CHD8 RNAseq

NIAID Data Ecosystem2026-03-11 收录

CHD8基因表达谱

神经发育障碍转录组学

数据链接：

https://www.omicsdi.org/dataset/ega/EGAS00001004270 数据链接链接失效反馈

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资源简介：

This study aims to conduct a landscape analysis of transcriptome from a patient with CHD8 deletion. RNAseq was conducted on a patient and normal sibling, each sample in triplicate.EGA study EGAS00001004270

创建时间：

2020-03-09

Table5_m6A Modification Involves in Enriched Environment-Induced Neurogenesis and Cognition Enhancement.XLSX

神经发育障碍转录组学

m6A甲基化调控

Although previous studies have shown that an enriched environment (EE) promotes neurogenesis and alters DNA and histone modifications, it remains largely unknown whether an EE affects epitranscriptome

NIAID Data Ecosystem80

An activity-mediated transition in transcription in early postnatal neurons [RNA-seq]. An activity-mediated transition in transcription in early postnatal neurons [RNA-seq]

出生后神经元转录调控

神经发育障碍转录组学

The maturation of the mammalian brain occurs after birth, and this stage of neuronal development is frequently impaired in neurological disorders, such as autism and schizophrenia. However, the mechan

NIAID Data Ecosystem60

Differential Gene Expression in Angelman syndrome deletion vs. int dup(15) Human Lymphocytes

Angelman综合征差异表达

神经发育障碍转录组学

Angelman syndrome (AS) and interstitial duplication 15q autism (int dup(15)) are reciprocal genomic disorders caused by maternal deletion or duplication of the 15q11.2-q13 region. While AS is caused

NIAID Data Ecosystem30

Bi-allelic SNAPC4 variants lead to altered global splicing and a neurodevelopmental disorder

剪接分析

神经发育障碍转录组学

To investigate the transcriptomic effects of deleterious SNAPC4 variants, patient-derived cells and SNAPC4-deficient HeLa cells were used to generate RNA-Seq data. Overall design: Four comparisons wer

NIAID Data Ecosystem80

Transcriptome data of temporal and cingulate cortex in the Rett syndrome brain. Transcriptome data of temporal and cingulate cortex in the Rett syndrome brain

Rett综合征分子病理机制

神经发育障碍转录组学

Rett syndrome is an X-linked neurodevelopmental disorder caused by mutation in the methyl-CpG-binding protein 2 gene in the majority of cases. We describe an RNA sequencing dataset of postmortem brain

NIAID Data Ecosystem50

CHD8 RNAseq

资源简介：

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