hydroxylase的例句大全

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。

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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。

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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。

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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。

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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

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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。

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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

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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；

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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

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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

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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。

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The essence of chicken can increased the ability of learning and memory of impairment in restraint stress mice, and the effect may be activation of the central serotonergic system through enhanced the level of 5-HT, tryptophan hydroxylase activity, tryptophan hydroxylase-2 mRNA expression to achieve.

鸡精能够提高拘束应激记忆障碍小鼠的学习能力，其作用可能是通过改善中枢5-羟色胺能系统，提高5-HT水平、色氨酸羟化酶活性和色氨酸羟化酶-2mRNA的表达来实现的。

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With the established transformation system, antisense orange β-carotene hydroxylase gene was introduced into kumquat in order to produce high β-carotene fruits.

应用所建立的转基因体系，成功地将甜橙β-胡萝卜素羟化酶反义基因导入金柑，旨在获得积累β-胡萝卜素的金柑新品种。

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Inductivity of aryl hydrocarbon hydroxylase in lymphocytes of patients with lung carcinoma

肺癌患者血淋巴细胞多环芳烃羟化酶的诱导性

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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

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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。

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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

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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

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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

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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。

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