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