A Low KmPhosphoenolpyruvate Mutant in the Amish with Red Cell Pyruvate Kinase Deficiency-Reference-Cited by-同舟云学术

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A Low KmPhosphoenolpyruvate Mutant in the Amish with Red Cell Pyruvate Kinase Deficiency

Published:1969-09 Issue:3 Volume:17 Page:289-297
ISSN:0007-1048
Container-title:British Journal of Haematology
language:en
Short-container-title:Br J Haematol

Author:

Oski Frank A.,Bowman Herbert

Publisher

Wiley

Subject

Hematology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2141.1969.tb01375.x/fullpdf

Reference25 articles.

1. Hereditary Non-spherocytic Hemolytic Anemia of the Pyruvate-kinase Deficient Type

2. D. Busch(1963 ). 'Erythrocyte metabolism in three persons with hereditary non-spherocytic hemolytic anemia, deficient in pyruvate-kinase.' Proc. Ninth Congr. Europ. Soc. Haemat., Lisbon, p.783 .

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1. Structure‐Based Design of AG‐946, a Pyruvate Kinase Activator;ChemMedChem;2024-02-02

2. AG-348 enhances pyruvate kinase activity in red blood cells from patients with pyruvate kinase deficiency;Blood;2017-09-14

3. A Deficient Pyruvate Kinase with an Electrophoretically Slow-Moving Component;Scandinavian Journal of Haematology;2009-04-24

4. Comparison of erythrocyte antioxidative enzyme activities between two types of haemoglobin H disease.;Journal of Clinical Pathology;1986-12-01

5. Mathematical modelling of metabolic pathways affected by an enzyme deficiency. A mathematical model of glycolysis in normal and pyruvate-kinase-deficient red blood cells;European Journal of Biochemistry;1985-05

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