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Two CRISPR/Cas9-mediated methods for targeting complex insertions, deletions, or replacements in mouse
Genetically modified model organisms are valuable tools for probing gene function, dissecting complex signaling networks, studying human disease, and more. CRISPR/Cas9 technology has significantly democratized and reduced the time and cost of generating genetically modified models to the point that...
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| Publicat a: | MethodsX |
|---|---|
| Autors principals: | , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Elsevier
2019
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6812322/ https://ncbi.nlm.nih.gov/pubmed/31667107 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.mex.2019.09.003 |
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