论文信息 - DNA repair: The bases for Cockayne syndrome

DNA repair: The bases for Cockayne syndrome

Cockayne syndrome is a rare, inherited human disease that can arise from mutations in any one of five genes, involved in different aspects of DNA repair. New results have now led to a model for how all of these different mutations result in the same disease.

Philip C. Hanawalt | P. Hanawalt

[1] M. Ljungman,et al. Blockage of RNA polymerase as a possible trigger for u.v. light-induced apoptosis. , 1996, Oncogene.

[2] P. Cooper,et al. Preferential repair of ionizing radiation-induced damage in the transcribed strand of an active human gene is defective in Cockayne syndrome. , 1993, Proceedings of the National Academy of Sciences of the United States of America.

[3] S. A. Leadon,et al. A common mutational pattern in Cockayne syndrome patients from xeroderma pigmentosum group G: implications for a second XPG function. , 1997, Proceedings of the National Academy of Sciences of the United States of America.

[4] A. Sarasin,et al. RETRACTED: Transcription-Coupled Repair of 8-oxoGuanine Requirement for XPG, TFIIH, and CSB and Implications for Cockayne Syndrome , 2000, Cell.

[5] S. Clarkson,et al. Defective Transcription-Coupled Repair of Oxidative Base Damage in Cockayne Syndrome Patients from XP Group G , 1997, Science.

[6] T. Lindahl,et al. Quality control by DNA repair. , 1999, Science.

[7] J. Hoeijmakers,et al. Engagement with transcription , 1993, Nature.

[8] P. Hanawalt,et al. Effect of DNA lesions on transcription elongation. , 1999, Biochimie.