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Defective repair of ionizing radiation damage in Cockayne's syndrome and xeroderma pigmentosum group G.

作者信息

Cooper P K, Leadon S A

机构信息

Life Sciences Division, Lawrence Berkeley Laboratory, Berkeley, California 94720.

出版信息

Ann N Y Acad Sci. 1994 Jul 29;726:330-2. doi: 10.1111/j.1749-6632.1994.tb52842.x.

DOI:10.1111/j.1749-6632.1994.tb52842.x
PMID:8092696
Abstract
摘要

相似文献

1
Defective repair of ionizing radiation damage in Cockayne's syndrome and xeroderma pigmentosum group G.科凯恩综合征和着色性干皮病G组中电离辐射损伤的修复缺陷
Ann N Y Acad Sci. 1994 Jul 29;726:330-2. doi: 10.1111/j.1749-6632.1994.tb52842.x.
2
Cross-sensitivity of certain xeroderma pigmentosum and Cockayne syndrome fibroblast strains to both ionizing radiation and ultraviolet light.某些着色性干皮病和成骨不全综合征成纤维细胞株对电离辐射和紫外线的交叉敏感性。
Mol Gen Genet. 1981;181(4):562-3. doi: 10.1007/BF00428755.
3
DNA repair and cancer: speculations based on studies with xeroderma pigmentosum, Cockayne's syndrome and trichothiodystrophy.DNA修复与癌症：基于着色性干皮病、科凯恩综合征和毛发硫营养不良症研究的推测
Carcinogenesis. 1989 Aug;10(8):1353-6. doi: 10.1093/carcin/10.8.1353.
4
Immune function, mutant frequency, and cancer risk in the DNA repair defective genodermatoses xeroderma pigmentosum, Cockayne's syndrome, and trichothiodystrophy.DNA修复缺陷型遗传性皮肤病（着色性干皮病、科凯恩综合征和毛发硫营养不良）中的免疫功能、突变频率和癌症风险。
J Invest Dermatol. 1990 Jan;94(1):94-100. doi: 10.1111/1523-1747.ep12873952.
5
Xeroderma pigmentosum, Cockayne's syndrome, helicases, and DNA repair: what's the relationship?
Cell. 1992 Dec 11;71(6):887-9. doi: 10.1016/0092-8674(92)90384-o.
6
Nuclear matrix associated DNA is preferentially repaired in normal human fibroblasts, exposed to a low dose of ultraviolet light but not in Cockayne's syndrome fibroblasts.与核基质相关的DNA在暴露于低剂量紫外线的正常人成纤维细胞中优先得到修复，但在科凯恩综合征成纤维细胞中则不然。
Nucleic Acids Res. 1988 Nov 25;16(22):10607-22. doi: 10.1093/nar/16.22.10607.
7
The Cockayne syndrome--an inherited multisystem disorder with cutaneous photosensitivity and defective repair of DNA. Comparison with xeroderma pigmentosum.科凯恩综合征——一种遗传性多系统疾病，伴有皮肤光敏性和DNA修复缺陷。与着色性干皮病的比较。
Am J Dermatopathol. 1985 Aug;7(4):387-92. doi: 10.1097/00000372-198508000-00013.
8
Preferential repair of ionizing radiation-induced damage in the transcribed strand of an active human gene is defective in Cockayne syndrome.活跃人类基因转录链中电离辐射诱导损伤的优先修复在科凯恩综合征中存在缺陷。
Proc Natl Acad Sci U S A. 1993 Nov 15;90(22):10499-503. doi: 10.1073/pnas.90.22.10499.
9
[DNA repair and related diseases].
Pathol Biol (Paris). 1992 Feb;40(2):169-77.
10
The relative expression of mutated XPB genes results in xeroderma pigmentosum/Cockayne's syndrome or trichothiodystrophy cellular phenotypes.突变的XPB基因的相对表达会导致着色性干皮病/科凯恩综合征或毛发硫营养不良细胞表型。
Hum Mol Genet. 1999 Jun;8(6):1125-33. doi: 10.1093/hmg/8.6.1125.

引用本文的文献

1
The ATPase domain but not the acidic region of Cockayne syndrome group B gene product is essential for DNA repair.科凯恩综合征B组基因产物的ATP酶结构域而非酸性区域对DNA修复至关重要。
Mol Biol Cell. 1999 Nov;10(11):3583-94. doi: 10.1091/mbc.10.11.3583.
2
Characterization of the DNA polymerase requirement of human base excision repair.人类碱基切除修复中DNA聚合酶需求的特征分析
Nucleic Acids Res. 1996 Oct 1;24(19):3763-70. doi: 10.1093/nar/24.19.3763.