(Q41448943)

30 September 2017

'GPI Roma', a new glucose phosphate isomerase deficient variant: in vivo occurrence of postsynthetic modifications of the mutant enzyme (English)

1 reference

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30 June 2022

author name string

G. Isacchi

1

1 reference

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30 June 2022

D. Cottreau

2

1 reference

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30 June 2022

F. Mandelli

3

1 reference

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30 June 2022

G. Papa

4

1 reference

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30 June 2022

F. Ciccone

5

1 reference

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30 June 2022

A. Kahn

6

1 reference

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30 June 2022

language of work or name

English

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=422204

30 June 2022

publication date

1 January 1979

1 reference

30 September 2017

25 January 1979

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=422204

30 June 2022

1 reference

30 September 2017

46

1 reference

30 September 2017

2

1 reference

30 September 2017

219-226

1 reference

https://scigraph.springernature.com/pub.10.1007/bf00291924

30 September 2017

0 references

cites work

Favism in a Portuguese family due to a deficient glucose-phosphate dehydrogenase variant (Canton) or (cpanton-like) type

1 reference

12 December 2020

Evidence against the occurrence of tissue-specific variants and isoenzymes of phosphoglucose isomerase

1 reference

12 December 2020

Inherited variations in human phosphohexose isomerase

1 reference

12 December 2020

Glucose phosphate isomerase deficiency with hereditary hemolytic anemia in a Spanish family: Clinical and familial studies

1 reference

12 December 2020

[Concerning tissue-specific isoenzymes of glucosephosphate isomerase in man (author's transl)]

1 reference

12 December 2020

Electrophoretic and kinetic studies of glucosephosphate isomerase (GPI) in two different Japanese families with GPI deficiency

1 reference

12 December 2020

Gd (−) Matam, an african glucose-6-phosphate dehydrogenase variant with enzyme deficiency. Biochemical and immunological properties in various hemopoietic tissues

1 reference

12 December 2020

Postsynthetic deamidation of hemoglobin Providence (beta 82 Lys replaced by Asn, Asp) and its effect on oxygen transport

1 reference

12 December 2020

Clinical and biochemical studies of glucosephosphate isomerase of normal human erythrocytes and in glucosephosphate isomerase deficiency

1 reference

12 December 2020

Glucose phosphate isomerase deficiency with congenital nonspherocytic hemolytic anemia: a new variant (type Nordhorn). II. Purification and biochemical properties of the defective enzyme

1 reference

12 December 2020

Molecular and functional anomalies in two new mutant glucose-phosphate-isomerase variants with enzyme deficiency and chronic hemolysis

1 reference

12 December 2020

Synthesis of haemoglobin Wayne in erythroid cells

1 reference

12 December 2020

Hereditary hemolytic anemia associated with glucosephosphate isomerase (GPI) deficiency--a new enzyme defect of human erythrocytes

1 reference

12 December 2020

Glucose-phosphate isomerase deficiency due to a new variant (GP I barcelona) and to a silent gene: Biochemical, immunological and genetic studies

1 reference

12 December 2020

A New variant of glucosephosphate isomerase deficiency: GPI-kortrijk

1 reference

12 December 2020

Genetic and Molecular Mechanisms of the Congenital Defects in Glucose Phosphate Isomerase Activity: Studies of Four Families

1 reference

12 December 2020

Congenital nonspherocytic hemolytic anemia associated with glucosephosphate isomerase deficiency: variant Paderborn

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00291924

1 reference

Dimensions Publication ID

30 September 2017

0 references

1 reference