Comment on: "Aldehyde dehydrogenases contribute to skeletal muscle homeostasis in healthy, aging, and Duchenne muscular dystrophy patients" by Etienne et al.

被引：0
|
作者：
Campos, Juliane C. [1 ]
Chen, Che-Hong [2 ]
Ferreira, Julio C. B. [1 ,2 ]
机构：
[1] Univ Sao Paulo, Inst Biomed Sci, Sao Paulo, Brazil
[2] Stanford Univ, Sch Med, Dept Chem & Syst Biol, Stanford, CA 94305 USA
来源：
JOURNAL OF CACHEXIA SARCOPENIA AND MUSCLE | 2020年 / 11卷 / 06期
基金：
巴西圣保罗研究基金会; 美国国家卫生研究院;
关键词：
ACTIVATION;
D O I：
10.1002/jcsm.12609
中图分类号：
R592 [老年病学]; C [社会科学总论];
学科分类号：
03 ; 0303 ; 100203 ;
摘要：
引用
收藏
页码：1858 / 1859
页数：2
相关论文
共 50 条
  • [1] The authors reply: Comment on: "Aldehyde dehydrogenases contribute to skeletal muscle homeostasis in healthy, aging, and Duchenne muscular dystrophy patients" by Etienne et al.
    Etienne, Jessy
    Joanne, Pierre
    Catelain, Cyril
    Riveron, Stephanie
    Bayer Wildberger, Alexandra
    Lafable, Jeremy
    Punzon, Isabel
    Blot, Stephane
    Agbulut, Onnik
    Vilquin, Jean-Thomas
    JOURNAL OF CACHEXIA SARCOPENIA AND MUSCLE, 2020, 11 (06) : 1860 - 1862
  • [2] Aldehyde dehydrogenases contribute to skeletal muscle homeostasis in healthy, aging, and Duchenne muscular dystrophy patients
    Etienne, Jessy
    Joanne, Pierre
    Catelain, Cyril
    Riveron, Stephanie
    Bayer, Alexandra Clarissa
    Lafable, Jeremy
    Punzon, Isabel
    Blot, Stephane
    Agbulut, Onnik
    Vilquin, Jean-Thomas
    JOURNAL OF CACHEXIA SARCOPENIA AND MUSCLE, 2020, 11 (04) : 1047 - 1069
  • [3] Evaluation of skeletal muscle DTI in patients with duchenne muscular dystrophy
    Hooijmans, M. T.
    Damon, B. M.
    Froeling, M.
    Versluis, M. J.
    Burakiewicz, J.
    Verschuuren, J. J. G. M.
    Niks, E. H.
    Webb, A. G.
    Kan, H. E.
    NMR IN BIOMEDICINE, 2015, 28 (11) : 1589 - 1597
  • [4] Response to Hamid et al., "Equitable Access of Delandistrogene Moxeparvovec for Patients With Duchenne Muscular Dystrophy"
    Urion, David K.
    Cabello, Juan Francisco
    Salinas, Rodrigo
    PEDIATRIC NEUROLOGY, 2024, 161 : 227 - 228
  • [5] Skeletal muscle homeostasis in Duchenne muscular dystrophy: modulating autophagy as a promising therapeutic strategy
    De Palma, Clara
    Perrotta, Cristiana
    Pellegrino, Paolo
    Clementi, Emilio
    Cervia, Davide
    FRONTIERS IN AGING NEUROSCIENCE, 2014, 6
  • [6] Comment on Smith et al., "Healthy Aging in China''
    Mohanty, Sanjay K.
    JOURNAL OF THE ECONOMICS OF AGEING, 2014, 4 : 44 - +
  • [7] ABNORMALITIES OF CREATINASE IN SKELETAL-MUSCLE OF PATIENTS WITH DUCHENNE MUSCULAR-DYSTROPHY
    MIYOSHI, K
    TAIRA, A
    YOSHIDA, K
    TAMURA, K
    UGA, S
    PROCEEDINGS OF THE JAPAN ACADEMY SERIES B-PHYSICAL AND BIOLOGICAL SCIENCES, 1980, 56 (02): : 99 - 101
  • [8] Repetitive elements transcription and mobilization contribute to human skeletal muscle differentiation and Duchenne muscular dystrophy progression
    Bodega, B.
    Geoff, F.
    Yoshihide, H.
    Piero, C.
    Valerio, O.
    FEBS JOURNAL, 2011, 278 : 75 - 76
  • [9] Repetitive elements transcription and mobilization contribute to human skeletal muscle differentiation and duchenne muscular dystrophy progression
    Bodega, B.
    Geoff, F.
    Yoshihide, H.
    Piero, C.
    Valerio, O.
    FEBS JOURNAL, 2011, 278 : 6 - 6
  • [10] Rebuttal to: Simvastatin Treatment Does Not Ameliorate Muscle Pathophysiology in a Mouse Model for Duchenne Muscular Dystrophy, Verhaart et al. 2020
    Whitehead, N. P.
    Kim, M. J.
    Bible, K. L.
    Adams, M. E.
    Froehner, S. C.
    JOURNAL OF NEUROMUSCULAR DISEASES, 2021, 8 (05) : 865 - 866
12345