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stress oxydatifSynonyme(s)oxidative stress |
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Antioxidant therapy for muscular dystrophy: caveat lector!
O'Halloran KD, Murphy KH, Burns DP
The Journal of physiology, 2018, 596, 4, p. 737-738
Reply from Gavin J. Pinniger, Jessica R. Terrill, Miranda D. Grounds and Peter G. Arthur.
Pinniger GJ, Terrill JR, Grounds MD, et al.
The Journal of physiology, 2018, 596, 4, p. 739
Pre-clinical evaluation of N-acetylcysteine reveals side effects in the mdx mouse model of Duchenne muscular dystrophy.
Pinniger GJ, Terrill JR, Assan EB, et al.
The Journal of physiology, 2017, 595, 23, p. 7093-7107
Edaravone is a candidate agent for spinal muscular atrophy: In vitro analysis using a human induced pluripotent stem cells-derived disease model.
Ando S, Funato M, Ohuchi K, et al.
European journal of pharmacology, 2017, Epub, 8 p.
Dystrophic phenotype improvement in the diaphragm muscle of mdx mice by diacerhein.
Mancio RD, Hermes TA, Macedo AB, et al.
Department of Structural and Functional Biology (Institute of Biology, State University of Campinas (UNICAMP), Campinas, Sao Paulo, Brazil., Department of Structural and Functional Biology, Institute of Biology, State University of Campinas (UNICAMP), Campinas, Sao Paulo, Brazil., Department of Structur)
PLoS ONE, 2017, e0182449, 13 p.
Une équipe de l'Institut de myologie primée par la fondation Prize4Life : La recherche : thérapeutiques
Dupuy-Maury F
VLM. Vaincre les myopathies, 2017, 181, p. 14-15
Sialic acid deficiency is associated with oxidative stress leading to muscle atrophy and weakness in the GNE myopathy.
Cho A, Malicdan MCV, Miyakawa M, et al.
Human molecular genetics, 2017, Epub, 13 p.
Pharmacological advances for treatment in Duchenne muscular dystrophy.
Guiraud S, Davies KE
Current opinion in pharmacology, 2017, 34, Epub, p. 36-48
Endoplasmic Reticulum Oxidative Stress Triggers Tgf-Beta-Dependent Muscle Dysfunction by Accelerating Ascorbic Acid Turnover.
Pozzer D, Favellato M, Bolis M, et al.
Scientific Reports, 2017, 7, p. 40993
Are Antioxidants a Potential Therapy for FSHD? A Review of the Literature.
Denny AP, Heather AK
Oxidative medicine and cellular longevity, 2017, 2017, 10 p.
Antioxidant Treatment Reduces Formation of Structural Cores and Improves Muscle Function in RYR1(Y522S/WT) Mice.
Michelucci A, De Marco A, Guarnier FA, et al.
Oxidative medicine and cellular longevity, 2017, 2017, 15 p.
Muscle redox disturbances and oxidative stress as pathomechanisms and therapeutic targets in early-onset myopathies
Moulin M, Ferreiro A
Seminars in cell & developmental biology, 2016, Epub, 30 p.
217th ENMC International Workshop: RYR1-related myopathies, Naarden, The Netherlands, 29-31 January 2016
Jungbluth H, Dowling JJ, Ferreiro A, et al.
Neuromuscular disorders : NMD, 2016, Epub, 10 p.
Quantitative proteome profiling of dystrophic dog skeletal muscle reveals a stabilized muscular architecture and protection against oxidative stress after systemic delivery of MuStem cells.
Lardenois A, Jagot S, Lagarrigue M, et al.
Proteomics, 2016, 24 p.
Impact d'un traitement antioxydant sur le transfert de gène par un vecteur AAVr dans un modèle murin de la dystrophie musculaire de Duchenne
Dupont JB, Tournaire B, Durand R, et al.
Les Cahiers de Myologie, 2016, 13, p. 99-101
Myology 2016 : 5th International Congress of Myology ; Symposium - Muscle Ageing
Sandri M, Butler-Browne G, Perdiguero E
Congrès : 5th International Congress of Myology (14-18 March 2016; Centre convention, Lyon, France)
2016, p. 20-21
A small-molecule Nrf1 and Nrf2 activator mitigates polyglutamine toxicity in spinal and bulbar muscular atrophy.
Bott LC, Badders NM, Chen KL, et al.
Human molecular genetics, 2016, Epub, 11 p.
Myology 2016 : 5th International Congress of Myology ; Posters n° 50 to 65 - Cardiac stem cells, cardiogenesis and cardiomyopathies
Congrès : 5th International Congress of Myology (14-18 March 2016; Centre convention, Lyon, France)
2016, p. 47-55
Myology 2016 : 5th International Congress of Myology ; Posters n° 275 to 283 - Muscle function
Congrès : 5th International Congress of Myology (14-18 March 2016; Centre convention, Lyon, France)
2016, p. 156-159
Myology 2016 : 5th International Congress of Myology ; Posters n° 388 to 423 - Young Investigator Posters
Congrès : 5th International Congress of Myology (14-18 March 2016; Centre convention, Lyon, France)
2016, p. 205-222
Facioscapulohumeral dystrophy myoblasts efficiently repair moderate levels of oxidative DNA damage.
Bou Saada Y, Dib C, Dmitriev P, et al.
Histochemistry and cell biology, 2016, Epub, 9 p.
A Study of a Cohort of X-Linked Myotubular Myopathy at the Clinical, Histologic, and Genetic Levels
Abath Neto O, Silva MR, Martins CA, et al.
Pediatric neurology, 2016, Epub, 6 p.
Improved Muscle Function in Duchenne Muscular Dystrophy through L-Arginine and Metformin: An Investigator-Initiated, Open-Label, Single-Center, Proof-Of-Concept-Study.
Hafner P, Bonati U, Erne B, et al.
PLoS ONE, 2016, 19 p.
The role of oxidative stress in skeletal muscle injury and regeneration: focus on antioxidant enzymes.
Kozakowska M, Pietraszek-Gremplewicz K, Jozkowicz A, et al.
Journal of muscle research and cell motility, 2016, Epub, 17 p.
