Cargando…
A functional sgRNA-CRISPR screening method for generating murine RET and NTRK1 rearranged oncogenes
CRISPR/Cas9 gene editing represents a powerful tool for investigating fusion oncogenes in cancer biology. Successful experiments require that sgRNAs correctly associate with their target sequence and initiate double stranded breaks which are subsequently repaired by endogenous DNA repair systems yie...
Autores principales: | Schubert, Laura, Le, Anh T., Hinz, Trista K., Navarro, Andre C., Nelson-Taylor, Sarah K., Nemenoff, Raphael A., Heasley, Lynn E., Doebele, Robert C. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Company of Biologists Ltd
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10445739/ https://www.ncbi.nlm.nih.gov/pubmed/37470475 http://dx.doi.org/10.1242/bio.059994 |
Ejemplares similares
-
A Rapid, Functional sgRNA Screening Method for Generating Murine RET and NTRK1 Fusion Oncogenes
por: Schubert, Laura, et al.
Publicado: (2023) -
A simple and rapid method for enzymatic synthesis of CRISPR-Cas9 sgRNA libraries
por: Yates, Joshua D, et al.
Publicado: (2021) -
CRISPR-STAT: an easy and reliable PCR-based method to evaluate target-specific sgRNA activity
por: Carrington, Blake, et al.
Publicado: (2015) -
AlleleAnalyzer: a tool for personalized and allele-specific sgRNA design
por: Keough, Kathleen C., et al.
Publicado: (2019) -
Refined sgRNA efficacy prediction improves large- and small-scale CRISPR–Cas9 applications
por: Labuhn, Maurice, et al.
Publicado: (2018)