Literature DB >> 2695933

Structural analysis of NADH-cytochrome b5 reductase in relation to hereditary methemoglobinemia.

T Yubisui1, K Murakami, K Shirabe, M Takeshita, S Zenno, S Tomatsu, Y Fukumaki.   

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Year:  1989        PMID： 2695933

Source DB:  PubMed          Journal:  Prog Clin Biol Res        ISSN： 0361-7742


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  3 in total

1.  Exonic point mutations in NADH-cytochrome B5 reductase genes of homozygotes for hereditary methemoglobinemia, types I and III: putative mechanisms of tissue-dependent enzyme deficiency.

Authors:  T Katsube; N Sakamoto; Y Kobayashi; R Seki; M Hirano; K Tanishima; A Tomoda; E Takazakura; T Yubisui; M Takeshita
Journal:  Am J Hum Genet       Date:  1991-04       Impact factor: 11.025

2.  Familial Congenital Methemoglobinemia in Pomeranian Dogs Caused by a Missense Variant in the NADH-Cytochrome B5 Reductase Gene.

Authors:  H Shino; Y Otsuka-Yamasaki; T Sato; K Ooi; O Inanami; R Sato; M Yamasaki
Journal:  J Vet Intern Med       Date:  2018-01-22       Impact factor: 3.333

3.  A new mutation of congenital methemoglobinemia exacerbated after methylene blue treatment.

Authors:  Fuminori Yamaji; Akio Soeda; Hiroki Shibata; Takuya Morikawa; Kodai Suzuki; Shozo Yoshida; Shinji Ogura
Journal:  Acute Med Surg       Date:  2018-02-15
  3 in total

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