Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4
|
pubmed:dateCreated |
1996-9-26
|
pubmed:databankReference |
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/D44499,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/D44500,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/D44501,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/D50292,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/D50293,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/D50294,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/D50295,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/D50296
|
pubmed:abstractText |
In order to further clarify the diversity of the HLA-B15 antigens and the correspondence of serological types with alleles in Asians, we screened various B15 serological splits by means of a polymerase chain reaction-single strand conformation polymorphism (PCR-SSCP) method. Subsequently, the genes encoding various B15 variants were sequenced. Two novel alleles, B*1528 and B*1529, were identified: the nucleotide sequence of the former contained a single-base substitution at position 263 in exon 2 as compared to that of the B*1501 allele, which results in an amino acid change at position 64 in the alpha 1 domain, and the nucleotide sequence of the latter differs from that of B*1518 by a single-base substitution at position 272 of exon 2 which results in an amino acid change at position 67 of the alpha 1 domain. One new allele, B*1521, described recently in Australian Aborigines was also identified in Asians in the present study. Moreover, the results of sequencing demonstrated that Asian HLA-B62, B70, and B77 antigens are encoded by B*1501, B*1518, and B*1513, respectively. Two splits of B75 antigens, B75V (TS-1) and B15N, which have been proposed to exist in the Japanese population were encoded by B*1511 and B*1502, respectively. Most of the B15 alleles detected in the present study showed positive associations with other locus antigens. Especially, B*1502 was strongly associated with Cw8, while B*1521 was strongly associated with A34 and Cw6.
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
Apr
|
pubmed:issn |
0001-2815
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
47
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
265-74
|
pubmed:dateRevised |
2004-11-17
|
pubmed:meshHeading | |
pubmed:year |
1996
|
pubmed:articleTitle |
Further molecular diversity in the HLA-B15 group.
|
pubmed:affiliation |
Department of Research, Japanese Red Cross Central Blood Center, Tokyo, Japan.
|
pubmed:publicationType |
Journal Article
|