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  • Bücher
  • Artikel  (4)
  • Mice, Inbred C57BL
  • 2010-2014
  • 1980-1984  (4)
  • 1950-1954
  • 1982  (4)
  • Biologie  (4)
  • Geographie
  • 1
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 1982-06-18
    Beschreibung: Responses of auditory neurons in the inferior colliculi of mice were studied longitudinally before and shortly after each animal was exposed to intense noise. Noise exposure caused expected losses in auditory sensitivity, but in 31 percent of the neurons studied, unexpected alterations of temporal patterns of action potentials were observed: certain suprathreshold stimuli that had evoked only transient "onset" responses or inhibition of spontaneous discharges prior to noise exposure came to elicit sustained excitation after exposure. Thus, noise-induced hearing loss can be associated with increases in neural responsivity and alterations of normal neural coding processes.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Willott, J F -- Lu, S M -- New York, N.Y. -- Science. 1982 Jun 18;216(4552):1331-4.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7079767" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): Acoustic Stimulation ; Action Potentials ; Animals ; Evoked Potentials, Auditory ; Hearing Loss, Noise-Induced/*physiopathology ; Inferior Colliculi/*physiopathology ; Mice ; Mice, Inbred C57BL ; Neurons/*physiology
    Print ISSN: 0036-8075
    Digitale ISSN: 1095-9203
    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
    Standort Signatur Erwartet Verfügbarkeit
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  • 2
    Publikationsdatum: 1982-07-09
    Beschreibung: Strain-specific unresponsiveness was induced in adult mice by immunizing them with donor blood treated with antiserum to Ia (I region-associated antigens) prior to the transplantation of islets of Langerhans. This regimen alone produced greater than 100-day survival of islet allografts transplanted across a major histocompatibility barrier.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Faustman, D -- Lacy, P -- Davie, J -- Hauptfeld, V -- AI-12734/AI/NIAID NIH HHS/ -- AM-01226/AM/NIADDK NIH HHS/ -- GM-07200/GM/NIGMS NIH HHS/ -- New York, N.Y. -- Science. 1982 Jul 9;217(4555):157-8.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/6806903" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): Animals ; Complement System Proteins ; Diabetes Mellitus, Experimental/immunology ; Erythrocytes/immunology ; Graft Survival ; Histocompatibility Antigens Class II/*immunology ; Immune Sera ; Immunization ; Immunosuppression ; *Islets of Langerhans Transplantation ; Lymphocytes/immunology ; Male ; Mice ; Mice, Inbred C57BL ; Transplantation, Homologous
    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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  • 3
    Publikationsdatum: 1982-08-06
    Beschreibung: The ability of tumor cells to metastasize may be related to their ability to promote aggregation of host platelets. The use of inhibitors of cysteine proteinases resulted in parallel inhibition of B16 amelanotic melanoma-induced platelet aggregation and of a cathepsin B activity. The antimetastatic agent prostacyclin inhibited platelet aggregation induced by the tumor cells and by papain, a cathepsin B-mimicking agent.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Honn, K V -- Cavanaugh, P -- Evens, C -- Taylor, J D -- Sloane, B F -- CA29405/CA/NCI NIH HHS/ -- CA29997/CA/NCI NIH HHS/ -- New York, N.Y. -- Science. 1982 Aug 6;217(4559):540-2.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7046053" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): Animals ; Cathepsin B ; Cathepsins/*metabolism ; Cells, Cultured ; Cysteine Endopeptidases ; Endopeptidases/*metabolism ; Epoprostenol/*pharmacology ; Humans ; Melanoma/metabolism ; Mice ; Mice, Inbred C57BL ; Neoplasms, Experimental/metabolism ; Papain/pharmacology ; Platelet Aggregation/*drug effects ; Prostaglandins/*pharmacology ; Protease Inhibitors/pharmacology
    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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  • 4
    Publikationsdatum: 1982-12-24
    Beschreibung: Monoclonal antibodies subcutaneously injected into mice track to regional lymph nodes and specifically label target cells there. The lymphatic route of administration can be expected to provide much higher sensitivity, higher target-to-background ratio, faster localization, and lower toxicity than the intravenous route when the aim is to diagnose or treat tumor metastases or lymphoma in the lymph nodes.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Weinstein, J N -- Parker, R J -- Keenan, A M -- Dower, S K -- Morse, H C 3rd -- Sieber, S M -- New York, N.Y. -- Science. 1982 Dec 24;218(4579):1334-7.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7146917" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): Animals ; *Antibodies, Monoclonal/administration & dosage ; Injections, Subcutaneous ; Lymph Nodes/*cytology ; Major Histocompatibility Complex ; Methods ; Mice ; Mice, Inbred C57BL ; Neoplasm Metastasis/*diagnosis
    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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