344 related articles for article (PubMed ID: 25823699)
1. Therapeutic options for hydrating airway mucus in cystic fibrosis.
Tildy BE; Rogers DF
Pharmacology; 2015; 95(3-4):117-32. PubMed ID: 25823699
[TBL] [Abstract][Full Text] [Related]
2. Unplugging Mucus in Cystic Fibrosis and Chronic Obstructive Pulmonary Disease.
Mall MA
Ann Am Thorac Soc; 2016 Apr; 13 Suppl 2():S177-85. PubMed ID: 27115954
[TBL] [Abstract][Full Text] [Related]
3. Insights into the mechanisms underlying CFTR channel activity, the molecular basis for cystic fibrosis and strategies for therapy.
Kim Chiaw P; Eckford PD; Bear CE
Essays Biochem; 2011 Sep; 50(1):233-48. PubMed ID: 21967060
[TBL] [Abstract][Full Text] [Related]
4. Model of mucociliary clearance in cystic fibrosis lungs.
Kurbatova P; Bessonov N; Volpert V; Tiddens HA; Cornu C; Nony P; Caudri D;
J Theor Biol; 2015 May; 372():81-8. PubMed ID: 25746843
[TBL] [Abstract][Full Text] [Related]
5. Strategies in early clinical development for the treatment of basic defects of cystic fibrosis.
Dhooghe B; Haaf JB; Noel S; Leal T
Expert Opin Investig Drugs; 2016; 25(4):423-36. PubMed ID: 26878157
[TBL] [Abstract][Full Text] [Related]
6. 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
[TBL] [Abstract][Full Text] [Related]
7. Treatment of cystic fibrosis airway cells with CFTR modulators reverses aberrant mucus properties
Morrison CB; Shaffer KM; Araba KC; Markovetz MR; Wykoff JA; Quinney NL; Hao S; Delion MF; Flen AL; Morton LC; Liao J; Hill DB; Drumm ML; O'Neal WK; Kesimer M; Gentzsch M; Ehre C
Eur Respir J; 2022 Feb; 59(2):. PubMed ID: 34172469
[TBL] [Abstract][Full Text] [Related]
8. TMEM16A Potentiation: A Novel Therapeutic Approach for the Treatment of Cystic Fibrosis.
Danahay HL; Lilley S; Fox R; Charlton H; Sabater J; Button B; McCarthy C; Collingwood SP; Gosling M
Am J Respir Crit Care Med; 2020 Apr; 201(8):946-954. PubMed ID: 31898911
[No Abstract] [Full Text] [Related]
9. Cystic fibrosis transmembrane conductance regulator is expressed in mucin granules from Calu-3 and primary human airway epithelial cells.
LeSimple P; Goepp J; Palmer ML; Fahrenkrug SC; O'Grady SM; Ferraro P; Robert R; Hanrahan JW
Am J Respir Cell Mol Biol; 2013 Oct; 49(4):511-6. PubMed ID: 23742042
[TBL] [Abstract][Full Text] [Related]
10. Rationale for hypertonic saline therapy for cystic fibrosis lung disease.
Tarran R; Donaldson S; Boucher RC
Semin Respir Crit Care Med; 2007 Jun; 28(3):295-302. PubMed ID: 17562499
[TBL] [Abstract][Full Text] [Related]
11. HGF stimulation of Rac1 signaling enhances pharmacological correction of the most prevalent cystic fibrosis mutant F508del-CFTR.
Moniz S; Sousa M; Moraes BJ; Mendes AI; Palma M; Barreto C; Fragata JI; Amaral MD; Matos P
ACS Chem Biol; 2013 Feb; 8(2):432-42. PubMed ID: 23148778
[TBL] [Abstract][Full Text] [Related]
12. Pharmacological rescue of mutant CFTR protein improves the viscoelastic properties of CF mucus.
Gianotti A; Capurro V; Scudieri P; Galietta LJ; Moran O; Zegarra-Moran O
J Cyst Fibros; 2016 May; 15(3):295-301. PubMed ID: 26677762
[TBL] [Abstract][Full Text] [Related]
13. Introduction to section I: overview of approaches to study cystic fibrosis pathophysiology.
Clunes MT; Boucher RC
Methods Mol Biol; 2011; 742():3-14. PubMed ID: 21547723
[TBL] [Abstract][Full Text] [Related]
14. Modulation of Ion Transport to Restore Airway Hydration in Cystic Fibrosis.
Reihill JA; Douglas LEJ; Martin SL
Genes (Basel); 2021 Mar; 12(3):. PubMed ID: 33810137
[TBL] [Abstract][Full Text] [Related]
15. New pharmacological approaches for cystic fibrosis: promises, progress, pitfalls.
Bell SC; De Boeck K; Amaral MD
Pharmacol Ther; 2015 Jan; 145():19-34. PubMed ID: 24932877
[TBL] [Abstract][Full Text] [Related]
16. Small Molecule Anion Carriers Correct Abnormal Airway Surface Liquid Properties in Cystic Fibrosis Airway Epithelia.
Gianotti A; Capurro V; Delpiano L; Mielczarek M; GarcĂa-Valverde M; Carreira-Barral I; Ludovico A; Fiore M; Baroni D; Moran O; Quesada R; Caci E
Int J Mol Sci; 2020 Feb; 21(4):. PubMed ID: 32098269
[TBL] [Abstract][Full Text] [Related]
17. Cigarette smoke exposure induces CFTR internalization and insolubility, leading to airway surface liquid dehydration.
Clunes LA; Davies CM; Coakley RD; Aleksandrov AA; Henderson AG; Zeman KL; Worthington EN; Gentzsch M; Kreda SM; Cholon D; Bennett WD; Riordan JR; Boucher RC; Tarran R
FASEB J; 2012 Feb; 26(2):533-45. PubMed ID: 21990373
[TBL] [Abstract][Full Text] [Related]
18. Regulation of airway surface liquid volume by human airway epithelia.
Boucher RC
Pflugers Arch; 2003 Jan; 445(4):495-8. PubMed ID: 12548395
[TBL] [Abstract][Full Text] [Related]
19. Altering airway surface liquid volume: inhalation therapy with amiloride and hyperosmotic agents.
Hirsh AJ
Adv Drug Deliv Rev; 2002 Dec; 54(11):1445-62. PubMed ID: 12458154
[TBL] [Abstract][Full Text] [Related]
20. The epithelium as a target for therapy in cystic fibrosis.
Thelin WR; Boucher RC
Curr Opin Pharmacol; 2007 Jun; 7(3):290-5. PubMed ID: 17475561
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]