hydroxylase信息详情
n.[生化]羟化酶
beryllium hydroxide───氢氧化铍
hydroxide acid───氢氧化物酸
hydroid diving helmet───潜水头盔
strontia springs hydro───斯通提亚水泉
anhydrous ether───n.无水乙醚
hydrothermal vent───深海热泉;深海热液喷口
hydroid build───水状建造
hydroxide formula───氢氧化物配方
diffusible hydrogen───扩散氢
oxyhydrogen lamp───氢氧灯
Dextromethorphan metabolic phenotyping provides a new information for debrisoquine 4-hydroxylase (CYP2D6) polymorphism in native Chinese.───右美沙芬的代谢表型研究为中国本地人的异丁喹4-羟化酶(CYP2D6)多态性提供了新的信息。
Objective To investigate the genotype in Chinese patients with nonclassical 21 hydroxylase deficiency (NC 21OHD).───目的对中国人非经典型21 羟化酶缺乏症(21 OHD)基因型进行研究。
Aniline hydroxylase was also high in the 9th week.───苯胺羟化酶在第9周也有升高。
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。
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。
Double fluorescence immunostain of tyrosine hydroxylase (TH) and glutamate (Glu) was used in midbrain sections of rat.───在大鼠中脑组织切片上进行酪氨酸羟化酶和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.───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。
Clinical and genetic analysis of tetrahydrobiopterin-responsive phenylalanine hydroxylase deficiency───四氢生物蝶呤反应性苯丙氨酸羟化酶缺乏症的临床与基因研究
Effects of beta-blocker on Expression of Tyrosine Hydroxylase mRNA and Electrophysiological Study in a Rabbit Myocardial Infarction Model───受体阻滞剂对兔心肌梗死后酪氨酸羟化酶mRNA表达及心脏电生理的影响
- jane moore
- hereisyourpresent
- language used in real life
- get a ticket for speed
- blood sampling
- anthraco-silicosis
- liver tonic
- liver transplantation
- fill it
- liver structure
- induced flow
- induced fit model
- horizontal gust
- blood sampling room
- induced flux
- illegal condemnation
- horizontal hair
- hydroxylate
- keepinrun
- goldball machine
- liverdetox