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⟩
-
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
35
Publications avec texte intégral
Open Access
61 %
Mots clés
Mitochondrial dysfunction
CNS
Mecp2
Brain damage
Cell stemness
Amyotrophie spinale
Early-onset sepsis
ASO
Aav10
Biomarkers
Brain development
FGR
Dicer
ERK1/2 signaling
ASOs
FTD
Intra-uterine growth restriction
DTI
DPRs
Disease heterogeneity
Brain MRI
Antisense oligonucleotides
Epigenetic changes
Clinical trial
Brain injury
Functional outcomes
GeneRide
Cofilin-1
Spinal muscular atrophy
Fabry disease lysosomal storage disorders adeno asociated virus-9
Maternal behavior
LMNA
Adult patients
MRI
CRISPR/SaCas9
Lentiviral vectors
MRNP assembly
Melatonin
Cellules souches musculaires
Effector T cells
Microglia
Les paramètres respiratoires
Adult SMA
IUGR
G-Secretase
Clinical markers
Mouse model
IPSCs
Longitudinal progression
Biological marker
ALS
Metabolic disorders
Prematurity
Amyotrophic Lateral Sclerosis
Duchenne Muscular Dystrophy
Methylosome
Brain imaging
Icv
Gene transfer
Gene therapy
Brain
Intra-CSF delivery
Adenosine
Albumin gene targeting
FOXO3a
Cartilage and bone regeneration
Coagulation factor IX
Inflammation
Blood brain barrier
Clinical trials
AICD
Glucocorticosteroid
Long-term handicap
IRM
Maladie neuromusculaire
Mitophagy
Errance diagnotique
Genetical therapy
Biomarker
Cell reprogramming
Calcium handling
MND
Chondrocytes
MUNIX
Modèle murin
Disease modifiers
Dilated cardiomyopathy
SMN
AAV
Extremely preterm infants
Diseases
3xTgAD Mice
Fetal growth restriction
MiRNA
Maternal malnutrition
C9orf72
Bone development
Bone involvement
Distal myopathy
GABA