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Data for: Application of a Hindi version of CNS to assess parental needs for children suffering from neurodevelopmental disorder: an Indian perspective

Mendeley Data2024-06-25 更新2024-06-26 收录

神经发育障碍

父母需求评估

数据链接：

https://data.mendeley.com/datasets/tg5j9xrw4g 数据链接链接失效反馈

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资源简介：

Statistical output of results

应用场景：

创建时间：

2024-01-23

基因敲除实验

神经发育障碍

K1, K2, K3 are knockout data. C1, C2, C3 are controls (FASTQ and MD5 files) - for full details see Chalkiadaki et al. 2024

Mendeley Data90

Imbalance of Excitatory_Inhibitory Neuron Differentiation in Neurodevelopmental Disorders with an NR2F1 Point Mutation

神经发育障碍

基因突变

WT and Mut human NPCs were subjected into transcriptome analysis with two biological replicates. ChIP-Seq was done by over-expressing an equal amount of pcDNA3.1-WT/Mut-NR2F1-Flag plasmids into WT hES

干细胞与再生医学数据中心2021-12-14 更新60

Common neuronal mechanisms underlying tics and hyperactivity

神经发育障碍

神经元电生理

Study data and code used in the article "Common neuronal mechanisms underlying tics and hyperactivity" (Israelashvili et al., under review)

NIAID Data Ecosystem50

关于IQSEC家族蛋白结构和功能研究

神经发育障碍

蛋白结构功能

IQSEC1-3，也被称为BRAG1-3，是ARF家族蛋白的鸟苷酸交换因子（GEF）。其中，IQSEC2是高置信度的综合征型自闭症风险基因，也是明确确定的神经发育障碍风险基因。目前，已经发现了100多种与中度到重度的智力障碍、癫痫和自闭症有关的IQSEC2致病突变。然而，现有研究尚未阐明确切的IQSEC2基因型-表型相关性及病理行为表型的分子机制。我们的研究解析了apoCaM/IQ/Sec7-PH

国家基础学科公共科学数据中心80

An Analysis of the Correlation Between Poor Short-Term Memory and Behavior in Children and Adolescents with Prader Willi Syndrome, 1996

神经发育障碍

认知行为

The purpose of the “An Analysis of the Correlation Between Poor Short-term Memory and Behavior in Children and Adolescents with Prader Willi Syndrome, 1996” was to investigate whether there were any c

DataCite Commons2023-02-28 更新50

Data for: Application of a Hindi version of CNS to assess parental needs for children suffering from neurodevelopmental disorder: an Indian perspective

资源简介：

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