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Examining the polymorphisms in the hypoxia pathway genes in relation to outcome in colorectal cancer.
Haja Mohideen, Asan M S; Hyde, Angela; Squires, Jessica; Wang, Jing; Dicks, Elizabeth; Younghusband, Ban; Parfrey, Patrick; Green, Roger; Savas, Sevtap.
Afiliação
  • Haja Mohideen AM; Discipline of Genetics, Faculty of Medicine, Memorial University of Newfoundland, St. John's, NL, Canada.
  • Hyde A; Discipline of Genetics, Faculty of Medicine, Memorial University of Newfoundland, St. John's, NL, Canada.
  • Squires J; Discipline of Genetics, Faculty of Medicine, Memorial University of Newfoundland, St. John's, NL, Canada.
  • Wang J; Division of Community Health and Humanities, Faculty of Medicine, Memorial University of Newfoundland, St. John's, NL, Canada.
  • Dicks E; Clinical Epidemiology Unit, Faculty of Medicine, Memorial University of Newfoundland, St. John's, NL, Canada.
  • Younghusband B; Discipline of Genetics, Faculty of Medicine, Memorial University of Newfoundland, St. John's, NL, Canada.
  • Parfrey P; Clinical Epidemiology Unit, Faculty of Medicine, Memorial University of Newfoundland, St. John's, NL, Canada.
  • Green R; Discipline of Genetics, Faculty of Medicine, Memorial University of Newfoundland, St. John's, NL, Canada.
  • Savas S; Discipline of Genetics, Faculty of Medicine, Memorial University of Newfoundland, St. John's, NL, Canada; Discipline of Oncology, Faculty of Medicine, Memorial University of Newfoundland, St. John's, NL, Canada.
PLoS One ; 9(11): e113513, 2014.
Article em En | MEDLINE | ID: mdl-25405996

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Colorretais / Transdução de Sinais / Polimorfismo de Nucleotídeo Único / Hipóxia Tipo de estudo: Diagnostic_studies / Etiology_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2014 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Colorretais / Transdução de Sinais / Polimorfismo de Nucleotídeo Único / Hipóxia Tipo de estudo: Diagnostic_studies / Etiology_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2014 Tipo de documento: Article