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Journal Abstract Search

348 related items for PubMed ID: 24885604

  • 21. Tgf-beta downregulation of distinct chloride channels in cystic fibrosis-affected epithelia.
    Sun H, Harris WT, Kortyka S, Kotha K, Ostmann AJ, Rezayat A, Sridharan A, Sanders Y, Naren AP, Clancy JP.
    PLoS One; 2014; 9(9):e106842. PubMed ID: 25268501
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  • 23. Exocytosis is not involved in activation of Cl- secretion via CFTR in Calu-3 airway epithelial cells.
    Loffing J, Moyer BD, McCoy D, Stanton BA.
    Am J Physiol; 1998 Oct; 275(4):C913-20. PubMed ID: 9755044
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  • 24. TMEM16A (ANO1) as a therapeutic target in cystic fibrosis.
    Galietta LJV.
    Curr Opin Pharmacol; 2022 Jun; 64():102206. PubMed ID: 35364521
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  • 30. 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 03; 95(5):2674-9. PubMed ID: 9482946
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  • 31. Glucose-Sensitive CFTR Suppresses Glucagon Secretion by Potentiating KATP Channels in Pancreatic Islet α Cells.
    Huang WQ, Guo JH, Zhang XH, Yu MK, Chung YW, Ruan YC, Chan HC.
    Endocrinology; 2017 Oct 01; 158(10):3188-3199. PubMed ID: 28977595
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  • 32. Glibenclamide stimulates fluid secretion in rodent cholangiocytes through a cystic fibrosis transmembrane conductance regulator-independent mechanism.
    Spirlì C, Fiorotto R, Song L, Santos-Sacchi J, Okolicsanyi L, Masier S, Rocchi L, Vairetti MP, De Bernard M, Melero S, Pozzan T, Strazzabosco M.
    Gastroenterology; 2005 Jul 01; 129(1):220-33. PubMed ID: 16012949
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  • 33. Clusters of Cl- channels in CFTR-expressing Sf9 cells switch spontaneously between slow and fast gating modes.
    Larsen EH, Price EM, Gabriel SE, Stutts MJ, Boucher RC.
    Pflugers Arch; 1996 Jul 01; 432(3):528-37. PubMed ID: 8766014
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  • 34. 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 01; 512 ( Pt 3)(Pt 3):765-77. PubMed ID: 9769420
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  • 35. Islet-intrinsic effects of CFTR mutation.
    Koivula FNM, McClenaghan NH, Harper AGS, Kelly C.
    Diabetologia; 2016 Jul 01; 59(7):1350-1355. PubMed ID: 27033560
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  • 36. Defective regulation of gap junctional coupling in cystic fibrosis pancreatic duct cells.
    Chanson M, Scerri I, Suter S.
    J Clin Invest; 1999 Jun 01; 103(12):1677-84. PubMed ID: 10377174
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  • 37. cAMP- but not Ca(2+)-regulated Cl- conductance in the oviduct is defective in mouse model of cystic fibrosis.
    Leung AY, Wong PY, Gabriel SE, Yankaskas JR, Boucher RC.
    Am J Physiol; 1995 Mar 01; 268(3 Pt 1):C708-12. PubMed ID: 7534985
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  • 38. Cystic fibrosis transmembrane regulator inhibitors CFTR(inh)-172 and GlyH-101 target mitochondrial functions, independently of chloride channel inhibition.
    Kelly M, Trudel S, Brouillard F, Bouillaud F, Colas J, Nguyen-Khoa T, Ollero M, Edelman A, Fritsch J.
    J Pharmacol Exp Ther; 2010 Apr 01; 333(1):60-9. PubMed ID: 20051483
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  • 39. CFTR: a hub for kinases and crosstalk of cAMP and Ca2+.
    Kunzelmann K, Mehta A.
    FEBS J; 2013 Sep 01; 280(18):4417-29. PubMed ID: 23895508
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  • 40. Regulation of plasma membrane recycling by CFTR.
    Bradbury NA, Jilling T, Berta G, Sorscher EJ, Bridges RJ, Kirk KL.
    Science; 1992 Apr 24; 256(5056):530-2. PubMed ID: 1373908
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