186 related articles for article (PubMed ID: 31050570)
1.
Saber A; Nakka SS; Hussain R; Hugosson S
Acta Otolaryngol; 2019 Jul; 139(7):652-658. PubMed ID: 31050570
[No Abstract] [Full Text] [Related]
2. Modulation of ENaC, CFTR, and iNOS expression in bronchial epithelial cells after stimulation with Staphylococcus epidermidis (94B080) and Staphylococcus aureus (90B083).
Hussain R; Oliynyk I; Roomans GM; Björkqvist M
APMIS; 2013 Sep; 121(9):814-26. PubMed ID: 23879620
[TBL] [Abstract][Full Text] [Related]
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
[TBL] [Abstract][Full Text] [Related]
4. Effects of rhinovirus infection on the expression and function of cystic fibrosis transmembrane conductance regulator and epithelial sodium channel in human nasal mucosa.
Kim JH; Kwon HJ; Jang YJ
Ann Allergy Asthma Immunol; 2012 Mar; 108(3):182-7. PubMed ID: 22374202
[TBL] [Abstract][Full Text] [Related]
5. Paranasal sinus size is decreased in CFTR heterozygotes with chronic rhinosinusitis.
Calton JB; Koripella PC; Willis AL; Le CH; Chiu AG; Chang EH
Int Forum Allergy Rhinol; 2017 Mar; 7(3):256-260. PubMed ID: 27860385
[TBL] [Abstract][Full Text] [Related]
6. Effect of cytosolic pH on epithelial Na+ channel in normal and cystic fibrosis sweat ducts.
Reddy MM; Wang XF; Quinton PM
J Membr Biol; 2008; 225(1-3):1-11. PubMed ID: 18937003
[TBL] [Abstract][Full Text] [Related]
7. Non-specific activation of the epithelial sodium channel by the CFTR chloride channel.
Nagel G; Szellas T; Riordan JR; Friedrich T; Hartung K
EMBO Rep; 2001 Mar; 2(3):249-54. PubMed ID: 11266369
[TBL] [Abstract][Full Text] [Related]
8. [Ion transport in nasal and paranasal sinus mucosa in mucoviscidosis and chronic sinusitis].
Rückes-Nilges C; Weber U; Popp C; Fryen A; Klimek T; Glanz H; Lindemann H; Münker G; Clauss W; Weber WM
HNO; 1999 Mar; 47(3):157-66. PubMed ID: 10231698
[TBL] [Abstract][Full Text] [Related]
9. Correlations between cystic fibrosis genotype and sinus disease severity in chronic rhinosinusitis.
Abuzeid WM; Song C; Fastenberg JH; Fang CH; Ayoub N; Jerschow E; Mohabir PK; Hwang PH
Laryngoscope; 2018 Aug; 128(8):1752-1758. PubMed ID: 29193105
[TBL] [Abstract][Full Text] [Related]
10. The epithelial sodium channel (ENaC) as a therapeutic target for cystic fibrosis lung disease.
Moore PJ; Tarran R
Expert Opin Ther Targets; 2018 Aug; 22(8):687-701. PubMed ID: 30028216
[TBL] [Abstract][Full Text] [Related]
11. Cl- transport by cystic fibrosis transmembrane conductance regulator (CFTR) contributes to the inhibition of epithelial Na+ channels (ENaCs) in Xenopus oocytes co-expressing CFTR and ENaC.
Briel M; Greger R; Kunzelmann K
J Physiol; 1998 May; 508 ( Pt 3)(Pt 3):825-36. PubMed ID: 9518736
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Cystic fibrosis transmembrane conductance regulator in the endolymphatic sac of the rat.
Matsubara A; Miyashita T; Inamoto R; Hoshikawa H; Mori N
Auris Nasus Larynx; 2014 Oct; 41(5):409-12. PubMed ID: 24598307
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. 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]
16. Cystic fibrosis transmembrane conductance regulator-dependent up-regulation of Kir1.1 (ROMK) renal K+ channels by the epithelial sodium channel.
Konstas AA; Koch JP; Tucker SJ; Korbmacher C
J Biol Chem; 2002 Jul; 277(28):25377-84. PubMed ID: 11994290
[TBL] [Abstract][Full Text] [Related]
17. The effect of NO-donors on chloride efflux, intracellular Ca(2+) concentration and mRNA expression of CFTR and ENaC in cystic fibrosis airway epithelial cells.
Oliynyk I; Hussain R; Amin A; Johannesson M; Roomans GM
Exp Mol Pathol; 2013 Jun; 94(3):474-80. PubMed ID: 23523754
[TBL] [Abstract][Full Text] [Related]
18. ENaC- and CFTR-dependent ion and fluid transport in human middle ear epithelial cells.
Choi JY; Son EJ; Kim JL; Lee JH; Park HY; Kim SH; Song MH; Yoon JH
Hear Res; 2006 Jan; 211(1-2):26-32. PubMed ID: 16226002
[TBL] [Abstract][Full Text] [Related]
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; 43():152-165. PubMed ID: 30340955
[TBL] [Abstract][Full Text] [Related]
20. New generation ENaC inhibitors detach cystic fibrosis airway mucus bundles via sodium/hydrogen exchanger inhibition.
Giorgetti M; Klymiuk N; Bähr A; Hemmerling M; Jinton L; Tarran R; Malmgren A; Åstrand A; Hansson GC; Ermund A
Eur J Pharmacol; 2021 Aug; 904():174123. PubMed ID: 33974881
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
