|
| Entrez Id: |
540 |
| Gene Symbol: |
ATP7B |
ATP7B
|
Hepatic Form of Wilson Disease
|
0.300 |
Biomarker |
CTD_human |
The plant decapeptide OSIP108 prevents copper-induced toxicity in various models for Wilson disease.
|
25134866 |
2014 |
|
| Entrez Id: |
540 |
| Gene Symbol: |
ATP7B |
ATP7B
|
Hepatic Form of Wilson Disease
|
0.300 |
Biomarker |
CTD_human |
Genetic defects in Indian Wilson disease patients and genotype-phenotype correlation.
|
24094725 |
2014 |
|
| Entrez Id: |
540 |
| Gene Symbol: |
ATP7B |
ATP7B
|
Hepatic Form of Wilson Disease
|
0.300 |
Biomarker |
CTD_human |
ATP7B activity is stimulated by PKCɛ in porcine liver.
|
25003971 |
2014 |
|
| Entrez Id: |
540 |
| Gene Symbol: |
ATP7B |
ATP7B
|
Hepatic Form of Wilson Disease
|
0.300 |
Biomarker |
CTD_human |
The effect of zinc and D-penicillamine in a stable human hepatoma ATP7B knockout cell line.
|
24892424 |
2014 |
|
| Entrez Id: |
540 |
| Gene Symbol: |
ATP7B |
ATP7B
|
Hepatic Form of Wilson Disease
|
0.300 |
Biomarker |
CTD_human |
Intestinal expression of metal transporters in Wilson's disease.
|
23963605 |
2013 |
|
| Entrez Id: |
540 |
| Gene Symbol: |
ATP7B |
ATP7B
|
Hepatic Form of Wilson Disease
|
0.300 |
Biomarker |
CTD_human |
Mutation analysis of ATP7B gene in Turkish Wilson disease patients: identification of five novel mutations.
|
23333878 |
2013 |
|
| Entrez Id: |
540 |
| Gene Symbol: |
ATP7B |
ATP7B
|
Hepatic Form of Wilson Disease
|
0.300 |
Biomarker |
CTD_human |
Wilson's disease: changes in methionine metabolism and inflammation affect global DNA methylation in early liver disease.
|
22945834 |
2013 |
|
| Entrez Id: |
540 |
| Gene Symbol: |
ATP7B |
ATP7B
|
Hepatic Form of Wilson Disease
|
0.300 |
Biomarker |
CTD_human |
Mutational analysis of ATP7B gene and the genotype-phenotype correlation in patients with Wilson's disease in Serbia.
|
23789284 |
2013 |
|
| Entrez Id: |
540 |
| Gene Symbol: |
ATP7B |
ATP7B
|
Hepatic Form of Wilson Disease
|
0.300 |
Biomarker |
CTD_human |
Mutational analysis of ATP7B in north Chinese patients with Wilson disease.
|
23235335 |
2013 |
|
| Entrez Id: |
540 |
| Gene Symbol: |
ATP7B |
ATP7B
|
Hepatic Form of Wilson Disease
|
0.300 |
Biomarker |
CTD_human |
Novel ATPase Cu(2+) transporting beta polypeptide mutations in Chinese families with Wilson's disease.
|
23843956 |
2013 |
|
| Entrez Id: |
540 |
| Gene Symbol: |
ATP7B |
ATP7B
|
Hepatic Form of Wilson Disease
|
0.300 |
Biomarker |
CTD_human |
Selective divalent copper chelation for the treatment of diabetes mellitus.
|
22455587 |
2012 |
|
| Entrez Id: |
540 |
| Gene Symbol: |
ATP7B |
ATP7B
|
Hepatic Form of Wilson Disease
|
0.300 |
Biomarker |
CTD_human |
Urinary copper elevation in a mouse model of Wilson's disease is a regulated process to specifically decrease the hepatic copper load.
|
22802922 |
2012 |
|
| Entrez Id: |
540 |
| Gene Symbol: |
ATP7B |
ATP7B
|
Hepatic Form of Wilson Disease
|
0.300 |
Biomarker |
CTD_human |
Clusterin and COMMD1 independently regulate degradation of the mammalian copper ATPases ATP7A and ATP7B.
