ロード中...
Arterial endoglin does not protect against arteriovenous malformations
INTRODUCTION: Endoglin (ENG) forms a receptor complex with ALK1 in endothelial cells (ECs) to promote BMP9/10 signalling. Loss of function mutations in either ENG or ALK1 genes lead to the inherited vascular disorder hereditary haemorrhagic telangiectasia (HHT), characterised by arteriovenous malfor...
保存先:
| 出版年: | Angiogenesis |
|---|---|
| 主要な著者: | , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Springer Netherlands
2020
|
| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7524831/ https://ncbi.nlm.nih.gov/pubmed/32506200 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s10456-020-09731-z |
| タグ: |
タグ追加
タグなし, このレコードへの初めてのタグを付けませんか!
|