Disease: Glucose-6-phosphate translocase deficiency
- A direct method for the diagnosis of human hepatic type 1b and type 1c glycogen-storage disease
- A gene on chromosome 11q23 coding for a putative glucose- 6-phosphate translocase is mutated in glycogen-storage disease types Ib and Ic
- A molecular link between the common phenotypes of type 1 glycogen storage disease and HNF1alpha-null mice
- A mutation in SLC37A4 causes a dominantly inherited congenital disorder of glycosylation characterized by liver dysfunction
- Acute myelogenous leukemia and glycogen storage disease 1b
- Cell death and stress signaling in glycogen storage disease type I
- Clinical characteristics and long-term outcomes of patients with glycogen storage disease type 1b: a retrospective multi-center experience in Poland
- CRISPR/Cas9 genome editing of SLC37A4 gene elucidates the role of molecular markers of endoplasmic reticulum stress and apoptosis in renal involvement in glycogen storage disease type Ib
- Diabetes affects similarly the catalytic subunit and putative glucose-6-phosphate translocase of glucose-6-phosphatase
- Diagnosis and management of glycogen storage disease type I: a practice guideline of the American College of Medical Genetics and Genomics
- Dietary P(i) deprivation in rats affects liver cAMP, glycogen, key steps of gluconeogenesis and glucose production
- Failure to eliminate a phosphorylated glucose analog leads to neutropenia in patients with G6PT and G6PC3 deficiency
- G6PC3 mutations are associated with a major defect of glycosylation: a novel mechanism for neutrophil dysfunction
- Gastric drip feeding in patients with glycogen storage disease type I: its effects on growth and plasma lipids and apolipoproteins
- Gene mutations and clinical manifestations in children with glycogen storage disease type Ib
- Genomic structure of the human glucose 6-phosphate translocase gene and novel mutations in the gene of a Japanese patient with glycogen storage disease type Ib
- Genotype-phenotype correlation and description of two novel mutations in Iranian patients with glycogen storage disease 1b (GSD1b)
- Glucocorticoids activate transcription of the gene for the glucose-6-phosphate transporter, deficient in glycogen storage disease type 1b
- Glucose release from GLUT2-null hepatocytes: characterization of a major and a minor pathway
- Glucose-6-phosphatase dependent substrate transport in the glycogen storage disease type-1a mouse
- Glucose-6-phosphatase mutation G188R confers an atypical glycogen storage disease type 1b phenotype
- Glucose-6-phosphate translocase deficiency--glycogen storage disease type 1 b
- Glycogen storage disease
- Glycogen storage disease type 1b due to a defect of glucose-6-phosphate translocase
- Glycogen storage disease type 1b: an early onset severe phenotype associated with a novel mutation (IVS4) in the glucose 6-phosphate translocase (SLC37A4) gene in a Turkish patient
- Glycogen storage disease type 1b: genetic disorder involving the transport system of intracellular membrane
- Glycogen storage disease type 1b: microsomal glucose-6-phosphatase system in two patients with different clinical findings
- Glycogen Storage Disease Type I
- Glycogen Storage Disease Type I
- Glycogen storage disease type Ib: a defect in the glucose-6-phosphate transport system in microsomal membrane (The Japan Society of Human Genetics Award lecture)
- Glycogen storage disease type Ib: role of glucose-6-phosphate transporter in cell metabolism and function
- Glycogen storage disease type Ib: the first case in Taiwan
- Glycogen storage disease: clinical, biochemical, and molecular heterogeneity
- Glycogen storage disease: recommendations for treatment
- Historical highlights and unsolved problems in glycogen storage disease type 1
- Human variant glucose-6-phosphate transporter is active in microsomal transport
- Identification, purification and genetic deficiencies of the glucose-6-phosphatase system transport proteins
