Literature DB >> 11020328

Analysis of gene-specific DNA damage and repair using quantitative polymerase chain reaction.

S Ayala-Torres1, Y Chen, T Svoboda, J Rosenblatt, B Van Houten.   

Abstract

Soon after discovery of the polymerase chain reaction (PCR), various laboratories have attempted to use quantitative PCR (QPCR) to detect DNA damage in specific gene segments. The development of techniques that facilitate long PCR increased the sensitivity of the assay so that biologically relevant doses of DNA-damaging agents could be assessed. QPCR has been used to survey DNA damage induced by different genotoxicants and to establish the repair kinetics of numerous genes. Current work seeks to analyze damage and repair in specific genes from animals exposed to specific DNA-damaging agents such as oxidative stress. Copyright 2000 Academic Press.

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Year:  2000        PMID: 11020328     DOI: 10.1006/meth.2000.1054

Source DB:  PubMed          Journal:  Methods        ISSN: 1046-2023            Impact factor:   3.608


  99 in total

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5.  The transition of closely opposed lesions to double-strand breaks during long-patch base excision repair is prevented by the coordinated action of DNA polymerase delta and Rad27/Fen1.

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9.  Oxidative damage of mitochondrial DNA in diabetes and its protection by manganese superoxide dismutase.

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Journal:  Free Radic Biol Med       Date:  2016-03-04       Impact factor: 7.376

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