Cystic Fibrosis Human Organs-on-a-Chip

Cystic fibrosis (CF) is an autosomal recessive disease caused by mutations in the cystic fibrosis transmembrane regulator (CFTR) gene: the gene product responsible for transporting chloride and bicarbonate ions through the apical membrane of most epithelial cells. Major clinical features of CF inclu...

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Detalles Bibliográficos
Autores principales: Ogden, Herbert Luke, Kim, Hoyeol, Wikenheiser-Brokamp, Kathryn A., Naren, Anjaparavanda P., Mun, Kyu Shik
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8305167/
https://www.ncbi.nlm.nih.gov/pubmed/34202364
http://dx.doi.org/10.3390/mi12070747

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8305167/
https://www.ncbi.nlm.nih.gov/pubmed/34202364
http://dx.doi.org/10.3390/mi12070747

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