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Lu Shen

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Wen-Juan Guan; Ji-Feng Guo; Hong Jiang; Jia-Da Li; Yu-Tao Liu; Yan-Tao Ma; Lu Shen; Jun-Ling Wang; Kun Xia; Ying Zhou; Bei-sha Tang
Spinocerebellar ataxia type 35 (SCA35)-associated transglutaminase 6 mutants sensitize cells to apoptosis.
Ya-Fang Zhou; Jing-Wei Chi; Juan Du; Hong Jiang; Li-Fang Lei; Shu-sheng Liao; Ying-Ying Luo; Bei-sha Tang; Jian-guang Tang; Jun-Ling Wang; Kun Xia; Lu Shen
SUMO-1 modification on K166 of polyQ-expanded ataxin-3 strengthens its stability and increases its cytotoxicity.
Yu-Tao Liu; Lu Shen; Yu-Ting Shi; Bei-sha Tang; Jun-Ling Wang; Kun Xia; Xin-Xiang Yan; Ying Zhou; Wen-Juan Guan; Hong Jiang
Spinocerebellar ataxia type 23 is an uncommon SCA subtype in the Chinese Han population.

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2013: Wen-Juan Guan; Ji-Feng Guo; Hong Jiang; Jia-Da Li; Yu-Tao Liu; Yan-Tao Ma; Lu Shen; Jun-Ling Wang; Kun Xia; Ying Zhou; Bei-sha Tang
Spinocerebellar ataxia type 35 (SCA35)-associated transglutaminase 6 mutants sensitize cells to apoptosis.
Biochemical and biophysical research communications 2013;430(2):780-6.
2013: Ya-Fang Zhou; Jing-Wei Chi; Juan Du; Hong Jiang; Li-Fang Lei; Shu-sheng Liao; Ying-Ying Luo; Bei-sha Tang; Jian-guang Tang; Jun-Ling Wang; Kun Xia; Lu Shen
SUMO-1 modification on K166 of polyQ-expanded ataxin-3 strengthens its stability and increases its cytotoxicity.
PloS one 2013;8(1):e54214.
2012: Yu-Tao Liu; Lu Shen; Yu-Ting Shi; Bei-sha Tang; Jun-Ling Wang; Kun Xia; Xin-Xiang Yan; Ying Zhou; Wen-Juan Guan; Hong Jiang
Spinocerebellar ataxia type 23 is an uncommon SCA subtype in the Chinese Han population.
Neuroscience letters 2012;528(1):51-4.
2012: Zi-xiong Zhan; Zhao-ting Hu; Lu Shen
[Strategies for exome sequence data analysis for discovering genes underlying autosomal recessive disorders].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2012;29(5):558-61.
2012: Jin-yong Tian; Xin-xiang Yan; Ri-li Yu; Kai Li; Zhan-yun Lv; Lu Shen; Chang-he Shi; Bei-sha Tang; Ji-feng Guo
Analysis of PLA2G6 gene mutation in sporadic early-onset parkinsonism patients from Chinese population.
Neuroscience letters 2012;514(2):156-8.
2012: Hai-nan Zhang; Chun-yu Wang; Ya-qin Wang; Xin-xiang Yan; Ji-feng Guo; Dan He; Li-fang Lei; Lu Shen; Li-ming Tan; Bei-sha Tang
Lower serum UA levels in Parkinson's disease patients in the Chinese population.
Neuroscience letters 2012;514(2):152-5.
2012: Sanxi Ai; Xiang Feng; Jifeng Guo; Lu Shen; Beisha Tang
DNA methylation as a biomarker for neuropsychiatric diseases.
The International journal of neuroscience 2012;122(4):165-76.
2012: Yacen Hu; Lu Shen; Changhe Shi; Qiying Sun; Liming Tan; Beisha Tang; Chunyu Wang; Lei Wang; Xintian Wu; Xinxiang Yan; Jifeng Guo; Liang Hu; Hainan Zhang
Variant in the 3' region of SNCA associated with Parkinson's disease and serum α-synuclein levels.
Journal of neurology 2012;259(3):497-504.
2012: Fu-Feng Zhang; Ya-Fang Zhou; Xin-Xiang Yan; Hong Jiang; Xiao-Qin Lu; Lu Shen; Bei-sha Tang
[Roles of axonal transport affected by K141N mutant HSP22 in the pathogenesis of CMT2L].
Zhonghua yi xue za zhi 2012;92(7):496-8.
