Mucus Aberrant Properties in CF: Insights from Cells and Animal Models

Cystic fibrosis (CF), an autosomal genetic disorder caused by the dysfunction of the cystic fibrosis transmembrane conductance regulator (CFTR) protein, is characterized by mucus accumulation in the lungs, the intestinal tract, and the pancreatic ducts. Mucins are high-molecular-weight glycoproteins...

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Detalles Bibliográficos
Autores principales: Ehre, Camille, Hansson, Gunnar C., Thornton, David J., Ostedgaard, Lynda S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10018425/
https://www.ncbi.nlm.nih.gov/pubmed/36117114
http://dx.doi.org/10.1016/j.jcf.2022.08.019

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10018425/
https://www.ncbi.nlm.nih.gov/pubmed/36117114
http://dx.doi.org/10.1016/j.jcf.2022.08.019

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