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PMID |
Sentence |
1 |
12175732
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Linkage disequilibrium between HLA-DPB1 alleles and retinoid X receptor beta haplotypes.
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2 |
12175732
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The human retinoid X receptor beta (RXRB) gene maps to the major histocompatibility complex (MHC) region, between KE4 and COL11A2, approximately 130-kb centromeric to HLA-DPB1.
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3 |
12175732
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We also reported strong linkage disequilibrium between the HLA-DPB1*0401 and RXRB+7*T alleles.
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4 |
12175732
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The data generated from this study were used to determine linkage disequilibrium between several MHC markers and the RXRB alleles and haplotypes.
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5 |
12175732
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Family studies revealed significant linkage disequilibrium between the RXRB alleles and a number of HLA-DPB1 alleles.
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6 |
18830248
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Conditional analyses on the T1DGC MHC dataset: novel associations with type 1 diabetes around HLA-G and confirmation of HLA-B.
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7 |
18830248
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The major histocompatibility complex (MHC) is known to harbour genetic risk factors for type 1 diabetes (T1D) additional to the class II determinants HLA-DRB1, -DQA1 and -DQB1, but strong linkage disequilibrium (LD) has made efforts to establish their location difficult.
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8 |
18830248
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A subset of polymorphisms that could explain most of the association in each region included single nucleotide polymorphisms (SNPs) in the vicinity of HLA-G, particular HLA-B and HLA-DPB1 alleles, and SNPs close to the COL11A2 and RING1 genes.
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9 |
18830248
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Apart from HLA-B and HLA-DPB1, all of these represent novel associations, and subpopulation analyses did not indicate large population-specific differences among Caucasians for our findings.
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10 |
18830248
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On account of the unusual genetic complexity of the MHC, further fine mapping is demanded, with the possible exception of HLA-B.
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