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  • Chemistry  (10,474)
  • Biochemistry and Biotechnology  (670)
  • Humans  (564)
  • FLUID MECHANICS AND HEAT TRANSFER
  • Fisheries
  • LUNAR AND PLANETARY EXPLORATION
  • Surface physics, nanoscale physics, low-dimensional systems
  • 2020-2022
  • 1995-1999  (11,042)
  • 1990-1994
  • 1985-1989
  • 1996  (11,042)
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  • 2020-2022
  • 1995-1999  (11,042)
  • 1990-1994
  • 1985-1989
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  • 1
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    In:  CASI
    Publication Date: 2019-07-20
    Description: We have investigated the interaction of Io, Jupiter's innermost Galilean satellite, with the Io plasma torus. The interaction of Io with the plasma surrounding it has been a subject of interest for almost 30 years, dating from the discovery by Bigg (1964) that radio emissions from the Jovian magnetosphere are controlled by Io's position. Since that time, both ground-based and spacecraft observations have shown that Io is a unique satellite that influences the Jovian magnetosphere in important ways. In particular, material from Io is a major source of plasma for the magnetosphere, and the energy that this plasma harnesses from Jupiter's co-rotating magnetic field is an important power source for the magnetosphere. It is apparent that the local interaction of the torus plasma with Io plays a key role in the formation, composition, and energetics of the Io torus; the interaction is also highly nonlinear. We have modeled this interaction using time-dependent three-dimensional magnetohydrodynamic (MHD) simulations. During this past year, we have used NASA support to develop a new MHD code to study the interaction. As part of the Galileo spacecraft's recent successful insertion into orbit around Jupiter, the spacecraft passed within 900 km of Io's surface. Our calculations have focused on using Galileo particles and fields data to examine a question that was not resolved by the Voyager observations: Does Io have an intrinsic magnetic field? In this progress summary, we describe our efforts on this problem to date.
    Keywords: LUNAR AND PLANETARY EXPLORATION
    Type: NASA-CR-200134 , NAS 1.26:200134 , SAIC-95/1381:APPAT-174 , NIPS-96-07877
    Format: application/pdf
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  • 2
    Publication Date: 2019-07-13
    Description: The NPARC Alliance is a partnership between the NASA Lewis Research Center (LeRC) and the USAF Arnold Engineering Development Center (AEDC) dedicated to the establishment of a national CFD capability, centered on the NPARC Navier-Stokes computer program. The three main tasks of the Alliance are user support, code development, and validation. The present paper is a status report on the validation effort. It describes the validation approach being taken by the Alliance. Representative results are presented for laminar and turbulent flat plate boundary layers, a supersonic axisymmetric jet, and a glancing shock/turbulent boundary layer interaction. Cases scheduled to be run in the future are also listed. The archive of validation cases is described, including information on how to access it via the Internet.
    Keywords: FLUID MECHANICS AND HEAT TRANSFER
    Type: NASA-TM-107134 , NAS 1.15:107134 , E-10064 , AIAA PAPER 96-0387 , NIPS-96-08124 , Aerospace Sciences Meeting and Exhibit; Jan 15, 1996 - Jan 18, 1996; Reno, NV; United States
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  • 3
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1996-12-20
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Cohen, J -- New York, N.Y. -- Science. 1996 Dec 20;274(5295):2005.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/8984656" target="_blank"〉PubMed〈/a〉
    Keywords: *AIDS Vaccines ; Acquired Immunodeficiency Syndrome/*prevention & control ; History, 20th Century ; Humans ; National Institutes of Health (U.S.)/*organization & administration ; United States
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 4
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1996-12-20
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉McFarland, H F -- New York, N.Y. -- Science. 1996 Dec 20;274(5295):2037-8.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Neuroimmunology Branch, National Institutes of Health, Bethesda, MD 20892, USA. henrymcf@helix.nih.gov〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/8984662" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Antigens/immunology ; Autoimmune Diseases/immunology/*therapy ; CD8-Positive T-Lymphocytes/*immunology ; Callithrix ; Cytokines/*immunology ; Diabetes Mellitus, Type 1/immunology/therapy ; Encephalomyelitis, Autoimmune, Experimental/immunology/therapy ; Humans ; Immune Tolerance ; Immunotherapy/*adverse effects ; Mice ; Myelin Proteins ; Myelin-Associated Glycoprotein/immunology ; Myelin-Oligodendrocyte Glycoprotein ; Ovalbumin/immunology ; Th1 Cells/*immunology ; Th2 Cells/*immunology
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 5
    Publication Date: 1996-12-20
    Description: The human Kv1.5 potassium channel (hKv1.5) contains proline-rich sequences identical to those that bind to Src homology 3 (SH3) domains. Direct association of the Src tyrosine kinase with cloned hKv1.5 and native hKv1.5 in human myocardium was observed. This interaction was mediated by the proline-rich motif of hKv1.5 and the SH3 domain of Src. Furthermore, hKv1.5 was tyrosine phosphorylated, and the channel current was suppressed, in cells coexpressing v-Src. These results provide direct biochemical evidence for a signaling complex composed of a potassium channel and a protein tyrosine kinase.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Holmes, T C -- Fadool, D A -- Ren, R -- Levitan, I B -- F32 NS009952/NS/NINDS NIH HHS/ -- New York, N.Y. -- Science. 1996 Dec 20;274(5295):2089-91.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Biochemistry and Volen Center for Complex Systems, Brandeis University, Waltham, MA 02254, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/8953041" target="_blank"〉PubMed〈/a〉
