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

94 related items for PubMed ID: 12459180

  • 1. The binding of the RyR2 calcium channel to its gating protein FKBP12.6 is oppositely affected by ARVD2 and VTSIP mutations.
    Tiso N, Salamon M, Bagattin A, Danieli GA, Argenton F, Bortolussi M.
    Biochem Biophys Res Commun; 2002 Dec 13; 299(4):594-8. PubMed ID: 12459180
    [Abstract] [Full Text] [Related]

  • 2. Enhanced store overload-induced Ca2+ release and channel sensitivity to luminal Ca2+ activation are common defects of RyR2 mutations linked to ventricular tachycardia and sudden death.
    Jiang D, Wang R, Xiao B, Kong H, Hunt DJ, Choi P, Zhang L, Chen SR.
    Circ Res; 2005 Nov 25; 97(11):1173-81. PubMed ID: 16239587
    [Abstract] [Full Text] [Related]

  • 3. Sudden death in familial polymorphic ventricular tachycardia associated with calcium release channel (ryanodine receptor) leak.
    Lehnart SE, Wehrens XH, Laitinen PJ, Reiken SR, Deng SX, Cheng Z, Landry DW, Kontula K, Swan H, Marks AR.
    Circulation; 2004 Jun 29; 109(25):3208-14. PubMed ID: 15197150
    [Abstract] [Full Text] [Related]

  • 4. Regulation of ryanodine receptors by FK506 binding proteins.
    Chelu MG, Danila CI, Gilman CP, Hamilton SL.
    Trends Cardiovasc Med; 2004 Aug 29; 14(6):227-34. PubMed ID: 15451514
    [Abstract] [Full Text] [Related]

  • 5. Identification of mutations in the cardiac ryanodine receptor gene in families affected with arrhythmogenic right ventricular cardiomyopathy type 2 (ARVD2).
    Tiso N, Stephan DA, Nava A, Bagattin A, Devaney JM, Stanchi F, Larderet G, Brahmbhatt B, Brown K, Bauce B, Muriago M, Basso C, Thiene G, Danieli GA, Rampazzo A.
    Hum Mol Genet; 2001 Feb 01; 10(3):189-94. PubMed ID: 11159936
    [Abstract] [Full Text] [Related]

  • 6. Involvement of the cardiac ryanodine receptor/calcium release channel in catecholaminergic polymorphic ventricular tachycardia.
    Marks AR, Priori S, Memmi M, Kontula K, Laitinen PJ.
    J Cell Physiol; 2002 Jan 01; 190(1):1-6. PubMed ID: 11807805
    [Abstract] [Full Text] [Related]

  • 7. Ryanodine receptor mutations associated with stress-induced ventricular tachycardia mediate increased calcium release in stimulated cardiomyocytes.
    George CH, Higgs GV, Lai FA.
    Circ Res; 2003 Sep 19; 93(6):531-40. PubMed ID: 12919952
    [Abstract] [Full Text] [Related]

  • 8. Dantrolene rescues aberrant N-terminus intersubunit interactions in mutant pro-arrhythmic cardiac ryanodine receptors.
    Seidel M, Thomas NL, Williams AJ, Lai FA, Zissimopoulos S.
    Cardiovasc Res; 2015 Jan 01; 105(1):118-28. PubMed ID: 25411383
    [Abstract] [Full Text] [Related]

  • 9. FKBPs facilitate the termination of spontaneous Ca2+ release in wild-type RyR2 but not CPVT mutant RyR2.
    Zhang JZ, Waddell HM, Wu E, Dholakia J, Okolo CA, McLay JC, Jones PP.
    Biochem J; 2016 Jul 15; 473(14):2049-60. PubMed ID: 27154203
    [Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11. Three-dimensional visualization of FKBP12.6 binding to an open conformation of cardiac ryanodine receptor.
    Sharma MR, Jeyakumar LH, Fleischer S, Wagenknecht T.
    Biophys J; 2006 Jan 01; 90(1):164-72. PubMed ID: 16214874
    [Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

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

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16. A novel mutation in FKBP12.6 binding region of the human cardiac ryanodine receptor gene (R2401H) in a Japanese patient with catecholaminergic polymorphic ventricular tachycardia.
    Aizawa Y, Ueda K, Komura S, Washizuka T, Chinushi M, Inagaki N, Matsumoto Y, Hayashi T, Takahashi M, Nakano N, Yasunami M, Kimura A, Hiraoka M, Aizawa Y.
    Int J Cardiol; 2005 Mar 18; 99(2):343-5. PubMed ID: 15749201
    [Abstract] [Full Text] [Related]

  • 17. Mechanisms of abnormal calcium homeostasis in mutations responsible for catecholaminergic polymorphic ventricular tachycardia.
    Iyer V, Hajjar RJ, Armoundas AA.
    Circ Res; 2007 Feb 02; 100(2):e22-31. PubMed ID: 17234962
    [Abstract] [Full Text] [Related]

  • 18. Central domain of the human cardiac muscle ryanodine receptor does not mediate interaction with FKBP12.6.
    Zissimopoulos S, Lai FA.
    Cell Biochem Biophys; 2005 Feb 02; 43(2):203-19. PubMed ID: 16049346
    [Abstract] [Full Text] [Related]

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

  • 20. A mechanism of ryanodine receptor modulation by FKBP12/12.6, protein kinase A, and K201.
    Blayney LM, Jones JL, Griffiths J, Lai FA.
    Cardiovasc Res; 2010 Jan 01; 85(1):68-78. PubMed ID: 19661110
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 5.