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EEPD1 Rescues Stressed Replication Forks and Maintains Genome Stability by Promoting End Resection and Homologous Recombination Repair.
Wu, Yuehan; Lee, Suk-Hee; Williamson, Elizabeth A; Reinert, Brian L; Cho, Ju Hwan; Xia, Fen; Jaiswal, Aruna Shanker; Srinivasan, Gayathri; Patel, Bhavita; Brantley, Alexis; Zhou, Daohong; Shao, Lijian; Pathak, Rupak; Hauer-Jensen, Martin; Singh, Sudha; Kong, Kimi; Wu, Xaiohua; Kim, Hyun-Suk; Beissbarth, Timothy; Gaedcke, Jochen; Burma, Sandeep; Nickoloff, Jac A; Hromas, Robert A.
Afiliação
  • Wu Y; Department of Medicine and the Cancer Center, University of Florida Health, Gainesville, Florida, United States of America.
  • Lee SH; Department of Biochemistry and Molecular Biology, Indiana University School of Medicine, Indianapolis, Indiana, United States of America.
  • Williamson EA; Department of Medicine and the Cancer Center, University of Florida Health, Gainesville, Florida, United States of America.
  • Reinert BL; Department of Medicine and the Cancer Center, University of Florida Health, Gainesville, Florida, United States of America.
  • Cho JH; Department of Radiation Oncology, Comprehensive Cancer Center, The Ohio State University, Columbus, Ohio, United States of America.
  • Xia F; Department of Radiation Oncology, Comprehensive Cancer Center, The Ohio State University, Columbus, Ohio, United States of America.
  • Jaiswal AS; Department of Medicine and the Cancer Center, University of Florida Health, Gainesville, Florida, United States of America.
  • Srinivasan G; Department of Medicine and the Cancer Center, University of Florida Health, Gainesville, Florida, United States of America.
  • Patel B; Department of Medicine and the Cancer Center, University of Florida Health, Gainesville, Florida, United States of America.
  • Brantley A; Department of Medicine and the Cancer Center, University of Florida Health, Gainesville, Florida, United States of America.
  • Zhou D; Department of Pharmaceutical Sciences, University of Arkansas for Medical Sciences, Little Rock, Arkansas, United States of America.
  • Shao L; Department of Pharmaceutical Sciences, University of Arkansas for Medical Sciences, Little Rock, Arkansas, United States of America.
  • Pathak R; Department of Pharmaceutical Sciences, University of Arkansas for Medical Sciences, Little Rock, Arkansas, United States of America.
  • Hauer-Jensen M; Department of Pharmaceutical Sciences, University of Arkansas for Medical Sciences, Little Rock, Arkansas, United States of America.
  • Singh S; Department of Medicine and the Cancer Center, University of Florida Health, Gainesville, Florida, United States of America.
  • Kong K; Department of Craniofacial Regeneration, College of Dental Medicine, Columbia University, New York, New York, United States of America.
  • Wu X; Department of Molecular and Experimental Medicine, Scripps Research Institute, La Jolla, California, United States of America.
  • Kim HS; Department of Biochemistry and Molecular Biology, Indiana University School of Medicine, Indianapolis, Indiana, United States of America.
  • Beissbarth T; Department of Medical Statistics, and General, Visceral, and Pediatric Surgery, University Medical Center Göttingen, Göttingen, Germany.
  • Gaedcke J; Department of Medical Statistics, and General, Visceral, and Pediatric Surgery, University Medical Center Göttingen, Göttingen, Germany.
  • Burma S; Department of Radiation Oncology, University of Texas Southwestern, Dallas, Texas, United States of America.
  • Nickoloff JA; Department of Environmental and Radiological Health Sciences, Colorado State University, Fort Collins, Colorado, United States of America.
  • Hromas RA; Department of Medicine and the Cancer Center, University of Florida Health, Gainesville, Florida, United States of America.
PLoS Genet ; 11(12): e1005675, 2015 Dec.
Article em En | MEDLINE | ID: mdl-26684013
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: DNA Helicases / Instabilidade Genômica / Peptídeos e Proteínas de Sinalização Intracelular / Endodesoxirribonucleases / Reparo de DNA por Recombinação / Recombinação Homóloga Limite: Humans Idioma: En Revista: PLoS Genet Assunto da revista: GENETICA Ano de publicação: 2015 Tipo de documento: Article País de afiliação: Estados Unidos País de publicação: Estados Unidos
Texto completo
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: DNA Helicases / Instabilidade Genômica / Peptídeos e Proteínas de Sinalização Intracelular / Endodesoxirribonucleases / Reparo de DNA por Recombinação / Recombinação Homóloga Limite: Humans Idioma: En Revista: PLoS Genet Assunto da revista: GENETICA Ano de publicação: 2015 Tipo de documento: Article País de afiliação: Estados Unidos País de publicação: Estados Unidos