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Copper Transporter ATP7A Protects Against Endothelial Dysfunction in Type 1 Diabetic Mice by Regulating Extracellular Superoxide Dismutase

Diabetes (New York, N.Y.), 2013-11, Vol.62 (11), p.3839-3850

2013

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Lack of ceruloplasmin expression alters aspects of copper transport to the fetus and newborn, as determined in mice

Biometals, 2012-04, Vol.25 (2), p.373-382

2012

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Chronological changes in tissue copper, zinc and iron in the toxic milk mouse and effects of copper loading

Biometals, 2006-10, Vol.19 (5), p.555-564

2006

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Heterozygous tx mice have an increased sensitivity to copper loading: Implications for Wilson's disease carriers

Biometals, 2007-10, Vol.20 (5), p.751-757

2007

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Copper Exposure Induces Trafficking of the Menkes Protein in Intestinal Epithelium of ATP7A Transgenic Mice

The Journal of nutrition, 2005-12, Vol.135 (12), p.2762-2766

2005

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Alteration of copper physiology in mice overexpressing the human Menkes protein ATP7A

American journal of physiology. Regulatory, integrative and comparative physiology, 2006-05, Vol.290 (5), p.R1460-R1467

2006

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Clusterin and COMMD1 Independently Regulate Degradation of the Mammalian Copper ATPases ATP7A and ATP7B

The Journal of biological chemistry, 2012-01, Vol.287 (4), p.2485-2499

2012

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ATP7A Transgenic and Nontransgenic Mice Are Resistant to High Copper Exposure

The Journal of nutrition, 2008-04, Vol.138 (4), p.693-697

2008

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The Potential of Bone Marrow Stem Cells to Correct Liver Dysfunction in a Mouse Model of Wilson's Disease

Cell transplantation, 2004-01, Vol.13 (7-8), p.765-774

2004

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Copper transport during lactation in transgenic mice expressing the human ATP7A protein

Biochemical and biophysical research communications, 2008-08, Vol.372 (4), p.613-617

2008

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Liver cell transplantation leads to repopulation and functional correction in a mouse model of Wilson's disease

Journal of gastroenterology and hepatology, 2004-11, Vol.19 (11), p.1283-1290

2004

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Characterizing the molecular phenotype of an Atp7a(T985I) conditional knock in mouse model for X-linked distal hereditary motor neuropathy (dHMNX)

Metallomics, 2016-09, Vol.8 (9), p.981-992

2016

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Menkes syndrome and animal models

The American journal of clinical nutrition, 1998-05, Vol.67 (5), p.1022S-1028S

Mercer, JF

1998

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The Toxic Milk Mouse is a Murine Model of Wilson Disease

Human molecular genetics, 1996-10, Vol.5 (10), p.1619-1624

1996

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Mutation spectrum of ATP7A, the gene defective in Menkes disease

Advances in experimental medicine and biology, 1999, Vol.448, p.83

1999

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Decreased carbonic anhydrase III levels in the liver of the mouse mutant 'toxic milk' (tx) due to copper accumulation

Biochemical journal, 1997-01, Vol.321 ( Pt 2) (2), p.341-346

1997

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Correction of a mouse model of Menkes disease by the human Menkes gene

Biochimica et biophysica acta, 2006-04, Vol.1762 (4), p.485-493

2006

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Molecular Basis of the Brindled Mouse Mutant (Mobr): A Murine Model of Menkes Disease

Human molecular genetics, 1997-07, Vol.6 (7), p.1037-1042

1997

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Intracellular Localization and Loss of Copper Responsiveness of Mnk, the Murine Homologue of the Menkes Protein, in Cells from Blotchy (Moblo) and Brindled (Mobr) Mouse Mutants

Human molecular genetics, 1999-06, Vol.8 (6), p.1069-1075

1999

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Developmental expression of the mouse mottled and toxic milk genes

Advances in experimental medicine and biology, 1999, Vol.448, p.109

1999

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Cloning and sequencing of a sheep metallothionein cDNA

European journal of biochemistry, 1984-01, Vol.143 (3), p.507-511

1984

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Copper levels are increased in the cerebral cortex and liver of APP and APLP2 knockout mice

Brain research, 1999-09, Vol.842 (2), p.439-444

1999

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Effect of the toxic milk mutation (tx) on the function and intracellular localization of Wnd, the murine homologue of the Wilson copper ATPase

Human molecular genetics, 2001-02, Vol.10 (4), p.361-370

2001

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Mutations in the murine homologue of the Menkes gene in dappled and blotchy mice

Nature genetics, 1994-04, Vol.6 (4), p.374-378

1994

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Copper Transporter ATP7A Protects Against Endothelial Dysfunction in Type 1 Diabetic Mice by Regulating Extracellular Superoxide Dismutase

Lack of ceruloplasmin expression alters aspects of copper transport to the fetus and newborn, as determined in mice

Chronological changes in tissue copper, zinc and iron in the toxic milk mouse and effects of copper loading

Heterozygous tx mice have an increased sensitivity to copper loading: Implications for Wilson's disease carriers

Copper Exposure Induces Trafficking of the Menkes Protein in Intestinal Epithelium of ATP7A Transgenic Mice

Alteration of copper physiology in mice overexpressing the human Menkes protein ATP7A

Clusterin and COMMD1 Independently Regulate Degradation of the Mammalian Copper ATPases ATP7A and ATP7B

ATP7A Transgenic and Nontransgenic Mice Are Resistant to High Copper Exposure

The Potential of Bone Marrow Stem Cells to Correct Liver Dysfunction in a Mouse Model of Wilson's Disease

Copper transport during lactation in transgenic mice expressing the human ATP7A protein

Oral treatment with Cu(II)(atsm) increases mutant SOD1 in vivo but protects motor neurons and improves the phenotype of a transgenic mouse model of amyotrophic lateral sclerosis

Liver cell transplantation leads to repopulation and functional correction in a mouse model of Wilson's disease

Characterizing the molecular phenotype of an Atp7a(T985I) conditional knock in mouse model for X-linked distal hereditary motor neuropathy (dHMNX)

Menkes syndrome and animal models

The Toxic Milk Mouse is a Murine Model of Wilson Disease

Mutation spectrum of ATP7A, the gene defective in Menkes disease

Decreased carbonic anhydrase III levels in the liver of the mouse mutant 'toxic milk' (tx) due to copper accumulation

Correction of a mouse model of Menkes disease by the human Menkes gene

Molecular Basis of the Brindled Mouse Mutant (Mobr): A Murine Model of Menkes Disease

Intracellular Localization and Loss of Copper Responsiveness of Mnk, the Murine Homologue of the Menkes Protein, in Cells from Blotchy (Moblo) and Brindled (Mobr) Mouse Mutants

Developmental expression of the mouse mottled and toxic milk genes

Cloning and sequencing of a sheep metallothionein cDNA

Copper levels are increased in the cerebral cortex and liver of APP and APLP2 knockout mice

Effect of the toxic milk mutation (tx) on the function and intracellular localization of Wnd, the murine homologue of the Wilson copper ATPase

Mutations in the murine homologue of the Menkes gene in dappled and blotchy mice

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