    Keywords: Amino Acid Sequence ; Cell Line ; Cloning, Molecular ; Humans ; Kv1.5 Potassium Channel ; Molecular Sequence Data ; Myocardium/chemistry ; Oncogene Protein pp60(v-src)/metabolism ; Patch-Clamp Techniques ; Phosphorylation ; Phosphotyrosine/metabolism ; Potassium Channels/chemistry/*metabolism ; *Potassium Channels, Voltage-Gated ; Recombinant Fusion Proteins/metabolism ; Signal Transduction ; Transfection ; src Homology Domains/*physiology ; src-Family Kinases/chemistry/*metabolism
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 6
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1996-12-20
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Enserink, M -- New York, N.Y. -- Science. 1996 Dec 20;274(5295):2004-5.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/8984655" target="_blank"〉PubMed〈/a〉
    Keywords: Aspirin/*therapeutic use ; Brain Diseases ; Cerebrovascular Disorders/*prevention & control ; Controlled Clinical Trials as Topic/*standards ; Dipyridamole/*therapeutic use ; Drug Therapy, Combination ; Ethics Committees, Research ; *Ethics, Medical ; Europe ; Humans ; Multicenter Studies as Topic ; Placebos ; Platelet Aggregation Inhibitors/*therapeutic use ; Recurrence ; Scientific Misconduct
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 7
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1996-12-20
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Bloom, F E -- New York, N.Y. -- Science. 1996 Dec 20;274(5295):1987.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/8984651" target="_blank"〉PubMed〈/a〉
    Keywords: Anti-HIV Agents/*therapeutic use ; Apoptosis ; Embryonic and Fetal Development ; HIV/*pathogenicity ; *HIV Infections/drug therapy/virology ; Humans ; Receptors, Cytokine/*physiology ; Receptors, HIV/*physiology
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 8
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1996-12-20
    Description: The origin of cholera has been elusive, even though scientific evidence clearly shows it is a waterborne disease. However, standard bacteriological procedures for isolation of the cholera vibrio from environmental samples, including water, between epidemics generally were unsuccessful. Vibrio cholerae, a marine vibrio, requiring salt for growth, enters into a dormant, viable but nonculturable stage when conditions are unfavorable for growth and reproduction. The association of Vibrio cholerae with plankton, notably copepods, provides further evidence for the environmental origin of cholera, as well as an explanation for the sporadic and erratic occurrence of cholera epidemics. On a global scale, cholera epidemics can now be related to climate and climatic events, such as El Nino, as well as the global distribution of the plankton host. Remote sensing, with the use of satellite imagery, offers the potential for predicting conditions conducive to cholera outbreaks or epidemics.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Colwell, R R -- SR01AI 1976-13/AI/NIAID NIH HHS/ -- New York, N.Y. -- Science. 1996 Dec 20;274(5295):2025-31.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉University of Maryland Biotechnology Institute, 4321 Hartwick Road, Suite 550, College Park, MD 20740, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/8953025" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Bangladesh/epidemiology ; Cholera/*epidemiology/history/microbiology/transmission ; *Climate ; Communicable Diseases/*epidemiology ; *Disease Outbreaks/history ; *Global Health ; History, 16th Century ; History, 19th Century ; History, 20th Century ; History, Ancient ; Humans ; Phytoplankton/growth & development ; Vibrio cholerae/classification/immunology/*pathogenicity ; Water Microbiology ; Zooplankton/growth & development/microbiology
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 9
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1996-12-20
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Grady, D -- New York, N.Y. -- Science. 1996 Dec 20;274(5295):2010.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/8984659" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; *Brain Chemistry ; Creutzfeldt-Jakob Syndrome/metabolism ; Humans ; Mice ; Mice, Transgenic ; Prion Diseases/*etiology/metabolism/transmission ; Prions/*chemistry/genetics ; *Protein Conformation ; *Protein Folding
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 10
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1996-12-20
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Balter, M -- New York, N.Y. -- Science. 1996 Dec 20;274(5295):1988-9.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/8984652" target="_blank"〉PubMed〈/a〉
    Keywords: Anti-HIV Agents/*therapeutic use ; Chemokines/physiology ; HIV/drug effects/physiology ; HIV Infections/*drug therapy/*virology ; HIV Protease Inhibitors/*therapeutic use ; Humans ; Membrane Proteins/physiology ; Receptors, CCR5 ; Receptors, CXCR4 ; Receptors, Cytokine/*physiology ; Receptors, HIV/*physiology ; Virus Replication/drug effects
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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