Identification of MAVS as a Novel Risk Factor for the Development of Osteoarthritis

Por Liu, Jie, Tang, Ling-yun, Wang, Yan-gui, Lu, Shun-yuan, Zhang, En-ning, Wang, Zhu-gang, Zhang, Hong-xin
Publicado no Aging Dis (2018)

Lacking of palladin leads to multiple cellular events changes which contribute to NTD

Por Tan, Juan, Chen, Xue-Jiao, Shen, Chun-Ling, Zhang, Hong-Xin, Tang, Ling-Yun, Lu, Shun-Yuan, Wu, Wen-Ting, Kuang, Ying, Fei, Jian, Wang, Zhu-Gang
Publicado no Neural Dev (2017)

DHTKD1 Deficiency Causes Charcot-Marie-Tooth Disease in Mice

Por Xu, Wang-Yang, Zhu, Houbao, Shen, Yan, Wan, Ying-Han, Tu, Xiao-Die, Wu, Wen-Ting, Tang, Lingyun, Zhang, Hong-Xin, Lu, Shun-Yuan, Jin, Xiao-Long, Fei, Jian, Wang, Zhu-Gang
Publicado no Mol Cell Biol (2018)

Deficiency of Adiponectin Protects against Ovariectomy-Induced Osteoporosis in Mice

Por Wang, Fang, Wang, Pei-xia, Wu, Xiao-lin, Dang, Su-ying, Chen, Yan, Ni, Ying-yin, Gao, Li-hong, Lu, Shun-yuan, Kuang, Ying, Huang, Lei, Fei, Jian, Wang, Zhu-gang, Pang, Xiao-fen
Publicado em 2013

Deletion of Gpr128 results in weight loss and increased intestinal contraction frequency

Por Ni, Ying-Yin, Chen, Yan, Lu, Shun-Yuan, Sun, Bi-Ying, Wang, Fang, Wu, Xiao-Lin, Dang, Su-Ying, Zhang, Guo-Hua, Zhang, Hong-Xin, Kuang, Yin, Fei, Jian, Gu, Ming-Min, Rong, Wei-Fang, Wang, Zhu-Gang
Publicado em 2014

Germinal Cell Aplasia in Kif18a Mutant Male Mice Due to Impaired Chromosome Congression and Dysregulated BubR1 and CENP-E

Por Liu, Xue-song, Zhao, Xu-dong, Wang, Xiaoxing, Yao, Yi-xin, Zhang, Liang-liang, Shu, Run-zhe, Ren, Wei-hua, Huang, Ying, Huang, Lei, Gu, Ming-min, Kuang, Ying, Wang, Long, Lu, Shun-yuan, Chi, Jun, Fen, Jing-sheng, Wang, Yi-fei, Fei, Jian, Dai, Wei, Wang, Zhu-Gang
Publicado em 2010

Rig-I regulates NF-κB activity through binding to Nf-κb1 3′-UTR mRNA

Por Zhang, Hong-Xin, Liu, Zi-Xing, Sun, Yue-Ping, Zhu, Jiang, Lu, Shun-Yuan, Liu, Xue-Song, Huang, Qiu-Hua, Xie, Yin-Yin, Zhu, Hou-Bao, Dang, Su-Ying, Chen, Hai-Feng, Zheng, Guang-Yong, Li, Yi-Xue, Kuang, Ying, Fei, Jian, Chen, Sai-Juan, Chen, Zhu, Wang, Zhu-Gang
Publicado em 2013

Multiple Synostoses Syndrome Is Due to a Missense Mutation in Exon 2 of FGF9 Gene

Por Wu, Xiao-lin, Gu, Ming-min, Huang, Lei, Liu, Xue-song, Zhang, Hong-xin, Ding, Xiao-yi, Xu, Jian-qiang, Cui, Bin, Wang, Long, Lu, Shun-yuan, Chen, Xiao-yi, Zhang, Hai-guo, Huang, Wei, Yuan, Wen-tao, Yang, Jiang-ming, Gu, Qun, Fei, Jian, Chen, Zhu, Yuan, Zhi-min, Wang, Zhu-gang
Publicado em 2009