Nano rare-earth oxides induced size-dependent vacuolization: an independent pathway from autophagy

por Zhang, Ying, Yu, Chenguang, Huang, Guanyi, Wang, Changli, Wen, Longping
Publicado 2010

Novel Partial Exon 51 Deletion in the Duchenne Muscular Dystrophy Gene Identified via Whole Exome Sequencing and Long-Read Whole-Genome Sequencing

por Li, Qianqian, Chen, Zhanni, Xiong, Hui, Li, Ranran, Yu, Chenguang, Meng, Jingjing, Shi, Panlai, Kong, Xiangdong
Publicado 2021

Kidney stone disease and cardiovascular events: a study on bidirectional causality based on mendelian randomization

por Zhao, Yuanyuan, Fan, Yang, Wang, Mengru, Yu, Chenguang, Zhou, Mengchen, Jiang, Dan, Du, Dunfeng, Chen, Shanshan, Tu, Xin
Publicado 2021

Case Report: A Novel Homozygous Mutation in MYF5 Due to Paternal Uniparental Isodisomy of Chromosome 12 in a Case of External Ophthalmoplegia With Rib and Vertebral Anomalies

por Li, Qianqian, Zhu, Xiaofan, Yu, Chenguang, Shang, Lin, Li, Ranran, Wang, Xia, Yang, Yaping, Meng, Jingjing, Kong, Xiangdong
Publicado 2022

miR-190a-5p Partially Represses the Abnormal Electrical Activity of SCN3B in Cardiac Arrhythmias by Downregulation of IL-2

por Li, Qianqian, Zhang, Ziguan, Chen, Shanshan, Huang, Zhengrong, Wang, Mengru, Zhou, Mengchen, Yu, Chenguang, Wang, Xiangyi, Chen, Yilin, Jiang, Dan, Du, Dunfeng, Huang, Yufeng, Tu, Xin, Chen, Zhishui, Zhao, Yuanyuan
Publicado 2022

Crosstalk between KIF1C and PRKAR1A in left atrial myxoma

por Zhou, Mengchen, Yao, Yan, Wang, Xiangyi, Zha, Lingfeng, Chen, Yilin, Li, Yanze, Wang, Mengru, Yu, Chenguang, Zhou, Yingchao, Li, Qianqian, Cao, Zhubing, Wu, Jianfei, Shi, Shumei, Jiang, Dan, Long, Deyong, Wang, Jiangang, Wang, Qing, Cheng, Xiang, Liao, Yuhua, Tu, Xin
Publicado 2023