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BMJ Open
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November 20, 2023
Chronotypes and their association with sleep quality among Chinese college students of Anhui Province: a cross-sectional study
Xin Tong, Mei-Mei Gao, Liu Zhang, et al.
Seizure
|
July 16, 2010
Milder phenotype with SCN1A truncation mutation other than SMEI
Mei-Juan Yu, Yi-Wu Shi, Mei-Mei Gao, et al.
Cellular and Molecular Neurobiology
|
June 6, 2020
Valproate-Induced Epigenetic Upregulation of Hypothalamic Fto Expression Potentially Linked with Weight Gain
Huan Zhang, Ping Lu, Hui-Ling Tang, et al.
Journal of Molecular Cell Biology
|
May 18, 2018
FTO is a transcriptional repressor to auto-regulate its own gene and potentially associated with homeostasis of body weight
Shu-Jing Liu, Hui-Ling Tang, Qian He, et al.
Brain Research Bulletin
|
February 13, 2021
The ALOXE3 gene variants from patients with Dravet syndrome decrease gene expression and enzyme activity
Mei-Mei Gao, Hao-Ying Huang, Si-Yu Chen, et al.
Neuroscience
|
March 5, 2017
A novel role of fragile X mental retardation protein in pre-mRNA alternative splicing through RNA-binding protein 14
Lin-Tao Zhou, Shun-Hua Ye, Hai-Xuan Yang, et al.
Neuropharmacology
|
November 7, 2016
GAPDH-mediated posttranscriptional regulations of sodium channel Scn1a and Scn3a genes under seizure and ketogenic diet conditions
Guo-Wang Lin, Ping Lu, Tao Zeng, et al.
Epilepsy Research
|
January 1, 2021
Ilepcimide inhibited sodium channel activity in mouse hippocampal neurons
Yang Zeng, Bing Qin, Yi-Wu Shi, et al.
Frontiers in Molecular Neuroscience
|
April 1, 2022
Clinical and Functional Features of Epilepsy-Associated In-Frame Deletion Variants in <i>SCN1A</i>
Jing-Yang Wang, Bin Tang, Wen-Xiang Sheng, 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 condition
Hai-Jun Li, Rui-Ping Wan, Ling-Jia Tang, et al.
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of 3
Search research articles
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Showing results (11-20 of 26) with videos related to
Sort By:
Page
of 3
BMJ Open
|
November 20, 2023
Chronotypes and their association with sleep quality among Chinese college students of Anhui Province: a cross-sectional study
Xin Tong, Mei-Mei Gao, Liu Zhang, et al.
Seizure
|
July 16, 2010
Milder phenotype with SCN1A truncation mutation other than SMEI
Mei-Juan Yu, Yi-Wu Shi, Mei-Mei Gao, et al.
Cellular and Molecular Neurobiology
|
June 6, 2020
Valproate-Induced Epigenetic Upregulation of Hypothalamic Fto Expression Potentially Linked with Weight Gain
Huan Zhang, Ping Lu, Hui-Ling Tang, et al.
Journal of Molecular Cell Biology
|
May 18, 2018
FTO is a transcriptional repressor to auto-regulate its own gene and potentially associated with homeostasis of body weight
Shu-Jing Liu, Hui-Ling Tang, Qian He, et al.
Brain Research Bulletin
|
February 13, 2021
The ALOXE3 gene variants from patients with Dravet syndrome decrease gene expression and enzyme activity
Mei-Mei Gao, Hao-Ying Huang, Si-Yu Chen, et al.
Neuroscience
|
March 5, 2017
A novel role of fragile X mental retardation protein in pre-mRNA alternative splicing through RNA-binding protein 14
Lin-Tao Zhou, Shun-Hua Ye, Hai-Xuan Yang, et al.
Neuropharmacology
|
November 7, 2016
GAPDH-mediated posttranscriptional regulations of sodium channel Scn1a and Scn3a genes under seizure and ketogenic diet conditions
Guo-Wang Lin, Ping Lu, Tao Zeng, et al.
Epilepsy Research
|
January 1, 2021
Ilepcimide inhibited sodium channel activity in mouse hippocampal neurons
Yang Zeng, Bing Qin, Yi-Wu Shi, et al.
Frontiers in Molecular Neuroscience
|
April 1, 2022
Clinical and Functional Features of Epilepsy-Associated In-Frame Deletion Variants in <i>SCN1A</i>
Jing-Yang Wang, Bin Tang, Wen-Xiang Sheng, 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 condition
Hai-Jun Li, Rui-Ping Wan, Ling-Jia Tang, et al.
Page
of 3