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Downregulation of SIRT1 signaling underlies hepatic autophagy impairment in glycogen storage disease type Ia

PLoS genetics, 2017-05, Vol.13 (5), p.e1006819-e1006819

2017

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Prevention of hepatocellular adenoma and correction of metabolic abnormalities in murine glycogen storage disease type Ia by gene therapy

Hepatology (Baltimore, Md.), 2012-11, Vol.56 (5), p.1719-1729

2012

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SLC37A1 and SLC37A2 are phosphate-linked, glucose-6-phosphate antiporters

PloS one, 2011-09, Vol.6 (9), p.e23157

2011

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glucose-6-phosphate transporter is a phosphate-linked antiporter deficient in glycogen storage disease type Ib and Ic

The FASEB journal, 2008-07, Vol.22 (7), p.2206-2213

2008

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A Glucose-6-phosphate Hydrolase, Widely Expressed Outside the Liver, Can Explain Age-dependent Resolution of Hypoglycemia in Glycogen Storage Disease Type Ia

The Journal of biological chemistry, 2003-11, Vol.278 (47), p.47098-47103

2003

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Normoglycemia alone is insufficient to prevent long-term complications of hepatocellular adenoma in glycogen storage disease type Ib mice

Journal of hepatology, 2009-11, Vol.51 (5), p.909-917

2009

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Generation of mice with a conditional allele for G6pc

Genesis (New York, N.Y. : 2000), 2009-09, Vol.47 (9), p.590-594

2009

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Minimal hepatic glucose-6-phosphatase-α activity required to sustain survival and prevent hepatocellular adenoma formation in murine glycogen storage disease type Ia

Molecular genetics and metabolism reports, 2015-06, Vol.3 (C), p.28-32

2015

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Structure–function study of the glucose-6-phosphate transporter, an eukaryotic antiporter deficient in glycogen storage disease type Ib

Molecular genetics and metabolism, 2009-01, Vol.96 (1), p.32-37

2009

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Glycogen storage disease type Ia mice with less than 2% of normal hepatic glucose-6-phosphatase-α activity restored are at risk of developing hepatic tumors

Molecular genetics and metabolism, 2017-03, Vol.120 (3), p.229-234

2017

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Complete Normalization of Hepatic G6PC Deficiency in Murine Glycogen Storage Disease Type Ia Using Gene Therapy

Molecular therapy, 2010-06, Vol.18 (6), p.1076-1084

2010

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Inactivation of the Glucose 6-Phosphate Transporter Causes Glycogen Storage Disease Type 1b

The Journal of biological chemistry, 1999-02, Vol.274 (9), p.5532-5536

1999

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Functional analysis of mutations in a severe congenital neutropenia syndrome caused by glucose-6-phosphatase-β deficiency

Molecular genetics and metabolism, 2015-01, Vol.114 (1), p.41-45

2015

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Impaired neutrophil activity and increased susceptibility to bacterial infection in mice lacking glucose-6-phosphatase-beta

The Journal of clinical investigation, 2007-03, Vol.117 (3), p.784-793

2007

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Mutations in the Glucose-6-Phosphatase Gene That Cause Glycogen Storage Disease Type 1a

Science (American Association for the Advancement of Science), 1993-10, Vol.262 (5133), p.580-583

1993

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The upstream enhancer elements of the G6PC promoter are critical for optimal G6PC expression in murine glycogen storage disease type Ia

Molecular genetics and metabolism, 2013-11, Vol.110 (3), p.275-280

2013

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A Potential New Role for Muscle in Blood Glucose Homeostasis

The Journal of biological chemistry, 2004-06, Vol.279 (25), p.26215-26219

2004

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Transmembrane Topology of Human Glucose 6-Phosphate Transporter

The Journal of biological chemistry, 1999-05, Vol.274 (20), p.13865-13869

1999

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Correction of Glycogen Storage Disease Type 1a in a Mouse Model by Gene Therapy

The Journal of biological chemistry, 2000-01, Vol.275 (2), p.828-832

2000

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Cloning and Characterization of cDNAs Encoding a Candidate Glycogen Storage Disease Type 1b Protein in Rodents

