英语释义

1. any of a group of enzymes that catalyze oxidation reactions in which one of the two atoms of molecular oxygen is incorporated into the substrate and the other is used to oxidize NADH or NADPH

片语

phenol hydroxylase酚羟化酶

Tryptophan Hydroxylase色氨酸羟化酶

prolyl hydroxylase脯氨酰羟化酶

tyrosine hydroxylase酪氨酸羟化酶

hydrocarbon hydroxylase芳香烃羟化酶

Aniline hydroxylase苯胺羟化酶

lysine hydroxylase及赖氨酰羟化酶

lysyl hydroxylaseLysyl hydroxylase (or procollagen-lysine 5-dioxygenase) is an oxygenase enzyme that catalyzes the hydroxylation of lysine to hydroxylysine. This reaction is necessary to the formation and stabilization of collage

benzene hydroxylase苯羟化酶

cholesterol hydroxylase胆固醇羟化酶

英汉例句

• Methods: By using GFP gene as a marker, to observe expression of human tyrosine hydroxylase type I (HTH1) gene in vitro or in brains.

  方法：以绿色荧光蛋白(GFP)作为标记，观察hth_1基因在体外和脑内的表达。

• To develop a fluorescent MGB probe real time PCR platform for detection the mutation of phenylalanine hydroxylase gene in patients with phenylketonuria.

  探讨荧光mgb探针实时P CR技术检测经典型苯丙酮尿癥的基因突变。

• Objective To investigate the genotype in Chinese patients with nonclassical 21 hydroxylase deficiency (NC 21OHD).

  目的对中国人非经典型21羟化酶缺乏癥（21OHD）基因型进行研究。

• Objective: To set the measuring method of tyrosine hydroxylase activity in the brain of conscious rats.

  中文摘要：目的：建立清醒自由活动大鼠脑内酪氨酸羟化酶活性的测定方法。

• AIM: To observe the relationship between the drug dependence behavior and levels of tyrosine hydroxylase (th) in drug acquisition process.

  目的：探讨药物依赖行为和酪氨酸羟化酶在成瘾过程中的相互关系。

• A polyketide synthase complex composed of polyketide synthase with 15 total modules, a non-ribosomal peptide synthetase with I module, and a cytochrome P450 hydroxylase is described.

  描述了包括总共具有15个组件的聚酮化合物合酶、具有1个组件的非核糖体肽合成酶和细胞色素P 450羟化酶组成的聚酮化合物合酶复合物。

• The results indicated the supplying method of carbon source seriously effecting on the hydroxylase activity.

  研究结果表明，菌体培养的碳源供应对菌体所产羟化酶的活力有重要影响。

• Aniline hydroxylase was also high in the 9th week.

  苯胺羟化酶在第9周也有升高。

• Objective Clinical data of 19 Chinese patients with 21 hydroxylase deficiency (21OHD) were analyzed to improve the diagnosis and treatment level.

  目的分析19例21羟化酶缺陷癥（21OHD）患者的临床和随访资料，提高该病的诊断和治疗水平。

• Objective to investigate the association among tryptophan hydroxylase (TPH) gene A218C polymorphism, unipolar depression (UPD) and symptom phenotypes in han nationality of Chinese.

  目的探讨中国汉族人色氨酸羟化酶(TPH)基因A 218c多态性与单相抑郁癥及其癥状表型的遗传关联性。

• CONCLUSION: NURR1 gene combined with NSC can effectively ameliorate PD models symptoms and elevate the number of tyrosine hydroxylase positive neurons after transplantation.

  结论：NURR1基因结合神经干细胞有效改善了帕金森病模型癥状，提高移植后酪氨酸羟化酶阳性神经元细胞的数量。

• To investigate the characteristic of V245V mutation of human phenylalanine hydroxylase gene in Tianjin area.

  目的：探讨天津地区苯丙氨酸羟化酶基因V245 V突变特点。

• Objective To diagnose and treat female pseudohermaphroditism caused by 21 - hydroxylase deficiencies.

  目的为了诊断和治疗21羟化酶缺乏导致的女性假两性畸形。

• Methods: Immunohistochemistry technology and high-pressure liquid chromatography with electrochemical detector (HPLC-EC) were used to evaluated tyrosine hydroxylase (TH) and DA .

  方法：采用免疫组化技术和高效液相-电化学法（ HPLC -EC）分别对酪氨酸羟化酶（TH）、DA进行了含量测定。