BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

610 related articles for article (PubMed ID: 22951447)

  • 1. CFTR, mucins, and mucus obstruction in cystic fibrosis.
    Kreda SM; Davis CW; Rose MC
    Cold Spring Harb Perspect Med; 2012 Sep; 2(9):a009589. PubMed ID: 22951447
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Cystic fibrosis transmembrane conductance regulator is expressed in mucin granules from Calu-3 and primary human airway epithelial cells.
    LeSimple P; Goepp J; Palmer ML; Fahrenkrug SC; O'Grady SM; Ferraro P; Robert R; Hanrahan JW
    Am J Respir Cell Mol Biol; 2013 Oct; 49(4):511-6. PubMed ID: 23742042
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Cystic fibrosis: an inherited disease affecting mucin-producing organs.
    Ehre C; Ridley C; Thornton DJ
    Int J Biochem Cell Biol; 2014 Jul; 52():136-45. PubMed ID: 24685676
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Airway mucus in cystic fibrosis.
    Puchelle E; Bajolet O; Abély M
    Paediatr Respir Rev; 2002 Jun; 3(2):115-9. PubMed ID: 12297057
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Mucus, mucins, and cystic fibrosis.
    Morrison CB; Markovetz MR; Ehre C
    Pediatr Pulmonol; 2019 Nov; 54 Suppl 3(Suppl 3):S84-S96. PubMed ID: 31715083
    [TBL] [Abstract][Full Text] [Related]  

  • 6. CFTR delivery to 25% of surface epithelial cells restores normal rates of mucus transport to human cystic fibrosis airway epithelium.
    Zhang L; Button B; Gabriel SE; Burkett S; Yan Y; Skiadopoulos MH; Dang YL; Vogel LN; McKay T; Mengos A; Boucher RC; Collins PL; Pickles RJ
    PLoS Biol; 2009 Jul; 7(7):e1000155. PubMed ID: 19621064
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Unplugging Mucus in Cystic Fibrosis and Chronic Obstructive Pulmonary Disease.
    Mall MA
    Ann Am Thorac Soc; 2016 Apr; 13 Suppl 2():S177-85. PubMed ID: 27115954
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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; 304(7):L469-80. PubMed ID: 23377346
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Cystic fibrosis mice lacking Muc1 have reduced amounts of intestinal mucus.
    Parmley RR; Gendler SJ
    J Clin Invest; 1998 Nov; 102(10):1798-806. PubMed ID: 9819365
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Mucin Production and Hydration Responses to Mucopurulent Materials in Normal versus Cystic Fibrosis Airway Epithelia.
    Abdullah LH; Coakley R; Webster MJ; Zhu Y; Tarran R; Radicioni G; Kesimer M; Boucher RC; Davis CW; Ribeiro CMP
    Am J Respir Crit Care Med; 2018 Feb; 197(4):481-491. PubMed ID: 29099608
    [TBL] [Abstract][Full Text] [Related]  

  • 11. The HDAC inhibitor SAHA does not rescue CFTR membrane expression in Cystic Fibrosis.
    Bergougnoux A; Petit A; Knabe L; Bribes E; Chiron R; De Sario A; Claustres M; Molinari N; Vachier I; Taulan-Cadars M; Bourdin A
    Int J Biochem Cell Biol; 2017 Jul; 88():124-132. PubMed ID: 28478266
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Mucus aberrant properties in CF: Insights from cells and animal models.
    Ehre C; Hansson GC; Thornton DJ; Ostedgaard LS
    J Cyst Fibros; 2023 Mar; 22 Suppl 1(Suppl 1):S23-S26. PubMed ID: 36117114
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Critical role of cytosolic phospholipase A2{alpha} in bronchial mucus hypersecretion in CFTR-deficient mice.
    Dif F; Wu YZ; Burgel PR; Ollero M; Leduc D; Aarbiou J; Borot F; Garcia-Verdugo I; Martin C; Chignard M; Israel-Biet D; Kita Y; Scholte BJ; Touqui L
    Eur Respir J; 2010 Nov; 36(5):1120-30. PubMed ID: 20413542
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Bicarbonate and functional CFTR channel are required for proper mucin secretion and link cystic fibrosis with its mucus phenotype.
    Gustafsson JK; Ermund A; Ambort D; Johansson ME; Nilsson HE; Thorell K; Hebert H; Sjövall H; Hansson GC
    J Exp Med; 2012 Jul; 209(7):1263-72. PubMed ID: 22711878
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Vector-specific complementation profiles of two independent primary defects in cystic fibrosis airways.
    Zhang Y; Jiang Q; Dudus L; Yankaskas JR; Engelhardt JF
    Hum Gene Ther; 1998 Mar; 9(5):635-48. PubMed ID: 9551612
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Identification and quantification of mucin expression.
    Thomsson KA; Hansson GC
    Methods Mol Biol; 2011; 742():127-41. PubMed ID: 21547730
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Treatment of cystic fibrosis airway cells with CFTR modulators reverses aberrant mucus properties
    Morrison CB; Shaffer KM; Araba KC; Markovetz MR; Wykoff JA; Quinney NL; Hao S; Delion MF; Flen AL; Morton LC; Liao J; Hill DB; Drumm ML; O'Neal WK; Kesimer M; Gentzsch M; Ehre C
    Eur Respir J; 2022 Feb; 59(2):. PubMed ID: 34172469
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Pharmacotherapy of the ion transport defect in cystic fibrosis: role of purinergic receptor agonists and other potential therapeutics.
    Kunzelmann K; Mall M
    Am J Respir Med; 2003; 2(4):299-309. PubMed ID: 14719996
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Mucins and CFTR: Their Close Relationship.
    Okuda K; Shaffer KM; Ehre C
    Int J Mol Sci; 2022 Sep; 23(18):. PubMed ID: 36142171
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Zinc Deficiency via a Splice Switch in Zinc Importer ZIP2/SLC39A2 Causes Cystic Fibrosis-Associated MUC5AC Hypersecretion in Airway Epithelial Cells.
    Kamei S; Fujikawa H; Nohara H; Ueno-Shuto K; Maruta K; Nakashima R; Kawakami T; Matsumoto C; Sakaguchi Y; Ono T; Suico MA; Boucher RC; Gruenert DC; Takeo T; Nakagata N; Li JD; Kai H; Shuto T
    EBioMedicine; 2018 Jan; 27():304-316. PubMed ID: 29289532
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 31.