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

页码：1858 / 1859

页数：2

共 50 条

[21] Expression of Heat Shock Proteins in Skeletal Muscle from Idiopathic Inflammatory Myopathy and Duchenne Muscular Dystrophy Patients
De Bleecker, Jan L.
Creus, Kim K.
Martin, Jean-Jacques
Weis, Joachim
De Paepe, Boel
NEUROLOGY, 2010, 74 (09) : A438 - A438
[22] Skeletal muscle of patients with Duchenne's muscular dystrophy: Evidence of a mitochondrial proteolytic factor responsible for calmitine deficiency
LucasHeron, B
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1996, 223 (01) : 31 - 35
[23] Poly A RNA status and expression of milli (m) and micro (μ) calpains in skeletal muscle of duchenne muscular dystrophy patients
Mangat H.
Hussain T.
Sundaram C.
Anandaraj M.P.J.S.
Indian Journal of Clinical Biochemistry, 2002, 17 (2) : 74 - 79
[24] Absence of a calmitine-specific protease inhibitor in skeletal muscle mitochondria of patients with Duchenne's muscular dystrophy
LucasHeron, B
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1996, 225 (03) : 701 - 704
[25] Reply to F. Muntoni et al.: "In response to PR Clemens et al., Efficacy and Safety of Viltolarsen in Boys with Duchenne Muscular Dystrophy: Results From the Phase 2, Open-Label, 4-Year Extension Study, and Long-Term Functional Efficacy and Safety of Viltolarsen in Patients with Duchenne Muscular Dystrophy
Clemens, Paula R.
Hoffman, Eric P.
JOURNAL OF NEUROMUSCULAR DISEASES, 2023, 10 (06) : 1155 - 1157
[26] ION CHANNELS AND RECEPTORS IN SKELETAL-MUSCLE CELL-LINES FROM DUCHENNE MUSCULAR-DYSTROPHY PATIENTS
CAVIEDES, P
CAVIEDES, R
LIBERONA, JL
JAIMOVICH, E
BIOPHYSICAL JOURNAL, 1994, 66 (02) : A90 - A90
[27] Expression of the gene for large subunit of m-calpain is elevated in skeletal muscle from Duchenne muscular dystrophy patients
Hussain, T
Mangath, H
Sundaram, C
Anandaraj, MPJS
JOURNAL OF GENETICS, 2000, 79 (02) : 77 - 80
[28] Expression of the gene for large subunit of m-calpain is elevated in skeletal muscle from Duchenne muscular dystrophy patients
Tajamul Hussain
Harleen Mangath
C. Sundaram
M. P. J. S. Anandaraj
Journal of Genetics, 2000, 79 : 77 - 80
[29] Neopterin/7,8-dihydroneopterin is elevated in Duchenne muscular dystrophy patients and protects mdx skeletal muscle function
Lindsay, Angus
Schmiechen, Alexandra
Chamberlain, Christopher M.
Ervasti, James M.
Lowe, Dawn A.
EXPERIMENTAL PHYSIOLOGY, 2018, 103 (07) : 995 - 1009
[30] Skeletal muscle water T2 as a biomarker of disease status and exercise effects in patients with Duchenne muscular dystrophy
Mankodi, Ami
Azzabou, Noura
Bulea, Thomas
Reyngoudt, Harmen
Shimellis, Hirity
Ren, Yupeng
Kim, Eunhee
Fischbeck, Kenneth H.
Carlier, Pierre G.
NEUROMUSCULAR DISORDERS, 2017, 27 (08) : 705 - 714

← 1 2 3 4 5 →