2011: Juan Du; Ya-Cen Hu; Hong Jiang; Ying-Ying Luo; Bei-sha Tang; Kun Xia; Zi-Xiong Zhan; Guo-hua Zhao; Chong Chen; Lu Shen
Expansion of the phenotypic spectrum of SPG6 caused by mutation in NIPA1.
Clinical neurology and neurosurgery 2011;113(6):480-2.
2011: Lifang Lei; Weihua Liao; Yunjie Liao; Lu Shen; Junling Wang; Yi Yuan; Jie Zhou; Hong Jiang; Beisha Tang
Magnetic resonance spectroscopy of the cerebellum in patients with spinocerebellar ataxia type 3/Machado-Joseph disease.
Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences 2011;36(6):511-9.
2011: Jie Zhou; Junling Wang; Hong Jiang; Lifang Lei; Lu Shen; Yuting Shi; Beisha Tang
Serum concentrations of NSE and S100B in spinocerebellar ataxia type 3/Machado-Joseph disease.
Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences 2011;36(6):504-10.
2011: Jie Zhou; Beisha Tang; Junling Wang; Hong Jiang; Lifang Lei; Xinxin Liao; Lu Shen
Related factors of ICARS and SARA scores on spinocerebellar ataxia type 3/Machado-Joseph disease.
Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences 2011;36(6):498-503.
2011: Junling Wang; Kun Xia; Qian Xu; Jie Zhou; Lifang Lei; Yutao Liu; Qian Pan; Lu Shen; Beisha Tang; Wenjuan Guan; Hong Jiang
Spinocerebellar ataxias in mainland China: an updated genetic analysis among a large cohort of familial and sporadic cases.
Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences 2011;36(6):482-9.
2011: Ling-Yan Yao; Ji-feng Guo; Lei Wang; Ren-He Yu; Qi-Ying Sun; Qian Pan; Kun Xia; Bei-sha Tang; Lu Shen
LRRK2 Pro755Leu variant in ethnic Chinese population with Parkinson's disease.
Neuroscience letters 2011;495(1):35-8.
2011: Lei Wang; Ji-feng Guo; Li-luo Nie; Linzi Luo; Xing Zuo; Lu Shen; Hong Jiang; Xin-xiang Yan; Kun Xia; Qian Pan; Bei-sha Tang
Case-control study of the UCH-L1 S18Y variant in sporadic Parkinson's disease in the Chinese population.
Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia 2011;18(4):541-4.
2010: Jun Ling Wang; Xu Yang; Kun Xia; Zheng Mao Hu; Ling Weng; Xin Jin; Hong Jiang; Peng Zhang; Lu Shen; Ji Feng Guo; Nan Li; Ying Rui Li; Li Fang Lei; Jie Zhou; Juan Du; Ya Fang Zhou; Qian Pan; Jian Wang; Jun Wang; Rui Qiang Li; Bei-sha Tang
TGM6 identified as a novel causative gene of spinocerebellar ataxias using exome sequencing.
Brain : a journal of neurology 2010;133(Pt 12):3510-8.
2010: Qian Xu; Dandan Jia; Junling Wang; Jifeng Guo; Hong Jiang; Lifang Lei; Lu Shen; Qian Pan; Kun Xia; Xinxiang Yan; Beisha Tang
Genetic analysis of Spinocerebellar ataxia type 17 in Parkinson's disease in Mainland China.
Parkinsonism & related disorders 2010;16(10):700-2.
2010: Xuejing Wang; Jifeng Guo; Hong Jiang; Lu Shen; Beisha Tang
[Direct interaction between BAG5 protein and Parkin protein].
Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences 2010;35(11):1156-61.
2010: Jun-ling Wang; Yun-qin Wu; Li-fang Lei; Lu Shen; Hong Jiang; Ya-fang Zhou; Ji-ping Yi; Jie Zhou; Xin-xiang Yan; Qian Pan; Kun Xia; Bei-sha Tang
[Polynucleotide repeat expansion of nine spinocerebellar ataxia subtypes and dentatorubral-pallidoluysian atrophy in healthy Chinese Han population].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2010;27(5):501-5.
2010: Xing Zuo; Hong Jiang; Ji-feng Guo; Ren-He Yu; Qi-Ying Sun; Liang Hu; Lei Wang; Ling-Yan Yao; Lu Shen; Qian Pan; Xiao-Xin Yan; Kun Xia; Bei-sha Tang
Screening for two SNPs of LINGO1 gene in patients with essential tremor or sporadic Parkinson's disease in Chinese population.
