Cargando…
CRISPR-SKIP: programmable gene splicing with single base editors
CRISPR gene editing has revolutionized biomedicine and biotechnology by providing a simple means to engineer genes through targeted double-strand breaks in the genomic DNA of living cells. However, given the stochasticity of cellular DNA repair mechanisms and the potential for off-target mutations,...
Autores principales: | Gapinske, Michael, Luu, Alan, Winter, Jackson, Woods, Wendy S., Kostan, Kurt A., Shiva, Nikhil, Song, Jun S., Perez-Pinera, Pablo |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6092781/ https://www.ncbi.nlm.nih.gov/pubmed/30107853 http://dx.doi.org/10.1186/s13059-018-1482-5 |
Ejemplares similares
-
Targeted exon skipping with AAV-mediated split adenine base editors
por: Winter, Jackson, et al.
Publicado: (2019) -
Targeting Duchenne muscular dystrophy by skipping DMD exon 45 with base editors
por: Gapinske, Michael, et al.
Publicado: (2023) -
Author Correction: Targeted exon skipping with AAV-mediated split adenine base editors
por: Winter, Jackson, et al.
Publicado: (2019) -
Multiplexed and tunable transcriptional activation by promoter insertion using nuclease-assisted vector integration
por: Brown, Alexander, et al.
Publicado: (2019) -
CRISPR/Cas9-mediated genome editing induces exon skipping by alternative splicing or exon deletion
por: Mou, Haiwei, et al.
Publicado: (2017)