Quantitative analysis of glucose-6-phosphate translocase gene expression in various human tissues and haematopoietic progenitor cells (Q73079656)

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1 November 2019

title

Quantitative analysis of glucose-6-phosphate translocase gene expression in various human tissues and haematopoietic progenitor cells (English)

1 reference

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1 November 2019

author name string

K Ihara

1

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1 November 2019

A Nomura

2

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1 November 2019

S Hikino

3

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1 November 2019

H Takada

4

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1 November 2019

T Hara

5

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1 November 2019

publication date

1 September 2000

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Journal of Inherited Metabolic Disease

1 November 2019

published in

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1 November 2019

volume

23

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1 November 2019

page(s)

583-592

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1 November 2019

issue

6

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https://scigraph.springernature.com/pub.10.1023/a:1005677912539

1 November 2019

exact match

0 references

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Type Ib glycogen storage disease is caused by a defect in the glucose-6-phosphate translocase of the microsomal glucose-6-phosphatase system

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Molecular analysis of glycogen storage disease type Ib: identification of a prevalent mutation among Japanese patients and assignment of a putative glucose-6-phosphate translocase gene to chromosome 11

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In vitro and in vivo effects of granulocyte colony-stimulating factor on neutrophils in glycogen storage disease type 1B: granulocyte colony-stimulating factor therapy corrects the neutropenia and the defects in respiratory burst activity and Ca2+ m

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Neutropenia and impaired neutrophil migration in type IB glycogen storage disease

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Defective neutrophil and monocyte functions in glycogen storage disease type Ib: a literature review

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The putative glucose 6-phosphate translocase gene is mutated in essentially all cases of glycogen storage disease type I non-a

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Structure and mutation analysis of the glycogen storage disease type 1b gene.

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A new variant of glycogen storage disease Type I probably due to a defect in the glucose-6-phosphate transport system

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A gene on chromosome 11q23 coding for a putative glucose- 6-phosphate translocase is mutated in glycogen-storage disease types Ib and Ic.

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Structure of the gene mutated in glycogen storage disease type Ib.

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