218 related articles for article (PubMed ID: 25329998)
1. Correlation of apical fluid-regulating channel proteins with lung function in human COPD lungs.
Zhao R; Liang X; Zhao M; Liu SL; Huang Y; Idell S; Li X; Ji HL
PLoS One; 2014; 9(10):e109725. PubMed ID: 25329998
[TBL] [Abstract][Full Text] [Related]
2. Enhancement of alveolar epithelial sodium channel activity with decreased cystic fibrosis transmembrane conductance regulator expression in mouse lung.
Lazrak A; Jurkuvenaite A; Chen L; Keeling KM; Collawn JF; Bedwell DM; Matalon S
Am J Physiol Lung Cell Mol Physiol; 2011 Oct; 301(4):L557-67. PubMed ID: 21743028
[TBL] [Abstract][Full Text] [Related]
3. Regulation of ENaC and CFTR expression with K+ channel modulators and effect on fluid absorption across alveolar epithelial cells.
Leroy C; Privé A; Bourret JC; Berthiaume Y; Ferraro P; Brochiero E
Am J Physiol Lung Cell Mol Physiol; 2006 Dec; 291(6):L1207-19. PubMed ID: 16891388
[TBL] [Abstract][Full Text] [Related]
4. Expression of ENaC subunits, chloride channels, and aquaporins in ovine fetal lung: ontogeny of expression and effects of altered fetal cortisol concentrations.
Jesse NM; McCartney J; Feng X; Richards EM; Wood CE; Keller-Wood M
Am J Physiol Regul Integr Comp Physiol; 2009 Aug; 297(2):R453-61. PubMed ID: 19515987
[TBL] [Abstract][Full Text] [Related]
5. 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; 287(20):16781-90. PubMed ID: 22442149
[TBL] [Abstract][Full Text] [Related]
6. The cystic fibrosis transmembrane conductance regulator impedes proteolytic stimulation of the epithelial Na+ channel.
Gentzsch M; Dang H; Dang Y; Garcia-Caballero A; Suchindran H; Boucher RC; Stutts MJ
J Biol Chem; 2010 Oct; 285(42):32227-32. PubMed ID: 20709758
[TBL] [Abstract][Full Text] [Related]
7. 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]
8.
Saber A; Nakka SS; Hussain R; Hugosson S
Acta Otolaryngol; 2019 Jul; 139(7):652-658. PubMed ID: 31050570
[No Abstract] [Full Text] [Related]
9. The CFTR and ENaC debate: how important is ENaC in CF lung disease?
Collawn JF; Lazrak A; Bebok Z; Matalon S
Am J Physiol Lung Cell Mol Physiol; 2012 Jun; 302(11):L1141-6. PubMed ID: 22492740
[TBL] [Abstract][Full Text] [Related]
10. Accumulation of metals in GOLD4 COPD lungs is associated with decreased CFTR levels.
Hassan F; Xu X; Nuovo G; Killilea DW; Tyrrell J; Da Tan C; Tarran R; Diaz P; Jee J; Knoell D; Boyaka PN; Cormet-Boyaka E
Respir Res; 2014 Jun; 15(1):69. PubMed ID: 24957904
[TBL] [Abstract][Full Text] [Related]
11. δβγ-ENaC is inhibited by CFTR but stimulated by cAMP in
Rauh R; Hoerner C; Korbmacher C
Am J Physiol Lung Cell Mol Physiol; 2017 Feb; 312(2):L277-L287. PubMed ID: 27941075
[TBL] [Abstract][Full Text] [Related]
12. Increased cystic fibrosis transmembrane conductance regulators expression and decreased epithelial sodium channel alpha subunits expression in early abortion: findings from a mouse model and clinical cases of abortion.
Zhou M; Fu J; Huang W; Shen L; Xiao L; Song Y; Liu Y
PLoS One; 2014; 9(6):e99521. PubMed ID: 24914548
[TBL] [Abstract][Full Text] [Related]
13. CFTR dysfunction in cystic fibrosis and chronic obstructive pulmonary disease.
Fernandez Fernandez E; De Santi C; De Rose V; Greene CM
Expert Rev Respir Med; 2018 Jun; 12(6):483-492. PubMed ID: 29750581
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Acquired cystic fibrosis transmembrane conductance regulator dysfunction in the lower airways in COPD.
Dransfield MT; Wilhelm AM; Flanagan B; Courville C; Tidwell SL; Raju SV; Gaggar A; Steele C; Tang LP; Liu B; Rowe SM
Chest; 2013 Aug; 144(2):498-506. PubMed ID: 23538783
[TBL] [Abstract][Full Text] [Related]
16. Molecular proximity of cystic fibrosis transmembrane conductance regulator and epithelial sodium channel assessed by fluorescence resonance energy transfer.
Berdiev BK; Cormet-Boyaka E; Tousson A; Qadri YJ; Oosterveld-Hut HM; Hong JS; Gonzales PA; Fuller CM; Sorscher EJ; Lukacs GL; Benos DJ
J Biol Chem; 2007 Dec; 282(50):36481-8. PubMed ID: 17913705
[TBL] [Abstract][Full Text] [Related]
17. Effects of the serine/threonine kinase SGK1 on the epithelial Na(+) channel (ENaC) and CFTR: implications for cystic fibrosis.
Wagner CA; Ott M; Klingel K; Beck S; Melzig J; Friedrich B; Wild KN; Bröer S; Moschen I; Albers A; Waldegger S; Tümmler B; Egan ME; Geibel JP; Kandolf R; Lang F
Cell Physiol Biochem; 2001; 11(4):209-18. PubMed ID: 11509829
[TBL] [Abstract][Full Text] [Related]
18. The KDEL receptor has a role in the biogenesis and trafficking of the epithelial sodium channel (ENaC).
Bikard Y; Viviano J; Orr MN; Brown L; Brecker M; Jeger JL; Grits D; Suaud L; Rubenstein RC
J Biol Chem; 2019 Nov; 294(48):18324-18336. PubMed ID: 31653700
[TBL] [Abstract][Full Text] [Related]
19. Fetal lung epithelial ion channels relocate in the cell membrane during late gestation.
Beard LL; Li T; Hu Y; Folkesson HG
Anat Rec (Hoboken); 2011 Sep; 294(9):1461-71. PubMed ID: 21809453
[TBL] [Abstract][Full Text] [Related]
20. Thickness of the airway surface liquid layer in the lung is affected in cystic fibrosis by compromised synergistic regulation of the ENaC ion channel.
Olivença DV; Fonseca LL; Voit EO; Pinto FR
J R Soc Interface; 2019 Aug; 16(157):20190187. PubMed ID: 31455163
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]