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Putative functional variants of XRCC1 identified by RegulomeDB were not associated with lung cancer risk in a Korean population.
Yoo, Seung Soo; Jin, Chengcheng; Jung, Deuk Kju; Choi, Yi Young; Choi, Jin Eun; Lee, Won Kee; Lee, Shin Yup; Lee, Jaehee; Cha, Seung Ick; Kim, Chang Ho; Seok, Yangki; Lee, Eungbae; Park, Jae Yong.
Afiliação
  • Yoo SS; Department of Internal Medicine, Kyungpook National University School of Medicine, Daegu, Korea.
  • Jin C; Department of Biochemistry and Cell Biology, Kyungpook National University School of Medicine, Daegu, Korea.
  • Jung DK; Department of Biochemistry and Cell Biology, Kyungpook National University School of Medicine, Daegu, Korea.
  • Choi YY; Department of Biochemistry and Cell Biology, Kyungpook National University School of Medicine, Daegu, Korea.
  • Choi JE; Department of Biochemistry and Cell Biology, Kyungpook National University School of Medicine, Daegu, Korea.
  • Lee WK; Department of Preventive Medicine, Kyungpook National University School of Medicine, Daegu, Korea.
  • Lee SY; Department of Internal Medicine, Kyungpook National University School of Medicine, Daegu, Korea.
  • Lee J; Department of Internal Medicine, Kyungpook National University School of Medicine, Daegu, Korea.
  • Cha SI; Department of Internal Medicine, Kyungpook National University School of Medicine, Daegu, Korea.
  • Kim CH; Department of Internal Medicine, Kyungpook National University School of Medicine, Daegu, Korea.
  • Seok Y; Department of Thoracic Surgery, Kyungpook National University School of Medicine, Daegu, Korea.
  • Lee E; Department of Thoracic Surgery, Kyungpook National University School of Medicine, Daegu, Korea.
  • Park JY; Department of Internal Medicine, Kyungpook National University School of Medicine, Daegu, Korea; Department of Biochemistry and Cell Biology, Kyungpook National University School of Medicine, Daegu, Korea. Electronic address: jaeyong@knu.ac.kr.
Cancer Genet ; 208(1-2): 19-24, 2015.
Article em En | MEDLINE | ID: mdl-25592768
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Predisposição Genética para Doença / Polimorfismo de Nucleotídeo Único / Bases de Dados Genéticas / Proteínas de Ligação a DNA / Neoplasias Pulmonares Tipo de estudo: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Aged / Humans / Male / Middle aged País/Região como assunto: Asia Idioma: En Ano de publicação: 2015 Tipo de documento: Article
Texto completo
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XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Predisposição Genética para Doença / Polimorfismo de Nucleotídeo Único / Bases de Dados Genéticas / Proteínas de Ligação a DNA / Neoplasias Pulmonares Tipo de estudo: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Aged / Humans / Male / Middle aged País/Região como assunto: Asia Idioma: En Ano de publicação: 2015 Tipo de documento: Article