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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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Muhammad Haseeb Iqbal, Jeanne Rosine Faratiana, Emeline Pradel, Varvara Gribova, Kamel Mamchaoui, et al.. Brush-Induced Orientation of Collagen Fibers in Layer-by-Layer Nanofilms: A Simple Method for the Development of Human Muscle Fibers. ACS Nano, In press, ⟨10.1021/acsnano.2c06329⟩. ⟨hal-03832239⟩
Chiffres clés
52
Publications avec texte intégral
Open Access
87 %
Mots clés
Antisense morpholino
Gene therapy
Dynamin 2
Lamin A/C nuclei
BMD
Dystrophin
Neuromuscular junction
Muscle
Allele-specific silencing therapy
Myotonic dystrophy
CXCR4
Fluorescence microscopy
Alternative splicing
Myotube
CFTR correctors
DNM2
Immortalized dystrophic canine myoblast
Becker muscular dystrophy BMD Duchenne muscular dystrophy DMD miRNA nNOS
Glucocorticoid-induced muscle atrophy
Autophagosome
3D co-culture
Duchenne muscular dystrophy
Immortalisation
DiPRO1
RNA interference
Exondys 51
Muscular dystrophy
Adhesion
Gel electrophoresis
Human muscle stem/progenitor cells
Allele-specific silencing
Conjugation
Motor neuron
FSHD
Bioinformatics
Exon skipping
Clinical trial candidate screening
Migration
BAF
Skeletal muscle
Biomimetism
Neuromuscular disease
CTG⋅CAGn repeat
DM1 myoblasts
Fear response
Atrial cardiac defects
Bile acid
Drisapersen
Human artificial chromosomes
Chromatin
Becker muscular dystrophy
LRP4
Gut microbiota
Centronuclear myopathy
Endocytosis
HDMD/Dmd-null mice
Myogenesis
Dominant centronuclear myopathy
Emerin
Gene Therapy
ICU-acquired weakness
LTβR
Cell biology
Flavonoid
Coculture
Insulin
Fibrosis
Computer software
DMD
Gene network analysis
Antisense oligonucleotide
Folding-defective proteins
DsDNA break repair
FoxO
Differentiation
Actin
Eteplirsen
Culture platform
CRISPR/Cas9
Adeno-associated viral vector
Exon-skipping
CMS
CXCL12
Canine X-linked muscular dystrophy in Japan CXMD J
Expanded repeats
Human
Autophagy
Cell-penetrating peptide
CLS
KLF15
Developmental biology
Genetics
Duchenne Muscular Dystrophy
Acetylcholine receptor subunit epsilon
Glucose
CDNA synthesis
Fibroblast
Exon Skipping
Cell Therapy
ITSN1