Yanyu Lu

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

H. Lv, Wei Zhang, Zhaoxia Wang, 2022, Frontiers in Genetics.

Pathogenic PSAT1 Variants and Autosomal Recessive Axonal Charcot-Marie-Tooth Disease With Ichthyosis.

H. Lv, Wei Zhang, Zhaoxia Wang, 2022, Pediatric neurology.

Role of S100A1 in hypoxia‐induced inflammatory response in cardiomyocytes via TLR4/ROS/NF‐κB pathway

Yapeng Li, Yanshen Li, Jiangkun Yu, 2015, The Journal of pharmacy and pharmacology.

Eupatilin attenuates doxorubicin-induced cardiotoxicity by activating the PI3K-AKT signaling pathway in mice.

Jianzeng Dong, Xiaoyan Zhao, Li Li, 2023, Molecular and cellular biochemistry.

Clinical, pathological, and genetic characterization in a large Chinese cohort with female dystrophinopathy

Wei Zhang, Wei Zhang, Zhaoxia Wang, 2023, Neuromuscular Disorders.

Clinical and genetic interpretation of uncertain DMD missense variants: evidence from mRNA and protein studies

Zhaoxia Wang, Zhiying Xie, Yawen Zhao, 2024, Orphanet journal of rare diseases.

A novel deep intronic variant introduce dystrophin pseudoexon in Becker muscular dystrophy: A case report

Zhiying Xie, Yawen Zhao, Jianwen Deng, 2024, Heliyon.

A new pseudoexon activation due to ultrarare branch point formation in Duchenne muscular dystrophy

Wei Zhang, Zhaoxia Wang, Zhiying Xie, 2023, Neuromuscular Disorders.