(Q28505378)

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Null mutation of the murine ATP7B (Wilson disease) gene results in intracellular copper accumulation and late-onset hepatic nodular transformation

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scholarly article

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PubMed publication ID

24 January 2017

Null mutation of the murine ATP7B (Wilson disease) gene results in intracellular copper accumulation and late-onset hepatic nodular transformation (English)

1 reference

PubMed publication ID

24 January 2017

ATPase, Cu++ transporting, beta polypeptide

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GOA release 2020-03-11

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O. I. Buiakova

1

1 reference

PubMed publication ID

24 January 2017

J. Xu

2

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24 January 2017

S. Lutsenko

3

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24 January 2017

S. Zeitlin

4

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24 January 2017

K. Das

5

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24 January 2017

S. Das

6

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24 January 2017

B. M. Ross

7

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24 January 2017

C. Mekios

8

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PubMed publication ID

24 January 2017

I. H. Scheinberg

9

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24 January 2017

T. C. Gilliam

10

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24 January 2017

language of work or name

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1 September 1999

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24 January 2017

Human Molecular Genetics

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24 January 2017

8

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24 January 2017

9

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24 January 2017

1665–1671

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PubMed publication ID

24 January 2017

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

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.9.1665

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.9.1665

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.9.1665

21 January 2018

Characterization of the Wilson disease gene encoding a P-type copper transporting ATPase: genomic organization, alternative splicing, and structure/function predictions

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.9.1665

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.9.1665

21 January 2018

Sequence, mapping and disruption of CCC2, a gene that cross-complements the Ca(2+)-sensitive phenotype of csg1 mutants and encodes a P-type ATPase belonging to the Cu(2+)-ATPase subfamily.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.9.1665

21 January 2018

Biochemical characterization of the Wilson disease protein and functional expression in the yeast Saccharomyces cerevisiae

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.9.1665

21 January 2018

Menkes disease mutations and response to early copper histidine treatment.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.9.1665

21 January 2018

Identification and analysis of mutations in the Wilson disease gene (ATP7B): population frequencies, genotype-phenotype correlation, and functional analyses

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.9.1665

21 January 2018

The Wilson disease gene: spectrum of mutations and their consequences

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.9.1665

21 January 2018

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/10.1093%2FHMG%2F8.9.1665

21 January 2018

Inherited copper toxicity in Long-Evans cinnamon rats exhibiting spontaneous hepatitis: a model of Wilson's disease

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.9.1665

21 January 2018

New mutation causing hereditary hepatitis in the laboratory rat.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.9.1665

21 January 2018

A pineal regulatory element (PIRE) mediates transactivation by the pineal/retina-specific transcription factor CRX

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.9.1665

21 January 2018

Expression of Menkes disease gene in mammary carcinoma cells.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.9.1665

21 January 2018

Toxic milk, a new mutation affecting cooper metabolism in the mouse

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.9.1665

21 January 2018

Developmental expression of the mouse mottled and toxic milk genes suggests distinct functions for the Menkes and Wilson disease copper transporters

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.9.1665

21 January 2018

Histochemical localization of copper in various organs of brindled mice

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.9.1665

21 January 2018

Identifiers

10.1093/HMG/8.9.1665

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Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

PubMed publication ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

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