نتایج جستجو برای: crispr

تعداد نتایج: 12099  

2015
Yumei Luo Detu Zhu Zhizhuo Zhang Yaoyong Chen Xiaofang Sun

Recently, the clustered regularly interspaced short palindromic repeats (CRISPR) system has emerged as a powerful customizable artificial nuclease to facilitate precise genetic correction for tissue regeneration and isogenic disease modeling. However, previous studies reported substantial off-target activities of CRISPR system in human cells, and the enormous putative off-target sites are labor...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2011
Ekaterina Semenova Matthijs M Jore Kirill A Datsenko Anna Semenova Edze R Westra Barry Wanner John van der Oost Stan J J Brouns Konstantin Severinov

Prokaryotic clustered regularly interspaced short palindromic repeat (CRISPR)/Cas (CRISPR-associated sequences) systems provide adaptive immunity against viruses when a spacer sequence of small CRISPR RNA (crRNA) matches a protospacer sequence in the viral genome. Viruses that escape CRISPR/Cas resistance carry point mutations in protospacers, though not all protospacer mutations lead to escape...

2018
Zubair Ahmed Ratan Young-Jin Son Mohammad Faisal Haidere Bhuiyan Mohammad Mahtab Uddin Md Abdullah Yusuf Sojib Bin Zaman Jong-Hoon Kim Laila Anjuman Banu Jae Youl Cho

Bacteria and archaea possess adaptive immunity against foreign genetic materials through clustered regularly interspaced short palindromic repeat (CRISPR) systems. The discovery of this intriguing bacterial system heralded a revolutionary change in the field of medical science. The CRISPR and CRISPR-associated protein 9 (Cas9) based molecular mechanism has been applied to genome editing. This C...

2017
Mei-Yi Yan Hai-Qin Yan Gai-Xian Ren Ju-Ping Zhao Xiao-Peng Guo Yi-Cheng Sun

Clustered regularly interspaced short palindromic repeat (CRISPR)-Cas12a (Cpf1) has emerged as an effective genome editing tool in many organisms. Here, we developed and optimized a CRISPR-Cas12a-assisted recombineering system to facilitate genetic manipulation in bacteria. Using this system, point mutations, deletions, insertions, and gene replacements can be easily generated on the chromosome...

2013
James E. DiCarlo Julie E. Norville Prashant Mali Xavier Rios John Aach George M. Church

Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR) and CRISPR-associated (Cas) systems in bacteria and archaea use RNA-guided nuclease activity to provide adaptive immunity against invading foreign nucleic acids. Here, we report the use of type II bacterial CRISPR-Cas system in Saccharomyces cerevisiae for genome engineering. The CRISPR-Cas components, Cas9 gene and a designer g...

2016
Alexander P. Hynes Simon J. Labrie Sylvain Moineau

UNLABELLED The adaptive immune system of prokaryotes, called CRISPR-Cas (clustered regularly interspaced short palindromic repeats and CRISPR-associated genes), results in specific cleavage of invading nucleic acid sequences recognized by the cell's "memory" of past encounters. Here, we exploited the properties of native CRISPR-Cas systems to program the natural "memorization" process, efficien...

Journal: :International journal of medical microbiology : IJMM 2013
Eva Schunder Kerstin Rydzewski Roland Grunow Klaus Heuner

Francisella tularensis is a zoonotic agent and the subspecies novicida is proposed to be a water-associated bacterium. The intracellular pathogen F. tularensis causes tularemia in humans and is known for its potential to be used as a biological threat. We analyzed the genome sequence of F. tularensis subsp. novicida U112 in silico for the presence of a putative functional CRISPR/Cas (clustered ...

Journal: :Science 2016
Omar O Abudayyeh Jonathan S Gootenberg Silvana Konermann Julia Joung Ian M Slaymaker David B T Cox Sergey Shmakov Kira S Makarova Ekaterina Semenova Leonid Minakhin Konstantin Severinov Aviv Regev Eric S Lander Eugene V Koonin Feng Zhang

The clustered regularly interspaced short palindromic repeat (CRISPR)-CRISPR-associated genes (Cas) adaptive immune system defends microbes against foreign genetic elements via DNA or RNA-DNA interference. We characterize the class 2 type VI CRISPR-Cas effector C2c2 and demonstrate its RNA-guided ribonuclease function. C2c2 from the bacterium Leptotrichia shahii provides interference against RN...

Journal: :Methods in molecular biology 2017
Kit-San Yuen Chi-Ping Chan Kin-Hang Kok Dong-Yan Jin

The clustered regularly interspaced short palindromic repeats (CRISPR)-CRISPR associated protein 9 nuclease (Cas9) system is a powerful genome-editing tool for both chromosomal and extrachromosomal DNA. DNA viruses such as Epstein-Barr virus (EBV), which undergoes episomal replication in human cells, can be effectively edited by CRISPR/Cas9. We have demonstrated targeted editing of the EBV geno...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2017
Chunlong Xu Xiaolan Qi Xuguang Du Huiying Zou Fei Gao Tao Feng Hengxing Lu Shenglan Li Xiaomeng An Lijun Zhang Yuanyuan Wu Ying Liu Ning Li Mario R Capecchi Sen Wu

CRISPR/Cas9 is becoming an increasingly important tool to functionally annotate genomes. However, because genome-wide CRISPR libraries are mostly constructed in lentiviral vectors, in vivo applications are severely limited as a result of difficulties in delivery. Here, we examined the piggyBac (PB) transposon as an alternative vehicle to deliver a guide RNA (gRNA) library for in vivo screening....

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