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The molecular basis of nucleotide excision repair syndromes.

作者信息

Bootsma D, Hoeijmakers J H

机构信息

Medical Genetics Centre, Department of Cell Biology and Genetics, Erasmus University Rotterdam, The Netherlands.

出版信息

Mutat Res. 1994 May 1;307(1):15-23. doi: 10.1016/0027-5107(94)90273-9.

DOI:10.1016/0027-5107(94)90273-9
PMID:7513792
Abstract
摘要

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引用本文的文献

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Mechanistic insights into the regulation of transcription and transcription-coupled DNA repair by Cockayne syndrome protein B.解析 Cockayne 综合征蛋白 B 调控转录和转录偶联 DNA 修复的机制研究
Nucleic Acids Res. 2018 Sep 6;46(15):7471-7479. doi: 10.1093/nar/gky660.
2
Unscheduled DNA synthesis: the clinical and functional assay for global genomic DNA nucleotide excision repair.非程序性DNA合成：全球基因组DNA核苷酸切除修复的临床及功能检测
Methods Mol Biol. 2014;1105:511-32. doi: 10.1007/978-1-62703-739-6_36.
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A novel and simple micro-irradiation technique for creating localized DNA double-strand breaks.
一种新颖而简单的微照射技术，用于产生局部 DNA 双链断裂。
Nucleic Acids Res. 2010 Jul;38(12):e129. doi: 10.1093/nar/gkq226. Epub 2010 Apr 12.
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Unscheduled DNA synthesis: a functional assay for global genomic nucleotide excision repair.非程序性DNA合成：一种用于全基因组核苷酸切除修复的功能检测方法。
Methods Mol Biol. 2005;291:303-20. doi: 10.1385/1-59259-840-4:303.
5
Restoration of nucleotide excision repair in a helicase-deficient XPD mutant from intragenic suppression by a trichothiodystrophy mutation.通过毛发硫营养不良突变实现基因内抑制，恢复解旋酶缺陷型XPD突变体中的核苷酸切除修复。
Mol Cell Biol. 2001 Nov;21(21):7355-65. doi: 10.1128/MCB.21.21.7355-7365.2001.
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Rapid changes of nucleotide excision repair gene expression following UV-irradiation and cisplatin treatment of Dictyostelium discoideum.紫外线照射和顺铂处理盘基网柄菌后核苷酸切除修复基因表达的快速变化
Nucleic Acids Res. 1998 Jul 15;26(14):3397-403. doi: 10.1093/nar/26.14.3397.
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Genetic analysis of twenty-two patients with Cockayne syndrome.
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Binding and repair of O6-ethylguanine in double-stranded oligodeoxynucleotides by recombinant human O6-alkylguanine-DNA alkyltransferase do not exhibit significant dependence on sequence context.重组人O6-烷基鸟嘌呤-DNA烷基转移酶对双链寡脱氧核苷酸中O6-乙基鸟嘌呤的结合与修复对序列背景没有显著依赖性。
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Defects in the DNA repair and transcription gene ERCC2(XPD) in trichothiodystrophy.毛发硫营养不良中DNA修复与转录基因ERCC2（XPD）的缺陷。
Am J Hum Genet. 1996 Feb;58(2):263-70.
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Cockayne syndrome complementation group B associated with xeroderma pigmentosum phenotype.与着色性干皮病表型相关的科凯恩综合征互补组B
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