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Dernières publications
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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
47
Publications avec texte intégral
Open Access
86 %
Mots clés
Allele-specific silencing therapy
Gene therapy
BAF
Exon skipping
Cell-penetrating peptide
Microarray
Expanded repeats
Dominant centronuclear myopathy
ITSN1
Mechano-transduction
3D co-culture
Glucose
Drisapersen
Fibroblast
Allele-specific silencing
Flavonoid
Neuromuscular junction
Exon-skipping
Duchenne muscular dystrophy
Insulin
Gene network analysis
Endocytosis
Gut microbiota
Antisense morpholino
HDMD/Dmd-null mice
Migration
CTG⋅CAGn repeat
Laminographie
Exondys 51
RNA interference
CXCR4
Lamin A/C nuclei
MT RNA/DNA Editing
Muscle
Actin
Adhesion
Eteplirsen
DM1 myoblasts
Glucocorticoid-induced muscle atrophy
DMD
CDNA synthesis
Autophagosome
Human artificial chromosomes
Dynamin 2
DsDNA break repair
LRP4
DNM2
Bile acid
CXCL12
CMS
Computer software
Motor neuron
Dystrophin
MSCs
CRISPR/Cas9
FoxO
Fibrosis
Acetylcholine receptor subunit epsilon
Emerin
ICU-acquired weakness
Myotube
Differentiation
Immortalized dystrophic canine myoblast
Folding-defective proteins
Becker muscular dystrophy
Human muscle stem/progenitor cells
LTβR
Conjugation
Lymphotoxin-β-receptor
Adeno-associated viral vector
Skeletal muscle
Mitochondrial ROS
Human
Developmental biology
BMD
Centronuclear myopathy
Autophagy
Fear response
Mdx52 mice
Canine X-linked muscular dystrophy in Japan CXMD J
Coculture
Gel electrophoresis
Atrial cardiac defects
FSHD
Myogenesis
Alternative splicing
Mechanisms of disease
Immortalisation
Lamina-associated domain
Cell biology
Machine learning
Myotonic dystrophy
Clinical trial candidate screening
Becker muscular dystrophy BMD Duchenne muscular dystrophy DMD miRNA nNOS
CFTR correctors
Mdx
KLF15
Antisense oligonucleotide
Chromatin
CLS