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