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Dernières publications
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Francesco Galli, Laricia Bragg, Maira Rossi, Daisy Proietti, Laura Perani, et al.. Cell-mediated exon skipping normalizes dystrophin expression and muscle function in a new mouse model of Duchenne Muscular Dystrophy. EMBO Molecular Medicine, 2024, 16 (4), pp.927 - 944. ⟨10.1038/s44321-024-00031-3⟩. ⟨hal-04603972⟩
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Ekaterina Kiseleva, Olesya Serbina, Anna Karpukhina, Vincent Mouly, Yegor S Vassetzky. Interaction between mesenchymal stem cells and myoblasts in the context of facioscapulohumeral muscular dystrophy contributes to the disease phenotype. Journal of Cellular Physiology, 2022, 237 (8), pp.3328-3337. ⟨10.1002/jcp.30789⟩. ⟨hal-03796151⟩
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Chiffres clés
52
Publications avec texte intégral
Open Access
87 %
Mots clés
LTβR
Genetics
Drisapersen
Flavonoid
Differentiation
Fibroblast
Neuromuscular disease
KLF15
Dystrophin
Gut microbiota
Atrial cardiac defects
Autophagosome
Cell-penetrating peptide
Exon Skipping
ITSN1
Human muscle stem/progenitor cells
Computer software
Fear response
Cell Therapy
Gene Therapy
Actin
DsDNA break repair
Exon skipping
CRISPR/Cas9
Chromatin
Allele-specific silencing
Skeletal muscle
DMD
Bioinformatics
Exondys 51
Lamin A/C nuclei
Centronuclear myopathy
Autophagy
Alternative splicing
Myotonic dystrophy
RNA interference
Canine X-linked muscular dystrophy in Japan CXMD J
Exon-skipping
Myogenesis
Acetylcholine receptor subunit epsilon
Insulin
Immortalized dystrophic canine myoblast
Muscular dystrophy
Folding-defective proteins
Antisense morpholino
Endocytosis
CMS
Expanded repeats
3D co-culture
Duchenne muscular dystrophy
Emerin
Conjugation
HDMD/Dmd-null mice
CXCR4
Gene therapy
Antisense oligonucleotide
Muscle
CLS
Fluorescence microscopy
LRP4
Dominant centronuclear myopathy
FoxO
Migration
Dynamin 2
Glucocorticoid-induced muscle atrophy
ICU-acquired weakness
Neuromuscular junction
Culture platform
Immortalisation
Developmental biology
Eteplirsen
Gel electrophoresis
DNM2
Myotube
DiPRO1
Cell biology
CTG⋅CAGn repeat
Glucose
CXCL12
Human
CDNA synthesis
Motor neuron
BMD
Gene network analysis
Allele-specific silencing therapy
Biomimetism
Human artificial chromosomes
BAF
CFTR correctors
Coculture
Clinical trial candidate screening
Fibrosis
Adhesion
DM1 myoblasts
Duchenne Muscular Dystrophy
Becker muscular dystrophy BMD Duchenne muscular dystrophy DMD miRNA nNOS
Becker muscular dystrophy
Adeno-associated viral vector
Bile acid
FSHD