Your browser doesn't support javascript.
loading
Identification of oncogenic driver mutations by genome-wide CRISPR-Cas9 dropout screening.
Kiessling, Michael K; Schuierer, Sven; Stertz, Silke; Beibel, Martin; Bergling, Sebastian; Knehr, Judith; Carbone, Walter; de Vallière, Cheryl; Tchinda, Joelle; Bouwmeester, Tewis; Seuwen, Klaus; Rogler, Gerhard; Roma, Guglielmo.
Afiliación
  • Kiessling MK; Department of Gastroenterology and Hepatology, University Hospital Zürich, Zürich, Switzerland.
  • Schuierer S; Novartis Institutes for Biomedical Research, Novartis Pharma AG, Basel, Switzerland.
  • Stertz S; Institute of Medical Virology, University of Zürich, Zürich, Switzerland.
  • Beibel M; Novartis Institutes for Biomedical Research, Novartis Pharma AG, Basel, Switzerland.
  • Bergling S; Novartis Institutes for Biomedical Research, Novartis Pharma AG, Basel, Switzerland.
  • Knehr J; Novartis Institutes for Biomedical Research, Novartis Pharma AG, Basel, Switzerland.
  • Carbone W; Novartis Institutes for Biomedical Research, Novartis Pharma AG, Basel, Switzerland.
  • de Vallière C; Department of Gastroenterology and Hepatology, University Hospital Zürich, Zürich, Switzerland.
  • Tchinda J; Department of Oncology, Children University Hospital Zürich, Zürich, Switzerland.
  • Bouwmeester T; Novartis Institutes for Biomedical Research, Novartis Pharma AG, Basel, Switzerland.
  • Seuwen K; Novartis Institutes for Biomedical Research, Novartis Pharma AG, Basel, Switzerland.
  • Rogler G; Department of Gastroenterology and Hepatology, University Hospital Zürich, Zürich, Switzerland. Gerhard.rogler@usz.ch.
  • Roma G; Novartis Institutes for Biomedical Research, Novartis Pharma AG, Basel, Switzerland. Guglielmo.roma@novartis.com.
BMC Genomics ; 17(1): 723, 2016 09 09.
Article en En | MEDLINE | ID: mdl-27613601
Asunto(s)
Palabras clave
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Oncogenes / Transformación Celular Neoplásica / Estudio de Asociación del Genoma Completo / Sistemas CRISPR-Cas / Mutación Tipo de estudio: Diagnostic_studies / Screening_studies Límite: Humans Idioma: En Revista: BMC Genomics Asunto de la revista: GENETICA Año: 2016 Tipo del documento: Article País de afiliación: Suiza
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Oncogenes / Transformación Celular Neoplásica / Estudio de Asociación del Genoma Completo / Sistemas CRISPR-Cas / Mutación Tipo de estudio: Diagnostic_studies / Screening_studies Límite: Humans Idioma: En Revista: BMC Genomics Asunto de la revista: GENETICA Año: 2016 Tipo del documento: Article País de afiliación: Suiza