BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

202 related articles for article (PubMed ID: 9435515)

  • 1. FLAG epitope positioned in an external loop preserves normal biophysical properties of CFTR.
    Schultz BD; Takahashi A; Liu C; Frizzell RA; Howard M
    Am J Physiol; 1997 Dec; 273(6):C2080-9. PubMed ID: 9435515
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Function of Xenopus cystic fibrosis transmembrane conductance regulator (CFTR) Cl channels and use of human-Xenopus chimeras to investigate the pore properties of CFTR.
    Price MP; Ishihara H; Sheppard DN; Welsh MJ
    J Biol Chem; 1996 Oct; 271(41):25184-91. PubMed ID: 8810276
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Severed molecules functionally define the boundaries of the cystic fibrosis transmembrane conductance regulator's NH(2)-terminal nucleotide binding domain.
    Chan KW; Csanády L; Seto-Young D; Nairn AC; Gadsby DC
    J Gen Physiol; 2000 Aug; 116(2):163-80. PubMed ID: 10919864
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Functional roles of nonconserved structural segments in CFTR's NH2-terminal nucleotide binding domain.
    Csanády L; Chan KW; Nairn AC; Gadsby DC
    J Gen Physiol; 2005 Jan; 125(1):43-55. PubMed ID: 15596536
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The two halves of CFTR form a dual-pore ion channel.
    Yue H; Devidas S; Guggino WB
    J Biol Chem; 2000 Apr; 275(14):10030-4. PubMed ID: 10744680
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Regulation of chloride secretion across porcine endometrial epithelial cells by prostaglandin E2.
    Deachapunya C; O'Grady SM
    J Physiol; 1998 Apr; 508 ( Pt 1)(Pt 1):31-47. PubMed ID: 9490813
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Intracellular loop between transmembrane segments IV and V of cystic fibrosis transmembrane conductance regulator is involved in regulation of chloride channel conductance state.
    Xie J; Drumm ML; Ma J; Davis PB
    J Biol Chem; 1995 Nov; 270(47):28084-91. PubMed ID: 7499295
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Deletion of phenylalanine 508 causes attenuated phosphorylation-dependent activation of CFTR chloride channels.
    Wang F; Zeltwanger S; Hu S; Hwang TC
    J Physiol; 2000 May; 524 Pt 3(Pt 3):637-48. PubMed ID: 10790148
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Cystic fibrosis transmembrane conductance regulator mediates sulphonylurea block of the inwardly rectifying K+ channel Kir6.1.
    Ishida-Takahashi A; Otani H; Takahashi C; Washizuka T; Tsuji K; Noda M; Horie M; Sasayama S
    J Physiol; 1998 Apr; 508 ( Pt 1)(Pt 1):23-30. PubMed ID: 9490811
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Mutations in the putative pore-forming domain of CFTR do not change anion selectivity of the cAMP activated Cl- conductance.
    Hipper A; Mall M; Greger R; Kunzelmann K
    FEBS Lett; 1995 Nov; 374(3):312-6. PubMed ID: 7589561
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Regulation of epithelial sodium channels by the cystic fibrosis transmembrane conductance regulator.
    Ismailov II; Awayda MS; Jovov B; Berdiev BK; Fuller CM; Dedman JR; Kaetzel M; Benos DJ
    J Biol Chem; 1996 Mar; 271(9):4725-32. PubMed ID: 8617738
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Two mechanisms of genistein inhibition of cystic fibrosis transmembrane conductance regulator Cl- channels expressed in murine cell line.
    Lansdell KA; Cai Z; Kidd JF; Sheppard DN
    J Physiol; 2000 Apr; 524 Pt 2(Pt 2):317-30. PubMed ID: 10766914
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Severed channels probe regulation of gating of cystic fibrosis transmembrane conductance regulator by its cytoplasmic domains.
    Csanády L; Chan KW; Seto-Young D; Kopsco DC; Nairn AC; Gadsby DC
    J Gen Physiol; 2000 Sep; 116(3):477-500. PubMed ID: 10962022
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Pyrophosphate stimulates wild-type and mutant cystic fibrosis transmembrane conductance regulator Cl- channels.
    Carson MR; Winter MC; Travis SM; Welsh MJ
    J Biol Chem; 1995 Sep; 270(35):20466-72. PubMed ID: 7544788
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Contribution of proline residues in the membrane-spanning domains of cystic fibrosis transmembrane conductance regulator to chloride channel function.
    Sheppard DN; Travis SM; Ishihara H; Welsh MJ
    J Biol Chem; 1996 Jun; 271(25):14995-5001. PubMed ID: 8663008
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Cystic fibrosis transmembrane conductance regulator (CFTR) anion binding as a probe of the pore.
    Mansoura MK; Smith SS; Choi AD; Richards NW; Strong TV; Drumm ML; Collins FS; Dawson DC
    Biophys J; 1998 Mar; 74(3):1320-32. PubMed ID: 9512029
    [TBL] [Abstract][Full Text] [Related]  

  • 18. cAMP-regulated trafficking of epitope-tagged CFTR.
    Howard M; Jilling T; DuVall M; Frizzell RA
    Kidney Int; 1996 Jun; 49(6):1642-8. PubMed ID: 8743469
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Sensitivity of a renal K+ channel (ROMK2) to the inhibitory sulfonylurea compound glibenclamide is enhanced by coexpression with the ATP-binding cassette transporter cystic fibrosis transmembrane regulator.
    McNicholas CM; Guggino WB; Schwiebert EM; Hebert SC; Giebisch G; Egan ME
    Proc Natl Acad Sci U S A; 1996 Jul; 93(15):8083-8. PubMed ID: 8755607
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A conserved region of the R domain of cystic fibrosis transmembrane conductance regulator is important in processing and function.
    Pasyk EA; Morin XK; Zeman P; Garami E; Galley K; Huan LJ; Wang Y; Bear CE
    J Biol Chem; 1998 Nov; 273(48):31759-64. PubMed ID: 9822639
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.