官方服务：
资源简介：
The details about this dataset and how to use them can be found here: https://aksimhal.github.io/astrocytes-synapses-fxs/
应用场景：
创建时间：
2019-04-22
相关数据集
RNA-sequencing in WT and Fmr1-/- (KO) neurons treated with Jq1 and THZ
Widespread epigenetic disruptions in FXS mice leads to transcriptional changes that likely contribute to the neuronal phenotpyes underlying FXS. Overall design: 7DIV cultured cortical neurons from WT
NIAID Data Ecosystem50
Additional file 2 of FMRP attenuates activity dependent modifications in the mitochondrial proteome
Additional file 2: Table S2. Ontological analyses of the proteome sensitive to activity deprivation and Fmr1−/y.
NIAID Data Ecosystem40
Table_8_Cytoplasmic Polyadenylation Element-Binding Protein 1 Post-transcriptionally Regulates Fragile X Mental Retardation 1 Expression Through 3′ Untranslated Region in Central Nervous System Neurons.XLSX
Fragile X syndrome (FXS) is an inherited intellectual disability caused by a deficiency in Fragile X mental retardation 1 (Fmr1) gene expression. Recent studies have proposed the importance of cytopla
NIAID Data Ecosystem20
Effects of Fmr1 gene mutations on sex differences in autism-like behavior and dendritic spine development in mice and transcriptomic studies. Effects of Fmr1 gene mutations on sex differences in autism-like behavior and dendritic spine development in mice and transcriptomic studies
Fragile X syndrome (FXS) is the most common single gene disorder contributing to autism spectrum disorder (ASD). Although significant sex differences are observed in FXS, few studies have focused on t
NIAID Data Ecosystem40
Knockdown and Overexpression of FMR4 in HEK293T cells at 6 and 24 hours
CGG repeat expansions in the Fragile X mental retardation 1 (FMR1) gene are responsible for a family of associated disorders characterized by either intellectual disability and autism (Fragile X Syndr
NIAID Data Ecosystem40
