Copper transporting P-type ATPases and human disease (Q28204507)

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scientific article (publication date: October 2002)

• Copper Transporting P-Type ATPases and Human Disease

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English	Copper transporting P-type ATPases and human disease	scientific article (publication date: October 2002)	Copper Transporting P-Type ATPases and Human Disease

Statements

instance of

scholarly article

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review article

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Europe PubMed Central

title

Copper transporting P-type ATPases and human disease (English)

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Copper Transporting P-Type ATPases and Human Disease (English)

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main subject

copper

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author name string

Diane W Cox

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1

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Steven D P Moore

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2

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Diane W. Cox

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1

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Steven D. P. Moore

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2

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language of work or name

English

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publication date

October 2002

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2002

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published in

Journal of Bioenergetics and Biomembranes

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volume

34

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issue

5

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page(s)

333-8

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333-338

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cites work

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

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/12539960

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12 December 2020

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Copper pumping ATPases: common concepts in bacteria and man.

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/12539960

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12 December 2020

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Metal Ion Chaperone Function of the Soluble Cu(I) Receptor Atx1

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/12539960

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12 December 2020

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Failure of copper incorporation into ceruloplasmin in the Golgi apparatus of LEC rat hepatocytes

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/12539960

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12 December 2020

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Localization of the Wilson's disease protein in human liver.

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/12539960

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12 December 2020

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Metallothionein messenger RNA levels in the macular mutant mouse: an animal model of Menkes' kinky-hair disease

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/12539960

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12 December 2020

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Genetic mapping of the copper toxicosis locus in Bedlington terriers to dog chromosome 10, in a region syntenic to human chromosome region 2p13-p16.

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/12539960

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12 December 2020

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Expression in mouse kidney of membrane copper transporters Atp7a and Atp7b

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/12539960

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12 December 2020

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The Menkes/Wilson disease gene homologue in yeast provides copper to a ceruloplasmin-like oxidase required for iron uptake

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/12539960

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12 December 2020

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Manifestations of copper excess

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/12539960

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12 December 2020

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The metallochaperone Atox1 plays a critical role in perinatal copper homeostasis

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/12539960

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12 December 2020

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In vivo characterization of renal iron transport in the anaesthetized rat.

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https://pubmed.ncbi.nlm.nih.gov/12539960

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12 December 2020

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Copper transport

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https://pubmed.ncbi.nlm.nih.gov/12539960

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12 December 2020

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Metallochaperone Atox1 transfers copper to the NH2-terminal domain of the Wilson's disease protein and regulates its catalytic activity

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/12539960

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12 December 2020

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Mechanism of hepatorenal syndrome in rats of Long-Evans Cinnamon strain, an animal model of fulminant Wilson's disease

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/12539960

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12 December 2020

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A Golgi localization signal identified in the Menkes recombinant protein

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/12539960

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12 December 2020

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inferred from PubMed ID database lookup

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

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/12539960

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12 December 2020

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inferred from PubMed ID database lookup

Renal tubular function of patients with classical Menkes disease

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/12539960

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12 December 2020

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A cytoplasmic sequence in human tyrosinase defines a second class of di-leucine-based sorting signals for late endosomal and lysosomal delivery

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https://pubmed.ncbi.nlm.nih.gov/12539960

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12 December 2020

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A mutation in the ceruloplasmin gene is associated with systemic hemosiderosis in humans

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/12539960

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12 December 2020

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A permease-oxidase complex involved in high-affinity iron uptake in yeast

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/12539960

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12 December 2020

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Refined genetic and comparative physical mapping of the canine copper toxicosis locus

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/12539960

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12 December 2020

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Hepatocyte-specific localization and copper-dependent trafficking of the Wilson's disease protein in the liver

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/12539960

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12 December 2020

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Menkes X-linked disease: prenatal diagnosis of hemizygous males and heterozygous females

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/12539960

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12 December 2020

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Mutation Analysis and Expression of the Mottled Gene in the Macular Mouse Model of Menkes Disease

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/12539960

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12 December 2020

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

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/12539960

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12 December 2020

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Copper-histidine therapy for Menkes disease

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/12539960

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12 December 2020

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The LEC rat has a deletion in the copper transporting ATPase gene homologous to the Wilson disease gene

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/12539960

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12 December 2020

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Mutation analysis provides additional proof that mottled is the mouse homologue of Menkes' disease

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https://pubmed.ncbi.nlm.nih.gov/12539960

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12 December 2020

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The toxic milk mouse is a murine model of Wilson disease

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/12539960

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The mottled gene is the mouse homologue of the Menkes disease gene

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12539960

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12539960

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/12539960

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/12539960

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12 December 2020

based on heuristic

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

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/12539960

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12 December 2020

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Endogenous intestinal metallothionein possibly contributes to the renal accumulation of cadmium

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12539960

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fetal copper uptake and a homolog (Atp7b) of the Wilson's disease gene in rats

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12539960

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Copper-induced apical trafficking of ATP7B in polarized hepatoma cells provides a mechanism for biliary copper excretion

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12539960

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Copper-dependent trafficking of Wilson disease mutant ATP7B proteins

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12539960

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Functional expression of the Wilson disease protein reveals mislocalization and impaired copper-dependent trafficking of the common H1069Q mutation

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12539960

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of a new copper metabolism gene by positional cloning in a purebred dog population

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12539960

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12539960

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Copper delivery by metallochaperone proteins

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12539960

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Aceruloplasminemia: molecular characterization of this disorder of iron metabolism

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12539960

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Menkes disease: underlying genetic defect and new diagnostic possibilities

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12539960

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Occipital horn syndrome and a mild Menkes phenotype associated with splice site mutations at the MNK locus

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12539960

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/12539960

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12 December 2020

based on heuristic

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Abnormalities of copper accumulation in cell lines established from nine different alleles of mottled are the same as those found in Menkes disease

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/12539960

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12 December 2020

based on heuristic

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The Jackson toxic milk mouse as a model for copper loading

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/12539960

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12 December 2020

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Clinical, morphologic, and chemical studies on copper toxicosis of Bedlington Terriers

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12539960

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutation spectrum of ATP7A, the gene defective in Menkes disease

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12539960

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12539960

retrieved

12 December 2020

based on heuristic

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Primary structure of two P-type ATPases involved in copper homeostasis in Enterococcus hirae

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/12539960

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12 December 2020

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Ligand-regulated transport of the Menkes copper P-type ATPase efflux pump from the Golgi apparatus to the plasma membrane: a novel mechanism of regulated trafficking

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12539960

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12 December 2020

based on heuristic

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A C-terminal di-leucine is required for localization of the Menkes protein in the trans-Golgi network

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12539960

retrieved

12 December 2020

based on heuristic

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Molecular characterization of a copper transport protein in S. cerevisiae: an unexpected role for copper in iron transport

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12539960

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12539960

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12539960

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Biochemical Characterization of the Wilson Disease Protein and Functional Expression in the Yeast Saccharomyces cerevisiae

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12539960

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

DOI

10.1023/A:1021293818125

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Dimensions Publication ID

1039981652

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PubMed publication ID

12539960

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