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Int J Mol Cell Med 2019, 8 - Suppl 1_Int J Mol Cell Med: 69-70 Back to browse issues page
The Pathway from Gene Therapy to Genome Editing: A Nightmare or Dream
Mandana Hasanzad1 , Bagher Larijani 2
1- Medical Genomics Research Center, Tehran Medical Sciences, Islamic Azad University, Tehran, Iran; Personalized Medicine Research Center, Endocrinology and Metabolism Clinical Sciences Institute, Tehran University of Medical Sciences, Tehran, Iran.
2- Personalized Medicine Research Center, Endocrinology and Metabolism Clinical Sciences Institute, Tehran University of Medical Sciences, Tehran, Iran. , Larijanib1340@gmail.com
Abstract:   (231 Views)
The gene therapy approach has largely been improved by the development of new methods in gene transfer and genome editing. The use of CART cells was first approved in 2018 by FDA for ex vivo treatment of B cell acute lymphoblastic leukemia and in vivo treatment of retinal dystrophy. This revolutionary trend is expected to continue as the clinical vision develops and the technical capacity improves.
Keywords: Gene Therapy, Genome Editing
Full-Text [PDF 335 kb]   (91 Downloads)    
Type of Study: Letters to the editor | Subject: Other
Received: 2019/03/13 | Accepted: 2019/11/9 | Published: 2020/01/1
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Hasanzad M, Larijani B. The Pathway from Gene Therapy to Genome Editing: A Nightmare or Dream. Int J Mol Cell Med. 2019; 8 (S1) :69-70
URL: http://ijmcmed.org/article-1-1042-en.html


Volume 8 - Suppl 1_Int J Mol Cell Med Back to browse issues page
International Journal of Molecular and Cellular Medicine (IJMCM) International Journal of Molecular and Cellular Medicine (IJMCM)
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