443 related articles for article (PubMed ID: 11309505)
1. 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]
2. 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]
3. CFTR-dependent and -independent swelling-activated K+ currents in primary cultures of mouse nephron.
Belfodil R; Barrière H; Rubera I; Tauc M; Poujeol C; Bidet M; Poujeol P
Am J Physiol Renal Physiol; 2003 Apr; 284(4):F812-28. PubMed ID: 12475745
[TBL] [Abstract][Full Text] [Related]
4. Antisense oligodeoxynucleotide to the cystic fibrosis transmembrane conductance regulator inhibits cyclic AMP-activated but not calcium-activated cell volume reduction in a human pancreatic duct cell line.
Kopelman H; Gauthier C; Bornstein M
J Clin Invest; 1993 Mar; 91(3):1253-7. PubMed ID: 7680666
[TBL] [Abstract][Full Text] [Related]
5. Turnover of the cystic fibrosis transmembrane conductance regulator (CFTR): slow degradation of wild-type and delta F508 CFTR in surface membrane preparations of immortalized airway epithelial cells.
Wei X; Eisman R; Xu J; Harsch AD; Mulberg AE; Bevins CL; Glick MC; Scanlin TF
J Cell Physiol; 1996 Aug; 168(2):373-84. PubMed ID: 8707873
[TBL] [Abstract][Full Text] [Related]
6. Activation of apical CFTR and basolateral Ca(2+)-activated K+ channels by tetramethylpyrazine in Caco-2 cell line.
Zhu JX; Zhang GH; Yang N; Rowlands DK; Wong HY; Tsang LL; Chung YW; Chan HC
Eur J Pharmacol; 2005 Mar; 510(3):187-95. PubMed ID: 15763242
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Modulation of Ca2+-activated Cl- secretion by basolateral K+ channels in human normal and cystic fibrosis airway epithelia.
Mall M; Gonska T; Thomas J; Schreiber R; Seydewitz HH; Kuehr J; Brandis M; Kunzelmann K
Pediatr Res; 2003 Apr; 53(4):608-18. PubMed ID: 12612194
[TBL] [Abstract][Full Text] [Related]
9. Volume regulation in the human airway epithelial cell line Calu-3.
Harron SA; Clarke CM; Jones CL; Babin-Muise D; Cowley EA
Can J Physiol Pharmacol; 2009 May; 87(5):337-46. PubMed ID: 19448731
[TBL] [Abstract][Full Text] [Related]
10. Transient receptor potential canonical channel 6 links Ca2+ mishandling to cystic fibrosis transmembrane conductance regulator channel dysfunction in cystic fibrosis.
Antigny F; Norez C; Dannhoffer L; Bertrand J; Raveau D; Corbi P; Jayle C; Becq F; Vandebrouck C
Am J Respir Cell Mol Biol; 2011 Jan; 44(1):83-90. PubMed ID: 20203293
[TBL] [Abstract][Full Text] [Related]
11. Defective formation of PKA/CnA-dependent annexin 2-S100A10/CFTR complex in DeltaF508 cystic fibrosis cells.
Borthwick LA; Riemen C; Goddard C; Colledge WH; Mehta A; Gerke V; Muimo R
Cell Signal; 2008 Jun; 20(6):1073-83. PubMed ID: 18346874
[TBL] [Abstract][Full Text] [Related]
12. Defective regulation of gap junctional coupling in cystic fibrosis pancreatic duct cells.
Chanson M; Scerri I; Suter S
J Clin Invest; 1999 Jun; 103(12):1677-84. PubMed ID: 10377174
[TBL] [Abstract][Full Text] [Related]
13. Direct interaction of a small-molecule modulator with G551D-CFTR, a cystic fibrosis-causing mutation associated with severe disease.
Pasyk S; Li C; Ramjeesingh M; Bear CE
Biochem J; 2009 Feb; 418(1):185-90. PubMed ID: 18945216
[TBL] [Abstract][Full Text] [Related]
14. [Ion channel mechanism of regulatory volume decrease in human epithelial cells].
Shi LP; Zang YM; Hou XL; Wang J
Zhongguo Ying Yong Sheng Li Xue Za Zhi; 2008 Aug; 24(3):356-60. PubMed ID: 21141603
[TBL] [Abstract][Full Text] [Related]
15. Rescue of DeltaF508-CFTR (cystic fibrosis transmembrane conductance regulator) by curcumin: involvement of the keratin 18 network.
Lipecka J; Norez C; Bensalem N; Baudouin-Legros M; Planelles G; Becq F; Edelman A; Davezac N
J Pharmacol Exp Ther; 2006 May; 317(2):500-5. PubMed ID: 16424149
[TBL] [Abstract][Full Text] [Related]
16. Disease-associated mutations in cytoplasmic loops 1 and 2 of cystic fibrosis transmembrane conductance regulator impede processing or opening of the channel.
Seibert FS; Jia Y; Mathews CJ; Hanrahan JW; Riordan JR; Loo TW; Clarke DM
Biochemistry; 1997 Sep; 36(39):11966-74. PubMed ID: 9305991
[TBL] [Abstract][Full Text] [Related]
17. Selective activation of cystic fibrosis transmembrane conductance regulator Cl- and HCO3- conductances.
Reddy MM; Quinton PM
JOP; 2001 Jul; 2(4 Suppl):212-8. PubMed ID: 11875262
[TBL] [Abstract][Full Text] [Related]
18. Swelling-activated Ca2+ entry via TRPV4 channel is defective in cystic fibrosis airway epithelia.
Arniges M; Vázquez E; Fernández-Fernández JM; Valverde MA
J Biol Chem; 2004 Dec; 279(52):54062-8. PubMed ID: 15489228
[TBL] [Abstract][Full Text] [Related]
19. Impaired Regulatory Volume Decrease and Characterization of Underlying Volume-Activated Currents in Cystic Fibrosis Human Cholangiocyte Cell Line.
Chen B; Jefferson DM; Cho WK
J Membr Biol; 2022 Jun; 255(2-3):261-276. PubMed ID: 35098342
[TBL] [Abstract][Full Text] [Related]
20. Rescuing cystic fibrosis transmembrane conductance regulator (CFTR)-processing mutants by transcomplementation.
Cormet-Boyaka E; Jablonsky M; Naren AP; Jackson PL; Muccio DD; Kirk KL
Proc Natl Acad Sci U S A; 2004 May; 101(21):8221-6. PubMed ID: 15141088
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
