|
| Entrez Id: |
635 |
| Gene Symbol: |
BHMT |
BHMT
|
0.300 |
Biomarker
|
disease |
CTD_human |
The early molecular processes underlying the neurological manifestations of an animal model of Wilson's disease.
|
23519153 |
2013 |
|
| Entrez Id: |
1356 |
| Gene Symbol: |
CP |
CP
|
0.300 |
Biomarker
|
disease |
CTD_human |
The early molecular processes underlying the neurological manifestations of an animal model of Wilson's disease.
|
23519153 |
2013 |
|
| Entrez Id: |
540 |
| Gene Symbol: |
ATP7B |
ATP7B
|
0.300 |
Biomarker
|
disease |
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
|
0.300 |
Biomarker
|
disease |
CTD_human |
Selective divalent copper chelation for the treatment of diabetes mellitus.
|
22455587 |
2012 |
|
| Entrez Id: |
540 |
| Gene Symbol: |
ATP7B |
ATP7B
|
0.300 |
Biomarker
|
disease |
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
|
0.300 |
Biomarker
|
disease |
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
|
0.300 |
Biomarker
|
disease |
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
|
0.300 |
Biomarker
|
disease |
CTD_human |
A systems approach implicates nuclear receptor targeting in the Atp7b(-/-) mouse model of Wilson's disease.
|
22565294 |
2012 |
|
| Entrez Id: |
1356 |
| Gene Symbol: |
CP |
CP
|
0.300 |
Biomarker
|
disease |
CTD_human |
Mutations in SLC33A1 cause a lethal autosomal-recessive disorder with congenital cataracts, hearing loss, and low serum copper and ceruloplasmin.
|
22243965 |
2012 |
|
| Entrez Id: |
540 |
| Gene Symbol: |
ATP7B |
ATP7B
|
0.300 |
Biomarker
|
disease |
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
|
0.300 |
Biomarker
|
disease |
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
|
0.300 |
Biomarker
|
disease |
CTD_human |
Liver mitochondrial membrane crosslinking and destruction in a rat model of Wilson disease.
|
21364284 |
2011 |
|
| Entrez Id: |
308 |
| Gene Symbol: |
ANXA5 |
ANXA5
|
0.300 |
Biomarker
|
disease |
CTD_human |
Proteomic analysis of the hepatic tissue of Long-Evans Cinnamon (LEC) rats according to the natural course of Wilson disease.
|
21751376 |
2011 |
|
| Entrez Id: |
540 |
| Gene Symbol: |
ATP7B |
ATP7B
|
0.300 |
Biomarker
|
disease |
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
|
0.300 |
Biomarker
|
disease |
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
|
0.300 |
Biomarker
|
disease |
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
|
0.300 |
Biomarker
|
disease |
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
|
0.300 |
Biomarker
|
disease |
CTD_human |
Role of copper transporters in copper homeostasis.
|
18779302 |
2008 |
|
| Entrez Id: |
540 |
| Gene Symbol: |
ATP7B |
ATP7B
|
0.300 |
Biomarker
|
disease |
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
|
0.300 |
Biomarker
|
disease |
CTD_human |
Molecular diagnosis of Wilson disease using prevalent mutations and informative single-nucleotide polymorphism markers.
|
17634212 |
2007 |
|
| Entrez Id: |
540 |
| Gene Symbol: |
ATP7B |
ATP7B
|
0.300 |
Biomarker
|
disease |
CTD_human |
Wilson's disease.
|
17276780 |
2007 |
|
| Entrez Id: |
540 |
| Gene Symbol: |
ATP7B |
ATP7B
|
0.300 |
Biomarker
|
disease |
CTD_human |
Distinct Wilson's disease mutations in ATP7B are associated with enhanced binding to COMMD1 and reduced stability of ATP7B.
|
17919502 |
2007 |
|
| Entrez Id: |
540 |
| Gene Symbol: |
ATP7B |
ATP7B
|
0.300 |
Biomarker
|
disease |
CTD_human |
Copper- and iron-rich matrices in hepatocellular lipofuscin particles of a young male patient: diagnostic ultrastructures for Wilson disease.
|
17182432 |
2007 |
|
| Entrez Id: |
540 |
| Gene Symbol: |
ATP7B |
ATP7B
|
0.300 |
Biomarker
|
disease |
CTD_human |
Wilson's disease: an update.
|
16932613 |
2006 |
|
| Entrez Id: |
540 |
| Gene Symbol: |
ATP7B |
ATP7B
|
0.300 |
Biomarker
|
disease |
CTD_human |
Profound midbrain atrophy in patients with Wilson's disease and neurological symptoms?
|
16607473 |
2006 |