ATP7B mediates vesicular sequestration of copper: insight into biliary copper excretion
about
Medical therapeutic agents for Wilson's diseaseCopper binding to the N-terminal metal-binding sites or the CPC motif is not essential for copper-induced trafficking of the human Wilson protein (ATP7B)Copper-dependent interaction of dynactin subunit p62 with the N terminus of ATP7B but not ATP7ABiochemical basis of regulation of human copper-transporting ATPasesCellular multitasking: the dual role of human Cu-ATPases in cofactor delivery and intracellular copper balanceMolecular pathogenesis of Wilson and Menkes disease: correlation of mutations with molecular defects and disease phenotypesCanine Models for Copper Homeostasis DisordersCopper directs ATP7B to the apical domain of hepatic cells via basolateral endosomesMetal Binding Domains 3 and 4 of the Wilson Disease Protein: Solution Structure and Interaction with the Copper(I) Chaperone HAH1 † ‡Identification of p38 MAPK and JNK as new targets for correction of Wilson disease-causing ATP7B mutantsPolarized sorting of the copper transporter ATP7B in neurons mediated by recognition of a dileucine signal by AP-1.The puzzle posed by COMMD1, a newly discovered protein binding Cu(II).Effects of graded levels of cupric citrate on growth performance, antioxidant status, serum lipid metabolites and immunity, and tissue residues of trace elements in weaned pigs.The plant decapeptide OSIP108 prevents copper-induced apoptosis in yeast and human cellsRole of glutaredoxin1 and glutathione in regulating the activity of the copper-transporting P-type ATPases, ATP7A and ATP7B.Clusterin (apolipoprotein J), a molecular chaperone that facilitates degradation of the copper-ATPases ATP7A and ATP7B.Critical roles for the COOH terminus of the Cu-ATPase ATP7B in protein stability, trans-Golgi network retention, copper sensing, and retrograde trafficking.The effect of zinc and D-penicillamine in a stable human hepatoma ATP7B knockout cell lineWilson's disease: a comprehensive review of the molecular mechanisms.Clusterin and COMMD1 independently regulate degradation of the mammalian copper ATPases ATP7A and ATP7BCanine models of copper toxicosis for understanding mammalian copper metabolism.Elevated copper impairs hepatic nuclear receptor function in Wilson's disease.Atomic Absorption Spectrometry in Wilson's Disease and Its Comparison with Other Laboratory Tests and Paraclinical FindingsATP7B expression in human breast epithelial cells is mediated by lactational hormones.Opportunities in multidimensional trace metal imaging: taking copper-associated disease research to the next levelCopper transport during lactation in transgenic mice expressing the human ATP7A protein.Xenobiotic transporters: ascribing function from gene knockout and mutation studies.Apical targeting and Golgi retention signals reside within a 9-amino acid sequence in the copper-ATPase, ATP7B.Diagnosis of Wilson disease in young children: molecular genetic testing and a paradigm shift from the laboratory diagnosis.Role of the P-Type ATPases, ATP7A and ATP7B in brain copper homeostasis.Copper as a target for prostate cancer therapeutics: copper-ionophore pharmacology and altering systemic copper distribution.Advances in the understanding of mammalian copper transporters.Golgi in copper homeostasis: a view from the membrane trafficking field.Physiological and molecular biochemical mechanisms of bile formation.Functional understanding of the versatile protein copper metabolism MURR1 domain 1 (COMMD1) in copper homeostasis.Targeting copper in cancer therapy: 'Copper That Cancer'.Increased copper levels in in vitro and in vivo models of Niemann-Pick C disease.Roles of COMM-domain-containing 1 in stability and recruitment of the copper-transporting ATPase in a mouse hepatoma cell line.Functional interactions of Cu-ATPase ATP7B with cisplatin and the role of ATP7B in the resistance of cells to the drug.Copper-induced translocation of the Wilson disease protein ATP7B independent of Murr1/COMMD1 and Rab7.
P2860
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P2860
ATP7B mediates vesicular sequestration of copper: insight into biliary copper excretion
description
2006 nî lūn-bûn
@nan
2006 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2006 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
2006年の論文
@ja
2006年論文
@yue
2006年論文
@zh-hant
2006年論文
@zh-hk
2006年論文
@zh-mo
2006年論文
@zh-tw
2006年论文
@wuu
name
ATP7B mediates vesicular sequestration of copper: insight into biliary copper excretion
@ast
ATP7B mediates vesicular sequestration of copper: insight into biliary copper excretion
@en
ATP7B mediates vesicular sequestration of copper: insight into biliary copper excretion
@en-gb
ATP7B mediates vesicular sequestration of copper: insight into biliary copper excretion
@nl
type
label
ATP7B mediates vesicular sequestration of copper: insight into biliary copper excretion
@ast
ATP7B mediates vesicular sequestration of copper: insight into biliary copper excretion
@en
ATP7B mediates vesicular sequestration of copper: insight into biliary copper excretion
@en-gb
ATP7B mediates vesicular sequestration of copper: insight into biliary copper excretion
@nl
prefLabel
ATP7B mediates vesicular sequestration of copper: insight into biliary copper excretion
@ast
ATP7B mediates vesicular sequestration of copper: insight into biliary copper excretion
@en
ATP7B mediates vesicular sequestration of copper: insight into biliary copper excretion
@en-gb
ATP7B mediates vesicular sequestration of copper: insight into biliary copper excretion
@nl
P2093
P3181
P1433
P1476
ATP7B mediates vesicular sequestration of copper: insight into biliary copper excretion
@en
P2093
Julian F B Mercer
Kristy Shield
Michael A Cater
Yolanda Deal
P304
P3181
P356
10.1053/J.GASTRO.2005.10.054
P407
P577
2006-02-01T00:00:00Z