About: Type I glycogen storage diseases: disorders of the glucose-6-phosphatase complex

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scientific article (publication date: March 2002)

Attributes	Values
rdf:type	Item
description	wissenschaftlicher Artikel (de) artículu científicu espublizáu en 2002 (ast) vědecký článek publikovaný v roce 2002 (cs) 2002 թուականի Մարտին հրատարակուած գիտական յօդուած (hyw) 2002 թվականի մարտին հրատարակված գիտական հոդված (hy) vedecký článok (publikovaný 2002-03) (sk) наукова стаття, опублікована в березні 2002 (uk) wetenschappelijk artikel (gepubliceerd in 2002-03) (nl) مقالة علمية (نشرت في مارس 2002) (ar) scientific article (publication date: March 2002) (en)
publication date	wds:Q28214516-B40B4747-C056-45D6-9E69-6024D4F70800
publication date	2002-03-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q28214516-4FCCEC50-20F7-4AB8-84B6-35F64149FF25
language of work or name	English
author name string	wds:Q28214516-1CFF5EC8-0ECC-4378-A187-4DA2BF186B41 wds:Q28214516-70DFCE1B-1BCD-4364-84CE-9433CF1F4846 wds:Q28214516-BA34EB94-1E89-42A9-B8DE-A530C17655B9
OpenCitations bibliographic resource ID	wds:Q28214516-692DF558-B1BA-402A-8171-8006207A3081
OpenCitations bibliographic resource ID	https://w3id.org/oc/corpus/br/4889057
author name string	Dietrich Matern Yuan-Tsong Chen Janice Yang Chou
OpenCitations bibliographic resource ID	4889057
rdfs:label	Type I glycogen storage diseases: disorders of the glucose-6-phosphatase complex (en) Type I glycogen storage diseases: disorders of the glucose-6-phosphatase complex (nl) Type I glycogen storage diseases: disorders of the glucose-6-phosphatase complex (ast)
skos:prefLabel	Type I glycogen storage diseases: disorders of the glucose-6-phosphatase complex (en) Type I glycogen storage diseases: disorders of the glucose-6-phosphatase complex (nl) Type I glycogen storage diseases: disorders of the glucose-6-phosphatase complex (ast)
name	Type I glycogen storage diseases: disorders of the glucose-6-phosphatase complex (en) Type I glycogen storage diseases: disorders of the glucose-6-phosphatase complex (nl) Type I glycogen storage diseases: disorders of the glucose-6-phosphatase complex (ast)
author	wds:Q28214516-7DCFA57A-72E9-49EB-A878-FCA9760AA0B1
author	Brian C Mansfield
title	wds:Q28214516-1AA4CB19-6F33-4395-9750-48C678830A6A
title	Type I glycogen storage diseases: disorders of the glucose-6-phosphatase complex (en)
page(s)	wds:Q28214516-367010B0-C2DE-48D0-B9A8-564179EFA775
page(s)	121-43
instance of	wds:Q28214516-2d0c644f-5949-4b3f-bb45-b373ab12e85e wds:Q28214516-F34877FF-9833-4492-ABFF-2D9D7064463F
instance of	review article scholarly article
main subject	wds:Q28214516-33EDEDE7-186D-4CB0-AFD1-79A8A0CB1982 wds:Q28214516-85266cc8-d69a-4893-81a2-ccbd5999db18
main subject	glycobiology glucose
PubMed ID	wds:Q28214516-F093D7E5-44D4-48A2-9EFA-EE914B351185
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/11949931
PubMed ID	11949931
published in	wds:Q28214516-A235E2F6-46A6-4133-8D41-785D9B164044
published in	Current Molecular Medicine
issue	wds:Q28214516-15846550-488C-4F8F-ADBF-2EC76F9077F4
volume	wds:Q28214516-BFC27180-4820-4076-90CE-683F4B31C063
issue	2
volume	2
DOI	wds:Q28214516-825C2BB6-772B-4375-97EA-BA220FC5A146
DOI	http://dx.doi.org/10.2174/1566524024605798
DOI	10.2174/1566524024605798
is owl:sameAs of	Type I glycogen storage diseases: disorders of the glucose-6-phosphatase complex
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q28214516
is cites work of	Reduction of hepatic glucocorticoid receptor and hexose-6-phosphate dehydrogenase expression ameliorates diet-induced obesity and insulin resistance in mice Specific reduction of G6PT may contribute to downregulation of hepatic 11β-HSD1 in diabetic mice SLC37A1 and SLC37A2 are phosphate-linked, glucose-6-phosphate antiporters Targeted deletion of kidney glucose-6 phosphatase leads to nephropathy. Glycine N-methyltransferase-/- mice develop chronic hepatitis and glycogen storage disease in the liver Tissue-specific dysregulation of hexose-6-phosphate dehydrogenase and glucose-6-phosphate transporter production in db/db mice as a model of type 2 diabetes. Brain contains a functional glucose-6-phosphatase complex capable of endogenous glucose production