Neuroscience letters 2010;481(2):69-72.
2010: Xuejing Wang; Hui Wang; Yujun Xia; Hong Jiang; Lu Shen; Shoubiao Wang; Ruowu Shen; Liang Huang; Junling Wang; Qian Xu; Xiaohui Li; Xuegang Luo; Beisha Tang
A neuropathological study at autopsy of early onset spinocerebellar ataxia 6.
Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia 2010;17(6):751-5.
2010: Nan Li; Haiyan Li; Hong Jiang; Lu Shen; Xinxiang Yan; Jifeng Guo; Yanmin Song; Qian Yang; Yaqin Wang; Xiaobo Li; Ruping Xiang; Xiaohong Zi; Xiaoyan Long; Zhengmao Hu; Qian Pan; Kun Xia; Beisha Tang
Mutation detection in candidate genes for benign familial infantile seizures on a novel locus.
The International journal of neuroscience 2010;120(3):217-21.
2010: Qian Xu; Qinghua Li; Junling Wang; Hong Jiang; Lu Shen; Xiaohui Li; Beisha Tang
A spinocerebellar ataxia family with expanded alleles in the TATA-binding protein gene and ataxin-3 gene.
The International journal of neuroscience 2010;120(2):159-61.
2010: Qian Xu; Xiaohui Li; Junling Wang; JiPing Yi; Lifang Lei; Lu Shen; Hong Jiang; Kun Xia; Qian Pan; Beisha Tang
Spinocerebellar ataxia type 11 in the Chinese Han population.
Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2010;31(1):107-9.
2009: Lei Wang; Ji-Feng Guo; Li-Luo Nie; Hai-Nan Zhang; Lu Shen; Hong Jiang; Qian Pan; Kun Xia; Bei-sha Tang; Xin-xiang Yan
A new variant of the ATP13A2 gene in Chinese patients with early-onset parkinsonism.
Chinese medical journal 2009;122(24):3082-5.
2009: Juan Du; Lu Shen; Beisha Tang
[Recent advances of study on hereditary spastic paraplegia type 11].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2009;26(6):670-3.
2009: Junling Wang; Qian Xu; Lifang Lei; Lu Shen; Hong Jiang; Xiaohui Li; Yafang Zhou; Jiping Yi; Jie Zhou; Xinxiang Yan; Qian Pan; Kun Xia; Beisha Tang
[Studies on the CAG repeat expansion in patients with hereditary spinocerebellar ataxia from Chinese Han].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2009;26(6):620-5.
2009: Jun-Ling Wang; Bin Xiao; Xiang-Xiang Cui; Ji-feng Guo; Li-Fang Lei; Xing-Wang Song; Lu Shen; Hong Jiang; Xin-xiang Yan; Qian Pan; Zhi-gao Long; Kun Xia; Bei-sha Tang
Analysis of SCA2 and SCA3/MJD repeats in Parkinson's disease in mainland China: genetic, clinical, and positron emission tomography findings.
Movement disorders : official journal of the Movement Disorder Society 2009;24(13):2007-11.
2009: Yin-guang Wang; Juan Du; Jun-ling Wang; Juan Chen; Chong Chen; Ying-ying Luo; Zhi-quan Xiao; Hong Jiang; Xin-xiang Yan; Kun Xia; Qian Pan; Bei-sha Tang; Lu Shen
Six cases of SCA3/MJD patients that mimic hereditary spastic paraplegia in clinic.
Journal of the neurological sciences 2009;285(1-2):121-4.
2009: Q Xu; X H Li; J L Wang; Hong Jiang; S Zhang; L F Lei; Lu Shen; Kun Xia; Qian Pan; Zhi-gao Long; Bei-sha Tang
Mutation analysis of the TATA box-binding protein (TBP) gene in Chinese Han patients with spinocerebellar ataxia.
Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia 2009;16(10):1374-5.
2009: Juan Du; Lu Shen; Guo-hua Zhao; Yin-guang Wang; Shu-sheng Liao; Chong Chen; Zhi-fan Zhou; Ying-ying Luo; Hong Jiang; Kun Xia; Bei-sha Tang
Receptor expression-enhancing protein 1 gene (SPG31) mutations are rare in Chinese Han patients with hereditary spastic paraplegia.
Chinese medical journal 2009;122(17):2064-6.
