BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

213 related articles for article (PubMed ID: 32978064)

  • 1. Evidence of early increased sialylation of airway mucins and defective mucociliary clearance in CFTR-deficient piglets.
    Caballero I; Ringot-Destrez B; Si-Tahar M; Barbry P; Guillon A; Lantier I; Berri M; Chevaleyre C; Fleurot I; Barc C; Ramphal R; Pons N; Paquet A; Lebrigand K; Baron C; Bähr A; Klymiuk N; Léonard R; Robbe-Masselot C
    J Cyst Fibros; 2021 Jan; 20(1):173-182. PubMed ID: 32978064
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Pseudomonas aeruginosa triggers CFTR-mediated airway surface liquid secretion in swine trachea.
    Luan X; Campanucci VA; Nair M; Yilmaz O; Belev G; Machen TE; Chapman D; Ianowski JP
    Proc Natl Acad Sci U S A; 2014 Sep; 111(35):12930-5. PubMed ID: 25136096
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Altered O-glycosylation and sulfation of airway mucins associated with cystic fibrosis.
    Xia B; Royall JA; Damera G; Sachdev GP; Cummings RD
    Glycobiology; 2005 Aug; 15(8):747-75. PubMed ID: 15994837
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Defective innate immunity and hyperinflammation in newborn cystic fibrosis transmembrane conductance regulator-knockout ferret lungs.
    Keiser NW; Birket SE; Evans IA; Tyler SR; Crooke AK; Sun X; Zhou W; Nellis JR; Stroebele EK; Chu KK; Tearney GJ; Stevens MJ; Harris JK; Rowe SM; Engelhardt JF
    Am J Respir Cell Mol Biol; 2015 Jun; 52(6):683-94. PubMed ID: 25317669
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Acquired Cystic Fibrosis Transmembrane Conductance Regulator Deficiency.
    Cho DY; Woodworth BA
    Adv Otorhinolaryngol; 2016; 79():78-85. PubMed ID: 27466849
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. 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]  

  • 8. Role of CFTR in airway disease.
    Pilewski JM; Frizzell RA
    Physiol Rev; 1999 Jan; 79(1 Suppl):S215-55. PubMed ID: 9922383
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Mucociliary Transport in Healthy and Cystic Fibrosis Pig Airways.
    Xie Y; Ostedgaard L; Abou Alaiwa MH; Lu L; Fischer AJ; Stoltz DA
    Ann Am Thorac Soc; 2018 Nov; 15(Suppl 3):S171-S176. PubMed ID: 30431346
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Pseudomonas aeruginosa pyocyanin modulates mucin glycosylation with sialyl-Lewis(x) to increase binding to airway epithelial cells.
    Jeffries JL; Jia J; Choi W; Choe S; Miao J; Xu Y; Powell R; Lin J; Kuang Z; Gaskins HR; Lau GW
    Mucosal Immunol; 2016 Jul; 9(4):1039-1050. PubMed ID: 26555707
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. The mucus bundles responsible for airway cleaning are retained in cystic fibrosis and by cholinergic stimulation.
    Ermund A; Meiss LN; Dolan B; Bähr A; Klymiuk N; Hansson GC
    Eur Respir J; 2018 Aug; 52(2):. PubMed ID: 29853489
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Impaired mucus detachment disrupts mucociliary transport in a piglet model of cystic fibrosis.
    Hoegger MJ; Fischer AJ; McMenimen JD; Ostedgaard LS; Tucker AJ; Awadalla MA; Moninger TO; Michalski AS; Hoffman EA; Zabner J; Stoltz DA; Welsh MJ
    Science; 2014 Aug; 345(6198):818-22. PubMed ID: 25124441
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Human airway mucin glycosylation: a combinatory of carbohydrate determinants which vary in cystic fibrosis.
    Lamblin G; Degroote S; Perini JM; Delmotte P; Scharfman A; Davril M; Lo-Guidice JM; Houdret N; Dumur V; Klein A; Rousse P
    Glycoconj J; 2001 Sep; 18(9):661-84. PubMed ID: 12386453
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Mucin glycosylation and sulphation in airway epithelial cells is not influenced by cystic fibrosis transmembrane conductance regulator expression.
    Leir SH; Parry S; Palmai-Pallag T; Evans J; Morris HR; Dell A; Harris A
    Am J Respir Cell Mol Biol; 2005 May; 32(5):453-61. PubMed ID: 15677769
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Modulation of Ion Transport to Restore Airway Hydration in Cystic Fibrosis.
    Reihill JA; Douglas LEJ; Martin SL
    Genes (Basel); 2021 Mar; 12(3):. PubMed ID: 33810137
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Regulation of cystic fibrosis transmembrane conductance regulator by microRNA-145, -223, and -494 is altered in ΔF508 cystic fibrosis airway epithelium.
    Oglesby IK; Chotirmall SH; McElvaney NG; Greene CM
    J Immunol; 2013 Apr; 190(7):3354-62. PubMed ID: 23436935
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Cystic fibrosis transmembrane conductance regulator regulates epithelial cell response to Aspergillus and resultant pulmonary inflammation.
    Chaudhary N; Datta K; Askin FB; Staab JF; Marr KA
    Am J Respir Crit Care Med; 2012 Feb; 185(3):301-10. PubMed ID: 22135344
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Mucociliary clearance in cystic fibrosis knockout mice infected with Pseudomonas aeruginosa.
    Cowley EA; Wang CG; Gosselin D; Radzioch D; Eidelman DH
    Eur Respir J; 1997 Oct; 10(10):2312-8. PubMed ID: 9387959
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 11.