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  • 1
    Electronic Resource
    Electronic Resource
    Lack of M-MuSV tumour regression associated with T lymphocyte tolerance (1980)
    [s.l.] : Nature Publishing Group
    Nature 285 (1980), S. 667-668 
    Details
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] CBA/Ca (CBA) male mice, 4 to 6 weeks old, were rendered numerically deficient in T cells by a sequence of adult thymectomy, 850 rad total-body irradiation and injection with syngeneic bone marrow cells, as detailed elsewhere5. The mice were transplanted with one thymus lobe under the kidney capsule ...
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1038/285667a0
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    Paper (German National Licenses)
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  • 2
    Electronic Resource
    Electronic Resource
    Biological and conformational studies on analogues of a synthetic peptide enhancing HIV-1 infection (1998)
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Peptide Science 4 (1998), S. 436-448 
    Details
    ISSN: 1075-2617
    Keywords: CD ; FT-IR ; gp120-CD4 interaction ; HIV-1 ; structure-function studies ; solid-phase peptide synthesis ; Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: We have previously demonstrated that a 23-amino acid peptide derived from the V3 loop of the surface glycoprotein of the HIV-1 strain MN is able to bind CD4 and to enhance HIV-1 infection. Further studies have suggested that the peptide/CD4 interaction induces an increase in both CD4 expression and CD4/gp120 binding affinity. This paper describes the biological and physico-chemical characterization of three analogues of reduced sequence that have been designed in order to identify the minimum active sequence of this peptide corresponding to the MN-HIV-1 principal neutralizing domain. Biological studies indicate that the entire sequence is required for biological activity and that the sequence 1-18 presents an inhibitory activity. CD and FT-IR absorption data are discussed here in order to identify possible structure-function correlations. © 1998 European Peptide Society and John Wiley & Sons, Ltd.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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    Paper (German National Licenses)
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