Capacity of UV-lrradiated Human Fibroblasts to Support Adenovirus DNA Synthesis Correlates with Transcription-Coupled Repair and is Reduced in SV40-Transformed Cells and Cells Expressing Mutant p53-Reference-Cited by-同舟云学术

Capacity of UV-lrradiated Human Fibroblasts to Support Adenovirus DNA Synthesis Correlates with Transcription-Coupled Repair and is Reduced in SV40-Transformed Cells and Cells Expressing Mutant p53

Published:1997-11 Issue:5 Volume:66 Page:659-664
ISSN:0031-8655
Container-title:Photochemistry and Photobiology
language:en
Short-container-title:Photochem Photobiol

Author:

McKay Bruce C.,Winrow Christopher,Rainbow Andrew J.

Publisher

Wiley

Subject

Physical and Theoretical Chemistry,General Medicine,Biochemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1751-1097.1997.tb03203.x/fullpdf

Reference54 articles.

1. DNA repair in an active gene: Removal of pyrimidine dimers from the DHFR gene of CHO cells is much more efficient than in the genome overall

2. Selective removal of transcription-blocking DNA damage from the transcribed strand of the mammalian DHFR gene

3. Repair of ribosomal RNA genes in hamster cells after UV irradiation, or treatment with cisplatin or alkylating agents

4. The residual repair capacity of xeroderma pigmentosum complementation group C fibroblasts is highly specific for transcriptionally active DNA

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