A platform to deliver single and bi-specific Cas9/guide RNA to perturb genes in vitro and in vivo-Reference-Cited by-同舟云学术

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A platform to deliver single and bi-specific Cas9/guide RNA to perturb genes in vitro and in vivo

Published:2024-07 Issue: Volume: Page:
ISSN:1525-0016
Container-title:Molecular Therapy
language:en
Short-container-title:Molecular Therapy

Author:

Li Yi-Jia,Chien Sheng-Hsuan,Huang Rui,Herrmann Andreas,Zhao Qianqian,Li Pei-Chuan,Zhang Chunyan,Martincuks Antons,Santiago Nicole Lugo,Zong Katherine,Swiderski Piotr,Okimoto Ross A.,Song Mihae,Rodriguez Lorna,Forman Stephen J.,Wang Xiuli,Yu Hua^ORCID

Funder

City of Hope Beckman Research Institute

Publisher

Elsevier BV

Reference108 articles.

1. The Potential of CRISPR/Cas9 Gene Editing as a Treatment Strategy for Inherited Diseases;Abdelnour;Front. Cell Dev. Biol.,2021

2. Landmark CRISPR trial shows promise against deadly disease;Ledford;Nature,2021

3. CRISPR/Cas: Advances, Limitations, and Applications for Precision Cancer Research;Yang;Front. Med.,2021

4. CRISPR off-targets: a question of context;Haeussler;Cell Biol. Toxicol.,2020

5. Off-target effects in CRISPR/Cas9 gene editing;Guo;Front. Bioeng. Biotechnol.,2023

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