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
34
Publications avec texte intégral
Open Access
61 %
Mots clés
Modèle murin
Mecp2
FOXO3a
MRNP assembly
Distal myopathy
MND
Intra-uterine growth restriction
DTI
Maternal behavior
Clinical trials
FGR
Melatonin
Long-term handicap
Mitophagy
Disease heterogeneity
Aav10
Microglia
Maternal malnutrition
Cofilin-1
Cell reprogramming
3xTgAD Mice
Extremely preterm infants
AAV
CNS
ALS
Bone involvement
Adenosine
Les paramètres respiratoires
ASO
Duchenne Muscular Dystrophy
Dilated cardiomyopathy
Clinical trial
Coagulation factor IX
Fetal growth restriction
Mouse model
Diseases
ERK1/2 signaling
IUGR
Amyotrophic Lateral Sclerosis
Adult SMA
Gene transfer
G-Secretase
ASOs
MiRNA
IRM
Functional outcomes
Antisense oligonucleotides
Adult patients
Blood brain barrier
CRISPR/SaCas9
Brain MRI
Metabolic disorders
Early-onset sepsis
Gene therapy
MUNIX
Chondrocytes
Calcium handling
Prematurity
Glucocorticosteroid
Epigenetic changes
Methylosome
Intra-CSF delivery
GABA
Lentiviral vectors
Brain imaging
Errance diagnotique
IPSCs
LMNA
Genetical therapy
Amyotrophie spinale
Biomarkers
MRI
Effector T cells
Mitochondrial dysfunction
Icv
Spinal muscular atrophy
Maladie neuromusculaire
Cartilage and bone regeneration
Brain
Clinical markers
Inflammation
Brain injury
Cell stemness
AICD
Bone development
Brain development
Brain damage
DPRs
Disease modifiers
Biological marker
C9orf72
Biomarker
Fabry disease lysosomal storage disorders adeno asociated virus-9
Cellules souches musculaires
Dicer
SMN
FTD
Albumin gene targeting
GeneRide
Longitudinal progression