Φορτώνει......
Transmembrane helical interactions in the CFTR channel pore
Mutations in the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) gene affect CFTR protein biogenesis or its function as a chloride channel, resulting in dysregulation of epithelial fluid transport in the lung, pancreas and other organs in cystic fibrosis (CF). Development of pharmaceutica...
Αποθηκεύτηκε σε:
| Τόπος έκδοσης: | PLoS Comput Biol |
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| Κύριοι συγγραφείς: | , , , , , |
| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
Public Library of Science
2017
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| Θέματα: | |
| Διαθέσιμο Online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5501672/ https://ncbi.nlm.nih.gov/pubmed/28640808 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pcbi.1005594 |
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