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PMID Allele Disease Population Drug Names SNP Class Sentence
9628455 HLA (HLA) myopathies NA NA NA unclassified
hla allele distribution distinguishes sporadic inclusion body myositis from hereditary inclusion body myopathies.
9628455 HLA (HLA) sporadic inclusion body myositis NA NA NA unclassified
hla allele distribution distinguishes sporadic inclusion body myositis from hereditary inclusion body myopathies.
9628455 HLA-CLASS II (HLA CLASS II) myopathies NA NA NA only_studied
we studied the hla class ii associations in patients with sporadic inclusion body myositis (s-ibm) and hereditary inclusion body myopathies (h-ibm) and attempted to distinguish these myopathies on the basis of hla allele assignments.
9628455 HLA-CLASS II (HLA CLASS II) sporadic inclusion body myositis NA NA NA only_studied
we studied the hla class ii associations in patients with sporadic inclusion body myositis (s-ibm) and hereditary inclusion body myopathies (h-ibm) and attempted to distinguish these myopathies on the basis of hla allele assignments.
23851103 HLA-DRB1*11 myopathies NA NA NA unclassified
unlike other necrotizing myopathies, statin-induced myopathy is associated with the presence of autoantibodies directed against 3-hydroxy-3-methylglutaryl- coenzyme a reductase (the enzyme target of statin therapies), and with human leukocyte antigen-drb1*11.
15496200 HLA-DR3 (BROAD ANTIGEN) sporadic inclusion body myositis Caucasian NA NA unclassified
two major histocompatibility complex haplotypes influence susceptibility to sporadic inclusion body myositis: critical evaluation of an association with hla-dr3.
15496200 HLA-A*01 sporadic inclusion body myositis Caucasian NA NA unclassified
previous studies of sporadic inclusion body myositis (sibm) have shown a strong association with hla-dr3 and other components of the 8.1 ancestral haplotype (ah) (hla-a1, b8, dr3), where the susceptibility locus has been mapped to the central major histocompatibility complex (mhc) region between hla-dr and c4.
15496200 HLA-DR3 (BROAD ANTIGEN) sporadic inclusion body myositis Caucasian NA NA unclassified
previous studies of sporadic inclusion body myositis (sibm) have shown a strong association with hla-dr3 and other components of the 8.1 ancestral haplotype (ah) (hla-a1, b8, dr3), where the susceptibility locus has been mapped to the central major histocompatibility complex (mhc) region between hla-dr and c4.
16564169 MHC (MHC) sporadic inclusion body myositis Japanese NA NA unclassified
sporadic inclusion body myositis in japanese is associated with the mhc ancestral haplotype 52.1.
16564169 HLA-B*35 sporadic inclusion body myositis Japanese NA NA unclassified
in caucasians, sporadic inclusion body myositis has been associated with the mhc ancestral haplotypes; hla-a1, b8, dr3 (8.1ah) and hla-b35, dr1 (35.2ah).
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