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

American journal of human genetics ·Vol. 22 ·No. 1 ·1970-01-00 ·Pages 100-4

Detter JC, Anderson JE, Giblett ER

Abstract

暂无摘要

MeSH Terms

Dihydrolipoamide Dehydrogenase/metabolism Electrophoresis Erythrocytes/enzymology Female Genes Genetic Variation Glutathione/metabolism Humans Male Methemoglobin/metabolism Methemoglobinemia/enzymology Pedigree

Chemicals

Methemoglobin Dihydrolipoamide Dehydrogenase Glutathione

Authors & Affiliations

3 authors, click to expand affiliations / ORCID

Detter J C

Anderson J E

Giblett E R

References (11)

11 references, click to expand

Hereditary partial deficiency of human-erythrocyte phosphogluconate dehydrogenase.
Biochem J. 1964 Dec;93(3):28C-30C PMID: 5839175
Hereditary methemoglobinemias associated with abnormalities in the metabolism of erythrocytes.
Am J Med. 1966 Nov;41(5):786-98 PMID: 5332175
Demonstration of an enzyme variant in a case of congenital methaemoglobinaemia.
Br Med J. 1967 Oct 28;4(5573):212-4 PMID: 6061565
A starch-gel electrophoretic method for the study of diaphorase isozymes and preliminary results with sheep and human erythrocytes.
Biochem Biophys Res Commun. 1967 Oct 26;29(2):198-204 PMID: 6066279
Electrophoretic study of glutathione reductase in human erythrocytes and leucocytes.
Nature. 1968 Jan 20;217(5125):256-8 PMID: 4384274
The absence of close linkage of methemoglobinemia and other loci.
Am J Hum Genet. 1969 Mar;21(2):194-5 PMID: 5770174
An improved procedure for starch-gel electrophoresis: further variations in the serum proteins of normal individuals.
Biochem J. 1959 Mar;71(3):585-7 PMID: 13638269
THE ABSENCE OF CLOSE LINKAGE OF METHEMOGLOBINEMIA AND BLOOD GROUP LOCI.
Am J Hum Genet. 1963 Dec;15:493-4 PMID: 14097243
The relation of diaphorase of human erythrocytes to inheritance of methemoglobinemia.
J Clin Invest. 1960 Jul;39:1176-9 PMID: 14444209
The reduction of methemoglobin in human erythrocytes incubated with purine nucleosides.
J Clin Invest. 1959 Sep;38:1555-63 PMID: 14406502
Electrophoresis of red cell NADH- and NADPH-diaphorases in normal subjects and patients with congenital methemoglobinemia.
Biochem Biophys Res Commun. 1967 Nov 30;29(4):605-10 PMID: 16496543

Article Info

Journal

American journal of human genetics

Abbr.

Am J Hum Genet

ISSN

0002-9297

Published

1970-01-00

Pages

100-4

Language

English

Region

United States

NLM ID

0370475

PMCID

PMC1706502

Subset

External Links

PubMed source PMC Full Text View journal details

Analysis Services

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

Contact

WeChat Official Account