×
Entrez Id:
1356
Gene Symbol:
CP
CP
0.300
Biomarker
disease
CTD_human
[Wilson's disease: physiopathology, therapeutic approach and case report].
7849148
1994
×
Entrez Id:
540
Gene Symbol:
ATP7B
ATP7B
0.300
Biomarker
disease
CTD_human
The impact of apolipoprotein E genotypes on age at onset of symptoms and phenotypic expression in Wilson's disease.
10686180
2000
×
Entrez Id:
348
Gene Symbol:
APOE
APOE
0.300
Biomarker
disease
CTD_human
The impact of apolipoprotein E genotypes on age at onset of symptoms and phenotypic expression in Wilson's disease.
10686180
2000
×
Entrez Id:
540
Gene Symbol:
ATP7B
ATP7B
0.300
Biomarker
disease
CTD_human
Mutational analysis of ATP7B and genotype-phenotype correlation in Japanese with Wilson's disease.
10790207
2000
×
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-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
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:
540
Gene Symbol:
ATP7B
ATP7B
0.300
Biomarker
disease
CTD_human
Mutation analysis and the correlation between genotype and phenotype of Arg778Leu mutation in chinese patients with Wilson disease.
11405812
2001
×
Entrez Id:
540
Gene Symbol:
ATP7B
ATP7B
0.300
Biomarker
disease
CTD_human
Haemolytic onset of Wilson disease in a patient with homozygous truncation of ATP7B at Arg1319.
11472373
2001
×
Entrez Id:
540
Gene Symbol:
ATP7B
ATP7B
0.300
Biomarker
disease
CTD_human
Reduction of copper and metallothionein in toxic milk mice by tetrathiomolybdate, but not deferiprone.
11803042
2002
×
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
Nuclear proteins that bind to metal response element a (MREa) in the Wilson disease gene promoter are Ku autoantigens and the Ku-80 subunit is necessary for basal transcription of the WD gene.
11985593
2002
×
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
Identification of novel mutations and the three most common mutations in the human ATP7B gene of Korean patients with Wilson disease.
12544487
2003
×
Entrez Id:
540
Gene Symbol:
ATP7B
ATP7B
0.300
Biomarker
disease
CTD_human
Mutation analysis of copper-transporting P-type adenosine triphosphatase (ATP7B) in human solid carcinomas.
12820478
2003
×
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
×
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:
540
Gene Symbol:
ATP7B
ATP7B
0.300
Biomarker
disease
CTD_human
Intracellular trafficking of the human Wilson protein: the role of the six N-terminal metal-binding sites.
14998371
2004
×
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
Molecular modelling of the nucleotide-binding domain of Wilson's disease protein: location of the ATP-binding site, domain dynamics and potential effects of the major disease mutations.
15147237
2004
×
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:
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
Molecular pathogenesis of Wilson disease: haplotype analysis, detection of prevalent mutations and genotype-phenotype correlation in Indian patients.
16133174
2005
×
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