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Rare missense mutations in RECQL and POLG associate with inherited predisposition to breast cancer.
Tervasmäki, Anna; Mantere, Tuomo; Hartikainen, Jaana M; Kauppila, Saila; Lee, Hang-Mao; Koivuluoma, Susanna; Grip, Mervi; Karihtala, Peeter; Jukkola-Vuorinen, Arja; Mannermaa, Arto; Winqvist, Robert; Pylkäs, Katri.
Affiliation
  • Tervasmäki A; Laboratory of Cancer Genetics and Tumor Biology, Cancer and Translational Medicine Research Unit and Biocenter Oulu, Northern Finland Laboratory Centre Nordlab Oulu, University of Oulu, Oulu, Finland.
  • Mantere T; Laboratory of Cancer Genetics and Tumor Biology, Cancer and Translational Medicine Research Unit and Biocenter Oulu, Northern Finland Laboratory Centre Nordlab Oulu, University of Oulu, Oulu, Finland.
  • Hartikainen JM; School of Medicine, Institute of Clinical Medicine, Pathology and Forensic Medicine, and Translational Cancer Research Area, University of Eastern Finland, Kuopio, Finland.
  • Kauppila S; Department of Clinical Pathology, Imaging Center, Kuopio University Hospital, Kuopio, Finland.
  • Lee HM; Department of Pathology, Oulu University Hospital and University of Oulu, Oulu, Finland.
  • Koivuluoma S; Biocenter Oulu and Faculty of Biochemistry and Molecular Medicine, University of Oulu, Oulu, Finland.
  • Grip M; Laboratory of Cancer Genetics and Tumor Biology, Cancer and Translational Medicine Research Unit and Biocenter Oulu, Northern Finland Laboratory Centre Nordlab Oulu, University of Oulu, Oulu, Finland.
  • Karihtala P; Department of Surgery, Oulu University Hospital and University of Oulu, Oulu, Finland.
  • Jukkola-Vuorinen A; Department of Oncology and Radiotherapy, Medical Research Center Oulu, Oulu University Hospital and University of Oulu, Oulu, Finland.
  • Mannermaa A; Department of Oncology and Radiotherapy, Medical Research Center Oulu, Oulu University Hospital and University of Oulu, Oulu, Finland.
  • Winqvist R; School of Medicine, Institute of Clinical Medicine, Pathology and Forensic Medicine, and Translational Cancer Research Area, University of Eastern Finland, Kuopio, Finland.
  • Pylkäs K; Department of Clinical Pathology, Imaging Center, Kuopio University Hospital, Kuopio, Finland.
Int J Cancer ; 142(11): 2286-2292, 2018 06 01.
Article de En | MEDLINE | ID: mdl-29341116
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Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Tumeurs du sein / Prédisposition génétique à une maladie / Mutation faux-sens / RecQ helicases / DNA Polymerase gamma Type d'étude: Observational_studies / Prognostic_studies / Risk_factors_studies Limites: Female / Humans Langue: En Journal: Int J Cancer Année: 2018 Type de document: Article Pays d'affiliation: Finlande
Texte intégral
Ajouter à My VHL
Imprimer
XML
PubMed Links
Recherche sur Google

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Tumeurs du sein / Prédisposition génétique à une maladie / Mutation faux-sens / RecQ helicases / DNA Polymerase gamma Type d'étude: Observational_studies / Prognostic_studies / Risk_factors_studies Limites: Female / Humans Langue: En Journal: Int J Cancer Année: 2018 Type de document: Article Pays d'affiliation: Finlande