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11 in total

1. THE ABSENCE OF CLOSE LINKAGE OF METHEMOGLOBINEMIA AND BLOOD GROUP LOCI.

Authors: E M SCOTT; M LEWIS; H KAITA; B CHOWN; E R GIBLETT
Journal: Am J Hum Genet Date: 1963-12 Impact factor: 11.025

2. An improved procedure for starch-gel electrophoresis: further variations in the serum proteins of normal individuals.

Authors: O SMITHIES
Journal: Biochem J Date: 1959-03 Impact factor: 3.857

3. The relation of diaphorase of human erythrocytes to inheritance of methemoglobinemia.

Authors: E M SCOTT
Journal: J Clin Invest Date: 1960-07 Impact factor: 14.808

4. The reduction of methemoglobin in human erythrocytes incubated with purine nucleosides.

Authors: E R JAFFE
Journal: J Clin Invest Date: 1959-09 Impact factor: 14.808

5. Electrophoretic study of glutathione reductase in human erythrocytes and leucocytes.

Authors: J C Kaplan; E Beutler
Journal: Nature Date: 1968-01-20 Impact factor: 49.962

Review 6. Hereditary methemoglobinemias associated with abnormalities in the metabolism of erythrocytes.

Authors: E R Jaffé
Journal: Am J Med Date: 1966-11 Impact factor: 4.965

7. The absence of close linkage of methemoglobinemia and other loci.

Authors: E M Scott; R C Wright
Journal: Am J Hum Genet Date: 1969-03 Impact factor: 11.025

8. Hereditary partial deficiency of human-erythrocyte phosphogluconate dehydrogenase.

Authors: C W Parr; L I Fitch
Journal: Biochem J Date: 1964-12 Impact factor: 3.857

9. 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

10. 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

9 in total

1. NAD(P) glycohydrolase deficiency in human erythrocytes and alteration of cytosol NADH-methemoglobin diaphorase by membrane NAD-glycohydrolase activity.

Authors: H Frischer; R Nelson; C Noyes; P E Carson; J E Bowman; K H Rieckmann; F Ajmar
Journal: Proc Natl Acad Sci U S A Date: 1973-08 Impact factor: 11.205

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

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

3. [Genetically determined variants of NADH-diaphorase].

Authors: G Tariverdian; H Ritter; G G Wendt
Journal: Humangenetik Date: 1970

4. Genic variation within and between the three major races of man, Caucasoids, Negroids, and Mongoloids.

Authors: M Nei; A K Roychoudhury
Journal: Am J Hum Genet Date: 1974-07 Impact factor: 11.025

5. Red blood cell NADH diaphorase in Italian populations.

Authors: P Lucarelli; M Di Mino; E Carapella; R Agostino; R Palmarino
Journal: Humangenetik Date: 1972

6. [Hb Tübingen. A new beta-chain variant (beta Tp 10-21) with increased spontaneous oxidation].

Authors: E Kleihauer; H D Waller; H C Benöhr; E Kohne; P Gelinsky
Journal: Klin Wochenschr Date: 1971-06-01

7. Hereditary methemoglobinemia associated with NADH diaphorase deficiency.

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

8. 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

9. Electrophoretic and functional variants of NADH-methemoglobin reductase in hereditary methemoglobinemia.

Authors: H S Hsieh; E R Jaffé
Journal: J Clin Invest Date: 1971-01 Impact factor: 14.808

9 in total