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。
Objective: To explore the association between anxiety disorder and polymorphism of catechol-O-methyltransferase(COMT).
【译】在DNA甲基转移酶基因DNMT3A突变引起的过度生长综合征与智力残疾。
Mutations in the DNA methyltransferase gene DNMT3A cause an overgrowth syndrome with intellectual disability.
目的探索多巴胺d3受体(DRD3)、多巴胺d2受体(DRD2)和儿茶酚氧位甲基转移酶(COMT)基因多态性与双相情感障碍的关系。
Objective To explore the relationship between dopamine D3 (DRD3), dopamine D2 (DRD2), catechol o methyltransferase (COMT) genes polymorphism and bipolar affective disorder.
DNA甲基化由DNA甲基转移酶催化，在多种调节因子的参与下，与组蛋白修饰相互作用，抑制基因转录，导致基因沉默。
DNA methylation catalyzed by DNA methyltransferases interacts with histone modification to inhibit gene transcription, induce gene silencing at the participation of many regulators.
大部分与安慰剂相关的SNP证据表明，基因编码的酶被称为儿茶酚- o -甲基转移酶和单胺氧化酶。
The genes for which most placebo-related SNP evidence exists encode enzymes called catechol-O-methyltransferase and monoamine oxidase.
大部分与安慰剂相关的SNP证据表明，基因编码的酶被称为儿茶酚- o -甲基转移酶和单胺氧化酶。
The genes for which most placebo-related SNP evidence exists encode enzymes called catechol-O-methyltransferase and monoamine oxidase.
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