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MMSET/WHSC1 enhances DNA damage repair leading to an increase in resistance to chemotherapeutic agents.
Shah, M Y; Martinez-Garcia, E; Phillip, J M; Chambliss, A B; Popovic, R; Ezponda, T; Small, E C; Will, C; Phillip, M P; Neri, P; Bahlis, N J; Wirtz, D; Licht, J D.
  • Shah MY; Division of Hematology/Oncology, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
  • Martinez-Garcia E; Division of Hematology/Oncology, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
  • Phillip JM; Department of Chemical and Biomolecular Engineering, Institute for Nanobiotechnology, Johns Hopkins University, Baltimore, MD, USA.
  • Chambliss AB; Department of Chemical and Biomolecular Engineering, Institute for Nanobiotechnology, Johns Hopkins University, Baltimore, MD, USA.
  • Popovic R; Division of Hematology/Oncology, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
  • Ezponda T; Division of Hematology/Oncology, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
  • Small EC; Division of Hematology/Oncology, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
  • Will C; Division of Hematology/Oncology, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
  • Phillip MP; Department of Chemical and Biomolecular Engineering, Institute for Nanobiotechnology, Johns Hopkins University, Baltimore, MD, USA.
  • Neri P; Departments of Oncology and Medicine, University of Calgary and Tom Baker Cancer Centre, Calgary, AB, Canada.
  • Bahlis NJ; Departments of Oncology and Medicine, University of Calgary and Tom Baker Cancer Centre, Calgary, AB, Canada.
  • Wirtz D; Department of Chemical and Biomolecular Engineering, Institute for Nanobiotechnology, Johns Hopkins University, Baltimore, MD, USA.
  • Licht JD; Department of Oncology and Pathology, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Oncogene ; 35(45): 5905-5915, 2016 11 10.
Article en En | MEDLINE | ID: mdl-27109101

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Proteínas Represoras / Daño del ADN / N-Metiltransferasa de Histona-Lisina / Resistencia a Antineoplásicos / Reparación del ADN / Antineoplásicos Tipo de estudio: Prognostic_studies Límite: Animals / Humans Idioma: En Año: 2016 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Proteínas Represoras / Daño del ADN / N-Metiltransferasa de Histona-Lisina / Resistencia a Antineoplásicos / Reparación del ADN / Antineoplásicos Tipo de estudio: Prognostic_studies Límite: Animals / Humans Idioma: En Año: 2016 Tipo del documento: Article