Literature DB >> 1349298

Localization of the nucleotide excision repair gene ERCC6 to human chromosome 10q11-q21.

C Troelstra1, R M Landsvater, J Wiegant, M van der Ploeg, G Viel, C H Buys, J H Hoeijmakers.   

Abstract

We have cloned the human DNA excision repair gene ERCC6 by virtue of its ability to correct the uv sensitivity of Chinese hamster overy cell mutant UV61. This mutant is a member of complementation group 6 of the nucleotide excision repair-deficient rodent mutants. By means of in situ hybridization and Southern blot analysis of mouse x human somatic cell hybrids, the gene was localized to human chromosome 10q11-q21. An RFLP detected within the ERCC6 locus can be helpful in linkage analysis.

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Year:  1992        PMID： 1349298     DOI： 10.1016/0888-7543(92)90304-b

Source DB:  PubMed          Journal:  Genomics        ISSN： 0888-7543            Impact factor:   5.736


  15 in total

1.  PTEN is a target of chromosome 10q loss in anaplastic oligodendrogliomas and PTEN alterations are associated with poor prognosis.

Authors:  H Sasaki; M C Zlatescu; R A Betensky; Y Ino; J G Cairncross; D N Louis
Journal:  Am J Pathol       Date:  2001-07       Impact factor: 4.307

2.  A variant of the Cockayne syndrome B gene ERCC6 confers risk of lung cancer.

Authors:  Zhongning Lin; Xuemei Zhang; Jingsheng Tuo; Yongli Guo; Bridgett Green; Chi-Chao Chan; Wen Tan; Ying Huang; Wenhua Ling; Fred F Kadlubar; Dongxin Lin; Baitang Ning
Journal:  Hum Mutat       Date:  2008-01       Impact factor: 4.878

Review 3.  Nucleotide excision repair in yeast.

Authors:  K S Sweder
Journal:  Curr Genet       Date:  1994-12       Impact factor: 3.886

Review 4.  Mechanisms of transcription-repair coupling and mutation frequency decline.

Authors:  C P Selby; A Sancar
Journal:  Microbiol Rev       Date:  1994-09

5.  Complete absence of Cockayne syndrome group B gene product gives rise to UV-sensitive syndrome but not Cockayne syndrome.

Authors:  Katsuyoshi Horibata; Yuka Iwamoto; Isao Kuraoka; Nicolaas G J Jaspers; Akihiro Kurimasa; Mitsuo Oshimura; Masamitsu Ichihashi; Kiyoji Tanaka
Journal:  Proc Natl Acad Sci U S A       Date:  2004-10-14       Impact factor: 11.205

Review 6.  Multiple interaction partners for Cockayne syndrome proteins: implications for genome and transcriptome maintenance.

Authors:  Maria D Aamann; Meltem Muftuoglu; Vilhelm A Bohr; Tinna Stevnsner
Journal:  Mech Ageing Dev       Date:  2013-04-09       Impact factor: 5.432

7.  Mutational analysis of the human nucleotide excision repair gene ERCC1.

Authors:  A M Sijbers; P J van der Spek; H Odijk; J van den Berg; M van Duin; A Westerveld; N G Jaspers; D Bootsma; J H Hoeijmakers
Journal:  Nucleic Acids Res       Date:  1996-09-01       Impact factor: 16.971

8.  The clinical implications of a positive calcitonin test for C-cell hyperplasia in genetically unaffected members of an MEN2A kindred.

Authors:  R M Landsvater; A G Rombouts; G J te Meerman; J M Schillhorn-van Veen; M J Berends; R A Geerdink; A Struyvenberg; C H Buys; C J Lips
Journal:  Am J Hum Genet       Date:  1993-02       Impact factor: 11.025

9.  Structure and expression of the excision repair gene ERCC6, involved in the human disorder Cockayne's syndrome group B.

Authors:  C Troelstra; W Hesen; D Bootsma; J H Hoeijmakers
Journal:  Nucleic Acids Res       Date:  1993-02-11       Impact factor: 16.971

Review 10.  The role of Cockayne Syndrome group B (CSB) protein in base excision repair and aging.

Authors:  Tinna Stevnsner; Meltem Muftuoglu; Maria Diget Aamann; Vilhelm A Bohr
Journal:  Mech Ageing Dev       Date:  2008-04-30       Impact factor: 5.432
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