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These datasets are generated and analyzed during the SynGAP study.
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Wu, Fengqi创建时间：
2024-06-14
相关数据集
Regulation of CHD2 expression by a long noncoding RNA is essential for mammalian development
Long noncoding RNAs (lncRNAs) are enriched in regions flanking transcription- and chromatin-associated genes, but the functional importance of such co-location events is largely unclear. Chromodomain
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Elevated Fibroblast Growth Factor Signaling Is Critical for the Pathogenesis of the Dwarfism in Evc2/Limbin Mutant Mice
Ellis-van Creveld (EvC) syndrome is a skeletal dysplasia, characterized by short limbs, postaxial polydactyly, and dental abnormalities. EvC syndrome is also categorized as a ciliopathy because of cil
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Additional file 2: of RNA sequencing and proteomics approaches reveal novel deficits in the cortex of Mecp2-deficient mice, a model for Rett syndrome
List of significant genes (p < 0.05) identified as RTT hits along with references. Information on WT and Mecp2 Jae/y FPKM values, Log2 fold change expression, p-value and q-value (FDR) are provided
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Transcriptome analysis of Chd8 S62X heterozygote mutant and wild-type mice
Autism spectrum disorders (ASD) are ~4-times more common in males than females, and CHD8 (a chromatin remodeler)-related ASD shows a strong male bias (~5:1), although the underlying mechanism remains
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Effect of DRP1 mutations on synaptic development during iPSC-derived cortical neuron maturation
With the advent of exome sequencing, a growing number of children are being identified with de novo loss of function mutations in the large GTPase essential for mitochondrial fission - Dynamin Related
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