Molecular characterization of MET fusions from a large real‐world Chinese population: A multicenter study

por Xia, Hui, Zhang, Junhua, Chen, Tong, Wang, Mingzhao, Chen, Dongna, Si, Tongguo, Liu, Yutao
Publicado 2023

Efficacy and safety of immunotherapy combined with single-agent chemotherapy as second- or later-line therapy for metastatic non-small cell lung cancer

por Chen, Dongna, Li, Lin, Wang, Mingzhao, Hu, Xingsheng, Jiang, Jun, Li, Weihua, Yang, Lin, Fan, Meng, Shi, Yuankai, Lv, Fang, Liu, Yutao
Publicado 2023

A novel gene ZNF862 causes hereditary gingival fibromatosis

por Wu, Juan, Chen, Dongna, Huang, Hui, Luo, Ning, Chen, Huishuang, Zhao, Junjie, Wang, Yanyan, Zhao, Tian, Huang, Siyuan, Ren, Yang, Zhai, Teng, Sun, Weibin, Li, Houxuan, Li, Wei
Publicado 2022

Novel mutations c.28G>T (p.Ala10Ser) and c.189G>T (p.Glu63Asp) in WDR62 associated with early onset acanthosis and hyperkeratosis in a patient with autosomal recessive microcephaly...

por Banerjee, Santasree, Chen, Huishuang, Huang, Hui, Wu, Jing, Yang, Zhiyun, Deng, Weiping, Chen, Dongna, Deng, Jianlian, Su, Yan, Li, Yang, Wu, Chao, Wang, Ye, Zeng, Hao, Wang, Yiming, Li, Xunhua
Publicado 2016

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 2017