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SLC37A4 gene

Known as: solute carrier family 37 member 4, SLC37A4, GLUCOSE-6-PHOSPHATE TRANSLOCASE 
National Institutes of Health

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2 relations
Glucose-6-phosphate transport defectSLC37A1 gene

Papers overview

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2011
2011
A novel mutation in SLC37A4 gene in a Sri Lankan boy with glycogen storage disease type Ib associated with very early onset neutropenia
Glycogen storage disease type Ib (GSD Ib) [MIM 232220] is caused by mutations in the gene encoding microsomal glucose-6-phosphate… 
2010
2010
Inhibition of Tubulogenesis and of Carcinogen‐mediated Signaling in Brain Endothelial Cells Highlight the Antiangiogenic Properties of a Mumbaistatin Analog
A better understanding of the metabolic adaptations of the vascular endothelial cells (EC) that mediate tumor vascularization… 
2009
2009
A case of glycogen storage disease type Ib
= Abstract = We report a case of an 18-month-old girl with glycogen storage disease type Ib (GSD Ib). Her neutrophil counts had… 
Review
2002
Review
2002
Historical highlights and unsolved problems in glycogen storage disease type 1
Abstract. Thirty-three years after Von Gierke described the first patient with glycogen storage disease type 1 (GSD1) in 1929… 
2001
2001
Glucose-6-phosphate translocase as a target for the design of antidiabetic agents
Highly Cited
1998
Highly Cited
1998
Plasma glucose levels are reduced in rats and mice treated with an inhibitor of glucose-6-phosphate translocase.
The activity of glucose-6-phosphatase (G-6-Pase) in isolated rat microsomes was inhibited by a new selective inhibitor of the… 
1995
1995
Multiple transport protein defects in a patient with glycogen storage disease type 1: GSD 1b/1cβ
SummaryA male child presented at 5 months of age with vomiting, diarrhoea, hypoglycaemia and hepatomegaly. Histology on a frozen… 
1988
1988
Analysis of glucose-6-phosphate translocase and hexose-6-phosphate phosphohydrolase, the two obligatory components of microsomal glucose-6-phosphatase system, in rat liver.
A membrane filter procedure developed by Igarashi et al. (1984) for the measurement of glucose 6-phosphate uptake by the… 
1982
1982
Glycogen storage disease type 1b due to a defect of glucose-6-phosphate translocase
AbstractsPatients with glycogen storage disease (GSD) type 1b have shown normal activity of glucose-6-phosphatase (EC 3.1.3.9) as… 
1978
1978
Four new electrophoretically slow‐moving glucose 6‐phosphate dehydrogenase variants associated with congenital nonspherocytic hemolytic anemia found in Japan: Gd(‐) Kurume, Gd(‐) Fukushima, Gd…
Four new glucose 6‐phosphate dehydrogenase (G6PD) variants which had electrophoretically slow‐moving characteristics associated… 
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