Assembly of CRISPR ribonucleoproteins with biotinylated oligonucleotides via an RNA aptamer for precise gene editing
Using CRISPR to write specific genetic sequences can sometimes be difficult due to the preference of mammalian cells to repair breaks using NHEJ. Here the authors form nanoparticles to localize the template sequence to the nuclease, shifting repair in favor of HDR.
Guardado en:
Autores principales: | Jared Carlson-Stevermer, Amr A. Abdeen, Lucille Kohlenberg, Madelyn Goedland, Kaivalya Molugu, Meng Lou, Krishanu Saha |
---|---|
Formato: | article |
Lenguaje: | EN |
Publicado: |
Nature Portfolio
2017
|
Materias: | |
Acceso en línea: | https://doaj.org/article/f08b65b2ded04098a2d3fda73679eeab |
Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|
Ejemplares similares
-
Design of efficacious somatic cell genome editing strategies for recessive and polygenic diseases
por: Jared Carlson-Stevermer, et al.
Publicado: (2020) -
Inhibition of CRISPR-Cas9 ribonucleoprotein complex assembly by anti-CRISPR AcrIIC2
por: Annoj Thavalingam, et al.
Publicado: (2019) -
Genome editing in maize directed by CRISPR–Cas9 ribonucleoprotein complexes
por: Sergei Svitashev, et al.
Publicado: (2016) -
CRISPRoff enables spatio-temporal control of CRISPR editing
por: Jared Carlson-Stevermer, et al.
Publicado: (2020) -
Systemic nanoparticle delivery of CRISPR-Cas9 ribonucleoproteins for effective tissue specific genome editing
por: Tuo Wei, et al.
Publicado: (2020)