Copper transport and its defect in Wilson disease: characterization of the copper-binding domain of Wilson disease ATPase.
about
Biochemical basis of regulation of human copper-transporting ATPasesHepatic transport systems.Copper transportion of WD protein in hepatocytes from Wilson disease patients in vitroDeactivation of human immunodeficiency virus type 1 in medium by copper oxide-containing filters.Mapping brain metals to evaluate therapies for neurodegenerative disease.The MXCXXC class of metallochaperone proteins: model studies.Increased tunel positive cells in CA1, CA2, and CA3 subfields of rat hippocampus due to copper and ethanol co-exposure.The metal chaperone Atox1 regulates the activity of the human copper transporter ATP7B by modulating domain dynamics.Living-related liver transplantation for Wilson's disease.
P2860
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P2860
Copper transport and its defect in Wilson disease: characterization of the copper-binding domain of Wilson disease ATPase.
description
2000 nî lūn-bûn
@nan
2000 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
2000 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
2000年の論文
@ja
2000年学术文章
@wuu
2000年学术文章
@zh-cn
2000年学术文章
@zh-hans
2000年学术文章
@zh-my
2000年学术文章
@zh-sg
2000年學術文章
@yue
name
Copper transport and its defec ...... main of Wilson disease ATPase.
@ast
Copper transport and its defec ...... main of Wilson disease ATPase.
@en
type
label
Copper transport and its defec ...... main of Wilson disease ATPase.
@ast
Copper transport and its defec ...... main of Wilson disease ATPase.
@en
prefLabel
Copper transport and its defec ...... main of Wilson disease ATPase.
@ast
Copper transport and its defec ...... main of Wilson disease ATPase.
@en
P1476
Copper transport and its defec ...... main of Wilson disease ATPase.
@en
P2093
P304
P356
10.1016/S0162-0134(99)00249-4
P577
2000-04-01T00:00:00Z