BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

355 related articles for article (PubMed ID: 33321047)

  • 1. Secretory Cells Dominate Airway CFTR Expression and Function in Human Airway Superficial Epithelia.
    Okuda K; Dang H; Kobayashi Y; Carraro G; Nakano S; Chen G; Kato T; Asakura T; Gilmore RC; Morton LC; Lee RE; Mascenik T; Yin WN; Barbosa Cardenas SM; O'Neal YK; Minnick CE; Chua M; Quinney NL; Gentzsch M; Anderson CW; Ghio A; Matsui H; Nagase T; Ostrowski LE; Grubb BR; Olsen JC; Randell SH; Stripp BR; Tata PR; O'Neal WK; Boucher RC
    Am J Respir Crit Care Med; 2021 May; 203(10):1275-1289. PubMed ID: 33321047
    [No Abstract]   [Full Text] [Related]  

  • 2. Ionocytes and CFTR Chloride Channel Expression in Normal and Cystic Fibrosis Nasal and Bronchial Epithelial Cells.
    Scudieri P; Musante I; Venturini A; Guidone D; Genovese M; Cresta F; Caci E; Palleschi A; Poeta M; Santamaria F; Ciciriello F; Lucidi V; Galietta LJV
    Cells; 2020 Sep; 9(9):. PubMed ID: 32933106
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Sonic Hedgehog Signaling Is Essential for Pulmonary Ionocyte Specification in Human and Ferret Airway Epithelia.
    Cai Q; Luo M; Tang Y; Yu M; Yuan F; Gasser GN; Liu X; Engelhardt JF
    Am J Respir Cell Mol Biol; 2023 Sep; 69(3):295-309. PubMed ID: 37141531
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. 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]  

  • 6. CFTR-rich ionocytes mediate chloride absorption across airway epithelia.
    Lei L; Traore S; Romano Ibarra GS; Karp PH; Rehman T; Meyerholz DK; Zabner J; Stoltz DA; Sinn PL; Welsh MJ; McCray PB; Thornell IM
    J Clin Invest; 2023 Oct; 133(20):. PubMed ID: 37581935
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Epithelial sodium channel silencing as a strategy to correct the airway surface fluid deficit in cystic fibrosis.
    Gianotti A; Melani R; Caci E; Sondo E; Ravazzolo R; Galietta LJ; Zegarra-Moran O
    Am J Respir Cell Mol Biol; 2013 Sep; 49(3):445-52. PubMed ID: 23600628
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Cystic Fibrosis and the Cells of the Airway Epithelium: What Are Ionocytes and What Do They Do?
    Shah VS; Chivukula RR; Lin B; Waghray A; Rajagopal J
    Annu Rev Pathol; 2022 Jan; 17():23-46. PubMed ID: 34437820
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Detargeting Lentiviral-Mediated CFTR Expression in Airway Basal Cells Using miR-106b.
    Choi SH; Reeves RE; Romano Ibarra GS; Lynch TJ; Shahin WS; Feng Z; Gasser GN; Winter MC; Evans TIA; Liu X; Luo M; Zhang Y; Stoltz DA; Devor EJ; Yan Z; Engelhardt JF
    Genes (Basel); 2020 Oct; 11(10):. PubMed ID: 33036232
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Tgf-beta downregulation of distinct chloride channels in cystic fibrosis-affected epithelia.
    Sun H; Harris WT; Kortyka S; Kotha K; Ostmann AJ; Rezayat A; Sridharan A; Sanders Y; Naren AP; Clancy JP
    PLoS One; 2014; 9(9):e106842. PubMed ID: 25268501
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Choice of Differentiation Media Significantly Impacts Cell Lineage and Response to CFTR Modulators in Fully Differentiated Primary Cultures of Cystic Fibrosis Human Airway Epithelial Cells.
    Saint-Criq V; Delpiano L; Casement J; Onuora JC; Lin J; Gray MA
    Cells; 2020 Sep; 9(9):. PubMed ID: 32967385
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Expression and function of Anoctamin 1/TMEM16A calcium-activated chloride channels in airways of in vivo mouse models for cystic fibrosis research.
    Hahn A; Salomon JJ; Leitz D; Feigenbutz D; Korsch L; Lisewski I; Schrimpf K; Millar-Büchner P; Mall MA; Frings S; Möhrlen F
    Pflugers Arch; 2018 Sep; 470(9):1335-1348. PubMed ID: 29860639
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The ΔF508-CFTR mutation inhibits wild-type CFTR processing and function when co-expressed in human airway epithelia and in mouse nasal mucosa.
    Tucker TA; Fortenberry JA; Zsembery A; Schwiebert LM; Schwiebert EM
    BMC Physiol; 2012 Sep; 12():12. PubMed ID: 22999299
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Spliceosome-mediated RNA trans-splicing with recombinant adeno-associated virus partially restores cystic fibrosis transmembrane conductance regulator function to polarized human cystic fibrosis airway epithelial cells.
    Liu X; Luo M; Zhang LN; Yan Z; Zak R; Ding W; Mansfield SG; Mitchell LG; Engelhardt JF
    Hum Gene Ther; 2005 Sep; 16(9):1116-23. PubMed ID: 16149910
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. In vitro platform to model the function of ionocytes in the human airway epithelium.
    Vilà-González M; Pinte L; Fradique R; Causa E; Kool H; Rodrat M; Morell CM; Al-Thani M; Porter L; Guo W; Maeshima R; Hart SL; McCaughan F; Granata A; Sheppard DN; Floto RA; Rawlins EL; Cicuta P; Vallier L
    Respir Res; 2024 Apr; 25(1):180. PubMed ID: 38664797
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Human cystic fibrosis airway epithelia have reduced Cl- conductance but not increased Na+ conductance.
    Itani OA; Chen JH; Karp PH; Ernst S; Keshavjee S; Parekh K; Klesney-Tait J; Zabner J; Welsh MJ
    Proc Natl Acad Sci U S A; 2011 Jun; 108(25):10260-5. PubMed ID: 21646513
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Amniotic mesenchymal stem cells: a new source for hepatocyte-like cells and induction of CFTR expression by coculture with cystic fibrosis airway epithelial cells.
    Paracchini V; Carbone A; Colombo F; Castellani S; Mazzucchelli S; Gioia SD; Degiorgio D; Seia M; Porretti L; Colombo C; Conese M
    J Biomed Biotechnol; 2012; 2012():575471. PubMed ID: 22315512
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Unimpaired lysosomal acidification in respiratory epithelial cells in cystic fibrosis.
    Haggie PM; Verkman AS
    J Biol Chem; 2009 Mar; 284(12):7681-6. PubMed ID: 19136560
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 18.