AbstractWe report the sequence of a human cDNA that encodes a 46 kDa transmembrane protein homologous to bacterial transporters for phosphate esters. This protein presents at its carboxy terminus the consensus motif for retention in the endoplasmic reticulum. Northern blots of rat tissues indicate that the corresponding mRNA is mostly expressed in liver and kidney. In two patients with glycogen storage disease type Ib, mutations were observed that either replaced a conserved Gly to Cys or introduced a premature stop codon. The encoded protein is therefore most likely the glucose 6-phosphate translocase that is functionally associated with glucose-6-phosphatase
AbstractThis study aimed at directly assessing glucose 6-phosphate (G6P) transport by intact rat liv...
Deficiency of a microsomal phosphate transporter in the liver has been suggested in some patients af...
AbstractThere are differences in the kinetic properties of the liver and brain microsomal glucose-6-...
We report the sequence of a human cDNA that encodes a 46 kDa transmembrane protein homologous to bac...
AbstractWe report the sequence of a human cDNA that encodes a 46 kDa transmembrane protein homologou...
Glucose 6-phosphate transport has been well characterized in liver microsomes. The transport is requ...
We report the structure of the human gene encoding the putative glucose 6-phosphate translocase that...
SummaryGlycogen-storage diseases type I (GSD type I) are due to a deficiency in glucose-6-phosphatas...
Glycogen storage disease (GSD) 1b is the deficiency of endoplasmic reticulum glucose-6-phosphate (G...
In liver endoplasmic reticulum the intralumenal glucose-6-phosphatase activity requires the operatio...
Glycogen storage disease (GSD) 1b is the deficiency of endoplasmic reticulum glucose-6-phosphate (G6...
Glycogen storage disease (GSD) 1b is the deficiency of endoplasmic reticulum glucose-6-phosphate (G6...
AbstractGlycogen storage disease (GSD) 1b is the deficiency of endoplasmic reticulum glucose-6-phosp...
Glycogen storage disease (GSD) 1b is the deficiency of endoplasmic reticulum glucose-6-phosphate (G6...
AbstractThis study aimed at directly assessing glucose 6-phosphate (G6P) transport by intact rat liv...
Deficiency of a microsomal phosphate transporter in the liver has been suggested in some patients af...
AbstractThere are differences in the kinetic properties of the liver and brain microsomal glucose-6-...
We report the sequence of a human cDNA that encodes a 46 kDa transmembrane protein homologous to bac...
AbstractWe report the sequence of a human cDNA that encodes a 46 kDa transmembrane protein homologou...
Glucose 6-phosphate transport has been well characterized in liver microsomes. The transport is requ...
We report the structure of the human gene encoding the putative glucose 6-phosphate translocase that...
SummaryGlycogen-storage diseases type I (GSD type I) are due to a deficiency in glucose-6-phosphatas...
Glycogen storage disease (GSD) 1b is the deficiency of endoplasmic reticulum glucose-6-phosphate (G...
In liver endoplasmic reticulum the intralumenal glucose-6-phosphatase activity requires the operatio...
Glycogen storage disease (GSD) 1b is the deficiency of endoplasmic reticulum glucose-6-phosphate (G6...
Glycogen storage disease (GSD) 1b is the deficiency of endoplasmic reticulum glucose-6-phosphate (G6...
AbstractGlycogen storage disease (GSD) 1b is the deficiency of endoplasmic reticulum glucose-6-phosp...
Glycogen storage disease (GSD) 1b is the deficiency of endoplasmic reticulum glucose-6-phosphate (G6...
AbstractThis study aimed at directly assessing glucose 6-phosphate (G6P) transport by intact rat liv...
Deficiency of a microsomal phosphate transporter in the liver has been suggested in some patients af...
AbstractThere are differences in the kinetic properties of the liver and brain microsomal glucose-6-...