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Using Oct4:MerCreMer Lineage Tracing to Monitor Endogenous Oct4 Expression During the Reprogramming of Fibroblasts into Induced Pluripotent Stem Cells (iPSCs).
Greder, Lucas V; Post, Jason; Dutton, James R.
Afiliación
  • Greder LV; MRC Molecular Haematology Unit, Weatherall Institute of Molecular Medicine, Radcliffe Department of Medicine, John Radcliffe Hospital, University of Oxford, Oxford, OX3 9DS, UK.
  • Post J; Stem Cell Institute, University of Minnesota, 2-220 MTRF, 2001 6th Street SE, Minneapolis, MN, 55455, USA.
  • Dutton JR; Stem Cell Institute, University of Minnesota, 2-220 MTRF, 2001 6th Street SE, Minneapolis, MN, 55455, USA. dutto015@umn.edu.
Methods Mol Biol ; 1357: 97-110, 2016.
Article en En | MEDLINE | ID: mdl-25687297
The reprogramming of somatic cells into induced pluripotent stem cells (iPSCs) using a combination of defined transcription factors has become one of the most widely used techniques in stem cell biology. A critical, early event in iPSC reprogramming is the induction of the endogenous transcription factor network that maintains pluripotency in iPSCs. Here we describe using a transgenic, conditional Oct4-Cre construct to investigate the spatial and temporal induction of endogenous Oct4 expression during the reprogramming of mouse fibroblasts into iPS cells.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Regulación de la Expresión Génica / Factor 3 de Transcripción de Unión a Octámeros / Reprogramación Celular / Células Madre Pluripotentes Inducidas / Fibroblastos / Técnicas de Reprogramación Celular Límite: Animals Idioma: En Revista: Methods Mol Biol Asunto de la revista: BIOLOGIA MOLECULAR Año: 2016 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Regulación de la Expresión Génica / Factor 3 de Transcripción de Unión a Octámeros / Reprogramación Celular / Células Madre Pluripotentes Inducidas / Fibroblastos / Técnicas de Reprogramación Celular Límite: Animals Idioma: En Revista: Methods Mol Biol Asunto de la revista: BIOLOGIA MOLECULAR Año: 2016 Tipo del documento: Article
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