C. Bagni

Discipline

Psychologie (4) Education (1) Economies et finances (1)

Type de document

Articles (19) Recensions (2)

Co-auteur

Date

Source

Mot-clé

Mice (11) Human beings (10) protéine (9) Phenotype (9) Fragile X syndrome (9) Animals (9) spectacle (8) Mental retardation (8) Neurons (7) Expression (7) Brain (7) Disabilities (7) Proteins (6) Proteins--Synthesis (6) Patients (6) Autism (6) Patients (6) cerveau (6) puits (5) risque (5) adulte (5) Risk (5) RNA (5) Example (5) Cells (5) Autism spectrum disorders (5) adulte (5) modèle (4) gène (4) règlement (4)

Documents écrit par C. Bagni (19) | parle de C. Bagni (0)

Cell-type-specific disruption of cortico-striatal circuitry drives repetitive patterns of behavior in fragile X syndrome model mice.
F. Longo et al. (29 août 2023)
Dendritic autophagy degrades postsynaptic proteins and is required for long-term synaptic depression in mice.
E. Kallergi et al. (3 févr. 2022)
Absence of RNA-binding protein FXR2P prevents prolonged phase of kainate-induced seizures.
A.C. Lo et al. (7 avr. 2021)
Modelling Learning and Memory in Drosophila to Understand Intellectual Disabilities.
V. Mariano et al. (1 oct. 2020)
Conserved Tao Kinase Activity Regulates Dendritic Arborization, Cytoskeletal Dynamics, and Sensory Function in Drosophila.
C. Hu et al. (26 févr. 2020)
The autism- and schizophrenia-associated protein CYFIP1 regulates bilateral brain connectivity and behaviour.
N. Domínguez-Iturza et al. (1 août 2019)
Detection of antisense protein (ASP) RNA transcripts in individuals infected with human immunodeficiency virus type 1 (HIV-1).
A. Mancarella et al.
A Synaptic Perspective of Fragile X Syndrome and Autism Spectrum Disorders.
C. Bagni et al. (20 mars 2019)
Disruption of mTOR and MAPK pathways correlates with severity in idiopathic autism.
E. Rosina et al. (31 janv. 2019)
Protein synthesis levels are increased in a subset of individuals with fragile X syndrome.
S. Jacquemont et al. (1 nov. 2018)
Protein synthesis levels are increased in a subset of individuals with fragile X syndrome.
S. Jacquemont et al. (15 juin 2018)
Alpha2-Containing Glycine Receptors Promote Neonatal Spontaneous Activity of Striatal Medium Spiny Neurons and Support Maturation of Glutamatergic Inputs
J. Comhair et al. (2018)
FXS-Like Phenotype in Two Unrelated Patients Carrying a Methylated Premutation of the FMR1 Gene.
E. Fernández et al. (2018)
The fragile X mental retardation protein regulates tumor invasiveness-related pathways in melanoma cells.
F. Zalfa et al. (16 nov. 2017)
Absence of the Fragile X Mental Retardation Protein results in defects of RNA editing of neuronal mRNAs in mouse.
A. Filippini et al. (2 nov. 2017)
The non-coding RNA BC1 regulates experience-dependent structural plasticity and learning.
V. Briz et al. (17 août 2017)
Mutant HSPB1 causes loss of translational repression by binding to PCBP1, an RNA binding protein with a possible role in neurodegenerative disease.
T. Geuens et al. (11 janv. 2017)
Clinical and Molecular Assessment in a Female with Fragile X Syndrome and Tuberous Sclerosis.
C.M. Yrigollen et al. (2016)
SnapShot: FMRP interacting proteins.
E. Pasciuto et al. (25 sept. 2014)