Identification of novel variations in the NTRK1 gene causing congenital insensitivity to pain with anhidrosis

por Li, Shang, Hu, Hua‐ying, Xu, Jun‐Jun, Feng, Zhan‐ke, Sun, Yong‐qing, Chen, Xu, Yang, Kai, Li, Ya‐zhou, Zhang, Dong‐liang
Publicado 2021

Investigation of a Novel LRP6 Variant Causing Autosomal-Dominant Tooth Agenesis

por Huang, Yan-xia, Gao, Chun-yan, Zheng, Chun-yan, Chen, Xu, Yan, You-sheng, Sun, Yong-qing, Dong, Xing-yue, Yang, Kai, Zhang, Dong-liang
Publicado 2021

Investigation of a Novel NTRK1 Variation Causing Congenital Insensitivity to Pain With Anhidrosis

por Yang, Kai, Xu, Yi-Cheng, Hu, Hua-Ying, Li, Ya-Zhou, Li, Qian, Luan, Ying-Yi, Liu, Yan, Sun, Yong-Qing, Feng, Zhan-Ke, Yan, You-Sheng, Yin, Cheng-Hong
Publicado 2021

Prenatal Cases Reflect the Complexity of the COL1A1/2 Associated Osteogenesis Imperfecta

por Yang, Kai, Liu, Yan, Wu, Jue, Zhang, Jing, Hu, Hua-ying, Yan, You-sheng, Chen, Wen-qi, Yang, Shu-fa, Sun, Li-juan, Sun, Yong-qing, Wu, Qing-qing, Yin, Cheng-hong
Publicado 2022

NTRK1 knockdown induces mouse cognitive impairment and hippocampal neuronal damage through mitophagy suppression via inactivating the AMPK/ULK1/FUNDC1 pathway

por Yang, Kai, Wu, Jue, Li, Shang, Wang, Shan, Zhang, Jing, Wang, Yi-peng, Yan, You-sheng, Hu, Hua-ying, Xiong, Ming-fang, Bai, Chao-bo, Sun, Yong-qing, Chen, Wen-qi, Zeng, Yang, Yuan, Jun-liang, Yin, Cheng-hong
Publicado 2023