1) Aniline hydroxylase
苯胺羟化酶
1.
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。
2) hydroxylamine oxidoreductase
羟胺氧化酶
1.
A probable novel gene coding hydroxylamine oxidoreductase (HAO) was acquired by PCR and gene sequencing in Acinetobactor sp.
YY-5的一种羟胺氧化酶(Hydroxylamine oxidored uctase,HAO)编码基因序列并进行生物信息学分析。
3) phenol hydroxylase
苯酚羟化酶
1.
Cloning and sequencing of phenol hydroxylase gene from Acinetobacter junii GXP04;
琼氏不动杆菌GXP04的苯酚羟化酶基因的克隆及序列分析
2.
PCR and electrophoresis analysis detected a typical band of DNA fragment of phenol hydroxylase.
利用PCR方法和琼脂糖凝胶电泳技术检测到 phen8菌中苯酚羟化酶基因片段的特异性条带 ,从基因水平上证实了 phen8菌的苯酚降解功能的遗传基础。
4) dopamine-β-hydroxylase
多巴胺β羟化酶
1.
Objective:To investigate the relationship of a G→A variation (G444A) in exon 2 of the dopamine-β-hydroxylase gene (DBH) and tardive dyskinesia (TD) in chronic schizophrenia.
目的:观察广州地区汉族人群中有或无迟发性运动障碍(TD)精神分裂症患者中,多巴胺β羟化酶 基因(dopamineβ hydroxylasegene,DBH)外显子2单核苷酸多态性G444A的分布,并探讨该多态与迟发性运动 障碍发生的关系。
5) Tyrosine hydroxylase
酪胺酸羟化酶
1.
Methods The distribution of VMAT2 and tyrosine hydroxylase (TH) in substantia nigra pars compacta(SNC), ventral tegmental ares(VTA) and locus coeruleus(LC) were examined by immunohistochemical staining and Western blot in human spontaneous abortion embryonic brains of different gestational age.
方法分别收集不同胎龄自然流产的新鲜胎儿脑组织,应用免疫组织化学方法和Western blot观察VMAT2和酪胺酸羟化酶(TH)在胎脑黑质致密部、腹侧被盖部和蓝斑分布的变化。
2.
Objective:To observe the expression of Tyrosine Hydroxylase(TH) of Hypothalamus in post-stroke depression rat model and effects of Yishen Tiaoqi decoction.
目的:观察脑缺血后抑郁模型大鼠下丘脑酪胺酸羟化酶(TH)表达及益肾调气方药的干预作用。
6) dopamine beta hydroxylase
多巴胺β羟化酶
1.
Objective To investigate the correlation between the polymorphism of dopamine beta hydroxylase(DBH) gene and the susceptibility of Shanghai Chinese Han population to Parkinson s disease(PD).
目的 探讨多巴胺β羟化酶 ( dopamine beta hydroxylase,DBH)基因内含子 5 Taq 多态性与帕金森病遗传易感性的关系。
补充资料：20-α羟化酶(22-β羟化酶，20、22断裂酶)缺乏症
20-α羟化酶(22-β羟化酶，20、22断裂酶)缺乏症
病名。先天性肾上腺性异常综合征之一。 指20-α羟化酶、22-β羟化酶、20、2 2断裂酶中任何一种酶的缺乏，均可导致各类皮质激素合成的第一阶段即胆固醇-孕烯醇 酮受阻，胆固醇聚积于肾上腺皮质，雄激素和雌激素产生障碍，男性和女性出生时，均表现 为 女性型外生殖器，出现失盐症状，多发性感染为特征的一种综合征。多于出生后不久因发生 肾上腺皮质功能不全而死亡。详见先天性肾上腺性异常综合征、肾上腺性异常综合征条。
说明：补充资料仅用于学习参考，请勿用于其它任何用途。
参考词条