Literature DB >> 3557459

Transferrin variants in Japan and New Zealand. Report of an unusually sialyzed TF variant.

I Yuasa, Y Saneshige, K Suenaga, K Ito, Y Gotoh.   

Abstract

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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Year:  1987        PMID: 3557459     DOI: 10.1159/000153672

Source DB:  PubMed          Journal:  Hum Hered        ISSN: 0001-5652            Impact factor:   0.444


  2 in total

1.  Transferrin D protein variants in the diagnosis of congenital disorders of glycosylation (CDG).

Authors:  Eliska Marklová; Ziad Albahri
Journal:  J Clin Lab Anal       Date:  2009       Impact factor: 2.352

2.  Transferrin mutations at the glycosylation site complicate diagnosis of congenital disorders of glycosylation type I.

Authors:  Mailys Guillard; Yoshinao Wada; Hana Hansikova; Isao Yuasa; Katerina Vesela; Nina Ondruskova; Machiko Kadoya; Alice Janssen; Lambertus P W J Van den Heuvel; Eva Morava; Jiri Zeman; Ron A Wevers; Dirk J Lefeber
Journal:  J Inherit Metab Dis       Date:  2011-03-23       Impact factor: 4.982

  2 in total

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