(Q42723820)

English

Mutation in the CPC motif-containing 6th transmembrane domain affects intracellular localization, trafficking and copper transport efficiency of ATP7A protein in mosaic mutant mice--an animal model of Menkes disease

scientific article published on 16 November 2011

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

5 November 2017

Mutation in the CPC motif-containing 6th transmembrane domain affects intracellular localization, trafficking and copper transport efficiency of ATP7A protein in mosaic mutant mice--an animal model of Menkes disease (English)

1 reference

Europe PubMed Central

PubMed publication ID

5 November 2017

transmembrane transport

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transmembrane protein

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2

object named as

Paweł Grzmil

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Europe PubMed Central

PubMed publication ID

5 November 2017

author name string

Małgorzata Lenartowicz

1

1 reference

Europe PubMed Central

PubMed publication ID

5 November 2017

Moneef Shoukier

3

1 reference

Europe PubMed Central

PubMed publication ID

5 November 2017

Rafał Starzyński

4

1 reference

Europe PubMed Central

PubMed publication ID

5 November 2017

Marcin Marciniak

5

1 reference

Europe PubMed Central

PubMed publication ID

5 November 2017

Paweł Lipiński

6

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Europe PubMed Central

PubMed publication ID

5 November 2017

publication date

16 November 2011

1 reference

Europe PubMed Central

PubMed publication ID

5 November 2017

1 reference

Europe PubMed Central

PubMed publication ID

5 November 2017

4

1 reference

Europe PubMed Central

PubMed publication ID

5 November 2017

2

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Europe PubMed Central

PubMed publication ID

5 November 2017

197-204

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Europe PubMed Central

PubMed publication ID

5 November 2017

Function and regulation of human copper-transporting ATPases

1 reference

https://api.crossref.org/works/10.1039%2FC1MT00134E

21 January 2018

Posttranslational regulation of copper transporters

1 reference

https://api.crossref.org/works/10.1039%2FC1MT00134E

21 January 2018

The multi-layered regulation of copper translocating P-type ATPases

1 reference

https://api.crossref.org/works/10.1039%2FC1MT00134E

21 January 2018

Human copper transporters: mechanism, role in human diseases and therapeutic potential

1 reference

https://api.crossref.org/works/10.1039%2FC1MT00134E

21 January 2018

Trafficking of the copper-ATPases, ATP7A and ATP7B: role in copper homeostasis

1 reference

https://api.crossref.org/works/10.1039%2FC1MT00134E

21 January 2018

Structural organization of human Cu-transporting ATPases: learning from building blocks

1 reference

https://api.crossref.org/works/10.1039%2FC1MT00134E

21 January 2018

Copper-induced trafficking of the cU-ATPases: a key mechanism for copper homeostasis

1 reference

https://api.crossref.org/works/10.1039%2FC1MT00134E

21 January 2018

Distinct functional roles for the Menkes and Wilson copper translocating P-type ATPases in human placental cells.

1 reference

https://api.crossref.org/works/10.1039%2FC1MT00134E

21 January 2018

The Menkes copper transporter is required for the activation of tyrosinase

1 reference

https://api.crossref.org/works/10.1039%2FC1MT00134E

21 January 2018

Molecular diagnosis of Menkes disease: genotype-phenotype correlation.

1 reference

https://api.crossref.org/works/10.1039%2FC1MT00134E

21 January 2018

Molecular pathogenesis of Wilson and Menkes disease: correlation of mutations with molecular defects and disease phenotypes

1 reference

https://api.crossref.org/works/10.1039%2FC1MT00134E

21 January 2018

Molecular correlates of epilepsy in early diagnosed and treated Menkes disease

1 reference

https://api.crossref.org/works/10.1039%2FC1MT00134E

21 January 2018

Functional copper transport explains neurologic sparing in occipital horn syndrome

1 reference

https://api.crossref.org/works/10.1039%2FC1MT00134E

21 January 2018

Distinctive Menkes disease variant with occipital horns: delineation of natural history and clinical phenotype.

1 reference

https://api.crossref.org/works/10.1039%2FC1MT00134E

21 January 2018

Missense mutations in the copper transporter gene ATP7A cause X-linked distal hereditary motor neuropathy

1 reference

https://api.crossref.org/works/10.1039%2FC1MT00134E

21 January 2018

Intracellular localization and loss of copper responsiveness of Mnk, the murine homologue of the Menkes protein, in cells from blotchy (Mo blo) and brindled (Mo br) mouse mutants

1 reference

https://api.crossref.org/works/10.1039%2FC1MT00134E

21 January 2018

Molecular basis of the brindled mouse mutant (Mo(br)): a murine model of Menkes disease

1 reference

https://api.crossref.org/works/10.1039%2FC1MT00134E

21 January 2018

Mutations in the murine homologue of the Menkes gene in dappled and blotchy mice

1 reference

https://api.crossref.org/works/10.1039%2FC1MT00134E

21 January 2018

Mutation analysis and expression of the mottled gene in the macular mouse model of Menkes disease

1 reference

https://api.crossref.org/works/10.1039%2FC1MT00134E

21 January 2018

Crystal structure of a copper-transporting PIB-type ATPase

1 reference

https://api.crossref.org/works/10.1039%2FC1MT00134E

21 January 2018

Functional characterization of missense mutations in ATP7B: Wilson disease mutation or normal variant?

1 reference

https://api.crossref.org/works/10.1039%2FC1MT00134E

21 January 2018

Menkes disease: recent advances and new aspects

1 reference

https://api.crossref.org/works/10.1039%2FC1MT00134E

21 January 2018

Copper-regulated trafficking of the Menkes disease copper ATPase is associated with formation of a phosphorylated catalytic intermediate

1 reference

https://api.crossref.org/works/10.1039%2FC1MT00134E

21 January 2018

Copper-metallothionein in the kidney of macular mice: a model for Menkes disease

1 reference

https://api.crossref.org/works/10.1039%2FC1MT00134E

21 January 2018

Phenotypic diversity of Menkes disease in mottled mice is associated with defects in localisation and trafficking of the ATP7A protein

1 reference

https://api.crossref.org/works/10.1039%2FC1MT00134E

21 January 2018

Intracellular localization of the Menkes and Wilson's disease proteins and their role in intracellular copper transport

1 reference

5 June 2022

https://opencitations.net/index/coci/api/v1/citations/10.1046/J.1442-200X.1999.01090.X

Identifiers

10.1039/C1MT00134E

1 reference

Europe PubMed Central

PubMed publication ID

5 November 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

5 November 2017

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