Bacterial metabolites directly modulate farnesoid X receptor activity

av Zhang, Xianqin, Osaka, Toshifumi, Tsuneda, Satoshi
I publikationen Nutr Metab (Lond) (2015)

The diagnostic role of microRNA-34a in breast cancer: a systematic review and meta-analysis

av Imani, Saber, Zhang, Xianqin, Hosseinifard, Hossein, Fu, Shangyi, Fu, Junjiang
I publikationen Oncotarget (2017)

SLCO4C1 promoter methylation is a potential biomarker for prognosis associated with biochemical recurrence-free survival after radical prostatectomy

av Li, Xin, Zhang, Wanfeng, Song, Jing, Zhang, Xianqin, Ran, Longke, He, Yunfeng
I publikationen Clin Epigenetics (2019)

Potential treatment with Chinese and Western medicine targeting NSP14 of SARS-CoV-2

av Liu, Chao, Zhu, Xiaoxiao, Lu, Yiyao, Zhang, Xianqin, Jia, Xu, Yang, Tai
I publikationen J Pharm Anal (2021)

Chinese College Students' Stress and Anxiety Levels Under COVID-19

av Zhan, Huali, Zheng, Chunmei, Zhang, Xianqin, Yang, Meng, Zhang, Lin, Jia, Xu
I publikationen Front Psychiatry (2021)

A novel donor splice-site mutation of major intrinsic protein gene associated with congenital cataract in a Chinese family

av Zeng, Lu, Liu, Wenqiang, Feng, Wenguo, Wang, Xing, Dang, Hui, Gao, Luna, Yao, Jing, Zhang, Xianqin
Publicerad 2013

LINC01272 Promotes Migration and Invasion of Gastric Cancer Cells via EMT

av Leng, Xue, Liu, Geli, Wang, Sen, Song, Jing, Zhang, Wanfeng, Zhang, Xianqin, Rong, Li, Ma, Yongping, Song, Fangzhou
I publikationen Onco Targets Ther (2020)

Novel mutations in ZP1 and ZP2 cause primary infertility due to empty follicle syndrome and abnormal zona pellucida

av Luo, Geng, Zhu, Lixia, Liu, Zhenxing, Yang, Xue, Xi, Qingsong, Li, Zhou, Duan, Jinliang, Jin, Lei, Zhang, Xianqin
I publikationen J Assist Reprod Genet (2020)

Novel compound heterozygous mutations in WEE2 causes female infertility and fertilization failure

av Zhou, Xiaopei, Zhu, Lixia, Hou, Meiqi, Wu, Yanling, Li, Zhou, Wang, Jiarui, Liu, Zhenxing, Zhang, Dazhi, Jin, Lei, Zhang, Xianqin
I publikationen J Assist Reprod Genet (2019)

ARHGEF38 as a novel biomarker to predict aggressive prostate cancer

av Liu, Kun, Wang, Aixiang, Ran, Longke, Zhang, Wanfeng, Jing, Song, Wang, Yujing, Zhang, Xianqin, Liu, Geli, Sen, Wang, Song, Fangzhou
I publikationen Genes Dis (2019)

Integrative analysis of the gastric cancer long non-coding RNA-associated competing endogenous RNA network

av Jiang, Yuyou, Zhang, Xianqin, Rong, Li, Hou, Yi, Song, Jing, Zhang, Wanfeng, He, Min, Xie, Yan, Li, Yue, Song, Fangzhou
I publikationen Oncol Lett (2021)

A novel DSPP mutation is associated with type II dentinogenesis Imperfecta in a chinese family

av Zhang, Xianqin, Chen, Lanying, Liu, Jingyu, Zhao, Zhen, Qu, Erjun, Wang, Xiaotao, Chang, Wei, Xu, Chengqi, Wang, Qing K, Liu, Mugen
Publicerad 2007

Protective effect of KCNH2 single nucleotide polymorphism K897T in LQTS families and identification of novel KCNQ1 and KCNH2 mutations

av Zhang, Xianqin, Chen, Shenghan, Zhang, Li, Liu, Mugen, Redfearn, Sharon, Bryant, Randall M, Oberti, Carlos, Vincent, G Michael, Wang, Qing K
Publicerad 2008

Novel homozygous mutations in PATL2 lead to female infertility with oocyte maturation arrest

av Liu, Zhenxing, Zhu, Lixia, Wang, Jiarui, Luo, Geng, Xi, Qingsong, Zhou, Xiaopei, Li, Zhou, Yang, Xue, Duan, Jinliang, Jin, Lei, Zhang, Xianqin
I publikationen J Assist Reprod Genet (2020)

MicroRNA-34a targets epithelial to mesenchymal transition-inducing transcription factors (EMT-TFs) and inhibits breast cancer cell migration and invasion

av Imani, Saber, Wei, Chunli, Cheng, Jingliang, Asaduzzaman Khan, Md., Fu, Shangyi, Yang, Luquan, Tania, Mousumi, Zhang, Xianqin, Xiao, Xiuli, Zhang, Xianning, Fu, Junjiang
I publikationen Oncotarget (2017)

p.His16Arg of STXBP1 (MUNC18-1) Associated With Syntaxin 3B Causes Autosomal Dominant Congenital Nystagmus

av Li, Yulei, Jiang, Lei, Wang, Lejin, Wang, Cheng, Liu, Chunjie, Guo, Anyuan, Liu, Mugen, Zhang, Luoying, Ma, Cong, Zhang, Xianqin, Gao, Shangbang, Liu, Jing Yu
I publikationen Front Cell Dev Biol (2020)

A novel mutation in ZP3 causes empty follicle syndrome and abnormal zona pellucida formation

av Zhang, Dazhi, Zhu, Lixia, Liu, Zhenxing, Ren, Xinling, Yang, Xue, Li, Dan, Luo, Yalin, Peng, Xuejie, Zhou, Xiaopei, Jia, Weimin, Hou, Meiqi, Li, Zhou, Jin, Lei, Zhang, Xianqin
I publikationen J Assist Reprod Genet (2020)

Novel CACNA1S mutation causes autosomal dominant hypokalemic periodic paralysis in a Chinese family

av Wang, Qiufen, Liu, Mugen, Xu, Chunsheng, Tang, Zhaohui, Liao, Yuhua, Du, Rong, Li, Wei, Wu, Xiaoyan, Wang, Xu, Liu, Ping, Zhang, Xianqin, Zhu, Jianfang, Ren, Xiang, Ke, Tie, Wang, Qing, Yang, Junguo
Publicerad 2005

Three novel compound heterozygous IL12RB1 mutations in Chinese patients with Mendelian susceptibility to mycobacterial disease

av Zhou, Xiaopei, Jia, Weimin, Ni, Zhengyi, Wang, Ali, Liu, Zhenxing, Hou, Meiqi, Zhou, Mi, Tang, Zhongwen, Zhang, Dazhi, Li, Lei, Han, Tiantian, Tan, Yang, Luo, Geng, Wang, Jiarui, Wu, Yanling, Zhang, Xianqin
I publikationen PLoS One (2019)

Genetic identification and molecular modeling characterization reveal a novel PROM1 mutation in Stargardt4-like macular dystrophy

av Imani, Saber, Cheng, Jingliang, Shasaltaneh, Marzieh Dehghan, Wei, Chunli, Yang, Lisha, Fu, Shangyi, Zou, Hui, Khan, Md. Asaduzzaman, Zhang, Xianqin, Chen, Hanchun, Zhang, Dianzheng, Duan, Chengxia, Lv, Hongbin, Li, Yumei, Chen, Rui, Fu, Junjiang
I publikationen Oncotarget (2017)