Loading...
Dernières publications
-
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⟩
-
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⟩
-
Ingo Riederer, Daniella Arêas Mendes-Da-Cruz, Guilherme Cordenonsi da Fonseca, Mariela Natacha González, Otavio Brustolini, et al.. Zika virus disrupts gene expression in human myoblasts and myotubes: Relationship with susceptibility to infection. PLoS Neglected Tropical Diseases, 2022, 16 (2), pp.e0010166. ⟨10.1371/journal.pntd.0010166⟩. ⟨hal-03832616⟩
Chiffres clés
98
Publications avec texte intégral
Open Access
59 %
Mots clés
Pax7
Calcium
Cell therapy
Actin
FSHD
Oculopharyngeal muscular dystrophy
Myotube
Dystrophie musculaire oculopharyngée
Biopsies humaines
Gene therapy
CD49d
Cross-bridge kinetics
Arbovirus
Muscle strength
Antiserum
FAPs
Annexin A2
Myopathies
Alzheimer's disease
Muscle
Bile salt hydrolases
Thérapie génique
Myoblast
Intercellular communication
BINDING SPECIFICITY
DNA methylation
Haploinsufficiency
Myosin
RNA
Akt
Dysferlinopathy
ALS
Ageing
Bioinformatics
Andermann syndrome
Transcriptomics
CNOT6L
Adipose tissue
AAV vectors
Gene replacement
OPMD
Bioinformatique
DMD
Triplet expansion disease
2-D PAGE
Skeletal muscle
APOPTOSIS
Functional genomics
Exon-skipping
Human
Fibrosis
Xenograft
Lamins
Muscle dystrophy
Biomarker
Dystrophin
Alphavirus
Myogenesis
Botulinum neurotoxin
Pharyngeal muscle
AChR antibodies
Aav-U7
CS
Agrégats de PABPN1
Neuromuscular junction NMJ
DUX4
Duchenne muscular dystrophy
Geriatric assessment
Sarcopenia
Myositis
Myopathy
Aggregate
Nuclear envelope
Anti-acetylcholine receptor antibodies
Satellite cells
Regeneration
Metabolism
Atrophy
ARN
Myoblasts
C2 domains
Muscle stem cells
MUTATIONS
Anti-fibrotic pharmacotherapies
GENE
Antisens oligonucleotides
C2C12 cells
PABPN1
Inflammation
Autoimmune diseases
Satellite cell
Aged
Muscle fibrosis
Dysferlin
AAV
Differentiation
Accelerometry
Autologous
AUTOPHAGY
PABPN1 agregates