hydroxylase

This study aimed to investigate the effect of BH4 and phenylalanine hydroxylase ( PAH) gene mutations in patients with BH4 responsive mild PKU and mild hyperphenylalaninemia ( HPA). Compared with W. Mainly discusses the architecture and principle of the.

本研究将探讨BH4和苯丙氨酸羟化酶（PAH）基因突变在对BH4有反应的轻度PKU和轻度高苯丙酸血症（HPA）患者中的作用。

Hepatic Microsomal Aniline Hydroxylase and Aminopyrine N-demethylase Activities in the Rat at Different Ages

不同鼠龄大鼠肝微粒体苯胺羟化酶及氨基比林N-脱甲基酶活性

Objective To explore the method for prenatal diagnosis of congenital adrenal hyperplasia ( CAH) with 21-hydroxylase deficiency ( 21-OHD).

目的探讨先天性肾上腺皮质增生症21羟化酶缺陷的产前诊断方法。

Mutations in Exon 7 of the Phenylalanine Hydroxylase ( PAH) Gene in Chinese Patients with Phenylketonuria

苯丙氨酸羟化酶（PAH）基因外显子7及其两侧内含子的突变研究

Histone Deacetylase Maybe Involved in the Mechanism of Inhibition of Tyrosine Hydroxylase Expression in α-Synuclein-Transfected Dopaminergic Neuronal Cells

组蛋白脱乙酰化酶在α-突触核蛋白抑制酪氨酸羟化酶表达中的作用

Objective: To explore the relationship between the hepatic depression syndrome and hyperpyrexia of liver syndrome disorder and polymorphisms in the serotonin transporter ( 5 HTT) and tryptophan hydroxylase ( TPH).

目的：探讨肝气郁结证、肝火上炎证与五羟色胺转运体（5HTT）、色氨酸羟化酶（TPH）基因三种多态性的相关性。

Exercise also decreased striatal DA transporter and tyrosine hydroxylase immunoreactivity in MPTP-lesioned mice.

运动也可以减少纹状体多巴胺转运体,还能抑制酪氨酸羟化酶的免疫反应性.

Association Study for Serotonin Transporter and Tryptophan Hydroxylase Gene Polymorphisms and Hepatic Depression Syndrome and Hyperpyrexia of Liver Syndrome Disorder

肝气郁结证、肝火上炎证患者情绪测量及与5-HTT，TPH，ACE基因多态性相关研究

AIM: To observe the expression of tyrosine hydroxylase ( TH) and dopamine beta hydroxylase ( DBH) in the lumbar sympathetic ganglia neurons of the patients with Buerger disease of lower limb.

目的：研究下肢Buerger病患者腰交感神经节神经元中去甲肾上腺素合成酶酪氨酸羟化酶（tyrosine hydroxylase，TH）和多巴胺β羟化酶（dopamine beta hydroxylase，DBH）的表达变化。

Studies on autoregulation of tyrosine hydroxylase in rat corpus striatum

大鼠纹状体突触体酪氨酸羟化酶自身调节的研究

Objective To obtain the mutation spectrum of exon 12 of the phenylalanine hydroxylase ( PAH) gene.

目的了解中国人苯丙酮尿症（phenylketonuria，PKU）患者的苯丙氨酸羟化酶（Phenylalanine hydroxylase，PAH）基因第12外显子点突变种类和频率。

Here reported is a female pseudohermaphroditism due to 11-β-hydroxylase deficit. Its clinical forms, diagnosis and treatment were discussed.

本文报道一例先天性肾上腺皮质增生症（11&β-羟化酶缺乏）的女性患者，并对本症的临床、诊断及治疗进行了讨论。

Hydroxylation by protoplasts of the strain indicated that its hydroxylase is endoenzyme which could be induced by steroid substrate and cell wall of this fungus is an important rate limitation factor.

原生质体的羟化反应实验表明，该菌的羟化酶属于胞内诱导酶，真菌细胞壁是甾体微生物转化的一个很重要的速率限制因子。

Four weeks after operation, experimental animals were gained, anesthetizing, filling, filleting, and then performing immunohistochemical reaction of tyroxine hydroxylase of midbrain.