2009: Shen Zhang; Jun-ling Wang; Qian Xu; Xiao-hui Li; Li-fang Lei; Hong Jiang; Lu Shen; Xin-xiang Yan; Qian Pan; Kun Xia; Bei-sha Tang
[Detection of the CAG trinucleotide repeats of MJD1 gene by recombinant DNA technology].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2009;26(4):406-9.
2009: Yin-guang Wang; Lu Shen
[AAA ATPases and hereditary spastic paraplegia].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2009;26(3):298-301.
2008: Shu-sheng Liao; Lu Shen; Juan Du; Guo-hua Zhao; Xiao-yi Wang; Yi Yang; Zi-quan Xiao; Yi Yuan; Hong Jiang; Nan Li; He-dong Sun; Jun-ling Wang; Chun-yu Wang; Ya-fang Zhou; Xiao-yun Mo; Kun Xia; Bei-sha Tang
Novel mutations of the SPG11 gene in hereditary spastic paraplegia with thin corpus callosum.
Journal of the neurological sciences 2008;275(1-2):92-9.
2008: Jun-Ling Wang; Hong Jiang; Shen Zhang; Qian Xu; Ya-Fang Zhou; Shu-Sheng Liao; Lu Shen; Xin-Xiang Yan; Huai-Xu Zhu; Qian Pan; Kun Xia; Bei-sha Tang
Lack of variation of ATTCT pentanucleotide repeats at ATXN10 gene between clinically diagnosed ataxia patients and normal individuals originated from Chinese Han.
Journal of genetics 2008;87(3):283-6.
2008: Ji-feng Guo; Bin Xiao; Bing Liao; xuewei zhang; Li-Luo Nie; Yu-Hu Zhang; Lu Shen; Hong Jiang; Kun Xia; Qian Pan; Xin-xiang Yan; Bei-sha Tang
Mutation analysis of Parkin, PINK1, DJ-1 and ATP13A2 genes in Chinese patients with autosomal recessive early-onset Parkinsonism.
Movement disorders : official journal of the Movement Disorder Society 2008;23(14):2074-9.
2008: Junling Wang; Shen Zhang; Qian Xu; Xiaohui Li; Xingwang Song; Hong Jiang; Lu Shen; Xinxiang Yan; Qian Pan; Kun Xia; Beisha Tang
[Studies on the CTA/CTG trinucleotide repeats of ATXN8OS gene in Chinese Hans].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2008;25(5):511-4.
2008: Guo-hua Zhao; Zhi-jun Ren; Xiao-min Liu; Shu-jian Li; Peng Guo; Lu Shen; Kun Xia; Bei-sha Tang
[The clinical characteristics of a pedigree with incompletely penetrated autosomal dominant hereditary spastic paraplegia and its exclusion analysis of genetic loci].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2008;25(3):304-7.
2008: Guo-hua Zhao; Zheng-mao Hu; Lu Shen; Hong Jiang; Zhi-jun Ren; Xiao-min Liu; Kun Xia; Peng Guo; Qian Pan; Bei-sha Tang
A novel candidate locus on chromosome 11p14.1-p11.2 for autosomal dominant hereditary spastic paraplegia.
Chinese medical journal 2008;121(5):430-4.
2008: Haiyan Li; Nan Li; Lu Shen; Hong Jiang; Qian Yang; Yanmin Song; Jifeng Guo; Kun Xia; Qian Pan; Beisha Tang
A novel mutation of KCNQ3 gene in a Chinese family with benign familial neonatal convulsions.
Epilepsy research 2008;79(1):1-5.
2007: Guo-hua Zhao; Peng Guo; Zhi-jun Ren; Xiao-min Liu; Lu Shen; Kun Xia; Bei-sha Tang
[Gene screening in five Chinese families with hereditary spastic paraplegia with thin corpus callosum].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2007;24(6):677-80.
2007: Jing Li; Bei-sha Tang; Ji-feng Guo; Yu-hu Zhang; Xin-xiang Yan; Ying-feng Mu; xuewei zhang; Kun Xia; Qian Pan; Lu Shen; Hong Jiang
[Mutation detection of parkin gene by denaturing high performance liquid chromatography].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2007;24(4):449-52.
2007: Jing Li; Bei-sha Tang; Ji-feng Guo; Yu-hu Zhang; Zhi-guo Xie; Xin-xiang Yan; Lu Shen; Hong Jiang; xuewei zhang; Kun Xia; Qian Pan
[Mutation analysis of GCH1 gene in Chinese patients with dopa responsive dystonia].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2007;24(3):302-4.
