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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
48
Publications with fulltext
Open Access
87 %
Mots clés
Exondys 51
Motor neuron
Canine X-linked muscular dystrophy in Japan CXMD J
Conjugation
Neuromuscular junction
CLS
Myotonic dystrophy
Autophagosome
Coculture
Fear response
Autophagy
DNM2
DsDNA break repair
BMD
Becker muscular dystrophy
Gene network analysis
CXCL12
Exon Skipping
Eteplirsen
MT RNA/DNA Editing
LTβR
Atrial cardiac defects
Antisense morpholino
Actin
Immortalized dystrophic canine myoblast
Fibroblast
Allele-specific silencing
CMS
Dystrophin
Lymphotoxin-β-receptor
Duchenne muscular dystrophy
Myogenesis
Flavonoid
Cell Therapy
CRISPR/Cas9
Insulin
Lamin A/C nuclei
Human artificial chromosomes
Acetylcholine receptor subunit epsilon
DMD
CTG⋅CAGn repeat
Exon-skipping
CFTR correctors
Lamina-associated domain
Drisapersen
Glucocorticoid-induced muscle atrophy
Becker muscular dystrophy BMD Duchenne muscular dystrophy DMD miRNA nNOS
CXCR4
Adhesion
Dynamin 2
Machine learning
Gene therapy
Human muscle stem/progenitor cells
Immortalisation
Myotube
CDNA synthesis
Migration
Differentiation
Emerin
Duchenne Muscular Dystrophy
Cell biology
Gel electrophoresis
Expanded repeats
Skeletal muscle
HDMD/Dmd-null mice
DM1 myoblasts
Bile acid
FoxO
Muscle
Cell-penetrating peptide
Antisense oligonucleotide
ITSN1
Glucose
MSCs
Endocytosis
RNA interference
Chromatin
Dominant centronuclear myopathy
LRP4
Gut microbiota
Clinical trial candidate screening
Gene Therapy
Mdx
Laminographie
Fibrosis
Adeno-associated viral vector
Alternative splicing
Human
Folding-defective proteins
Exon skipping
KLF15
Developmental biology
Mdx52 mice
BAF
3D co-culture
FSHD
Centronuclear myopathy
Allele-specific silencing therapy
ICU-acquired weakness
Computer software