Cargando…
Genome editing: the road of CRISPR/Cas9 from bench to clinic
Molecular scissors engineered for site-specific modification of the genome hold great promise for effective functional analyses of genes, genomes and epigenomes and could improve our understanding of the molecular underpinnings of disease states and facilitate novel therapeutic applications. Several...
Autores principales: | Eid, Ayman, Mahfouz, Magdy M |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5099421/ https://www.ncbi.nlm.nih.gov/pubmed/27741224 http://dx.doi.org/10.1038/emm.2016.111 |
Ejemplares similares
-
CRISPR base editors: genome editing without double-stranded breaks
por: Eid, Ayman, et al.
Publicado: (2018) -
CRISPR/Cas9-mediated target validation of the splicing inhibitor Pladienolide B
por: Aouida, Mustapha, et al.
Publicado: (2016) -
Efficient CRISPR/Cas9-Mediated Genome Editing Using a Chimeric Single-Guide RNA Molecule
por: Butt, Haroon, et al.
Publicado: (2017) -
Strategies in the delivery of Cas9 ribonucleoprotein for CRISPR/Cas9 genome editing
por: Zhang, Song, et al.
Publicado: (2021) -
CRISPR-Cas9: from Genome Editing to Cancer Research
por: Chen, Si, et al.
Publicado: (2016)