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Transcriptome profiling of mutant embryos from the Mouse Genetics Project DMDD

ChEBI2014-09-02 更新2026-07-21 收录

胚胎发育转录组学

小鼠疾病模型

数据链接：

https://www.ebi.ac.uk/biostudies/ArrayExpress/studies/E-ERAD-272 数据链接链接失效反馈

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资源简介：

Transcriptome profiling of mutant embryos from the Mouse Genetics Project DMDD

应用场景：

创建时间：

2014-09-02

胚胎发育转录组学

器官发生分子网络

We here report transcriptome profiles of human embryos at six successive developmental stages (i.e., Carnegie Stages 9 to 14), representing the first comprehensive gene expression database of early hu

NIAID Data Ecosystem50

Transcriptomic landscape of developing Presomitic mesoderm (PSM)

胚胎发育转录组学

干细胞定向分化模型

Stem cell-derived tissues have wide potential for modelling developmental and pathological processes as well as cell-based therapy. However, it has proven difficult to generate several key cell types

NIAID Data Ecosystem30

RNA-seq profiling of neural tissue from mouse embryos with combined loss of p53 and Bim

神经管缺陷分子机制

胚胎发育转录组学

Neural tube defects (NTDs) are common birth defects in humans and show an unexplained female bias. Female mice lacking the tumor suppressor p53 display NTDs with incomplete penetrance. We found that t

NIAID Data Ecosystem10

Validated urine metabolites that were differentially abundant in RM as compared to CM in Atm-KO and WT mice.

代谢组学分析

小鼠疾病模型

Validated urine metabolites that were differentially abundant in RM as compared to CM in Atm-KO and WT mice.

NIAID Data Ecosystem40

Summary statistics for Fig 3B.

运动神经元疾病

小鼠疾病模型

Motor neuron diseases, such as amyotrophic lateral sclerosis (ALS) and progressive bulbar palsy, involve loss of muscle control resulting from death of motor neurons. Although the exact pathogenesis o

NIAID Data Ecosystem30

Transcriptome profiling of mutant embryos from the Mouse Genetics Project DMDD

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