Structure–function study of the glucose-6-phosphate transporter, an eukaryotic antiporter deficient in glycogen storage disease type Ib
Author:
Publisher
Elsevier BV
Subject
Endocrinology,Genetics,Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism
Reference30 articles.
1. Type I glycogen storage diseases: disorders of the glucose-6-phosphatase complex;Chou;Curr. Mol. Med.,2002
2. Glucose-6-phosphate transporter: the key to glycogen storage disease type Ib;Chou,2003
3. Glucose-6-phosphate hydrolase, widely expressed outside the liver, can explain age-dependent resolution of hypoglycemia in glycogen storage disease type Ia;Shieh;J. Biol. Chem.,2003
4. Histidine-167 is the phosphate acceptor in glucose-6-phosphatase-β forming a phosphohistidine–enzyme intermediate during catalysis;Ghosh;J. Biol. Chem.,2004
5. Impaired neutrophil activity and increased susceptibility to bacterial infection in mice lacking glucose-6-phosphatase-β;Cheung;J. Clin. Invest.,2007
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