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Gene Expression Analysis in an Animal Model of Cortical Dysplasia-CONTROL GROUP

ChEBI2008-12-09 更新2026-07-21 收录

神经发育疾病基因

动物模型对照组数据

数据链接：

https://www.ebi.ac.uk/biostudies/ArrayExpress/studies/E-GEOD-13676 数据链接链接失效反馈

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资源简介：

Gene Expression Analysis in an Animal Model of Cortical Dysplasia-CONTROL GROUP

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创建时间：

2008-12-09

癫痫遗传学

神经发育疾病基因

Lennox-Gastaut syndrome (LGS) is a severe type of childhood-onset epilepsy characterized by multiple types of seizures, specific discharges on electroencephalography, and intellectual disability. Most

NIAID Data Ecosystem70

Data: Gene expression of Mowat-Wilson syndrome patient derived GABAergic interneurons

神经发育疾病基因

GABA能神经元

IPSC lines established from fibroblasts of both sibling (MW1=26, MW2=27) and two healthy donors (Ctl2=K02 and Ctl8=K08). Neurocortical differentiation of iPSCs (samples IPS) was carried out as de

DataCite Commons2025-01-16 更新40

RNA_CoIP_HEK_N2a_unfiltered.xlsx

RNA-蛋白相互作用

神经发育疾病基因

In this study, we identified novel interaction partners of wt and truncated MAGEL2.

Figshare2024-06-13 更新10

Multiplex Epigenome Editing of MECP2 to Rescue Rett Syndrome Neurons (WGBS). Multiplex Epigenome Editing of MECP2 to Rescue Rett Syndrome Neurons (WGBS)

神经发育疾病基因

表观基因组学

Rett syndrome (RTT) is an X-linked neurodevelopmental disorder caused by loss-of-function heterozygous mutations of MECP2. Reactivation of the silent wild-type MECP2 allele on the inactive X chromosom

NIAID Data Ecosystem60

L1 Retrotransposition in Tissues of Rett Patients and Healthy Individuals. Homo sapiens

神经发育疾病基因

反转录转座子

We used HAT-seq bulk sequencing to perform genome-wide L1Hs insertion profiling of 20 postmortem tissues from five patients with Rett syndrome and their matched healthy controls. The aims of this stud

NIAID Data Ecosystem30

Gene Expression Analysis in an Animal Model of Cortical Dysplasia-CONTROL GROUP

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