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483 related items for PubMed ID: 9463368
1. CFTR Cl- channel and CFTR-associated ATP channel: distinct pores regulated by common gates. Sugita M, Yue Y, Foskett JK. EMBO J; 1998 Feb 16; 17(4):898-908. PubMed ID: 9463368 [Abstract] [Full Text] [Related]
2. Protein kinase A regulates ATP hydrolysis and dimerization by a CFTR (cystic fibrosis transmembrane conductance regulator) domain. Howell LD, Borchardt R, Kole J, Kaz AM, Randak C, Cohn JA. Biochem J; 2004 Feb 15; 378(Pt 1):151-9. PubMed ID: 14602047 [Abstract] [Full Text] [Related]
3. Potentiation of cystic fibrosis transmembrane conductance regulator (CFTR) Cl- currents by the chemical solvent tetrahydrofuran. Hughes LK, Ju M, Sheppard DN. Mol Membr Biol; 2008 Sep 15; 25(6-7):528-38. PubMed ID: 18989824 [Abstract] [Full Text] [Related]
4. Regulation of the cystic fibrosis transmembrane conductance regulator chloride channel by MgATP. Welsh MJ, Anderson MP. Soc Gen Physiol Ser; 1993 Sep 15; 48():119-27. PubMed ID: 7684867 [Abstract] [Full Text] [Related]
5. Prolonged nonhydrolytic interaction of nucleotide with CFTR's NH2-terminal nucleotide binding domain and its role in channel gating. Basso C, Vergani P, Nairn AC, Gadsby DC. J Gen Physiol; 2003 Sep 15; 122(3):333-48. PubMed ID: 12939393 [Abstract] [Full Text] [Related]
6. Cl- absorption across the thick ascending limb is not altered in cystic fibrosis mice. A role for a pseudo-CFTR Cl- channel. Marvão P, De Jesus Ferreira MC, Bailly C, Paulais M, Bens M, Guinamard R, Moreau R, Vandewalle A, Teulon J. J Clin Invest; 1998 Dec 01; 102(11):1986-93. PubMed ID: 9835624 [Abstract] [Full Text] [Related]
7. Down-regulation of volume-sensitive Cl- channels by CFTR is mediated by the second nucleotide-binding domain. Ando-Akatsuka Y, Abdullaev IF, Lee EL, Okada Y, Sabirov RZ. Pflugers Arch; 2002 Nov 01; 445(2):177-86. PubMed ID: 12457238 [Abstract] [Full Text] [Related]
8. Inhibition of heterologously expressed cystic fibrosis transmembrane conductance regulator Cl- channels by non-sulphonylurea hypoglycaemic agents. Cai Z, Lansdell KA, Sheppard DN. Br J Pharmacol; 1999 Sep 01; 128(1):108-18. PubMed ID: 10498841 [Abstract] [Full Text] [Related]
9. Direct block of the cystic fibrosis transmembrane conductance regulator Cl(-) channel by niflumic acid. Scott-Ward TS, Li H, Schmidt A, Cai Z, Sheppard DN. Mol Membr Biol; 2004 Sep 01; 21(1):27-38. PubMed ID: 14668136 [Abstract] [Full Text] [Related]
10. CFTR-like chloride channels in non-ciliated bronchiolar epithelial (Clara) cells. Chinet TC, Gabriel SE, Penland CM, Sato M, Stutts MJ, Boucher RC, Van Scott MR. Biochem Biophys Res Commun; 1997 Jan 13; 230(2):470-5. PubMed ID: 9016805 [Abstract] [Full Text] [Related]
11. Stimulation of CFTR activity by its phosphorylated R domain. Winter MC, Welsh MJ. Nature; 1997 Sep 18; 389(6648):294-6. PubMed ID: 9305845 [Abstract] [Full Text] [Related]
12. Control of dynamic CFTR selectivity by glutamate and ATP in epithelial cells. Reddy MM, Quinton PM. Nature; 2003 Jun 12; 423(6941):756-60. PubMed ID: 12802335 [Abstract] [Full Text] [Related]
13. Walker mutations reveal loose relationship between catalytic and channel-gating activities of purified CFTR (cystic fibrosis transmembrane conductance regulator). Ramjeesingh M, Li C, Garami E, Huan LJ, Galley K, Wang Y, Bear CE. Biochemistry; 1999 Feb 02; 38(5):1463-8. PubMed ID: 9931011 [Abstract] [Full Text] [Related]
14. CFTR chloride channels in human and simian heart. Warth JD, Collier ML, Hart P, Geary Y, Gelband CH, Chapman T, Horowitz B, Hume JR. Cardiovasc Res; 1996 Apr 02; 31(4):615-24. PubMed ID: 8689654 [Abstract] [Full Text] [Related]
15. ATP hydrolysis cycles and the gating of CFTR Cl- channels. Gadsby DC, Dousmanis AG, Nairn AC. Acta Physiol Scand Suppl; 1998 Aug 02; 643():247-56. PubMed ID: 9789567 [Abstract] [Full Text] [Related]
17. Regulation of CFTR Cl- channel gating by ADP and ATP analogues. Schultz BD, Venglarik CJ, Bridges RJ, Frizzell RA. J Gen Physiol; 1995 Mar 02; 105(3):329-61. PubMed ID: 7539480 [Abstract] [Full Text] [Related]
18. Regulation of the gating of cystic fibrosis transmembrane conductance regulator C1 channels by phosphorylation and ATP hydrolysis. Hwang TC, Nagel G, Nairn AC, Gadsby DC. Proc Natl Acad Sci U S A; 1994 May 24; 91(11):4698-702. PubMed ID: 7515176 [Abstract] [Full Text] [Related]
19. 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 30; 36(39):11966-74. PubMed ID: 9305991 [Abstract] [Full Text] [Related]
20. Gating of cystic fibrosis transmembrane conductance regulator chloride channels by adenosine triphosphate hydrolysis. Quantitative analysis of a cyclic gating scheme. Zeltwanger S, Wang F, Wang GT, Gillis KD, Hwang TC. J Gen Physiol; 1999 Apr 30; 113(4):541-54. PubMed ID: 10102935 [Abstract] [Full Text] [Related] Page: [Next] [New Search]