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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
Allele-specific silencing therapy
Actin
BAF
Gel electrophoresis
DiPRO1
Eteplirsen
Glucocorticoid-induced muscle atrophy
Emerin
Immortalized dystrophic canine myoblast
Differentiation
Drisapersen
LTβR
Developmental biology
Adeno-associated viral vector
Exon-skipping
Insulin
Computer software
Conjugation
Myotube
CDNA synthesis
Antisense oligonucleotide
3D co-culture
Machine learning
LRP4
Antisense morpholino
Cell Therapy
BMD
Gene Therapy
DsDNA break repair
Flavonoid
Canine X-linked muscular dystrophy in Japan CXMD J
FSHD
Myotonic dystrophy
CMS
Human artificial chromosomes
CXCL12
Human
Fear response
Myogenesis
Autophagy
Laminographie
MT RNA/DNA Editing
CRISPR/Cas9
Dominant centronuclear myopathy
Expanded repeats
Gene network analysis
DM1 myoblasts
Lamina-associated domain
CXCR4
Skeletal muscle
Adhesion
FoxO
Chromatin
Bile acid
Neuromuscular junction
ICU-acquired weakness
Duchenne Muscular Dystrophy
Fibroblast
Allele-specific silencing
Folding-defective proteins
Becker muscular dystrophy
Migration
Dystrophin
CFTR correctors
Glucose
Motor neuron
Exon Skipping
Mdx
Lamin A/C nuclei
Coculture
DMD
CTG⋅CAGn repeat
Gut microbiota
Autophagosome
Immortalisation
Becker muscular dystrophy BMD Duchenne muscular dystrophy DMD miRNA nNOS
MSCs
Gene therapy
Exondys 51
ITSN1
Centronuclear myopathy
Exon skipping
Muscle
Alternative splicing
Atrial cardiac defects
KLF15
Dynamin 2
HDMD/Dmd-null mice
Duchenne muscular dystrophy
Fibrosis
Acetylcholine receptor subunit epsilon
CLS
Human muscle stem/progenitor cells
Endocytosis
Cell-penetrating peptide
Lymphotoxin-β-receptor
DNM2
RNA interference
Cell biology
Clinical trial candidate screening