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.
苯胺羟化酶在第9周也有升高。
介绍了近年来苯直接羟化合成苯酚的研究进展和合成方法。
Recent progress and synthesis methods on direct hydroxylation of benzene to phenol are systematically introduced.
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.
目的观察中国人CYP2C19基因型与奥美拉唑羟化代谢的关系。
AIM to study the relation of CYP2C19 genotype to omeprazole metabolism in Chinese healthy subjects.
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.
苯酚直接羟化制备苯二酚为液固相的强放热快反应，催化剂的活性衰减很快。
The hydroxylation of phenol to produce dihydric phenol is a rapid and strongly exothermal reaction, the activity of the complex-oxide catalyst decreased rapidly.
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).
通过比较认为，氧化还原法是未来实现苯直接羟化合成苯酚工业化的优选方法。
And it is considered that the reduction-oxidation method would be the optimum method for realizing in industry direct hydroxylation of benzene to phenol.
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.
通过与已报道环氧木脂素类化合物碳谱数值比较，得到了木脂素羟化和苷化位移效应规律。
The rule of hydroxylation and glycosidation shift effects on bisepoxy lignans were obtained by comparing the information of 13C NMR with known analogous.
系统阐述了羟化反应机理，并指出加氧酶活性中心少数氨基酸残基是影响羟化反应的关键因素。
Some amino acid residues in the active center of mono-oxygenases were pointed out to be the main factors to the hydroxylation.
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.
在实验中我们观察到苯酚羟化反应中不仅有苯醌生成 ，而且生成的苯醌还能促进羟化反应 。
The charge transfer interactions of dobutamine with p benzoquinone and chloranil were investigated in ethanol medium, the reactions of Dobutamine with p benzoquinone and chloranil are complete.
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.
本发明涉及一种用于制备链烯基化的羟化芳族化合物、苯并二氢吡喃化合物和其酰化衍生物的方法。
The present invention relates to a process for the manufacture of alkenylated hydroxylated aromatic compounds, of chroman compounds and of their acylated derivatives.
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.
槲皮素竞争性抑制CYP3A2右美沙芬N脱甲基反应，非竞争性抑制CYP2E1氯唑沙宗6羟化反应。
QU exhibited competitive inhibition of CYP3A2 dextromethorphan N-demethylation reaction and expressed noncompetitive inhibition of CYP2E1 chlorzoxazone-6-hydroxylation reaction.
介绍了锰及锰卟啉对超氧化物、羟化自由基、脂质过氧化等自由基的抑制作用，并初步讨论了它们的作用机理。
This paper mainly introduces the inhibition function of manganese and manganese porphyrins to superoxide and hydroxyl radicals, lipid peroxidation.
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.
研究小组发现血清VDR的基因型并不影响血清25-羟化维生素D25-hydroxyvitaminD水平。
The team found no differences in serum 25-hydroxyvitamin D by VDR genotype.
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.
其位移效应规律对于双环氧四氢呋喃木脂素的结构确定，尤其糖的连接位置和羟化位置的指定，提供了一定的判断依据。
The rules of displacement provided suggestion for the confirmation of double-tetrahydrofuran lignans, especially the position of hydroxylation and glycosylation.
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).
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).
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