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Gain and loss of function variants in EZH1 disrupt neurogenesis and cause overlapping neurodevelopmental disorders.

NIAID Data Ecosystem2026-05-01 收录

发育遗传学

EZH1基因功能变异

数据链接：

https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE227016 数据链接链接失效反馈

官方服务：

资源简介：

This SuperSeries is composed of the SubSeries listed below. Refer to individual Series

应用场景：

创建时间：

2023-08-03

发育遗传学

基因功能验证

Additional file 12: Source Data File 1. Zip file with the raw unedited blot images. Sections of these 3 images were used to create Supplemental Fig. 2.

DataCite Commons2023-05-05 更新120

Genomic integration of Wnt/b-catenin and BMP/Smad1 coordinates the transcriptional program of foregut and hindgut progenitors. Genomic integration of Wnt/b-catenin and BMP/Smad1 coordinates the transcriptional program of foregut and hindgut progenitors

发育遗传学

转录组调控

This SuperSeries is composed of the SubSeries listed below. Overall design: Refer to individual Series

NIAID Data Ecosystem50

Procrustes distances between neonatal mean shapes.

形态测量学

发育遗传学

All comparisons are significant at p UG1c, which is significant at p = 0.0102. Abbreviations: OG = Pten overgrowth model; OGc = overgrowth control, UG1 = Trsp undergrowth model; UG1c = Trsp undergrowt

Figshare2015-12-03 更新40

E-GEOD-1482

发育遗传学

转录组分析

Transcription profiling of mouse NF+/- and control samples to determine the molecular basis of the neurodevelopmental changes that result from the primary gene mutation

NIAID Data Ecosystem70

Slc25a21_expression_profile

基因表达分析

发育遗传学

Homozygosity for Slc25a21 results in mice exhibiting orofacial abnormalities, alterations in carpal and rugae structures, and hearing impairment and inflammation in the middle ear. Unexpectedly, after

NIAID Data Ecosystem50

Gain and loss of function variants in EZH1 disrupt neurogenesis and cause overlapping neurodevelopmental disorders.

资源简介：

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