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Protocollagen lysyl hydroxylase deficiency 前胶原赖氨酸羟化酶缺乏
lysyl hydroxylase 赖氨酸羟化酶; 原胶原-赖氨酸; 2-酮戊二酸5-双(加)氧酶
The invention also relates to tyrosine hydroxylase revulsant. 本发明化合物是酪氨酸羟化酶诱导剂。
OBJECTIVE To study the expression of lysyl oxidase gene (LOX) in atherosclerotic artery. 摘要[目的]观察赖氨酰氧化酶基因(LOX)在动脉粥样硬化血管壁中的表达情况。
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。
Exercise also decreased striatal DA transporter and tyrosine hydroxylase immunoreactiity 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。
Tyrosine hydroxylase (TH), the limited enzyme in the synthesis process of NE, has much to do with depressive disorder. 酪氨酸羟化酶(TH)作为NE合成的限速酶，与抑郁症密切相关。
Phenylketonuria(PKU) is one kinds of autusomal recessive disease caused by phenylalanine hydroxylase(PAH) gene mutation. 苯丙酮尿症是由于苯丙氨酸羟化酶基因突变引起的常染色体隐性遗传病。
After labeled by tyrosine hydroxylase, the differentiated dopaminergic neuron proportion was detected by a flow cytometer. 酪氨酸羟化酶染色标记后通过流式细胞仪检测分化的多巴胺能神经元比率。
Objective: To study the relationship between the expression of tyrosine hydroxylase (TH) in adrenals and adrenal medulla hyperplasia (AMH) in rats. 目的 :探讨酪氨酸羟化酶 (TH)蛋白在肾上腺髓质增生 (AMH)大鼠肾上腺组织中的表达与肾上腺髓质增生的关系。
Abstract: Phenylketonria (PKU ) is one kind of autosomal recessive disease caused by phenylalanine hydroxylase(PAH ) gene mutation. 苯丙酮尿症是由于苯丙氨酸羟化酶基因突变引起的常染色体隐性遗传病。
Abstract: Phenylketonuria(PKU) is one kinds of autusomal recessive disease caused by phenylalanine hydroxylase(PAH) gene mutation. 苯丙酮尿症是由于苯丙氨酸羟化酶基因突变引起的常染色体隐性遗传病。
Such graft-derived functional effects were accompanied 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。
A pair of specific primers of gene encoding phenol hydroxylase was designed by oligonucleotide high conservative sequence. 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。
To investigate the effect of Molybdenum on liver microsomal fraction aniline hydroxylase in rats,50 rats were randomly divided into 5 groups. 为研究钼对大鼠肝微粒体中苯胺羟化酶的影响,将50只大鼠随机分为5个组,4个试验组每天分别灌服剂量为8。
Objective To investigate the point mutation features of exon 11 and 12 in phenylalanine hydroxylase(PAH)gene of the patients with phenylketonuria(PKU)in Xinjiang. 目的分析新疆地区苯丙酮尿症(PKU)患者中苯丙氨酸羟化酶(PAH)基因第11、12外显子点突变。
Objective To investigate the point mutation features of exon 11 and 12 in phenylalanine hydroxylase (PAH) gene of the patients with phenylketonuria (PKU) in Xinjiang. 摘要目的分析新疆地区苯丙酮尿症(PKU)患者中苯丙氨酸羟化酶(PAH)基因第11、12外显子点突变。
Methods: Immunohistochemistry technology and high-pressure liquid chromatography with electrochemical detector (HPLC-EC) were used to evaluated tyrosine hydroxylase (TH) and DA . 方法:采用免疫组化技术和高效液相-电化学法(HPLC-EC)分别对酪氨酸羟化酶(TH)、DA进行了含量测定。
Objective:To study the mutations of the phenylalanine hydroxylase(PAH)gene and enhance the gene diagnosis of classical phenylketonuria(PKU) in Inner Mongolia. 目的:研究内蒙古地区经典型苯丙酮尿症(PKU)苯丙氨酸羟化酶(PAH)基因突变的特点和频率,以提高该地区PKU的基因诊断率。