Aberrant Respiratory Control in the Mdx Mouse Model of Duchenne Muscular Dystrophy

被引:0
|
作者
Burns, David P. [1 ]
Lucking, Eric [1 ]
Roy, Arijit [2 ]
Murphy, Kevin [1 ]
McDonald, Fiona B. [2 ]
Wilson, Richard [2 ]
Edge, Deirdre [3 ]
O'Halloran, Ken D. [1 ]
机构
[1] Univ Coll Cork, Physiol, Cork, Ireland
[2] Univ Calgary, Physiol & Pharmacol, Calgary, AB, Canada
[3] Trinity Coll Dublin, Physiol, Dublin, Ireland
来源
FASEB JOURNAL | 2017年 / 31卷
关键词
D O I
暂无
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
873.2
引用
收藏
页数:1
相关论文
共 50 条
  • [31] Cerebellar dysfunction in the mdx mouse model of Duchenne muscular dystrophy: An electrophysiological and behavioural study
    Prigogine, Cynthia
    Ruiz, Javier Marquez
    Cebolla, Ana Maria
    Deconinck, Nicolas
    Servais, Laurent
    Gailly, Philippe
    Dan, Bernard
    Cheron, Guy
    EUROPEAN JOURNAL OF NEUROSCIENCE, 2024, 60 (10) : 6470 - 6489
  • [32] Sildenafil Ameliorates Skeletal Muscle Pathology in the mdx Mouse Model of Duchenne Muscular Dystrophy
    Percival, Justin
    Whitehead, Nicholas
    Siegel, Michael
    Gray, Heidi
    Adamo, Candace
    Marcinek, David
    Beavo, Joseph
    Froehner, Stanley
    FASEB JOURNAL, 2011, 25
  • [33] Body-wide gene therapy of Duchenne muscular dystrophy in the mdx mouse model
    Denti, MA
    Rosa, A
    D'Antona, G
    Sthandier, O
    De Angelis, FG
    Nicoletti, C
    Allocca, M
    Pansarasa, O
    Parente, V
    Musarò, A
    Auricchio, A
    Bottinelli, R
    Bozzoni, I
    PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2006, 103 (10) : 3758 - 3763
  • [34] Resveratrol ameliorates skeletal muscle function in the mdx mouse, a model of Duchenne muscular dystrophy
    Sebori, Rio
    Kuno, Atsushi
    Hayashi, Takashi
    Hosoda, Ryusuke
    Hori, Yusuke
    Horio, Yoshiyuki
    JOURNAL OF PHARMACOLOGICAL SCIENCES, 2013, 121 : 69P - 69P
  • [35] Altered visual processing in the mdx52 mouse model of Duchenne muscular dystrophy
    Salgueiro Barboni, Mirella Telles
    Passos Liber, Andre Mauricio
    Joachimsthaler, Anneka
    Saoudi, Amel
    Goyenvalle, Aurelie
    Rendon, Alvaro
    Roger, Jerome E.
    Ventura, Dora Fix
    Kremers, Jan
    Vaillend, Cyrille
    NEUROBIOLOGY OF DISEASE, 2021, 152
  • [36] Ventilatory Chemosensory Drive Is Blunted in the mdx Mouse Model of Duchenne Muscular Dystrophy (DMD)
    Mosqueira, Matias
    Baby, Santhosh M.
    Lahiri, Sukhamay
    Khurana, Tejvir S.
    PLOS ONE, 2013, 8 (07):
  • [37] In vivo cerebellar circuit function is disrupted in an mdx mouse model of Duchenne muscular dystrophy
    Stay, Trace L.
    Miterko, Lauren N.
    Arancillo, Marife
    Lin, Tao
    Sillitoe, Roy, V
    DISEASE MODELS & MECHANISMS, 2020, 13 (02)
  • [38] Klotho gene silencing promotes pathology in the mdx mouse model of Duchenne muscular dystrophy
    Wehling-Henricks, Michelle
    Li, Zhenzhi
    Lindsey, Catherine
    Wang, Ying
    Welc, Steven S.
    Ramos, Julian N.
    Khanlou, Negar
    Kuro-o, Makoto
    Tidball, James G.
    HUMAN MOLECULAR GENETICS, 2016, 25 (12) : 2465 - 2482
  • [39] Resveratrol decreases inflammation and oxidative stress in the mdx mouse model of duchenne muscular dystrophy
    Gordon, Bradley Scott
    Weed, Patti
    Learner, Emily
    Schoenling, Drew
    Kostek, Matthew C.
    FASEB JOURNAL, 2012, 26
  • [40] Effective correction of the mdx dystrophin gene mutation in the mouse model of Duchenne muscular dystrophy
    Todaro, M
    Wong, SHA
    Kita, M
    Quigley, AF
    Lowes, KN
    Marotta, R
    Cook, MJ
    Kornberg, AJ
    Kapsa, RMI
    NEUROMUSCULAR DISORDERS, 2005, 15 (9-10) : 714 - 714