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PMID Allele Disease Population Drug Names SNP Class Sentence
9258386 HLA (HLA) berylliosis NA NA NA positive
the presence of the marker was associated with higher prevalence (hla-dpb1glu69-positive machinists 25%; hla-dpb1glu69-negative machinists 3.2%, p = 0.05) and predicted berylliosis independent of machining history (odds ratios 11.8 and 10.1).
11423174 NA (NA) berylliosis NA NA NA unclassified
beryllium binding to hla-dp molecule carrying the marker of susceptibility to berylliosis glutamate beta 69.
11423174 NA (NA) berylliosis NA NA NA unclassified
susceptibility to berylliosis has been associated with the supratypic variant of hla-dp gene coding for glutamate at position beta69 (hla-dpbetaglu69).
15127972 NA (NA) berylliosis NA NA NA positive
two gene markers have been previously associated with berylliosis: hla-dp allelic variants carrying glutamate in position 69 of the beta-chain and the high tnf-alpha production-associated tnf-alpha promoter allele tnfa2.
17017386 HLA (HLA) berylliosis NA NA NA unclassified
the high response to beryllium in the lymphocytes proliferation test and the hla typing which revealed the presence of the two susceptibility markers hla-dpglu69 and hla-drphe47 led to a diagnosis of berylliosis.
19191908 NA (NA) berylliosis NA NA NA unclassified
role of high-affinity hla-dp specific clip-derived peptides in beryllium binding to the hla-dpglu69 berylliosis-associated molecules and presentation to beryllium-sensitized t cells.
19191908 DP (HAPLOTYPE) berylliosis NA NA NA unclassified
berylliosis is driven by the accumulation in the lung of beryllium-specific t helper type 1 (th1) cells recognizing beryllium as antigen when presented principally by human leucocyte antigen dp molecules carrying a glutamate at position beta69 (hla-dpglu69).
19191908 NA (NA) berylliosis NA NA NA unclassified
overall, these data support the proposal that hla-dp high-affinity peptides might be used as a model for specific berylliosis therapy.
28518476 HLA (HLA) petechiae NA NA NA positive
platelet characterization showed a lack of aggregation to all agonists (adp, asp, and collagen), increased activation with increased expression of surface marker (hla-abc), and an absence of surface receptor gpix during clinical episodes of petechiae and ecchymoses, even in the presence of normal platelet counts.
28518476 HLA (HLA) ecchymoses NA NA NA positive
platelet characterization showed a lack of aggregation to all agonists (adp, asp, and collagen), increased activation with increased expression of surface marker (hla-abc), and an absence of surface receptor gpix during clinical episodes of petechiae and ecchymoses, even in the presence of normal platelet counts.
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