(Q28505378)

English

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

scientific journal article

In more languages

Statements

scholarly article

1 reference

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

24 January 2017

ATPase, Cu++ transporting, beta polypeptide

1 reference

GOA release 2020-03-11

0 references

1 reference

based on heuristic

inferred from title

author name string

O. I. Buiakova

1

1 reference

24 January 2017

J. Xu

2

1 reference

24 January 2017

S. Lutsenko

3

1 reference

24 January 2017

S. Zeitlin

4

1 reference

24 January 2017

K. Das

5

1 reference

24 January 2017

S. Das

6

1 reference

24 January 2017

B. M. Ross

7

1 reference

24 January 2017

C. Mekios

8

1 reference

24 January 2017

I. H. Scheinberg

9

1 reference

24 January 2017

T. C. Gilliam

10

1 reference

24 January 2017

language of work or name

1 reference

based on heuristic

inferred from title

publication date

1 September 1999

1 reference

24 January 2017

Human Molecular Genetics

1 reference

24 January 2017

8

1 reference

24 January 2017

1665–1671

1 reference

24 January 2017

9

1 reference

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

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q28505378&oldid=1899903040"