Frataxin gene editing rescues Friedreich’s ataxia pathology in dorsal root ganglia organoid-derived sensory neurons
Friedreich’s ataxia (FRDA) is an autosomal-recessive disorder. Here the authors describe a DRG organoid from patient derived-neurons and co-culture with muscle cells to mimic the disorder in vitro and demonstrate potential correction of the phenotype by CRISPR based editing.
Guardado en:
Autores principales: | Pietro Giuseppe Mazzara, Sharon Muggeo, Mirko Luoni, Luca Massimino, Mattia Zaghi, Parisa Tajalli-Tehrani Valverde, Simone Brusco, Matteo Jacopo Marzi, Cecilia Palma, Gaia Colasante, Angelo Iannielli, Marianna Paulis, Chiara Cordiglieri, Serena Gea Giannelli, Paola Podini, Cinzia Gellera, Franco Taroni, Francesco Nicassio, Marco Rasponi, Vania Broccoli |
---|---|
Formato: | article |
Lenguaje: | EN |
Publicado: |
Nature Portfolio
2020
|
Materias: | |
Acceso en línea: | https://doaj.org/article/b91a2f099cbf40dd993de29571b96be7 |
Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|
Ejemplares similares
-
Activating frataxin expression by repeat-targeted nucleic acids
por: Liande Li, et al.
Publicado: (2016) -
Two factor-based reprogramming of rodent and human fibroblasts into Schwann cells
por: Pietro Giuseppe Mazzara, et al.
Publicado: (2017) -
Cofilin dysregulation alters actin turnover in frataxin-deficient neurons
por: Diana C. Muñoz-Lasso, et al.
Publicado: (2020) -
Friedreichs ataxia in a diabetic patient
por: Inna Igorevna Klefortova, et al.
Publicado: (2010) -
Current and emerging treatment options in the management of Friedreich ataxia
por: Michelangelo Mancuso, et al.
Publicado: (2010)