Mots-clés
 > MYOBASE > BIOLOGIE > biologie par discipline > physiologie > métabolisme > catabolisme > stress oxydatif
stress oxydatifSynonyme(s)oxidative stress |
trié(s) par (Pertinence décroissant(e), Date de parution décroissant(e), Date de parution décroissant(e), Système de projection du document croissant(e)) | Mettre toutes les notices dans le panier | Faire une suggestion | Ajouter un critère de rechercheEtendre la recherche sur niveau(x) vers le bas
Temporary Reduction of Membrane CD4 with the Antioxidant MnTBAP Is Sufficient to Prevent Immune Responses Induced by Gene Transfer
Da Rocha S, Bigot J, Onodi F, et al.
Molecular therapy. Methods & clinical development, 2019, 14, p 285
Antioxidant therapy for muscular dystrophy: caveat lector!
O'Halloran KD, Murphy KH, Burns DP
The Journal of physiology, 2018, 596, 4, p 737
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
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
Muscle redox disturbances and oxidative stress as pathomechanisms and therapeutic targets in early-onset myopathies
Moulin M, Ferreiro A
Seminars in cell & developmental biology, 2017, 64, p 213
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
Pharmacological advances for treatment in Duchenne muscular dystrophy
Guiraud S, Davies KE
Current opinion in pharmacology, 2017, 34, p 36
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, 26, 16, p 3081
Are Antioxidants a Potential Therapy for FSHD? A Review of the Literature
Denny AP, Heather AK
Oxidative medicine and cellular longevity, 2017, 2017
Dystrophic phenotype improvement in the diaphragm muscle of mdx mice by diacerhein
Mancio RD, Hermes TA, Macedo AB, et al.
PLoS ONE, 2017, 12, 8
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, 814, p 161
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
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
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
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, 145, 4, p 475
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, 11, 1
Absence of Dystrophin Disrupts Skeletal Muscle Signaling: Roles of Ca2+, Reactive Oxygen Species, and Nitric Oxide in the Development of Muscular Dystrophy
Allen DG, Whitehead NP, Froehner SC
Physiological reviews, 2016, 96, 1, p 253
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, 58, p 107
Linkage of Stress with Neuromuscular Disorders
Ashraf GM, Ali A, Tabrez S, et al.
CNS & neurological disorders drug targets, 2016, 15, 3, p 321
