Hepatic Form of Wilson Disease
|
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 |
Hepatic Form of Wilson Disease
|
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 |
Hepatic Form of Wilson Disease
|
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 |
Hepatic Form of Wilson Disease
|
0.300 |
Biomarker
|
disease |
CTD_human |
Mutational analysis of ATP7B and genotype-phenotype correlation in Japanese with Wilson's disease.
|
10790207 |
2000 |
Hepatic Form of Wilson Disease
|
0.300 |
Biomarker
|
disease |
CTD_human |
Haemolytic onset of Wilson disease in a patient with homozygous truncation of ATP7B at Arg1319.
|
11472373 |
2001 |
Hepatic Form of Wilson Disease
|
0.300 |
Biomarker
|
disease |
CTD_human |
Copper transportion of WD protein in hepatocytes from Wilson disease patients in vitro.
|
11854914 |
2001 |
Hepatic Form of Wilson Disease
|
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 |
Hepatic Form of Wilson Disease
|
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 |
Hepatic Form of Wilson Disease
|
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 |
Hepatic Form of Wilson Disease
|
0.300 |
Biomarker
|
disease |
CTD_human |
Reduction of copper and metallothionein in toxic milk mice by tetrathiomolybdate, but not deferiprone.
|
11803042 |
2002 |
Hepatic Form of Wilson Disease
|
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 |
Hepatic Form of Wilson Disease
|
0.300 |
Biomarker
|
disease |
CTD_human |
Mutation analysis of copper-transporting P-type adenosine triphosphatase (ATP7B) in human solid carcinomas.
|
12820478 |
2003 |
Hepatic Form of Wilson Disease
|
0.300 |
Biomarker
|
disease |
CTD_human |
Gene expression in the liver of Long-Evans cinnamon rats during the development of hepatitis.
|
14574444 |
2003 |
Hepatic Form of Wilson Disease
|
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 |
Hepatic Form of Wilson Disease
|
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 |
Hepatic Form of Wilson Disease
|
0.300 |
Biomarker
|
disease |
CTD_human |
A comparison of the mutation spectra of Menkes disease and Wilson disease.
|
14579150 |
2004 |
Hepatic Form of Wilson Disease
|
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 |
Hepatic Form of Wilson Disease
|
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 |
Hepatic Form of Wilson Disease
|
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 |
Hepatic Form of Wilson Disease
|
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 |
Hepatic Form of Wilson Disease
|
0.300 |
Biomarker
|
disease |
CTD_human |
Wilson's disease: an update.
|
16932613 |
2006 |
Hepatic Form of Wilson Disease
|
0.300 |
Biomarker
|
disease |
CTD_human |
Profound midbrain atrophy in patients with Wilson's disease and neurological symptoms?
|
16607473 |
2006 |
Hepatic Form of Wilson Disease
|
0.300 |
Biomarker
|
disease |
CTD_human |
Mitochondrial involvement in genetically determined transition metal toxicity II. Copper toxicity.
|
16824500 |
2006 |
Hepatic Form of Wilson Disease
|
0.300 |
Biomarker
|
disease |
CTD_human |
Molecular diagnosis of Wilson disease using prevalent mutations and informative single-nucleotide polymorphism markers.
|
17634212 |
2007 |
Hepatic Form of Wilson Disease
|
0.300 |
Biomarker
|
disease |
CTD_human |
Wilson's disease.
|
17276780 |
2007 |