Oxidative-phosphorylation defects in liver of patients with Wilson's disease (Q74301118)

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10 November 2019

title

Oxidative-phosphorylation defects in liver of patients with Wilson's disease (English)

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10 November 2019

A H Schapira

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10 November 2019

J M Cooper

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10 November 2019

M Gu

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10 November 2019

P Butler

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10 November 2019

A P Walker

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10 November 2019

P K Mistry

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10 November 2019

J S Dooley

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10 November 2019

language of work or name

English

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publication date

1 August 2000

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10 November 2019

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10 November 2019

volume

356

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10 November 2019

issue

9228

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10 November 2019

page(s)

469-474

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Biochemical Characterization of the Wilson Disease Protein and Functional Expression in the Yeast Saccharomyces cerevisiae

10 November 2019

cites work

1 reference

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7 January 2021

Localization of the Wilson's disease protein product to mitochondria

1 reference

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7 January 2021

Failure of copper incorporation into ceruloplasmin in the Golgi apparatus of LEC rat hepatocytes

1 reference

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7 January 2021

Biliary copper excretion by hepatocyte lysosomes in the rat. Major excretory pathway in experimental copper overload

1 reference

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7 January 2021

Intracellular distribution of the Wilson’s disease gene product (atpase7b) after in vitro and in vivo exogenous expression in hepatocytes from the LEC rat, an animal model of Wilson’s disease

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2800%2902556-3

7 January 2021

Mitochondrial disease in superoxide dismutase 2 mutant mice

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7 January 2021

Deficit of in vivo mitochondrial ATP production in patients with Friedreich ataxia

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7 January 2021

Clinical, biochemical and molecular genetic correlations in Friedreich's ataxia

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7 January 2021

Friedreich's ataxia: autosomal recessive disease caused by an intronic GAA triplet repeat expansion

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7 January 2021

Respiratory deficiency due to loss of mitochondrial DNA in yeast lacking the frataxin homologue

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7 January 2021

Oxidant injury to hepatic mitochondrial lipids in rats with dietary copper overload. Modification by vitamin E deficiency

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7 January 2021

Mitochondrial complex I deficiency in Parkinson's disease

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7 January 2021

Biochemical abnormalities and excitotoxicity in Huntington's disease brain.

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7 January 2021

The Wilson disease gene: spectrum of mutations and their consequences

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7 January 2021

Premature oxidative aging of hepatic mitochondrial DNA in Wilson's disease

1 reference

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7 January 2021

Plasma copper and antioxidant status in Wilson's disease

1 reference

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7 January 2021

Spontaneous hepatic copper accumulation in Long-Evans Cinnamon rats with hereditary hepatitis. A model of Wilson's disease

1 reference

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7 January 2021

The LEC rat has a deletion in the copper transporting ATPase gene homologous to the Wilson disease gene

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2800%2902556-3

7 January 2021

Association of copper to metallothionein in hepatic lysosomes of Long-Evans cinnamon (LEC) rats during the development of hepatitis [se e comments]

1 reference

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7 January 2021

Abnormal hepatic mitochondrial respiration and cytochrome C oxidase activity in rats with long-term copper overload

1 reference

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7 January 2021

Hepatic copper content is normal in early primary biliary cirrhosis and primary sclerosing cholangitis

1 reference

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7 January 2021

Characterization of the Menkes protein copper-binding domains and their role in copper-induced protein relocalization

1 reference

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7 January 2021

Studies in vivo of the effect of unconjugated bilirubin on hepatic phosphorylation and respiration

1 reference

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7 January 2021

Clinical pharmacokinetics of D-penicillamine

1 reference

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7 January 2021

10.1016/S0140-6736(00)02556-3

Identifiers

DOI

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10 November 2019

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