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Journal Abstract Search

506 related items for PubMed ID: 17012353

  • 1. Intracellular calcium handling in ventricular myocytes from mdx mice.
    Williams IA, Allen DG.
    Am J Physiol Heart Circ Physiol; 2007 Feb; 292(2):H846-55. PubMed ID: 17012353
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  • 3. Exacerbation of dystrophic cardiomyopathy by phospholamban deficiency mediated chronically increased cardiac Ca2+ cycling in vivo.
    Law ML, Prins KW, Olander ME, Metzger JM.
    Am J Physiol Heart Circ Physiol; 2018 Dec 01; 315(6):H1544-H1552. PubMed ID: 30118340
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  • 6. Calcium current properties in dystrophin-deficient ventricular cardiomyocytes from aged mdx mice.
    Rubi L, Todt H, Kubista H, Koenig X, Hilber K.
    Physiol Rep; 2018 Jan 01; 6(1):. PubMed ID: 29333726
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  • 7. Differential expression of genes involved in the calcium homeostasis in masticatory muscles of MDX mice.
    Kunert-Keil CH, Gredes T, Lucke S, Botzenhart U, Dominiak M, Gedrange T.
    J Physiol Pharmacol; 2014 Apr 01; 65(2):317-24. PubMed ID: 24781740
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  • 8. Increased constitutive nitric oxide production by whole body periodic acceleration ameliorates alterations in cardiomyocytes associated with utrophin/dystrophin deficiency.
    Lopez JR, Kolster J, Zhang R, Adams J.
    J Mol Cell Cardiol; 2017 Jul 01; 108():149-157. PubMed ID: 28623080
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  • 9. Cardiovascular phenotype of the Dmdmdx rat - a suitable animal model for Duchenne muscular dystrophy.
    Szabó PL, Ebner J, Koenig X, Hamza O, Watzinger S, Trojanek S, Abraham D, Todt H, Kubista H, Schicker K, Remy S, Anegon I, Kiss A, Podesser BK, Hilber K.
    Dis Model Mech; 2021 Feb 22; 14(2):. PubMed ID: 33619211
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  • 13. Ryanodine receptor dysfunction causes senescence and fibrosis in Duchenne dilated cardiomyopathy.
    Souidi M, Resta J, Dridi H, Sleiman Y, Reiken S, Formoso K, Colombani S, Amédro P, Meyer P, Charrabi A, Vincenti M, Liu Y, Soni RK, Lezoualc'h F, Stéphane Blot DVM, Rivier F, Cazorla O, Parini A, Marks AR, Mialet-Perez J, Lacampagne A, Meli AC.
    J Cachexia Sarcopenia Muscle; 2024 Apr 22; 15(2):536-551. PubMed ID: 38221511
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  • 16. Simvastatin provides long-term improvement of left ventricular function and prevents cardiac fibrosis in muscular dystrophy.
    Kim MJ, Bible KL, Regnier M, Adams ME, Froehner SC, Whitehead NP.
    Physiol Rep; 2019 Mar 22; 7(6):e14018. PubMed ID: 30912308
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  • 17. Effects of stretch-activated channel blockers on [Ca2+]i and muscle damage in the mdx mouse.
    Yeung EW, Whitehead NP, Suchyna TM, Gottlieb PA, Sachs F, Allen DG.
    J Physiol; 2005 Jan 15; 562(Pt 2):367-80. PubMed ID: 15528244
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  • 18. Hierarchical accumulation of RyR post-translational modifications drives disease progression in dystrophic cardiomyopathy.
    Kyrychenko S, Poláková E, Kang C, Pocsai K, Ullrich ND, Niggli E, Shirokova N.
    Cardiovasc Res; 2013 Mar 15; 97(4):666-75. PubMed ID: 23263329
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  • 19. Calcium handling dysfunction and cardiac damage following acute ventricular preload challenge in the dystrophin-deficient mouse heart.
    Haffner V, Nourian Z, Boerman EM, Lambert MD, Hanft LM, Krenz M, Baines CP, Duan D, McDonald KS, Domeier TL.
    Am J Physiol Heart Circ Physiol; 2023 Nov 01; 325(5):H1168-H1177. PubMed ID: 37737731
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