Cargando…
Precise in vivo functional analysis of DNA variants with base editing using ACEofBASEs target prediction
Single nucleotide variants (SNVs) are prevalent genetic factors shaping individual trait profiles and disease susceptibility. The recent development and optimizations of base editors, rubber and pencil genome editing tools now promise to enable direct functional assessment of SNVs in model organisms...
Autores principales: | Cornean, Alex, Gierten, Jakob, Welz, Bettina, Mateo, Juan Luis, Thumberger, Thomas, Wittbrodt, Joachim |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9033269/ https://www.ncbi.nlm.nih.gov/pubmed/35373735 http://dx.doi.org/10.7554/eLife.72124 |
Ejemplares similares
-
CRISPR-based knockout and base editing confirm the role of MYRF in heart development and congenital heart disease
por: Doering, Lino, et al.
Publicado: (2023) -
Boosting targeted genome editing using the hei-tag
por: Thumberger, Thomas, et al.
Publicado: (2022) -
In vivo identification and validation of novel potential predictors for human cardiovascular diseases
por: Hammouda, Omar T., et al.
Publicado: (2021) -
Natural genetic variation quantitatively regulates heart rate and dimension
por: Gierten, Jakob, et al.
Publicado: (2023) -
De novo PAM generation to reach initially inaccessible target sites for base editing
por: Pakari, Kaisa, et al.
Publicado: (2023)