Exploring the potential of cell-derived vesicles for transient delivery of gene editing payloads

[Display omitted] Gene editing technologies have the potential to correct genetic disorders by modifying, inserting, or deleting specific DNA sequences or genes, paving the way for a new class of genetic therapies. While gene editing tools continue to be improved to increase their precision and effi...

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Veröffentlicht in:	Advanced drug delivery reviews 2024-08, Vol.211, p.115346-115346, Article 115346
Hauptverfasser:	Leandro, Kevin, Rufino-Ramos, David, Breyne, Koen, Di Ianni, Emilio, Lopes, Sara M., Jorge Nobre, Rui, Kleinstiver, Benjamin P., Perdigão, Pedro R.L., Breakefield, Xandra O., Pereira de Almeida, Luís
Format:	Artikel
Sprache:	eng
Schlagworte:	Animals Biovesicles Cre recombinase CRISPR-Cas9 Delivery vehicles Extracellular vesicles Extracellular Vesicles - metabolism Gene Editing - methods Gene Transfer Techniques Genetic Therapy - methods Humans Virus-like particles
Online-Zugang:	Volltext
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