These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
3. Characterization of cystic fibrosis airway smooth muscle cell proliferative and contractile activities. Jang JH; Panariti A; O'Sullivan MJ; Pyrch M; Wong C; Lauzon AM; Martin JG Am J Physiol Lung Cell Mol Physiol; 2019 Nov; 317(5):L690-L701. PubMed ID: 31508974 [TBL] [Abstract][Full Text] [Related]
4. Reduced expression of Tis7/IFRD1 protein in murine and human cystic fibrosis airway epithelial cell models homozygous for the F508del-CFTR mutation. Blanchard E; Marie S; Riffault L; Bonora M; Tabary O; Clement A; Jacquot J Biochem Biophys Res Commun; 2011 Aug; 411(3):471-6. PubMed ID: 21723850 [TBL] [Abstract][Full Text] [Related]
6. Ileal smooth muscle dysfunction and remodeling in cystic fibrosis. Risse PA; Kachmar L; Matusovsky OS; Novali M; Gil FR; Javeshghani S; Keary R; Haston CK; Michoud MC; Martin JG; Lauzon AM Am J Physiol Gastrointest Liver Physiol; 2012 Jul; 303(1):G1-8. PubMed ID: 22538405 [TBL] [Abstract][Full Text] [Related]
7. Defective regulatory volume decrease in human cystic fibrosis tracheal cells because of altered regulation of intermediate conductance Ca2+-dependent potassium channels. Vázquez E; Nobles M; Valverde MA Proc Natl Acad Sci U S A; 2001 Apr; 98(9):5329-34. PubMed ID: 11309505 [TBL] [Abstract][Full Text] [Related]
8. CFTR regulation of intracellular calcium in normal and cystic fibrosis human airway epithelia. Walsh DE; Harvey BJ; Urbach V J Membr Biol; 2000 Oct; 177(3):209-19. PubMed ID: 11014859 [TBL] [Abstract][Full Text] [Related]
9. Quantitative fluorescence measurements of chloride secretion in native airway epithelium from CF and non-CF subjects. Stern M; Munkonge FM; Caplen NJ; Sorgi F; Huang L; Geddes DM; Alton EW Gene Ther; 1995 Dec; 2(10):766-74. PubMed ID: 8750017 [TBL] [Abstract][Full Text] [Related]
10. The low PLC-δ1 expression in cystic fibrosis bronchial epithelial cells induces upregulation of TRPV6 channel activity. Vachel L; Norez C; Jayle C; Becq F; Vandebrouck C Cell Calcium; 2015 Jan; 57(1):38-48. PubMed ID: 25477137 [TBL] [Abstract][Full Text] [Related]
11. 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]
12. Purinergic signaling underlies CFTR control of human airway epithelial cell volume. Braunstein GM; Zsembery A; Tucker TA; Schwiebert EM J Cyst Fibros; 2004 Jun; 3(2):99-117. PubMed ID: 15463893 [TBL] [Abstract][Full Text] [Related]
13. Expression of delta F508 cystic fibrosis transmembrane conductance regulator protein and related chloride transport properties in the gallbladder epithelium from cystic fibrosis patients. Dray-Charier N; Paul A; Scoazec JY; Veissière D; Mergey M; Capeau J; Soubrane O; Housset C Hepatology; 1999 Jun; 29(6):1624-34. PubMed ID: 10347100 [TBL] [Abstract][Full Text] [Related]
16. How the airway smooth muscle in cystic fibrosis reacts in proinflammatory conditions: implications for airway hyper-responsiveness and asthma in cystic fibrosis. McCuaig S; Martin JG Lancet Respir Med; 2013 Apr; 1(2):137-47. PubMed ID: 24429094 [TBL] [Abstract][Full Text] [Related]