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- Cytoehrome P450 expoxygenase 细胞色素表氧化酶
- Objective To observe the effect of arachidonic acid cytochrome P450 expoxygenases (CYP450) metabolite, epoxyeicosatrienoic acids (EETs), on the apoptosis of primarily cultured bovine aortic endothelial cells (BAECs) induced by lipopolysaccharide (IPS). 目的研究花生四烯酸经细胞色素P450表氧化酶代谢产物一表氧化二十碳三烯酸 (epoxyeicosatrienoic acids,EETs)对脂多糖(lipopolysaccharide,LPS)诱导的牛主动脉内皮细胞(bovine aortic endothelial cells,BAECs)凋亡的影响。
- Cytoehrome P450 细胞色素P450
- Cytochrome P450 enzyme system shown to activate many carcinogens. 细胞色素P450酶系统可以激活多种癌基因.
- Cytochrome P450 enzyme system shown to actiate many carcinogens. 细胞色素P450酶系统可以激活多种癌基因.
- They also bind tightly to some of the TB P450 enzymes and inactivate them. 氮杂茂可与结核菌内的一些P450酶类紧密结合使其失活。
- They also bind tightly to some of the TB P450 enzymes and inactiate them. 氮杂茂可与结核菌内的一些P450酶类紧密结合使其失活。
- At present, more than 90 genes for cytochromes P450 in plants are cloned. 目前已克隆90多个植物细胞色素P450基因。
- Cytochrome P450 enzymes are very important for metabolism function in body. 细胞色素P450酶是体内代谢转换的重要酶系。
- Sequence analysis of genomes has revealed that P450 is a gene super-family. 生物基因组序列分析表明,它是一个基因超家族。
- Cytochrome P450 monooxygenase which is composed of various kinds of components is an oxidase system widely exists in aerobic organisms. 细胞色素P450单加氧酶系是一种广泛分布于各种需氧生物体内的氧化酶系,由多种成分组成。
- Phenobarbital (PB) and dexamethasone (DEX) are P450 inducers while troleandomycin (TAO) can inhibit P4503A activity. 苯巴比妥(phenobarbital,PB)是P4502B、P4502C和3A的强诱导剂; 而地塞米松(dexamethasone,DEX)和三乙酰竹桃霉素(troleandomycin,TAO)则分别是P4503A的强诱导剂和抑制剂。
- Cytochrome P450 2D6 (CYP2D6) is an important hepatic microsomal enzyme which metabolizes clinical drugs. CYP2D6在临床重要药物代谢中具有重要作用。
- The research progress of expression of plant P450 gene family is discussed in rela... 本文概述了植物P450基因表达调控与环境、发育、组织特异性关系的研究进展。
- An example of a flavoprotein undergoing a one-electron transfer is with the microsomal NADPH-cytochrome P450 reductase. 的一个经历一个单电子转移黄素蛋白的例子是与微粒NADPH -细胞色素P450还原酶。
- Regardless, both ligand-bound states lead to P450 inactiation by actie site occlusion. 不管怎样,这两种配体结合的状态都可以导致P450的活性位点被占据而失活。
- Expression of a wheat cytochrome P450 monooxygenase in yeast and its inhibition by glyphosate. Wen-Sheng Xiang; Xiang-Jing Wang; Tian-Rui Ren(通讯作者) & Xiu-Lian Ju.
- METHODS The ultraviolet spectrophotometric method was used to measure P450 concentration of hepatic microsomes. 方法紫外分光光度法测定大鼠肝微粒体P450含量;
- Proton pump inhibitors were metabolized with the sub-enzyme CYP2C19 of microsomes P450. 质子泵抑制剂奥美拉唑、兰索拉唑和盘托拉唑主要经细胞色素P450(CYP)的异构酶CYP2C19代谢消除。
- Cytochrome P450 3A(CYP3A) is one of the key isoenzymes involved in the metabolism of clinical drugs. 摘要 细胞色素P450 3A(CYP3A)是参与临床药物代谢的主要CYP同工酶之一。
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