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