193 related articles for article (PubMed ID: 11597908)
1. Partial correction of defective Cl(-) secretion in cystic fibrosis epithelial cells by an analog of squalamine.
Jiang C; Lee ER; Lane MB; Xiao YF; Harris DJ; Cheng SH
Am J Physiol Lung Cell Mol Physiol; 2001 Nov; 281(5):L1164-72. PubMed ID: 11597908
[TBL] [Abstract][Full Text] [Related]
2. Na+ and Cl- conductances in airway epithelial cells: increased Na+ conductance in cystic fibrosis.
Kunzelmann K; Kathöfer S; Greger R
Pflugers Arch; 1995 Nov; 431(1):1-9. PubMed ID: 8584404
[TBL] [Abstract][Full Text] [Related]
3. Role of K(V)LQT1 in cyclic adenosine monophosphate-mediated Cl(-) secretion in human airway epithelia.
Mall M; Wissner A; Schreiber R; Kuehr J; Seydewitz HH; Brandis M; Greger R; Kunzelmann K
Am J Respir Cell Mol Biol; 2000 Sep; 23(3):283-9. PubMed ID: 10970817
[TBL] [Abstract][Full Text] [Related]
4. Chlorzoxazone or 1-EBIO increases Na(+) absorption across cystic fibrosis airway epithelial cells.
Gao L; Yankaskas JR; Fuller CM; Sorscher EJ; Matalon S; Forman HJ; Venglarik CJ
Am J Physiol Lung Cell Mol Physiol; 2001 Nov; 281(5):L1123-9. PubMed ID: 11597903
[TBL] [Abstract][Full Text] [Related]
5. Polarized distribution of HCO3- transport in human normal and cystic fibrosis nasal epithelia.
Paradiso AM; Coakley RD; Boucher RC
J Physiol; 2003 Apr; 548(Pt 1):203-18. PubMed ID: 12562898
[TBL] [Abstract][Full Text] [Related]
6. Normalization of raised sodium absorption and raised calcium-mediated chloride secretion by adenovirus-mediated expression of cystic fibrosis transmembrane conductance regulator in primary human cystic fibrosis airway epithelial cells.
Johnson LG; Boyles SE; Wilson J; Boucher RC
J Clin Invest; 1995 Mar; 95(3):1377-82. PubMed ID: 7533790
[TBL] [Abstract][Full Text] [Related]
7. Human cystic fibrosis airway epithelia have reduced Cl- conductance but not increased Na+ conductance.
Itani OA; Chen JH; Karp PH; Ernst S; Keshavjee S; Parekh K; Klesney-Tait J; Zabner J; Welsh MJ
Proc Natl Acad Sci U S A; 2011 Jun; 108(25):10260-5. PubMed ID: 21646513
[TBL] [Abstract][Full Text] [Related]
8. Resveratrol ameliorates abnormalities of fluid and electrolyte secretion in a hypoxia-Induced model of acquired CFTR deficiency.
Woodworth BA
Laryngoscope; 2015 Oct; 125 Suppl 7(0 7):S1-S13. PubMed ID: 25946147
[TBL] [Abstract][Full Text] [Related]
9. cAMP regulation of Cl(-) and HCO(-)(3) secretion across rat fetal distal lung epithelial cells.
Lazrak A; Thome U; Myles C; Ware J; Chen L; Venglarik CJ; Matalon S
Am J Physiol Lung Cell Mol Physiol; 2002 Apr; 282(4):L650-8. PubMed ID: 11880289
[TBL] [Abstract][Full Text] [Related]
10. Sensitivity of chloride efflux vs. transepithelial measurements in mixed CF and normal airway epithelial cell populations.
