Wilson disease patient with rare heterozygous mutations in ATP7B accompanied by distinctive nocturnal enuresis: A case report

por Zhang, Shijie, Li, Liangyong, Wang, Jiuxiang
Publicado 2020

Study on the Mechanism of Compound Kidney-Invigorating Granule for Osteoporosis based on Network Pharmacology and Experimental Verification

por Lv, Hao, Wang, Jiuxiang, Zhu, Yujun, Jiang, Ting
Publicado 2022

Analyses of key gene networks controlling carotenoid metabolism in Xiangfen 1 banana

por Dong, Chen, Wang, Jiuxiang, Hu, Yulin, Xiao, Weijun, Hu, Huigang, Xie, Jianghui
Publicado 2022

Association between osteoporosis or osteopenia and taking antiplatelet agents in general US population of NHANES

por Lv, Hao, Wang, Jiuxiang, Zhu, Yujun, Hu, Zhimu, Wang, Ziwen, Qiao, Mingzhu, Jiang, Ting
Publicado 2022

Discussion on the Mechanism of Gandoufumu Decoction Attenuates Liver Damage of Wilson's Disease by Inhibiting Autophagy through the PI3K/Akt/mTOR Pathway Based on Network Pharmacol...

por Tang, Lulu, Zhao, Chenling, Zhang, Jing, Dong, Ting, Chen, Huaizhen, Wei, Taohua, Wang, Jiuxiang, Yang, Wenming
Publicado 2023

Case Report: Identification of a De novo C19orf12 Variant in a Patient With Mitochondrial Membrane Protein–Associated Neurodegeneration

por Yang, Yue, Zhang, Shijie, Yang, Wenming, Wei, Taohua, Hao, Wenjie, Cheng, Ting, Wang, Jiuxiang, Dong, Wei, Qian, Nannan
Publicado 2022

Clinical manifestations and genetic analysis of a newborn with Arboleda−Tham syndrome

por Zeng, Feng, Yang, Yue, Xu, Zhaohui, Wang, Ziwen, Ke, Huan, Zhang, Jianhong, Dong, Tongtong, Yang, Wenming, Wang, Jiuxiang
Publicado 2022

Case Report: Late-Onset Autosomal Recessive Cerebellar Ataxia Associated With SYNE1 Mutation in a Chinese Family

por Qian, Nannan, Wei, Taohua, Yang, Wenming, Wang, Jiuxiang, Zhang, Shijie, Jin, Shan, Dong, Wei, Hao, Wenjie, Yang, Yue, Huang, Ru
Publicado 2022

FRMD7 Mutations Disrupt the Interaction with GABRA2 and May Result in Infantile Nystagmus Syndrome

por Jiang, Lei, Li, Yulei, Yang, Kangjuan, Wang, Yuping, Wang, Jiuxiang, Cui, Xiaoniu, Mao, Jinglin, Gao, Yong, Yi, Ping, Wang, Lejin, Liu, Jing Yu
Publicado 2020

Identification of mutations in the ATP7B gene in 14 Wilson disease children: Case series

por Wang, Jiuxiang, Tang, Lulu, Xu, Anqi, Zhang, Shijie, Jiang, Hailin, Pei, Pei, Li, Hongmei, Lv, Tingting, Yang, Yue, Qian, Nannan, Naidu, Keegan, Yang, Wenming
Publicado 2021

Whole exome sequencing identifies a novel NRL mutation in a Chinese family with autosomal dominant retinitis pigmentosa

por Gao, Meng, Zhang, Su, Liu, Chunjie, Qin, Yayun, Archacki, Stephen, Jin, Ling, Wang, Yong, Liu, Fei, Chen, Jiaxiang, Liu, Ying, Wang, Jiuxiang, Huang, Mi, Liao, Shengjie, Tang, Zhaohui, Guo, An Yuan, Jiang, Fagang, Liu, Mugen
Publicado 2016

Loss-of-function Mutation in PMVK Causes Autosomal Dominant Disseminated Superficial Porokeratosis

por Wang, Jiuxiang, Liu, Ying, Liu, Fei, Huang, Changzheng, Han, Shanshan, Lv, Yuexia, Liu, Chun-Jie, Zhang, Su, Qin, Yayun, Ling, Lei, Gao, Meng, Yu, Shanshan, Li, Chang, Huang, Mi, Liao, Shengjie, Hu, Xuebin, Lu, Zhaojing, Liu, Xiliang, Jiang, Tao, Tang, Zhaohui, Zhang, Huiping, Guo, An-Yuan, Liu, Mugen
Publicado 2016