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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⟩
Chiffres clés
50
Publications avec texte intégral
Open Access
87 %
Mots clés
Gene Therapy
Glucose
Allele-specific silencing therapy
Conjugation
Exondys 51
CXCR4
Motor neuron
ICU-acquired weakness
Cell-penetrating peptide
LRP4
Emerin
Lamina-associated domain
Gene network analysis
Endocytosis
Expanded repeats
Skeletal muscle
Exon-skipping
Alternative splicing
CFTR correctors
Human
CDNA synthesis
Gel electrophoresis
Migration
Muscle
Clinical trial candidate screening
Adeno-associated viral vector
CRISPR/Cas9
Fear response
Immortalisation
DNM2
CMS
Becker muscular dystrophy
DM1 myoblasts
DiPRO1
Glucocorticoid-induced muscle atrophy
Autophagosome
Bile acid
Insulin
Centronuclear myopathy
Machine learning
FSHD
Antisense morpholino
3D co-culture
Gut microbiota
Autophagy
Dystrophin
Canine X-linked muscular dystrophy in Japan CXMD J
Coculture
CTG⋅CAGn repeat
Mdx
Myotonic dystrophy
Gene therapy
LTβR
Atrial cardiac defects
Exon skipping
Lamin A/C nuclei
Neuromuscular junction
Computer software
Duchenne muscular dystrophy
Antisense oligonucleotide
Dominant centronuclear myopathy
BAF
Allele-specific silencing
RNA interference
Folding-defective proteins
Lymphotoxin-β-receptor
Fibrosis
Myogenesis
Drisapersen
DsDNA break repair
Myotube
Developmental biology
Laminographie
Adhesion
Fibroblast
MT RNA/DNA Editing
Flavonoid
Human muscle stem/progenitor cells
Human artificial chromosomes
HDMD/Dmd-null mice
BMD
Becker muscular dystrophy BMD Duchenne muscular dystrophy DMD miRNA nNOS
ITSN1
Exon Skipping
Dynamin 2
Cell Therapy
Actin
CLS
FoxO
Cell biology
Eteplirsen
Differentiation
KLF15
Chromatin
CXCL12
DMD
Duchenne Muscular Dystrophy
MSCs
Immortalized dystrophic canine myoblast
Acetylcholine receptor subunit epsilon