(Q28575487)

31 January 2017

title

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

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31 January 2017

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J. Wu

1

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31 January 2017

J. R. Forbes

series ordinal

2

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31 January 2017

H. S. Chen

series ordinal

3

1 reference

31 January 2017

D. W. Cox

series ordinal

4

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31 January 2017

language of work or name

English

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publication date

1 August 1994

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31 January 2017

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31 January 2017

volume

7

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31 January 2017

issue

4

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31 January 2017

page(s)

541–545

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The Wilson disease gene is a copper transporting ATPase with homology to the Menkes disease gene

31 January 2017

cites work

1 reference

Isolation of a candidate gene for Menkes disease and evidence that it encodes a copper-transporting ATPase

21 April 2017

1 reference

Isolation of a partial candidate gene for Menkes disease by positional cloning

21 April 2017

1 reference

Isolation of a candidate gene for Menkes disease that encodes a potential heavy metal binding protein

21 April 2017

1 reference

Molecular characterization of a copper transport protein in S. cerevisiae: an unexpected role for copper in iron transport

21 April 2017

1 reference

The Wilson disease gene is a putative copper transporting P-type ATPase similar to the Menkes gene

21 April 2017

1 reference

https://api.crossref.org/works/10.1038%2FNG0894-541

Isolation and characterization of a human liver cDNA as a candidate gene for Wilson disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0894-541

Hereditary low level of plasma ceruloplasmin in LEC rats associated with spontaneous development of hepatitis and liver cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0894-541

Hepatocarcinogenesis is the sequel to hepatitis in Z#2 alpha 1-antitrypsin transgenic mice: histopathological and DNA ploidy studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0894-541

Wilson disease and Menkes disease: new handles on heavy-metal transport.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0894-541

7 January 2021

New mutation causing hereditary hepatitis in the laboratory rat.

1 reference

https://api.crossref.org/works/10.1038%2FNG0894-541

7 January 2021

Hereditary hepatitis of LEC rats is controlled by a single autosomal recessive gene

1 reference

https://api.crossref.org/works/10.1038%2FNG0894-541

7 January 2021

Phenotype of preneoplastic and neoplastic liver lesions during spontaneous liver carcinogenesis of LEC rats

1 reference

https://api.crossref.org/works/10.1038%2FNG0894-541

7 January 2021

Genetic linkage between copper accumulation and hepatitis/hepatoma development in LEC rats

1 reference

https://api.crossref.org/works/10.1038%2FNG0894-541

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0894-541

7 January 2021

Correction of the genetic defect in hepatocytes from the Watanabe heritable hyperlipidemic rabbit.

1 reference

https://api.crossref.org/works/10.1038%2FNG0894-541

7 January 2021

Mutagenesis by the autoxidation of iron with isolated DNA

1 reference

https://api.crossref.org/works/10.1038%2FNG0894-541

7 January 2021

A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity

1 reference

https://api.crossref.org/works/10.1038%2FNG0894-541

7 January 2021

Identifiers

1 reference

Dimensions Publication ID

31 January 2017

1042289397

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1 reference

DOI.org query endpoint

https://doi.org/10.1666%2F0094-8373%282008%29034%5B0179%3AHGWCTI%5D2.0.CO%3B2