Molecular basis of an autoantibody-associated restriction fragment length polymorphism that confers susceptibility to autoimmune diseases
about
Epitope-specific antibody response is controlled by immunoglobulin V H polymorphismsChromosome localization and RFLP analysis of PDC-E2: the major autoantigen of primary biliary cirrhosisMolecular mimicry between bacterial and self antigen in a patient with systemic lupus erythematosus.Chromosomal organization of the heavy chain variable region gene segments comprising the human fetal antibody repertoire.The frequency of homozygous deletion of a developmentally regulated Vh gene (Humhv3005) is increased in patients with chronic idiopathic thrombocytopenic purpura.Analysis of human antitopoisomerase-I idiotypesFunctional activities and immunoglobulin variable regions of human and murine monoclonal antibodies specific for the P1.7 PorA protein loop of Neisseria meningitidisGenetic studies of human lupus in families.Human organ-specific autoimmune disease. Molecular cloning and expression of an autoantibody gene repertoire for a major autoantigen reveals an antigenic immunodominant region and restricted immunoglobulin gene usage in the target organDefining the genetic origins of three rheumatoid synovium-derived IgG rheumatoid factors.Population and family studies of three disease-related polymorphic genes in systemic lupus erythematosus.The immunoglobulin heavy chain locus: genetic variation, missing data, and implications for human disease.The NOD mouse as a model of SLE.Immunopathology and the gene therapy of lupus.A fetally expressed immunoglobulin VH1 gene belongs to a complex set of alleles.Superantigen properties of a human sialoprotein involved in gut-associated immunity.Revenge of the microbes. Superantigens of the T and B cell lineageClonal evolution of B cells in transformation from low- to high-grade lymphoma.Genetic analysis of self-associating immunoglobulin G rheumatoid factors from two rheumatoid synovia implicates an antigen-driven responseThe structural basis of germline-encoded VH3 immunoglobulin binding to staphylococcal protein ADiversification, not use, of the immunoglobulin VH gene repertoire is restricted in DiGeorge syndrome.Complete haplotype sequence of the human immunoglobulin heavy-chain variable, diversity, and joining genes and characterization of allelic and copy-number variationHuman immunodeficiency virus-1 (HIV-1) gp120 superantigen-binding serum antibodies. A host factor in homosexual HIV-1 transmission.Characterization of a germline Vk gene encoding cationic anti-DNA antibody and role of receptor editing for development of the autoantibody in patients with systemic lupus erythematosus.Restricted use of fetal VH3 immunoglobulin genes by unselected B cells in the adult. Predominance of 56p1-like VH genes in common variable immunodeficiency.V region gene analysis of human IgM hybridoma monoclonal anti-Sm antibodies.Susceptibility to coeliac disease in Tunisian children and GM immunoglobulin allotypes.Immunoglobulin gene sequence analysis to further assess B-cell origin of multiple myeloma.Germline variable region gene segment derivation of human monoclonal anti-Rh(D) antibodies. Evidence for affinity maturation by somatic hypermutation and repertoire shift.Immunoglobulin allotypes (GM and KM) and their interactions with HLA antigens in autoimmune diseases: a review.Molecular characterization of monoclonal IgM derived from human B cell lines expressing the 4C9 rheumatoid factor associated idiotype.Molecular analysis of human immunoglobulin heavy chain variable genes (IgVH) in normal and malignant B cellsAssociation of homozygous deletion of the Humhv3005 and the VH3-30.3 genes with renal involvement in systemic lupus erythematosus.Analysis of the V genes coding for a monospecific human antibody to myosin and functional expression of single chain Fv fragments.Analysis of the V kappa I family: germline genes from an SLE patient and expressed autoantibodies.Expression of Rheumatoid Factor Idiotypes 17.109, 6b6.6 and 4c9 in the Sera of Pima Indians
P2860
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P2860
Molecular basis of an autoantibody-associated restriction fragment length polymorphism that confers susceptibility to autoimmune diseases
description
1991 nî lūn-bûn
@nan
1991 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
1991 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
1991年の論文
@ja
1991年論文
@yue
1991年論文
@zh-hant
1991年論文
@zh-hk
1991年論文
@zh-mo
1991年論文
@zh-tw
1991年论文
@wuu
name
Molecular basis of an autoanti ...... ibility to autoimmune diseases
@ast
Molecular basis of an autoanti ...... ibility to autoimmune diseases
@en
Molecular basis of an autoanti ...... ibility to autoimmune diseases
@nl
type
label
Molecular basis of an autoanti ...... ibility to autoimmune diseases
@ast
Molecular basis of an autoanti ...... ibility to autoimmune diseases
@en
Molecular basis of an autoanti ...... ibility to autoimmune diseases
@nl
prefLabel
Molecular basis of an autoanti ...... ibility to autoimmune diseases
@ast
Molecular basis of an autoanti ...... ibility to autoimmune diseases
@en
Molecular basis of an autoanti ...... ibility to autoimmune diseases
@nl
P2093
P2860
P356
P1476
Molecular basis of an autoanti ...... ibility to autoimmune diseases
@en
P2093
D A Carson
K A Siminovitch
P2860
P304
P356
10.1172/JCI115277
P407
P577
1991-07-01T00:00:00Z