Illek B; Lei D; Fischer H; Gruenert DC
Cell Physiol Biochem; 2010; 26(6):983-90. PubMed ID: 21220929
[TBL] [Abstract][Full Text] [Related]
11. Correlating genotype with phenotype using CFTR-mediated whole-cell Cl
Noel S; Servel N; Hatton A; Golec A; Rodrat M; Ng DRS; Li H; Pranke I; Hinzpeter A; Edelman A; Sheppard DN; Sermet-Gaudelus I
J Physiol; 2022 Mar; 600(6):1515-1531. PubMed ID: 34761808
[TBL] [Abstract][Full Text] [Related]
12. Increased contact time improves adenovirus-mediated CFTR gene transfer to nasal epithelium of CF mice.
Jiang C; Akita GY; Colledge WH; Ratcliff RA; Evans MJ; Hehir KM; St George JA; Wadsworth SC; Cheng SH
Hum Gene Ther; 1997 Apr; 8(6):671-80. PubMed ID: 9113507
[TBL] [Abstract][Full Text] [Related]
13. Extracellular zinc and ATP restore chloride secretion across cystic fibrosis airway epithelia by triggering calcium entry.
Zsembery A; Fortenberry JA; Liang L; Bebok Z; Tucker TA; Boyce AT; Braunstein GM; Welty E; Bell PD; Sorscher EJ; Clancy JP; Schwiebert EM
J Biol Chem; 2004 Mar; 279(11):10720-9. PubMed ID: 14701827
[TBL] [Abstract][Full Text] [Related]
14. Expression and function of Anoctamin 1/TMEM16A calcium-activated chloride channels in airways of in vivo mouse models for cystic fibrosis research.
Hahn A; Salomon JJ; Leitz D; Feigenbutz D; Korsch L; Lisewski I; Schrimpf K; Millar-Büchner P; Mall MA; Frings S; Möhrlen F
Pflugers Arch; 2018 Sep; 470(9):1335-1348. PubMed ID: 29860639
[TBL] [Abstract][Full Text] [Related]
15. Parallel improvement of sodium and chloride transport defects by miglustat (n-butyldeoxynojyrimicin) in cystic fibrosis epithelial cells.
Noël S; Wilke M; Bot AG; De Jonge HR; Becq F
J Pharmacol Exp Ther; 2008 Jun; 325(3):1016-23. PubMed ID: 18309088
[TBL] [Abstract][Full Text] [Related]
16. Guanabenz, an alpha2-selective adrenergic agonist, activates Ca2+-dependent chloride currents in cystic fibrosis human airway epithelial cells.
Norez C; Vandebrouck C; Antigny F; Dannhoffer L; Blondel M; Becq F
Eur J Pharmacol; 2008 Sep; 592(1-3):33-40. PubMed ID: 18640110
[TBL] [Abstract][Full Text] [Related]
17. Spiperone, identified through compound screening, activates calcium-dependent chloride secretion in the airway.
Liang L; MacDonald K; Schwiebert EM; Zeitlin PL; Guggino WB
Am J Physiol Cell Physiol; 2009 Jan; 296(1):C131-41. PubMed ID: 18987251
[TBL] [Abstract][Full Text] [Related]
18. Nitric oxide has no beneficial effects on ion transport defects in cystic fibrosis human nasal epithelium.
Rückes-Nilges C; Lindemann H; Klimek T; Glanz H; Weber WM
Pflugers Arch; 2000 Nov; 441(1):133-7. PubMed ID: 11205052
[TBL] [Abstract][Full Text] [Related]
19. Lack of correlation between CFTR expression, CFTR Cl- currents, amiloride-sensitive Na+ conductance, and cystic fibrosis phenotype.
Beck S; Kühr J; Schütz VV; Seydewitz HH; Brandis M; Greger R; Kunzelmann K
Pediatr Pulmonol; 1999 Apr; 27(4):251-9. PubMed ID: 10230924
[TBL] [Abstract][Full Text] [Related]
20. SERCA pump inhibitors do not correct biosynthetic arrest of deltaF508 CFTR in cystic fibrosis.
Grubb BR; Gabriel SE; Mengos A; Gentzsch M; Randell SH; Van Heeckeren AM; Knowles MR; Drumm ML; Riordan JR; Boucher RC
Am J Respir Cell Mol Biol; 2006 Mar; 34(3):355-63. PubMed ID: 16284361
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
