T. Su

发表

Expression Pattern of ALOXE3 in Mouse Brain Suggests Its Relationship with Seizure Susceptibility

Mei-Mei Gao, Hui-Ling Tang, Si-Yu Chen, 2020, Cellular and molecular neurobiology.

Altered expression of voltage-gated potassium channel 4.2 and voltage-gated potassium channel 4-interacting protein, and changes in intracellular calcium levels following lithium-pilocarpine-induced status epilepticus

W. Sun, W. Liao, T. Su, 2008, Neuroscience.

Study of Antiepileptic Effect of Extracts from Acorus tatarinowii Schott

Mei-Mei Gao, W. Liao, Wei-Wen Sun, 2005, Epilepsia.

ADGRV1 Variants in Febrile Seizures/Epilepsy With Antecedent Febrile Seizures and Their Associations With Audio-Visual Abnormalities

Xiaoyun Lei, N. He, Hankui Liu, 2022, Frontiers in Molecular Neuroscience.

Neuroprotection of lamotrigine on hypoxic-ischemic brain damage in neonatal rats: Relations to administration time and doses

W. Liao, Wei-Wen Sun, T. Su, 2008, Biologics : targets & therapy.

Paroxysmal hypnogenic dyskinesia is associated with mutations in the PRRT2 gene

Yi-wu Shi, Xiao-Rong Liu, W. Liao, 2016, Neurology: Genetics.

Evaluating the pathogenic potential of genes with de novo variants in epileptic encephalopathies

Yi-wu Shi, Xiao-Rong Liu, W. Liao, 2018, Genetics in Medicine.

CHD4 variants are associated with childhood idiopathic epilepsy with sinus arrhythmia

Yi-wu Shi, Xiao-Rong Liu, W. Liao, 2021, CNS neuroscience & therapeutics.

Clinical and Functional Features of Epilepsy-Associated In-Frame Deletion Variants in SCN1A

Mei-Mei Gao, N. He, T. Su, 2022, Frontiers in Molecular Neuroscience.

The SCN1A Mutation Database: Updating Information and Analysis of the Relationships among Genotype, Functional Alteration, and Phenotype

B. Li, Yi-wu Shi, Xiao-Rong Liu, 2015, Human mutation.

Identification of the promoter region and the 5′‐untranslated exons of the human voltage‐gated sodium channel Nav1.1 gene (SCN1A) and enhancement of gene expression by the 5′‐untranslated exons

Yi-wu Shi, W. Liao, T. Su, 2008, Journal of neuroscience research.

Heterozygous PGM3 Variants Are Associated With Idiopathic Focal Epilepsy With Incomplete Penetrance

Yi-wu Shi, Xiao-Rong Liu, W. Liao, 2020, Frontiers in Genetics.

Early continuous inhibition of group 1 mGlu signaling partially rescues dendritic spine abnormalities in the Fmr1 knockout mouse model for fragile X syndrome

Mei-Mei Gao, Wei-Wen Sun, T. Su, 2011, Psychopharmacology.

Human transcription factor genes involved in neuronal development tend to have high GC content and CpG elements in the proximal promoter region.

W. Liao, T. Su, Y. Long, 2011, Journal of genetics and genomics = Yi chuan xue bao.

Evaluation of cell damage in organotypic hippocampal slice culture from adult mouse: A potential model system to study neuroprotection

B. Paradiso, W. Liao, M. Simonato, 2011, Brain Research.

Functional Differences Between Two Kv1.1 RNA Editing Isoforms: a Comparative Study on Neuronal Overexpression in Mouse Prefrontal Cortex

P. Zhu, W. Liao, T. Su, 2021, Molecular Neurobiology.

P. Zhu, W. Liao, T. Su, 2018, Progress in Neuro-Psychopharmacology and Biological Psychiatry.

GRIN2A Variants Associated With Idiopathic Generalized Epilepsies

Yi-wu Shi, Xiao-Rong Liu, W. Liao, 2021, Frontiers in Molecular Neuroscience.

Optimization of in silico tools for predicting genetic variants: individualizing for genes with molecular sub-regional stratification

Na He, Bin Li, Xiao-Rong Liu, 2020, Briefings Bioinform..

Ion Channel Genes and Epilepsy: Functional Alteration, Pathogenic Potential, and Mechanism of Epilepsy

Yi-wu Shi, W. Liao, N. He, 2017, Neuroscience Bulletin.

Identification of the transcriptional promoters in the proximal regions of human microRNA genes

Yue-Sheng Long, Yong-Hong Yi, Tao Su, 2011, Molecular Biology Reports.

Exaggerated activities of TRPM7 underlie bupivacaine‐induced neurotoxicity in the SH‐SY5Y cells preconditioned with high glucose

T. Su, Shi-Yuan Xu, Yawen Li, 2021, Journal of biochemical and molecular toxicology.

Functional Investigation of a GRIN2A Variant Associated with Rolandic Epilepsy

Yi-wu Shi, Xiao-Rong Liu, W. Liao, 2018, Neuroscience Bulletin.

Homozygous missense TPP1 mutation associated with mild late infantile neuronal ceroid lipofuscinosis and the genotype-phenotype correlation

Xiao-Rong Liu, Liu Liu, T. Su, 2019, Seizure.

