Literature DB >> 3834200

Electrophoretic variants of blood proteins in Japanese. VI. Transferrin.

M Fujita, C Satoh, J Asakawa, Y Nagahata, Y Tanaka, R Hazama, T Krasteff.   

Abstract

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Year:  1985        PMID： 3834200     DOI： 10.1007/BF01876469

Source DB:  PubMed          Journal:  Jinrui Idengaku Zasshi        ISSN： 0021-5074


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  5 in total

1.  Heterozygosity and ethnic variation in Japanese platelet proteins.

Authors:  J Asakawa; J V Neel; N Takahashi; C Satoh; S Kaneoka; E Nishikori; M Fujita
Journal:  Hum Genet       Date:  1988-01       Impact factor: 4.132

2.  Protein variants in Hiroshima and Nagasaki: tales of two cities.

Authors:  J V Neel; C Satoh; P Smouse; J Asakawa; N Takahashi; K Goriki; M Fujita; T Kageoka; R Hazama
Journal:  Am J Hum Genet       Date:  1988-12       Impact factor: 11.025

3.  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

4.  Dissecting Total Plasma and Protein-Specific Glycosylation Profiles in Congenital Disorders of Glycosylation.

Authors:  Agnes L Hipgrave Ederveen; Noortje de Haan; Melissa Baerenfaenger; Dirk J Lefeber; Manfred Wuhrer
Journal:  Int J Mol Sci       Date:  2020-10-15       Impact factor: 5.923

Review 5.  Insights into complexity of congenital disorders of glycosylation.

Authors:  Sandra Supraha Goreta; Sanja Dabelic; Jerka Dumic
Journal:  Biochem Med (Zagreb)       Date:  2012       Impact factor: 2.313
  5 in total

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