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RNAseq of iPSC derived cardiomyocytes in response to endothelin-1 as a model for cardiac hypertrophy

ChEBI2020-09-01 更新2026-07-12 收录

心肌肥大模型研究

干细胞转录组学

数据链接：

https://www.ebi.ac.uk/biostudies/ArrayExpress/studies/E-MTAB-8548 数据链接链接失效反馈

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RNAseq of iPSC derived cardiomyocytes in response to endothelin-1 as a model for cardiac hypertrophy

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创建时间：

2020-09-01

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

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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. 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

Transcription profiling of hematopoietic and adipose tissue-derived stem cells

干细胞转录组学

造血与脂肪干细胞研究

Transcription profiling of hematopoietic and adipose tissue-derived stem cells

ChEBI2006-10-15 更新10

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).

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RNAseq of iPSC derived cardiomyocytes in response to endothelin-1 as a model for cardiac hypertrophy

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