Polymorphisms in estrogen receptors predict the risk of male infertility: a meta-analysis

por Li, Tian-Fu, Wu, Qiu-Yue, Zhang, Cui, Li, Wei-Wei, Li, Na, Cui, Ying-Xia, Li, Xiao-Jun, Xia, Xin-Yi
Publicado 2014

Clinical, molecular and cytogenetic analysis of 46, XX testicular disorder of sex development with SRY-positive

por Wu, Qiu-Yue, Li, Na, Li, Wei-Wei, Li, Tian-Fu, Zhang, Cui, Cui, Ying-Xia, Xia, Xin-Yi, Zhai, Jin-Sheng
Publicado 2014

The clinicopathological features of ganglioglioma with CD34 expression and BRAF mutation in patients with epilepsy

por Xie, Ming-Guo, Wang, Xiong-Fei, Qiao, Jiao, Zhou, Jian, Guan, Yu-Guang, Li, Tian-Fu, Qi, Xue-Ling, Luan, Guo-Ming
Publicado 2023

The long‐term surgical outcomes of low‐grade epilepsy‐associated neuroepithelial tumors

por Xie, Ming‐Guo, Wang, Xiong‐Fei, Qiao, Jiao, Zhou, Jian, Guan, Yu‐Guang, Liu, Chang‐Qing, Zhao, Meng, Li, Tian‐Fu, Luan, Guo‐Ming
Publicado 2022

46,XX testicular disorder of sexual development with SRY-negative caused by some unidentified mechanisms: a case report and review of the literature

por Li, Tian-Fu, Wu, Qiu-Yue, Zhang, Cui, Li, Wei-Wei, Zhou, Qing, Jiang, Wei-Jun, Cui, Ying-Xia, Xia, Xin-Yi, Shi, Yi-Chao
Publicado 2014

A duplication upstream of SOX9 was not positively correlated with the SRY-negative 46,XX testicular disorder of sex development: A case report and literature review

por XIA, XIN-YI, ZHANG, CUI, LI, TIAN-FU, WU, QIU-YUE, LI, NA, LI, WEI-WEI, CUI, YING-XIA, LI, XIAO-JUN, SHI, YI-CHAO
Publicado 2015

Overexpression of kinesin superfamily members as prognostic biomarkers of breast cancer

por Li, Tian-Fu, Zeng, Hui-Juan, Shan, Zhen, Ye, Run-Yi, Cheang, Tuck-Yun, Zhang, Yun-Jian, Lu, Si-Hong, Zhang, Qi, Shao, Nan, Lin, Ying
Publicado 2020

A novel P20R mutation in the alpha-B crystallin gene causes autosomal dominant congenital posterior polar cataracts in a Chinese family

por Xia, Xin-Yi, Wu, Qiu-Yue, An, Li-Mei, Li, Wei-Wei, Li, Na, Li, Tian-Fu, Zhang, Cui, Cui, Ying-Xia, Li, Xiao-Jun, Xue, Chun-Yan
Publicado 2014

A novel COL4A1 gene mutation results in autosomal dominant non-syndromic congenital cataract in a Chinese family

por Xia, Xin-Yi, Li, Na, Cao, Xiang, Wu, Qiu-Yue, Li, Tian-Fu, Zhang, Cui, Li, Wei-Wei, Cui, Ying-Xia, Li, Xiao-Jun, Xue, Chun-Yan
Publicado 2014

A parthenogenetic maternal and double paternal contribution to an ovotesticular disorder of sex development

por Xia, Xin-Yi, Wang, Wei-Ping, Li, Tian-Fu, Li, Wei-Wei, Wu, Qiu-Yue, Li, Na, Zhang, Cui, Gao, Hong-Liu, Li, Xiao-Jun, Cui, Ying-Xia
Publicado 2014

A Novel p. Gly630Ser Mutation of COL2A1 in a Chinese Family with Presentations of Legg–Calvé–Perthes Disease or Avascular Necrosis of the Femoral Head

por Li, Na, Yu, Jian, Cao, Xiang, Wu, Qiu-Yue, Li, Wei-Wei, Li, Tian-Fu, Zhang, Cui, Cui, Ying-Xia, Li, Xiao-Jun, Yin, Zhi-Min, Xia, Xin-Yi
Publicado 2014

A patient with unusual features and a 69.5 Mb duplication from a de novo extra der (9): A case report

por ZHOU, YU-CHUN, ZHANG, CUI, ZHAI, JIN-SHENG, LI, TIAN-FU, WU, QIU-YUE, LI, WEI-WEI, LI, NA, LI, XIAO-JUN, HUANG, YU-FENG, CUI, YING-XIA, XIA, XIN-YI
Publicado 2015

Rasmussen’s encephalitis is characterized by relatively lower production of IFN-β and activated cytotoxic T cell upon herpes viruses infection

por Wang, Yi-Song, Liu, Dong, Wang, Xin, Luo, Qiao-Li, Ding, Ling, Fan, Dong-Ying, Cai, Qi-Liang, Tang, Chong-Yang, Yang, Wei, Guan, Yu-Guang, Li, Tian-Fu, Wang, Pei-Gang, Luan, Guo-Ming, An, Jing
Publicado 2022

Translocation of High Mobility Group Box 1 From the Nucleus to the Cytoplasm in Depressed Patients With Epilepsy

por Li, Xiao-Li, Wang, Shu, Tang, Chong-Yang, Ma, Hao-Wei, Cheng, Zi-Zhang, Zhao, Meng, Sun, Wei-Jin, Wang, Xiong-Fei, Wang, Meng-Yang, Li, Tian-Fu, Qi, Xue-Ling, Zhou, Jian, Luan, Guo-Ming, Guan, Yu-Guang
Publicado 2022