The Wilson disease gene is a putative copper transporting P-type ATPase similar to the Menkes gene.
about
Urinary copper elevation in a mouse model of Wilson's disease is a regulated process to specifically decrease the hepatic copper loadCharacterization of the interaction between the Wilson and Menkes disease proteins and the cytoplasmic copper chaperone, HAH1pPenicinillamine for Wilson's diseaseThe Wilson disease protein ATP7B resides in the late endosomes with Rab7 and the Niemann-Pick C1 proteinAlteration of copper physiology in mice overexpressing the human Menkes protein ATP7ACopper binding to the N-terminal metal-binding sites or the CPC motif is not essential for copper-induced trafficking of the human Wilson protein (ATP7B)Binding of copper(I) by the Wilson disease protein and its copper chaperoneThe copper chaperone for superoxide dismutaseCharacterization of COMMD protein-protein interactions in NF-kappaB signallinghCTR1: a human gene for copper uptake identified by complementation in yeastHAH1 is a copper-binding protein with distinct amino acid residues mediating copper homeostasis and antioxidant defenseBiochemical characterization and intracellular localization of the Menkes disease proteinBiochemical characterization and subcellular localization of human copper transporter 1 (hCTR1)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 traffickingAceruloplasminemia: molecular characterization of this disorder of iron metabolismPrionsMolecular pathogenesis of Wilson and Menkes disease: correlation of mutations with molecular defects and disease phenotypesThe zntA gene of Escherichia coli encodes a Zn(II)-translocating P-type ATPaseClinical presentation, diagnosis and long-term outcome of Wilson's disease: a cohort studyIdentification of point mutations in 41 unrelated patients affected with Menkes diseaseDifferential expression of copper-associated and oxidative stress related proteins in a new variant of copper toxicosis in Doberman pinschersAnimal models of copper-associated liver diseaseSex and ceruloplasmin modulate the response to copper exposure in healthy individuals.Molecular mechanism of copper transport in Wilson disease.Biomarkers for diagnosis of Wilson's diseaseCanine Models for Copper Homeostasis DisordersMolecular imaging and therapy targeting copper metabolism in hepatocellular carcinomaPharmacogenomics of cisplatin sensitivity in non-small cell lung cancerCongential scoliosis in Wilson's disease: case report and review of the literatureCellular function and pathological role of ATP13A2 and related P-type transport ATPases in Parkinson's disease and other neurological disordersBiochemical characterization of P-type copper ATPasesSolution structure of the yeast copper transporter domain Ccc2a in the apo and Cu(I)-loaded statesStructural basis for the function of the N-terminal domain of the ATPase CopA from Bacillus subtilisMetal Binding Domains 3 and 4 of the Wilson Disease Protein: Solution Structure and Interaction with the Copper(I) Chaperone HAH1 † ‡Conformations of the apo-, substrate-bound and phosphate-bound ATP-binding domain of the Cu(II) ATPase CopB illustrate coupling of domain movement to the catalytic cycleCopper-transporting P-type ATPases use a unique ion-release pathwayThe complete inventory of the yeast Saccharomyces cerevisiae P-type transport ATPasesA role for the Saccharomyces cerevisiae ATX1 gene in copper trafficking and iron transport.The Menkes/Wilson disease gene homologue in yeast provides copper to a ceruloplasmin-like oxidase required for iron uptake.Restriction of copper export in Saccharomyces cerevisiae to a late Golgi or post-Golgi compartment in the secretory pathway.
P2860
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P2860
The Wilson disease gene is a putative copper transporting P-type ATPase similar to the Menkes gene.
description
1993 nî lūn-bûn
@nan
1993 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
1993 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
1993年の論文
@ja
1993年論文
@yue
1993年論文
@zh-hant
1993年論文
@zh-hk
1993年論文
@zh-mo
1993年論文
@zh-tw
1993年论文
@wuu
name
The Wilson disease gene is a p ...... se similar to the Menkes gene.
@ast
The Wilson disease gene is a p ...... se similar to the Menkes gene.
@en
The Wilson disease gene is a p ...... se similar to the Menkes gene.
@nl
type
label
The Wilson disease gene is a p ...... se similar to the Menkes gene.
@ast
The Wilson disease gene is a p ...... se similar to the Menkes gene.
@en
The Wilson disease gene is a p ...... se similar to the Menkes gene.
@nl
prefLabel
The Wilson disease gene is a p ...... se similar to the Menkes gene.
@ast
The Wilson disease gene is a p ...... se similar to the Menkes gene.
@en
The Wilson disease gene is a p ...... se similar to the Menkes gene.
@nl
P2093
P356
P1433
P1476
The Wilson disease gene is a p ...... se similar to the Menkes gene.
@en
P2093
P2888
P304
P356
10.1038/NG1293-327
P407
P577
1993-12-01T00:00:00Z
P5875
P6179
1002629743