Modeling Rett Syndrome Using TALEN-Edited MECP2 Mutant Cynomolgus Monkeys
Cell2017Vol. 169(5), pp. 945–955.e10
Citations Over TimeTop 1% of 2017 papers
Yongchang Chen, Juehua Yu, Yuyu Niu, Dongdong Qin, Hailiang Liu, Gang Li, Yingzhou Hu, Jiaojian Wang, Yi Lü, Yu Kang, Yong Jiang, Kunhua Wu, Siguang Li, Jingkuan Wei, Jing He, Junbang Wang, Xiaojing Liu, Yuping Luo, Chenyang Si, Raoxian Bai, Kunshan Zhang, Jie Liu, Shaoyong Huang, Zhenzhen Chen, Shuang Wang, Xiaoying Chen, Xinhua Bao, Qingping Zhang, Fuxing Li, Rui Geng, Aibin Liang, Dinggang Shen, Tianzi Jiang, Xintian Hu, Yuanye Ma, Weizhi Ji, Yi Eve Sun
Related Papers
- → A mouse Mecp2-null mutation causes neurological symptoms that mimic Rett syndrome(2001)1,559 cited
- → FOXG1 Is Responsible for the Congenital Variant of Rett Syndrome(2008)432 cited
- → MeCP2 Dysfunction in Humans and Mice(2005)90 cited
- → Ocular MECP2 Protein Expression in Patients With and Without Rett Syndrome(2010)17 cited
- → Can we relate MeCP2 deficiency to the structural and chemical abnormalities in the Rett brain?(2005)18 cited