Molecular lesion affecting the ADP-combining site in a mutant isozyme of erythrocyte pyruvate kinase (Q35468694)

8 August 2017

title

Molecular lesion affecting the ADP-combining site in a mutant isozyme of erythrocyte pyruvate kinase (English)

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8 August 2017

D E Paglia

1

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8 August 2017

W N Valentine

series ordinal

2

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8 August 2017

language of work or name

English

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publication date

1 August 1981

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Proceedings of the National Academy of Sciences of the United States of America

8 August 2017

published in

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8 August 2017

volume

78

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8 August 2017

issue

8

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8 August 2017

page(s)

5175-5179

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An inherited molecular lesion of erythrocyte pyruvate kinase. Identification of a kinetically aberrant isozyme associated with premature hemolysis

8 August 2017

cites work

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Kinetic differences between human red cell and leucocyte pyruvate kinase

27 July 2018

1 reference

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International Committee for Standardization in Haematology: recommended methods for red-cell enzyme analysis.

27 July 2018

1 reference

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Hemolytic anemia due to pyruvate kinase deficiency: characterization of the enzymatic activity from eight patients

27 July 2018

1 reference

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Significance of the electrophoretic modifications of defective pyruvate kinase variants. Study of six new observations

27 July 2018

1 reference

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Concomitance of an Active and an Inactive Mutant of Red Cell Pyruvate Kinase (PK)

27 July 2018

1 reference

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Advances in hereditary red cell enzyme anomalies

27 July 2018

1 reference

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Thirteen cases of pyruvate kinase deficiency found in Japan.

27 July 2018

1 reference

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A specific erythrocyte glycolytic enzyme defect (pyruvate kinase) in three subjects with congenital non-spherocytic hemolytic anemia

26 September 2018

1 reference

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Studies on erythrocyte glycolysis. I. Determination of the glycolytic intermediates in human erythrocytes

15 November 2018

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12 December 2020

Stabilization, partial purification, and effects of activating cations, ADP, and phosphoenolpyruvate on the reaction rates of an erythrocyte pyruvate kinase

1 reference

12 December 2020

Evidence for molecular alteration of pyruvate kinase as a consequence of erythrocyte aging

1 reference

12 December 2020

Human erythrocyte pyruvate kinase. Its purification and some properties

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12 December 2020

Pyruvate kinase deficiency

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12 December 2020

Hereditary erythrocyte pyruvate kinase deficiency: molecular and functional studies of four mutant PK variants detected in Spain

1 reference

12 December 2020

Human erythrocyte pyruvate kinase deficiency: The use of a kinetic study of mutant enzymes for the detection of heterozygotes

1 reference

12 December 2020

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12 December 2020

Seven pyruvate kinase variants characterized by the ICSH recommended methods

1 reference

12 December 2020

Pyruvate kinase deficiency hemolytic anemia: enzymatic characterization studies in twelve patients

1 reference

12 December 2020

The primary cause of hemolysis in enzymopathies of anaerobic glycolysis: a viewpoint

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12 December 2020

Studies on spontaneous in vitro autohemolysis in hemolytic disorders

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12 December 2020

The correlation of reaction kinetics and substrate binding with the mechanism of pyruvate kinase

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12 December 2020

Pyruvate kinase (PK) deficiency hereditary nonspherocytic hemolytic anemia

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12 December 2020

Improved method for the determination of blood glutathione

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12 December 2020

Identifiers

DOI

10.1073/PNAS.78.8.5175

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8 August 2017

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8 August 2017

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