279 related articles for article (PubMed ID: 9547020)
1. Expression of cystic fibrosis transmembrane conductance regulator alters the responses to hypotonic cell swelling and ATP of Chinese hamster ovary cells.
Thiele IE; Hug MJ; Hübner M; Greger R
Cell Physiol Biochem; 1998; 8(1-2):61-74. PubMed ID: 9547020
[TBL] [Abstract][Full Text] [Related]
2. The role of exocytosis in the activation of the chloride conductance in Chinese hamster ovary cells (CHO) stably expressing CFTR.
Hug MJ; Thiele IE; Greger R
Pflugers Arch; 1997 Nov; 434(6):779-84. PubMed ID: 9306012
[TBL] [Abstract][Full Text] [Related]
3. CFTR channels expressed in CHO cells do not have detectable ATP conductance.
Grygorczyk R; Tabcharani JA; Hanrahan JW
J Membr Biol; 1996 May; 151(2):139-48. PubMed ID: 8661502
[TBL] [Abstract][Full Text] [Related]
4. No evidence for direct activation of the cystic fibrosis transmembrane conductance regulator by 8-cyclopentyl-1,3-dipropylxanthine.
Kunzelmann K; Briel M; Schreiber R; Ricken S; Nitschke R; Greger R
Cell Physiol Biochem; 1998; 8(4):185-93. PubMed ID: 9694345
[TBL] [Abstract][Full Text] [Related]
5. The delta F508 mutation decreases the stability of cystic fibrosis transmembrane conductance regulator in the plasma membrane. Determination of functional half-lives on transfected cells.
Lukacs GL; Chang XB; Bear C; Kartner N; Mohamed A; Riordan JR; Grinstein S
J Biol Chem; 1993 Oct; 268(29):21592-8. PubMed ID: 7691813
[TBL] [Abstract][Full Text] [Related]
6. Comparison of the gating behaviour of human and murine cystic fibrosis transmembrane conductance regulator Cl- channels expressed in mammalian cells.
Lansdell KA; Delaney SJ; Lunn DP; Thomson SA; Sheppard DN; Wainwright BJ
J Physiol; 1998 Apr; 508 ( Pt 2)(Pt 2):379-92. PubMed ID: 9508803
[TBL] [Abstract][Full Text] [Related]
7. Cystic fibrosis transmembrane conductance regulator (CFTR) and renal function.
Stanton BA
Wien Klin Wochenschr; 1997 Jun; 109(12-13):457-64. PubMed ID: 9261986
[TBL] [Abstract][Full Text] [Related]
8. Expression of cystic fibrosis transmembrane conductance regulator in a model epithelium.
Sheppard DN; Carson MR; Ostedgaard LS; Denning GM; Welsh MJ
Am J Physiol; 1994 Apr; 266(4 Pt 1):L405-13. PubMed ID: 7513963
[TBL] [Abstract][Full Text] [Related]
9. Pyridine nucleotide redox potential modulates cystic fibrosis transmembrane conductance regulator Cl- conductance.
Stutts MJ; Gabriel SE; Price EM; Sarkadi B; Olsen JC; Boucher RC
J Biol Chem; 1994 Mar; 269(12):8667-74. PubMed ID: 7510695
[TBL] [Abstract][Full Text] [Related]
10. Cytoplasmic loop three of cystic fibrosis transmembrane conductance regulator contributes to regulation of chloride channel activity.
Seibert FS; Linsdell P; Loo TW; Hanrahan JW; Riordan JR; Clarke DM
J Biol Chem; 1996 Nov; 271(44):27493-9. PubMed ID: 8910333
[TBL] [Abstract][Full Text] [Related]
11. Small-conductance Cl- channels in HT29 cells: activation by Ca2+, hypotonic cell swelling and 8-Br-cGMP.
Kunzelmann K; Kubitz R; Grolik M; Warth R; Greger R
Pflugers Arch; 1992 Jun; 421(2-3):238-46. PubMed ID: 1382268
[TBL] [Abstract][Full Text] [Related]
12. Apical and basolateral ATP stimulates tracheal epithelial chloride secretion via multiple purinergic receptors.
Hwang TH; Schwiebert EM; Guggino WB
Am J Physiol; 1996 Jun; 270(6 Pt 1):C1611-23. PubMed ID: 8764143
[TBL] [Abstract][Full Text] [Related]
13. Effect of ATP-sensitive K+ channel regulators on cystic fibrosis transmembrane conductance regulator chloride currents.
Sheppard DN; Welsh MJ
J Gen Physiol; 1992 Oct; 100(4):573-91. PubMed ID: 1281220
[TBL] [Abstract][Full Text] [Related]
14. Chloride channel and chloride conductance regulator domains of CFTR, the cystic fibrosis transmembrane conductance regulator.
Schwiebert EM; Morales MM; Devidas S; Egan ME; Guggino WB
Proc Natl Acad Sci U S A; 1998 Mar; 95(5):2674-9. PubMed ID: 9482946
[TBL] [Abstract][Full Text] [Related]
15. Generation of cAMP-activated chloride currents by expression of CFTR.
Anderson MP; Rich DP; Gregory RJ; Smith AE; Welsh MJ
Science; 1991 Feb; 251(4994):679-82. PubMed ID: 1704151
[TBL] [Abstract][Full Text] [Related]
16. Mutant (delta F508) cystic fibrosis transmembrane conductance regulator Cl- channel is functional when retained in endoplasmic reticulum of mammalian cells.
Pasyk EA; Foskett JK
J Biol Chem; 1995 May; 270(21):12347-50. PubMed ID: 7539001
[TBL] [Abstract][Full Text] [Related]
17. The cystic fibrosis transmembrane conductance regulator attenuates the endogenous Ca2+ activated Cl- conductance of Xenopus oocytes.
Kunzelmann K; Mall M; Briel M; Hipper A; Nitschke R; Ricken S; Greger R
Pflugers Arch; 1997 Dec; 435(1):178-81. PubMed ID: 9359918
[TBL] [Abstract][Full Text] [Related]
18. Failure of the cystic fibrosis transmembrane conductance regulator to conduct ATP.
Reddy MM; Quinton PM; Haws C; Wine JJ; Grygorczyk R; Tabcharani JA; Hanrahan JW; Gunderson KL; Kopito RR
Science; 1996 Mar; 271(5257):1876-9. PubMed ID: 8596959
[TBL] [Abstract][Full Text] [Related]
19. External ATP and its analogs activate the cystic fibrosis transmembrane conductance regulator by a cyclic AMP-independent mechanism.
Cantiello HF; Prat AG; Reisin IL; Ercole LB; Abraham EH; Amara JF; Gregory RJ; Ausiello DA
J Biol Chem; 1994 Apr; 269(15):11224-32. PubMed ID: 7512560
[TBL] [Abstract][Full Text] [Related]
20. Swelling and Ca2+-activated anion conductances in C127 epithelial cells expressing WT and delta F508-CFTR.
Xia Y; Krouse ME; Fang RH; Wine JJ
J Membr Biol; 1996 Jun; 151(3):269-78. PubMed ID: 8661514
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]