2006: Xing-wang Song; Bei-sha Tang; Hong Jiang; Lu Shen; Qian Yang; Shu-sheng Liao; Qing-hua Li; Jian-guang Tang
[Frequency of different subtypes of spinocerebellar ataxia in the Han nationality of Hunan province in China].
Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences 2006;31(5):702-5.
2006: Hai-yan Li; Bei-sha Tang; Xin-xiang Yan; Ji-feng Guo; Lu Shen; Yan-min Song; Hong Jiang; Kun Xia; Zhi-guo Xie; Qi-an Yang
[Clinical and mutational analysis of KCNQ3 gene in a Chinese family with benign familial neonatal convulsions].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2006;23(4):374-7.
2006: Xing-Wang Song; Bei-sha Tang; Hong Jiang; Lu Shen; Qian Yang; Shu-sheng Liao; Qing-hua Li; Xiao-chun Liang; Jian-guang Tang
[Clinical characteristics and molecular biology of hereditary spinocerebellar ataxia type 7: study of 3 Chinese families].
Zhonghua yi xue za zhi 2006;86(25):1755-8.
2006: Ji-feng Guo; Bei-sha Tang; Jing Li; Yu-hu Zhang; xuewei zhang; Tao Chen; Kun Xia; Xin-xiang Yan; Li Cao; Fang Cai; Qian Pan; Lu Shen; Hong Jiang
[Exon rearrangement analysis of parkin gene in patients with isolated early-onset parkinsonism using semi-quantitative PCR].
Zhonghua yi xue za zhi 2006;86(21):1447-9.
2006: Hong Jiang; Beisha Tang; Kun Xia; Zhengmao Hu; Lu Shen; Jianguang Tang; Guohua Zhao; Yuhu Zhang; Fang Cai; Qian Pan; Zhigao Long; Guo Wang; Heping Dai
Mutation analysis of the ATM gene in two Chinese patients with ataxia telangiectasia.
Journal of the neurological sciences 2006;241(1-2):1-6.
2006: Lu Shen; Bei-sha Tang; Jian-guang Tang; Hong Jiang; Cheng Wang; Hai-yan Fang
[Screening for proteins interacting with ataxin-3, the gene product of SCA3/MJD].
Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences 2006;31(1):40-4.
2006: Ji-feng Guo; Bei-sha Tang; Yu-hu Zhang; Hong-jian Liu; Xin-xiang Yan; Tao Chen; Lu Shen; Hong Jiang; Kun Xia; Fang Cai; Qian Pan
[Genotype and phenotype analyses of three families with autosomal recessive juvenile parkinsonism].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2006;23(1):70-3.
2005: Jian-guang Tang; Bei-sha Tang; Lu Shen; Hong Jiang; Zhi-ping Hu; Li Cao; Kun Xia; Fang Cai
[Construction of the eukaryotic expression vector of MJD1 and its expression in SH-SY5Y cells].
Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences 2005;30(6):640-4.
2005: Ji-feng Guo; Bei-sha Tang; Yu-hu Zhang; Kun Xia; Fang Cai; Qian Pan; Lu Shen; Hong Jiang; Guo-hua Zhao; Xin-xiang Yan; Li Cao
[Mutation analysis of DJ1 gene in patients with autosomal recessive early-onset Parkinsonism].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2005;22(6):641-3.
2005: Xiao-min Liu; Bei-sha Tang; Guo-hua Zhao; Kun Xia; Fu-feng Zhang; Qian Pan; Fang Cai; Zheng-mao Hu; Cheng Zhang; Piu Chan; Lu Shen; Ru-xu Zhang; Hong Jiang
[Mutation analysis of small heat shock protein 27 gene in Chinese patients with Charcot-Marie-Tooth disease].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2005;22(5):510-3.
2005: Hong Jiang; Beisha Tang; Kun Xia; Yongxin Zhou; Bo Xu; Guohua Zhao; Haiyan Li; Lu Shen; Qian Pan; Fang Cai
Spinocerebellar ataxia type 6 in Mainland China: molecular and clinical features in four families.
Journal of the neurological sciences 2005;236(1-2):25-9.
2005: Peng Guo; Bei-sha Tang; Guo-hua Zhao; Xiao-min Liu; Fu-feng Zhang; Ru-xu Zhang; Lu Shen; Hong Jiang; Jing-hui Liang
[Analysis of the pathological features and gene mutations of Chinese patients with Charcot-Marie-Tooth disease].
