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