1 Molecular Mechanisms of RNA Targeting by Cas13-containing Type VI CRISPR-Cas Systems
来源:J MOL BIOL( P 0022-2836 E 1089-8638 ) 发表时间: 2019/01
类型:期刊论文 为本人加分:28592.411584
2 Programmable RNA recognition and cleavage by CRISPR/Cas9
来源:NATURE( P 0028-0836 E 1476-4687 ) 发表时间: 2014/12
类型:期刊论文 为本人加分:24514.913369
3 Two distinct RNase activities of CRISPR-C2c2 enable guide-RNA processing and RNA detection
来源:NATURE( P 0028-0836 E 1476-4687 ) 发表时间: 2016/10
类型:期刊论文 为本人加分:16967.843765
贡献度:参与作者
4 Csx28 is a membrane pore that enhances CRISPR-Cas13b-dependent antiphage defense
来源:SCIENCE( P 0036-8075 E 1095-9203 ) 发表时间: 2023/04
类型:期刊论文 为本人加分:15981.895004
5 RNA Binding and HEPN-Nuclease Activation Are Decoupled in CRISPR-Cas13a
来源:CELL REP( P 2211-1247 E ) 发表时间: 2018/07
类型:期刊论文 为本人加分:4630.292435
6 RNA Targeting by Functionally Orthogonal Type VI-A CRISPR-Cas Enzymes
来源:MOL CELL( P 1097-2765 E 1097-4164 ) 发表时间: 2017/05
类型:期刊论文 为本人加分:4131.971331
7 Programmable RNA Tracking in Live Cells with CRISPR/Cas9
来源:CELL( P 0092-8674 E 1097-4172 ) 发表时间: 2016/04
类型:期刊论文 为本人加分:2435.354456
8 New design strategies for ultra-specific CRISPR-Cas13a-based RNA detection with single-nucleotide mi..
来源:NUCLEIC ACIDS RES( P 0305-1048 E 1362-4962 ) 发表时间: 2024/01
类型:期刊论文 为本人加分:1975.794199
9 THUMPD1 bi-allelic variants cause loss of tRNA acetylation and a syndromic neurodevelopmental disord..
来源:AM J HUM GENET( P 0002-9297 E 1537-6605 ) 发表时间: 2022/04
类型:期刊论文 为本人加分:1784.045633
10 Unveiling the RNA-mediated allosteric activation discloses functional hotspots in CRISPR-Cas13a
来源:NUCLEIC ACIDS RES( P 0305-1048 E 1362-4962 ) 发表时间: 2024/01
类型:期刊论文 为本人加分:1704.630009