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Molecular Neurobiology|June 8, 2014
A MicroRNA Profile in Fmr1 Knockout Mice Reveals MicroRNA Expression Alterations with Possible Roles in Fragile X SyndromeTing Liu, Rui-Ping Wan, Ling-Jia Tang, et al.
Biochimica Et Biophysica Acta|December 3, 2014
Alteration of Scn3a expression is mediated via CpG methylation and MBD2 in mouse hippocampus during postnatal development and seizure conditionHai-Jun Li, Rui-Ping Wan, Ling-Jia Tang, et al.
Molecular Neurobiology|March 20, 2016
Involvement of FMRP in Primary MicroRNA Processing via Enhancing Drosha TranslationRui-Ping Wan, Lin-Tao Zhou, Hai-Xuan Yang, et al.
Molecular Neurobiology|January 18, 2014
Transcription of the human sodium channel SCN1A gene is repressed by a scaffolding protein RACK1Zhao-Fei Dong, Ling-Jia Tang, Guang-Fei Deng, et al.
Human Genetics|January 28, 2014
A novel variant in the 3' UTR of human SCN1A gene from a patient with Dravet syndrome decreases mRNA stability mediated by GAPDH's bindingTao Zeng, Zhao-Fei Dong, Shu-Jing Liu, et al.
Frontiers in Neurology|August 12, 2022
PRRT2 gene mutations associated with infantile convulsions induced by sucking and the genotype-phenotype correlationDe-Tian Liu, Xue-Qing Tang, Rui-Ping Wan, et al.
Human Molecular Genetics|August 24, 2022
YWHAZ variation causes intellectual disability and global developmental delay with brain malformationRui-Ping Wan, Zhi-Gang Liu, Xiao-Fei Huang, et al.
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