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.
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.
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.
20. Methods: Immunohistochemistry technology and high-pressure liquid chromatography with electrochemical detector (HPLC-EC) were used to evaluated tyrosine hydroxylase (TH) and DA .
21. Objective to investigate the association among tryptophan hydroxylase (TPH) gene A218C polymorphism, unipolar depression (UPD) and symptom phenotypes in han nationality of Chinese.
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.
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).
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).
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。
