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

Author:

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

Publisher

Elsevier BV

Reference250 articles.

1. Applications of genome editing technology in the targeted therapy of human diseases: mechanisms, advances and prospects;Li;Signal Transduct Target Ther,2020

2. The promise and challenge of therapeutic genome editing;Doudna;Nature,2020

3. Therapeutic in vivo delivery of gene editing agents;Raguram;Cell,2022

4. Enhanced proofreading governs CRISPR-Cas9 targeting accuracy;Chen;Nature,2017

5. Directed evolution of CRISPR-Cas9 to increase its specificity;Lee;Nat Commun,2018

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