miR‐181a/b downregulation: a mutation‐independent therapeutic approach for inherited retinal diseases

Inherited retinal diseases (IRDs) are a group of diseases whose common landmark is progressive photoreceptor loss. The development of gene‐specific therapies for IRDs is hampered by their wide genetic heterogeneity. Mitochondrial dysfunction is proving to constitute one of the key pathogenic events...

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Detalles Bibliográficos
Autores principales: Carrella, Sabrina, Di Guida, Martina, Brillante, Simona, Piccolo, Davide, Ciampi, Ludovica, Guadagnino, Irene, Garcia Piqueras, Jorge, Pizzo, Mariateresa, Marrocco, Elena, Molinari, Marta, Petrogiannakis, Georgios, Barbato, Sara, Ezhova, Yulia, Auricchio, Alberto, Franco, Brunella, De Leonibus, Elvira, Surace, Enrico Maria, Indrieri, Alessia, Banfi, Sandro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9641422/
https://www.ncbi.nlm.nih.gov/pubmed/36194668
http://dx.doi.org/10.15252/emmm.202215941

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9641422/
https://www.ncbi.nlm.nih.gov/pubmed/36194668
http://dx.doi.org/10.15252/emmm.202215941

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