手术后4周，取实验动物，麻醉，灌注，切片，再行中脑抗酪氨酸羟化酶免疫组织化学反应。

Abnormal expression of tyrosine hydroxylase in the cerebellum of Niemann-Pick type c mice

酪氨酸羟化酶在C型尼曼-匹克病小鼠小脑中的异常表达

Aniline hydroxylase was also high in the 9th week.

苯胺羟化酶在第9周也有升高。

Tyrosine hydroxylase are mainly found in glomerular layer, few in external plexiform layer.

结果表明：tyrosine hydroxylase主要出现在嗅球的小球层，在外网织层有很少的阳性细胞；

By the experiment of melanin synthesis inhibition in vitro observing appearance changes in integument, the paper demonstrate it is an important reaction step in melanin synthesis and metabolism of silkworm that tyrosine hydroxylase catalyse tyrosine into dopa. 4.

通过眠蚕离体培养体壁组织的黑色素合成抑制试验观察到的体壁外观性状变化，证明了酪氨酸羟化酶催化酪氨酸转化成多巴是家蚕黑色素合成代谢途径上的重要反应步骤。

Objective To explore new mutation in phenylalanine hydroxylase ( PAH) gene.

目的检测中国苯丙酮尿症（phenylketonuria，PKU）患者苯丙氨酸羟化酶（Phenylalanine hydroxylase，PAH）基因新的突变位点。

Expression of tyrosine hydroxylase and dopamine beta hydroxylase in lumbar sympathetic ganglia neurons in patients with Buerger disease of lower limb

下肢Buerger病患者腰交感神经节神经元TH和DBH的表达

Such graft-derived functional effects by preservation of tyrosine hydroxylase ( TH ) immunoreactivity along the nigrostriatal pathway.

黑质纹状体通路上酪氨酸 羟 化酶免疫活性可随移植衍生物机能效应得以保存.

The present study was undertaken to define whether the effects of capsaicin were induced by activating the catecholaminergic neurons by double immunohistochemical method for Fos and tyrosine hydroxylase ( TH).

在外周压力感受器去神经支配的大鼠上，用Fos蛋白和酪氨酸羟化酶（TH）的双重免疫组化方法，研究辣椒素的效应是否通过激活脑干核团内儿茶酚胺能神经元而诱发。

Effect of Aluminum on Expression of Tyrosine Hydroxylase mRNA in the Rat Nigra

铝对大鼠黑质酪氨酸羟化酶mRNA表达的影响

A polymorphic tetranucleotide short tandem repeat ( STR) sequence in intron 3 of the phenylalanine hydroxylase ( PAH) gene was analysed in 52 normal individuals and 23 Phenylketonuria ( PKU) families by PCR amplification and silver staining.

应用PCR结合银染显色法分析了苯丙氨酸羟化酶基因内含子3中1个四核苷酸（TCTA）重复序列的多态性。

The effect of antibiotics and an inhibitor of hydroxylase on selective Nocardia oxidation of cholesterol

羟化酶抑制剂与抗生素在诺卡菌选择性氧化胆甾醇中的作用

The phenylalanine hydroxylase activities of 23 cirrhotic patients ( 8 compensated and 15 decompensated) and 8 normal adults were measured with a deuterated phenylalanine loading test.

采用~2H-苯丙氨酸（~2H-Phenylalanine）负荷试验，对8例正常人和23例肝硬化病人（8例代偿性，15例失代偿）的苯丙氨酸羟化酶活力进行了测定。

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

【目的】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。

Objective: To study the mutations of phenylalanine hydroxylase ( PAH) gene in phenylketonuria ( PKU) patients.

目的：探讨苯丙酮尿症（PKU）患者PAH基因突变特点。

Follow-Up on Puberty Development and Final Height in 41 Children with Simple Virilizing Form of 21-Hydroxylase Deficiency

单纯男性化型21羟化酶缺乏症患儿41例青春发育与最终身高随访

Interleukin 1 α( IL 1 α) Inhibits the Activity of 17 α hydroxylase/ C 17 20 Lyase Cytochrome P_ ( 450) Enzyme

白细胞介素-1α对睾酮合成酶P（450）17α活性的抑制