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。
Dextromethorphan metabolic phenotyping provides a new information for debrisoquine 4-hydroxylase (CYP2D6) polymorphism in native Chinese.
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。
Objective To diagnose and treat female pseudohermaphroditism caused by 21 - hydroxylase deficiencies.
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。
A pair of specific primers of gene encoding phenol hydroxylase was designed by oligonucleotide high conservative sequence.
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。
AIM: To observe the relationship between the drug dependence behavior and levels of tyrosine hydroxylase (th) in drug acquisition process.
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。
Objective: To set the measuring method of tyrosine hydroxylase activity in the brain of conscious rats.
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。
Objective To investigate the genotype in Chinese patients with nonclassical 21 hydroxylase deficiency (NC 21OHD).
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。
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.
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。
The salicylate hydroxylase, a important enzyme in bacterial naphthalene degradation pathway, catalyzes the decarboxylative hydroxylation of salicylate to form catechol.
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。
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。
Conclusion DNA analysis of amniocytes was a feasible method for the prenatal diagnosis of congenital adrenal hyperplasia with 21-hydroxylase deficiency.
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。
Objective:To observe the expression of Tyrosine Hydroxylase(TH) of Hypothalamus in post-stroke depression rat model and effects of Yishen Tiaoqi decoction.
这是首次用热不对称交错pcr法从木本植物的基因组dna克隆到类黄酮3'-羟化酶基因。
This was the first time to clone flavonoid 3 '-hydroxy-lase gene from genomic DNA of woody plants by thermal asymmetric interlaced PCR.
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。
Objective Clinical data of 19 Chinese patients with 21 hydroxylase deficiency (21OHD) were analyzed to improve the diagnosis and treatment level.
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。
Objective to investigate the association among tryptophan hydroxylase (TPH) gene A218C polymorphism, unipolar depression (UPD) and symptom phenotypes in han nationality of Chinese.
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。
CONCLUSION: NURR1 gene combined with NSC can effectively ameliorate PD models symptoms and elevate the number of tyrosine hydroxylase positive neurons after transplantation.
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)。
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).
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。
Methods: Immunohistochemistry technology and high-pressure liquid chromatography with electrochemical detector (HPLC-EC) were used to evaluated tyrosine hydroxylase (TH) and DA .
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。
Objective:To study the mutations of the phenylalanine hydroxylase(PAH)gene and enhance the gene diagnosis of classical phenylketonuria(PKU) in Inner Mongolia.
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。
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。
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.
应用推荐