Loading...
Dernières publications
-
Anna Underhill, Samuel Webb, Fiorella Grandi, Jing-Yi Jeng, Jacques de Monvel, et al.. MYO7A is required for the functional integrity of the mechanoelectrical transduction complex in hair cells of the adult cochlea. Proceedings of the National Academy of Sciences of the United States of America, 2025, 122 (1), pp.e2414707122. ⟨10.1073/pnas.2414707122⟩. ⟨hal-04905455⟩
-
-
-
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⟩
-
-
-
-
-
-
Chiffres clés
39
Publications avec texte intégral
Open Access
62 %
Mots clés
Dicer
Clinical trial
Cellules souches musculaires
Prematurity
Spinal muscular atrophy
Effector T cells
Skeletal muscle
Les paramètres respiratoires
Gene therapy
Biomarkers
Fabry disease lysosomal storage disorders adeno asociated virus-9
Dilated cardiomyopathy
Bone development
FGR
Disease modifiers
IUGR
Distal myopathy
Chondrocytes
Biomarker
AICD
Intra-uterine growth restriction
MRI
Clinical markers
Genetics
Cochlea
Modèle murin
Cartilage and bone regeneration
ALS
DPRs
Clinical trials
Calcium handling
Maladie neuromusculaire
ASO
IRM
Brain
Extremely preterm infants
Biological marker
ASOs
AAV
SMN
Early-onset sepsis
Amyotrophic Lateral Sclerosis
Glucocorticosteroid
Brain imaging
Neuromuscular disease
Hearing loss
CRISPR/SaCas9
GeneRide
LMNA
IPSCs
ERK1/2 signaling
Intra-CSF delivery
Brain MRI
Microglia
Diseases
Aav10
MRNP assembly
FTD
Cofilin-1
Brain injury
Disease heterogeneity
Lentiviral vectors
Coagulation factor IX
GABA
Mouse model
DTI
Gene transfer
Albumin gene targeting
Amyotrophie spinale
Cell stemness
3xTgAD Mice
Adult patients
CNS
Bioinformatics
Epigenetic changes
Icv
Blood brain barrier
Maternal behavior
Brain damage
G-Secretase
Adenosine
Brain development
FOXO3a
Adult SMA
Fetal growth restriction
Cell reprogramming
Errance diagnotique
Antisense oligonucleotides
Bone involvement
MND
Longitudinal progression
MiRNA
Long-term handicap
Duchenne Muscular Dystrophy
Functional outcomes
Inflammation
Hair cell
MUNIX
C9orf72
Genetical therapy