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mitochondrieSynonyme(s)mitochondrion mitochondriaVoir aussi |
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Physical and Functional Cross Talk Between Endo-Sarcoplasmic Reticulum and Mitochondria in Skeletal Muscle
Boncompagni S, Pozzer D, Viscomi C, et al.
Antioxidants & redox signaling, 2019
Functional Interplay between Cristae Biogenesis, Mitochondrial Dynamics and Mitochondrial DNA Integrity
Kondadi AK, Anand R, Reichert AS
International Journal of molecular sciences, 2019, 20, 17
Des recommandations pour établir l’histoire naturelle des maladies mitochondriales
Urtizberea JA
2018
Mitochondrial content is preserved throughout disease progression in the mdx mouse model of Duchenne muscular dystrophy, regardless of taurine supplementation
Barker RG, Wyckelsma VL, Xu H, et al.
American journal of physiology. Cell physiology, 2018, 314, 4, p 483
Structure, function, and regulation of mitofusin-2 in health and disease
Chandhok G, Lazarou M, Neumann B
Biological reviews of the Cambridge Philosophical Society, 2018, 93, 2, p 933
A novel mechanism causing imbalance of mitochondrial fusion and fission in human myopathies
Bartsakoulia M, Pyle A, Troncosco D, et al.
Human molecular genetics, 2018, 27, 7, p 1186
Dysregulated autophagy in restrictive cardiomyopathy due to Pro209Leu mutation in BAG3
Schänzer A, Rupp S, Graf S, et al.
Molecular genetics and metabolism, 2018, 123, 3, p 388
Prévenir la transmission des mutations de l'ADN mitochondrial par don de cytoplasme : où en est-on ?
Steffann J, Bonnefont JP, Frydman N
médecine/sciences, 2017, 33, 6-7, p 642
IFN-beta-induced reactive oxygen species and mitochondrial damage contribute to muscle impairment and inflammation maintenance in dermatomyositis
Meyer A, Laverny G, Allenbach Y, et al.
Acta neuropathologica, 2017, 134, 4, p 655
Advances in understanding the role of disease-associated proteins in spinal muscular atrophy
Hosseinibarkooie S, Schneider S, Wirth B
Expert review of proteomics, 2017, 14, 7, p 581
Riboflavin Responsive Mitochondrial Dysfunction in Neurodegenerative Diseases
Udhayabanu T, Manole A, Rajeshwari M, et al.
Journal of clinical medicine, 2017, 6, 5
A newly distal hereditary motor neuropathy caused by a rare AIFM1 mutation
Sancho P, Sánchez-Monteagudo A, Collado A, et al.
Neurogenetics, 2017, 18, 4, p 245
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
Bioenergetic status modulates motor neuron vulnerability and pathogenesis in a zebrafish model of spinal muscular atrophy
Boyd PJ, Tu WY, Shorrock HK, et al.
PLoS Genetics, 2017, 13, 4
Peptide-mediated delivery of donor mitochondria improves mitochondrial function and cell viability in human cybrid cells with the MELAS A3243G mutation
Chang JC, Hoel F, Liu KH, et al.
Scientific Reports, 2017, 7, 1
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
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 ; Symposium - Mitochondria
Hashemolhosseini S, Jimenez-Mallebrera C, Rötig A
Congrès : 5th International Congress of Myology (14-18 March 2016; Centre convention, Lyon, France)
2016, p. 3
Myology 2016 : 5th International Congress of Myology ; Posters n° 1 to 17 - Adult muscle regeneration / muscle regeneration
Congrès : 5th International Congress of Myology (14-18 March 2016; Centre convention, Lyon, France)
2016, p. 26-33
Myology 2016 : 5th International Congress of Myology ; Posters n° 189 to 207 - Metabolic and Mitochondrial Disorders
Congrès : 5th International Congress of Myology (14-18 March 2016; Centre convention, Lyon, France)
2016, p. 113-122
Myology 2016 : 5th International Congress of Myology ; Posters n° 66 to 75 - Congenital muscular dystrophies / Dystrophinopathies
Congrès : 5th International Congress of Myology (14-18 March 2016; Centre convention, Lyon, France)
2016, p. 55-59
Bicyclic-Capped Histone Deacetylase 6 Inhibitors with Improved Activity in a Model of Axonal Charcot-Marie-Tooth Disease
Shen S, Benoy V, Bergman JA, et al.
ACS chemical neuroscience, 2016, 7, 2, p 240
Downstream effects of plectin mutations in epidermolysis bullosa simplex with muscular dystrophy
Winter L, Türk M, Harter PN, et al.
Acta neuropathologica communications, 2016, 4, 1
The Biochemistry and Physiology of Mitochondrial Fatty Acid Beta-Oxidation and Its Genetic Disorders
Houten SM, Violante S, Ventura FV, et al.
Annual review of physiology, 2016, 78, p 23
Zebrafish Tg(hb9:MTS-Kaede): a new in vivo tool for studying the axonal movement of mitochondria
Bergamin G, Cieri D, Vazza G, et al.
Biochimica et biophysica acta, 2016, 1860, 6, p 1247
