Loading...
Dernières publications
-
-
-
-
-
-
-
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⟩
-
-
-
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
Myopathy
FSHD
Lamins
Neuromuscular junction NMJ
Transcriptomics
MND
DMD
Mass spectrometry
Actin
DUX4
AUTOPHAGY
Functional genomics
AChR antibodies
Geriatric assessment
Anti-acetylcholine receptor antibodies
Haploinsufficiency
Epigenetics
Amyotrophic Lateral Sclerosis
Metabolism
Dystrophin
Myoblasts
Myositis
Human
QUIESCENCE
ARN
Myoblast
Effector T cells
Exon-skipping
Secreted vesicles
AAV vectors
Sarcopenia
APOPTOSIS
DNA methylation
Gene therapy
FAPs
OPMD
Gene replacement
Alzheimer's disease
Accelerometry
Adipose tissue
Oculopharyngeal muscular dystrophy
Agrégats de PABPN1
AAV
NICHE
Muscular dystrophy
Muscle fibrosis
Regulatory T cells
Regenerative medicine
Nuclear envelope
PABPN1
Muscle strength
Dystrophie musculaire oculopharyngée
Myotube
Inflammation
Skeletal muscle
Muscle stem cells
Andermann syndrome
MEGF10
Aav-U7
2-D PAGE
Pax7
Thérapie génique
Calcium
Cell therapy
Omics
Alphavirus
Cross-bridge kinetics
Myosin
ALS
Akt
Myopathies
Aged
Aggregate
SATELLITE CELLS
Triplet expansion disease
MYOPATHY
Duchenne muscular dystrophy
Fibrosis
Muscle dystrophy
Satellite cell
Biomarker
GENE
RNA
Ageing
Differentiation
Dysferlinopathy
Satellite cells
Sporadic ALS
Pharyngeal muscle
Intercellular communication
Neuromuscular disease
Muscle
Myogenesis
Regeneration
Annexin A2
Xenograft
Dysferlin
MUTATIONS
PABPN1 agregates
MAINTENANCE