Article
New insight into the development of synpolydactyly caused by expansion of HOXD13 polyalanine based on weighted gene co-expression network analysis.
BMC medical genomics - 29 Oct 2024
Chen Xiumin, Shen Xiaofang, Yang Tao, Cao Yixuan, Zhao Xiuli
Abstract excerpt
BACKGROUND: Synpolydactyly (SPD) is mainly caused by mutations of polyalanine expansion (PAE) in the transcription factor gene HOXD13 and the involved cell types and signal pathway are still not clear possible pathways and single-cell expression characteristics of limb bud in HOXD13 PAE mice was analyzed in this study. METHOD: We investigated a previous study of a mouse model with SPD and conducted weighted gene...
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