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Global gene expression profiles of iPSC from SMA patient, unaffected father and iPS 19.9 compared to transcriptomic data obtained by corresponding fibroblasts

ChEBI2013-01-04 更新2026-07-21 收录

iPSC疾病模型

脊髓损伤转录组学

数据链接：

https://www.ebi.ac.uk/biostudies/ArrayExpress/studies/E-GEOD-27206 数据链接链接失效反馈

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资源简介：

Global gene expression profiles of iPSC from SMA patient, unaffected father and iPS 19.9 compared to transcriptomic data obtained by corresponding fibroblasts

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创建时间：

2013-01-04

ALS疾病分子机制

iPSC疾病模型

We established iPSCs from healthy donors, FUS-ALS and SOD1-ALS patients. Using our differentiation protocol originally developed by Reinhardt et al.,2013, we diferentiated these iPSCs toward spinal mo

NIAID Data Ecosystem100

Genome wide analysis of thoracic spinal cord at 5 days after T9 hemisection injury.

脊髓损伤转录组学

硬膜外电刺激效应

The goal of this study is to elucidate the influence of hemisection injury at thoracic spinal cord (T9) and epidural electrical spinal stimulation (L2-S1) on transcriptome of injured thoracic spinal c

NIAID Data Ecosystem50

Additional file 8: Table S6. of Transcriptome profile of rat genes in injured spinal cord at different stages by RNA-sequencing

脊髓损伤转录组学

基因功能富集分析

GO enrichment result of the down-regulated genes. (XLSX 58 kb)

Figshare2017-02-16 更新30

Genome wide analysis of the upper lumbar spinal cord at 4 days after T9 hemisection injury. Genome wide analysis of the upper lumbar spinal cord at 4 days after T9 hemisection injury

脊髓损伤转录组学

急性期基因表达

The goal of this study is to elucidate the influence of hemisection injury at thoracic spinal cord (T9) on the upper transcriptome of the upper lumbar spinal cord at acute phase. mRNA profiles of spin

NIAID Data Ecosystem100

Elucidating the role of miRNA in the modulation of Survival Motor Neuron (SMN) genes in both fibroblasts and firboblast-derived iPSCs.. Elucidating the role of miRNA in the modulation of Survival Motor Neuron (SMN) genes in both fibroblasts and firboblast-derived iPSCs.

脊髓性肌萎缩症分子机制

iPSC疾病模型

Spinal muscular atrophy (SMA) is a devastating neuromuscular disorder that affects the spinal motor neurons and leads to progressive muscle wasting and atrophy. It is caused by a reduction in SMN prot

NIAID Data Ecosystem40

Global gene expression profiles of iPSC from SMA patient, unaffected father and iPS 19.9 compared to transcriptomic data obtained by corresponding fibroblasts

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