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Journal Abstract Search

888 related items for PubMed ID: 31344409

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  • 3. The effect of ambroxol on chloride transport, CFTR and ENaC in cystic fibrosis airway epithelial cells.
    Varelogianni G, Hussain R, Strid H, Oliynyk I, Roomans GM, Johannesson M.
    Cell Biol Int; 2013 Nov; 37(11):1149-56. PubMed ID: 23765701
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  • 4. 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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  • 6. ENaC inhibitors and airway re-hydration in cystic fibrosis: state of the art.
    Althaus M.
    Curr Mol Pharmacol; 2013 Mar; 6(1):3-12. PubMed ID: 23547930
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  • 9. AMPK agonists ameliorate sodium and fluid transport and inflammation in cystic fibrosis airway epithelial cells.
    Myerburg MM, King JD, Oyster NM, Fitch AC, Magill A, Baty CJ, Watkins SC, Kolls JK, Pilewski JM, Hallows KR.
    Am J Respir Cell Mol Biol; 2010 Jun; 42(6):676-84. PubMed ID: 19617399
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  • 12. Pharmacotherapy of the ion transport defect in cystic fibrosis: role of purinergic receptor agonists and other potential therapeutics.
    Kunzelmann K, Mall M.
    Am J Respir Med; 2003 Jun; 2(4):299-309. PubMed ID: 14719996
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  • 17. SPLUNC1 degradation by the cystic fibrosis mucosal environment drives airway surface liquid dehydration.
    Webster MJ, Reidel B, Tan CD, Ghosh A, Alexis NE, Donaldson SH, Kesimer M, Ribeiro CMP, Tarran R.
    Eur Respir J; 2018 Oct; 52(4):. PubMed ID: 30190268
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  • 18. Low temperature and chemical rescue affect molecular proximity of DeltaF508-cystic fibrosis transmembrane conductance regulator (CFTR) and epithelial sodium channel (ENaC).
    Qadri YJ, Cormet-Boyaka E, Rooj AK, Lee W, Parpura V, Fuller CM, Berdiev BK.
    J Biol Chem; 2012 May 11; 287(20):16781-90. PubMed ID: 22442149
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