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Journal of Shanghai Jiaotong University(Medical Science) ; (12): 361-362, 2018.
Article Dans Chinois | WPRIM | ID: wpr-695671

Résumé

Wdpcp,a planar cell polarity (PCP) effector gene,plays essential roles in organogenesis during embryonic development through regulating collective cell movement and ciliogenesis.WDPCP mutations are associated with Bardet-Biedl syndrome and Meckel-Gruber syndrome in human.This study revealed a novel role of Wdpcp in regulating coronary artery development in mouse,demonstrating a new pathogenic phenotype associated with mutations of this gene in human.Results of this study may help us to understand the etiology of coronary artery disease.

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