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Missense Mutations in the Copper Transporter Gene ATP7A Cause X-Linked Distal Hereditary Motor Neuropathy

American journal of human genetics, 2010-03, Vol.86 (3), p.343-352

2010

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Copper accumulation by cultured astrocytes

Neurochemistry international, 2010-02, Vol.56 (3), p.451-460

2010

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Altered intracellular localization and valosin-containing protein (p97 VCP) interaction underlie ATP7A-related distal motor neuropathy

Human molecular genetics, 2012-04, Vol.21 (8), p.1794-1807

2012

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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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Neuronal expression of copper transporter 1 in rat dorsal root ganglia: association with platinum neurotoxicity

Cancer chemotherapy and pharmacology, 2009-09, Vol.64 (4), p.847-856

2009

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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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Copper-transporting P-type ATPase, ATP7A, confers multidrug resistance and its expression is related to resistance to SN-38 in clinical colon cancer

Cancer research (Chicago, Ill.), 2007-05, Vol.67 (10), p.4860-4868

2007

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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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Molecular and Cellular Aspects of Copper Transport in Developing Mammals

The Journal of nutrition, 2003-05, Vol.133 (5), p.1481S-1484S

2003

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Defective Copper-Induced Trafficking and Localization of the Menkes Protein in Patients With Mild and Copper-Treated Classical Menkes Disease

Human molecular genetics, 1999-08, Vol.8 (8), p.1547-1555

1999

Volltextzugriff (PDF)

Copper in disorders with neurological symptoms: Alzheimer’s, Menkes, and Wilson diseases

Brain research bulletin, 2001-05, Vol.55 (2), p.175-185

2001

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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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The Menkes copper transporter is required for the activation of tyrosinase

Human molecular genetics, 2000-11, Vol.9 (19), p.2845-2851

2000

Volltextzugriff (PDF)

A C-Terminal Di-Leucine is Required for Localization of the Menkes Protein in the trans-Golgi Network

Human molecular genetics, 1998-12, Vol.7 (13), p.2063-2071

1998

Volltextzugriff (PDF)

Menkes syndrome and animal models

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

Mercer, JF

1998

Volltextzugriff (PDF)

The Toxic Milk Mouse is a Murine Model of Wilson Disease

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

1996

Volltextzugriff (PDF)

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

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

2001

Volltextzugriff (PDF)

Functional Analysis and Intracellular Localization of the Human Menkes Protein (MNK) Stably Expressed from a cDNA Construct in Chinese Hamster Ovary Cells (CHO-K1)

Human molecular genetics, 1998-08, Vol.7 (8), p.1293-1300

1998

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

Copper is taken up efficiently from albumin and α2-macroglobulin by cultured human cells by more than one mechanism

American Journal of Physiology: Cell Physiology, 2008, Vol.64 (3)

2008

Volltextzugriff (PDF)

Cloning and sequencing of a sheep metallothionein cDNA

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

1984

Volltextzugriff (PDF)

Primary structure of the (1 leads to 3,1 leads to 4)-beta-D-glucan 4-glucohydrolase from barley aleurone

Proceedings of the National Academy of Sciences - PNAS, 1986-04, Vol.83 (7), p.2081-2085

1986

Volltextzugriff (PDF)

The sheep metallothionein gene family: structure, sequence and evolutionary relationship of five linked genes

European journal of biochemistry, 1988-06, Vol.174 (2), p.417-424

1988

Volltextzugriff (PDF)

Differential expression of four linked sheep metallothionein genes

European journal of biochemistry, 1988-06, Vol.174 (2), p.425-429

1988

Volltextzugriff (PDF)

Analysis of hepatic copper, zinc, metallothionein and metallothionein-Ia mRNA in developing sheep

European journal of biochemistry, 1990-05, Vol.190 (1), p.149-154

1990

Volltextzugriff (PDF)

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Missense Mutations in the Copper Transporter Gene ATP7A Cause X-Linked Distal Hereditary Motor Neuropathy

Copper accumulation by cultured astrocytes

Altered intracellular localization and valosin-containing protein (p97 VCP) interaction underlie ATP7A-related distal motor neuropathy

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

Neuronal expression of copper transporter 1 in rat dorsal root ganglia: association with platinum neurotoxicity

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

Copper-transporting P-type ATPase, ATP7A, confers multidrug resistance and its expression is related to resistance to SN-38 in clinical colon cancer

ATP7A Transgenic and Nontransgenic Mice Are Resistant to High Copper Exposure

Molecular and Cellular Aspects of Copper Transport in Developing Mammals

Defective Copper-Induced Trafficking and Localization of the Menkes Protein in Patients With Mild and Copper-Treated Classical Menkes Disease

Copper in disorders with neurological symptoms: Alzheimer’s, Menkes, and Wilson diseases

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

The Menkes copper transporter is required for the activation of tyrosinase

A C-Terminal Di-Leucine is Required for Localization of the Menkes Protein in the trans-Golgi Network

Menkes syndrome and animal models

The Toxic Milk Mouse is a Murine Model of Wilson Disease

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

Functional Analysis and Intracellular Localization of the Human Menkes Protein (MNK) Stably Expressed from a cDNA Construct in Chinese Hamster Ovary Cells (CHO-K1)

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

Copper is taken up efficiently from albumin and α2-macroglobulin by cultured human cells by more than one mechanism

Cloning and sequencing of a sheep metallothionein cDNA

Primary structure of the (1 leads to 3,1 leads to 4)-beta-D-glucan 4-glucohydrolase from barley aleurone

The sheep metallothionein gene family: structure, sequence and evolutionary relationship of five linked genes

Differential expression of four linked sheep metallothionein genes

Analysis of hepatic copper, zinc, metallothionein and metallothionein-Ia mRNA in developing sheep

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