Mots-clés
 > MYOBASE > BIOLOGIE > biologie par appareil > appareil locomoteur > muscle > tissu musculaire > muscle squelettique
muscle squelettiqueSynonyme(s)muscle strié ;striated muscle ;muscle volontaire ;voluntary muscle skeletal muscle |
Mettre toutes les notices dans le panier Faire une suggestion Ajouter un critère de rechercheEtendre la recherche sur niveau(x) vers le bas
Inhibition of cyclooxygenase-1 by nonsteroidal anti-inflammatory drugs demethylates MeR2 enhancer and promotes Mbnl1 transcription in myogenic cells
Huang K, Masuda A, Chen G, et al.
Scientific Reports, 2020, 10, 1
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
Increased Muscleblind levels by chloroquine treatment improve myotonic dystrophy type 1 phenotypes in in vitro and in vivo models
Bargiela A, Sabater-Arcis M, Espinosa-Espinosa J, et al.
Proceedings of the national Academy of sciences of the United States of America, 2019
An embryonic CaVbeta1 isoform promotes muscle mass maintenance via GDF5 signaling in adult mouse
Traoré M, Gentil C, Benedetto C, et al.
Science translational medicine, 2019, 11, 517
Deficiency of Anoctamin 5/TMEM16E causes nuclear positioning defect and impairs Ca(2+) signaling of differentiated C2C12 myotubes
Phuong TTT, An J, Park SH, et al.
The Korean journal of physiology & pharmacology : official journal of the Korean Physiological Society and the Korean Society of Pharmacology, 2019, 23, 6, p 539
Myopathie avec déficit en TK2 : une étude espagnole sur les formes à début tardif
Urtizberea JA
2019
MR fingerprinting for water T1 and fat fraction quantification in fat infiltrated skeletal muscles
Marty B, Carlier PG
Magnetic resonance in medicine, 2019
240th ENMC workshop: The involvement of skeletal muscle stem cells in the pathology of muscular dystrophies 25-27 January 2019, Hoofddorp, The Netherlands
Morgan J, Butler-Browne G, Muntoni F, et al.
Neuromuscular disorders : NMD, 2019, 29, 9, p 704
Phosphorylase Kinase Deficiency : Synonyms: Glycogen Storage Disease Type IX, GSDIX, PhK Deficiency, Phosphorylase b Kinase Deficiency
Herbert M, Goldstein JL, Rehder C, et al.
GeneReviews® [Internet], 2018
Eteplirsen treatment for Duchenne muscular dystrophy: Exon skipping and dystrophin production
Charleston JS, Schnell FJ, Dworzak J, et al.
Neurology, 2018
Muscle MRI in patients with dysferlinopathy: pattern recognition and implications for clinical trials
Diaz-Manera J, Fernández-Torrón R, Llauger J, et al.
Journal of neurology, neurosurgery, and psychiatry, 2018
MicroRNAs in hereditary and sporadic premature aging syndromes and other laminopathies
Frankel D, Delecourt V, Harhouri K, et al.
Aging cell, 2018
Congenital titinopathy: Comprehensive characterisation and pathogenic insights
Oates EC, Jones KJ, Donkervoort S, et al.
Annals of neurology, 2018
Characterization of congenital myopathies at a Korean neuromuscular center
Park YE, Shin JH, Kim HS, et al.
Muscle & Nerve, 2018
Muscle ultrasound elastography and MRI in preschool children with Duchenne muscular dystrophy
Pichiecchio A, Alessandrino F, Bortolotto C, et al.
Neuromuscular disorders : NMD, 2018
Retrospective natural history of thymidine kinase 2 deficiency
Garone C, Taylor RW, Nascimento A, et al.
Journal of medical genetics, 2018
Quantification of lectin fluorescence in GNE myopathy muscle biopsies
Leoyklang P, Class B, Noguchi S, et al.
Muscle & Nerve, 2018
Pompe disease: An Indian series diagnosed on muscle biopsy by ultrastructural characterization
Kakkar A, Sharma MC, Nambirajan A, et al.
Ultrastructural pathology, 2018
Prevalence and mutation spectrum of skeletal muscle channelopathies in the Netherlands
Stunnenberg BC, Raaphorst J, Deenen JCW, et al.
Neuromuscular disorders : NMD, 2018
Progressive fat replacement of muscle contributes to the disease mechanism of patients with single, large-scale deletions of mitochondrial DNA
Hedermann G, Dahlqvist JR, Lokken N, et al.
Neuromuscular disorders : NMD, 2018
Single Intramuscular Injection of AAV-shRNA Reduces DNM2 and Prevents Myotubular Myopathy in Mice
Tasfaout H, Lionello VM, Kretz C, et al.
Molecular therapy : the journal of the American Society of Gene Therapy, 2018
Small-molecule flunarizine increases SMN protein in nuclear Cajal bodies and motor function in a mouse model of spinal muscular atrophy.
Sapaly D, Dos Santos M, Delers P, et al.
Scientific Reports, 2018, 8, 1, p. 2075
Dystrophinopathy muscle biopsies in the genetic testing ERA: One center's data
Carlson CR, Moore SA, Mathews KD
Muscle & Nerve, 2018
