Hepatic copper metabolism: Insights from genetic disease

被引：129

作者：

Tao, TY ^{[1
]}

Gitlin, JA ^{[1
]}

机构：

[1] Washington Univ, Sch Med, Edward Mallinckrodt Dept Pediat, St Louis, MO 63110 USA

来源：

HEPATOLOGY | 2003年 / 37卷 / 06期

关键词：

D O I：

10.1053/jhep.2003.50281

中图分类号：

R57 [消化系及腹部疾病];

学科分类号：

摘要：

引用

页码：1241 / 1247

页数：7

共 76 条

[1]

[Anonymous], 2001, METABOLIC MOL BASES

[2] Hepatobiliary transport: Molecular mechanisms of development and cholestasis [J].

Arrese, M ;

Ananthananarayanan, M ;

Suchy, FJ .

PEDIATRIC RESEARCH, 1998, 44 (02) :141-147

[3] Null mutation of the murine ATP7B (Wilson disease) gene results in intracellular copper accumulation and late-onset hepatic nodular transformation [J].

Buiakova, OI ;

Xu, J ;

Lutsenko, S ;

Zeitlin, S ;

Das, K ;

Das, S ;

Ross, BM ;

Mekios, C ;

Scheinberg, IH ;

Gilliam, TC .

HUMAN MOLECULAR GENETICS, 1999, 8 (09) :1665-1671

[4] THE WILSON DISEASE GENE IS A PUTATIVE COPPER TRANSPORTING P-TYPE ATPASE SIMILAR TO THE MENKES GENE [J].

BULL, PC ;

THOMAS, GR ;

ROMMENS, JM ;

FORBES, JR ;

COX, DW .

NATURE GENETICS, 1993, 5 (04) :327-337

[5] The Jackson toxic milk mouse as a model for copper loading [J].

Coronado, V ;

Nanji, M ;

Cox, DW .

MAMMALIAN GENOME, 2001, 12 (10) :793-795

[6] MOLECULAR CHARACTERIZATION OF A COPPER TRANSPORT PROTEIN IN SACCHAROMYCES-CEREVISIAE - AN UNEXPECTED ROLE FOR COPPER IN IRON TRANSPORT [J].

DANCIS, A ;

YUAN, DS ;

HAILE, D ;

ASKWITH, C ;

EIDE, D ;

MOEHLE, C ;

KAPLAN, J ;

KLAUSNER, RD .

CELL, 1994, 76 (02) :393-402

[7] Chloride is an allosteric effector of copper assembly for the yeast multicopper oxidase Fet3p: An unexpected role for intracellular chloride channels [J].

Davis-Kaplan, SR ;

Askwith, CC ;

Bengtzen, AC ;

Radisky, D ;

Kaplan, J .

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (23) :13641-13645

[8] THE VACUOLAR H+-ATPASE OF SACCHAROMYCES-CEREVISIAE IS REQUIRED FOR EFFICIENT COPPER DETOXIFICATION, MITOCHONDRIAL-FUNCTION, AND IRON-METABOLISM [J].

EIDE, DJ ;

BRIDGHAM, JT ;

ZHAO, Z ;

MATTOON, JR .

MOLECULAR AND GENERAL GENETICS, 1993, 241 (3-4) :447-456

[9] Role of the copper-binding domain in the copper transport function of ATP7B, the P-type ATPase defective in Wilson disease [J].

Forbes, JR ;

Hsi, G ;

Cox, DW .

JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (18) :12408-12413

[10] Functional characterization of missense mutations in ATP7B:: Wilson disease mutation or normal variant? [J].

Forbes, JR ;

Cox, DW .

AMERICAN JOURNAL OF HUMAN GENETICS, 1998, 63 (06) :1663-1674

← 1 2 3 4 5 6 7 8 →