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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 Ciona intestinalis demonstrated a critical role for ETS1 in heart cell fate determination and cell migration, sugges...
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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MDPI
2022
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9319889/ https://www.ncbi.nlm.nih.gov/pubmed/35877581 http://dx.doi.org/10.3390/jcdd9070219 |