A Novel G542X CFTR Rat Model of Cystic Fibrosis Is Sensitive to Nonsense Mediated Decay

Nonsense mutations that lead to the insertion of a premature termination codon (PTC) in the cystic fibrosis transmembrane conductance regulator (CFTR) transcript affect 11% of patients with cystic fibrosis (CF) worldwide and are associated with severe disease phenotype. While CF rat models have cont...

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Detalles Bibliográficos
Autores principales: Sharma, Jyoti, Abbott, Joseph, Klaskala, Lauren, Zhao, Guojun, Birket, Susan E., Rowe, Steven M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Physiology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7772197/
https://www.ncbi.nlm.nih.gov/pubmed/33391025
http://dx.doi.org/10.3389/fphys.2020.611294

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7772197/
https://www.ncbi.nlm.nih.gov/pubmed/33391025
http://dx.doi.org/10.3389/fphys.2020.611294

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