| Literature DB >> 20225040 |
Abstract
Human Embryonic stem cells (hESCs) offer an invaluable tool for revealing human biology and a potential source of functional cells/tissues for regenerative medicine. The utility of hESCs will likely be significantly enhanced and broadened by our ability to build versatile genetically modified hESC lines. Here, we describe an efficient lentiviral vector mediated method to establish stable transgenic hESCs.Entities:
Mesh：
Year: 2010 PMID： 20225040 DOI： 10.1007/978-1-60761-533-0_8
Source DB: PubMed Journal: Methods Mol Biol ISSN： 1064-3745