Chronic sciatic nerve compression induces fibrosis in dorsal root ganglia

Por LI, QINWEN, CHEN, JIANGHAI, CHEN, YANHUA, CONG, XIAOBIN, CHEN, ZHENBING
Publicado no Mol Med Rep (2016)

Association of apolipoprotein A1 -75 G/A polymorphism with susceptibility to the development of acute lung injury after cardiopulmonary bypass surgery

Por Tu, Jie, Zhang, Bingdong, Chen, Yanhua, Liang, Beiwei, Liang, Dongke, Liu, Guofeng, He, Fang
Publicado em 2013

Identification of a novel missense mutation of MIP in a Chinese family with congenital cataracts by target region capture sequencing

Por Jiang, Bo, chen, Yanhua, Xu, Baisheng, Hong, Nan, Liu, Rongrong, Qi, Ming, Shen, Liping
Publicado no Sci Rep (2017)

Microwave-Assisted Synthesis of Arene Ru(II) Complexes Induce Tumor Cell Apoptosis Through Selectively Binding and Stabilizing bcl-2 G-Quadruplex DNA

Por Chen, Yanhua, Wu, Qiong, Wang, Xicheng, Xie, Qiang, Tang, Yunyun, Lan, Yutao, Zhang, Shuangyan, Mei, Wenjie
Publicado no Materials (Basel) (2016)

Global metabolomics reveals potential urinary biomarkers of esophageal squamous cell carcinoma for diagnosis and staging

Por Xu, Jing, Chen, Yanhua, Zhang, Ruiping, He, Jiuming, Song, Yongmei, Wang, Jingbo, Wang, Huiqing, Wang, Luhua, Zhan, Qimin, Abliz, Zeper
Publicado no Sci Rep (2016)

Identification of A Novel SBF2 Frameshift Mutation in Charcot–Marie–Tooth Disease Type 4B2 Using Whole-exome Sequencing

Por Chen, Meiyan, Wu, Jing, Liang, Ning, Tang, Lihui, Chen, Yanhua, Chen, Huishuang, Wei, Wei, Wei, Tianying, Huang, Hui, Yi, Xin, Qi, Ming
Publicado no Genomics Proteomics Bioinformatics (2014)

Decrement of Sugar Consumption in Rice Young Panicle Under High Temperature Aggravates Spikelet Number Reduction

Por Wang Yaliang, Zhang Yikai, Shi Qinghua, Chen Huizhe, Xiang Jing, Hu Guohui, Chen Yanhua, Wang Xiaodan, Wang Junke, Yi Zihao, Zhu Defeng, Zhang Yuping
Publicado em 2020-01-01

Global and Targeted Metabolomics of Esophageal Squamous Cell Carcinoma Discovers Potential Diagnostic and Therapeutic Biomarkers

Por Xu, Jing, Chen, Yanhua, Zhang, Ruiping, Song, Yongmei, Cao, Jianzhong, Bi, Nan, Wang, Jingbo, He, Jiuming, Bai, Jinfa, Dong, Lijia, Wang, Luhua, Zhan, Qimin, Abliz, Zeper
Publicado em 2013

Targeted next generation sequencing identified novel mutations in RPGRIP1 associated with both retinitis pigmentosa and Leber’s congenital amaurosis in unrelated Chinese patients

Por Huang, Hui, Wang, Ying, Chen, Huishuang, Chen, Yanhua, Wu, Jing, Chiang, Pei-Wen, Fan, Ning, Su, Yan, Deng, Jianlian, Chen, Dongna, Li, Yang, Zhang, Xinxin, Zhang, Mengxin, Liang, Shengran, Banerjee, Santasree, Qi, Ming, Liu, Xuyang
Publicado no Oncotarget (2017)

Whole-exome sequencing identifies OR2W3 mutation as a cause of autosomal dominant retinitis pigmentosa

Por Ma, Xiangyu, Guan, Liping, Wu, Wei, Zhang, Yao, Zheng, Wei, Gao, Yu-Tang, Long, Jirong, Wu, Na, Wu, Long, Xiang, Ying, Xu, Bin, Shen, Miaozhong, Chen, Yanhua, Wang, Yuewen, Yin, Ye, Li, Yingrui, Xu, Haiwei, Xu, Xun, Li, Yafei
Publicado no Sci Rep (2015)