CLONING THE WILSON DISEASE GENE

被引：45

作者：

CHELLY, J

MONACO, AP

机构：

[1] Imperial Cancer Research Fund Laboratories, Institute of Molecular Medicine, John Radcliffe Hospital Headington, Oxford

来源：

NATURE GENETICS | 1993年 / 5卷 / 04期

关键词：

D O I：

10.1038/ng1293-317

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

[No abstract available]

引用

页码：317 / 318

页数：2

共 13 条

[1] 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

[2]

Bush A. J., 1993, Society for Neuroscience Abstracts, V19, P19

[3] ISOLATION OF A CANDIDATE GENE FOR MENKES DISEASE THAT ENCODES A POTENTIAL HEAVY-METAL BINDING-PROTEIN [J].

CHELLY, J ;

TUMER, Z ;

TONNESEN, T ;

PETTERSON, A ;

ISHIKAWABRUSH, Y ;

TOMMERUP, N ;

HORN, N ;

MONACO, AP .

NATURE GENETICS, 1993, 3 (01) :14-19

[4]

Danks DM, 1989, METABOLIC BASIS INHE, P1411

[5] ASSIGNMENT OF THE GENE FOR WILSON DISEASE TO CHROMOSOME-13 - LINKAGE TO THE ESTERASE-D LOCUS [J].

FRYDMAN, M ;

BONNETAMIR, B ;

FARRER, LA ;

CONNEALLY, PM ;

MAGAZANIK, A ;

ASHBEL, S ;

GOLDWITCH, Z .

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1985, 82 (06) :1819-1821

[6] ISOLATION OF A PARTIAL CANDIDATE GENE FOR MENKES DISEASE BY POSITIONAL CLONING [J].

MERCER, JFB ;

LIVINGSTON, J ;

HALL, B ;

PAYNTER, JA ;

BEGY, C ;

CHANDRASEKHARAPPA, S ;

LOCKHART, P ;

GRIMES, A ;

BHAVE, M ;

SIEMIENIAK, D ;

GLOVER, TW .

NATURE GENETICS, 1993, 3 (01) :20-25

[7] MAPPING, CLONING AND GENETIC-CHARACTERIZATION OF THE REGION CONTAINING THE WILSON DISEASE GENE [J].

PETRUKHIN, K ;

FISCHER, SG ;

PIRASTU, M ;

TANZI, RE ;

CHERNOV, I ;

DEVOTO, M ;

BRZUSTOWICZ, LM ;

CAYANIS, E ;

VITALE, E ;

RUSSO, JJ ;

MATSEOANE, D ;

BOUKHGALTER, B ;

WASCO, W ;

FIGUS, AL ;

LOUDIANOS, J ;

CAO, A ;

STERNLIEB, I ;

EVGRAFOV, O ;

PARANO, E ;

PAVONE, L ;

WARBURTON, D ;

OTT, J ;

PENCHASZADEH, GK ;

SCHEINBERG, IH ;

GILLIAM, TC .

NATURE GENETICS, 1993, 5 (04) :338-343

[8] DEFICIENCY OF CERULOPLASMIN IN PATIENTS WITH HEPATOLENTICULAR DEGENERATION (WILSONS DISEASE) [J].

SCHEINBERG, IH ;

GITLIN, D .

SCIENCE, 1952, 116 (3018) :484-485

[9] HUMAN MENKES X-CHROMOSOME DISEASE AND THE STAPHYLOCOCCAL CADMIUM-RESISTANCE ATPASE - A REMARKABLE SIMILARITY IN PROTEIN SEQUENCES [J].

SILVER, S ;

NUCIFORA, G ;

PHUNG, LT .

MOLECULAR MICROBIOLOGY, 1993, 10 (01) :7-12

[10] THE WILSON DISEASE GENE IS A COPPER TRANSPORTING ATPASE WITH HOMOLOGY TO THE MENKES DISEASE GENE [J].

TANZI, RE ;

PETRUKHIN, K ;

CHERNOV, I ;

PELLEQUER, JL ;

WASCO, W ;

ROSS, B ;

ROMANO, DM ;

PARANO, E ;

PAVONE, L ;

BRZUSTOWICZ, LM ;

DEVOTO, M ;

PEPPERCORN, J ;

BUSH, AI ;

STERNLIEB, I ;

PIRASTU, M ;

GUSELLA, JF ;

EVGRAFOV, O ;

PENCHASZADEH, GK ;

HONIG, B ;

EDELMAN, IS ;

SOARES, MB ;

SCHEINBERG, IH ;

GILLIAM, TC .

NATURE GENETICS, 1993, 5 (04) :344-350

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