|
22130675 |
2012 |
|
| Entrez Id: |
540 |
| Gene Symbol: |
ATP7B |
ATP7B
|
Hepatic Form of Wilson Disease
|
0.300 |
Biomarker |
CTD_human |
Molecular analysis of Wilson patients: direct sequencing and MLPA analysis in the ATP7B gene and Atox1 and COMMD1 gene analysis.
|
22677543 |
2012 |
|
| Entrez Id: |
540 |
| Gene Symbol: |
ATP7B |
ATP7B
|
Hepatic Form of Wilson Disease
|
0.300 |
Biomarker |
CTD_human |
A systems approach implicates nuclear receptor targeting in the Atp7b(-/-) mouse model of Wilson's disease.
|
22565294 |
2012 |
|
| Entrez Id: |
540 |
| Gene Symbol: |
ATP7B |
ATP7B
|
Hepatic Form of Wilson Disease
|
0.300 |
Biomarker |
CTD_human |
Functional significance of the copper transporter ATP7 in peptidergic neurons and endocrine cells in Drosophila melanogaster.
|
22981378 |
2012 |
|
| Entrez Id: |
540 |
| Gene Symbol: |
ATP7B |
ATP7B
|
Hepatic Form of Wilson Disease
|
0.300 |
Biomarker |
CTD_human |
Elevated copper remodels hepatic RNA processing machinery in the mouse model of Wilson's disease.
|
21146535 |
2011 |
|
| Entrez Id: |
540 |
| Gene Symbol: |
ATP7B |
ATP7B
|
Hepatic Form of Wilson Disease
|
0.300 |
Biomarker |
CTD_human |
Liver mitochondrial membrane crosslinking and destruction in a rat model of Wilson disease.
|
21364284 |
2011 |
|
| Entrez Id: |
540 |
| Gene Symbol: |
ATP7B |
ATP7B
|
Hepatic Form of Wilson Disease
|
0.300 |
Biomarker |
CTD_human |
Cellular copper levels determine the phenotype of the Arg875 variant of ATP7B/Wilson disease protein.
|
21406592 |
2011 |
|
| Entrez Id: |
540 |
| Gene Symbol: |
ATP7B |
ATP7B
|
Hepatic Form of Wilson Disease
|
0.300 |
Biomarker |
CTD_human |
Clusterin (apolipoprotein J), a molecular chaperone that facilitates degradation of the copper-ATPases ATP7A and ATP7B.
|
21242307 |
2011 |
|
| Entrez Id: |
540 |
| Gene Symbol: |
ATP7B |
ATP7B
|
Hepatic Form of Wilson Disease
|
0.300 |
Biomarker |
CTD_human |
Wilson disease at a single cell level: intracellular copper trafficking activates compartment-specific responses in hepatocytes.
|
20647314 |
2010 |
|
| Entrez Id: |
540 |
| Gene Symbol: |
ATP7B |
ATP7B
|
Hepatic Form of Wilson Disease
|
0.300 |
Biomarker |
CTD_human |
Regulation of heme synthesis and proteasomal activity by copper: possible implications for Wilson's disease.
|
19888908 |
2009 |
|
| Entrez Id: |
540 |
| Gene Symbol: |
ATP7B |
ATP7B
|
Hepatic Form of Wilson Disease
|
0.300 |
Biomarker |
CTD_human |
Role of copper transporters in copper homeostasis.
|
18779302 |
2008 |
|
| Entrez Id: |
540 |
| Gene Symbol: |
ATP7B |
ATP7B
|
Hepatic Form of Wilson Disease
|
0.300 |
Biomarker |
CTD_human |
Genotyping microarray as a novel approach for the detection of ATP7B gene mutations in patients with Wilson disease.
|
18371106 |
2008 |
|
| Entrez Id: |
540 |
| Gene Symbol: |
ATP7B |
ATP7B
|
Hepatic Form of Wilson Disease
|
0.300 |
Biomarker |
CTD_human |
Molecular diagnosis of Wilson disease using prevalent mutations and informative single-nucleotide polymorphism markers.
|
17634212 |
2007 |