An in‐frame pseudoexon activation caused by a novel deep‐intronic variant in the dysferlin gene

por Sun, Chengyue, Xie, Zhiying, Cong, Lu, Xu, Yan, Liu, Zunjing
Publicado 2022

Simulation of the Particle Transport Behaviors in Nanoporous Matter

por Wu, You, Ju, Dandan, Wang, Hao, Sun, Chengyue, Wu, Yiyong, Cao, Zhengli, Tolochko, Oleg V
Publicado 2022

Value of muscle magnetic resonance imaging in the differential diagnosis of muscular dystrophies related to the dystrophin-glycoprotein complex

por Xie, Zhiying, Xie, Zhihao, Yu, Meng, Zheng, Yiming, Sun, Chengyue, Liu, Yilin, Ling, Chen, Zhu, Ying, Zhang, Wei, Xiao, Jiangxi, Wang, Zhaoxia, Yuan, Yun
Publicado 2019

Exonization of a deep intronic long interspersed nuclear element in Becker muscular dystrophy

por Xie, Zhiying, Liu, Chang, Lu, Yanyu, Sun, Chengyue, Liu, Yilin, Yu, Meng, Shu, Junlong, Meng, Lingchao, Deng, Jianwen, Zhang, Wei, Wang, Zhaoxia, Lv, He, Yuan, Yun
Publicado 2022

Splicing Characteristics of Dystrophin Pseudoexons and Identification of a Novel Pathogenic Intronic Variant in the DMD Gene

por Xie, Zhiying, Tang, Liuqin, Xie, Zhihao, Sun, Chengyue, Shuai, Haoyue, Zhou, Chao, Liu, Yilin, Yu, Meng, Zheng, Yiming, Meng, Lingchao, Zhang, Wei, Leal, Suzanne M., Wang, Zhaoxia, Schrauwen, Isabelle, Yuan, Yun
Publicado 2020

Long‐read whole‐genome sequencing for the genetic diagnosis of dystrophinopathies

por Xie, Zhiying, Sun, Chengyue, Zhang, Siwen, Liu, Yilin, Yu, Meng, Zheng, Yiming, Meng, Lingchao, Acharya, Anushree, Cornejo‐Sanchez, Diana M, Wang, Gao, Zhang, Wei, Schrauwen, Isabelle, Leal, Suzanne M., Wang, Zhaoxia, Yuan, Yun
Publicado 2020

First Identification of Rare Exonic and Deep Intronic Splice-Altering Variants in Patients With Beta-Sarcoglycanopathy

por Xie, Zhiying, Sun, Chengyue, Liu, Chang, Chu, Xujun, Gang, Qiang, Yu, Meng, Zheng, Yiming, Meng, Lingchao, Li, Fan, Xia, Dongliang, Wang, Li, Li, Ying, Deng, Jianwen, Lv, He, Wang, Zhaoxia, Zhang, Wei, Yuan, Yun
Publicado 2022