Literature DB >> 2558854

Refined mapping of the three DNA repair genes, ERCC1, ERCC2, and XRCC1, on human chromosome 19.

H W Mohrenweiser1, A V Carrano, A Fertitta, B Perry, L H Thompson, J D Tucker, C A Weber.   

Abstract

Three DNA repair genes, ERCC1, ERCC2, and XRCC1, have been regionally mapped on human chromosome 19. ERCC2 and XRCC1 have been assigned to bands q13.2----q13.3 by in situ hybridization using fluorescently-labeled cosmid probes. ERCC1 and ERCC2 have been found to be separated by less than 250 kb by large fragment restriction enzyme site mapping.

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Year:  1989        PMID： 2558854     DOI： 10.1159/000132829

Source DB:  PubMed          Journal:  Cytogenet Cell Genet        ISSN： 0301-0171


  19 in total

Review 1.  Comparative map for mice and humans.

Authors:  J H Nadeau; M T Davisson; D P Doolittle; P Grant; A L Hillyard; M R Kosowsky; T H Roderick
Journal:  Mamm Genome       Date:  1992       Impact factor: 2.957

2.  Assembly and analysis of cosmid contigs in the CEA-gene family region of human chromosome 19.

Authors:  K Tynan; A Olsen; B Trask; P de Jong; J Thompson; W Zimmermann; A Carrano; H Mohrenweiser
Journal:  Nucleic Acids Res       Date:  1992-04-11       Impact factor: 16.971

3.  Localization of a DNA repair gene (XRCC5) involved in double-strand-break rejoining to human chromosome 2.

Authors:  P A Jeggo; M Hafezparast; A F Thompson; B C Broughton; G P Kaur; M Z Zdzienicka; R S Athwal
Journal:  Proc Natl Acad Sci U S A       Date:  1992-07-15       Impact factor: 11.205

Review 4.  Comparative map for mice and humans.

Authors:  J H Nadeau; M T Davisson; D P Doolittle; P Grant; A L Hillyard; M Kosowsky; T H Roderick
Journal:  Mamm Genome       Date:  1991       Impact factor: 2.957

5.  Correction of xeroderma pigmentosum complementation group D mutant cell phenotypes by chromosome and gene transfer: involvement of the human ERCC2 DNA repair gene.

Authors:  W L Flejter; L D McDaniel; D Johns; E C Friedberg; R A Schultz
Journal:  Proc Natl Acad Sci U S A       Date:  1992-01-01       Impact factor: 11.205

6.  Cloning and characterization of p52, the fifth subunit of the core of the transcription/DNA repair factor TFIIH.

Authors:  J C Marinoni; R Roy; W Vermeulen; P Miniou; Y Lutz; G Weeda; T Seroz; D M Gomez; J H Hoeijmakers; J M Egly
Journal:  EMBO J       Date:  1997-03-03       Impact factor: 11.598

Review 7.  Association between DNA repair gene polymorphisms and risk of glioma: a systematic review and meta-analysis.

Authors:  Maral Adel Fahmideh; Judith Schwartzbaum; Paolo Frumento; Maria Feychting
Journal:  Neuro Oncol       Date:  2014-02-04       Impact factor: 12.300

Review 8.  Coordination of DNA single strand break repair.

Authors:  Rachel Abbotts; David M Wilson
Journal:  Free Radic Biol Med       Date:  2016-11-24       Impact factor: 7.376

9.  Molecular cloning of the human XRCC1 gene, which corrects defective DNA strand break repair and sister chromatid exchange.

Authors:  L H Thompson; K W Brookman; N J Jones; S A Allen; A V Carrano
Journal:  Mol Cell Biol       Date:  1990-12       Impact factor: 4.272

10.  AKT2, a putative oncogene encoding a member of a subfamily of protein-serine/threonine kinases, is amplified in human ovarian carcinomas.

Authors:  J Q Cheng; A K Godwin; A Bellacosa; T Taguchi; T F Franke; T C Hamilton; P N Tsichlis; J R Testa
Journal:  Proc Natl Acad Sci U S A       Date:  1992-10-01       Impact factor: 11.205
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