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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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Valentin Jacquier, Manon Prévot, Thierry Gostan, Rémy Bordonné, Sofia Benkhelifa-Ziyyat, et al.. Splicing efficiency of minor introns in a mouse model of SMA predominantly depends on their branchpoint sequence and can involve the contribution of major spliceosome components. RNA, 2022, 28 (3), pp.303-319. ⟨10.1261/rna.078329.120⟩. ⟨hal-03687098⟩
Chiffres clés
38
Publications avec texte intégral
Open Access
62 %
Mots clés
AICD
Brain imaging
Clinical trials
Cell reprogramming
GABA
Long-term handicap
Les paramètres respiratoires
DPRs
Lentiviral vectors
ALS
Brain injury
IRM
SMN
Mouse model
IPSCs
CNS
Clinical trial
Disease modifiers
Effector T cells
Bioinformatics
Dicer
Spinal muscular atrophy
Gene transfer
LMNA
Aav10
Epigenetic changes
Inflammation
Cartilage and bone regeneration
Brain development
Cofilin-1
C9orf72
Amyotrophic Lateral Sclerosis
ERK1/2 signaling
ASO
Melatonin
Bone involvement
IUGR
Coagulation factor IX
FGR
Amyotrophie spinale
Cellules souches musculaires
Duchenne Muscular Dystrophy
Skeletal muscle
MiRNA
Clinical markers
Gene therapy
Fetal growth restriction
AAV
Cell stemness
Maladie neuromusculaire
Antisense oligonucleotides
Prematurity
Biological marker
MUNIX
FOXO3a
Extremely preterm infants
Modèle murin
Genetical therapy
Biomarker
Distal myopathy
Albumin gene targeting
ASOs
Adenosine
Functional outcomes
Adult SMA
Diseases
GeneRide
MND
Chondrocytes
Biomarkers
Brain MRI
DTI
Bone development
Icv
Blood brain barrier
Brain damage
Dilated cardiomyopathy
FTD
Neuromuscular disease
Maternal malnutrition
G-Secretase
3xTgAD Mice
Calcium handling
Mecp2
Intra-CSF delivery
Maternal behavior
Longitudinal progression
MRI
Early-onset sepsis
Errance diagnotique
Brain
Intra-uterine growth restriction
Fabry disease lysosomal storage disorders adeno asociated virus-9
Microglia
Glucocorticosteroid
Disease heterogeneity
CRISPR/SaCas9
MRNP assembly
Adult patients
Genetics