載入...
Crispr-mediated Gene Targeting of Human Induced Pluripotent Stem Cells
CRISPR / Cas9 nuclease systems can create double-stranded DNA breaks at specific sequences to efficiently and precisely disrupt, excise, mutate, insert, or replace genes. However, human embryonic stem or induced pluripotent stem cells (iPSCs) are more difficult to transfect and less resilient to DNA...
Na minha lista:
| 發表在: | Curr Protoc Stem Cell Biol |
|---|---|
| Main Authors: | , |
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
2015
|
| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4772967/ https://ncbi.nlm.nih.gov/pubmed/26949444 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/9780470151808.sc05a08s35 |
| 標簽: |
添加標簽
沒有標簽, 成為第一個標記此記錄!
|