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