hydroxylase

hydroxylase

美 [haɪ'drɒksɪleɪs]  英 [haɪ'drɒksɪleɪs]

  • n.羟化酶;氢氧酶
  • 网络羟基化酶;羟化脢;羟基酶

英汉解释

n.
1.
羟化酶
2.
氢氧酶

例句

Tyrosine hydroxylase (TH), the limited enzyme in the synthesis process of NE, has much to do with depressive disorder.

酪氨酸TH作为NE合成抑郁症密切相关

After labeled by tyrosine hydroxylase, the differentiated dopaminergic neuron proportion was detected by a flow cytometer .

酪氨酸染色标记通过式细胞仪检测分化多巴神经元比率

Double fluorescence immunostain of tyrosine hydroxylase (TH) and glutamate (Glu) was used in midbrain sections of rat.

中脑组织切片进行酪氨酸谷氨酸双重免疫荧光染色

Phenylketonuria (PKU) is one kinds of autosomal recessive disease caused by phenylalanine hydroxylase(PAH) gene mutation.

丙酮尿由于丙氨酸基因突变引起常染色体隐性遗传

Clinical and genetic analysis of tetrahydrobiopterin-responsive phenylalanine hydroxylase deficiency

生物蝶呤反应丙氨缺乏临床基因研究

Effects of beta-blocker on Expression of Tyrosine Hydroxylase mRNA and Electrophysiological Study in a Rabbit Myocardial Infarction Model

受体阻滞心肌死后酪氨酸mRNA表达心脏电生理影响

Clinical and gene detection of tetrahydrobiopterin-responsive phenylalanine hydroxylase deficiency

生物蝶呤反应丙氨缺乏临床基因检测

Distribution of the positive immunoreactive products of the dopamine and tyrosine hydroxylase in the marginal division of the rat striatum

大鼠纹状边缘多巴免疫阳性反应分布

Expression of prolyl-4-hydroxylase gene in placenta of patients with pregnancy induced hypertension and its clinical significance

-4-基因高征胎盘表达及其临床意义

Identification of novel mutations in the phenylalanine hydroxylase gene of classical phenylketonuria

经典型丙酮尿丙氨基因突变鉴定

Cloning of Human Phenylalanine Hydroxylase Gene and Construction of Prokaryotic Expression Plasmid

丙氨基因克隆及其原核表达质粒构建

Expression of endogenous dopamine toxicity induced by human tyrosine hydroxylase in mouse pituitary tumor cells

小鼠垂体细胞表达酪氨酸诱导产生多巴细胞毒性作用

Expression and Significance of Tyrosine Hydroxylase in Adrenals of Adrenal Medulla Hyperplasia Rats

酪氨酸肾上腺髓质增生大鼠肾上腺组织表达意义

Expression of enhanced green fluorescent protein and tyrosine hydroxylase genes in bone marrow stromal cells

绿色荧光蛋白酪氨酸骨髓基质细胞表达

Expression and assessment of double genes of tyrosine hydroxylase gene and aromatic L-amino acid decarboxylase gene in vitro

酪氨酸芳香氨基酸羧酶基因细胞表达活性检测

The correlation of genotypes and phenotypes for two novel mutations in phenylalanine hydroxylase gene

丙氨酸基因突变临床关系

Genotype and clinical characteristics of Chinese patients with nonclassical steroid 21-hydroxylase deficiency

经典21-缺乏基因临床特征

The differentiation of neural stem cells after tyrosine hydroxylase gene transferring

神经干细胞酪氨酸基因分化

A Study on the Tyrosine Hydroxylase Gene Polymorphism in Hypertension with the Hyperactive Liver-yang

高血压亢证酪氨酸基因多态分析

Comparison of phenotype and genotype distribution among three types of Chinese patients with 21 - hydroxylase deficiency

不同类型21-缺乏临床基因对比研究

Expression of immortalized fibroblasts genetically modified by tyrosine hydroxylase gene and GTP cyclohydrolase-1 gene

酪氨酸GTP水解-1基因修饰永生成纤维细胞及其表达研究

Distribution of Tyrosine Hydroxylase Positive Cell in Lymphoid Organs

淋巴器官酪氨酸阳性细胞分布研究

Expression of Tyrosine Hydroxylase Gene in the Adrenal of Adrenal Medulla Hyperplasia Rat

肾上腺髓质增生大鼠模型基因表达

Prenatal diagnosis of congenital adrenal hyperplasia with 21-hydroxylase deficiency

先天性肾上腺皮质增生症21-缺陷产前诊断

Screening nonclassical 21-hydroxylase deficiency in androgen excess women of Chinese Han nationality

汉族雄激素过多女性筛查经典21-缺乏

Effects of Nurr1 down-regulation on the expression of tyrosine hydroxylase and neurite extension in dopaminergic cells

受体相关因子1表达下调多巴胺细胞酪氨酸神经突起生长影响

Study on characteristics of phenotype and genotype of Chinese carriers of steroid 21-hydroxylase deficiency

中国人21-缺乏携带者基因临床特点研究

Screening 21-hydroxylase deficiency carriers in androgen excess women of Chinese Han nationality

中国汉族雄激素过多女性21-缺陷携带基因检测

Effect of peroxovanadate-nicotinic acid on phenylalanine hydroxylase activity in diabetic rats

糖尿病活性影响

cloning and sequence analysis of - carotene hydroxylase gene fro

胡萝卜素基因克隆序列分析

The Measurement of Tyrosine Hydroxylase Activity in the Brain of Conscious Rats

清醒自由活动大鼠酪氨酸活性测定

Effect of Molybdenum on Aniline Hydroxylase of Liver Microsomal Fraction in Rats

大鼠微粒体苯胺活力影响

Mutations in the promoter region of 21-hydroxylase gene of patients with congenital adrenal hyperplasia

先天性肾上腺皮质增生症患者21-基因启动子区域突变初步研究

Study on Gene Mutation of 21-hydroxylase Deficiency in Congenital Adrenal Hyperplasia

先天性肾上腺皮质增生21基因突变研究

The effect of proton pump inhibitor on intragastric acidity and it relation to S-mephenytoin hydroxylase genetic polymorphism

质子抑制剂效果肝药基因关系

Study on the Purification and Activity of L-proline Hydroxylase

L-脯氨羟基提纯活性研究

Combined treatment of female pseudohermaphroditism caused by 21-hydroxylase deficiency

21缺乏女性假两性畸形治疗效果

Current progress on cellular oxygen sensors: the family of hypoxia inducible factor-1 prolyl hydroxylase

细胞感受缺氧诱导因子-1脯氨酰研究进展

A Concise Synthesis of L-3-(o-Methoxybenzoyl)alanine, a Selective Kynurenine Hydroxylase Inhibitor

尿选择性抑制剂L-3-(酰基简捷合成

A discuss on risk factors of final height in 21-hydroxylase deficiency patients

21缺乏患者最终身高影响因素探讨