The metallochaperone Atox1 plays a critical role in perinatal copper homeostasis (Q28590480)

Antioxidant 1 copper chaperone

GOA release 2020-03-11

1 reference

GOA release 2020-03-11

copper

0 references

author name string

I. Hamza

1

1 reference

31 January 2017

A. Faisst

2

1 reference

31 January 2017

J. Prohaska

3

1 reference

31 January 2017

J. Chen

4

1 reference

31 January 2017

P. Gruss

5

1 reference

31 January 2017

J. D. Gitlin

Proceedings of the National Academy of Sciences of the United States of America

6

1 reference

31 January 2017

language of work or name

English

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publication date

5 June 2001

1 reference

31 January 2017

1 reference

31 January 2017

98

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31 January 2017

12

1 reference

31 January 2017

6848–6852

1 reference

31 January 2017

The copper transport protein Atox1 promotes neuronal survival

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=34441

Interaction of the copper chaperone HAH1 with the Wilson disease protein is essential for copper homeostasis

17 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=34441

Characterization of the interaction between the Wilson and Menkes disease proteins and the cytoplasmic copper chaperone, HAH1p

17 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=34441

Crystal structure of the Atx1 metallochaperone protein at 1.02 A resolution

17 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=34441

Metal ion chaperone function of the soluble Cu(I) receptor Atx1.

17 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=34441

A role for the Saccharomyces cerevisiae ATX1 gene in copper trafficking and iron transport

17 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=34441

A murine model of Menkes disease reveals a physiological function of metallothionein

17 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=34441

Undetectable intracellular free copper: the requirement of a copper chaperone for superoxide dismutase

17 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=34441

Essential role for mammalian copper transporter Ctr1 in copper homeostasis and embryonic development

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=34441

Long-term functional consequences of malnutrition during brain development: copper

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=34441

Mitf from neural crest to melanoma: signal transduction and transcription in the melanocyte lineage.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=34441

Metallochaperones, an intracellular shuttle service for metal ions

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=34441

A delicate balance: homeostatic control of copper uptake and distribution

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=34441

Efficient gene trap screening for novel developmental genes using IRES beta geo vector and in vitro preselection

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=34441

Folic acid and the prevention of birth defects

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=34441

Structure, expression, and chromosomal localization of the mouse Atox1 gene

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=34441

Menkes syndrome and animal models.

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=34441

Delivering copper inside yeast and human cells

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=34441

Copper metabolism in mottled mouse mutants. Defective placental transfer of 64Cu to foetal brindled (Mobr) mice

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=34441

Tricarboxylic acid cycle flux and enzyme activities in the isolated working rat heart

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=34441

Bodenin: a novel murine gene expressed in restricted areas of the brain.

3 June 2018

1 reference

Crossref

https://api.crossref.org/works/10.1073%2FPNAS.111058498

Absorption and Excretion of Copper in Mice

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1073%2FPNAS.111058498

Altered copper metabolism in cultured cells from human Menkes' syndrome and mottled mouse mutants

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/11391006

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Changes in Tissue Growth, Concentrations of Copper, Iron, Cytochrome Oxidase and Superoxide Dismutase Subsequent to Dietary or Genetic Copper Deficiency in Mice

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/11391006

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Pathogenesis of the platinum (cp) mutation, a model for oculocutaneous albinism

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/11391006

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1073/PNAS.111058498

1 reference

140125

ADS bibcode

2001PNAS...98.6848H

0 references

140125

1 reference

1 reference

1 reference