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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
Lamin A/C nuclei
Becker muscular dystrophy BMD Duchenne muscular dystrophy DMD miRNA nNOS
Fibroblast
Gut microbiota
Skeletal muscle
CDNA synthesis
Lamina-associated domain
Motor neuron
Flavonoid
Coculture
FoxO
Glucose
Acetylcholine receptor subunit epsilon
Muscle
LTβR
Exondys 51
Human artificial chromosomes
Becker muscular dystrophy
DM1 myoblasts
Folding-defective proteins
LRP4
CRISPR/Cas9
Dystrophin
Machine learning
Differentiation
Myotonic dystrophy
Fear response
Mdx
Emerin
MSCs
Drisapersen
Eteplirsen
Antisense morpholino
Developmental biology
Fibrosis
BMD
ICU-acquired weakness
Exon Skipping
Gel electrophoresis
Lymphotoxin-β-receptor
Dynamin 2
Exon skipping
Gene network analysis
Centronuclear myopathy
CXCR4
CMS
Adhesion
Myotube
Allele-specific silencing
Duchenne Muscular Dystrophy
CTG⋅CAGn repeat
Human
Autophagy
CFTR correctors
Adeno-associated viral vector
Gene Therapy
ITSN1
Mdx52 mice
Alternative splicing
Bile acid
Duchenne muscular dystrophy
Autophagosome
Conjugation
Canine X-linked muscular dystrophy in Japan CXMD J
BAF
KLF15
Insulin
Cell-penetrating peptide
Actin
DNM2
Endocytosis
DsDNA break repair
Computer software
Clinical trial candidate screening
Allele-specific silencing therapy
FSHD
Immortalisation
Expanded repeats
Gene therapy
Atrial cardiac defects
CLS
Cell biology
Neuromuscular junction
Glucocorticoid-induced muscle atrophy
Immortalized dystrophic canine myoblast
Exon-skipping
Migration
CXCL12
Cell Therapy
Laminographie
DMD
Dominant centronuclear myopathy
MT RNA/DNA Editing
Chromatin
HDMD/Dmd-null mice
Human muscle stem/progenitor cells
Antisense oligonucleotide
Myogenesis
RNA interference
3D co-culture