Benefit of transcription-coupled nucleotide excision repair for gene expression in u.v.-damaged Escherichia coli
Author:
Publisher
Wiley
Subject
Molecular Biology,Microbiology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2958.1995.mmi_18040615.x/fullpdf
Cited by 6 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Mfd Is Required for Rapid Recovery of Transcription following UV-Induced DNA Damage but Not Oxidative DNA Damage in Escherichia coli;Journal of Bacteriology;2012-03-16
2. The DNA-Mismatch Repair Enzyme hMSH2 Modulates UV-B-Induced Cell Cycle Arrest and Apoptosis in Melanoma Cells;Journal of Investigative Dermatology;2008-01
3. Reduced host cell reactivation of oxidative DNA damage in human cells deficient in the mismatch repair gene hMSH2;Mutagenesis;2007-03-09
4. DNA Mismatch Repair Protein Msh6 Is Required for Optimal Levels of Ultraviolet-B-Induced Apoptosis in Primary Mouse Fibroblasts;Journal of Investigative Dermatology;2003-10
5. DNA Mismatch Repair Proteins: Potential Guardians Against Genomic Instability and Tumorigenesis Induced by Ultraviolet Photoproducts;Journal of Investigative Dermatology;2003-09
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