首页/数据集/Transcriptional profiling of hair follicle stem cells in the presence and absence of Regulatory T-cells

Transcriptional profiling of hair follicle stem cells in the presence and absence of Regulatory T-cells

ChEBI2017-04-28 更新2026-07-12 收录

干细胞转录组学

妊娠免疫微环境调控

数据链接：

https://www.ebi.ac.uk/biostudies/ArrayExpress/studies/E-GEOD-76102 数据链接链接失效反馈

官方服务：

资源简介：

Transcriptional profiling of hair follicle stem cells in the presence and absence of Regulatory T-cells

应用场景：

创建时间：

2017-04-28

干细胞转录组学

细胞适应性

Transcriptome profile was obtained from a set of human embryonic stem cell (hESCs) line (WA09: H9) with different passage numbers (P1: 40s, P2: 100s, P3: 200s, P4: 300s passage). Culture adaptation oc

NIAID Data Ecosystem70

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

脊髓性肌萎缩症机制研究

干细胞转录组学

Spinal Muscular Atrophy (SMA) is an autosomal recessive motor neuron disease and is the second most common genetic disorder leading to death in childhood. Motoneurons derived from induced pluripotent

NIAID Data Ecosystem60

CD73-Dependent Adenosine Signaling through Adora2b Drives Immunosuppression in Ductal Pancreatic Cancer

癌症分子机制

妊娠免疫微环境调控

Kras and Trp53 mutations promote transformation in pancreatic acinar and ductal cells. We wanted to evaluate whole transcriptomic profiles of acinar and ductal derived tumors. In addition, we studied

NIAID Data Ecosystem30

RNA-seq study of human long-term and short-term hematopoietic stem cells from umblical cord blood with lentiviral overexpression of S1PR3

干细胞转录组学

S1PR3基因功能研究

To investigate the molecular and biological pathways altered by S1PR3OE in human hematopoietic stem cells (HSC), we performed RNA-sequencing (RNA-seq) of LT- and ST-HSC 3 days after transduction with

NIAID Data Ecosystem60

Human iPSC-derived neuronal cells from CTBP1-mutated patients reveal altered expression of neurodevelopmental gene networks

神经疾病模型

干细胞转录组学

A recurrent de novo mutation in the transcriptional corepressor CTBP1 is associated with neurodevelopmental disabilities in children (Beck et al., 2016; Beck et al., 2019; Sommerville et al., 2017).

NIAID Data Ecosystem40

Transcriptional profiling of hair follicle stem cells in the presence and absence of Regulatory T-cells

资源简介：

相关数据集