Zhonghua yi xue za zhi 2005;85(34):2382-5.
2005: Beisha Tang; Xiaomin Liu; Guohua Zhao; Wei Luo; Kun Xia; Qian Pan; Fang Cai; Zhengmao Hu; Cheng Zhang; Piu Chan; Fufeng Zhang; Lu Shen; Ruxu Zhang; Hong Jiang
Mutation analysis of the small heat shock protein 27 gene in chinese patients with Charcot-Marie-Tooth disease.
Archives of neurology 2005;62(8):1201-7.
2005: Lu Shen; Jian-guang Tang; Bei-sha Tang; Hong Jiang; Guo-hua Zhao; Kun Xia; Yu-hu Zhang; Fang Cai; Li-ming Tan; Qian Pan
Research on screening and identification of proteins interacting with ataxin-3.
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2005;22(3):242-7.
2005: Hong Jiang; Bei-sha Tang; Bo Xu; Guo-hua Zhao; Lu Shen; Jian-guang Tang; Qing-hua Li; Kun Xia
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;118(10):837-43.
2005: Hong Jiang; Beisha Tang; Zhengmao Hu; Kun Xia; Bo Xu; Jianguang Tang; Lu Shen
[ATM gene mutations in Chinese patients with ataxia telangiectasia].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2005;22(2):121-4.
2005: Ru-xu Zhang; Wei Luo; Xiao-hong Zi; Kun Xia; Fang Cai; Jian-feng Xiao; Guo-hua Zhao; Fu-feng Zhang; Lu Shen; Hong Jiang; Bei-sha Tang
Mutation screening of Cx32 in Han Chinese patients with Charcot-Marie-Tooth disease.
Beijing da xue xue bao. Yi xue ban = Journal of Peking University. Health sciences 2005;37(1):68-71.
2005: Hong Jiang; Beisha Tang; Bo Xu; Guo-hua Zhao; Lu Shen; Jian-guang Tang; Qing-hua Li; Kun Xia
[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 = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2005;22(1):1-4.
2005: Bei-sha Tang; Guo-hua Zhao; Wei Luo; Kun Xia; Fang Cai; Qian Pan; Ru-xu Zhang; Fu-feng Zhang; Xiao-min Liu; Piu Chan; Cheng Zhang; Lu Shen; Hong Jiang; Zhi-gao Long; He-ping Dai
Small heat-shock protein 22 mutated in autosomal dominant Charcot-Marie-Tooth disease type 2L.
Human genetics 2005;116(3):222-4.
2004: Bei-sha Tang; Xin Chen; Guo-hua Zhao; Lu Shen; Xin-xiang Yan; Hong Jiang; Wei Luo
Clinical features of hereditary spastic paraplegia with thin corpus callosum: report of 5 Chinese cases.
Chinese medical journal 2004;117(7):1002-5.
2004: Beisha Tang; Haiyan Li; Kun Xia; Hong Jiang; Qian Pan; Lu Shen; Zhigao Long; Guohua Zhao; Fang Cai
A novel mutation in KCNQ2 gene causes benign familial neonatal convulsions in a Chinese family.
Journal of the neurological sciences 2004;221(1-2):31-4.
2004: Bei-sha Tang; Wei Luo; Kun Xia; Jian-feng Xiao; Hong Jiang; Lu Shen; Jian-guang Tang; Guo-hua Zhao; Fang Cai; Qian Pan; He-ping Dai; Qi-dong Yang; Jia-hui Xia; Oleg V Evgrafov
A new locus for autosomal dominant Charcot-Marie-Tooth disease type 2 (CMT2L) maps to chromosome 12q24.
Human genetics 2004;114(6):527-33.
2004: Beisha Tang; Guohua Zhao; Kun Xia; Qian Pan; Wei Luo; Lu Shen; Zhigao Long; Heping Dai; Xiaohong Zi; Hong Jiang
Three novel mutations of the spastin gene in Chinese patients with hereditary spastic paraplegia.
Archives of neurology 2004;61(1):49-55.
2003: Hai-yan Li; Bei-sha Tang; Ai-mei Zhang; Qiu-hui Cao; Gui-lian Meng; Hong Jiang; Lu Shen
[A novel mutation of KCNQ2 gene in a Chinese family with benign familial neonatal convulsions].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2003;20(6):482-5.