Nomenclature for factors of the HLA system, 1994

Bodmer, Julia G.; Marsh, Steven G.E.; Albert, E. D.; Bodmer, Walter F.; Dupont, Bo; Erlich, Henry A.; Mach, Bernard; Mayr, Wolfgang R.; Parham, Peter; Sasazuki, Takehiko; Schreuder, G. M. T.; Strominger, Jack L.; Svejgaard, A.; Terasaki, Paul I.

doi:10.1016/0198-8859(94)90077-9

Cited by 57 publications

(10 citation statements)

References 149 publications

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“…All laboratory procedures, primers, and probes utilized were modified versions of those presented at the XI International Histocompatibility Workshop. The nomenclature used was that of the World Health Organization Nomenclature Committee for Factors of the HLA System ( Bodmer et al ., 1994 ).…”

Section: Methodsmentioning

confidence: 99%

The HLA–DQ associations with Graves' disease in Chinese children

Wong

Cheng

Dorman

1999

Clinical Endocrinology

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Section: Methodsmentioning

confidence: 99%

The HLA–DQ associations with Graves' disease in Chinese children

Wong

Cheng

Dorman

1999

Clinical Endocrinology

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“…In some instances when the SSO typing did not yield conclusive data, further typing was performed either by manual sequencing-based typing (23), or by allele-specific amplification using the The latest recommendations of the WHO Committee for Factors of the HLA System were employed using four digits (24). When only the "broad" allele was defined, only two digits were used.…”

Section: Genomic Typing For Class II Genesmentioning

confidence: 99%

The HLA‐DQ(α10102, β10602) heterodimer may confer susceptibility to multiple sclerosis in the absence of the HLA‐DR(α101, β11501) heterodimer

Spurkland

Knutsen

et al. 1997

Tissue Antigens

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The frequencies of DR2, DQ6-related DRB1, DQA1, DQB1 haplotypes were compared in 181 multiple sclerosis patients and 294 controls in Norway. All individuals carried either DR2 or DQ6, i.e., the DQ(alpha 1*0102, beta 1*0602) heterodimer. The DR(alpha 1*01, beta 1*1501) and the DQ(alpha 1*0102, beta 1*0602) heterodimers were carried by 171 of the patients (94%) and 289 (98%) of the controls. Seven of the patients and one of the controls carried the DQ(alpha 1*0102, beta 1*0603) heterodimer together with the DR(alpha 1*01, beta 1*1501) heterodimer. Two patients carried the DQ(alpha 1*0102, beta 1*0602) heterodimer in the absence of the DR( alpha 1*01, beta 1*1501) heterodimer. The DR(alpha 1*01, beta 1*1501) heterodimer was not observed in the absence of the DQ(alpha 1*0102, beta 1*0602) heterodimer or the DQ(alpha 1*0102, beta 1*0603) heterodimer, neither in the patients nor in the controls. Our findings indicate that the genes encoding the DQ(alpha 1*0102, beta 1*0602) heterodimer may confer susceptibility to developing multiple sclerosis in the absence of the DRB1*1501 allele.

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“…The African-American LMP allele frequencies did not differ from a sample of Europeans (26) at these two loci. TAPl and TAP2 each had three alleles (Table 1); all except one has been assigned official nomenclature (35) designations in parenthesis): TAP1*0101 (IA), TAP1*0201 (IB), TAPl*O301 (lC), TAP2*0101 (lA), TAP2*0201 (lB), and TAP2 (2C) (36). The African-American frequencies differed significantly from Europeans (34) at both loci.…”

Section: Frequency Of Alleles Relative To Parental Populationsmentioning

confidence: 99%

African‐American HLA class II allele and haplotype diversity

et al. 1997

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Molecular genetic techniques were used to type nine loci in the HLA class II region in 241 unrelated African-Americans from New York City (NYC). Several effects attributable to recent genetic admixture were evident: the number of distinct class II alleles and haplotypes was larger in the African-Americans than in people of African or European origin, the allele frequencies were more consistently even, and linkage disequilibrium was present across the entire class II region. The African-American DRB1 allele frequencies almost always fell between frequencies among samples from northern Europe and the Gambia, two possible founding populations. The exceptions are attributed to the contribution of other genetically dissimilar African groups to the African-American gene pool. DRB1 allele frequencies (specifically DRB1*1501) and some haplotypes of DRB1-DPB1 were different in our NYC and the 11th International Histocompatibility Workshop (IHW) samples of African-Americans. The high level of allele and haplotype diversity found in African-Americans has important implications for the construction of pools of unrelated potential donors for tissue transplantation.

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Nomenclature for factors of the HLA system, 1994

Cited by 57 publications

References 149 publications

The HLA–DQ associations with Graves' disease in Chinese children

The HLA–DQ associations with Graves' disease in Chinese children

The HLA‐DQ(α10102, β10602) heterodimer may confer susceptibility to multiple sclerosis in the absence of the HLA‐DR(α101, β11501) heterodimer

African‐American HLA class II allele and haplotype diversity

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Nomenclature for factors of the HLA system, 1994

Cited by 57 publications

References 149 publications

The HLA–DQ associations with Graves' disease in Chinese children

The HLA–DQ associations with Graves' disease in Chinese children

The HLA‐DQ(α1*0102, β1*0602) heterodimer may confer susceptibility to multiple sclerosis in the absence of the HLA‐DR(α1*01, β1*1501) heterodimer

African‐American HLA class II allele and haplotype diversity

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Resources

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The HLA‐DQ(α10102, β10602) heterodimer may confer susceptibility to multiple sclerosis in the absence of the HLA‐DR(α101, β11501) heterodimer