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Functional interrogation of Lynch syndrome-associated MSH2 missense variants via CRISPR-Cas9 gene editing in human embryonic stem cells.
Rath, Abhijit; Mishra, Akriti; Ferreira, Victoria Duque; Hu, Chaoran; Omerza, Gregory; Kelly, Kevin; Hesse, Andrew; Reddi, Honey V; Grady, James P; Heinen, Christopher D.
Afiliación
  • Rath A; Center for Molecular Oncology and Institute for Systems Genomics, UConn Health, Farmington, Connecticut.
  • Mishra A; Department of Molecular and Cell Biology, University of Connecticut, Storrs, Connecticut.
  • Ferreira VD; University of St. Joseph, West Hartford, Connecticut.
  • Hu C; Department of Statistics, University of Connecticut, Storrs, Connecticut.
  • Omerza G; Connecticut Institute for Clinical and Translational Science, UConn Health, Farmington, Connecticut.
  • Kelly K; Clinical Genomics Laboratory, The Jackson Laboratory for Genomic Medicine, Farmington, Connecticut.
  • Hesse A; Clinical Genomics Laboratory, The Jackson Laboratory for Genomic Medicine, Farmington, Connecticut.
  • Reddi HV; Clinical Genomics Laboratory, The Jackson Laboratory for Genomic Medicine, Farmington, Connecticut.
  • Grady JP; Clinical Genomics Laboratory, The Jackson Laboratory for Genomic Medicine, Farmington, Connecticut.
  • Heinen CD; Connecticut Institute for Clinical and Translational Science, UConn Health, Farmington, Connecticut.
Hum Mutat ; 40(11): 2044-2056, 2019 11.
Article en En | MEDLINE | ID: mdl-31237724
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Neoplasias Colorrectales Hereditarias sin Poliposis / Mutación Missense / Proteína 2 Homóloga a MutS / Sistemas CRISPR-Cas / Células Madre Embrionarias Humanas / Edición Génica Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Hum Mutat Asunto de la revista: GENETICA MEDICA Año: 2019 Tipo del documento: Article
Texto completo
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Neoplasias Colorrectales Hereditarias sin Poliposis / Mutación Missense / Proteína 2 Homóloga a MutS / Sistemas CRISPR-Cas / Células Madre Embrionarias Humanas / Edición Génica Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Hum Mutat Asunto de la revista: GENETICA MEDICA Año: 2019 Tipo del documento: Article