Abstract:
:Advances in Clustered Regularly Interspaced Short Palindromic Repeats/CRISPR associated system (CRISPR/Cas9) has dramatically reshaped our ability to edit genomes. The scientific community is using CRISPR/Cas9 for various biotechnological and medical purposes. One of its most important uses is developing potential therapeutic strategies against diseases. CRISPR/Cas9 based approaches have been increasingly applied to the treatment of human diseases like cancer, genetic, immunological and neurological disorders and viral diseases. These strategies using CRISPR/Cas9 are not only therapy oriented but can also be used for disease modeling as well, which in turn can lead to the improved understanding of mechanisms of various infectious and genetic diseases. In addition, CRISPR/Cas9 system can also be used as programmable antibiotics to kill the bacteria sequence specifically and therefore can bypass multidrug resistance. Furthermore, CRISPR/Cas9 based gene drive may also hold the potential to limit the spread of vector borne diseases. This bacterial and archaeal adaptive immune system might be a therapeutic answer to previous incurable diseases, of course rigorous testing is required to corroborate these claims. In this review, we provide an insight about the recent developments using CRISPR/Cas9 against various diseases with respect to disease modeling and treatment, and what future perspectives should be noted while using this technology.
journal_name
J Biomed Scijournal_title
Journal of biomedical scienceauthors
Khan S,Mahmood MS,Rahman SU,Zafar H,Habibullah S,Khan Z,Ahmad Adoi
10.1186/s12929-018-0425-5subject
Has Abstractpub_date
2018-03-28 00:00:00pages
29issue
1eissn
1021-7770issn
1423-0127pii
10.1186/s12929-018-0425-5journal_volume
25pub_type
杂志文章,评审abstract::The Tat proteins of human immunodeficiency virus types 1 (HIV-1) and 2 (HIV-2), termed Tat-1 and Tat-2, respectively, are essential for efficient viral replication. Tat proteins activate viral transcription by binding to the TAR RNA stem-loop structure at the 5' end of viral transcripts. We used an in vitro selection ...
journal_title:Journal of biomedical science
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pub_type: 杂志文章,评审
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pub_type: 杂志文章
doi:10.1186/1423-0127-17-23
更新日期:2010-03-31 00:00:00
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pub_type: 杂志文章
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更新日期:2013-07-01 00:00:00
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journal_title:Journal of biomedical science
pub_type: 杂志文章
doi:10.1007/BF02253469
更新日期:1998-01-01 00:00:00
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journal_title:Journal of biomedical science
pub_type: 杂志文章
doi:10.1007/s11373-007-9164-4
更新日期:2007-09-01 00:00:00
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journal_title:Journal of biomedical science
pub_type: 杂志文章
doi:10.1007/s11373-005-9043-9
更新日期:2006-05-01 00:00:00
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pub_type: 杂志文章
doi:10.1186/s12929-020-00683-6
更新日期:2020-08-27 00:00:00
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pub_type: 杂志文章
doi:10.1186/s12929-019-0526-9
更新日期:2019-05-11 00:00:00
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pub_type: 杂志文章
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更新日期:2008-11-01 00:00:00
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pub_type: 杂志文章,评审
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journal_title:Journal of biomedical science
pub_type: 杂志文章
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更新日期:1998-11-01 00:00:00
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pub_type: 杂志文章
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更新日期:2004-07-01 00:00:00
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pub_type: 杂志文章,评审
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pub_type: 已发布勘误
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pub_type: 杂志文章
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