Introduction to discussion of regulation of erythrocyte glycolysis (Q40002956)

16 September 2017

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title

Introduction to discussion of regulation of erythrocyte glycolysis (English)

1 reference

https://api.crossref.org/works/10.1016/S0014-4835(71)80039-8

22 March 2023

1 reference

https://api.crossref.org/works/10.1016/S0014-4835(71)80039-8

22 March 2023

W. N. Valentine

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A4941673

22 March 2023

language of work or name

English

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National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=4941673

22 March 2023

publication date

1 May 1971

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full work available at URL

16 September 2017

https://api.elsevier.com/content/article/PII:S0014483571800398?httpAccept=text/xml

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https://api.crossref.org/works/10.1016/S0014-4835(71)80039-8

https://api.elsevier.com/content/article/PII:S0014483571800398?httpAccept=text/plain

22 March 2023

1 reference

https://api.crossref.org/works/10.1016/S0014-4835(71)80039-8

Experimental Eye Research

22 March 2023

published in

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16 September 2017

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16 September 2017

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16 September 2017

page(s)

273-279

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Effect of flavin compounds on glutathione reductase activity: in vivo and in vitro studies

16 September 2017

cites work

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Glutathione reductase: stimulation in normal subjects by riboflavin supplementation

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[D-2,3-DIPHOSPHOGLYCERATE-2-PHOSPHOHYDROLASE DEFICIENCY AS A POSSIBLE CAUSE OF INCREASED ATP LEVELS]

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Hemolytic anemia with impaired hexokinase activity

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Red cell phosphoglycerate kinase deficiency. A new cause of non-spherocytic hemolytic anemia

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Muscle Phosphofructokinase Deficiency

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Occurrence of Defective Hexosephosphate Isomerization in Human Erythrocytes and Leukocytes

7 January 2021

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

7 January 2021

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Red-cell metabolism in non-spherocytic congenital haemolytic anaemia

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HEREDITARY HEMOLYTIC ANEMIA WITH TRIOSEPHOSPHATE ISOMERASE DEFICIENCY

7 January 2021

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Congenital non-spherocytic hemolytic anemia by 2,3-diphosphoglycerate mutase deficiency of the erythrocytes in early infancy

7 January 2021

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PHOSPHOFRUCTOKINASE DEFICIENCY IN SKELETAL MUSCLE. A NEW TYPE OF GLYCOGENOSIS.

7 January 2021

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Enzymatic basis for the coexistence of myopathy and hemolytic disease in inherited muscle phosphofructokinase deficiency

7 January 2021

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Hereditary hemolytic anemia associated with phosphoglycerate kinase deficiency in erythrocytes and leukocytes. A probable X-chromosome-linked syndrome

7 January 2021

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Hereditary hemolytic anemia with hexokinase deficiency. Role of hexokinase in erythrocyte aging

7 January 2021

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22 March 2023

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22 March 2023

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https://api.crossref.org/works/10.1016/S0014-4835(71)80039-8

22 March 2023

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22 March 2023

Identifiers

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16 September 2017

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