet Verfügbarkeit
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  • 193
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 1990-01-05
    Beschreibung: Feeding behavior of Aplysia is associated with an arousal state characterized by a constellation of maintained behaviors and by a potentiation or depression of responses to specific stimuli. A neuron (the cerebral-pedal regulator or CPR) that has widespread actions on various systems connected with feeding has been identified. CPR excites neurons that modulate or drive (i) body posture, (ii) biting, and (iii) cardiovascular behaviors. CPR also inhibits neurons concerned with defensive responses. Food stimuli, which elicit food arousal in the animal, produce prolonged excitation of the CPR. The results suggest that the CPR may evoke a central motive state representing the neuronal correlate of feeding motivation.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Teyke, T -- Weiss, K R -- Kupfermann, I -- GM-320099/GM/NIGMS NIH HHS/ -- MH 35564/MH/NIMH NIH HHS/ -- New York, N.Y. -- Science. 1990 Jan 5;247(4938):85-7.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Center for Neurobiology and Behavior, College of Physicians and Surgeons, Columbia University, New York, NY 10032.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/2294596" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): Animals ; Aplysia/*physiology ; Arousal/physiology ; Cardiovascular Physiological Phenomena ; Feeding Behavior/physiology ; Muscles/physiology ; Neurons/*physiology
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    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
    Standort Signatur Erwartet Verfügbarkeit
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  • 194
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    Unbekannt
    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 1990-10-05
    Beschreibung: Silicified peritidal carbonate rocks of the 1250- to 750-million-year-old Hunting Formation, Somerset Island, arctic Canada, contain fossils of well-preserved bangiophyte red algae. Morphological details, especially the presence of multiseriate filaments composed of radially arranged wedge-shaped cells derived by longitudinal divisions from disc-shaped cells in uniseriate filaments, indicate that the fossils are related to extant species in the genus Bangia. Such taxonomic resolution distinguishes these fossils from other pre-Ediacaran eukaryotes and contributes to growing evidence that multicellular algae diversified well before the Ediacaran radiation of large animals.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Butterfield, N J -- Knoll, A H -- Swett, K -- New York, N.Y. -- Science. 1990 Oct 5;250:104-7.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Botanical Museum, Harvard University, Cambridge, MA 02138, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/11538072" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): *Biological Evolution ; Canada ; *Fossils ; Geological Phenomena ; Geology ; Paleontology ; Rhodophyta/*classification/cytology
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    Standort Signatur Erwartet Verfügbarkeit
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  • 195
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 1990-09-21
    Beschreibung: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Lauterbur, P C -- Burke, J E -- New York, N.Y. -- Science. 1990 Sep 21;249(4975):1375.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17812160" target="_blank"〉PubMed〈/a〉
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    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
    Standort Signatur Erwartet Verfügbarkeit
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  • 196
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 1990-01-19
    Beschreibung: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Leakey, R E -- New York, N.Y. -- Science. 1990 Jan 19;247(4940):271.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17735827" target="_blank"〉PubMed〈/a〉
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    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
    Standort Signatur Erwartet Verfügbarkeit
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  • 197
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    Unbekannt
    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 1990-08-17
    Beschreibung: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Nicholson, R S -- New York, N.Y. -- Science. 1990 Aug 17;249(4970):721.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17756769" target="_blank"〉PubMed〈/a〉
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    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
    Standort Signatur Erwartet Verfügbarkeit
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  • 198
    Publikationsdatum: 1990-08-03
    Beschreibung: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Ritter, R C -- New York, N.Y. -- Science. 1990 Aug 3;249(4968):572.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17735294" target="_blank"〉PubMed〈/a〉
    Print ISSN: 0036-8075
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    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
    Standort Signatur Erwartet Verfügbarkeit
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  • 199
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    Unbekannt
    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 1990-10-12
    Beschreibung: Europa and Ganymede may have undergone an episode of chaotic motion before the establishment of the current Laplace resonance involving the three inner Galilean satellites. During this episode, the orbital eccentricities of both satellites may have increased dramatically. As a result, the mechanical stresses due to tidal deformation of the satellites' icy lithospheres may have been large enough to result in extensive fracturing, and tidal heating may have melted water ice in the mantles of both satellites, triggering the geological activity that has modified their surfaces since the heavy cratering period. The tidal effects on Ganymede during this episode provide an explanation of the dichotomy between it and Callisto, which have similar bulk properties but very different geological histories.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Tittemore, W C -- New York, N.Y. -- Science. 1990 Oct 12;250(4978):263-7.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17797308" target="_blank"〉PubMed〈/a〉
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    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
    Standort Signatur Erwartet Verfügbarkeit
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  • 200
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    Unbekannt
    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 1990-01-19
    Beschreibung: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉New York, N.Y. -- Science. 1990 Jan 19;247(4940):284.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17735840" target="_blank"〉PubMed〈/a〉
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    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
    Standort Signatur Erwartet Verfügbarkeit
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