These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
109 related articles for article (PubMed ID: 4285251)
21. [Hereditary methemoglobinemia due to NADH cytochrome b5 abnormality--clinical importance of the enzyme in leukocytes and platelets]. Tomita Y; Inagaki M; Taki M; Miura T; Saito N; Meguro T; Yamada K; Fujii H; Takizawa T; Miwa S Rinsho Ketsueki; 1986 Mar; 27(3):412-9. PubMed ID: 3735692 [No Abstract] [Full Text] [Related]
22. [A family with congenital methemoglobinemia due to diaphorase deficiency]. Frick PG; Bachmann F; Schmid JR Acta Haematol; 1965 Oct; 34(4):215-27. PubMed ID: 4955559 [No Abstract] [Full Text] [Related]
23. Automated determination of red cell methaemoglobin reductase activity by a continuous-flow system for screening hereditary methaemoglobinaemia. Tanishima K; Fukuda N; Takeshita M; Takizawa Y; Kitamura T; Yoneyama Y J Clin Pathol; 1979 Jun; 32(6):584-9. PubMed ID: 469015 [TBL] [Abstract][Full Text] [Related]
24. Effects of chloride and bicarbonate on methemoglobin reduction in mouse erythrocytes. Klurfeld G; Smith RP Biochem Pharmacol; 1968 Jun; 17(6):1067-77. PubMed ID: 5661344 [No Abstract] [Full Text] [Related]
25. Determination of concentration of cytosolic NADH-cytochrome b5 reductase in erythrocytes from normal Chinese adults, neonates and patients with hereditary methemoglobinemia by double-antibody sandwich ELISA. Lan F; Tang Y; Huang C; Zhu Z Acta Haematol; 1998; 100(1):44-8. PubMed ID: 9691146 [TBL] [Abstract][Full Text] [Related]
26. [Cyanosis in children caused by inherited methemoglobinemia due to deficiency of NADH-dependent methemoglobin reductase in erythrocytes]. Jabłońska-Skwiecińska E; Wierzbicka M; Kubicka K Pediatr Pol; 1989 Jan; 64(1):53-9. PubMed ID: 2812907 [TBL] [Abstract][Full Text] [Related]
28. Enzymopenic hereditary methemoglobinemia: a clinical/biochemical classification. Jaffé ER Blood Cells; 1986; 12(1):81-90. PubMed ID: 3539237 [TBL] [Abstract][Full Text] [Related]
29. Nicotinamide-adenine dinucleotide dehydrogenase activity of human erythrocyte membranes. Zamudio I; Canessa M Biochim Biophys Acta; 1966 May; 120(1):165-9. PubMed ID: 4289762 [No Abstract] [Full Text] [Related]
30. Structural analysis of NADH-cytochrome b5 reductase in relation to hereditary methemoglobinemia. Yubisui T; Murakami K; Shirabe K; Takeshita M; Zenno S; Tomatsu S; Fukumaki Y Prog Clin Biol Res; 1989; 319():107-19; discussion 120-1. PubMed ID: 2695933 [No Abstract] [Full Text] [Related]
31. Species differences in methemoglobin reductase activity. Stolk JM; Smith RP Biochem Pharmacol; 1966 Mar; 15(3):343-51. PubMed ID: 4380376 [No Abstract] [Full Text] [Related]
32. Hereditary methemoglobinemic cyanosis due to diaphorase deficiency in three successive generations. Ozsoylu S Acta Haematol; 1967; 37(5):276-83. PubMed ID: 4963515 [No Abstract] [Full Text] [Related]
33. Reduction of methemoglobin in human adult and cord blood erythrocytes incubated with glucose or inosine. Lee WM; Bragg FE; Jaffé ER Proc Soc Exp Biol Med; 1967 Jan; 124(1):214-6. PubMed ID: 6017769 [No Abstract] [Full Text] [Related]
35. [Isoelectric focusing of NADH: methemoglobin reductase and NAD(P)H: diaphorases of human erythrocytes]. Sonnet J; de Noyette JP; Steichen-Defalque M Clin Chim Acta; 1971 Mar; 32(1):5-16. PubMed ID: 5096427 [No Abstract] [Full Text] [Related]
36. [Hereditary methemoglobinemic cyanosis]. Păsculescu G Med Interna (Bucur); 1972 Apr; 24(4):413-21. PubMed ID: 5027787 [No Abstract] [Full Text] [Related]
37. Electrophoretic and functional variants of NADH-methemoglobin reductase in hereditary methemoglobinemia. Hsieh HS; Jaffé ER J Clin Invest; 1971 Jan; 50(1):196-202. PubMed ID: 5543874 [TBL] [Abstract][Full Text] [Related]
38. Rapid method for detection of erythrocyte NADH-methemoglobin reductase deficiency. Rogers LE Am J Clin Pathol; 1972 Feb; 57(2):186-7. PubMed ID: 4333282 [No Abstract] [Full Text] [Related]
39. The structure of the S127P mutant of cytochrome b5 reductase that causes methemoglobinemia shows the AMP moiety of the flavin occupying the substrate binding site. Bewley MC; Davis CA; Marohnic CC; Taormina D; Barber MJ Biochemistry; 2003 Nov; 42(45):13145-51. PubMed ID: 14609324 [TBL] [Abstract][Full Text] [Related]