KDM2A and KDM3B as Potential Targets for the Rescue of F508del-CFTR

Cystic fibrosis (CF) is caused by mutations in the gene encoding of the cystic fibrosis transmembrane conductance regulator (CFTR), an anion-selective plasma membrane channel that mainly regulates chloride transport in a variety of epithelia. More than 2000 mutations, most of which presumed to be di...

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Detalles Bibliográficos
Autores principales: D’Amore, Claudio, Borgo, Christian, Bosello Travain, Valentina, Salvi, Mauro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9455907/
https://www.ncbi.nlm.nih.gov/pubmed/36077010
http://dx.doi.org/10.3390/ijms23179612

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9455907/
https://www.ncbi.nlm.nih.gov/pubmed/36077010
http://dx.doi.org/10.3390/ijms23179612

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