Your browser doesn't support javascript.
loading
Precise therapeutic gene correction by a simple nuclease-induced double-stranded break.
Iyer, Sukanya; Suresh, Sneha; Guo, Dongsheng; Daman, Katelyn; Chen, Jennifer C J; Liu, Pengpeng; Zieger, Marina; Luk, Kevin; Roscoe, Benjamin P; Mueller, Christian; King, Oliver D; Emerson, Charles P; Wolfe, Scot A.
  • Iyer S; Department of Molecular, Cell and Cancer Biology, University of Massachusetts Medical School, Worcester, MA, USA.
  • Suresh S; Department of Molecular, Cell and Cancer Biology, University of Massachusetts Medical School, Worcester, MA, USA.
  • Guo D; Department of Neurology, University of Massachusetts Medical School, Worcester, MA, USA.
  • Daman K; Wellstone Muscular Dystrophy Program, University of Massachusetts Medical School, Worcester, MA, USA.
  • Chen JCJ; Department of Neurology, University of Massachusetts Medical School, Worcester, MA, USA.
  • Liu P; Wellstone Muscular Dystrophy Program, University of Massachusetts Medical School, Worcester, MA, USA.
  • Zieger M; Department of Neurology, University of Massachusetts Medical School, Worcester, MA, USA.
  • Luk K; Wellstone Muscular Dystrophy Program, University of Massachusetts Medical School, Worcester, MA, USA.
  • Roscoe BP; Office of the Vice-Principal (Research), Queen's University, Kingston, Ontario, Canada.
  • Mueller C; Department of Molecular, Cell and Cancer Biology, University of Massachusetts Medical School, Worcester, MA, USA.
  • King OD; Horae Gene Therapy Center, University of Massachusetts Medical School, Worcester, MA, USA.
  • Emerson CP; Li Weibo Institute for Rare Diseases Research, University of Massachusetts Medical School, Worcester, MA, USA.
  • Wolfe SA; Department of Molecular, Cell and Cancer Biology, University of Massachusetts Medical School, Worcester, MA, USA.
Nature ; 568(7753): 561-565, 2019 04.
Article en En | MEDLINE | ID: mdl-30944467
Asunto(s)
Texto completo
Imprimir
XML
PubMed Links
Search on Google

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Síndrome de Hermanski-Pudlak / Distrofia Muscular de Cinturas / Roturas del ADN de Doble Cadena / Reparación del ADN por Unión de Extremidades / Conectina / Proteínas Asociadas a CRISPR Límite: Humans Idioma: En Año: 2019 Tipo del documento: Article
Texto completo
Imprimir
XML
PubMed Links
Search on Google

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Síndrome de Hermanski-Pudlak / Distrofia Muscular de Cinturas / Roturas del ADN de Doble Cadena / Reparación del ADN por Unión de Extremidades / Conectina / Proteínas Asociadas a CRISPR Límite: Humans Idioma: En Año: 2019 Tipo del documento: Article