HUMAN DISORDERS SHOWING INCREASED SENSITIVITY TO INDUCTION OF GENETIC DAMAGE

被引：199
作者：
ARLETT, CF
LEHMANN, AR
机构：
来源：
ANNUAL REVIEW OF GENETICS | 1978年 / 12卷
关键词：
D O I：
10.1146/annurev.ge.12.120178.000523
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：95 / 115
页数：21
相关论文
共 126 条
[1]  
AGARWAL SS, 1977, CANCER RES, V37, P3594
[2]   REMOVAL OF ACETYLAMINOFLUORENE FROM DNA OF CONTROL AND REPAIR-DEFICIENT HUMAN FIBROBLASTS [J].
AMACHER, DE ;
LIEBERMAN, MW .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1977, 74 (01) :285-290
[3]  
ANDREWS A D, 1976, Lancet, V1, P1318
[4]   HUMAN SUBJECT WITH A NEW DEFECT IN REPAIR OF ULTRAVIOLET DAMAGE [J].
ARLETT, CF ;
LEHMANN, AR ;
GIANNELLI, F ;
RAMSAY, CA .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1978, 70 (04) :173-177
[5]   CARCINOGEN-INDUCED CHROMOSOME BREAKAGE IN FANCONIS ANEMIA HETEROZYGOUS CELLS [J].
AUERBACH, AD ;
WOLMAN, SR .
NATURE, 1978, 271 (5640) :69-71
[6]   SUSCEPTIBILITY OF FANCONIS ANEMIA FIBROBLASTS TO CHROMOSOME-DAMAGE BY CARCINOGENS [J].
AUERBACH, AD ;
WOLMAN, SR .
NATURE, 1976, 261 (5560) :494-496
[7]   UV-SPECIFIC ENDONUCLEOLYTIC ACTIVITY PRESENT IN HUMAN CELL EXTRACTS [J].
BACCHETTI, S ;
VANDERPL.A ;
VELDHUISEN, G .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1972, 48 (03) :662-+
[8]   CHROMATID EXCHANGES IN ATAXIA TELANGIECTASIA, BLOOM SYNDROME, WERNER SYNDROME, AND XERODERMA PIGMENTOSUM [J].
BARTRAM, CR ;
KOSKEWESTPHAL, T ;
PASSARGE, E .
ANNALS OF HUMAN GENETICS, 1976, 40 (JUL) :79-86
[9]  
BEARD MEJ, 1976, CONGENITAL DISORDERS, V37, P103
[10]  
BERGER R, 1975, CR ACAD SCI D NAT, V281, P297
12345678910