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régulation métaboliqueSynonyme(s)metabolic regulation |
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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
WANTED - Dead or alive: Myotubularins, a large disease-associated protein family
Raess MA, Friant S, Cowling BS, et al.
Advances in biological regulation, 2017, 63, p 49
Dp71 is regulated by phosphorylation and ubiquitin-proteasome system in neuronal cells
Fujimoto T, Yaoi T, Fushiki S, et al.
Biochemical and biophysical research communications, 2017, 492, 3, p 349
Facioscapulohumeral Muscular Dystrophy
DeSimone AM, Pakula A, Lek A, et al.
Comprehensive Physiology, 2017, 7, 4, p 1229
Molecular combing reveals complex 4q35 rearrangements in Facioscapulohumeral dystrophy
Nguyen K, Puppo F, Roche S, et al.
Human mutation, 2017, 38, 10, p 1432
SMCHD1 regulates a limited set of gene clusters on autosomal chromosomes
Mason AG, Slieker RC, Balog J, et al.
Skeletal Muscle, 2017, 7, 1
Elevated Expression of Moesin in Muscular Dystrophies
Pines M, Levi O, Genin O, et al.
The American journal of pathology, 2017, 187, 3, p 654
Chimeric protein repair of laminin polymerization ameliorates muscular dystrophy phenotype
McKee KK, Crosson SC, Meinen S, et al.
The Journal of clinical investigation, 2017, 127, 3, p 1075
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° 323 to 330 - Nuclear envelopathies (lamin A/C, emerin, others)
Congrès : 5th International Congress of Myology (14-18 March 2016; Centre convention, Lyon, France)
2016, p. 178-181
Myology 2016 : 5th International Congress of Myology ; Posters n° 331 to 337 - Pharmacological therapies
Congrès : 5th International Congress of Myology (14-18 March 2016; Centre convention, Lyon, France)
2016, p. 181-185
Dissecting the role of the myofilament in diaphragm dysfunction during the development of heart failure in mice
Gillis TE, Klaiman JM, Foster A, et al.
American journal of physiology. Heart and circulatory physiology, 2016, 310, 5, p 572
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
Riboflavin transport and metabolism in humans
Barile M, Giancaspero TA, Léone P, et al.
Journal of inherited metabolic disease, 2016, 39, 4, p 545
Targeted Molecular Therapies for SBMA
Rinaldi C, Malik B, Greensmith L
Journal of molecular neuroscience, 2016, 58, 3, p 335
Adenylyl cyclase activating polypeptide reduces phosphorylation and toxicity of the polyglutamine-expanded androgen receptor in spinobulbar muscular atrophy
Polanco MJ, Parodi S, Piol D, et al.
Science translational medicine, 2016, 8, 370
Choline Acetyltransferase Mutations Causing Congenital Myasthenic Syndrome: Molecular Findings and Genotype-Phenotype Correlations.
Arredondo J, Lara M, Gospe SM, et al.
Human mutation, 2015, Epub
Preventing proteostasis diseases by selective inhibition of a phosphatase regulatory subunit
Das I, Krzyzosiak A, Schneider K, et al.
Science, 2015, 348, 6231, p. 239-242
SAM68 is a physiological regulator of SMN2 splicing in spinal muscular atrophy
Pagliarini V, Pelosi L, Bustamante MB, et al.
Journal of cell biology, 2015, 211, 1, p 77
Responses to Fasting and Glucose Loading in a Cohort of Well Children with Spinal Muscular Atrophy Type II
Davis RH, Miller EA, Zhang RZ, et al.
The Journal of pediatrics, 2015, 167, 6, p 1362
High content screening identifies small molecules that remove nuclear foci, affect MBNL distribution and CELF1 protein levels via a PKC independent pathway in myotonic dystrophy cell lines
Ketley A, Chen CZ, Li X, et al.
Human molecular genetics, 2014, 23, 6, p. 1551-1562
Activation of muscle enhancers by MyoD and epigenetic modifiers
Blum R
Journal of cellular biochemistry, 2014, 115, 11, p 1855
Dystrophie myotonique : 2 nouveaux composés capables d’éliminer les agrégats nucléaires
Cukierman L
2013
Phagocytose et cytocinèse : des thèmes communs et des différences
Deschamps C, Echard A, Niedergang F
médecine/sciences, 2013, 29, 11, p. 1004-1009
