Molecular mechanism of copper transport in Wilson disease.
about
Cellular multitasking: the dual role of human Cu-ATPases in cofactor delivery and intracellular copper balanceNew perspectives on oxidized genome damage and repair inhibition by pro-oxidant metals in neurological diseasesGenetic polymorphisms are associated with hair, blood, and urine mercury levels in the American Dental Association (ADA) study participantsWilson's disease: a comprehensive review of the molecular mechanisms.Proteomics of metal transport and metal-associated diseases.Metals in membranes.Treatment with D-penicillamine or zinc sulphate affects copper metabolism and improves but not normalizes antioxidant capacity parameters in Wilson disease.Carboplatin/taxane-induced gastrointestinal toxicity: a pharmacogenomics study on the SCOTROC1 trial.The genetics of Wilson disease.An Amidochlorin-Based Colorimetric Fluorescent Probe for Selective Cu(2+) Detection.Frameshift and nonsense mutations in the gene for ATPase7B are associated with severe impairment of copper metabolism and with an early clinical manifestation of Wilson's disease.Sex Differences in Clinical Characteristics and Brain MRI Change in Patients With Wilson's Disease in a Chinese Population
P2860
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P2860
Molecular mechanism of copper transport in Wilson disease.
description
2002 nî lūn-bûn
@nan
2002 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2002 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2002年の論文
@ja
2002年論文
@yue
2002年論文
@zh-hant
2002年論文
@zh-hk
2002年論文
@zh-mo
2002年論文
@zh-tw
2002年论文
@wuu
name
Molecular mechanism of copper transport in Wilson disease
@nl
Molecular mechanism of copper transport in Wilson disease.
@ast
Molecular mechanism of copper transport in Wilson disease.
@en
type
label
Molecular mechanism of copper transport in Wilson disease
@nl
Molecular mechanism of copper transport in Wilson disease.
@ast
Molecular mechanism of copper transport in Wilson disease.
@en
prefLabel
Molecular mechanism of copper transport in Wilson disease
@nl
Molecular mechanism of copper transport in Wilson disease.
@ast
Molecular mechanism of copper transport in Wilson disease.
@en
P2860
P921
P356
P1476
Molecular mechanism of copper transport in Wilson disease.
@en
P2093
Bibudhendra Sarkar
Negah Fatemi
P2860
P304
P356
10.1289/EHP.02110S5695
P407
P478
110 Suppl 5
P577
2002-10-01T00:00:00Z