BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

230 related articles for article (PubMed ID: 23609890)

  • 1. Proteomic and ionomic profiling reveals significant alterations of protein expression and calcium homeostasis in cystic fibrosis cells.
    Ciavardelli D; D'Orazio M; Pieroni L; Consalvo A; Rossi C; Sacchetta P; Di Ilio C; Battistoni A; Urbani A
    Mol Biosyst; 2013 Jun; 9(6):1117-26. PubMed ID: 23609890
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Transient receptor potential canonical channel 6 links Ca2+ mishandling to cystic fibrosis transmembrane conductance regulator channel dysfunction in cystic fibrosis.
    Antigny F; Norez C; Dannhoffer L; Bertrand J; Raveau D; Corbi P; Jayle C; Becq F; Vandebrouck C
    Am J Respir Cell Mol Biol; 2011 Jan; 44(1):83-90. PubMed ID: 20203293
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Purinergic signaling underlies CFTR control of human airway epithelial cell volume.
    Braunstein GM; Zsembery A; Tucker TA; Schwiebert EM
    J Cyst Fibros; 2004 Jun; 3(2):99-117. PubMed ID: 15463893
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The low PLC-δ1 expression in cystic fibrosis bronchial epithelial cells induces upregulation of TRPV6 channel activity.
    Vachel L; Norez C; Jayle C; Becq F; Vandebrouck C
    Cell Calcium; 2015 Jan; 57(1):38-48. PubMed ID: 25477137
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Expression of delta F508 cystic fibrosis transmembrane conductance regulator protein and related chloride transport properties in the gallbladder epithelium from cystic fibrosis patients.
    Dray-Charier N; Paul A; Scoazec JY; Veissière D; Mergey M; Capeau J; Soubrane O; Housset C
    Hepatology; 1999 Jun; 29(6):1624-34. PubMed ID: 10347100
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Effect of duramycin on chloride transport and intracellular calcium concentration in cystic fibrosis and non-cystic fibrosis epithelia.
    Oliynyk I; Varelogianni G; Roomans GM; Johannesson M
    APMIS; 2010 Dec; 118(12):982-90. PubMed ID: 21091780
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Calcium-dependent regulation of NF-(kappa)B activation in cystic fibrosis airway epithelial cells.
    Tabary O; Boncoeur E; de Martin R; Pepperkok R; Clément A; Schultz C; Jacquot J
    Cell Signal; 2006 May; 18(5):652-60. PubMed ID: 16084692
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The effect of NO-donors on chloride efflux, intracellular Ca(2+) concentration and mRNA expression of CFTR and ENaC in cystic fibrosis airway epithelial cells.
    Oliynyk I; Hussain R; Amin A; Johannesson M; Roomans GM
    Exp Mol Pathol; 2013 Jun; 94(3):474-80. PubMed ID: 23523754
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The proteome speciation of an immortalized cystic fibrosis cell line: New perspectives on the pathophysiology of the disease.
    Puglia M; Landi C; Gagliardi A; Breslin L; Armini A; Brunetti J; Pini A; Bianchi L; Bini L
    J Proteomics; 2018 Jan; 170():28-42. PubMed ID: 28970102
    [TBL] [Abstract][Full Text] [Related]  

  • 10. CFTR: a hub for kinases and crosstalk of cAMP and Ca2+.
    Kunzelmann K; Mehta A
    FEBS J; 2013 Sep; 280(18):4417-29. PubMed ID: 23895508
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. CFTR chloride channel activity modulates the mitochondrial morphology in cultured epithelial cells.
    García R; Falduti C; Clauzure M; Jara R; Massip-Copiz MM; de Los Ángeles Aguilar M; Santa-Coloma TA; Valdivieso ÁG
    Int J Biochem Cell Biol; 2021 Jun; 135():105976. PubMed ID: 33845203
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Episomal expression of wild-type CFTR corrects cAMP-dependent chloride transport in respiratory epithelial cells.
    Lei DC; Kunzelmann K; Koslowsky T; Yezzi MJ; Escobar LC; Xu Z; Ellison AR; Rommens JM; Tsui L-C ; Tykocinski M; Gruenert DC
    Gene Ther; 1996 May; 3(5):427-36. PubMed ID: 9156804
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Reduced expression of Tis7/IFRD1 protein in murine and human cystic fibrosis airway epithelial cell models homozygous for the F508del-CFTR mutation.
    Blanchard E; Marie S; Riffault L; Bonora M; Tabary O; Clement A; Jacquot J
    Biochem Biophys Res Commun; 2011 Aug; 411(3):471-6. PubMed ID: 21723850
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Macromolecular interactions and ion transport in cystic fibrosis.
    Guggino WB; Banks-Schlegel SP
    Am J Respir Crit Care Med; 2004 Oct; 170(7):815-20. PubMed ID: 15447951
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Turnover of the cystic fibrosis transmembrane conductance regulator (CFTR): slow degradation of wild-type and delta F508 CFTR in surface membrane preparations of immortalized airway epithelial cells.
    Wei X; Eisman R; Xu J; Harsch AD; Mulberg AE; Bevins CL; Glick MC; Scanlin TF
    J Cell Physiol; 1996 Aug; 168(2):373-84. PubMed ID: 8707873
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Normal function of the cystic fibrosis conductance regulator protein can be associated with homozygous (Delta)F508 mutation.
    Sermet-Gaudelus I; Vallée B; Urbin I; Torossi T; Marianovski R; Fajac A; Feuillet MN; Bresson JL; Lenoir G; Bernaudin JF; Edelman A
    Pediatr Res; 2002 Nov; 52(5):628-35. PubMed ID: 12409506
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A cystic fibrosis respiratory epithelial cell chronically treated by miglustat acquires a non-cystic fibrosis-like phenotype.
    Norez C; Antigny F; Noel S; Vandebrouck C; Becq F
    Am J Respir Cell Mol Biol; 2009 Aug; 41(2):217-25. PubMed ID: 19131642
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Abnormal spatial diffusion of Ca2+ in F508del-CFTR airway epithelial cells.
    Antigny F; Norez C; Cantereau A; Becq F; Vandebrouck C
    Respir Res; 2008 Oct; 9(1):70. PubMed ID: 18973672
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Expression of cystic fibrosis transmembrane conductance regulator in human gallbladder epithelial cells.
    Dray-Charier N; Paul A; Veissiere D; Mergey M; Scoazec JY; Capeau J; Brahimi-Horn C; Housset C
    Lab Invest; 1995 Dec; 73(6):828-36. PubMed ID: 8558844
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.