Mediterranean glucose 6-phosphate dehydrogenase (G6PD) deficiency - Near normal decay of the mutant enzyme protein in circulating erythrocytes
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1600-0609.1984.tb02389.x/fullpdf
Reference34 articles.
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2. In vivo lability of glucose-6-phosphate dehydrogenase in Gd A- and Gd Mediterranean deficiency;Piomelli;J Clin Invest,1968
3. Negro variant of glucose-6-phosphate dehydrogenase deficiency (A-) in man;Yoshida;Science,1967
4. Biochemical mechanisms of glucose 6-phosphate dehydrogenase deficiency;Morelli;Proc Natl Acad Sci USA,1978
5. Favism: Erythrocyte metabolism during haemolysis and reticulocytosis;Gaetani;Br J Haematol,1979
Cited by 5 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Oxidative inactivation of the calcium-stimulated neutral proteinase from human red blood cells by divicine and intracellular protection by reduced glutathione;Archives of Biochemistry and Biophysics;1986-11
2. INTRAERYTHROCYTIC STABILITY OF NORMAL AND MUTANT G6PD11Supported in part by grants from the Special Project “Ingegneria Genetica e Basi Molecolari delle Malattie Ereditarie”, C.N.R., Rome, and from the Ministry of Education, Rome.;Glucose-6-phosphate Dehydrogenase;1986
3. The Role of Plasma in Oxidative Haemolysis;Free Radical Research Communications;1986-01
4. Hexose monophosphate shunt-stimulated reduction of methemoglobin by divicine;Archives of Biochemistry and Biophysics;1985-11
5. Impairment of the calcium pump of human erythrocytes by divicine;Archives of Biochemistry and Biophysics;1985-06
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