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Targeted sequencing of genes associated with the mismatch repair pathway in patients with endometrial cancer.
Singh, Ashish Kumar; Talseth-Palmer, Bente; McPhillips, Mary; Lavik, Liss Anne Solberg; Xavier, Alexandre; Drabløs, Finn; Sjursen, Wenche.
Afiliação
  • Singh AK; Department of Medical Genetics, St. Olavs Hospital, Trondheim, Norway.
  • Talseth-Palmer B; Department of Clinical and Molecular Medicine, Faculty of Medicine and Health Sciences, NTNU-Norwegian University of Science and Technology, Trondheim, Norway.
  • McPhillips M; Department of Medical Genetics, St. Olavs Hospital, Trondheim, Norway.
  • Lavik LAS; School of Biomedical Science and Pharmacy, Faculty of Health and Medicine, University of Newcastle and Hunter Medical Research Institute, Newcastle, Australia.
  • Xavier A; Department of Research and Development, Møre og Romsdal Hospital Trust, Molde, Norway.
  • Drabløs F; NSW Health Pathology, Molecular Medicine, John Hunter Hospital, Newcastle, NSW, Australia.
  • Sjursen W; Department of Medical Genetics, St. Olavs Hospital, Trondheim, Norway.
PLoS One ; 15(7): e0235613, 2020.
Article em En | MEDLINE | ID: mdl-32634176
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias do Endométrio / Proteína 2 Homóloga a MutS / Reparo de Erro de Pareamento de DNA / Endonuclease PMS2 de Reparo de Erro de Pareamento / Proteína 1 Homóloga a MutL Tipo de estudo: Etiology_studies / Prognostic_studies / Risk_factors_studies Limite: Female / Humans Idioma: En Ano de publicação: 2020 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: Neoplasias do Endométrio / Proteína 2 Homóloga a MutS / Reparo de Erro de Pareamento de DNA / Endonuclease PMS2 de Reparo de Erro de Pareamento / Proteína 1 Homóloga a MutL Tipo de estudo: Etiology_studies / Prognostic_studies / Risk_factors_studies Limite: Female / Humans Idioma: En Ano de publicação: 2020 Tipo de documento: Article