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Tissue-Specific Delivery of CRISPR Therapeutics: Strategies and Mechanisms of Non-Viral Vectors

The Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR) genome editing system has been the focus of intense research in the last decade due to its superior ability to desirably target and edit DNA sequences. The applicability of the CRISPR-Cas system to in vivo genome editing has acqu...

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Detalles Bibliográficos
Autores principales:	Shalaby, Karim, Aouida, Mustapha, El-Agnaf, Omar
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	MDPI 2020
Materias:	Review
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7583726/ https://www.ncbi.nlm.nih.gov/pubmed/33027946 http://dx.doi.org/10.3390/ijms21197353

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