hydroxylase
英[haɪ'drɒksɪleɪs]
美[haɪ'drɒksɪleɪs]
- n. [化]羟化酶
双语例句
- 1. Dextromethorphan metabolic phenotyping provides a new information for debrisoquine 4-hydroxylase (CYP2D6) polymorphism in native Chinese.
- 右美沙芬的代谢表型研究为中国本地人的异丁喹4-羟化酶（CYP2D6）多态性提供了新的信息。
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- 2. Aniline hydroxylase was also high in the 9th week.
- 苯胺羟化酶在第9周也有升高。
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- 3. 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。
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- 4. 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。
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- 5. 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。
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- 6. 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羟化酶缺乏症（21OHD）基因型进行研究。
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- 7. A pair of specific primers of gene encoding phenol hydroxylase was designed by oligonucleotide high conservative sequence.
- 根据苯酚羟化酶基因高度保守序列设计一对该基因的特异引物。
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- 8. 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。
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- 9. 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。
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- 10. DNA analysis of amniocytes was a feasible method for the prenatal diagnosis of congenital adrenal hyperplasia with 21-hydroxylase deficiency.
- 羊水细胞DNA分析是先天性肾上腺皮质增生症21-羟化酶缺陷的产前诊断的可靠方法。
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- 11. 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羟化酶缺陷症（21OHD）患者的临床和随访资料，提高该病的诊断和治疗水平。
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- 12. In mice and tobacco, this was overcome by over-expression of prolyl hydroxylase, analogous to what has been done in yeast and insect cell culture.
- 在小鼠和烟草中，这是通过过渡表达聚羟化酶来实现的，类似于酵母和昆虫细胞培养。
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- 13. Methods To introduce DNA encoding the wild- type and mutant channel into immortalized tyrosine hydroxylase- positive CNS- derived neurons, CAD cells.
- 方法给一类酪氨酸脱氢酶阳性的神经细胞（一种中枢神经源细胞），又称CAD细胞，引入由DNA编码的野生型和突变型离子通道。
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- 14. Conclusion DNA analysis of amniocytes was a feasible method for the prenatal diagnosis of congenital adrenal hyperplasia with 21-hydroxylase deficiency.
- 结论羊水细胞DNA分析是先天性肾上腺皮质增生症2 1羟化酶缺陷的产前诊断的可靠方法。
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- 15. 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PCR技术检测经典型苯丙酮尿症的基因突变。
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- 16. Objective:To observe the expression of Tyrosine Hydroxylase(TH) of Hypothalamus in post-stroke depression rat model and effects of Yishen Tiaoqi decoction.
- 目的：观察脑缺血后抑郁模型大鼠下丘脑酪胺酸羟化酶（TH）表达及益肾调气方药的干预作用。
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- 17. Objective:To study the mutations of the phenylalanine hydroxylase(PAH)gene and enhance the gene diagnosis of classical phenylketonuria(PKU) in Inner Mongolia.
- 目的：研究内蒙古地区经典型苯丙酮尿症（PKU）苯丙氨酸羟化酶（PAH）基因突变的特点和频率，以提高该地区PKU的基因诊断率。
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- 18. The salicylate hydroxylase, a important enzyme in bacterial naphthalene degradation pathway, catalyzes the decarboxylative hydroxylation of salicylate to form catechol.
- 水杨酸羟化酶是细菌萘降解途径中的关键酶，它能催化水杨酸脱羟和羟化，生成儿茶酚。
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- 19. 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症状，提高移植后酪氨酸羟化酶阳性神经元细胞的数量。
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- 20. 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。
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- 21. 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多态性与单相抑郁症及其症状表型的遗传关联性。
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- 22. 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。
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- 23. Increased EGR1 expression activates transcription of other signaling molecules, including CDK5 and tyrosine hydroxylase, and exerts long term effects on neural cell growth and differentiation (2, 3).
- 增加EGR1表达可以激活其他信号分子的转录，包括CDK5和酪氨酸羟化酶，对神经细胞生长和分化有长期影响(2,3)。
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- 24. Increased EGR1 expression activates transcription of other signaling molecules, including CDK5 and tyrosine hydroxylase, and exerts long term effects on neural cell growth and differentiation (2, 3).
- 增加EGR1表达可以激活其他信号分子的转录，包括CDK5和酪氨酸羟化酶，对神经细胞生长和分化有长期影响(2,3)。
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- The invention also relates to tyrosine hydroxylase revulsant.
本发明化合物是酪氨酸羟化酶诱导剂。 - A pair of specific primers of gene encoding phenol hydroxylase was designed by oligonucleotide high conservative sequence.
根据苯酚羟化酶基因高度保守序列设计一对该基因的特异引物。
用作名词 (n.)
用法讲解
- aryl hydrocarbon hydroxylase 芳烃羟化酶
- imidazole acetate hydroxylase 咪唑转乙酰基酶...
- cholesterol hydroxylase 胆固醇羟化酶...
- aniline hydroxylase 苯胺羟化酶
- arylhydrocarbon hydroxylase 芳香烃羟基化酶...
- collagen hydroxylase 胶原羟化酶
- fatty acid hydroxylase 脂肪酸羟化酶...
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