hydroxylase

hydroxylase

美 [ha?'dr?ks?le?s]  英 [ha?'dr?ks?le?s]

  • n.羥化酶;氫氧酶
  • 網絡羥基化酶;羥化脢;羥基酶

英漢解釋

n.
1.
羥化酶
2.
氫氧酶

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作為NE合成抑郁癥密切相關

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

酪氨酸染色標記通過式細胞儀檢測分化多巴神經元比率

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

中腦組織切片進行酪氨酸谷氨酸雙重免疫熒光染色

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變引起常染色體隱性遺傳

Clinical and genetic analysis of tetrahydrobiopterin-responsive phenylalanine hydroxylase deficiency

生物蝶呤反應丙氨缺乏臨床基因研究

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

受體阻滯心肌死后酪氨酸mRNA表達心臟電生理影響

Clinical and gene detection of tetrahydrobiopterin-responsive phenylalanine hydroxylase deficiency

生物蝶呤反應丙氨缺乏臨床基因檢測

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

大鼠紋狀邊緣多巴免疫陽性反應分布

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

-4-基因高征胎盤表達及其臨床意義

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

經典型丙酮尿丙氨基因突變鑒定

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

丙氨基因克隆及其原核表達質粒構建

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

小鼠垂體細胞表達酪氨酸誘導產生多巴細胞毒性作用

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

酪氨酸腎上腺髓質增生大鼠腎上腺組織表達意義

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

綠色熒光蛋白酪氨酸骨髓基質細胞表達

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細胞表達活性檢測

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

丙氨酸基因突變臨床關系

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

經典21-缺乏基因臨床特征

The differentiation of neural stem cells after tyrosine hydroxylase gene transferring

神經干細胞酪氨酸基因分化

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

高血壓亢證酪氨酸基因多態分析

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

不同類型21-缺乏臨床基因對比研究

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

酪氨酸GTP水解-1基因修飾永生成纖維細胞及其表達研究

Distribution of Tyrosine Hydroxylase Positive Cell in Lymphoid Organs

淋巴器官酪氨酸陽性細胞分布研究

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

腎上腺髓質增生大鼠模型基因表達

Prenatal diagnosis of congenital adrenal hyperplasia with 21-hydroxylase deficiency

先天性腎上腺皮質增生癥21-缺陷產前診斷

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

漢族雄激素過多女性篩查經典21-缺乏

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

受體相關因子1表達下調多巴胺細胞酪氨酸神經突起生長影響

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

中國人21-缺乏攜帶者基因臨床特點研究

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

中國漢族雄激素過多女性21-缺陷攜帶基因檢測

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

糖尿病活性影響

cloning and sequence analysis of - carotene hydroxylase gene fro

胡蘿卜素基因克隆序列分析

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

清醒自由活動大鼠酪氨酸活性測定

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

大鼠微粒體苯胺活力影響

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

先天性腎上腺皮質增生癥患者21-基因啟動子區域突變初步研究

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

先天性腎上腺皮質增生21基因突變研究

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

質子抑制劑效果肝藥基因關系

Study on the Purification and Activity of L-proline Hydroxylase

L-脯氨羥基提純活性研究

Combined treatment of female pseudohermaphroditism caused by 21-hydroxylase deficiency

21缺乏女性假兩性畸形治療效果

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

細胞感受缺氧誘導因子-1脯氨酰研究進展

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

尿選擇性抑制劑L-3-(酰基簡捷合成

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

21缺乏患者最終身高影響因素探討