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Journal Abstract Search

161 related items for PubMed ID: 34610318

  • 21.
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  • 25. The cystic fibrosis transmembrane conductance regulator impedes proteolytic stimulation of the epithelial Na+ channel.
    Gentzsch M, Dang H, Dang Y, Garcia-Caballero A, Suchindran H, Boucher RC, Stutts MJ.
    J Biol Chem; 2010 Oct 15; 285(42):32227-32. PubMed ID: 20709758
    [Abstract] [Full Text] [Related]

  • 26. 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 15; 49(5):837-44. PubMed ID: 23782101
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  • 27. Effects of purinergic stimulation, CFTR and osmotic stress on amiloride-sensitive Na+ transport in epithelia and Xenopus oocytes.
    Schreiber R, König J, Sun J, Markovich D, Kunzelmann K.
    J Membr Biol; 2003 Mar 15; 192(2):101-10. PubMed ID: 12682798
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  • 29. Effect of cytosolic pH on epithelial Na+ channel in normal and cystic fibrosis sweat ducts.
    Reddy MM, Wang XF, Quinton PM.
    J Membr Biol; 2008 Mar 15; 225(1-3):1-11. PubMed ID: 18937003
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  • 31. Inhibition of epithelial Na+ currents by intracellular domains of the cystic fibrosis transmembrane conductance regulator.
    Kunzelmann K, Kiser GL, Schreiber R, Riordan JR.
    FEBS Lett; 1997 Jan 06; 400(3):341-4. PubMed ID: 9009227
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  • 32. Sustained inhibition of ENaC in CF: Potential RNA-based therapies for mutation-agnostic treatment.
    Kota P.
    Curr Opin Pharmacol; 2022 Jun 06; 64():102209. PubMed ID: 35483215
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  • 33. Loss of Cftr function exacerbates the phenotype of Na(+) hyperabsorption in murine airways.
    Livraghi-Butrico A, Kelly EJ, Wilkinson KJ, Rogers TD, Gilmore RC, Harkema JR, Randell SH, Boucher RC, O'Neal WK, Grubb BR.
    Am J Physiol Lung Cell Mol Physiol; 2013 Apr 01; 304(7):L469-80. PubMed ID: 23377346
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  • 34. The cytosolic termini of the beta- and gamma-ENaC subunits are involved in the functional interactions between cystic fibrosis transmembrane conductance regulator and epithelial sodium channel.
    Ji HL, Chalfant ML, Jovov B, Lockhart JP, Parker SB, Fuller CM, Stanton BA, Benos DJ.
    J Biol Chem; 2000 Sep 08; 275(36):27947-56. PubMed ID: 10821834
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  • 36. ENaC- and CFTR-dependent ion and fluid transport in mammary epithelia.
    Blaug S, Hybiske K, Cohn J, Firestone GL, Machen TE, Miller SS.
    Am J Physiol Cell Physiol; 2001 Aug 08; 281(2):C633-48. PubMed ID: 11443063
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  • 37. Isobutylmethylxanthine fails to stimulate chloride secretion in cystic fibrosis airway epithelia.
    Grubb B, Lazarowski E, Knowles M, Boucher R.
    Am J Respir Cell Mol Biol; 1993 Apr 08; 8(4):454-60. PubMed ID: 7682824
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  • 38. Effect of nitric oxide on epithelial ion transports in noncystic fibrosis and cystic fibrosis human proximal and distal airways.
    Blouquit-Laye S, Dannhoffer L, Braun C, Dinh-Xuan AT, Sage E, Chinet T.
    Am J Physiol Lung Cell Mol Physiol; 2012 Oct 01; 303(7):L617-25. PubMed ID: 22773693
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  • 39. Does epithelial sodium channel hyperactivity contribute to cystic fibrosis lung disease?
    Hobbs CA, Da Tan C, Tarran R.
    J Physiol; 2013 Sep 15; 591(18):4377-87. PubMed ID: 23878362
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  • 40. The effect of ambroxol on chloride transport, CFTR and ENaC in cystic fibrosis airway epithelial cells.
    Varelogianni G, Hussain R, Strid H, Oliynyk I, Roomans GM, Johannesson M.
    Cell Biol Int; 2013 Nov 15; 37(11):1149-56. PubMed ID: 23765701
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