Detalhe da pesquisa
1.
A High-Throughput Platform to Identify Small-Molecule Inhibitors of CRISPR-Cas9.
Cell;
177(4): 1067-1079.e19, 2019 05 02.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31051099
2.
Enhanced Bacterial Immunity and Mammalian Genome Editing via RNA-Polymerase-Mediated Dislodging of Cas9 from Double-Strand DNA Breaks.
Mol Cell;
71(1): 42-55.e8, 2018 07 05.
Artigo
em Inglês
| MEDLINE
| ID: mdl-29979968
3.
Mutations in Cas9 Enhance the Rate of Acquisition of Viral Spacer Sequences during the CRISPR-Cas Immune Response.
Mol Cell;
65(1): 168-175, 2017 Jan 05.
Artigo
em Inglês
| MEDLINE
| ID: mdl-28017588
4.
Cas9 specifies functional viral targets during CRISPR-Cas adaptation.
Nature;
519(7542): 199-202, 2015 Mar 12.
Artigo
em Inglês
| MEDLINE
| ID: mdl-25707807
5.
Adapting to new threats: the generation of memory by CRISPR-Cas immune systems.
Mol Microbiol;
93(1): 1-9, 2014 Jul.
Artigo
em Inglês
| MEDLINE
| ID: mdl-24806524
6.
A unique alkaline pH-regulated and fatty acid-activated tandem pore domain potassium channel (K2P) from a marine sponge.
J Exp Biol;
215(Pt 14): 2435-44, 2012 Jul 15.
Artigo
em Inglês
| MEDLINE
| ID: mdl-22723483
7.
Spacer Acquisition Rates Determine the Immunological Diversity of the Type II CRISPR-Cas Immune Response.
Cell Host Microbe;
25(2): 242-249.e3, 2019 02 13.
Artigo
em Inglês
| MEDLINE
| ID: mdl-30709780
8.
Homology model and targeted mutagenesis identify critical residues for arachidonic acid inhibition of Kv4 channels.
Channels (Austin);
7(2): 74-84, 2013.
Artigo
em Inglês
| MEDLINE
| ID: mdl-23334377