×
Entrez Id:
540
Gene Symbol:
ATP7B
ATP7B
0.300
Biomarker
disease
CTD_human
A comparison of the mutation spectra of Menkes disease and Wilson disease.
14579150
2004
×
Entrez Id:
3569
Gene Symbol:
IL6
IL6
0.300
Biomarker
disease
CTD_human
A study of oxidative stress, cytokines and glutamate in Wilson disease and their asymptomatic siblings.
25002079
2014
×
Entrez Id:
3576
Gene Symbol:
CXCL8
CXCL8
0.300
Biomarker
disease
CTD_human
A study of oxidative stress, cytokines and glutamate in Wilson disease and their asymptomatic siblings.
25002079
2014
×
Entrez Id:
3586
Gene Symbol:
IL10
IL10
0.300
Biomarker
disease
CTD_human
A study of oxidative stress, cytokines and glutamate in Wilson disease and their asymptomatic siblings.
25002079
2014
×
Entrez Id:
7124
Gene Symbol:
TNF
TNF
0.300
Biomarker
disease
CTD_human
A study of oxidative stress, cytokines and glutamate in Wilson disease and their asymptomatic siblings.
25002079
2014
×
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:
4015
Gene Symbol:
LOX
LOX
0.300
Biomarker
disease
CTD_human
Abnormal deposition of collagen around hepatocytes in Wilson's disease is associated with hepatocyte specific expression of lysyl oxidase and lysyl oxidase like protein-2.
16023247
2005
×
Entrez Id:
4017
Gene Symbol:
LOXL2
LOXL2
0.300
Biomarker
disease
CTD_human
Abnormal deposition of collagen around hepatocytes in Wilson's disease is associated with hepatocyte specific expression of lysyl oxidase and lysyl oxidase like protein-2.
16023247
2005
×
Entrez Id:
540
Gene Symbol:
ATP7B
ATP7B
0.300
Biomarker
disease
CTD_human
ATP7B activity is stimulated by PKCɛ in porcine liver.
25003971
2014
×
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
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
Copper transport and its defect in Wilson disease: characterization of the copper-binding domain of Wilson disease ATPase.
10830865
2000
×
Entrez Id:
540
Gene Symbol:
ATP7B
ATP7B
0.300
Biomarker
disease
CTD_human
Copper transportion of WD protein in hepatocytes from Wilson disease patients in vitro.
11854914
2001
×
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
Copper-induced apical trafficking of ATP7B in polarized hepatoma cells provides a mechanism for biliary copper excretion.
10982773
2000
×
Entrez Id:
540
Gene Symbol:
ATP7B
ATP7B
0.300
Biomarker
disease
CTD_human
Copper-regulated trafficking of the Menkes disease copper ATPase is associated with formation of a phosphorylated catalytic intermediate.
12228238
2002
×
Entrez Id:
540
Gene Symbol:
ATP7B
ATP7B
0.300
Biomarker
disease
CTD_human
Dietary polyunsaturated fatty acids suppress acute hepatitis, alter gene expression and prolong survival of female Long-Evans Cinnamon rats, a model of Wilson disease.
15135151
2004
×
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
Effect of the toxic milk mutation (tx) on the function and intracellular localization of Wnd, the murine homologue of the Wilson copper ATPase.
11157799
2001
×
Entrez Id:
7076
Gene Symbol:
TIMP1
TIMP1
0.300
Biomarker
disease
CTD_human
Elevated copper impairs hepatic nuclear receptor function in Wilson's disease.
26241054
2015
×
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
Ferrous and ferric iron accumulates in the brain of aged Long-Evans Cinnamon rats, an animal model of Wilson's disease.
15911138
2005
×
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
Gene expression in the liver of Long-Evans cinnamon rats during the development of hepatitis.
14574444
2003