Resultados de búsqueda - Jianwen Deng

A novel SPAST gene mutation identified in a Chinese family with hereditary spastic paraplegia por Weiwei Yu, Haiqiang Jin, Jianwen Deng, Ding Nan, Yining Huang

Connect to this object online.

First Identification of Rare Exonic and Deep Intronic Splice-Altering Variants in Patients With Beta-Sarcoglycanopathy por Zhiying Xie, Chengyue Sun, Chang Liu, Xujun Chu, Qiang Gang, Meng Yu, Yiming Zheng, Lingchao Meng, Fan Li, Dongliang Xia, Li Wang, Ying Li, Jianwen Deng, He Lv, Zhaoxia Wang, Wei Zhang, Yun Yuan

Connect to this object online.

A novel biomarker of fibrofatty replacement in dystrophinopathies identified by integrating transcriptome, magnetic resonance imaging, and pathology data por Zhihao Xie, Chang Liu, Chengyue Sun, Yanyu Lu, Shiyi Wu, Yilin Liu, Qi Wang, Yalan Wan, Yikang Wang, Meng Yu, Lingchao Meng, Jianwen Deng, Wei Zhang, Zhaoxia Wang, Chunxia Yang, Yun Yuan, Zhiying Xie

Connect to this object online.

Effect of Dl-3-n-butylphthalide on mitochondrial Cox7c in models of cerebral ischemia/reperfusion injury por Jingjing Jia, Jingjing Jia, Jianwen Deng, Haiqiang Jin, Jie Yang, Ding Nan, Ding Nan, Zemou Yu, Zemou Yu, Weiwei Yu, Weiwei Yu, Zhiyuan Shen, Yuxuan Lu, Ran Liu, Zhaoxia Wang, Xiaozhong Qu, Dong Qiu, Zhenzhong Yang, Yining Huang

Connect to this object online.