New insight into the development of synpolydactyly caused by expansion of HOXD13 polyalanine based on weighted gene co-expression network analysis

Abstract 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...

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主要な著者:	Xiumin Chen, Xiaofang Shen, Tao Yang, Yixuan Cao, Xiuli Zhao
フォーマット:	Artigo
言語:	Inglês
出版事項:	BMC 2024-10-01
シリーズ:	BMC Medical Genomics
主題:	Synpolydactyly HOXD13 Polyalanine expansion Single-cell RNA sequencing Immune response
オンライン･アクセス:	https://doi.org/10.1186/s12920-024-01974-9
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