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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⟩
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Elena Marchesi, Matteo Bovolenta, Lorenzo Preti, Massimo L Capobianco, Kamel Mamchaoui, et al.. Synthesis and Exon-Skipping Properties of a 3′-Ursodeoxycholic Acid-Conjugated Oligonucleotide Targeting DMD Pre-mRNA: Pre-Synthetic versus Post-Synthetic Approach. Molecules, 2021, 26 (24), pp.7662. ⟨10.3390/molecules26247662⟩. ⟨hal-03510261⟩
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Manuel Schmidt, Anja Weidemann, Christine Poser, Anne Bigot, Julia von Maltzahn. Stimulation of Non-canonical NF-κB Through Lymphotoxin-β-Receptor Impairs Myogenic Differentiation and Regeneration of Skeletal Muscle. Frontiers in Cell and Developmental Biology, 2021, 9, ⟨10.3389/fcell.2021.721543⟩. ⟨hal-03405959⟩
Chiffres clés
Open Access
87 %
Mots clés
DNM2
Gene therapy
KLF15
CXCR4
Emerin
Expanded repeats
Exon skipping
Chromatin
Mdx
Gut microbiota
LTβR
Dynamin 2
Cell Therapy
Coculture
Autophagy
Gene Therapy
Gel electrophoresis
Dominant centronuclear myopathy
Cell-penetrating peptide
Folding-defective proteins
Myotonic dystrophy
Eteplirsen
HDMD/Dmd-null mice
DMD
Adeno-associated viral vector
BMD
Glucose
Lamina-associated domain
MT RNA/DNA Editing
Exondys 51
FSHD
Exon Skipping
Motor neuron
Laminographie
Fibrosis
Insulin
MSCs
Fear response
Actin
Flavonoid
Glucocorticoid-induced muscle atrophy
Differentiation
Muscle
Neuromuscular junction
Clinical trial candidate screening
Immortalized dystrophic canine myoblast
Human artificial chromosomes
Lamin A/C nuclei
Fibroblast
CDNA synthesis
Exon-skipping
Alternative splicing
Adhesion
Mdx52 mice
Dystrophin
Migration
Becker muscular dystrophy BMD Duchenne muscular dystrophy DMD miRNA nNOS
Antisense morpholino
CRISPR/Cas9
Developmental biology
CLS
Computer software
Duchenne Muscular Dystrophy
Myogenesis
Antisense oligonucleotide
Acetylcholine receptor subunit epsilon
Skeletal muscle
CXCL12
DsDNA break repair
Human
FoxO
Human muscle stem/progenitor cells
Allele-specific silencing therapy
BAF
CFTR correctors
Lymphotoxin-β-receptor
Allele-specific silencing
Immortalisation
CMS
Duchenne muscular dystrophy
RNA interference
Drisapersen
Canine X-linked muscular dystrophy in Japan CXMD J
Gene network analysis
Atrial cardiac defects
ITSN1
3D co-culture
LRP4
CTG⋅CAGn repeat
Endocytosis
Conjugation
Bile acid
Machine learning
Becker muscular dystrophy
Autophagosome
Myotube
Cell biology
ICU-acquired weakness
Centronuclear myopathy
DM1 myoblasts