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Cancer Research|May 20, 2016
Decreased Mitochondrial Mutagenesis during Transformation of Human Breast Stem Cells into Tumorigenic CellsEun Hyun Ahn, Seung Hyuk Lee, Joon Yup Kim, et al.Proceedings of the National Academy of Sciences of the United States of America|August 21, 2016
Why Cockayne syndrome patients do not get cancer despite their DNA repair deficiencyKate S Reid-Bayliss, Sarah T Arron, Lawrence A Loeb, et al.The Journal of Biological Chemistry|July 4, 2008
The Werner syndrome protein binds replication fork and holliday junction DNAs as an oligomerSarah A Compton, Gökhan Tolun, Ashwini S Kamath-Loeb, et al.DNA Repair|August 19, 2008
Substrate binding pocket residues of human alkyladenine-DNA glycosylase critical for methylating agent survivalCheng-Yao Chen, Haiwei H Guo, Dharini Shah, et al.International Journal of Cancer|July 11, 2006
Mutations in DNA polymerase eta are not detected in squamous cell carcinoma of the skinEitan Glick, Lisa M White, Nathan A Elliott, et al.Nature Genetics|June 18, 2013
An in-frame deletion at the polymerase active site of POLD1 causes a multisystem disorder with lipodystrophyMichael N Weedon, Sian Ellard, Marc J Prindle, et al.Plos One|August 26, 2015
Detection of Ultra-Rare Mitochondrial Mutations in Breast Stem Cells by Duplex SequencingEun Hyun Ahn, Kensen Hirohata, Brendan F Kohrn, et al.Journal of Molecular Medicine (Berlin, Germany)|March 30, 2010
Mitochondrial mutagenesis induced by tumor-specific radiation bystander effectsSheeona Gorman, Edward Fox, Diarmuid O'Donoghue, et al.The Journal of Biological Chemistry|July 15, 2010
Active site mutations in mammalian DNA polymerase delta alter accuracy and replication fork progressionMichael W Schmitt, Ranga N Venkatesan, Marie-Jeanne Pillaire, et al.Proceedings of the National Academy of Sciences of the United States of America|August 3, 2012
Detection of ultra-rare mutations by next-generation sequencingMichael W Schmitt, Scott R Kennedy, Jesse J Salk, et al.Pageof 11