CRISPR/Cas9 a simple, inexpensive and effective technique for gene editing.
CRISPR/Cas9 a simple, inexpensive and effective technique for gene editing.
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CRISPR/Cas9是一种用于基因编辑的简单、廉价且有效的技术。
DOI:
10.1007/s11033-022-07442-w
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发表时间:
2022-07
影响因子:
2.8
通讯作者:
Choupina, Altino Branco
中科院分区:
文献类型:
--
作者:
Ferreira, Patrick;Choupina, Altino Branco
In recent years, the number of tools and techniques that enable genetic material to be added, removed or altered at specific locations in the genome has increased significantly. The objective is to know the structure of genomes, the function of genes and improve gene therapy. In this work we intend to explain the functioning of the CRISPR/Cas9 (Clustered Regularly Interspaced Short Palindromic Repeats/CRISPR associated protein 9) and the advantages that this technique may have compared to previously developed techniques, such as RNA interference (RNAi), Zinc Finger Nucleases (ZFNs) and transcription activator-like effector nucleases (TALENs) in gene and genome editing. We will start with the story of the discovery, then its biological function in the adaptive immune system of bacteria against bacteriophage attack, and ending with a description of the mechanism of action and its use in gene editing. We will also discuss other Cas enzymes with great potential for use in genome editing as an alternative to Cas9. CRISPR/Cas9 is a simple, inexpensive, and effective technique for gene editing with multiple applications from the development of functional genomics and epigenetics. This technique will, in the near future, have great applications in the development of cell models for use in medical and pharmaceutical processes, in targeted therapy, and improvement of agricultural and environmental species.
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影响因子:
64.8
作者:
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通讯作者:
Naldini, Luigi
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64.8
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56.9
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通讯作者:
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3.2
作者:
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通讯作者:
Moineau, Sylvain
影响因子:
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作者:
Krueger, Ute;Bergauer, Tobias;Konrad, Juliane
通讯作者:
Konrad, Juliane