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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⟩
Chiffres clés
52
Publications avec texte intégral
Open Access
87 %
Mots clés
Actin
Genetics
Duchenne Muscular Dystrophy
Fibrosis
Cell Therapy
CXCL12
Allele-specific silencing therapy
Alternative splicing
Dynamin 2
DM1 myoblasts
Drisapersen
CTG⋅CAGn repeat
Migration
Gut microbiota
Antisense oligonucleotide
DMD
Adhesion
Antisense morpholino
Human
Muscular dystrophy
Exon Skipping
Differentiation
Atrial cardiac defects
Dominant centronuclear myopathy
Canine X-linked muscular dystrophy in Japan CXMD J
3D co-culture
Emerin
Exon skipping
DsDNA break repair
DiPRO1
Muscle
Gene network analysis
Insulin
FoxO
Immortalized dystrophic canine myoblast
KLF15
Human muscle stem/progenitor cells
Coculture
Duchenne muscular dystrophy
CFTR correctors
Myogenesis
Adeno-associated viral vector
Becker muscular dystrophy BMD Duchenne muscular dystrophy DMD miRNA nNOS
Chromatin
BAF
Allele-specific silencing
Myotube
Computer software
Autophagosome
Becker muscular dystrophy
HDMD/Dmd-null mice
Developmental biology
Centronuclear myopathy
Endocytosis
Fluorescence microscopy
Gene therapy
BMD
FSHD
Exondys 51
Folding-defective proteins
CLS
Eteplirsen
Fear response
CXCR4
LRP4
Flavonoid
Neuromuscular junction
Myotonic dystrophy
Biomimetism
Cell biology
Autophagy
Expanded repeats
Human artificial chromosomes
Skeletal muscle
Gene Therapy
RNA interference
CRISPR/Cas9
Gel electrophoresis
CDNA synthesis
Cell-penetrating peptide
Bioinformatics
Lamin A/C nuclei
Glucose
Immortalisation
Dystrophin
ICU-acquired weakness
CMS
Clinical trial candidate screening
LTβR
Conjugation
Neuromuscular disease
Glucocorticoid-induced muscle atrophy
Acetylcholine receptor subunit epsilon
Exon-skipping
Motor neuron
Culture platform
DNM2
ITSN1
Bile acid
Fibroblast