[PDF] ntu.edu.tw

[引用][C] CYP1A1, CYP2E1, COMT 及MAO-B 基因之多形性與巴金森氏病易感性之相關研究

吳瑞美 - 2000 - ntur.lib.ntu.edu.tw
Reports suggest that COMTL/L (Val158/Met) and MAOB intron 13 genotype polymorphism is
associated with Parkinson's disease (PD). To understand the ethnicityspecific effects of …
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The COMT L allele modifies the association between MAOB polymorphism and PD in Taiwanese

RM Wu, CW Cheng, KH Chen, SL Lu, DE Shan, YF Ho… - Neurology, 2001 - AAN Enterprises
Objective: Reports suggest that catechol-O-methyltransferase (COMTL/L)(Val158/Met) and
monoamine oxidase B (MAOB) intron 13 genotype polymorphism is associated with PD. To …
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Association of Catechol-O-Methyltransferase and monoamine oxidase B gene polymorphisms with motor complications in parkinson's disease in a Chinese …

H Hao, M Shao, J An, C Chen, X Feng, S Xie… - Parkinsonism & Related …, 2014 - Elsevier
Abstract Background Catechol-O-Methyltransferase (COMT) and Monoamine oxidase B
(MAO-B) are the main enzymes that metabolize dopamine in the brain. The polymorphisms …
被引用次数：40 相关文章 所有 7 个版本

COMT Val158Met polymorphism and Parkinson's disease risk: A pooled analysis in different populations

Y Wang, Y Zou, J Xiao, C Pan, S Jiang… - Neurological …, 2019 - Taylor & Francis
Objective: Many studies have analyzed the association between the catechol-O-
methyltransferase (COMT) Val158Met polymorphism and Parkinson's disease (PD), which …
被引用次数：13 相关文章 所有 3 个版本

Association of COMT rs4680 and MAO-B rs1799836 polymorphisms with levodopa-induced dyskinesia in Parkinson's disease—a meta-analysis

Y Yin, Y Liu, M Xu, XM Zhang, C Li - Neurological Sciences, 2021 - Springer
Background and purpose Polymorphisms of the catechol-O-methyl transferase (COMT) or
monoamine oxidase B (MAO-B) genes may affect the occurrence of dyskinesia in …
被引用次数：14 相关文章 所有 5 个版本
[PDF] termedia.pl

Association of monoamine oxidase B and catechol-O-methyltransferase polymorphisms with sporadic Parkinson's disease in an Iranian population

A Torkaman-Boutorabi, GA Shahidi, S Choopani… - Folia …, 2012 - termedia.pl
Genetic polymorphisms have been shown to be involved in dopaminergic
neurotransmission. This may influence susceptibility to Parkinson's disease (PD). We …
被引用次数：25 相关文章 所有 10 个版本

Polymorphisms of catechol-0-methyltransferase (COMT), monoamine oxidase B (MAOB), N-acetyltransferase 2 (NAT2) and cytochrome P450 2D6 (CYP2D6) gene in …

M Bialecka, G Klodowska-Duda, K Honczarenko… - Parkinsonism & related …, 2007 - Elsevier
The aim of the present study was to evaluate the contribution of MAOB, COMT, NAT2 and
CYP2D6 gene polymorphisms to early onset Parkinson's disease (PD). The study enrolled …
被引用次数：48 相关文章 所有 6 个版本
[PDF] springer.com

Genetic polymorphisms involved in dopaminergic neurotransmission and risk for Parkinson's disease in a Japanese population

C Kiyohara, Y Miyake, M Koyanagi, T Fujimoto… - BMC neurology, 2011 - Springer
Background Parkinson's disease (PD) is characterized by alterations in dopaminergic
neurotransmission. Genetic polymorphisms involved in dopaminergic neurotransmission …
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[PDF] niscpr.res.in

Impact of COMT H108L, MAOB int 13 A> G and DRD2 haplotype on the susceptibility to Parkinson's Dise ase in South Indian subjects

N Kumudini, A Uma, YP Devi, SM Naushad, R Mridula… - 2013 - nopr.niscpr.res.in
In view of documented evidence demonstrating the association of dopaminergic metabolism
and neurotransmission with Parkinson's disease (PD), a case-control study was conducted …
被引用次数：13 相关文章 所有 9 个版本

Functional polymorphisms of the MAO gene with Parkinson disease susceptibility: a meta-analysis

YX Sun, XH Wang, AH Xu, JH Zhao - Journal of the neurological sciences, 2014 - Elsevier
Objective We carried out a meta-analysis focusing on the relationships between rs1137070
C> T and rs1799836 A> G polymorphisms in the MAO gene as a modifier of Parkinson …
被引用次数：18 相关文章 所有 5 个版本