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