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RNA-Seq of Homo sapiens: HUVEC treated with FK506/Tacrolimus, ALK1Fc and DMSO

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NIAID Data Ecosystem2026-03-10 收录
下载链接:
https://www.ncbi.nlm.nih.gov/bioproject/PRJNA381813
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资源简介:
Hereditary hemorrhagic telangiectasia (HHT) is a life-threatening vascular disorder arising from aberrant endothelial cell-driven hypervascularization, and caused by loss-of-function mutations in the BMP9-ALK1- Smad1/5/8 signaling pathway. We interrogated the whole-transcriptome in human umbilical vein endothelial cells (HUVECs).
创建时间:
2017-04-05
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