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pro vyhledávání: '"Joost vanHaasteren"'
Autor:
Joost vanHaasteren, Stephen L. Hart, Aristides D. Tagalakis, David McCarthy, Luca Rosa, Mustafa M. Munye, Ahmad Aldossary
Publikováno v:
Molecular Therapy. 24:S11
Cystic fibrosis (CF) is caused by mutations in the cystic fibrosis conductance regulator (CFTR) gene, which encodes for a chloride channel. Loss of CFTR upregulates the epithelial sodium channel (ENaC) causing hyperabsorption of sodium, reducing the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::57f9b484bcdef70f5d7c2f54a4036af5
https://doi.org/10.1016/s1525-0016(16)32832-5
https://doi.org/10.1016/s1525-0016(16)32832-5
