| Literature DB >> 32006418 |
Benjamin Dannenmann1, Masoud Nasri1, Karl Welte1, Julia Skokowa2.
Abstract
Research on patient-derived induced pluripotent stem cells (iPSCs) could immensely benefit from the implementation of CRISPR/Cas9 genome editing of iPSCs, creating unique opportunities such as the establishment of isogenic iPSC lines for disease modeling or personalized patient-specific drug screenings. Here we describe a stepwise protocol of safe, efficient, and selection-free CRISPR/Cas9-mediated gene correction or knockout in human iPSCs followed by 3D spin-embryoid body (EB)-based hematopoietic/neutrophilic iPSC-differentiation.Entities:
Keywords: CRISPR/Cas9; Genome editing; Hematopoietic, and neutrophilic differentiation of iPSCs; Human-induced pluripotent stem cells; Ribonucleoprotein; iPSC differentiation
Year: 2020 PMID: 32006418 DOI: 10.1007/978-1-0716-0290-4_27
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745