CHD7 regulates definitive endodermal and mesodermal development from human embryonic stem cells
Abstract Background CHD7 encodes an ATP-dependent chromodomain helicase DNA binding protein; mutations in this gene lead to multiple developmental disorders, including CHARGE (Coloboma, Heart defects, Atresia of the choanae, Retardation of growth and development, Genital hypoplasia, and Ear anomalie...
Tallennettuna:
| Päätekijät: | , , , , , , |
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| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
BMC
2025-06-01
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| Sarja: | Stem Cell Research & Therapy |
| Aiheet: | |
| Linkit: | https://doi.org/10.1186/s13287-025-04437-9 |
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