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There are 7584 results for: content related to: The heart in Duchenne muscular dystrophy: early detection of contractile performance alteration

  1. You have full text access to this OnlineOpen article
    Disease course in mdx:utrophin+/− mice: comparison of three mouse models of Duchenne muscular dystrophy

    Physiological Reports

    Volume 3, Issue 4, April 2015, Abby A. McDonald, Sadie L. Hebert, Matthew D. Kunz, Steven J. Ralles and Linda K. McLoon

    Version of Record online : 28 APR 2015, DOI: 10.14814/phy2.12391

  2. Small Fractions of Muscular Dystrophy Embryonic Stem Cells Yield Severe Cardiac and Skeletal Muscle Defects in Adult Mouse Chimeras

    STEM CELLS

    Volume 35, Issue 3, March 2017, Pages: 597–610, J. Patrick Gonzalez, Sergii Kyrychenko, Viktoriia Kyrychenko, Joel S. Schneider, Celine J. Granier, Eric Himelman, Kevin C. Lahey, Qingshi Zhao, Ghassan Yehia, Yuan-Xiang Tao, Mantu Bhaumik, Natalia Shirokova and Diego Fraidenraich

    Version of Record online : 2 NOV 2016, DOI: 10.1002/stem.2518

  3. You have free access to this content
    Activated calcineurin ameliorates contraction-induced injury to skeletal muscles of mdx dystrophic mice

    The Journal of Physiology

    Volume 575, Issue 2, September 2006, Pages: 645–656, Nicole Stupka, David R. Plant, Jonathan D. Schertzer, Tennent M. Emerson, Rhonda Bassel-Duby, Eric N. Olson and Gordon S. Lynch

    Version of Record online : 24 AUG 2006, DOI: 10.1113/jphysiol.2006.108472

  4. Postnatal Hyperplasic Effects of ActRIIB Blockade in a Severely Dystrophic Muscle

    Journal of Cellular Physiology

    Volume 232, Issue 7, July 2017, Pages: 1774–1793, Cory Nielsen, Ross M. Potter, Christopher Borowy, Kimberly Jacinto, Ravi Kumar and C. George Carlson

    Version of Record online : 16 FEB 2017, DOI: 10.1002/jcp.25694

  5. You have free access to this content
    Low Six4 and Six5 gene dosage improves dystrophic phenotype and prolongs life span of mdx mice

    Development, Growth & Differentiation

    Volume 58, Issue 6, August 2016, Pages: 546–561, Hiroshi Yajima and Kiyoshi Kawakami

    Version of Record online : 25 MAY 2016, DOI: 10.1111/dgd.12290

  6. Restoration of pharyngeal dilator muscle force in dystrophin-deficient (mdx) mice following co-treatment with neutralizing interleukin-6 receptor antibodies and urocortin 2

    Experimental Physiology

    Volume 102, Issue 9, 1 September 2017, Pages: 1177–1193, David P. Burns, Jane Rowland, Leonie Canavan, Kevin H. Murphy, Molly Brannock, Dervla O'Malley, Ken D. O'Halloran and Deirdre Edge

    Version of Record online : 6 AUG 2017, DOI: 10.1113/EP086232

  7. Sildenafil reduces respiratory muscle weakness and fibrosis in the mdx mouse model of Duchenne muscular dystrophy

    The Journal of Pathology

    Volume 228, Issue 1, September 2012, Pages: 77–87, Justin M Percival, Nicholas P Whitehead, Marvin E Adams, Candace M Adamo, Joseph A Beavo and Stanley C Froehner

    Version of Record online : 18 JUL 2012, DOI: 10.1002/path.4054

  8. You have free access to this content
    Sensorimotor control of breathing in the mdx mouse model of Duchenne muscular dystrophy

    The Journal of Physiology

    Volume 595, Issue 21, 1 November 2017, Pages: 6653–6672, David P. Burns, Arijit Roy, Eric F. Lucking, Fiona B. McDonald, Sam Gray, Richard J. Wilson, Deirdre Edge and Ken D. O'Halloran

    Version of Record online : 9 OCT 2017, DOI: 10.1113/JP274792

  9. You have free access to this content
    Increasing taurine intake and taurine synthesis improves skeletal muscle function in the mdx mouse model for Duchenne muscular dystrophy

    The Journal of Physiology

    Volume 594, Issue 11, 1 June 2016, Pages: 3095–3110, Jessica R. Terrill, Gavin J. Pinniger, Jamie A. Graves, Miranda D. Grounds and Peter G. Arthur

    Version of Record online : 18 JAN 2016, DOI: 10.1113/JP271418

  10. T and B lymphocyte depletion has a marked effect on the fibrosis of dystrophic skeletal muscles in the scid/mdx mouse

