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

PUBMED FOR HANDHELDS

Journal Abstract Search

411 related items for PubMed ID: 19050039

  • 1. Dominant-negative inhibition of Ca2+ influx via TRPV2 ameliorates muscular dystrophy in animal models.
    Iwata Y, Katanosaka Y, Arai Y, Shigekawa M, Wakabayashi S.
    Hum Mol Genet; 2009 Mar 01; 18(5):824-34. PubMed ID: 19050039
    [Abstract] [Full Text] [Related]

  • 2. A novel mechanism of myocyte degeneration involving the Ca2+-permeable growth factor-regulated channel.
    Iwata Y, Katanosaka Y, Arai Y, Komamura K, Miyatake K, Shigekawa M.
    J Cell Biol; 2003 Jun 09; 161(5):957-67. PubMed ID: 12796481
    [Abstract] [Full Text] [Related]

  • 3. Protective effects of Ca2+ handling drugs against abnormal Ca2+ homeostasis and cell damage in myopathic skeletal muscle cells.
    Iwata Y, Katanosaka Y, Shijun Z, Kobayashi Y, Hanada H, Shigekawa M, Wakabayashi S.
    Biochem Pharmacol; 2005 Sep 01; 70(5):740-51. PubMed ID: 16009351
    [Abstract] [Full Text] [Related]

  • 4.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 5. Targeted inhibition of Ca2+ /calmodulin signaling exacerbates the dystrophic phenotype in mdx mouse muscle.
    Chakkalakal JV, Michel SA, Chin ER, Michel RN, Jasmin BJ.
    Hum Mol Genet; 2006 May 01; 15(9):1423-35. PubMed ID: 16551657
    [Abstract] [Full Text] [Related]

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

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8. Drastic reduction of sarcalumenin in Dp427 (dystrophin of 427 kDa)-deficient fibres indicates that abnormal calcium handling plays a key role in muscular dystrophy.
    Dowling P, Doran P, Ohlendieck K.
    Biochem J; 2004 Apr 15; 379(Pt 2):479-88. PubMed ID: 14678011
    [Abstract] [Full Text] [Related]

  • 9. Enhanced Ca²⁺ influx from STIM1-Orai1 induces muscle pathology in mouse models of muscular dystrophy.
    Goonasekera SA, Davis J, Kwong JQ, Accornero F, Wei-LaPierre L, Sargent MA, Dirksen RT, Molkentin JD.
    Hum Mol Genet; 2014 Jul 15; 23(14):3706-15. PubMed ID: 24556214
    [Abstract] [Full Text] [Related]

  • 10. Dystrophic cardiomyopathy: role of TRPV2 channels in stretch-induced cell damage.
    Lorin C, Vögeli I, Niggli E.
    Cardiovasc Res; 2015 Apr 01; 106(1):153-62. PubMed ID: 25616416
    [Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12. TRPV2 is a component of osmotically sensitive cation channels in murine aortic myocytes.
    Muraki K, Iwata Y, Katanosaka Y, Ito T, Ohya S, Shigekawa M, Imaizumi Y.
    Circ Res; 2003 Oct 31; 93(9):829-38. PubMed ID: 14512441
    [Abstract] [Full Text] [Related]

  • 13. Translocation of calcium-permeable TRPV2 channel to the podosome: Its role in the regulation of podosome assembly.
    Nagasawa M, Kojima I.
    Cell Calcium; 2012 Feb 31; 51(2):186-93. PubMed ID: 22226146
    [Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15. Dystrophic cardiomyopathy: amplification of cellular damage by Ca2+ signalling and reactive oxygen species-generating pathways.
    Jung C, Martins AS, Niggli E, Shirokova N.
    Cardiovasc Res; 2008 Mar 01; 77(4):766-73. PubMed ID: 18056762
    [Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No 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 21.