7TH COMPLEMENTATION GROUP IN EXCISION-DEFICIENT XERODERMA PIGMENTOSUM

被引：149
作者：
KEIJZER, W
JASPERS, NGJ
ABRAHAMS, PJ
TAYLOR, AMR
ARLETT, CF
ZELLE, B
TAKEBE, H
KINMONT, PDS
BOOTSMA, D
机构：
[1] KYOTO UNIV, CTR RADIAT BIOL, KYOTO 606, JAPAN
[2] NOTTINGHAM GEN HOSP, DEPT DERMATOL, NOTTINGHAM NG1 6HA, ENGLAND
[3] SYLVIUS LABS, PHYSIOL CHEM LAB, LEIDEN, NETHERLANDS
[4] MED SCH BIRMINGHAM, DEPT CANC STUDIES, BIRMINGHAM B15 3TJ, ENGLAND
[5] UNIV SUSSEX, CELL & MUTAT UNIT, BRIGHTON BN1 9QH, E SUSSEX, ENGLAND
[6] TNO, MED BIOL LAB, RIJSWIJK, NETHERLANDS
来源：
MUTATION RESEARCH | 1979年 / 62卷 / 01期
关键词：
D O I：
10.1016/0027-5107(79)90231-8
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
Cells from a xeroderma pigmentosum patient XP2BI who has reached 17 years of age with no keratoses or skin tumours constitute a new, 7th complementation group G. These cells exhibit a low residual level of excision repair, 2% of normal after a UV dose of 5 J/m2 and an impairment of post-replication repair characteristic of excision-defective XPs. They are also sensitive to the lethal effects of UV and defective in host-cell reactivation of UV-irradiated SV40 DNA. © 1979.
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页码：183 / 190
页数：8
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