    The Journal of Pathology

    Volume 213, Issue 2, October 2007, Pages: 229–238, A Farini, M Meregalli, M Belicchi, M Battistelli, D Parolini, G D'Antona, M Gavina, L Ottoboni, G Constantin, R Bottinelli and Y Torrente

    Version of Record online : 31 JUL 2007, DOI: 10.1002/path.2213

  11. You have free access to this content
    Force and power output of fast and slow skeletal muscles from mdx mice 6-28 months old

    The Journal of Physiology

    Volume 535, Issue 2, September 2001, Pages: 591–600, Gordon S. Lynch, Richard T. Hinkle, Jeffrey S. Chamberlain, Susan V. Brooks and John A. Faulkner

    Version of Record online : 5 AUG 2004, DOI: 10.1111/j.1469-7793.2001.00591.x

  12. Impaired respiratory function in mdx and mdx/utrn+/− mice

    Muscle & Nerve

    Volume 43, Issue 2, February 2011, Pages: 263–267, Ping Huang, Georgiana Cheng, Haiyan Lu, Mark Aronica, Richard M. Ransohoff and Lan Zhou

    Version of Record online : 19 JAN 2011, DOI: 10.1002/mus.21848

  13. You have full text access to this OnlineOpen article
    Disruption of action potential and calcium signaling properties in malformed myofibers from dystrophin-deficient mice

    Physiological Reports

    Volume 3, Issue 4, April 2015, Erick O. Hernández-Ochoa, Stephen J. P. Pratt, Karla P. Garcia-Pelagio, Martin F. Schneider and Richard M. Lovering

    Version of Record online : 23 APR 2015, DOI: 10.14814/phy2.12366

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    Long-term dietary quercetin enrichment as a cardioprotective countermeasure in mdx mice

    Experimental Physiology

    Volume 102, Issue 6, 1 June 2017, Pages: 635–649, Christopher Ballmann, Thomas Denney, Ronald J. Beyers, Tiffany Quindry, Matthew Romero, Joshua T. Selsby and John C. Quindry

    Version of Record online : 30 MAR 2017, DOI: 10.1113/EP086091

  15. Characterization of neuromuscular synapse function abnormalities in multiple Duchenne muscular dystrophy mouse models

    European Journal of Neuroscience

    Volume 43, Issue 12, June 2016, Pages: 1623–1635, Elizabeth M. van der Pijl, Maaike van Putten, Erik H. Niks, Jan J. G. M. Verschuuren, Annemieke Aartsma-Rus and Jaap J. Plomp

    Version of Record online : 9 MAY 2016, DOI: 10.1111/ejn.13249

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    Branched fibres in old dystrophic mdx muscle are associated with mechanical weakening of the sarcolemma, abnormal Ca2+ transients and a breakdown of Ca2+ homeostasis during fatigue

    Experimental Physiology

    Volume 95, Issue 5, May 2010, Pages: 641–656, Stewart I. Head

    Version of Record online : 13 APR 2010, DOI: 10.1113/expphysiol.2009.052019

  17. You have free access to this content
    Utrophin regulates modal gating of mechanosensitive ion channels in dystrophic skeletal muscle

    The Journal of Physiology

    Volume 592, Issue 15, 1 August 2014, Pages: 3303–3323, Nhi Tan and Jeffry B. Lansman

    Version of Record online : 25 JUN 2014, DOI: 10.1113/jphysiol.2014.274332

  18. You have free access to this content
    Endogenous Mesenchymal Stromal Cells in Bone Marrow Are Required to Preserve Muscle Function in mdx Mice

    STEM CELLS

    Volume 33, Issue 3, March 2015, Pages: 962–975, Ryo Fujita, Katsuto Tamai, Eriko Aikawa, Keisuke Nimura, Saki Ishino, Yasushi Kikuchi and Yasufumi Kaneda

    Version of Record online : 17 FEB 2015, DOI: 10.1002/stem.1900

  19. You have free access to this content
    N-Acetylcysteine ameliorates skeletal muscle pathophysiology in mdx mice

    The Journal of Physiology

    Volume 586, Issue 7, April 2008, Pages: 2003–2014, Nicholas P. Whitehead, Catherine Pham, Othon L. Gervasio and David G. Allen

    Version of Record online : 31 MAR 2008, DOI: 10.1113/jphysiol.2007.148338

  20. Muscle function and running activity in mouse models of hereditary muscle dystrophy: Impact of double knockout for dystrophin and the transcription factor MyoD

    Muscle & Nerve

    Volume 45, Issue 4, April 2012, Pages: 544–551, Norman Mangner, Volker Adams, Marcus Sandri, Robert Hoellriegel, Rainer Hambrecht, Gerhard Schuler and Stephan Gielen

    Version of Record online : 16 MAR 2012, DOI: 10.1002/mus.22318