Association Study between Polymorphism of Catechol-O-methyltransferase Gene and Attention Deficit Hyperactivity Disorder, Cognitive Function of Attention Deficit Hyperactivity Disorder 注意缺陷多动障碍认知功能与儿茶酚胺氧位甲基转移酶基因多态性的关联分析
Study on Catechol-O-Methyltransferase Activity in Rat Liver by RP-HPLC RP-HPLC法测定鼠肝组织儿茶酚氧位甲基转移酶活性的研究
Association study of polymorphism of catechol-O-methyltransferase and anxiety disorder 儿茶酚邻甲基转移酶基因多态性与焦虑症的关联研究
Synergistic role of polymorphisms of dopamine beta hydroxylase gene and catechol-o-methyltransferase gene in genetic susceptibility to Parkinson disease 帕金森病遗传易感性与儿茶酚胺氧位甲基转移酶和多巴胺β羟化酶基因多态协同作用的关系
Objective: To explore the association between anxiety disorder and polymorphism of catechol-O-methyltransferase ( COMT). 目的探讨焦虑症与儿茶酚邻甲基转移酶基因多态性的相关性。
In this paper we study the catechol-O-methyltransferase ( COMT) gene and the dopamine transporter ( DAT) gene with the proposal to found the relationship among these genes, the children general ability ( g) and the children mental retardation ( MR). 本论文旨在探讨儿茶酚胺氧甲基转移酶(COMT)基因和多巴胺转运蛋白(DAT)基因的多态性与秦巴山区儿童一般认知能力及儿童精神发育迟滞(MR)的关系。
Measurement of catechol-O-methyltransferase activity in erythrocytes of Chinese Han people 正常中国汉人红细胞中儿茶酚氧位甲基转移酶的活性测定
Association analysis of dopamine D_2 receptor and catechol-O-methyltransferase genes with bipolar affective disorder in different age groups 不同年龄双相情感性精神障碍与多巴胺D2、儿茶酚氧位甲基转移酶基因多态性的关联分析
Objective: To explore the relation between polymorphism of catechol-O-methyltransferase ( COMT) gene and clinical characters of obsessive-compulsive disorder ( OCD). 目的:探索儿茶酚邻甲基转移酶(COMT)基因多态性同强迫症临床特征的关系。
OBJECTIVE To explore the normal range of catechol-O-methyltransferase ( COMT) activity in erythrocyte of Chinese Han people. 目的测定正常中国人群红细胞儿茶酚氧位甲基转移酶(COMT)活性浓度值,为研究COMT活性变化在疾病诊断中的应用提供依据。