604 related articles for article (PubMed ID: 8584404)
1. 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]
2. 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]
3. The amiloride-inhibitable Na+ conductance is reduced by the cystic fibrosis transmembrane conductance regulator in normal but not in cystic fibrosis airways.
Mall M; Bleich M; Greger R; Schreiber R; Kunzelmann K
J Clin Invest; 1998 Jul; 102(1):15-21. PubMed ID: 9649552
[TBL] [Abstract][Full Text] [Related]
4. Culture-dependent expression of Na+ conductances in airway epithelial cells.
Kunzelmann K; Kathöfer S; Hipper A; Gruenert DC; Gregner R
Pflugers Arch; 1996 Feb; 431(4):578-86. PubMed ID: 8596702
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. [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]
7. 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]
8. 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]
9. 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]
10. 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]
11. 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]
12. cAMP stimulates CFTR-like Cl- channels and inhibits amiloride-sensitive Na+ channels in mouse CCD cells.
Letz B; Korbmacher C
Am J Physiol; 1997 Feb; 272(2 Pt 1):C657-66. PubMed ID: 9124310
[TBL] [Abstract][Full Text] [Related]
13. Ca2+ and cAMP-activated Cl- conductances mediate Cl- secretion in a mouse renal inner medullary collecting duct cell line.
Boese SH; Glanville M; Aziz O; Gray MA; Simmons NL
J Physiol; 2000 Mar; 523 Pt 2(Pt 2):325-38. PubMed ID: 10699078
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Altered fluid transport across airway epithelium in cystic fibrosis.
Jiang C; Finkbeiner WE; Widdicombe JH; McCray PB; Miller SS
Science; 1993 Oct; 262(5132):424-7. PubMed ID: 8211164
[TBL] [Abstract][Full Text] [Related]
16. Minor role of Cl- secretion in non-cystic fibrosis and cystic fibrosis human nasal epithelium.
Rückes-Nilges C; Weber U; Lindemann H; Münker G; Clauss W; Weber WM
Cell Physiol Biochem; 1999; 9(1):1-10. PubMed ID: 10352340
[TBL] [Abstract][Full Text] [Related]
17. Bioelectric properties of chloride channels in human, pig, ferret, and mouse airway epithelia.
Liu X; Luo M; Zhang L; Ding W; Yan Z; Engelhardt JF
Am J Respir Cell Mol Biol; 2007 Mar; 36(3):313-23. PubMed ID: 17008635
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Evidence for reduced Cl- and increased Na+ permeability in cystic fibrosis human primary cell cultures.
Boucher RC; Cotton CU; Gatzy JT; Knowles MR; Yankaskas JR
J Physiol; 1988 Nov; 405():77-103. PubMed ID: 3255805
[TBL] [Abstract][Full Text] [Related]
20. In vivo nasal potential difference: techniques and protocols for assessing efficacy of gene transfer in cystic fibrosis.
Knowles MR; Paradiso AM; Boucher RC
Hum Gene Ther; 1995 Apr; 6(4):445-55. PubMed ID: 7542031
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]