Target identification of small molecules using large-scale CRISPR-Cas mutagenesis scanning of essential genes
Cancer therapy drugs are designed to target genetic vulnerabilities, but loss-of-function screens often fail to identify essential genes in drug mechanism studies. Here the authors demonstrate CRISPRres, which exploits in-frame variation generated by indel formation to discover gene-drug interaction...
Guardado en:
Autores principales: | Jasper Edgar Neggers, Bert Kwanten, Tim Dierckx, Hiroki Noguchi, Arnout Voet, Lotte Bral, Kristien Minner, Bob Massant, Nicolas Kint, Michel Delforge, Thomas Vercruysse, Erkan Baloglu, William Senapedis, Maarten Jacquemyn, Dirk Daelemans |
---|---|
Formato: | article |
Lenguaje: | EN |
Publicado: |
Nature Portfolio
2018
|
Materias: | |
Acceso en línea: | https://doaj.org/article/9dbf9e90c64d440ea8f766544059bc01 |
Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|
Ejemplares similares
-
Mapping the binding interface between an HIV-1 inhibiting intrabody and the viral protein Rev.
por: Thomas Vercruysse, et al.
Publicado: (2013) -
Mutagenesis
Publicado: (1986) -
FraC nanopores with adjustable diameter identify the mass of opposite-charge peptides with 44 dalton resolution
por: Gang Huang, et al.
Publicado: (2019) -
Antimicrobials, stress and mutagenesis.
por: Alexandro Rodríguez-Rojas, et al.
Publicado: (2014) -
Electrostatic similarities between protein and small molecule ligands facilitate the design of protein-protein interaction inhibitors.
por: Arnout Voet, et al.
Publicado: (2013)