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Dernières publications
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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⟩
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Nicolas Vignier, Maria Chatzifrangkeskou, Luca Pinton, Hugo Wioland, Thibaut Marais, et al.. The non-muscle ADF/cofilin-1 controls sarcomeric actin filament integrity and force production in striated muscle laminopathies. Cell Reports, 2021, 36 (8), pp.109601. ⟨10.1016/j.celrep.2021.109601⟩. ⟨hal-03350074⟩
Chiffres clés
32
Publications avec texte intégral
Open Access
60 %
Mots clés
Intra-CSF delivery
ALS
Extremely preterm infants
Cellules souches musculaires
Albumin gene targeting
Chondrocytes
SMN
Brain imaging
Aav10
Early-onset sepsis
Genetical therapy
FOXO3a
MiRNA
Maternal malnutrition
Antisense oligonucleotides
Methylosome
Dilated cardiomyopathy
AAV
Clinical markers
Clinical trial
Gene therapy
Distal myopathy
Biological marker
Icv
Brain MRI
Diseases
Mouse model
Maternal behavior
Dicer
Brain
GeneRide
Calcium handling
IRM
Bone development
CNS
GABA
Lentiviral vectors
Spinal muscular atrophy
G-Secretase
Epigenetic changes
Brain damage
Amyotrophie spinale
FGR
Murine model
Mecp2
Melatonin
ASOs
Functional outcomes
Errance diagnotique
DPRs
Adult SMA
Longitudinal progression
Cartilage and bone regeneration
ASO
Modèle murin
FTD
Cell reprogramming
Mitophagy
Clinical trials
Disease heterogeneity
AICD
Brain injury
Cell stemness
Adult patients
Blood brain barrier
Adenosine
MND
Motor neurons
Les paramètres respiratoires
Intra-uterine growth restriction
Disease modifiers
Fetal growth restriction
LMNA
Gene transfer
IPSCs
Brain development
IUGR
Maladie neuromusculaire
MRI
Cofilin-1
3xTgAD Mice
Coagulation factor IX
Glucocorticosteroid
Biomarker
CRISPR/SaCas9
Bone involvement
Metabolic disorders
Fabry disease lysosomal storage disorders adeno asociated virus-9
Biomarkers
Inflammation
Mitochondrial dysfunction
Prematurity
Motoneurone
Long-term handicap
MUNIX
C9orf72
ERK1/2 signaling
MRNP assembly
Microglia
DTI