83 related articles for article (PubMed ID: 12711306)
1. Functional analysis of CFTR chloride channel activity in cells with elevated MDR1 expression.
Cao L; Owsianik G; Jaspers M; Janssens A; Cuppens H; Cassiman JJ; Nilius B
Biochem Biophys Res Commun; 2003 May; 304(2):248-52. PubMed ID: 12711306
[TBL] [Abstract][Full Text] [Related]
2. Co-ordinate regulation of the cystic fibrosis and multidrug resistance genes in cystic fibrosis knockout mice.
Trezise AE; Ratcliff R; Hawkins TE; Evans MJ; Freeman TC; Romano PR; Higgins CF; Colledge WH
Hum Mol Genet; 1997 Apr; 6(4):527-37. PubMed ID: 9097955
[TBL] [Abstract][Full Text] [Related]
3. Adenosine triphosphate-binding cassette superfamily transporter gene expression in severe male infertility.
Larriba S; Bassas L; Egozcue S; Giménez J; Ramos MD; Briceño O; Estivill X; Casals T
Biol Reprod; 2001 Aug; 65(2):394-400. PubMed ID: 11466205
[TBL] [Abstract][Full Text] [Related]
4. The first-nucleotide binding domain of the cystic-fibrosis transmembrane conductance regulator is important for inhibition of the epithelial Na+ channel.
Schreiber R; Hopf A; Mall M; Greger R; Kunzelmann K
Proc Natl Acad Sci U S A; 1999 Apr; 96(9):5310-5. PubMed ID: 10220462
[TBL] [Abstract][Full Text] [Related]
5. Functional characterization of the CFTR R domain using CFTR/MDR1 hybrid and deletion constructs.
Vankeerberghen A; Lin W; Jaspers M; Cuppens H; Nilius B; Cassiman JJ
Biochemistry; 1999 Nov; 38(45):14988-98. PubMed ID: 10555981
[TBL] [Abstract][Full Text] [Related]
6. Activation of a CFTR-mediated chloride current in a rabbit corneal epithelial cell line.
Al-Nakkash L; Reinach PS
Invest Ophthalmol Vis Sci; 2001 Sep; 42(10):2364-70. PubMed ID: 11527951
[TBL] [Abstract][Full Text] [Related]
7. Inhibition of volume-regulated anion channels by expression of the cystic fibrosis transmembrane conductance regulator.
Vennekens R; Trouet D; Vankeerberghen A; Voets T; Cuppens H; Eggermont J; Cassiman JJ; Droogmans G; Nilius B
J Physiol; 1999 Feb; 515 ( Pt 1)(Pt 1):75-85. PubMed ID: 9925879
[TBL] [Abstract][Full Text] [Related]
8. Activation of cAMP-dependent C1- currents in guinea-pig paneth cells without relevant evidence for CFTR expression.
Tsumura T; Hazama A; Miyoshi T; Ueda S; Okada Y
J Physiol; 1998 Nov; 512 ( Pt 3)(Pt 3):765-77. PubMed ID: 9769420
[TBL] [Abstract][Full Text] [Related]
9. Capsaicin potentiates wild-type and mutant cystic fibrosis transmembrane conductance regulator chloride-channel currents.
Ai T; Bompadre SG; Wang X; Hu S; Li M; Hwang TC
Mol Pharmacol; 2004 Jun; 65(6):1415-26. PubMed ID: 15155835
[TBL] [Abstract][Full Text] [Related]
10. Two cystic fibrosis transmembrane conductance regulator mutations have different effects on both pulmonary phenotype and regulation of outwardly rectified chloride currents.
Fulmer SB; Schwiebert EM; Morales MM; Guggino WB; Cutting GR
Proc Natl Acad Sci U S A; 1995 Jul; 92(15):6832-6. PubMed ID: 7542778
[TBL] [Abstract][Full Text] [Related]
11. Expression of cystic fibrosis transmembrane conductance regulator in rat efferent duct epithelium.
Leung GP; Gong XD; Cheung KH; Cheng-Chew SB; Wong PY
Biol Reprod; 2001 May; 64(5):1509-15. PubMed ID: 11319159
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. A mutation in the cystic fibrosis transmembrane conductance regulator gene associated with elevated sweat chloride concentrations in the absence of cystic fibrosis.
Mickle JE; Macek M; Fulmer-Smentek SB; Egan MM; Schwiebert E; Guggino W; Moss R; Cutting GR
Hum Mol Genet; 1998 Apr; 7(4):729-35. PubMed ID: 9499426
[TBL] [Abstract][Full Text] [Related]
14. Functional activity of the CFTR Cl- channel in human myocardium.
Yajima T; Nagashima H; Tsutsumi-Sakai R; Hagiwara N; Hosoda S; Quertermous T; Kasanuki H; Kawana M
Heart Vessels; 1997; 12(6):255-61. PubMed ID: 9860191
[TBL] [Abstract][Full Text] [Related]
15. The CLIC1 chloride channel is regulated by the cystic fibrosis transmembrane conductance regulator when expressed in Xenopus oocytes.
Edwards JC
J Membr Biol; 2006; 213(1):39-46. PubMed ID: 17347778
[TBL] [Abstract][Full Text] [Related]
16. Altered pHi regulation in 3T3/CFTR clones and their chemotherapeutic drug-selected derivatives.
Wei LY; Hoffman MM; Roepe PD
Am J Physiol; 1997 May; 272(5 Pt 1):C1642-53. PubMed ID: 9176156
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Digoxin up-regulates MDR1 in human colon carcinoma Caco-2 cells.
Takara K; Tsujimoto M; Ohnishi N; Yokoyama T
Biochem Biophys Res Commun; 2002 Mar; 292(1):190-4. PubMed ID: 11890691
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. CFTR-mediated chloride permeability is regulated by type III phosphodiesterases in airway epithelial cells.
Kelley TJ; al-Nakkash L; Drumm ML
Am J Respir Cell Mol Biol; 1995 Dec; 13(6):657-64. PubMed ID: 7576703
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]