Human microsomal glucose-6-phosphatase system

No abstract is available for this paper.

• Publication year

  2005

• Venue

  European Journal of Pediatrics

• Publication date

  Unknown publication date

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1007/BF02072079PMID 8391443
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• Glycogen storage diseases

  1991cited by this paper
• Molecular pathology of glucose‐6‐phosphatase 1

  1990cited by this paper
• The Glycogen-Storage Diseases

  1990cited by this paper
• The microsomal glucose‐6‐phosphatase enzyme of human gall‐bladder

  1989cited by this paper
• Hepatic microsomal glucose-6-phosphatase system and sudden infant death syndrome.

  1989cited by this paper
• Glucose-6-phosphatase: two concepts of membrane-function relationship.

  1989cited by this paper
• Multiple forms of type I glycogen storage disease: underlying mechanisms

  1986cited by this paper
• Evidence for changes in the conformational status of rat liver microsomal glucose-6-phosphate:phosphohydrolase during detergent-dependent membrane modification. Effect of p-mercuribenzoate and organomercurial agarose gel on glucose-6-phosphatase of native and detergent-modified microsomes.

  1986cited by this paper
• Fine tuning of blood glucose concentrations

  1985cited by this paper
• Type Ic, a novel glycogenosis. Underlying mechanism.

  1983cited by this paper
• Mitochondrial-reticular cytostructure in liver cells.

  1983cited by this paper
• In vivo evidence for defective activity of glucose-6-phosphatase in type IB glycogenosis.

  1980cited by this paper
• Neutropenia and impaired neutrophil migration in type IB glycogen storage disease.

  1980cited by this paper
• Evidence for the participation of independent translocation for phosphate and glucose 6-phosphate in the microsomal glucose-6-phosphatase system. Interactions of the system with orthophosphate, inorganic pyrophosphate, and carbamyl phosphate.

  1980cited by this paper
• Type Ib glycogen storage disease is caused by a defect in the glucose-6-phosphate translocase of the microsomal glucose-6-phosphatase system.

  1980cited by this paper
• Disordered intestinal function in glycogen storage disease

  1978cited by this paper
• A new variant of glycogen storage disease type I probably due to a defect in the glucose-6-phosphate transport system.

  1978cited by this paper
• Futile cycles in the metabolism of glucose.

  1976cited by this paper
• On the involvement of a glucose 6-phosphate transport system in the function of microsomal glucose 6-phosphatase

  1975cited by this paper
• Mammalian carbamyl phosphate : glucose phosphotransferase and glucose-6-phosphate phosphohydrolase: extended tissue distribution.

  1975cited by this paper
• Utile and futile cycles in the liver.

  1974cited by this paper
• Human liver carbamyl phosphate‐glucose phosphotransferase activity: Catalytic properties and physiological phosphorylative potential

  1971cited by this paper
• 22 Glucose-6-Phosphatase, Hydrolytic and Synthetic Activities

  1971cited by this paper
• Studies of liver glycogenoses, with particular reference to the metabolism of intravenously administered glycerol.

  1968cited by this paper
• The inhibition by phlorizin of kidney microsomal inorganic pyrophosphate-glucose phosphotransferase and glucose 6-phosphatase.

  1967cited by this paper
• Glucose-6-phosphatase deficiency glycogen storage disease. Studies on the interrelationships of carbohydrate, lipid, and purine abnormalities.

  1962cited by this paper
• Glucose-6-phosphatase of the liver in glycogen storage disease.

  1952cited by this paper
• Phosphatases of liver. I. Glucose-6-phosphatase.

  1950cited by this paper
• The hexose-monophosphatase system (glucose-6-phosphatase) of liver.

  1948cited by this paper
• DEPHOSPHORYLATION IN LIVER EXTRACTS

  1945cited by this paper
• THE RÔLE OF GLUCOSE-1-PHOSPHATE IN THE FORMATION OF BLOOD SUGAR AND SYNTHESIS OF GLYCOGEN IN THE LIVER

  1939cited by this paper
• Formation and breakdown of glycogen in the liver.

  1939cited by this paper

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  2013cites this paper
• Peroxyvanadium compounds inhibit glucose-6-phosphatase activity and glucagon-stimulated hepatic glucose output in the rat in vivo.

  1999cites this paper
• Prevention of hypoglycaemia in a patient with type Ib glycogen storage disease by an amylase (α‐glucosidase) inhibitor

  1998cites this paper
• Hepatocellular expression of glucose-6-phosphatase is unaltered during hepatic regeneration.

  1998cites this paper
• Calcium kinetics in glycogen storage disease type 1a

  1996cites this paper
• Glycogen Storage Disease Type Ia in Two Littermate Maltese Puppies

  1995cites this paper