Cargando…
Rapid and efficient CRISPR/Cas9 gene inactivation in human neurons during human pluripotent stem cell differentiation and direct reprogramming
The CRISPR/Cas9 system is a rapid and customizable tool for gene editing in mammalian cells. In particular, this approach has widely opened new opportunities for genetic studies in neurological disease. Human neurons can be differentiated in vitro from hPSC (human Pluripotent Stem Cells), hNPCs (hum...
Autores principales: | Rubio, Alicia, Luoni, Mirko, Giannelli, Serena G., Radice, Isabella, Iannielli, Angelo, Cancellieri, Cinzia, Di Berardino, Claudia, Regalia, Giulia, Lazzari, Giovanna, Menegon, Andrea, Taverna, Stefano, Broccoli, Vania |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5114606/ https://www.ncbi.nlm.nih.gov/pubmed/27857203 http://dx.doi.org/10.1038/srep37540 |
Ejemplares similares
-
Two factor-based reprogramming of rodent and human fibroblasts into Schwann cells
por: Mazzara, Pietro Giuseppe, et al.
Publicado: (2017) -
Whole brain delivery of an instability-prone Mecp2 transgene improves behavioral and molecular pathological defects in mouse models of Rett syndrome
por: Luoni, Mirko, et al.
Publicado: (2020) -
Coenzyme A corrects pathological defects in human neurons of PANK2‐associated neurodegeneration
por: Orellana, Daniel I, et al.
Publicado: (2016) -
Modeling native and seeded Synuclein aggregation and related cellular dysfunctions in dopaminergic neurons derived by a new set of isogenic iPSC lines with SNCA multiplications
por: Iannielli, Angelo, et al.
Publicado: (2022) -
Human pluripotent reprogramming with CRISPR activators
por: Weltner, Jere, et al.
Publicado: (2018)