Hepatocyte nuclear factor-4 alpha mediates the stimulatory effect of peroxisome proliferator-activated receptor gamma co-activator-1 alpha (PGC-1 alpha) on glucose-6-phosphatase catalytic subunit gene transcription in H4IIE cells Lack of glucose recycling between endoplasmic reticulum and cytoplasm underlies cellular dysfunction in glucose-6-phosphatase-beta-deficient neutrophils in a congenital neutropenia syndrome G6PC3 mutations are associated with a major defect of glycosylation: a novel mechanism for neutrophil dysfunction Identification and characterisation of a new human glucose-6-phosphatase isoform Impaired neutrophil activity and increased susceptibility to bacterial infection in mice lacking glucose-6-phosphatase-beta Genotype/phenotype correlation in glycogen storage disease type 1b: a multicentre study and review of the literature Deletion of the gene encoding the ubiquitously expressed glucose-6-phosphatase catalytic subunit-related protein (UGRP)/glucose-6-phosphatase catalytic subunit-beta results in lowered plasma cholesterol and elevated glucagon. Strategies of bacterial over expression of membrane transporters relevant in human health: the successful case of the three members of OCTN subfamily Evidence for transcriptional regulation of the glucose-6-phosphate transporter by HIF-1alpha: Targeting G6PT with mumbaistatin analogs in hypoxic mesenchymal stromal cells MT1-MMP down-regulates the glucose 6-phosphate transporter expression in marrow stromal cells: a molecular link between pro-MMP-2 activation, chemotaxis, and cell survival. 11beta-Hydroxysteroid Dehydrogenase Type 1 Regulation by Intracellular Glucose 6-Phosphate Provides Evidence for a Novel Link between Glucose Metabolism and Hypothalamo-Pituitary-Adrenal Axis Function Glycogen storage disease type Ia in Argentina: two novel glucose-6-phosphatase mutations affecting protein stability Inborn errors of metabolism: the flux from Mendelian to complex diseases. Glycogen storage disease type I and G6Pase-β deficiency: etiology and therapy Complete normalization of hepatic G6PC deficiency in murine glycogen storage disease type Ia using gene therapy Neutropenia in type Ib glycogen storage disease Glucose-6-phosphate transporter gene therapy corrects metabolic and myeloid abnormalities in glycogen storage disease type Ib mice Control of blood glucose in the absence of hepatic glucose production during prolonged fasting in mice: induction of renal and intestinal gluconeogenesis by glucagon Immunocytochemical localization of glucose 6-phosphatase and cytosolic phosphoenolpyruvate carboxykinase in gluconeogenic tissues reveals unsuspected metabolic zonation. Adeno-associated virus-mediated correction of a canine model of glycogen storage disease type Ia. Neutrophilia and elevated serum cytokines are implicated in glycogen storage disease type Ia. Long-term correction of murine glycogen storage disease type Ia by recombinant adeno-associated virus-1-mediated gene transfer Coffee intake is associated with lower rates of liver disease progression in chronic hepatitis C. Sequence variation between the mouse and human glucose-6-phosphatase catalytic subunit gene promoters results in differential activation by peroxisome proliferator activated receptor gamma coactivator-1alpha Cooperativity between 11beta-hydroxysteroid dehydrogenase type 1 and hexose-6-phosphate dehydrogenase in the lumen of the endoplasmic reticulum Clinical Outcome of Hepatocyte Transplantation in Four Pediatric Patients with Inherited Metabolic Diseases Practical aspects of overexpressing bacterial secondary membrane transporters for structural studies. A Sleeping Beauty mutagenesis screen reveals a tumor suppressor role for Ncoa2/Src-2 in liver cancer. Direct regulation of glucose and not insulin on hepatic hexose-6-phosphate dehydrogenase and 11β-hydroxysteroid dehydrogenase type 1 Angiotensin mediates renal fibrosis in the nephropathy of glycogen storage disease type Ia Glucose-6-phosphatase-β, implicated in a congenital neutropenia syndrome, is essential for macrophage energy homeostasis and functionality. Neutrophil stress and apoptosis underlie myeloid dysfunction in glycogen storage disease type Ib

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