BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

129 related articles for article (PubMed ID: 2859414)

  • 1. Persistence of abnormal chloride ion permeability in cystic fibrosis nasal epithelial cells in heterologous culture.
    Yankaskas JR; Knowles MR; Gatzy JT; Boucher RC
    Lancet; 1985 Apr; 1(8435):954-6. PubMed ID: 2859414
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Evidence for reduced Cl- and increased Na+ permeability in cystic fibrosis human primary cell cultures.
    Boucher RC; Cotton CU; Gatzy JT; Knowles MR; Yankaskas JR
    J Physiol; 1988 Nov; 405():77-103. PubMed ID: 3255805
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Increased ion transport in cultured nasal polyp epithelial cells.
    Bernstein JM; Yankaskas JR
    Arch Otolaryngol Head Neck Surg; 1994 Sep; 120(9):993-6. PubMed ID: 8074828
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Chloride transport in cultured nasal epithelium of cystic fibrosis patients.
    Verbeek E; de Jonge HR; Bijman J; Keulemans J; Sinaasappel M; van der Kamp AW; Scholte BJ
    Pflugers Arch; 1990 Feb; 415(5):540-6. PubMed ID: 2158065
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Cystic fibrosis decreases the apical membrane chloride permeability of monolayers cultured from cells of tracheal epithelium.
    Widdicombe JH; Welsh MJ; Finkbeiner WE
    Proc Natl Acad Sci U S A; 1985 Sep; 82(18):6167-71. PubMed ID: 3862125
    [TBL] [Abstract][Full Text] [Related]  

  • 6. In vivo nasal potential difference: techniques and protocols for assessing efficacy of gene transfer in cystic fibrosis.
    Knowles MR; Paradiso AM; Boucher RC
    Hum Gene Ther; 1995 Apr; 6(4):445-55. PubMed ID: 7542031
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Minor role of Cl- secretion in non-cystic fibrosis and cystic fibrosis human nasal epithelium.
    Rückes-Nilges C; Weber U; Lindemann H; Münker G; Clauss W; Weber WM
    Cell Physiol Biochem; 1999; 9(1):1-10. PubMed ID: 10352340
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Activation by extracellular nucleotides of chloride secretion in the airway epithelia of patients with cystic fibrosis.
    Knowles MR; Clarke LL; Boucher RC
    N Engl J Med; 1991 Aug; 325(8):533-8. PubMed ID: 1857389
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Relative ion permeability of normal and cystic fibrosis nasal epithelium.
    Knowles M; Gatzy J; Boucher R
    J Clin Invest; 1983 May; 71(5):1410-7. PubMed ID: 6853720
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Protocols for in vivo measurement of the ion transport defects in cystic fibrosis nasal epithelium.
    Middleton PG; Geddes DM; Alton EW
    Eur Respir J; 1994 Nov; 7(11):2050-6. PubMed ID: 7875281
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Abnormal apical cell membrane in cystic fibrosis respiratory epithelium. An in vitro electrophysiologic analysis.
    Cotton CU; Stutts MJ; Knowles MR; Gatzy JT; Boucher RC
    J Clin Invest; 1987 Jan; 79(1):80-5. PubMed ID: 3793933
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Abnormal ion permeation through cystic fibrosis respiratory epithelium.
    Knowles MR; Stutts MJ; Spock A; Fischer N; Gatzy JT; Boucher RC
    Science; 1983 Sep; 221(4615):1067-70. PubMed ID: 6308769
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Cellular Cl- transport in cultured cystic fibrosis airway epithelium.
    Willumsen NJ; Davis CW; Boucher RC
    Am J Physiol; 1989 May; 256(5 Pt 1):C1045-53. PubMed ID: 2719094
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Nitric oxide has no beneficial effects on ion transport defects in cystic fibrosis human nasal epithelium.
    Rückes-Nilges C; Lindemann H; Klimek T; Glanz H; Weber WM
    Pflugers Arch; 2000 Nov; 441(1):133-7. PubMed ID: 11205052
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The amiloride-inhibitable Na+ conductance is reduced by the cystic fibrosis transmembrane conductance regulator in normal but not in cystic fibrosis airways.
    Mall M; Bleich M; Greger R; Schreiber R; Kunzelmann K
    J Clin Invest; 1998 Jul; 102(1):15-21. PubMed ID: 9649552
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Activation of an apical Cl- conductance by Ca2+ ionophores in cystic fibrosis airway epithelia.
    Willumsen NJ; Boucher RC
    Am J Physiol; 1989 Feb; 256(2 Pt 1):C226-33. PubMed ID: 2465689
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Chloride uptake into cultured airway epithelial cells from cystic fibrosis patients and normal individuals.
    Stutts MJ; Cotton CU; Yankaskas JR; Cheng E; Knowles MR; Gatzy JT; Boucher RC
    Proc Natl Acad Sci U S A; 1985 Oct; 82(19):6677-81. PubMed ID: 3863120
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Insights into the variability of nasal potential difference, a biomarker of CFTR activity.
    Kyrilli S; Henry T; Wilschanski M; Fajac I; Davies JC; Jais JP; Sermet-Gaudelus I
    J Cyst Fibros; 2020 Jul; 19(4):620-626. PubMed ID: 31699569
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Polarized distribution of HCO3- transport in human normal and cystic fibrosis nasal epithelia.
    Paradiso AM; Coakley RD; Boucher RC
    J Physiol; 2003 Apr; 548(Pt 1):203-18. PubMed ID: 12562898
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Nasal potential difference in congenital bilateral absence of the vas deferens.
    Pradal U; Castellani C; Delmarco A; Mastella G
    Am J Respir Crit Care Med; 1998 Sep; 158(3):896-901. PubMed ID: 9731023
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.