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  • 1
    ISSN: 1749-6632
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Natural Sciences in General
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 305 (1983), S. 541-543 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] Two murine monoclonal antibodies specific for determinants on the HLA-DR-encoded p29,34 bimolecular complex were used in this study: antibody 7.2 reacts with a framework determinant of the DR molecule, and binds DR antigens on cells from donors of all DR haplotypes8. Antibody 17.15 reacts with a ...
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1432-1211
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract Two-dimensional (2D) gel electrophoresis of immunoprecipitated HLA-DR antigens from eight homozygous typing cells (HTC) expressing the HLA-DRw8 specificity revealed a clustering of polymorphic β chain patterns into distinct electrophoretic variants. The variant patterns correlate with three discrete HLA-D clusters that are defined in the mixed leukocyte culture reaction (MLR) using DRw8-positive HTC. These HLA-D clusters have been provisionally designated Dw“8.1”, detected primarily in Caucasoids, Dw“8.2”, detected primarily in American Indians, and Dw“8.3”, detected predominantly in Orientals. All three HLA-Dw“8.1” cell lines express a single DR-locus product as defined by immunoprecipitation with a DR-specific monoclonal antibody, P4.1. This DR β chain is identical among the Dw“8.1” cell lines and different from the DR β chains of the Dw“8.2” and Dw“8.3” cell lines. Two separate Dw“8.2” HTC express a shared DR β chain that is slightly more basic than the 8.1 DR molecule; interestingly, one of these lines also expresses an additional DR-like β chain not found in the other cells. Thus, the two lines defining the Dw“8.2” cluster share one distinct class 11 molecule, but differ in another and therefore are not biochemically HLA-identical. Cells from the Dw“8.3” cluster are likewise distinct from all other Dw8 clusters. One additional DRw8-positive HTC has been analyzed and found to be distinct from the Dw“8.1”, “8.2” and “8.3” clusters by both MLR and 2D gels. lmmunoprecipitates using monoclonal antibody 1B5 [anti-DR and anti-DQ(DS)] identify additional polymorphic class II variants among the cell lines tested. These data indicate that HLA-DRw8 is a public serologic specificity present on class II molecules expressed on multiple distinct haplotypes. These haplotypes differ from each other in expression of polymorphic class II molecules encoded by at least two HLA loci. They also differ in HLA-D, even though they all type as HLA-DRw8 homozygous. In Dw“8.2”, variation in expressed β chains is not reflected in variation in HLA-D, indicating that MLR, as well as serologic typing, does not detect the full degree of allelic polymorphism within HLA.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Journal of clinical immunology 7 (1987), S. 1-7 
    ISSN: 1573-2592
    Keywords: Rheumatoid arthritis ; HLA-DR ; major histocompatibility complex
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract The association of HLA-DR4 with rheumatoid arthritis strongly implicates genes of the major histocompatibility complex (MHC) as contributing to disease susceptibility. Molecular analysis of MHC genes expressed on haplotypes in association with HLA-DR4 reveals that at least six different alleles of the DRβ1 locus and at least three different alleles of the DQβ locus occur on different DR4+ haplotypes. Some of these allelic differences are quite substantial, and others are rather subtle, involving as few as two amino acids. The analysis of individual DR and DQ alleles in rheumatoid arthritis identifies some DR4+ genes strongly associated with disease susceptibility and some DR4+ genes which are not. The Dw4(DR4) and Dw14(DR4) DRβ1 genes appear to represent specific alleles which confer disease risk in RA; other DRβ1 genes, such as Dw10(DR4), may represent DRβ genes altered during evolution which have lost their contribution to RA susceptibility. DQβ 3.1(DQw3) and DQβ 3.2(DQw3) DQβ genes, which are present on DR4+ haplotypes, represent discrete variable alleles not directly implicated in RA, but which account for HLA-DR4 associations with other diseases, such as the association of DQβ 3.2(DQw3) with Type I diabetes.
    Type of Medium: Electronic Resource
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