NKX2-5 mutations causative for congenital heart disease retain functionality and are directed to hundreds of targets
We take a functional genomics approach to congenital heart disease mechanism. We used DamID to establish a robust set of target genes for NKX2-5 wild type and disease associated NKX2-5 mutations to model loss-of-function in gene regulatory networks. NKX2-5 mutants, including those with a crippled ho...
Tallennettuna:
| Päätekijät: | , , , , , , , , , , , , , , , , , |
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| Aineistotyyppi: | Artigo |
| Kieli: | englanti |
| Julkaistu: |
2015
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| Linkit: | https://doi.org/10.7554/elife.06942 |
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