These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

256 related articles for article (PubMed ID: 19289574)

  • 21. Na+/H+ exchanger regulatory factor isoform 1 overexpression modulates cystic fibrosis transmembrane conductance regulator (CFTR) expression and activity in human airway 16HBE14o- cells and rescues DeltaF508 CFTR functional expression in cystic fibrosis cells.
    Guerra L; Fanelli T; Favia M; Riccardi SM; Busco G; Cardone RA; Carrabino S; Weinman EJ; Reshkin SJ; Conese M; Casavola V
    J Biol Chem; 2005 Dec; 280(49):40925-33. PubMed ID: 16203733
    [TBL] [Abstract][Full Text] [Related]  

  • 22. CFTR channels in immortalized human airway cells.
    Haws C; Krouse ME; Xia Y; Gruenert DC; Wine JJ
    Am J Physiol; 1992 Dec; 263(6 Pt 1):L692-707. PubMed ID: 1282304
    [TBL] [Abstract][Full Text] [Related]  

  • 23. 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; 107(13):6082-7. PubMed ID: 20231442
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Role of K(V)LQT1 in cyclic adenosine monophosphate-mediated Cl(-) secretion in human airway epithelia.
    Mall M; Wissner A; Schreiber R; Kuehr J; Seydewitz HH; Brandis M; Greger R; Kunzelmann K
    Am J Respir Cell Mol Biol; 2000 Sep; 23(3):283-9. PubMed ID: 10970817
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Cl transport in complemented CF bronchial epithelial cells correlates with CFTR mRNA expression levels.
    Illek B; Maurisse R; Wahler L; Kunzelmann K; Fischer H; Gruenert DC
    Cell Physiol Biochem; 2008; 22(1-4):57-68. PubMed ID: 18769032
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Inhibition of protein kinase CK2 closes the CFTR Cl channel, but has no effect on the cystic fibrosis mutant deltaF508-CFTR.
    Treharne KJ; Xu Z; Chen JH; Best OG; Cassidy DM; Gruenert DC; Hegyi P; Gray MA; Sheppard DN; Kunzelmann K; Mehta A
    Cell Physiol Biochem; 2009; 24(5-6):347-60. PubMed ID: 19910675
    [TBL] [Abstract][Full Text] [Related]  

  • 27. 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]  

  • 28. Generation and functional characterization of epithelial cells with stable expression of SLC26A9 Cl- channels.
    Salomon JJ; Spahn S; Wang X; Füllekrug J; Bertrand CA; Mall MA
    Am J Physiol Lung Cell Mol Physiol; 2016 Apr; 310(7):L593-602. PubMed ID: 26801567
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Bioelectric characterization of epithelia from neonatal CFTR knockout ferrets.
    Fisher JT; Tyler SR; Zhang Y; Lee BJ; Liu X; Sun X; Sui H; Liang B; Luo M; Xie W; Yi Y; Zhou W; Song Y; Keiser N; Wang K; de Jonge HR; Engelhardt JF
    Am J Respir Cell Mol Biol; 2013 Nov; 49(5):837-44. PubMed ID: 23782101
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Failure of cAMP agonists to activate rescued deltaF508 CFTR in CFBE41o- airway epithelial monolayers.
    Bebok Z; Collawn JF; Wakefield J; Parker W; Li Y; Varga K; Sorscher EJ; Clancy JP
    J Physiol; 2005 Dec; 569(Pt 2):601-15. PubMed ID: 16210354
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Spliceosome-mediated RNA trans-splicing with recombinant adeno-associated virus partially restores cystic fibrosis transmembrane conductance regulator function to polarized human cystic fibrosis airway epithelial cells.
    Liu X; Luo M; Zhang LN; Yan Z; Zak R; Ding W; Mansfield SG; Mitchell LG; Engelhardt JF
    Hum Gene Ther; 2005 Sep; 16(9):1116-23. PubMed ID: 16149910
    [TBL] [Abstract][Full Text] [Related]  

  • 32. The ΔF508-CFTR mutation inhibits wild-type CFTR processing and function when co-expressed in human airway epithelia and in mouse nasal mucosa.
    Tucker TA; Fortenberry JA; Zsembery A; Schwiebert LM; Schwiebert EM
    BMC Physiol; 2012 Sep; 12():12. PubMed ID: 22999299
    [TBL] [Abstract][Full Text] [Related]  

  • 33. CFTR and Anoctamin 1 (ANO1) contribute to cAMP amplified exocytosis and insulin secretion in human and murine pancreatic beta-cells.
    Edlund A; Esguerra JL; Wendt A; Flodström-Tullberg M; Eliasson L
    BMC Med; 2014 May; 12():87. PubMed ID: 24885604
    [TBL] [Abstract][Full Text] [Related]  

  • 34. cAMP and genistein stimulate HCO3- conductance through CFTR in human airway epithelia.
    Illek B; Yankaskas JR; Machen TE
    Am J Physiol; 1997 Apr; 272(4 Pt 1):L752-61. PubMed ID: 9142951
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Pyridine nucleotide redox potential modulates cystic fibrosis transmembrane conductance regulator Cl- conductance.
    Stutts MJ; Gabriel SE; Price EM; Sarkadi B; Olsen JC; Boucher RC
    J Biol Chem; 1994 Mar; 269(12):8667-74. PubMed ID: 7510695
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Human cystic fibrosis airway epithelia have reduced Cl- conductance but not increased Na+ conductance.
    Itani OA; Chen JH; Karp PH; Ernst S; Keshavjee S; Parekh K; Klesney-Tait J; Zabner J; Welsh MJ
    Proc Natl Acad Sci U S A; 2011 Jun; 108(25):10260-5. PubMed ID: 21646513
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Bypassing CFTR dysfunction in cystic fibrosis with alternative pathways for anion transport.
    Li H; Salomon JJ; Sheppard DN; Mall MA; Galietta LJ
    Curr Opin Pharmacol; 2017 Jun; 34():91-97. PubMed ID: 29065356
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Cystic fibrosis gene modifier SLC26A9 modulates airway response to CFTR-directed therapeutics.
    Strug LJ; Gonska T; He G; Keenan K; Ip W; Boëlle PY; Lin F; Panjwani N; Gong J; Li W; Soave D; Xiao B; Tullis E; Rabin H; Parkins MD; Price A; Zuberbuhler PC; Corvol H; Ratjen F; Sun L; Bear CE; Rommens JM
    Hum Mol Genet; 2016 Oct; 25(20):4590-4600. PubMed ID: 28171547
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Functional interaction of the cystic fibrosis transmembrane conductance regulator with members of the SLC26 family of anion transporters (SLC26A8 and SLC26A9): physiological and pathophysiological relevance.
    El Khouri E; Touré A
    Int J Biochem Cell Biol; 2014 Jul; 52():58-67. PubMed ID: 24530837
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Chloride transporting capability of Calu-3 epithelia following persistent knockdown of the cystic fibrosis transmembrane conductance regulator, CFTR.
    MacVinish LJ; Cope G; Ropenga A; Cuthbert AW
    Br J Pharmacol; 2007 Apr; 150(8):1055-65. PubMed ID: 17339840
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 13.