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PMID Allele Disease Population Drug Names SNP Class Sentence
14630515 HUMAN LEUKOCYTE ANTIGEN (HUMAN LEUKOCYTE ANTIGEN) beryllium disease NA NA NA unclassified
the pathobiology of chronic beryllium disease (cbd) involves the major histocompatibility complex class ii human leukocyte antigen (hla).
14662898 MHC (MHC) beryllium disease NA NA NA unclassified
influence of mhc class ii in susceptibility to beryllium sensitization and chronic beryllium disease.
14662898 HLA-DPB1 (HLA-DPB1) beryllium disease NA NA NA unclassified
a glutamic acid at residue 69(glu(69)) in the hla-dpb1 gene (glu(69)) is associated with chronic beryllium disease (cbd) and possibly beryllium sensitization (bes).
15273960 HLA (HLA) beryllium disease NA NA NA unclassified
the association between hla-dpb1glu69 and chronic beryllium disease and beryllium sensitization.
15273960 HLA-DPB1 (HLA-DPB1) beryllium disease NA NA NA unclassified
several case-control studies have found an association between chronic beryllium disease (cbd) and hla-dpb1 gene variants.
15273960 HLA-DPB1 (HLA-DPB1) occupational disease NA NA NA unclassified
follow-up of this cohort, scrutiny of hla-dpb1 haplotypes, and evaluation of gene-environment and gene-gene interactions will be important for fully understanding the immunogenetic nature of this occupational disease.
16054169 HLA (HLA) beryllium disease NA NA NA unclassified
it was shown that anti-hla antibodies could block the beryllium-specific response in the beryllium lymphocyte proliferation test, thereby implicating hla genes in chronic beryllium disease.
16054169 HLA-DPB1 (HLA-DPB1) beryllium disease NA NA NA positive
a supratypic genetic marker, hla-dpb1*e69, was found to be strongly associated with immunologic sensitization to beryllium and chronic beryllium disease in beryllium workers.
16054169 HLA-DPB1 (HLA-DPB1) beryllium disease NA NA NA positive
the purpose of the study was to evaluate the evidence for potential differential susceptibility that may be associated with the physical characteristics of hla protein molecules for which different hla-dpb1*e69 variants code; that is, do some hla-dpb1*e69 variants convey higher risk of beryllium sensitization and chronic beryllium disease than others.
16054169 HLA-DPB1*17 beryllium disease NA NA NA unclassified
among the 40 hla-dpb1 gene variants that code for e69, molecular epidemiological studies have suggested a risk hierarchy, where some variants appear to convey low to moderate risk of chronic beryllium disease (e.g., hla-dpb1*0201, approximately 3-fold increased risk), some convey an intermediate risk (e.g., hla-dpb1*1901, approximately 5-fold) and others convey high risk (e.g., hla-dpb1*1701, >10-fold).
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