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Case Report: Mutant SCN9A Susceptible to Charcot Neuroarthropathy in a Patient With Congenital Insensitivity to Pain

Frontiers in neuroscience, 2021-07, Vol.15

2021

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A Clinical Study Investigating Whether the Tongue-Out Position Improves the Quality of the Anatomical Appearance of the Pharynx on CT Imaging

Frontiers in surgery, 2021-09, Vol.8, p.732607-732607

2021

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SUMO-1 modification on K166 of polyQ-expanded ataxin-3 strengthens its stability and increases its cytotoxicity

PloS one, 2013-01, Vol.8 (1), p.e54214-e54214

2013

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Behaviors of Photosensitive Mechanisms in a Low-Loss Fiber at Different Energy Densities

Journal of lightwave technology, 2022-04, Vol.40 (8), p.2530-2534

2022

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Myasthenia gravis coexisting with HINT1-related motor axonal neuropathy without neuromyotonia: a case report

BMC neurology, 2022-05, Vol.22 (1), p.168-168, Article 168

2022

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Expression and immunogenicity of hepatitis E virus-like particles based on recombinant truncated ORF2 capsid protein

Protein expression and purification, 2023-03, Vol.203, p.106214-106214, Article 106214

2023

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Preliminary study of hsa-miR-626 change in the cerebrospinal fluid of Parkinson’s disease patients

Journal of clinical neuroscience, 2019-12, Vol.70, p.198-201

2019

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Preliminary Study of hsa-mir-626 Change in the Cerebrospinal Fluid in Parkinson's Disease

Neurology India, 2021-01, Vol.69 (1), p.115-118

2021

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A Novel Homozygous SACS Mutation Identified by Whole-Exome Sequencing in a Consanguineous Family with Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay

Cytogenetic and genome research, 2017, Vol.152 (1), p.16-21

2017

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Imaging manifestations of renal primary neuroectodermal tumors

Chinese medical journal, 2012-10, Vol.125 (19), p.3595-3597

2012

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The advances in research on phosphorylation of polyglutamine disease

Zhonghua yi xue yi chuan xue za zhi, 2008-08, Vol.25 (4), p.414

2008

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A new locus for autosomal dominant Charcot-Marie-Tooth disease type 2 (CMT2L) maps to chromosome 12q24

Human genetics, 2004-05, Vol.114 (6), p.527-533

2004

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Metabolic pathways of OGCP and the influence of parkin protein on the metabolism of OGCP

Sichuan da xue xue bao. Journal of Sichuan University. Yi xue ban, 2011-03, Vol.42 (2), p.157

2011

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BAG5 Interacts with DJ-1 and Inhibits the Neuroprotective Effects of DJ-1 to Combat Mitochondrial Oxidative Damage

Oxidative medicine and cellular longevity, 2017-01, Vol.2017, p.5094934-10

2017

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Protective effect of over-expression OGCP on HEK293 cells treated by rotenone and mutant Parkin protein

Sichuan da xue xue bao. Journal of Sichuan University. Yi xue ban, 2010-07, Vol.41 (4), p.604

2010

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Genetic variations of Omi / HTRA2 in Chinese patients with Parkinson's disease

Brain research, 2011-04, Vol.1385, p.293-297

2011

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Polyglutamine-expanded ataxin-3 is degraded by autophagy

Zhonghua yi xue yi chuan xue za zhi, 2010-02, Vol.27 (1), p.23

2010

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Screening for proteins interacting with ataxin-3, the gene product of SCA3/MJD

Zhong nan da xue xue bao. Journal of Central South University. Yi xue ban, 2006-02, Vol.31 (1), p.40-44

2006

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Frequency analysis of autosomal dominant spinocerebellar ataxias in mainland Chinese patients and clinical and molecular characterization of spinocerebellar ataxia type 6

Chinese medical journal, 2005-05, Vol.118 (10), p.837-843

2005

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Frequency of different subtypes of spinocerebellar ataxia in the Han nationality of Hunan province in China

Zhong nan da xue xue bao. Journal of Central South University. Yi xue ban, 2006-10, Vol.31 (5), p.702-705

2006

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Construction of the eukaryotic expression vector of MJD1 and its expression in SH-SY5Y cells

Zhong nan da xue xue bao. Journal of Central South University. Yi xue ban, 2005-12, Vol.30 (6), p.640-644

2005

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Clinical characteristics and molecular biology of hereditary spinocerebellar ataxia type 7: study of 3 Chinese families

Zhong hua yi xue za zhi, 2006-07, Vol.86 (25), p.1755-1758

2006

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Frequency analysis of autosomal dominant spinocerebellar ataxias in Han population in the Chinese mainland and clinical and molecular characterization of spinocerebellar ataxia type 6

Zhonghua yi xue yi chuan xue za zhi, 2005-02, Vol.22 (1), p.1

2005

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Case Report: Mutant SCN9A Susceptible to Charcot Neuroarthropathy in a Patient With Congenital Insensitivity to Pain

A Clinical Study Investigating Whether the Tongue-Out Position Improves the Quality of the Anatomical Appearance of the Pharynx on CT Imaging

SUMO-1 modification on K166 of polyQ-expanded ataxin-3 strengthens its stability and increases its cytotoxicity

Behaviors of Photosensitive Mechanisms in a Low-Loss Fiber at Different Energy Densities

The Phenotypic and Genetic Spectrum of Paroxysmal Kinesigenic Dyskinesia in China

TMEM151A Variants Cause Paroxysmal Kinesigenic Dyskinesia: A Large‐Sample Study

Myasthenia gravis coexisting with HINT1-related motor axonal neuropathy without neuromyotonia: a case report

Expression and immunogenicity of hepatitis E virus-like particles based on recombinant truncated ORF2 capsid protein

Preliminary study of hsa-miR-626 change in the cerebrospinal fluid of Parkinson’s disease patients

Preliminary Study of hsa-mir-626 Change in the Cerebrospinal Fluid in Parkinson's Disease

A Novel Homozygous SACS Mutation Identified by Whole-Exome Sequencing in a Consanguineous Family with Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay

Imaging manifestations of renal primary neuroectodermal tumors

The advances in research on phosphorylation of polyglutamine disease

A new locus for autosomal dominant Charcot-Marie-Tooth disease type 2 (CMT2L) maps to chromosome 12q24

Metabolic pathways of OGCP and the influence of parkin protein on the metabolism of OGCP

BAG5 Interacts with DJ-1 and Inhibits the Neuroprotective Effects of DJ-1 to Combat Mitochondrial Oxidative Damage

Protective effect of over-expression OGCP on HEK293 cells treated by rotenone and mutant Parkin protein

Genetic variations of Omi / HTRA2 in Chinese patients with Parkinson's disease

Polyglutamine-expanded ataxin-3 is degraded by autophagy

Screening for proteins interacting with ataxin-3, the gene product of SCA3/MJD

Frequency analysis of autosomal dominant spinocerebellar ataxias in mainland Chinese patients and clinical and molecular characterization of spinocerebellar ataxia type 6

Frequency of different subtypes of spinocerebellar ataxia in the Han nationality of Hunan province in China

Construction of the eukaryotic expression vector of MJD1 and its expression in SH-SY5Y cells

Clinical characteristics and molecular biology of hereditary spinocerebellar ataxia type 7: study of 3 Chinese families

Frequency analysis of autosomal dominant spinocerebellar ataxias in Han population in the Chinese mainland and clinical and molecular characterization of spinocerebellar ataxia type 6

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