The genetic basis for the association of the 8.1 ancestral haplotype (A1, B8, DR3) with multiple immunopathological diseases.
about
Genetic analysis of completely sequenced disease-associated MHC haplotypes identifies shuffling of segments in recent human history.HLA-A and -B alleles and haplotypes in 240 index patients with common variable immunodeficiency and selective IgG subclass deficiency in central AlabamaElevation of IgG antibodies against tissue transglutaminase as a diagnostic tool for coeliac disease in selective IgA deficiencyPleiotropic effects of the 8.1 HLA haplotype in patients with autoimmune myasthenia gravis and thymus hyperplasiaThe human Major Histocompatibility Complex as a paradigm in genomics researchScan of human genome reveals no new Loci under ancient balancing selectionScience review: Genetic variability in the systemic inflammatory responseGenotyping in the MHC locus: potential for defining predictive markers in sarcoidosisGenetics of rheumatoid arthritis: confronting complexity.Human leukocyte antigen class I, class II, and tumor necrosis factor-alpha polymorphisms in a healthy elder Mexican Mestizo populationDiametrical diseases reflect evolutionary-genetic tradeoffs: Evidence from psychiatry, neurology, rheumatology, oncology and immunologyInterrogating the major histocompatibility complex with high-throughput genomicsGenetic correlates influencing immunopathogenesis of HIV infectionPredictors of shingles reports at diagnosis of common variable immunodeficiency and selective immunoglobulin G subclass deficiency in 212 Alabama adultsThe genetics of complex cholestatic disordersHuman leukocyte antigen class I alleles and the disease course in sarcoidosis patientsThe central MHC gene, BAT1, may encode a protein that down-regulates cytokine productionGenome-wide association study identifies multiple susceptibility loci for diffuse large B cell lymphomaHLA haplotype map of river valley populations with hemochromatosis traced through five centuries in Central SwedenThe emergence of human-evolutionary medical genomicsRisk for myasthenia gravis maps to a (151) Pro→Ala change in TNIP1 and to human leukocyte antigen-B*08HLA-DPB1*04:01 Protects Genetically Susceptible Children from Celiac Disease Autoimmunity in the TEDDY Study.HLA-DRB1*07:01 is associated with a higher risk of asparaginase allergies.Serological assessment for celiac disease in IgA deficient adults.Evidence for association between the HLA-DQA locus and abdominal aortic aneurysms in the Belgian population: a case control studyMHC haplotype matching for unrelated hematopoietic cell transplantation.Pathology of Puumala hantavirus infection in macaquesPoly-autoimmunity in patients with myasthenia gravis: A single-center experience.HLA-DRB3*01:01 is a predictor of immunization against human platelet antigen-1a but not of the severity of fetal and neonatal alloimmune thrombocytopenia.Differences in the risk of celiac disease associated with HLA-DQ2.5 or HLA-DQ2.2 are related to sustained gluten antigen presentation.Immunogenetic characteristics of patients with autoimmune gastritis.Genetic polymorphisms in TNF genes and tuberculosis in North Indians.HLAscan: genotyping of the HLA region using next-generation sequencing data.HLA-A*01:03, HLA-A*24:02, HLA-B*08:01, HLA-B*27:05, HLA-B*35:01, HLA-B*44:02, and HLA-C*07:01 monochain transgenic/H-2 class I null mice: novel versatile preclinical models of human T cell responses.Whole-genome molecular haplotyping of single cellsAn integrated haplotype map of the human major histocompatibility complex.Influence of HLA DRB1 alleles in the susceptibility of rheumatoid arthritis and the regulation of antibodies against citrullinated proteins and rheumatoid factorAncient haplotypes of the HLA Class II region.Complexes of two cohorts of CLIP peptides and HLA-DQ2 of the autoimmune DR3-DQ2 haplotype are poor substrates for HLA-DMCeliac disease: how complicated can it get?
P2860
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P2860
The genetic basis for the association of the 8.1 ancestral haplotype (A1, B8, DR3) with multiple immunopathological diseases.
description
1999 nî lūn-bûn
@nan
1999 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
1999 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
1999年の論文
@ja
1999年論文
@yue
1999年論文
@zh-hant
1999年論文
@zh-hk
1999年論文
@zh-mo
1999年論文
@zh-tw
1999年论文
@wuu
name
The genetic basis for the asso ...... e immunopathological diseases.
@ast
The genetic basis for the asso ...... e immunopathological diseases.
@en
type
label
The genetic basis for the asso ...... e immunopathological diseases.
@ast
The genetic basis for the asso ...... e immunopathological diseases.
@en
prefLabel
The genetic basis for the asso ...... e immunopathological diseases.
@ast
The genetic basis for the asso ...... e immunopathological diseases.
@en
P2093
P2860
P1476
The genetic basis for the asso ...... e immunopathological diseases.
@en
P2093
Christiansen F
P2860
P304
P356
10.1111/J.1600-065X.1999.TB01398.X
P577
1999-02-01T00:00:00Z