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