The Journal of biological chemistry, 1998-11, Vol.273 (48), p.31656-31660

1998

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Structural Requirements for the Stability and Microsomal Transport Activity of the Human Glucose 6-Phosphate Transporter

The Journal of biological chemistry, 2000-11, Vol.275 (44), p.34280-34286

2000

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Ontogeny of the Murine Glucose-6-Phosphatase System

Archives of biochemistry and biophysics, 1998-10, Vol.358 (1), p.17-24

1998

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Identification of mutations in the gene for glucose-6-phosphatase, the enzyme deficient in glycogen storage disease type 1A

The Journal of clinical investigation, 1994-05, Vol.93 (5), p.1994-1999

1994

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Histidine 167 Is the Phosphate Acceptor in Glucose-6-phosphatase-β Forming a Phosphohistidine Enzyme Intermediate during Catalysis

The Journal of biological chemistry, 2004-03, Vol.279 (13), p.12479-12483

2004

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Functional analysis of mutations in the glucose-6-phosphate transporter that cause glycogen storage disease type Ib

Molecular genetics and metabolism, 2008-12, Vol.95 (4), p.220-223

2008

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Downregulation of SIRT1 signaling underlies hepatic autophagy impairment in glycogen storage disease type Ia

Prevention of hepatocellular adenoma and correction of metabolic abnormalities in murine glycogen storage disease type Ia by gene therapy

SLC37A1 and SLC37A2 are phosphate-linked, glucose-6-phosphate antiporters

glucose-6-phosphate transporter is a phosphate-linked antiporter deficient in glycogen storage disease type Ib and Ic

A Glucose-6-phosphate Hydrolase, Widely Expressed Outside the Liver, Can Explain Age-dependent Resolution of Hypoglycemia in Glycogen Storage Disease Type Ia

Normoglycemia alone is insufficient to prevent long-term complications of hepatocellular adenoma in glycogen storage disease type Ib mice

Generation of mice with a conditional allele for G6pc

Minimal hepatic glucose-6-phosphatase-α activity required to sustain survival and prevent hepatocellular adenoma formation in murine glycogen storage disease type Ia

Structure–function study of the glucose-6-phosphate transporter, an eukaryotic antiporter deficient in glycogen storage disease type Ib

Glycogen storage disease type Ia mice with less than 2% of normal hepatic glucose-6-phosphatase-α activity restored are at risk of developing hepatic tumors

Complete Normalization of Hepatic G6PC Deficiency in Murine Glycogen Storage Disease Type Ia Using Gene Therapy

Inactivation of the Glucose 6-Phosphate Transporter Causes Glycogen Storage Disease Type 1b

Functional analysis of mutations in a severe congenital neutropenia syndrome caused by glucose-6-phosphatase-β deficiency

Impaired neutrophil activity and increased susceptibility to bacterial infection in mice lacking glucose-6-phosphatase-beta

Mutations in the Glucose-6-Phosphatase Gene That Cause Glycogen Storage Disease Type 1a

The upstream enhancer elements of the G6PC promoter are critical for optimal G6PC expression in murine glycogen storage disease type Ia

A Potential New Role for Muscle in Blood Glucose Homeostasis

Transmembrane Topology of Human Glucose 6-Phosphate Transporter

Correction of Glycogen Storage Disease Type 1a in a Mouse Model by Gene Therapy

Cloning and Characterization of cDNAs Encoding a Candidate Glycogen Storage Disease Type 1b Protein in Rodents

Structural Requirements for the Stability and Microsomal Transport Activity of the Human Glucose 6-Phosphate Transporter

Ontogeny of the Murine Glucose-6-Phosphatase System

Identification of mutations in the gene for glucose-6-phosphatase, the enzyme deficient in glycogen storage disease type 1A

Histidine 167 Is the Phosphate Acceptor in Glucose-6-phosphatase-β Forming a Phosphohistidine Enzyme Intermediate during Catalysis

Functional analysis of mutations in the glucose-6-phosphate transporter that cause glycogen storage disease type Ib

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