(Q21134543)

16 August 2022

Jack H Kaplan

8

Jack H

Kaplan

1 reference

16 August 2022

Lawrence W Gray

1

Lawrence W

Gray

1 reference

16 August 2022

Shannon A Molloy

3

Shannon A

Molloy

1 reference

16 August 2022

Venkata S Pendyala

4

Venkata S

Pendyala

1 reference

16 August 2022

Abigael Muchenditsi

5

Abigael

Muchenditsi

1 reference

16 August 2022

Otto Muzik

6

Otto

Muzik

1 reference

16 August 2022

Jaekwon Lee

7

Jaekwon

Lee

1 reference

16 August 2022

Svetlana Lutsenko

9

Svetlana

Lutsenko

1 reference

Creative Commons Attribution 4.0 International

16 August 2022

language of work or name

English

0 references

publication date

2012

0 references

published in

PLOS One

0 references

volume

7

0 references

issue

6

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page(s)

e38327

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copyright license

start time

22 June 2012

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

cites work

Mitochondrial matrix copper complex used in metallation of cytochrome oxidase and superoxide dismutase

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3390108

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

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3390108

The copper-transporting ATPases, menkes and wilson disease proteins, have distinct roles in adult and developing cerebellum

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3390108

Copper-stimulated endocytosis and degradation of the human copper transporter, hCtr1

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3390108

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

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3390108

Consequences of copper accumulation in the livers of the Atp7b-/- (Wilson disease gene) knockout mice

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3390108

Specificity protein 1 (sp1) oscillation is involved in copper homeostasis maintenance by regulating human high-affinity copper transporter 1 expression

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3390108

Systems biology approach to Wilson's disease

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3390108

Liver mitochondrial membrane crosslinking and destruction in a rat model of Wilson disease

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3390108

Ctr1 is an apical copper transporter in mammalian intestinal epithelial cells in vivo that is controlled at the level of protein stability

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3390108

Wilson disease at a single cell level: intracellular copper trafficking activates compartment-specific responses in hepatocytes.

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3390108

Cardiac copper deficiency activates a systemic signaling mechanism that communicates with the copper acquisition and storage organs

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3390108

Copper-dependent recycling of hCTR1, the human high affinity copper transporter.

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3390108

Copper transport in mammalian cells: special care for a metal with special needs.

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3390108

Deletion of hepatic Ctr1 reveals its function in copper acquisition and compensatory mechanisms for copper homeostasis

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3390108

Transcription factor Sp1 plays an important role in the regulation of copper homeostasis in mammalian cells

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3390108

Copper-dependent degradation of the Saccharomyces cerevisiae plasma membrane copper transporter Ctr1p in the apparent absence of endocytosis.

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3390108

Mapping, cloning and genetic characterization of the region containing the Wilson disease gene.

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3390108

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

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3390108

High copper selectively alters lipid metabolism and cell cycle machinery in the mouse model of Wilson disease.

12 September 2017

1 reference

Crossref

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0038327

Determination of copper and iron in biological samples of viral hepatitis (A-E) female patients

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0038327

O-linked glycosylation at threonine 27 protects the copper transporter hCTR1 from proteolytic cleavage in mammalian cells.

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0038327

Evaluation of arsenic, cadmium, lead, and nickel in biological samples (scalp hair, serum, blood, and urine) of Pakistani viral hepatitis (A - E) patients and controls

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3390108

Imaging copper metabolism imbalance in Atp7b (-/-) knockout mouse model of Wilson's disease with PET-CT and orally administered 64CuCl2.

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3390108

Urinary copper excretion and hepatic copper concentrations in liver disease

29 November 2018

1 reference

12 December 2020

Metallothionein and copper in liver disease with copper retention--a histopathological study

1 reference

12 December 2020

Increased urinary zinc and copper excretion in colorectal cancer

1 reference

12 December 2020

Urinary copper excretion in pregnancy

1 reference

12 December 2020

Intracellular targeting of copper-transporting ATPase ATP7A in a normal and Atp7b-/- kidney

1 reference

12 December 2020

1 reference

12 December 2020

1 reference

12 December 2020

1 reference

12 December 2020

The pattern of urinary copper excretion and its response to treatment in patients with Wilson's disease

1 reference

12 December 2020

10.1371/JOURNAL.PONE.0038327

Identifiers

DOI

1 reference

ADS bibcode

2012PLoSO...738327G

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1 reference

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