Partial epilepsy with antecedent febrile seizures and seizure aggravation by antiepileptic drugs: Associated with loss of function of Nav1.1

S. Duan, Yi-wu Shi, Xiao-Rong Liu, 2010, Epilepsia.

Ion Channel Genes and Epilepsy: Functional Alteration, Pathogenic Potential, and Mechanism of Epilepsy

Yi-wu Shi, W. Liao, N. He, 2017, Neuroscience Bulletin.

DEPDC5 Variants Associated Malformations of Cortical Development and Focal Epilepsy With Febrile Seizure Plus/Febrile Seizures: The Role of Molecular Sub-Regional Effect

Xiao-Rong Liu, W. Liao, N. He, 2020, Frontiers in Neuroscience.

RYR2 Mutations Are Associated With Benign Epilepsy of Childhood With Centrotemporal Spikes With or Without Arrhythmia

Yi-wu Shi, Xiao-Rong Liu, W. Liao, 2021, Frontiers in Neuroscience.

ARHGEF9 mutations in epileptic encephalopathy/intellectual disability: toward understanding the mechanism underlying phenotypic variation

Yi-wu Shi, Xiao-Rong Liu, W. Liao, 2017, neurogenetics.

Autism in Dravet syndrome: Prevalence, features, and relationship to the clinical characteristics of epilepsy and mental retardation

Xiao-Rong Liu, W. Liao, T. Su, 2011, Epilepsy & Behavior.

CELSR3 variants are associated with febrile seizures and epilepsy with antecedent febrile seizures

Jing Zhu, Yi-wu Shi, Xiao-Rong Liu, 2021, CNS neuroscience & therapeutics.

MDH2 is an RNA binding protein involved in downregulation of sodium channel Scn1a expression under seizure condition.

Mei-Mei Gao, Tao Zeng, Hui-Ling Tang, 2017, Biochimica et biophysica acta. Molecular basis of disease.

Promoter Analysis of Mouse Scn3a Gene and Regulation of the Promoter Activity by GC Box and CpG Methylation

Yi-wu Shi, Xiao-Rong Liu, Mei-juan Yu, 2011, Journal of Molecular Neuroscience.

HLA-A*24:02 as a common risk factor for antiepileptic drug–induced cutaneous adverse reactions

C. Ng, K. Lim, Jie Pan, 2017, Neurology.

Localized delivery of fibroblast growth factor–2 and brain-derived neurotrophic factor reduces spontaneous seizures in an epilepsy model

E. Magri, B. Paradiso, P. Fabene, 2009, Proceedings of the National Academy of Sciences.

FTO is a transcriptional repressor to auto-regulate its own gene and potentially associated with homeostasis of body weight

S. Duan, Yan Luo, Mei-Mei Gao, 2019, Journal of molecular cell biology.

Novel PRRT2 mutations in paroxysmal dyskinesia patients with variant inheritance and phenotypes

W. Liao, N. He, T. Su, 2013, Genes, brain, and behavior.

Bystander Effect on Brain Tissue of Mesoangioblasts Producing Neurotrophins

B. Paradiso, A. Cattaneo, R. Scardigli, 2012, Cell transplantation.

Localized overexpression of FGF‐2 and BDNF in hippocampus reduces mossy fiber sprouting and spontaneous seizures up to 4 weeks after pilocarpine‐induced status epilepticus

B. Paradiso, P. Fabene, M. Simonato, 2011, Epilepsia.

Evaluating the pathogenic potential of genes with de novo variants in epileptic encephalopathies

Yi-wu Shi, Xiao-Rong Liu, W. Liao, 2018, Genetics in Medicine.

Common genetic epilepsies, pathogenicity of genes/variants, and genetic dependence

W. Liao, N. He, T. Su, 2023, Seizure: European Journal of Epilepsy.

Critical Role of E1623 Residue in S3-S4 Loop of Nav1.1 Channel and Correlation Between Nature of Substitution and Functional Alteration

Xiao-Rong Liu, W. Liao, T. Su, 2022, Frontiers in Molecular Neuroscience.

UNC13B variants associated with partial epilepsy with favourable outcome

Yanhui Chen, Yi-wu Shi, Xiao-Rong Liu, 2021, Brain : a journal of neurology.

Genetic Dependence and Genetic Diseases

Yi-wu Shi, W. Liao, N. He, 2023, bioRxiv.

Expression changes of microtubule associated protein 1B in the brain of Fmr1 knockout mice

W. Liao, Yong-jie Bai, Rong Wang, 2007, Neuroscience bulletin.

HCFC1 variants in the proteolysis domain are associated with X‐linked idiopathic partial epilepsy: Exploring the underlying mechanism

B. Tang, D. Zhou, Yi-wu Shi, 2023, Clinical and translational medicine.

Variants in SBF1, CELSR2, and TENM1 are associated with childhood epileptic encephalopathies

Sheng, J. Chen, Yinwei Qu, 2023, medRxiv.

Altered intrinsic properties and bursting activities of neurons in layer IV of somatosensory cortex from Fmr-1 knockout mice

Meng Li, P. Zhu, W. Liao, 2016, Experimental Neurology.

Localized overexpression of FGF‐2 and BDNF in hippocampus reduces mossy fiber sprouting and spontaneous seizures up to 4 weeks after pilocarpine‐induced status epilepticus

P. Fabene, M. Simonato, P. Marconi, 2011, Epilepsia.

Partial epilepsy with febrile seiure plus: A subtype of GFS+ or SM?

Mei-juan Yu, W. Liao, T. Su, 2007 .