about
Misregulation of Alternative Splicing in a Mouse Model of Rett SyndromeMethyl-CpG-Binding Protein MBD1 Regulates Neuronal Lineage Commitment through Maintaining Adult Neural Stem Cell IdentityHuman pluripotent stem cell models of Fragile X syndrome.Establishment of Reporter Lines for Detecting Fragile X Mental Retardation (FMR1) Gene Reactivation in Human Neural Cells.Identifying molecular mediators of environmentally enhanced neurogenesis.Imaging Voltage in Genetically Defined Neuronal Subpopulations with a Cre Recombinase-Targeted Hybrid Voltage Sensor.Reducing histone acetylation rescues cognitive deficits in a mouse model of Fragile X syndrome.Loss of MeCP2 in immature neurons leads to impaired network integrationHippocampal deficits in neurodevelopmental disordersRegulatory discrimination of mRNAs by FMRP controls mouse adult neural stem cell differentiationCRISPR/Cas9 editing of APP C-terminus attenuates β-cleavage and promotes α-cleavageHuman Models Are Needed for Studying Human Neurodevelopmental Disorders.Identification of FMR1-regulated molecular networks in human neurodevelopmentReduced mitochondrial fusion and Huntingtin levels contribute to impaired dendritic maturation and behavioral deficits in Fmr1-mutant mice
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description
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Xinyu Zhao
@ast
Xinyu Zhao
@en
Xinyu Zhao
@es
Xinyu Zhao
@nl
type
label
Xinyu Zhao
@ast
Xinyu Zhao
@en
Xinyu Zhao
@es
Xinyu Zhao
@nl
prefLabel
Xinyu Zhao
@ast
Xinyu Zhao
@en
Xinyu Zhao
@es
Xinyu Zhao
@nl
P106
P31
P496
0000-0002-5128-4424