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