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Journal of Immunology (Baltimore, Md. : 1950)|April 26, 2015
miR-155 Deficiency Ameliorates Autoimmune Inflammation of Systemic Lupus Erythematosus by Targeting S1pr1 in Faslpr/lpr MiceQian Xin, Jiangxia Li, Jie Dang, et al.
Pediatric Research|August 26, 2022
In the developing cerebral cortex: axonogenesis, synapse formation, and synaptic plasticity are regulated by SATB2 target genesQiufang Guo, Yaqiong Wang, Qing Wang, et al.
Nucleic Acids Research|June 12, 2016
A primary role of TET proteins in establishment and maintenance of De Novo bivalency at CpG islandsLingchun Kong, Li Tan, Ruitu Lv, et al.
Translational Pediatrics|January 3, 2022
Characteristics and outcomes of glomerulonephritis with membranoproliferative pattern in childrenLinan Xu, Fengfang Wei, Jiayan Feng, et al.
Molecular Genetics & Genomic Medicine|June 17, 2020
COQ8B nephropathy: Early detection and optimal treatmentXiaoxiang Song, Xiaoyan Fang, Xiaoshan Tang, et al.
Frontiers in Pediatrics|March 20, 2023
Further delineation of EBF3-related syndromic neurodevelopmental disorder in twelve Chinese patientsJitao Zhu, Wenhui Li, Sha Yu, et al.
Clinical and Translational Medicine|July 9, 2022
WDR62 variants contribute to congenital heart disease by inhibiting cardiomyocyte proliferationLili Hao, Jing Ma, Feizhen Wu, et al.
Human Genetics|November 8, 2023
Genetic spectrums and clinical profiles of critically ill neonates with congenital auricular deformity in the China Neonatal Genomes ProjectFeifan Xiao, Bingbing Wu, Chenbin Dong, et al.
BMC Medical Genomics|October 26, 2021
Phenotypic spectrum and genetics of PAX2-related disorder in the Chinese cohortXue Yang, Yaqi Li, Ye Fang, et al.
European Journal of Medical Genetics|September 6, 2020
Early diagnosis of WT1 nephropathy and follow up in a Chinese multicenter cohortShuzhen Sun, Linan Xu, Yunli Bi, et al.
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