ETS1 and HLHS: Implications for the Role of the Endocardium
We have identified the ETS1 gene as the cause of congenital heart defects, including an unprecedented high frequency of HLHS, in the chromosomal disorder Jacobsen syndrome. Studies in <i>Ciona intestinalis</i> demonstrated a critical role for ETS1 in heart cell fate determination and cell migration,...
保存先:
| 第一著者: | |
|---|---|
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
MDPI AG
2022-07-01
|
| シリーズ: | Journal of Cardiovascular Development and Disease |
| 主題: | |
| オンライン･アクセス: | https://www.mdpi.com/2308-3425/9/7/219 |
| タグ: |
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!
|