Cargando…
Developing ABEmax-NG with Precise Targeting and Expanded Editing Scope to Model Pathogenic Splice Site Mutations In Vivo
RNA splicing is related to many human diseases; however, lack of efficient genetic approaches to modulate splicing has prevented us from dissecting their functions in human diseases. Recently developed base editors (BEs) offer a new strategy to modulate RNA splicing by converting conservative splice...
Autores principales: | Huang, Shisheng, Liao, Zhaodi, Li, Xiangyang, Liu, Zhen, Li, Guanglei, Li, Jianan, Lu, Zongyang, Zhang, Yu, Li, Xiajun, Ma, Xu, Sun, Qiang, Huang, Xingxu |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6548941/ https://www.ncbi.nlm.nih.gov/pubmed/31130518 http://dx.doi.org/10.1016/j.isci.2019.05.008 |
Ejemplares similares
-
Efficient generation of mouse models of human diseases via ABE- and BE-mediated base editing
por: Liu, Zhen, et al.
Publicado: (2018) -
Efficient Generation of Pathogenic A-to-G Mutations in Human Tripronuclear Embryos via ABE-Mediated Base Editing
por: Li, Guanglei, et al.
Publicado: (2019) -
Highly efficient and precise base editing in discarded human tripronuclear embryos
por: Li, Guanglei, et al.
Publicado: (2017) -
Correction of the Marfan Syndrome Pathogenic FBN1 Mutation by Base Editing in Human Cells and Heterozygous Embryos
por: Zeng, Yanting, et al.
Publicado: (2018) -
Harnessing A3G for efficient and selective C-to-T conversion at C-rich sequences
por: Yu, Wenxia, et al.
Publicado: (2021)