Literature DB >> 34391646

Current advances in overcoming obstacles of CRISPR/Cas9 off-target genome editing.

Guillermo Aquino-Jarquin1.   

Abstract

CRISPR/Cas9-based technology has revolutionized biomedical research by providing a high-fidelity gene-editing method, foreshadowing a significant impact on the therapeutics of many human genetic disorders previously considered untreatable. However, off-target events represent a critical hurdle before genome editing can be fully established in clinical practice. This mini-review recapitulates some recent advances for detecting and overcoming off-target effects mediated by the CRISPR/Cas9 system that could increase the likelihood of clinical success of the CRISPR-based approaches.
Copyright © 2021 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Anti-CRISPR proteins; Base editors; CRISPR/Cas9; Genome-editing; Off-target effects; Prime editing

Mesh:

Year:  2021        PMID: 34391646     DOI: 10.1016/j.ymgme.2021.08.002

Source DB:  PubMed          Journal:  Mol Genet Metab        ISSN: 1096-7192            Impact factor:   4.797


  4 in total

1.  CRISPR/Cas9-induced gene conversion between ATAD3 paralogs.

Authors:  Shira Yanovsky-Dagan; Ayala Frumkin; James R Lupski; Tamar Harel
Journal:  HGG Adv       Date:  2022-01-25

Review 2.  [Precision medicine in pediatric neurology exemplified by the new treatment forms].

Authors:  Andreas Ziegler
Journal:  Nervenarzt       Date:  2022-01-17       Impact factor: 1.297

Review 3.  Therapeutic Applications of the CRISPR-Cas System.

Authors:  Kyungmin Kang; Youngjae Song; Inho Kim; Tae-Jung Kim
Journal:  Bioengineering (Basel)       Date:  2022-09-15

Review 4.  CRISPR/Cas9-A Promising Therapeutic Tool to Cure Blindness: Current Scenario and Future Prospects.

Authors:  Irshad Ahmad
Journal:  Int J Mol Sci       Date:  2022-09-29       Impact factor: 6.208

  4 in total

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