Alteration of NADH-diaphorase and cytochrome b5 reductase activities of erythrocytes, platelets, and leucocytes in hereditary methaemoglobinaemia with and without mental retardation.

مواد مشابهة

• Analyis of met-form haemoglobins in human erythrocytes of normal adults and of a patient with hereditary methaemoglobinaemia due to deficiency of NADH-cytochrome b5 reductase.
  بواسطة: Tomoda, A, وآخرون
  منشور في: (1979)
• Automated determination of red cell methaemoglobin reductase activity by a continuous-flow system for screening hereditary methaemoglobinaemia.
  بواسطة: Tanishima, K, وآخرون
  منشور في: (1979)
• The opposite effect of bivalent cations on cytochrome b5 reduction by NADH:cytochrome b5 reductase and NADPH:cytochrome c reductase.
  بواسطة: Tamura, M, وآخرون
  منشور في: (1988)
• Age-dependent decay of cytochrome b5 and cytochrome b5 reductase in human erythrocytes.
  بواسطة: Matsuki, T, وآخرون
  منشور في: (1981)
• 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
  بواسطة: Katsube, Takanori, وآخرون
  منشور في: (1991)