Identification of potential molecular mechanism related to craniofacial dysmorphism caused by FOXI3 deficiency

ConclusionThe craniofacial dysmorphism caused by the deficiency ofFoxi3 may be related to the expression ofAkt2 and PI3K-Akt signaling pathway. This study laid a foundation for understanding the function ofFOXI3 and the pathogenesis and treatment of related craniofacial dysmorphism caused byFOXI3 dysfunction.

Source: Molecular Genetics & Genomic Medicine - March 4, 2024 Category: Genetics & Stem Cells Authors: Xiao ‐Liang Xing, Ziqiang Zeng, Yana Wang, Bo Pan, Xueshuang Huang Tags: ORIGINAL ARTICLE Source Type: research