Literature DB >> 4321430

[Genetically determined variants of NADH-diaphorase].

G Tariverdian, H Ritter, G G Wendt.   

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Year:  1970        PMID: 4321430     DOI: 10.1007/bf00296308

Source DB:  PubMed          Journal:  Humangenetik        ISSN: 0018-7348


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  4 in total

1.  Electrophoresis of red cell NADH- and NADPH-diaphorases in normal subjects and patients with congenital methemoglobinemia.

Authors:  J C Kaplan; E Beutler
Journal:  Biochem Biophys Res Commun       Date:  1967-11-30       Impact factor: 3.575

2.  NADH diaphorase: an inherited variant associated with normal methemoglobin reduction.

Authors:  J C Detter; J E Anderson; E R Giblett
Journal:  Am J Hum Genet       Date:  1970-01       Impact factor: 11.025

3.  Demonstration of an enzyme variant in a case of congenital methaemoglobinaemia.

Authors:  C A West; B D Gomperts; E R Huehns; I Kessel; J R Ashby
Journal:  Br Med J       Date:  1967-10-28

4.  A starch-gel electrophoretic method for the study of diaphorase isozymes and preliminary results with sheep and human erythrocytes.

Authors:  G J Brewer; J W Eaton; C S Knutsen; C C Beck
Journal:  Biochem Biophys Res Commun       Date:  1967-10-26       Impact factor: 3.575

  4 in total
  4 in total

1.  [Polymorphism of red cell NADH-diaphorase in Western German population].

Authors:  B G Potrafki; H Hellenbroich; G Pulverer
Journal:  Humangenetik       Date:  1972

2.  [Transspecific variability of NADH-diaphorases in primates].

Authors:  J Schmitt; G Tariverdian; H Ritter
Journal:  Humangenetik       Date:  1971

3.  Hereditary methemoglobinemia associated with NADH diaphorase deficiency.

Authors:  H Ritter; K Schmidt; J Schmitt
Journal:  Humangenetik       Date:  1973

4.  Investigations on the polymorphism of sperm diaphorase in man. Evidence for a third common allele, SD.

Authors:  P Kühnl; U Langanke; W Spielmann; M Neubauer
Journal:  Hum Genet       Date:  1977-12-29       Impact factor: 4.132

  4 in total

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