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Dernières publications
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Julia Pereira Lemos, Liliane Patrícia Gonçalves Tenório, Vincent Mouly, Gillian Butler-Browne, Daniella Arêas Mendes-Da-Cruz, et al.. T cell biology in neuromuscular disorders: a focus on Duchenne Muscular Dystrophy and Amyotrophic Lateral Sclerosis. Frontiers in Immunology, 2023, 14, pp.120283. ⟨10.3389/fimmu.2023.1202834⟩. ⟨hal-04603915⟩
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Fanny Roth, Jamila Dhiab, Alexis Boulinguiez, Hadidja-Rose Mouigni, Saskia Lassche, et al.. Assessment of PABPN1 nuclear inclusions on a large cohort of patients and in a human xenograft model of oculopharyngeal muscular dystrophy. Acta Neuropathologica, 2022, ⟨10.1007/s00401-022-02503-7⟩. ⟨hal-03832636⟩
Chiffres clés
107
Publications avec texte intégral
Open Access
61 %
Mots clés
Satellite cells
Neuromuscular junction NMJ
Intercellular communication
Myopathies
Muscle stem cells
QUIESCENCE
Functional genomics
Sarcopenia
Xenograft
Lamins
Satellite cell
Neuromuscular disease
Cell therapy
Dysferlin
Cross-bridge kinetics
Sporadic ALS
DUX4
Amyotrophic Lateral Sclerosis
Actin
Epigenetics
GENE
Geriatric assessment
Annexin A2
Skeletal muscle
Exon-skipping
Muscle dystrophy
Myosin
Duchenne muscular dystrophy
Calcium
Myopathy
Dysferlinopathy
DMD
MUTATIONS
Regulatory T cells
Pharyngeal muscle
Transcriptomics
Biomarker
AAV vectors
Oculopharyngeal muscular dystrophy
Alphavirus
Agrégats de PABPN1
Regeneration
Gene therapy
RNA
FAPs
AChR antibodies
Alzheimer's disease
Gene replacement
Dystrophin
OPMD
Myogenesis
Accelerometry
Ageing
SATELLITE CELLS
PABPN1 agregates
ALS
Aav-U7
Differentiation
AUTOPHAGY
Fibrosis
Regenerative medicine
Human
Myositis
Inflammation
Aged
PABPN1
Akt
Muscle fibrosis
2-D PAGE
AAV
MEGF10
MND
Muscle strength
Muscular dystrophy
FSHD
DNA methylation
Omics
Effector T cells
APOPTOSIS
Andermann syndrome
MAINTENANCE
Myoblast
Mass spectrometry
Haploinsufficiency
Anti-acetylcholine receptor antibodies
Muscle
Myoblasts
Dystrophie musculaire oculopharyngée
Myotube
ARN
Nuclear envelope
Adipose tissue
Pax7
Secreted vesicles
Aggregate
NICHE
MYOPATHY
Metabolism
Triplet expansion disease
Thérapie génique