2017
DOI: 10.1080/13102818.2017.1406823
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CRISPR genome editing and its medical applications

Abstract: Genome editing has always been a challenging area as a means to provide more efficient ways to create a meaningful change in the genome. Today, the CRISPR (clustered regularly interspaced short palindromic repeat) restoration system is considered as one of the suitable and promising options for genome editing. This system has many advantages compared to the previous geneediting methods developed in this area. Compared to the previous systems, CRISPR can deactivate or eliminate a gene without interfering with i… Show more

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Cited by 13 publications
(8 citation statements)
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“…Complex algorithms and health apps will utilise AI and large, linked datasets to adapt all aspects of healthcare to patient subgroups and individuals in order to improve health outcomes. Additional technologies that were not discussed by experts or in the literature, such as the genome editing technique clustered regularly interspaced short palindromic repeats (CRISPR) [ 75 ], are also likely to fall under the umbrella of precision medicine as their application in healthcare is developed.…”
Section: Discussionmentioning
confidence: 99%
“…Complex algorithms and health apps will utilise AI and large, linked datasets to adapt all aspects of healthcare to patient subgroups and individuals in order to improve health outcomes. Additional technologies that were not discussed by experts or in the literature, such as the genome editing technique clustered regularly interspaced short palindromic repeats (CRISPR) [ 75 ], are also likely to fall under the umbrella of precision medicine as their application in healthcare is developed.…”
Section: Discussionmentioning
confidence: 99%
“…While genome sequencing helps to dissect the genome and identify its function, by introducing CRISPR, scientists are now able to manipulate genes, create new sequences, and introduce them to the genome, such as the work done on the schistosome genome [88,89]. Recently, gene-editing platforms have emerged as a treatment for parasitic diseases, which can modify the host genes required by the parasite or target the parasitic genes needed for replication [90][91][92]. This system uses Cas9 endonuclease to create a double-strand break (DSB) at a selected locus in the genome.…”
Section: Crispr and Its Application In Parasitologymentioning
confidence: 99%
“…Compared to the previous systems, CRISPR can deactivate or eliminate a gene without interfering with intracellular mechanisms. The system can be used in the treatment of diseases and in related research by identifying the performance of defective genes in these diseases [129]. However, the search for such recombinant DNA technology and genotyping tools regarding thermophilic microorganisms is in its infancy.…”
Section: Crispr Cas Systemsmentioning
confidence: 99%