Significance of the electrophoretic modifications of defective pyruvate kinase variants. Study of six new observations
Author:
Publisher
Elsevier BV
Subject
Biochemistry (medical),Clinical Biochemistry,Biochemistry,General Medicine
Reference20 articles.
1. The genetic system of the L-type pyruvate kinase forms in man Subunit structure, interrelation and kinetic characteristics of the pyruvate kinase enzymes from erythrocytes and liver
2. Evidence for a postsynthetic proteolytic transformation of human erythrocyte pyruvate kinase into L-type enzyme
3. Further evidence of molecular alteration and aberration of erythrocyte pyruvate kinase
4. Electrophoretic and Kinetic Studies of Mutant Erythrocyte Pyruvate Kinases
5. Pyruvate kinase isozymes in man
Cited by 8 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. Hereditary disorders of red cell enzymes in the embden-meyerhof pathway;American Journal of Hematology;1983-06
2. Molecular lesion affecting the ADP-combining site in a mutant isozyme of erythrocyte pyruvate kinase.;Proceedings of the National Academy of Sciences;1981-08-01
3. Three Pyruvate Kinase Variants with Increased Affinity for PEP;British Journal of Haematology;1981-03
4. Pyruvate Kinase Deficiency and Other Enzymopathies of the Embden—Meyerhof Pathway;Clinics in Haematology;1981-02
5. Hereditary erythrocyte pyruvate-kinase (PK) deficiency and chronic hemolytic anemia: Clinical, genetic and molecular studies in six new Spanish patients;Human Genetics;1980-03
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