Tbx1 represses Mef2c gene expression and is correlated with histone 3 deacetylation of the anterior heart field enhancer
The TBX1 gene is haploinsufficient in 22q11.2 deletion syndrome (22q11.2DS), and genetic evidence from human patients and mouse models points to a major role of this gene in the pathogenesis of this syndrome. Tbx1 can activate and repress transcription, and previous work has shown that one of its fu...
Furkejuvvon:
| Váldodahkkit: | , , , , , , |
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| Materiálatiipa: | Artigo |
| Giella: | Inglês |
| Almmustuhtton: |
The Company of Biologists
2018-09-01
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| Ráidu: | Disease Models & Mechanisms |
| Fáttát: | |
| Liŋkkat: | http://dmm.biologists.org/content/11/9/dmm029967 |
| Fáddágilkorat: |
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