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- immunoreactive prolyl hydroxylase protein 免疫反应性脯氨酰羟化酶蛋白
- Keywords Prolyl hydroxylase;Hypoxia-inducible factor;Immunohistochemistry; 脯氨酸羟化酶;缺氧诱导因子;免疫组织化学;
- Keywords hypoxia-inducible factor;aryl hydrocarbon receptor nuclear translocator;variant;prolyl hydroxylase domain; 乏氧诱导因子;芳烃受体核转位蛋白;变体;辅氨酰羟化酶;
- prolyl hydroxylase 脯氨酰羟化酶
- The invention also relates to tyrosine hydroxylase revulsant. 本发明化合物是酪氨酸羟化酶诱导剂。
- 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。
- In addition to Beijing roast duck States prolyl these products, there are more characteristics of it? 摘要: 除了烤鸭国脯这些北京特产，有没有更有特色的呢？
- 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。
- Exposure of prolyl endopeptidases to bile acids made them more susceptible to pancreatic proteases under simulated intestinal conditions. 在模拟肠内环境中，胆汁酸存在时可以使脯氨酰(基)内肽酶更已被胰蛋白酶分解。
- Day "for the soldier's pay cut of chicken, cattle and sheep cooking dishes and more miscellaneous prolyl cut out cleaning very fine. 每天“割鸡为饷，肴多烹牛羊杂割脯而出，甚精洁。”
- However, research on bacterial digestive enzymes identified a prolyl endopeptidase that can break the chain into innocuous components. 但是，对名为脯氨基(月太)内切脢的细菌性消化脢进行研究发现，其能将(月太)链分解成无毒成分。
- 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。
