Učitavanje...
Combining CRISPR/Cas9 and rAAV Templates for Efficient Gene Editing
Altering endogenous genes in cells is an integral tool of modern cell biology. The ease-of-use of the CRISPR/Cas9 system to introduce genomic DNA breaks at specific sites in vivo has led to its rapid and wide adoption. In the absence of a DNA template, the lesion is repaired by nonhomologous end joi...
Spremljeno u:
| Izdano u: | Nucleic Acid Ther |
|---|---|
| Glavni autori: | , |
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
Mary Ann Liebert, Inc.
2015
|
| Teme: | |
| Online pristup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4657517/ https://ncbi.nlm.nih.gov/pubmed/26540648 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1089/nat.2015.0545 |
| Oznake: |
Dodaj oznaku
Bez oznaka, Budi prvi tko označuje ovaj zapis!
|