The immunogenetics of glomerulonephritis (Q40743666)

23 September 2017

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title

The immunogenetics of glomerulonephritis (English)

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23 September 2017

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Rees AJ

1

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23 September 2017

language of work or name

English

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publication date

1 February 1994

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23 September 2017

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23 September 2017

volume

45

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23 September 2017

issue

2

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23 September 2017

page(s)

377-383

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The biochemistry and cell biology of antigen processing and presentation

23 September 2017

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Human T-cell clonal anergy is induced by antigen presentation in the absence of B7 costimulation

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Subsets of CD4+T Cells and their Roles in the Induction and Prevention of Autoimmunity

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Regulatory role of OX22high T cells in mercury-induced autoimmunity in the brown Norway rat.

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Major histocompatibility complex (MHC) control of CD4 T cell subset activation. II. A single peptide induces either humoral or cell-mediated responses in mice of distinct MHC genotype

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Genetic control of innate resistance to mycobacterial infections

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Genetic variation in the stress response: susceptibility to experimental allergic encephalomyelitis and implications for human inflammatory disease

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Mercuric chloride-induced anti-glomerular basement membrane antibodies in the rat Genetic control

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Requirement of H-2 heterozygosity for autoimmunity in (NZB X NZW)F1 hybrid mice

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The contribution of NZW genes to lupus-like disease in (NZB x NZW)F1 mice

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Genetic analysis of the imperfect association of H-2 haplotype with lupus-like autoimmune disease

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T-cell-receptor beta- and I-A beta-chain genes of normal SWR mice are linked with the development of lupus nephritis in NZB x SWR crosses

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Gene conversion between murine class II major histocompatibility complex loci. Functional and molecular evidence from the bm 12 mutant

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Mixed haplotypes and autoimmunity

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A large deletion within the T-cell receptor beta-chain gene complex in New Zealand white mice

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Delineation of a defect in T cell receptor beta genes of NZW mice predisposed to autoimmunity

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Murine T-cell receptor mutants with deletions of beta-chain variable region genes

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Spontaneous murine lupus-like syndromes. Clinical and immunopathological manifestations in several strains

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Lymphoproliferation disorder in mice explained by defects in Fas antigen that mediates apoptosis

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Genetic analysis of MRL-lpr mice: relationship of the Fas apoptosis gene to disease manifestations and renal disease-modifying loci

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A new allele of the lpr locus, lprcg, that complements the gld gene in induction of lymphadenopathy in the mouse

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Lpr and gld: single gene models of systemic autoimmunity and lymphoproliferative disease

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Enforced BCL2 expression in B-lymphoid cells prolongs antibody responses and elicits autoimmune disease

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Genetic selection for crescent formation yields mouse strain with rapidly progressive glomerulonephritis and small vessel vasculitis

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Nomenclature for factors of theHLA system, 1991

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MHC class-II molecules and autoimmunity

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Structure of the human class I histocompatibility antigen, HLA-A2

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Three-dimensional structure of the human class II histocompatibility antigen HLA-DR1.

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Allele-specific motifs revealed by sequencing of self-peptides eluted from MHC molecules

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Peptides presented to the immune system by the murine class II major histocompatibility complex molecule I-Ad

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Specificity and promiscuity among naturally processed peptides bound to HLA-DR alleles

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Molecular cloning of the human Goodpasture antigen demonstrates it to be the alpha 3 chain of type IV collagen

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Strong association between HLA-DRW2 and antibody-mediated Goodpasture's syndrome

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The influence of HLA-linked genes on the severity of anti-GBM antibody-mediated nephritis

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Strong association between idiopathic membranous nephropathy and HLA-DRW3

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Strong association of HLA-DR2 and MT1 with idiopathic membranous nephropathy in Japan

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Strong association of idiopathic membranous nephropathy with HLA-DR2 and MT1 in Japanese

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7 January 2021

A DQA1 allele is strongly associated with idiopathic membranous nephropathy

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The DQw7 allele at the HLA-DQB locus is associated with susceptibility to IgA nephropathy in Caucasians

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Association of HLA-DQw4 with IgA Nephropathy in the Japanese Population

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Familial IgA nephropathy: a study of HLA class II allogenotypes in a Chinese kindred

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HLA-DP region gene polymorphism in primary IgA nephropathy: no association

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HLA class II specificities in vasculitis with antibodies to neutrophil cytoplasmic antigens

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Association between rapidly progressive glomerulonephritis and the properdin factor BfF and different HLA-D region products

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HLA antigen frequencies in systemic vasculitis: increase in HLA-DR2 in wegener's granulomatosis

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Major histocompatibility complex genes and susceptibility to systemic lupus erythematosus in southern chinese

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Genetic aspects of human lupus

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Inherited deficiency of the second component of complement. Rheumatic disease associations

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Complement allotyping in SLE: association with C4A null

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Null alleles of the fourth component of complement and HLA haplotypes in familial systemic lupus erythematosus.

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Relationship between C4 null genes, HLA-D region antigens, and genetic susceptibility to systemic lupus erythematosus in Caucasian and black Americans.

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Deletion of C4A genes in patients with systemic lupus erythematosus

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7 January 2021

Identifiers

DOI

10.1038/KI.1994.48

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23 September 2017

1 reference