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Molecular Therapy : the Journal of the American Society of Gene Therapy|March 5, 2026
Low-Dose AAV9-SMN1 with CNS-Selective Expression Delivers Efficacy and Favorable Safety in Spinal Muscular AtrophyYongguo Yu, Xiji Qin, Mengxia Jing, et al.
Pain|August 12, 2024
Transient receptor potential melastatin 8 contributes to the interleukin-33-mediated cold allodynia in a mouse model of neuropathic painLixia Du, Jianyu Zhu, Shenbin Liu, et al.
JCI Insight|April 26, 2022
Heteroplasmic and homoplasmic m.616T>C in mitochondria tRNAPhe promote isolated chronic kidney disease and hyperuricemiaChengxian Xu, Lingxiao Tong, Jia Rao, et al.
Cell Reports|December 27, 2025
IgG2c subclass dominance drives fatal lupus-like nephritis via FcγR and complement activationYingying Luan, Pengfei Dai, Ying Wang, et al.
Frontiers in Pediatrics|May 17, 2021
Integrating Population Variants and Protein Structural Analysis to Improve Clinical Genetic Diagnosis and Treatment in Nephrogenic Diabetes InsipidusPanli Liao, Tianchao Xiang, Hongxia Li, et al.
Pediatric Nephrology (Berlin, Germany)|September 19, 2017
Analysis of 24 genes reveals a monogenic cause in 11.1% of cases with steroid-resistant nephrotic syndrome at a single centerWeizhen Tan, Svjetlana Lovric, Shazia Ashraf, et al.
Nature Communications|May 14, 2026
Maternal obesity induces macrophage to myofibroblast transition in kidneys of male offspring through a pathway driven by 20-hydroxyeicosatetraenoic acidFengbo Zhong, Xingyu Huang, Huiru Sun, et al.
NPJ Genomic Medicine|July 3, 2021
An accessible insight into genetic findings for transplantation recipients with suspected genetic kidney diseaseZhigang Wang, Hongen Xu, Tianchao Xiang, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|October 9, 2018
Panel sequencing distinguishes monogenic forms of nephritis from nephrosis in childrenDavid Schapiro, Ankana Daga, Jennifer A Lawson, et al.
Frontiers in Medicine|December 3, 2021
Genetic Variations and Clinical Features of NPHS1-Related Nephrotic Syndrome in Chinese Children: A Multicenter, Retrospective StudyLiping Rong, Lizhi Chen, Jia Rao, et al.
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