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Journal Abstract Search

1066 related items for PubMed ID: 14719996

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  • 2. Pharmacotherapy of the ion transport defect in cystic fibrosis.
    Kunzelmann K, Mall M.
    Clin Exp Pharmacol Physiol; 2001 Nov; 28(11):857-67. PubMed ID: 11703384
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  • 4. Ursodeoxycholic acid inhibits ENaC and Na/K pump activity to restore airway surface liquid height in cystic fibrosis bronchial epithelial cells.
    Mroz MS, Harvey BJ.
    Steroids; 2019 Nov; 151():108461. PubMed ID: 31344409
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  • 5. Pharmacological approaches to correcting the ion transport defect in cystic fibrosis.
    Roomans GM.
    Am J Respir Med; 2003 Nov; 2(5):413-31. PubMed ID: 14719993
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  • 7. Relationships between cystic fibrosis transmembrane conductance regulator, extracellular nucleotides and cystic fibrosis.
    Marcet B, Boeynaems JM.
    Pharmacol Ther; 2006 Dec; 112(3):719-32. PubMed ID: 16828872
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  • 11. Epithelial sodium channel silencing as a strategy to correct the airway surface fluid deficit in cystic fibrosis.
    Gianotti A, Melani R, Caci E, Sondo E, Ravazzolo R, Galietta LJ, Zegarra-Moran O.
    Am J Respir Cell Mol Biol; 2013 Sep; 49(3):445-52. PubMed ID: 23600628
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  • 13. Mathematical model reveals role of nucleotide signaling in airway surface liquid homeostasis and its dysregulation in cystic fibrosis.
    Sandefur CI, Boucher RC, Elston TC.
    Proc Natl Acad Sci U S A; 2017 Aug 29; 114(35):E7272-E7281. PubMed ID: 28808008
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  • 19. The epithelial sodium channel (ENaC) as a therapeutic target for cystic fibrosis.
    Shei RJ, Peabody JE, Kaza N, Rowe SM.
    Curr Opin Pharmacol; 2018 Dec 29; 43():152-165. PubMed ID: 30340955
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  • 20. [CFTR and transepithelial ionic transport abnormalities in cystic fibrosis].
    Becq F.
    Arch Pediatr; 2003 Sep 29; 10 Suppl 2():325s-332s. PubMed ID: 14671929
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