نمایش پرونده ساده آیتم

dc.contributor.authorSafari, F
dc.contributor.authorFarajnia, S
dc.contributor.authorGhasemi, Y
dc.contributor.authorZarghami, N
dc.date.accessioned2018-08-26T04:54:15Z
dc.date.available2018-08-26T04:54:15Z
dc.date.issued2017
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/38104
dc.description.abstractRNA-guided endonuclease as a versatile genome editing technology opened new windows in various fields of biology. The simplicity of this revolutionary technique provides a promising future for its application in a broad range of approaches from functional annotation of genes to diseases, to genetic manipulation and gene therapy. Besides the site-specific activity of Cas9 endonuclease, the unintended cleavage known as off-target effect is still a major challenge for this genome editing technique.Various strategies have been developed to resolve this bottleneck including development of new softwares for designing optimized guide RNA (gRNA), engineering Cas9 enzyme, improvement in off-target detection assays, etc. Results: This review dedicated to discuss on methods that have been used for optimizing Cas9, specificity with the aim of improving this technology for therapeutic applications.In addition, the applications and novel breakthroughs in the field of CRISPR technology will be described.
dc.language.isoEnglish
dc.relation.ispartofCurrent pharmaceutical biotechnology
dc.subjectAnimals
dc.subjectBacterial Proteins
dc.subjectCRISPR-Cas Systems
dc.subjectClustered Regularly Interspaced Short Palindromic Repeats
dc.subjectEndonucleases
dc.subjectHumans
dc.subjectRNA, Guide
dc.titleNew Developments in CRISPR Technology: Improvements in Specificity and Efficiency.
dc.typearticle
dc.citation.volume18
dc.citation.issue13
dc.citation.spage1038
dc.citation.epage1054
dc.citation.indexPubmed
dc.identifier.DOIhttps://doi.org/10.2174/1389201019666180209120533


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