- Impact of hematopoietic stem cell transplantation in glycogen storage disease type Ib: A single-subject research design using <sup>13</sup>C-glucose breath test
- Impaired glucose homeostasis, neutrophil trafficking and function in mice lacking the glucose-6-phosphate transporter
- Impaired glucose transport in polymorphonuclear leukocytes in glycogen storage disease Ib
- Inactivation of the glucose 6-phosphate transporter causes glycogen storage disease type 1b
- Intestinal glucose transport: evidence for a membrane traffic-based pathway in humans
- Molecular biology and gene therapy for glycogen storage disease type Ib
- Molecular diagnosis of glycogen storage disease type I: a review
- Molecular diagnosis of type 1c glycogen storage disease
- Molecular genetics of type 1 glycogen storage disease
- Mouse heat shock transcription factor 1 deficiency alters cardiac redox homeostasis and increases mitochondrial oxidative damage
- Multiple transport protein defects in a patient with glycogen storage disease type 1: GSD 1b/1c beta
- Mutation in the SLC37A4 gene of glycogen storage disease type Ib in 15 families of the mainland of China
- Neutrophil metabolic dysfunction in genetically heterogeneous patients with glycogen storage disease type 1b
- New insights into the organisation and intracellular localisation of the two subunits of glucose-6-phosphatase
- Normal kinetics of intestinal glucose absorption in the absence of GLUT2: evidence for a transport pathway requiring glucose phosphorylation and transfer into the endoplasmic reticulum
- Normoglycemia alone is insufficient to prevent long-term complications of hepatocellular adenoma in glycogen storage disease type Ib mice
- Novel mutation of SLC37A4 in a glycogen storage disease type Ib patient with neutropenia, horseshoe kidney, and arteriovenous malformation: a case report
- Ontogeny of the murine glucose-6-phosphatase system
- Partial correction of neutrophil dysfunction by oral galactose therapy in glycogen storage disease type Ib
- Periodontal Manifestation of Type Ib Glycogen Storage Disease: A Rare Case Report
- Prenatal diagnosis of glycogen storage disease type 1b using denaturing high performance liquid chromatography
- Prolonged blood glucose reduction in mrp-2 deficient rats (GY/TR(-)) by the glucose-6-phosphate translocase inhibitor S 3025
- SGLT5 is the renal transporter for 1,5-anhydroglucitol, a major player in two rare forms of neutropenia
- Silencing of the human microsomal glucose-6-phosphate translocase induces glioma cell death: potential new anticancer target for curcumin
- SLGT2 Inhibitor Rescues Myelopoiesis in G6PC3 Deficiency
- Structural requirements for the stability and microsomal transport activity of the human glucose 6-phosphate transporter
- Structure and mutation analysis of the glycogen storage disease type 1b gene
- Structure-function analysis of the glucose-6-phosphate transporter deficient in glycogen storage disease type Ib
- Successful use of empagliflozin to treat neutropenia in two G6PC3-deficient children: Impact of a mutation in SGLT5
- The benefits of liver transplantation in glycogenosis type Ib
- The Physiopathological Role of the Exchangers Belonging to the SLC37 Family
- The signature motif in human glucose-6-phosphate transporter is essential for microsomal transport of glucose-6-phosphate
- The SLC37 family of phosphate-linked sugar phosphate antiporters
- Transmembrane topology of human glucose 6-phosphate transporter
- Type Ib glycogen storage disease is caused by a defect in the glucose-6-phosphate translocase of the microsomal glucose-6-phosphatase system
- Type-1c glycogen storage disease is not caused by mutations in the glucose-6-phosphate transporter gene
- Unusual oral manifestations and evolution in glycogen storage disease type Ib
- Up-regulation of liver glucose-6-phosphatase in rats fed with a P(i)-deficient diet
- Up-regulation of liver glucose-6-phosphatase in x-linked hypophosphatemic mice
- Urinary excretion of lactate, 2-oxoglutarate, citrate, and glycerol in patients with glycogenosis type I