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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
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pubmed:dateCreated |
1987-5-12
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pubmed:abstractText |
The genetic polymorphism of transferrin (TF) was studied in 2,167 Japanese individuals and in 448 New Zealanders. The three TF C subtypes were identified, but TF C3 was absent from Japanese populations. In addition, three TF B and six TF D variants were observed, each of which occurred either in Japanese or in New Zealanders. Stepwise removal of N-acetyl-neuraminic acid (NANA) with neuraminidase revealed that the most cathodal variant TF DShinnanyo found in a Japanese family was characterized by having only two NANA residues.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:issn |
0001-5652
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
37
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
20-5
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pubmed:dateRevised |
2011-11-17
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pubmed:meshHeading |
pubmed-meshheading:3557459-Gene Frequency,
pubmed-meshheading:3557459-Humans,
pubmed-meshheading:3557459-Japan,
pubmed-meshheading:3557459-New Zealand,
pubmed-meshheading:3557459-Polymorphism, Genetic,
pubmed-meshheading:3557459-Sialic Acids,
pubmed-meshheading:3557459-Sialoglycoproteins,
pubmed-meshheading:3557459-Transferrin
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pubmed:year |
1987
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pubmed:articleTitle |
Transferrin variants in Japan and New Zealand. Report of an unusually sialyzed TF variant.
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pubmed:publicationType |
Journal Article
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