Beyond the promise: evaluating and mitigating off-target effects in CRISPR gene editing for safer therapeutics
Over the last decade, CRISPR has revolutionized drug development due to its potential to cure genetic diseases that currently do not have any treatment. CRISPR was adapted from bacteria for gene editing in human cells in 2012 and, remarkably, only 11 years later has seen it’s very first approval as...
Main Authors: | Rui Lopes, Megana K. Prasad |
---|---|
Format: | Article |
Language: | English |
Published: |
Frontiers Media S.A.
2024-01-01
|
Series: | Frontiers in Bioengineering and Biotechnology |
Subjects: | |
Online Access: | https://www.frontiersin.org/articles/10.3389/fbioe.2023.1339189/full |
Similar Items
-
CRISPR/Cas Systems in Genome Editing: Methodologies and Tools for sgRNA Design, Off‐Target Evaluation, and Strategies to Mitigate Off‐Target Effects
by: Hakim Manghwar, et al.
Published: (2020-03-01) -
Off-target effects in CRISPR/Cas9 gene editing
by: Congting Guo, et al.
Published: (2023-03-01) -
Optimizing CRISPR Cas9 Genome Editing System: A Review
by: Meen Bahadur Budhthoki, et al.
Published: (2017-03-01) -
Recent Advancements in Reducing the Off-Target Effect of CRISPR-Cas9 Genome Editing
by: Asmamaw Mengstie M, et al.
Published: (2024-01-01) -
Plant genome editing: CRISPR, base editing, prime editing, and beyond
by: Yujie Xie, et al.
Published: (2022-12-01)