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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
36
Publications avec texte intégral
Open Access
61 %
Mots clés
Amyotrophic Lateral Sclerosis
Disease modifiers
Bone involvement
MiRNA
MUNIX
Brain imaging
Biomarker
Brain damage
Intra-CSF delivery
Calcium handling
MND
Brain
Gene transfer
Early-onset sepsis
Microglia
Adult SMA
Adult patients
SMN
Brain development
Cellules souches musculaires
Melatonin
Amyotrophie spinale
Diseases
Metabolic disorders
Les paramètres respiratoires
IPSCs
Functional outcomes
Prematurity
Errance diagnotique
Maternal malnutrition
LMNA
AICD
Distal myopathy
Mecp2
Modèle murin
G-Secretase
Biomarkers
Dilated cardiomyopathy
ERK1/2 signaling
Epigenetic changes
Disease heterogeneity
GABA
Brain injury
Extremely preterm infants
GeneRide
Cofilin-1
CRISPR/SaCas9
Methylosome
Clinical trial
Mitophagy
Intra-uterine growth restriction
Brain MRI
FOXO3a
Blood brain barrier
3xTgAD Mice
Dicer
ASO
Icv
Albumin gene targeting
Antisense oligonucleotides
Fetal growth restriction
Mitochondrial dysfunction
Mouse model
Effector T cells
Coagulation factor IX
Clinical markers
Cell stemness
FTD
Glucocorticosteroid
Aav10
DPRs
ALS
ASOs
Bone development
Cartilage and bone regeneration
Cell reprogramming
Duchenne Muscular Dystrophy
MRI
Maladie neuromusculaire
Inflammation
Biological marker
CNS
IUGR
Lentiviral vectors
IRM
C9orf72
Genetical therapy
Long-term handicap
Chondrocytes
DTI
Adenosine
Gene therapy
FGR
AAV
Fabry disease lysosomal storage disorders adeno asociated virus-9
Clinical trials
Longitudinal progression
Spinal muscular atrophy
MRNP assembly
Maternal behavior