Zhuo-lin Liu

发表

Association study of dopamine D2, D3 receptor gene polymorphisms with motor fluctuations in PD

Jian Wang, Zhuo-lin Liu, Biao Chen, 2001, Neurology.

HtrA2/Omi is Involved in 6-OHDA-Induced Endoplasmic Reticulum Stress in SH-SY5Y Cells

Zhi-bin Chen, Yi Li, Xiaowu Chen, 2012, Journal of Molecular Neuroscience.

SNP rs7684318 of the α-synuclein gene is associated with Parkinson's disease in the Han Chinese population

Fayun Hu, Meirong Zhu, Yan-ming Xu, 2010, Brain Research.

Knockdown of glycogen synthase kinase 3 beta attenuates 6-hydroxydopamine-induced apoptosis in SH-SY5Y cells

Yi Li, P. Xu, Lei Wei, 2011, Neuroscience Letters.

Polymorphisms of dopamine receptor and transporter genes and hallucinations in Parkinson's disease

Biao Chen, Jian Wang, Chunying Zhao, 2004, Neuroscience Letters.

LRRK2 G2385R and LRRK2 R1628P increase risk of Parkinson's disease in a Han Chinese population from Southern Mainland China.

J. Zeng, Z. Pei, Ling Chen, 2013, Parkinsonism & related disorders.

Association of the COQ2 V393A Variant with Parkinson's Disease: A Case-Control Study and Meta-Analysis

Xinglong Yang, Ran An, Quanzhen Zhao, 2015, PloS one.

[A new point mutation on exon 2 of parkin gene in Parkinson's disease].

Biao Chen, E. Tao, Yan-ming Xu, 2002, Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics.

Activation of Wnt/β-catenin Pathway by Exogenous Wnt1 Protects SH-SY5Y Cells Against 6-Hydroxydopamine Toxicity

Shaomin Li, L. Ding, L. Yi, 2012, Journal of Molecular Neuroscience.

LRRK2 R1628P contributes to Parkinson's disease susceptibility in Chinese Han populations from mainland China

Yan Liu, Ling Liu, Fayun Hu, 2009, Brain Research.

HLA-DRB1 Alleles Are Associated with the Susceptibility to Sporadic Parkinson’s Disease in Chinese Han Population

Feiqi Zhu, P. Xu, Lei Wei, 2012, PloS one.

Association Studies of MMP-9 in Parkinson’s Disease and Amyotrophic Lateral Sclerosis

Ran An, Yan-ming Xu, X. Yao, 2013, PloS one.

Polymorphism in the Vesicular Monoamine Transporter 2 Gene Decreases the Risk of Parkinson's Disease in Han Chinese Men

Xinglong Yang, Ran An, Quanzhen Zhao, 2015, Parkinson's disease.

Lack of association between cytochrome P450 2E1 gene polymorphisms and Parkinson's disease in a Chinese population

Z. Liu, J. Wang, P. Chan, 2000, Movement disorders : official journal of the Movement Disorder Society.

Distinct novel mutations affecting the same base in the NIPA1 gene cause autosomal dominant hereditary spastic paraplegia in two Chinese families

Jiandong Sun, P. Maxwell, D. Geng, 2005, Human mutation.

Prevalence of pre-diagnostic symptoms did not differ between LRRK2-related, GBA-related and idiopathic patients with Parkinson's disease.

A. Xie, P. Chan, Baorong Zhang, 2018, Parkinsonism & related disorders.

[Effect of the oil from ganoderma lucidum spores on pathological changes in the substantia nigra and behaviors of MPTP-treated mice].

A. Xie, Wei-wen Zhu, Wen-zheng Chu, 2005, Di 1 jun yi da xue xue bao = Academic journal of the first medical college of PLA.

Cognitive impairment is common in Parkinson's disease without dementia in the early and middle stages in a Han Chinese cohort.

J. Zeng, Z. Pei, Hong-yan Zhou, 2012, Parkinsonism & related disorders.

ACT and UCH‐L1 polymorphisms in Parkinson's disease and age of onset

Biao Chen, Jian Wang, Chunying Zhao, 2002, Movement disorders : official journal of the Movement Disorder Society.

Cholecystokinin, cholecystokinin-A receptor and cholecystokinin-B receptor gene polymorphisms in Parkinson's disease.

Jian Wang, Yan-mei Si, Long Yu, 2003, Pharmacogenetics.

LRRK2 R1398H polymorphism is associated with decreased risk of Parkinson's disease in a Han Chinese population.

J. Zeng, Z. Pei, Hong-yan Zhou, 2011, Parkinsonism & related disorders.

Dopamine D5 receptor gene polymorphism and the risk of levodopa-induced motor fluctuations in patients with Parkinson's disease

Biao Chen, Jian Wang, Zhuo-lin Liu, 2001, Neuroscience Letters.

No association between paraoxonase 1 (PON1) gene polymorphisms and susceptibility to Parkinson's disease in a Chinese population

Z. Liu, J. Wang, Zhuo-lin Liu, 2000, Movement disorders : official journal of the Movement Disorder Society.

HtrA2/Omi is Involved in 6-OHDA-Induced Endoplasmic Reticulum Stress in SH-SY5Y Cells

Zhi-bin Chen, Yi Li, Xiaowu Chen, 2012, Journal of Molecular Neuroscience.

[Significant improvement of motor symptoms by deep brain stimulation of bilateral subthalamic nucleus in patients with moderate or advanced Parkinson's disease].

Z. Pei, Hong-yan Zhou, Ling Chen, 2011, Zhonghua yi xue za zhi.

Association of serum uric acid levels with the progression of Parkinson's disease in Chinese patients.

P. Xu, W. Le, Fei-Fei Luo, 2012, Chinese medical journal.

Dopamine Agonists Exert Nurr1-inducing Effect in Peripheral Blood Mononuclear Cells of Patients with Parkinson's Disease

L. Yi, P. Xu, W. Le, 2015, Chinese medical journal.

Corrigendum to “Polymorphisms of dopamine receptor and transporter genes and hallucinations in Parkinson’s disease” [Neurosci. Lett. 355 (2004) 193–196]

Biao Chen, Jian Wang, Chunying Zhao, 2004, Neuroscience Letters.

Activation of Wnt/β-catenin Pathway by Exogenous Wnt1 Protects SH-SY5Y Cells Against 6-Hydroxydopamine Toxicity

Shaomin Li, L. Ding, L. Yi, 2012, Journal of Molecular Neuroscience.