Hepatic copper metabolism: insights from genetic disease.
about
Biochemical basis of regulation of human copper-transporting ATPasesRedox mechanisms in hepatic chronic wound healing and fibrogenesisRapid and reliable diagnosis of Wilson disease using X-ray fluorescence.A cadmium-transporting P1B-type ATPase in yeast Saccharomyces cerevisiae.The copper toxicosis gene product Murr1 directly interacts with the Wilson disease proteinThe puzzle posed by COMMD1, a newly discovered protein binding Cu(II).Clinical and molecular characterization of Wilson's disease in China: identification of 14 novel mutations.A series of tripodal cysteine derivatives as water-soluble chelators that are highly selective for copper(I).Review article: diagnosis and current therapy of Wilson's disease.Mechanisms of the copper-dependent turnover of the copper chaperone for superoxide dismutase.Acquisition of dietary copper: a role for anion transporters in intestinal apical copper uptake.Cisplatin binds human copper chaperone Atox1 and promotes unfolding in vitroImpairment of interrelated iron- and copper homeostatic mechanisms in brain contributes to the pathogenesis of neurodegenerative disorders.Expressional control of a cadmium-transporting P1B-type ATPase by a metal sensing degradation signal.Deletion of hepatic Ctr1 reveals its function in copper acquisition and compensatory mechanisms for copper homeostasis.Genotype phenotype correlation in Wilson's disease within families--a report on four south Indian families.Mapping brain metals to evaluate therapies for neurodegenerative disease.Species-specific toxicity of copper nanoparticles among mammalian and piscine cell lines.Organ-specific regulation of ATP7A abundance is coordinated with systemic copper homeostasis.Ameliorative Influence of Green Tea Extract on Copper Nanoparticle-Induced Hepatotoxicity in Rats.Copper supplementation at 8 mg neither affects circulating lipids nor liver function in apparently healthy Chilean men.Haemolysis during sodium dimercaptosulphonate therapy for Wilson's disease in G6PD-deficient patients: First report of two cases.Isotopic evidence of unaccounted for Fe and Cu erythropoietic pathways.Comprehensive analysis on clinical features of Wilson's disease: an experience over 28 years with 133 cases.
P2860
Q24569563-B67EDDF4-0EEF-4486-8A7B-B6274DD66B01Q24656684-EC8700C1-F10E-4B2F-A36F-523B50CA2C5EQ27338256-461CC496-060C-4775-83F0-CA371ED3E75FQ27935630-06ACAA1C-0934-411D-9DD5-16AF049FD997Q28206233-CC369F18-219F-4D8A-BDC8-22E1F6696178Q33350537-79F7D60C-5B24-41DE-8A56-EB9CE16F6987Q33789624-15F52F29-6817-486A-AD94-EE874E819BF4Q33849917-87A8A9F5-9CE2-4D4A-88E6-D260939CC607Q34289864-B6E4DC3F-F10B-48C1-8D51-B30B629A9B56Q34501464-521C073C-3999-4279-86E4-52C34FFE483EQ34717962-8C51589D-4CB5-4335-B45E-1D08D61BCC37Q34880501-7F4271A8-B1EB-428E-A60A-7E787222C7A2Q36275015-157D540F-1E2A-4216-BB3B-9A759A87C2F9Q36968395-DA0057A8-E471-4644-A4E8-15378F3EE801Q37100217-D27A9AEE-D405-493D-9401-3C7A565597B2Q37335118-9571A4FD-2736-41D7-9E43-2C34482DA767Q37765635-C7692C71-8B13-4EDB-A328-EEDA6FDD8F0EQ39163806-345E5B42-8223-4D04-818E-90983E50D74DQ41697129-38AD167C-0637-4846-992F-EDD61607AF5BQ41807280-5A4D6322-06F6-48CB-9378-9363CFE804C2Q45174983-AAB4A547-7934-43C9-80DB-499081AC1CC0Q50204526-3E032585-5FF3-4CFE-BE4B-888573634096Q50528765-49E25819-C661-431E-A825-4AF562860D4BQ50686859-354285E8-32C1-4F54-92C1-6F116703DAE9
P2860
Hepatic copper metabolism: insights from genetic disease.
description
2003 nî lūn-bûn
@nan
2003 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2003 թվականի հունիսին հրատարակված գիտական հոդված
@hy
2003年の論文
@ja
2003年論文
@yue
2003年論文
@zh-hant
2003年論文
@zh-hk
2003年論文
@zh-mo
2003年論文
@zh-tw
2003年论文
@wuu
name
Hepatic copper metabolism: insights from genetic disease.
@ast
Hepatic copper metabolism: insights from genetic disease.
@en
type
label
Hepatic copper metabolism: insights from genetic disease.
@ast
Hepatic copper metabolism: insights from genetic disease.
@en
prefLabel
Hepatic copper metabolism: insights from genetic disease.
@ast
Hepatic copper metabolism: insights from genetic disease.
@en
P356
P1433
P1476
Hepatic copper metabolism: insights from genetic disease.
@en
P2093
Jonathan D Gitlin
Ting Y Tao
P304
P356
10.1053/JHEP.2003.50281
P407
P577
2003-06-01T00:00:00Z