Impaired nuclear localization of defective DNA helicases in Werner's syndrome

被引：158
作者：
Matsumoto, T
Shimamoto, A
Goto, M
Furuichi, Y
机构：
[1] AGENE RES INST,KAMAKURA,KANAGAWA 247,JAPAN
[2] TOKYO METROPOLITAN OTSUKA HOSP,DEPT RHEUMATOL,TOSHIMA KU,TOKYO 170,JAPAN
来源：
NATURE GENETICS | 1997年 / 16卷 / 04期
关键词：
D O I：
10.1038/ng0897-335
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
[No abstract available]
引用
收藏
页码：335 / 336
页数：2
相关论文
共 14 条
[1]   Human genetics - Mutation-causing mutations [J].
Ellis, NA .
NATURE, 1996, 381 (6578) :110-111
[2]   THE BLOOMS-SYNDROME GENE-PRODUCT IS HOMOLOGOUS TO RECQ HELICASES [J].
ELLIS, NA ;
GRODEN, J ;
YE, TZ ;
STRAUGHEN, J ;
LENNON, DJ ;
CIOCCI, S ;
PROYTCHEVA, M ;
GERMAN, J .
CELL, 1995, 83 (04) :655-666
[3]   WERNERS SYNDROME - A REVIEW OF ITS SYMPTOMATOLOGY NATURAL HISTORY PATHOLOGIC FEATURES GENETICS AND RELATIONSHIP TO NATURAL AGING PROCESS [J].
EPSTEIN, CJ ;
MARTIN, GM ;
SCHULTZ, AL ;
MOTULSKY, AG .
MEDICINE, 1966, 45 (03) :177-+
[4]   NUCLEAR-PROTEIN LOCALIZATION [J].
GARCIABUSTOS, J ;
HEITMAN, J ;
HALL, MN .
BIOCHIMICA ET BIOPHYSICA ACTA, 1991, 1071 (01) :83-101
[5]   Analysis of helicase gene mutations in Japanese Werner's syndrome patients [J].
Goto, M ;
Imamura, O ;
Kuromitsu, J ;
Matsumoto, T ;
Yamabe, Y ;
Tokutake, Y ;
Suzuki, N ;
Mason, B ;
Drayna, D ;
Sugawara, M ;
Sugimoto, M ;
Furuichi, Y .
HUMAN GENETICS, 1997, 99 (02) :191-193
[6]  
Goto M, 1996, CANCER EPIDEM BIOMAR, V5, P239
[7]  
GOTO M, 1981, CLIN GENET, V19, P8
[8]  
LOHMAN TM, 1993, J BIOL CHEM, V268, P2269
[9]   Mutation and haplotype analyses of the Werner's syndrome gene based on its genomic structure: Genetic epidemiology in the Japanese population [J].
Matsumoto, T ;
Imamura, O ;
Yamabe, Y ;
Kuromitsu, J ;
Tokutake, Y ;
Shimamoto, A ;
Suzuki, N ;
Satoh, M ;
Kitao, S ;
Ichikawa, K ;
Kataoka, H ;
Sugawara, K ;
Thomas, W ;
Mason, B ;
Tsuchihashi, Z ;
Drayna, D ;
Sugawara, M ;
Sugimoto, M ;
Furuichi, Y ;
Goto, M .
HUMAN GENETICS, 1997, 100 (01) :123-130
[10]   Homozygous and compound heterozygous mutations at the Werner syndrome locus [J].
Oshima, J ;
Yu, CE ;
Piussan, C ;
Klein, G ;
Jabkowski, J ;
Balci, S ;
Miki, T ;
Nakura, J ;
Ogihara, T ;
Ells, J ;
Smith, MDC ;
Melaragno, MI ;
Fraccaro, M ;
Scappaticci, S ;
Matthews, J ;
Ouais, S ;
Jarzebowicz, A ;
Schellenberg, GD ;
Martin, GM .
HUMAN MOLECULAR GENETICS, 1996, 5 (12) :1909-1913
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