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...

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Bibliographic Details
Main Authors: Luna Simona Pane (Author), Filomena Gabriella Fulcoli (Author), Andrea Cirino (Author), Alessandra Altomonte (Author), Rosa Ferrentino (Author), Marchesa Bilio (Author), Antonio Baldini (Author)
Format: Book
Published: The Company of Biologists, 2018-09-01T00:00:00Z.
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3rd Floor Main Library

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Call Number: A1234.567
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