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.


PUBMED FOR HANDHELDS

Journal Abstract Search


677 related items for PubMed ID: 21907281

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2. Anoctamin 1 dysregulation alters bronchial epithelial repair in cystic fibrosis.
    Ruffin M, Voland M, Marie S, Bonora M, Blanchard E, Blouquit-Laye S, Naline E, Puyo P, Le Rouzic P, Guillot L, Corvol H, Clement A, Tabary O.
    Biochim Biophys Acta; 2013 Dec; 1832(12):2340-51. PubMed ID: 24080196
    [Abstract] [Full Text] [Related]

  • 3. Pseudomonas aeruginosa Homoserine lactone activates store-operated cAMP and cystic fibrosis transmembrane regulator-dependent Cl- secretion by human airway epithelia.
    Schwarzer C, Wong S, Shi J, Matthes E, Illek B, Ianowski JP, Arant RJ, Isacoff E, Vais H, Foskett JK, Maiellaro I, Hofer AM, Machen TE.
    J Biol Chem; 2010 Nov 05; 285(45):34850-63. PubMed ID: 20739289
    [Abstract] [Full Text] [Related]

  • 4. 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 30; 9(1):70. PubMed ID: 18973672
    [Abstract] [Full Text] [Related]

  • 5. Maintaining low Ca2+ level in the endoplasmic reticulum restores abnormal endogenous F508del-CFTR trafficking in airway epithelial cells.
    Norez C, Antigny F, Becq F, Vandebrouck C.
    Traffic; 2006 May 30; 7(5):562-73. PubMed ID: 16643279
    [Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7. CFTR: a hub for kinases and crosstalk of cAMP and Ca2+.
    Kunzelmann K, Mehta A.
    FEBS J; 2013 Sep 30; 280(18):4417-29. PubMed ID: 23895508
    [Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9. The effect of ambroxol on chloride transport, CFTR and ENaC in cystic fibrosis airway epithelial cells.
    Varelogianni G, Hussain R, Strid H, Oliynyk I, Roomans GM, Johannesson M.
    Cell Biol Int; 2013 Nov 30; 37(11):1149-56. PubMed ID: 23765701
    [Abstract] [Full Text] [Related]

  • 10. Calcium homeostasis is abnormal in cystic fibrosis airway epithelial cells but is normalized after rescue of F508del-CFTR.
    Antigny F, Norez C, Becq F, Vandebrouck C.
    Cell Calcium; 2008 Feb 30; 43(2):175-83. PubMed ID: 17590432
    [Abstract] [Full Text] [Related]

  • 11. Calumenin contributes to ER-Ca2+ homeostasis in bronchial epithelial cells expressing WT and F508del mutated CFTR and to F508del-CFTR retention.
    Philippe R, Antigny F, Buscaglia P, Norez C, Huguet F, Castelbou C, Trouvé P, Becq F, Frieden M, Férec C, Mignen O.
    Cell Calcium; 2017 Mar 30; 62():47-59. PubMed ID: 28189267
    [Abstract] [Full Text] [Related]

  • 12. Normalization of raised sodium absorption and raised calcium-mediated chloride secretion by adenovirus-mediated expression of cystic fibrosis transmembrane conductance regulator in primary human cystic fibrosis airway epithelial cells.
    Johnson LG, Boyles SE, Wilson J, Boucher RC.
    J Clin Invest; 1995 Mar 30; 95(3):1377-82. PubMed ID: 7533790
    [Abstract] [Full Text] [Related]

  • 13. 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 Mar 30; 9(9):e106842. PubMed ID: 25268501
    [Abstract] [Full Text] [Related]

  • 14. Relationship of a non-cystic fibrosis transmembrane conductance regulator-mediated chloride conductance to organ-level disease in Cftr(-/-) mice.
    Clarke LL, Grubb BR, Yankaskas JR, Cotton CU, McKenzie A, Boucher RC.
    Proc Natl Acad Sci U S A; 1994 Jan 18; 91(2):479-83. PubMed ID: 7507247
    [Abstract] [Full Text] [Related]

  • 15. 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 18; 470(9):1335-1348. PubMed ID: 29860639
    [Abstract] [Full Text] [Related]

  • 16. The anion transporter SLC26A9 localizes to tight junctions and is degraded by the proteasome when co-expressed with F508del-CFTR.
    Sato Y, Thomas DY, Hanrahan JW.
    J Biol Chem; 2019 Nov 29; 294(48):18269-18284. PubMed ID: 31645438
    [Abstract] [Full Text] [Related]

  • 17. CFTR induces extracellular acid sensing in Xenopus oocytes which activates endogenous Ca²⁺-activated Cl⁻ conductance.
    Kongsuphol P, Schreiber R, Kraidith K, Kunzelmann K.
    Pflugers Arch; 2011 Sep 29; 462(3):479-87. PubMed ID: 21647592
    [Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]


    Page: [Next] [New Search]
    of 34.