The Cmah-/-mdx mouse: an early onset model of cardiomyopathy for Duchenne muscular dystrophy

被引：0
|
作者：
Betts, C. A. [1 ]
Healicon, R. [1 ]
van Westering, T. L. E. [1 ]
Ball, V. [1 ]
Tyler, D. J. [1 ]
Wood, M. J. A. [1 ]
机构：
[1] Univ Oxford, Dept Physiol Anat & Genet, South Parks Rd, Oxford OX1 3QX, England
来源：
NEUROMUSCULAR DISORDERS | 2016年 / 26卷
关键词：
D O I：
暂无
中图分类号：
R74 [神经病学与精神病学];
学科分类号：
摘要：
P09
引用
收藏
页码：S6 / S7
页数：2
相关论文
共 50 条
  • [1] The aging mdx mouse as a model of cardiomyopathy for Duchenne muscular dystrophy
    Hoey, A
    van Erp, C
    Laws, N
    [J]. JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 2004, 37 (01) : 174 - 174
  • [2] Hypoventilation in the Mdx Mouse Model of Duchenne Muscular Dystrophy
    Burns, David P.
    Arijit, Roy
    McDonald, Fiona
    Wilson, Richard J.
    O'Halloran, Ken D.
    [J]. FASEB JOURNAL, 2016, 30
  • [3] The mdx mouse model as a surrogate for Duchenne muscular dystrophy
    Partridge, Terence A.
    [J]. FEBS JOURNAL, 2013, 280 (17) : 4177 - 4186
  • [4] Spermatogenesis in Mdx Mouse Model of Duchenne Muscular Dystrophy
    Braz, Anine F.
    Gomes, Vilessa A.
    Siman, Veronica A.
    Matta, Sergio L. P.
    Clebis, Naianne K.
    Oliveira, Moacir F.
    Morais, Danielle B.
    Moura, Carlos Eduardo B.
    [J]. ANALYTICAL AND QUANTITATIVE CYTOPATHOLOGY AND HISTOPATHOLOGY, 2018, 40 (03): : 125 - 131
  • [5] A Human-Specific Deletion in Mouse Cmah Increases Disease Severity in the mdx Model of Duchenne Muscular Dystrophy
    Chandrasekharan, Kumaran
    Yoon, Jung Hae
    Xu, Ying
    deVries, Sarah
    Camboni, Marybeth
    Janssen, Paulus M. L.
    Varki, Ajit
    Martin, Paul T.
    [J]. SCIENCE TRANSLATIONAL MEDICINE, 2010, 2 (42)
  • [6] Peptide-conjugated phosphodiamidate oligomer-mediated exon skipping has benefits for cardiac function in mdx and Cmah-/-mdx mouse models of Duchenne muscular dystrophy
    Blain, Alison M.
    Greally, Elizabeth
    McClorey, Graham
    Manzano, Raquel
    Bette, Corinne A.
    Godfrey, Caroline
    O'Donovan, Liz
    Coursindel, Thibault
    Gait, Mike J.
    Wood, Matthew J.
    MacGowan, Guy A.
    Straub, Volker W.
    [J]. PLOS ONE, 2018, 13 (06):
  • [7] THE MDX MOUSE MYOPATHY AS A MODEL DUCHENNE MUSCULAR-DYSTROPHY
    COULTON, G
    CURTIN, N
    MORGAN, J
    PARTIDGE, T
    SLOPER, J
    [J]. JOURNAL OF PATHOLOGY, 1987, 151 (01): : A92 - A92
  • [8] Respiratory Control in the mdx Mouse Model of Duchenne Muscular Dystrophy
    Burns, David P.
    Edge, Deirdre
    O'Malley, Dervla
    O'Halloran, Ken D.
    [J]. ARTERIAL CHEMORECEPTORS IN PHYSIOLOGY AND PATHOPHYSIOLOGY, 2015, 860 : 239 - 244
  • [9] SURAMIN ATTENUATES DYSTROPHIN-DEFICIENT CARDIOMYOPATHY IN THE mdx MOUSE MODEL OF DUCHENNE MUSCULAR DYSTROPHY
    Moreira, Drielen De Oliveira
    Pereira, Juliano Alves
    Tiemi Taniguti, Ana Paula
    Matsumura, Cintia Yuri
    Ferreira Ramos, Luis Alberto
    Areas, Miguel Arcanjo
    Neto, Humberto Santo
    Marques, Maria Julia
    [J]. MUSCLE & NERVE, 2013, 48 (06) : 911 - 919
  • [10] A gene therapy approach to treat cardiomyopathy in the mdx mouse model of Duchenne muscular dystrophy (DMD)
    Rodino-Klapac, Louise
    Joshi, Mandar S.
    Montgomery, Chrystal L.
    Shontz, Kim M.
    Bauer, John Anthony
    Clark, K. Reed
    Mendell, Jerry
    [J]. NEUROLOGY, 2008, 70 (11) : A249 - A249
12345