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 *

155 related articles for article (PubMed ID: 34674574)

  • 41. The microbial community of the cystic fibrosis airway is disrupted in early life.
    Renwick J; McNally P; John B; DeSantis T; Linnane B; Murphy P;
    PLoS One; 2014; 9(12):e109798. PubMed ID: 25526264
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Composition of nasal airway surface liquid in cystic fibrosis and other airway diseases determined by X-ray microanalysis.
    Vanthanouvong V; Kozlova I; Johannesson M; Nääs E; Nordvall SL; Dragomir A; Roomans GM
    Microsc Res Tech; 2006 Apr; 69(4):271-6. PubMed ID: 16586482
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Assessment of airway microbiota and inflammation in cystic fibrosis using multiple sampling methods.
    Zemanick ET; Wagner BD; Robertson CE; Stevens MJ; Szefler SJ; Accurso FJ; Sagel SD; Harris JK
    Ann Am Thorac Soc; 2015 Feb; 12(2):221-9. PubMed ID: 25474078
    [TBL] [Abstract][Full Text] [Related]  

  • 44. No detectable improvements in cystic fibrosis transmembrane conductance regulator by nasal aminoglycosides in patients with cystic fibrosis with stop mutations.
    Clancy JP; Rowe SM; Bebok Z; Aitken ML; Gibson R; Zeitlin P; Berclaz P; Moss R; Knowles MR; Oster RA; Mayer-Hamblett N; Ramsey B
    Am J Respir Cell Mol Biol; 2007 Jul; 37(1):57-66. PubMed ID: 17347447
    [TBL] [Abstract][Full Text] [Related]  

  • 45. 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]  

  • 46. Efficacy and tolerability of a new nasal spray formulation containing hyaluronate and tobramycin in cystic fibrosis patients with bacterial rhinosinusitis.
    Di Cicco M; Alicandro G; Claut L; Cariani L; Luca N; Defilippi G; Costantini D; Colombo C
    J Cyst Fibros; 2014 Jul; 13(4):455-60. PubMed ID: 24656944
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Loss of CFTR function is associated with reduced bitter taste receptor-stimulated nitric oxide innate immune responses in nasal epithelial cells and macrophages.
    Carey RM; Palmer JN; Adappa ND; Lee RJ
    Front Immunol; 2023; 14():1096242. PubMed ID: 36742335
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Changes in Airway Microbiome and Inflammation with Ivacaftor Treatment in Patients with Cystic Fibrosis and the G551D Mutation.
    Harris JK; Wagner BD; Zemanick ET; Robertson CE; Stevens MJ; Heltshe SL; Rowe SM; Sagel SD
    Ann Am Thorac Soc; 2020 Feb; 17(2):212-220. PubMed ID: 31604026
    [No Abstract]   [Full Text] [Related]  

  • 49. Small Molecule Anion Carriers Correct Abnormal Airway Surface Liquid Properties in Cystic Fibrosis Airway Epithelia.
    Gianotti A; Capurro V; Delpiano L; Mielczarek M; García-Valverde M; Carreira-Barral I; Ludovico A; Fiore M; Baroni D; Moran O; Quesada R; Caci E
    Int J Mol Sci; 2020 Feb; 21(4):. PubMed ID: 32098269
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Corynebacterium pseudodiphtheriticum Exploits Staphylococcus aureus Virulence Components in a Novel Polymicrobial Defense Strategy.
    Hardy BL; Dickey SW; Plaut RD; Riggins DP; Stibitz S; Otto M; Merrell DS
    mBio; 2019 Jan; 10(1):. PubMed ID: 30622190
    [TBL] [Abstract][Full Text] [Related]  

  • 51. 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]  

  • 52. Gene therapy for cystic fibrosis using E1-deleted adenovirus: a phase I trial in the nasal cavity. The University of North Carolina at Chapel Hill.
    Boucher RC; Knowles MR; Johnson LG; Olsen JC; Pickles R; Wilson JM; Engelhardt J; Yang Y; Grossman M
    Hum Gene Ther; 1994 May; 5(5):615-39. PubMed ID: 7519885
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Airway surface liquid homeostasis in cystic fibrosis: pathophysiology and therapeutic targets.
    Haq IJ; Gray MA; Garnett JP; Ward C; Brodlie M
    Thorax; 2016 Mar; 71(3):284-7. PubMed ID: 26719229
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Ivacaftor Reduces Inflammatory Mediators in Upper Airway Lining Fluid From Cystic Fibrosis Patients With a G551D Mutation: Serial Non-Invasive Home-Based Collection of Upper Airway Lining Fluid.
    Mainz JG; Arnold C; Wittstock K; Hipler UC; Lehmann T; Zagoya C; Duckstein F; Ellemunter H; Hentschel J
    Front Immunol; 2021; 12():642180. PubMed ID: 34025651
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Effects of airway surface liquid pH on host defense in cystic fibrosis.
    Berkebile AR; McCray PB
    Int J Biochem Cell Biol; 2014 Jul; 52():124-9. PubMed ID: 24560894
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Effects of Elexacaftor/Tezacaftor/Ivacaftor Therapy on CFTR Function in Patients with Cystic Fibrosis and One or Two
    Graeber SY; Vitzthum C; Pallenberg ST; Naehrlich L; Stahl M; Rohrbach A; Drescher M; Minso R; Ringshausen FC; Rueckes-Nilges C; Klajda J; Berges J; Yu Y; Scheuermann H; Hirtz S; Sommerburg O; Dittrich AM; Tümmler B; Mall MA
    Am J Respir Crit Care Med; 2022 Mar; 205(5):540-549. PubMed ID: 34936849
    [No Abstract]   [Full Text] [Related]  

  • 57. Nasal and exhaled nitric oxide is reduced in adult patients with cystic fibrosis and does not correlate with cystic fibrosis genotype.
    Thomas SR; Kharitonov SA; Scott SF; Hodson ME; Barnes PJ
    Chest; 2000 Apr; 117(4):1085-9. PubMed ID: 10767244
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Long-term therapeutic and reporter gene expression in lentiviral vector treated cystic fibrosis mice.
    Cmielewski P; Donnelley M; Parsons DW
    J Gene Med; 2014; 16(9-10):291-9. PubMed ID: 25130650
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Infection of polarized airway epithelial cells by normal and small-colony variant strains of Staphylococcus aureus is increased in cells with abnormal cystic fibrosis transmembrane conductance regulator function and is influenced by NF-κB.
    Mitchell G; Grondin G; Bilodeau G; Cantin AM; Malouin F
    Infect Immun; 2011 Sep; 79(9):3541-51. PubMed ID: 21708986
    [TBL] [Abstract][Full Text] [Related]  

  • 60. A placebo-controlled study of liposome-mediated gene transfer to the nasal epithelium of patients with cystic fibrosis.
    Gill DR; Southern KW; Mofford KA; Seddon T; Huang L; Sorgi F; Thomson A; MacVinish LJ; Ratcliff R; Bilton D; Lane DJ; Littlewood JM; Webb AK; Middleton PG; Colledge WH; Cuthbert AW; Evans MJ; Higgins CF; Hyde SC
    Gene Ther; 1997 Mar; 4(3):199-209. PubMed ID: 9135733
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.