Is MTHFD1 polymorphism rs 2236225 (c.1958G>A) associated with the susceptibility of NSCL/P? A systematic review and meta-analysis

por Zhao, Huaxiang, Zhang, Jieni, Zhang, Mengqi, Deng, Feng, Zheng, Leilei, Zheng, Hui, Chen, Feng, Lin, Jiuxiang
Publicado 2016

Functional Characterization of a Novel IRF6 Frameshift Mutation From a Van Der Woude Syndrome Family

por Zhang, Mengqi, Zhang, Jieni, Zhao, Huaxiang, Ievlev, Vitaly, Zhong, Wenjie, Huang, Wenbin, Cornell, Robert A., Lin, Jiuxiang, Chen, Feng
Publicado 2020

A novel FZD6 mutation revealed the cause of cleft lip and/or palate in a Chinese family

por Zhang, Jieni, Zhao, Huaxiang, Huang, Wenbin, Song, Fengqi, Zhong, Wenjie, Zhang, Mengqi, Zhang, Yunfan, Zhou, Zhibo, Lin, Jiuxiang, Chen, Feng
Publicado 2019

Three GLI2 mutations combined potentially underlie non‐syndromic cleft lip with or without cleft palate in a Chinese pedigree

por Meng, Peiqi, Zhao, Huaxiang, Huang, Wenbin, Zhang, Yunfan, Zhong, Wenjie, Zhang, Mengqi, Jia, Peizeng, Zhou, Zhibo, Maimaitili, Gulibaha, Chen, Feng, Zhang, Jieni, Lin, Jiuxiang
Publicado 2019

Identification of rare PTCH1 nonsense variant causing orofacial cleft in a Chinese family and an up-to-date genotype-phenotype analysis

por Zhong, Wenjie, Zhao, Huaxiang, Huang, Wenbin, Zhang, Mengqi, Zhang, Qian, Zhang, Yue, Chen, Chong, Nueraihemaiti, Zulihumaer, Tuerhong, Dilifeire, Huang, Huizhe, Maimaitili, Gulibaha, Chen, Feng, Lin, Jiuxiang
Publicado 2020

The cytokine FAM3B/PANDER is an FGFR ligand that promotes posterior development in Xenopus

por Zhang, Fangfang, Zhu, Xuechen, Wang, Pan, He, Qing, Huang, Huimei, Zheng, Tianrui, Li, Yongyu, Jia, Hong, Xu, Linping, Zhao, Huaxiang, Colozza, Gabriele, Tao, Qinghua, De Robertis, Edward M., Ding, Yi
Publicado 2021