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Jpn J Cancer Res. 1992 Nov;83(11):1117-9. doi: 10.1111/j.1349-7006.1992.tb02731.x.
2
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本文引用的文献

1
Characterization of Giemsa dark- and light-band DNA.吉姆萨深染带和浅染带DNA的特征分析
Cell. 1982 Nov;31(1):121-9. doi: 10.1016/0092-8674(82)90411-1.
2
Replication timing of genes and middle repetitive sequences.基因与中度重复序列的复制时间
Science. 1984 May 18;224(4650):686-92. doi: 10.1126/science.6719109.
3
Human chromosome 13 compensates a DNA repair defect in UV-sensitive mouse cells by mouse--human cell hybridization.人类13号染色体通过小鼠-人类细胞杂交补偿了紫外线敏感小鼠细胞中的DNA修复缺陷。
Proc Natl Acad Sci U S A. 1983 Sep;80(18):5655-9. doi: 10.1073/pnas.80.18.5655.
4
Identification of nucleotide-excision-repair genes on human chromosomes 2 and 13 by functional complementation in hamster-human hybrids.通过仓鼠-人类杂种细胞中的功能互补鉴定人类2号和13号染色体上的核苷酸切除修复基因。
Somat Cell Mol Genet. 1987 Sep;13(5):539-51. doi: 10.1007/BF01534495.
5
An eighth complementation group of rodent cells hypersensitive to ultraviolet radiation.对紫外线辐射敏感的啮齿动物细胞的第八个互补群。
Somat Cell Mol Genet. 1988 Nov;14(6):605-12. doi: 10.1007/BF01535314.
6
Cell fusion-mediated improvement in transfection competence for repair-deficient mutant of mouse T cell line.
Somat Cell Mol Genet. 1988 Mar;14(2):195-203. doi: 10.1007/BF01534404.
7
Molecular cloning and biological characterization of a human gene, ERCC2, that corrects the nucleotide excision repair defect in CHO UV5 cells.一种可纠正中国仓鼠卵巢细胞UV5株核苷酸切除修复缺陷的人类基因ERCC2的分子克隆及生物学特性研究
Mol Cell Biol. 1988 Mar;8(3):1137-46. doi: 10.1128/mcb.8.3.1137-1146.1988.
8
Molecular characterization of the human excision repair gene ERCC-1: cDNA cloning and amino acid homology with the yeast DNA repair gene RAD10.人类切除修复基因ERCC-1的分子特征：cDNA克隆及与酵母DNA修复基因RAD10的氨基酸同源性
Cell. 1986 Mar 28;44(6):913-23. doi: 10.1016/0092-8674(86)90014-0.
9
Isolation of the functional human excision repair gene ERCC5 by intercosmid recombination.
Genomics. 1990 Dec;8(4):623-33. doi: 10.1016/0888-7543(90)90248-s.
10
R-banding and nonisotopic in situ hybridization: precise localization of the human type II collagen gene (COL2A1).R带和非同位素原位杂交：人类Ⅱ型胶原基因（COL2A1）的精确定位
Hum Genet. 1990 Nov;86(1):14-6. doi: 10.1007/BF00205165.

通过直接R带荧光原位杂交将切除修复基因ERCC5精确定位于人类染色体13q32.3 - q33.1。

Precise localization of the excision repair gene, ERCC5, to human chromosome 13q32.3-q33.1 by direct R-banding fluorescence in situ hybridization.

作者信息

Takahashi E, Shiomi N, Shiomi T

机构信息

Division of Genetics, National Institute of Radiological Sciences, Chiba.

出版信息

Jpn J Cancer Res. 1992 Nov;83(11):1117-9. doi: 10.1111/j.1349-7006.1992.tb02731.x.

DOI:10.1111/j.1349-7006.1992.tb02731.x
PMID:1483924
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5918714/
Abstract

The genomic DNA fragment encoding the excision repair gene, ERCC5, was mapped by direct R-banding fluorescence in situ hybridization. The signals were localized to human chromosome 13q32.3-q33.1. This result was in agreement with previous reports, and the gene was assigned to a narrower region.

摘要

通过直接R显带荧光原位杂交对编码切除修复基因ERCC5的基因组DNA片段进行了定位。信号定位于人类染色体13q32.3-q33.1。这一结果与先前的报道一致，并且该基因被定位到了一个更窄的区域。