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Long-term Effects of Recurrent Neonatal Seizures on Neurobehavioral Function and Related Gene Expression and Its Intervention by Inhibitor of Cathepsin B

Neurochemical research, 2012-01, Vol.37 (1), p.31-39

2012

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MECP2 and CDKL5 gene mutation analysis in Chinese patients with Rett syndrome

Journal of human genetics, 2007, Vol.52 (1), p.38-47

2007

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Functional Characterization and Neuronal Modeling of the Effects of Childhood Absence Epilepsy Variants of CACNA1H, a T-Type Calcium Channel

The Journal of neuroscience, 2005-05, Vol.25 (19), p.4844-4855

2005

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Neural (N-) cadherin, a synaptic adhesion molecule, is induced in hippocampal mossy fiber axonal sprouts by seizure

Journal of neuroscience research, 2002-08, Vol.69 (3), p.292-304

2002

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Genotype and early development in Rett syndrome: The value of international data

Brain & development (Tokyo. 1979), 2005-11, Vol.27, p.S59-S68

2005

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Clinical and laboratory survey of 65 Chinese patients with Leigh syndrome

Chinese medical journal, 2006-03, Vol.119 (5), p.373-377

2006

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Pay Attention to Late Onset Childhood Epilepsy due to Inborn Errors of Metabolism

Epilepsy & Seizure, 2008, Vol.1(1), pp.11-13

Wu, Xi-Ru

2008

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Proteolipid protein 1 gene mutation in nine patients with Pelizaeus-Merzbacher disease

Chinese medical journal, 2008-09, Vol.121 (17), p.1638-1642

2008

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Dynamic pattern of gene expression of ZnT-1, ZnT-3 and PRG-1 in rat brain following flurothyl-induced recurrent neonatal seizures

Toxicology letters, 2010-05, Vol.194 (3), p.86-93

2010

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Acute Phase Expression Pattern of ZnTs, LC3, and Beclin-1 in Rat Hippocampus and Its Regulation by 3-Methyladenine Following Recurrent Neonatal Seizures

Biological trace element research, 2011-10, Vol.143 (1), p.320-331

2011

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ZnT-1, ZnT-3, CaMK II, PRG-1 expressions in hippocampus following neonatal seizure-induced cognitive deficit in rats

Toxicology letters, 2009-02, Vol.184 (3), p.145-150

2009

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Genotype/phenotype of 6 Chinese cases with Niemann–Pick disease type C

Gene, 2012-05, Vol.498 (2), p.332-335

2012

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Effects of penicillin-induced developmental epilepticus on hippocampal regenerative sprouting, related gene expression and cognitive deficits in rats

Toxicology letters, 2009-07, Vol.188 (2), p.161-166

2009

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MECP2 gene mutation analysis in Chinese patients with Rett syndrome

European journal of human genetics : EJHG, 2002-08, Vol.10 (8), p.484-486

2002

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X Chromosome Inactivation in Rett Syndrome and Its Correlations With MeCP2 Mutations and Phenotype

Journal of child neurology, 2008-01, Vol.23 (1), p.22-25

2008

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Novel collagen VI mutations identified in Chinese patients with Ullrich congenital muscular dystrophy

World journal of pediatrics : WJP, 2014-05, Vol.10 (2), p.126-132

2014

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Nonsingular Terminal Sliding Mode Control of Mobile Robot Using Support Vector Machines

Applied Mechanics and Materials, 2012-07, Vol.190-191, p.705-709

2012

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Epigenetics and neurodevelopmental diseases

Zhonghua er ke za zhi, 2009-06, Vol.47 (6), p.429

Wu, Xi-ru

2009

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Spinal Cord Demyelination Associated with Biotinidase Deficiency in 3 Chinese Patients

Journal of child neurology, 2007-02, Vol.22 (2), p.156-160

2007

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Neural network modeling of hysteresis for harmonic drive in industrial robots

Guang xue, jing mi gong cheng, 2019, Vol.27 (3), p.694-701

2019

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Clinical, pathological and molecular biological characteristics of mitochondrial encephalomyopathy with lactic acidosis and stroke-like episode in children

Zhonghua er ke za zhi, 2013-02, Vol.51 (2), p.130

2013

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Recent developments in studies on ion channels and genetics of epilepsy

Zhonghua er ke za zhi, 2008-06, Vol.46 (6), p.434

Wu, Xi-ru

2008

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c-Fos, N-methyl- d-aspartate receptor 2C, GABA-A-α1 immonoreactivity, seizure latency and neuronal injury following single or recurrent neonatal seizures in hippocampus of Wistar rat

Neuroscience letters, 2005-05, Vol.380 (1), p.149-154

2005

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Effects on oligodendrocytic function resulting from proteolipid protein 1 gene mutations

Sheng li kʻo hsüeh chin chan, 2012-08, Vol.43 (4), p.271

2012

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Niemann-Pick disease type C: analysis of 7 patients

World journal of pediatrics : WJP, 2012-02, Vol.8 (1), p.61-66

2012

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Long-term Effects of Recurrent Neonatal Seizures on Neurobehavioral Function and Related Gene Expression and Its Intervention by Inhibitor of Cathepsin B

MECP2 and CDKL5 gene mutation analysis in Chinese patients with Rett syndrome

Functional Characterization and Neuronal Modeling of the Effects of Childhood Absence Epilepsy Variants of CACNA1H, a T-Type Calcium Channel

Neural (N-) cadherin, a synaptic adhesion molecule, is induced in hippocampal mossy fiber axonal sprouts by seizure

Genotype and early development in Rett syndrome: The value of international data

Clinical and laboratory survey of 65 Chinese patients with Leigh syndrome

Pay Attention to Late Onset Childhood Epilepsy due to Inborn Errors of Metabolism

Proteolipid protein 1 gene mutation in nine patients with Pelizaeus-Merzbacher disease

Dynamic pattern of gene expression of ZnT-1, ZnT-3 and PRG-1 in rat brain following flurothyl-induced recurrent neonatal seizures

Acute Phase Expression Pattern of ZnTs, LC3, and Beclin-1 in Rat Hippocampus and Its Regulation by 3-Methyladenine Following Recurrent Neonatal Seizures

ZnT-1, ZnT-3, CaMK II, PRG-1 expressions in hippocampus following neonatal seizure-induced cognitive deficit in rats

Genotype/phenotype of 6 Chinese cases with Niemann–Pick disease type C

Effects of penicillin-induced developmental epilepticus on hippocampal regenerative sprouting, related gene expression and cognitive deficits in rats

MECP2 gene mutation analysis in Chinese patients with Rett syndrome

X Chromosome Inactivation in Rett Syndrome and Its Correlations With MeCP2 Mutations and Phenotype

Novel collagen VI mutations identified in Chinese patients with Ullrich congenital muscular dystrophy

Nonsingular Terminal Sliding Mode Control of Mobile Robot Using Support Vector Machines

Epigenetics and neurodevelopmental diseases

Spinal Cord Demyelination Associated with Biotinidase Deficiency in 3 Chinese Patients

Neural network modeling of hysteresis for harmonic drive in industrial robots

Clinical, pathological and molecular biological characteristics of mitochondrial encephalomyopathy with lactic acidosis and stroke-like episode in children

Recent developments in studies on ion channels and genetics of epilepsy

c-Fos, N-methyl- d-aspartate receptor 2C, GABA-A-α1 immonoreactivity, seizure latency and neuronal injury following single or recurrent neonatal seizures in hippocampus of Wistar rat

Effects on oligodendrocytic function resulting from proteolipid protein 1 gene mutations

Niemann-Pick disease type C: analysis of 7 patients

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