Differential expression of ABCB5 in BRAF inhibitor-resistant melanoma cell lines

Por Xiao, Jingjing, Egger, Michael E., McMasters, Kelly M., Hao, Hongying
Publicado no BMC Cancer (2018)

Platinum covalent shell cross-linked micelles designed to deliver doxorubicin for synergistic combination cancer therapy

Por Zhu, Caiying, Xiao, Jingjing, Tang, Ming, Feng, Hua, Chen, Wulian, Du, Ming
Publicado no Int J Nanomedicine (2017)

Overcoming HBV immune tolerance to eliminate HBsAg-positive hepatocytes via pre-administration of GM-CSF as a novel adjuvant for a hepatitis B vaccine in HBV transgenic mice

Por Wang, Xianzheng, Dong, Aihua, Xiao, Jingjing, Zhou, Xingjun, Mi, Haili, Xu, Hanqian, Zhang, Jiming, Wang, Bin
Publicado no Cell Mol Immunol (2016)

A Novel COL4A5 Mutation Identified in a Chinese Han Family Using Exome Sequencing

Por Xiu, Xiaofei, Yuan, Jinzhong, Deng, Xiong, Xiao, Jingjing, Xu, Hongbo, Zeng, Zhaoyang, Guan, Liping, Xu, Fengping, Deng, Sheng
Publicado em 2014

Biomimetic Beetle-Inspired Flapping Air Vehicle Actuated by Ionic Polymer-Metal Composite Actuator

Por Zhao, Yang, Xu, Di, Sheng, Jiazheng, Meng, Qinglong, Wu, Dezhi, Wang, Lingyun, Xiao, Jingjing, Lv, Wenlong, Chen, Qinnan, Sun, Daoheng
Publicado no Appl Bionics Biomech (2018)

Identification of a Novel Missense FBN2 Mutation in a Chinese Family with Congenital Contractural Arachnodactyly Using Exome Sequencing

Por Deng, Hao, Lu, Qian, Xu, Hongbo, Deng, Xiong, Yuan, Lamei, Yang, Zhijian, Guo, Yi, Lin, Qiongfen, Xiao, Jingjing, Guan, Liping, Song, Zhi
Publicado no PLoS One (2016)

Identification of a novel collagen type IV alpha-4 (COL4A4) mutation in a Chinese family with autosomal dominant Alport syndrome using exome sequencing

Por Deng, Sheng, Xu, Hongbo, Yuan, Jinzhong, Xiao, Jingjing, Yuan, Lamei, Deng, Xiong, Guan, Liping, Zhu, Anding, Rong, Pengfei, Zhang, Jianguo, Deng, Hao
Publicado no Indian J Med Res (2016)

Dysfunction of Myosin Light‐Chain 4 (MYL4) Leads to Heritable Atrial Cardiomyopathy With Electrical, Contractile, and Structural Components: Evidence From Genetically‐Engineered Ra...

Por Peng, Wenhui, Li, Miaoxin, Li, Hailing, Tang, Kai, Zhuang, Jianhui, Zhang, Jianguo, Xiao, Jingjing, Jiang, Hui, Li, Dali, Yu, Yongchun, Sham, Pak C., Nattel, Stanley, Xu, Yawei
Publicado no J Am Heart Assoc (2017)

Exome Sequencing Identifies a Novel CEACAM16 Mutation Associated with Autosomal Dominant Nonsyndromic Hearing Loss DFNA4B in a Chinese Family

Por Wang, Honghan, Wang, Xinwei, He, Chufeng, Li, Haibo, Qing, Jie, Grati, Mhamed, Hu, Zhengmao, Li, Jiada, Hu, Yiqiao, Xia, Kun, Mei, Lingyun, Wang, Xingwei, Yu, Jianjun, Chen, Hongsheng, Jiang, Lu, Liu, Yalan, Men, Meichao, Zhang, Hailin, Guan, Liping, Xiao, Jingjing, Zhang, Jianguo, Liu, Xuezhong, Feng, Yong
Publicado no J Hum Genet (2015)

Identification of CHIP as a Novel Causative Gene for Autosomal Recessive Cerebellar Ataxia

Por Shi, Yuting, Wang, Junling, Li, Jia-Da, Ren, Haigang, Guan, Wenjuan, He, Miao, Yan, Weiqian, Zhou, Ying, Hu, Zhengmao, Zhang, Jianguo, Xiao, Jingjing, Su, Zheng, Dai, Meizhi, Wang, Jun, Jiang, Hong, Guo, Jifeng, Zhou, Yafang, Zhang, Fufeng, Li, Nan, Du, Juan, Xu, Qian, Hu, Yacen, Pan, Qian, Shen, Lu, Wang, Guanghui, Xia, Kun, Zhang, Zhuohua, Tang, Beisha
Publicado em 2013