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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⟩
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Elisa Negroni, Maria Kondili, Laura Muraine, Mona Bensalah, Gillian Sandra Butler-Browne, et al.. Muscle fibro-adipogenic progenitors from a single-cell perspective: Focus on their “virtual” secretome. Frontiers in Cell and Developmental Biology, 2022, 10, ⟨10.3389/fcell.2022.952041⟩. ⟨hal-03830589⟩
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Chiffres clés
103
Publications avec texte intégral
Open Access
61 %
Mots clés
Triplet expansion disease
Geriatric assessment
Anti-acetylcholine receptor antibodies
MUTATIONS
Alphavirus
Fibrosis
PABPN1 agregates
Accelerometry
Anti-fibrotic pharmacotherapies
Gene replacement
Aggregate
AAV
Myotube
GENE
Transcriptomics
Epigenetics
RNA
Duchenne muscular dystrophy
Antiserum
Metabolism
Cell therapy
Human
PABPN1
Muscle stem cells
Mass spectrometry
Satellite cell
Arbovirus
Muscle strength
Oculopharyngeal muscular dystrophy
Effector T cells
Muscle dystrophy
Alzheimer's disease
Pharyngeal muscle
Autologous
Regenerative medicine
Akt
Intercellular communication
OPMD
Actin
Myopathy
Myositis
FSHD
Myoblast
Aav-U7
Dystrophie musculaire oculopharyngée
Ageing
FAPs
Lamins
Aged
Skeletal muscle
Dysferlin
ALS
2-D PAGE
Inflammation
Muscle
Neuromuscular disease
Myogenesis
Calcium
Thérapie génique
Satellite cells
Amyotrophic Lateral Sclerosis
AUTOPHAGY
Pax7
Dysferlinopathy
Omics
Gene therapy
Andermann syndrome
Adipose tissue
Biomarker
BINDING SPECIFICITY
Myosin
Antisens oligonucleotides
ARN
Atrophy
Exon-skipping
Muscle fibrosis
Sarcopenia
Autoimmune diseases
Haploinsufficiency
Nuclear envelope
Xenograft
Annexin A2
Agrégats de PABPN1
Regeneration
Bile salt hydrolases
Differentiation
Cross-bridge kinetics
APOPTOSIS
Regulatory T cells
AAV vectors
DNA methylation
AChR antibodies
Neuromuscular junction NMJ
DMD
Muscular dystrophy
Myoblasts
DUX4
Myopathies
Dystrophin
Functional genomics