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Bioorganic & Medicinal Chemistry Letters|October 22, 2008
The design, synthesis and biological evaluation of 7-alkoxy-4-heteroarylamino-3-cyanoquinolines as dual inhibitors of c-Src and iNOSXin Cao, Qi-Dong You, Zhi-Yu Li, et al.Zhongguo Zhong Yao Za Zhi = Zhongguo Zhongyao Zazhi = China Journal of Chinese Materia Medica|December 19, 2023
[Research progress on Rhododendron molle in treatment of rheumatoid arthritis]Wen-Ya Mei, Xiang-Dan Liu, Zhi-Hui Wang, et al.Basic & Clinical Pharmacology & Toxicology|February 22, 2012
Association between HLA and Stevens-Johnson syndrome induced by carbamazepine in Southern Han Chinese: genetic markers besides B*1502?Yi-Wu Shi, Fu-Li Min, Bin Qin, et al.Briefings in Bioinformatics|November 6, 2019
Optimization of in silico tools for predicting genetic variants: individualizing for genes with molecular sub-regional stratificationBin Tang, Bin Li, Liang-Di Gao, et al.Frontiers in Genetics|September 19, 2022
Genome-wide comparison and <i>in silico</i> analysis of splicing factor SYF2/NTC31/p29 in eukaryotes: Special focus on vertebratesBao-Xing Huang, Zi-Chang Jia, Xue Yang, et al.Journal of Medical Genetics|January 5, 2023
Variants in <i>BSN</i> gene associated with epilepsy with favourable outcomeTingting Ye, Jiwei Zhang, Jie Wang, et al.Scientific Reports|October 27, 2024
Association of LONP1 gene with epilepsy and the sub-regional effectSi-Xiu Li, Na He, Jian-Xiang Liao, et al.Seizure|August 13, 2023
ATP6V1A variants are associated with childhood epilepsy with favorable outcomeBin Li, Song Lan, Xiao-Rong Liu, et al.Journal of Neurodevelopmental Disorders|March 22, 2018
Few individuals with Lennox-Gastaut syndrome have autism spectrum disorder: a comparison with Dravet syndromeNa He, Bing-Mei Li, Zhao-Xia Li, et al.Seizure|July 16, 2010
Milder phenotype with SCN1A truncation mutation other than SMEIMei-Juan Yu, Yi-Wu Shi, Mei-Mei Gao, et al.Pageof 12