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Journal Abstract Search
548 related items for PubMed ID: 18989824
1. 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; 25(6-7):528-38. PubMed ID: 18989824 [Abstract] [Full Text] [Related]
2. Discovery of pyrrolo[2,3-b]pyrazines derivatives as submicromolar affinity activators of wild type, G551D, and F508del cystic fibrosis transmembrane conductance regulator chloride channels. Noel S, Faveau C, Norez C, Rogier C, Mettey Y, Becq F. J Pharmacol Exp Ther; 2006 Oct; 319(1):349-59. PubMed ID: 16829626 [Abstract] [Full Text] [Related]
3. Discovery of alpha-aminoazaheterocycle-methylglyoxal adducts as a new class of high-affinity inhibitors of cystic fibrosis transmembrane conductance regulator chloride channels. Routaboul C, Norez C, Melin P, Molina MC, Boucherle B, Bossard F, Noel S, Robert R, Gauthier C, Becq F, Décout JL. J Pharmacol Exp Ther; 2007 Sep; 322(3):1023-35. PubMed ID: 17578899 [Abstract] [Full Text] [Related]
4. 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; 21(1):27-38. PubMed ID: 14668136 [Abstract] [Full Text] [Related]
5. Defective formation of PKA/CnA-dependent annexin 2-S100A10/CFTR complex in DeltaF508 cystic fibrosis cells. Borthwick LA, Riemen C, Goddard C, Colledge WH, Mehta A, Gerke V, Muimo R. Cell Signal; 2008 Jun; 20(6):1073-83. PubMed ID: 18346874 [Abstract] [Full Text] [Related]
6. [Butyl-p-hydroxybenzoate stimulates cystic fibrosis transmembrane conductance regulator Cl- transport]. Ge H, Hou TT, Sun JJ, Yang H. Yao Xue Xue Bao; 2009 Jan; 44(1):32-7. PubMed ID: 19350818 [Abstract] [Full Text] [Related]
7. 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]
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 16; 128(1):108-18. PubMed ID: 10498841 [Abstract] [Full Text] [Related]
9. 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]
11. Direct interaction of a small-molecule modulator with G551D-CFTR, a cystic fibrosis-causing mutation associated with severe disease. Pasyk S, Li C, Ramjeesingh M, Bear CE. Biochem J; 2009 Feb 15; 418(1):185-90. PubMed ID: 18945216 [Abstract] [Full Text] [Related]
13. Dual regulation of cardiac Na+-K+ pumps and CFTR Cl- channels by protein kinases A and C. Erlenkamp S, Glitsch HG, Kockskämper J. Pflugers Arch; 2002 May 15; 444(1-2):251-62. PubMed ID: 11976939 [Abstract] [Full Text] [Related]
14. Impact of the F508del mutation on ovine CFTR, a Cl- channel with enhanced conductance and ATP-dependent gating. Cai Z, Palmai-Pallag T, Khuituan P, Mutolo MJ, Boinot C, Liu B, Scott-Ward TS, Callebaut I, Harris A, Sheppard DN. J Physiol; 2015 Jun 01; 593(11):2427-46. PubMed ID: 25763566 [Abstract] [Full Text] [Related]
19. 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 01; 42(10):2364-70. PubMed ID: 11527951 [Abstract] [Full Text] [Related]
20. Mouse cystic fibrosis transmembrane conductance regulator forms cAMP-PKA-regulated apical chloride channels in cortical collecting duct. Lu M, Dong K, Egan ME, Giebisch GH, Boulpaep EL, Hebert SC. Proc Natl Acad Sci U S A; 2010 Mar 30; 107(13):6082-7. PubMed ID: 20231442 [Abstract] [Full Text] [Related] Page: [Next] [New Search]