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Expansion of Human-Specific GGC Repeat in Neuronal Intranuclear Inclusion Disease-Related Disorders

American journal of human genetics, 2019-07, Vol.105 (1), p.166-176

2019

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The Protective Effects of Osteocyte‐Derived Extracellular Vesicles Against Alzheimer's Disease Diminished with Aging

Advanced science, 2022-06, Vol.9 (17), p.e2105316-n/a

2022

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Mutations in GBA, SNCA, and VPS35 are not associated with Alzheimer's disease in a Chinese population: a case-control study

Neural regeneration research, 2022-03, Vol.17 (3), p.682-689

2022

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Associations of multiple visual rating scales based on structural magnetic resonance imaging with disease severity and cerebrospinal fluid biomarkers in patients with Alzheimer’s disease

Frontiers in aging neuroscience, 2022-07, Vol.14, p.906519-906519

2022

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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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Effectiveness of Combined Immunoglobulin and Glucocorticoid Treatments in a Patient With Stiff Limb Syndrome: Case Report and Review of the Literature

Frontiers in neurology, 2020-05, Vol.11

2020

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Multinodule abnormalities of the tracheobronchus: bronchoscopy findings and clinical diagnosis

The clinical respiratory journal, 2017-07, Vol.11 (4), p.440-447

2017

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Inclusion interaction of chloramphenicol and heptakis (2,6-di- O-methyl)-β-cyclodextrin: Phase solubility and spectroscopic methods

Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 2011-12, Vol.83 (1), p.570-574

2011

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ABCC2 rs2273697 is associated with valproic acid concentrations in patients with epilepsy on valproic acid monotherapy

Pharmazie, 2018-05, Vol.73 (5), p.279-282

2018

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C9orf72 mutation is rare in Alzheimer's disease, Parkinson's disease, and essential tremor in China

Frontiers in cellular neuroscience, 2013-09, Vol.7, p.164-164

2013

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TGM6 identified as a novel causative gene of spinocerebellar ataxias using exome sequencing

Brain (London, England : 1878), 2010-12, Vol.133 (12), p.3510-3518

2010

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Novel mutations of the SPG11 gene in hereditary spastic paraplegia with thin corpus callosum

Journal of the neurological sciences, 2008-12, Vol.275 (1), p.92-99

2008

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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, 2010-10, Vol.27 (5), p.501

2010

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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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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, 2008-12, Vol.87 (3), p.283-286

2008

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Improving the diagnosis of AUS/FLUS thyroid nodules using an algorithm with combination of BRAFV600E mutation analysis and ultrasound pattern-based risk stratification

Clinical hemorheology and microcirculation, 2021-01, Vol.77 (3), p.273-285

2021

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Spectroscopic study of globular clusters in the halo of M31 with the Xinglong 2.16 m telescope

Research in astronomy and astrophysics, 2011-11, Vol.11 (11), p.1298-1310

2011

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Spectroscopic study of globular clusters in the halo of M31 with the Xinglong 2.16 m telescope II: dynamics, metallicity and age

Research in astronomy and astrophysics, 2012-07, Vol.12 (7), p.829-844

2012

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Mutations in GBA, SNCA, and VPS35 are not associated with Alzheimer 's disease in a Chinese population: a case-control study

中国神经再生研究（英文版）, 2022, Vol.17 (3), p.682-689

2022

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Roles of axonal transport affected by K141N mutant HSP22 in the pathogenesis of CMT2L

Zhong hua yi xue za zhi, 2012-02, Vol.92 (7), p.496-498

2012

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Study on establishing the comprehensive evaluation system of sub-health and analysing the risk factors

Zhou, Ya Fang

2010

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Investigation of star formation toward the Sharpless 155 H II region

Research in astronomy and astrophysics, 2014-10, Vol.14 (10), p.1269-1278

2014

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Study on the single-nucleotide substitution (c.-16C to T) of the PURATROPHIN-1 gene in Chinese patients with spinocerebellar ataxia

Zhonghua yi xue yi chuan xue za zhi, 2008-12, Vol.25 (6), p.646

2008

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Serum inducible kinase is a positive regulator of cortical dendrite development and is required for BDNF-promoted dendritic arborization

Cell research, 2012-02, Vol.22 (2), p.387-398

2012

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Effectiveness of Combined Immunoglobulin and Glucocorticoid Treatments in a Patient With Stiff Limb Syndrome: Case Report and Review of the Literature

Frontiers in neurology, 2020, Vol.11, p.284-284

2020

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Expansion of Human-Specific GGC Repeat in Neuronal Intranuclear Inclusion Disease-Related Disorders

The Protective Effects of Osteocyte‐Derived Extracellular Vesicles Against Alzheimer's Disease Diminished with Aging

Mutations in GBA, SNCA, and VPS35 are not associated with Alzheimer's disease in a Chinese population: a case-control study

Associations of multiple visual rating scales based on structural magnetic resonance imaging with disease severity and cerebrospinal fluid biomarkers in patients with Alzheimer’s disease

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

Effectiveness of Combined Immunoglobulin and Glucocorticoid Treatments in a Patient With Stiff Limb Syndrome: Case Report and Review of the Literature

Multinodule abnormalities of the tracheobronchus: bronchoscopy findings and clinical diagnosis

Inclusion interaction of chloramphenicol and heptakis (2,6-di- O-methyl)-β-cyclodextrin: Phase solubility and spectroscopic methods

ABCC2 rs2273697 is associated with valproic acid concentrations in patients with epilepsy on valproic acid monotherapy

C9orf72 mutation is rare in Alzheimer's disease, Parkinson's disease, and essential tremor in China

TGM6 identified as a novel causative gene of spinocerebellar ataxias using exome sequencing

Novel mutations of the SPG11 gene in hereditary spastic paraplegia with thin corpus callosum

Polynucleotide repeat expansion of nine spinocerebellar ataxia subtypes and dentatorubral-pallidoluysian atrophy in healthy Chinese Han population

The advances in research on phosphorylation of polyglutamine disease

Lack of variation of ATTCT pentanucleotide repeats at ATXN10 gene between clinically diagnosed ataxia patients and normal individuals originated from Chinese Han

Improving the diagnosis of AUS/FLUS thyroid nodules using an algorithm with combination of BRAFV600E mutation analysis and ultrasound pattern-based risk stratification

Spectroscopic study of globular clusters in the halo of M31 with the Xinglong 2.16 m telescope

Spectroscopic study of globular clusters in the halo of M31 with the Xinglong 2.16 m telescope II: dynamics, metallicity and age

Mutations in GBA, SNCA, and VPS35 are not associated with Alzheimer 's disease in a Chinese population: a case-control study

Roles of axonal transport affected by K141N mutant HSP22 in the pathogenesis of CMT2L

Study on establishing the comprehensive evaluation system of sub-health and analysing the risk factors

Investigation of star formation toward the Sharpless 155 H II region

Study on the single-nucleotide substitution (c.-16C to T) of the PURATROPHIN-1 gene in Chinese patients with spinocerebellar ataxia

Serum inducible kinase is a positive regulator of cortical dendrite development and is required for BDNF-promoted dendritic arborization

Effectiveness of Combined Immunoglobulin and Glucocorticoid Treatments in a Patient With Stiff Limb Syndrome: Case Report and Review of the Literature

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