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本发明化合物是酪氨酸羟化酶诱导剂。The invention also relates to tyrosine hydroxylase revulsant.

苏尼替尼是一种新型的多靶点酪氨酸激酶抑制剂。Sunitinb is a novel multitargeted receptor tyrosine kinase inhibitor.

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蛋白质酪氨酸硝化是一氧化氮依赖的氧化应激的生物标志。Protein tyrosine nitration is a biomarker of NO-dependent oxidative stress.

多项研究表明，酪氨酸还能有效防止疲劳。In a number of studies, tyrosine has also been effective at fighting fatigue.

本抗体可能与其它酪氨酸位点被磷酸化的激活受体发生交叉反应。This antibody may cross-react with other activated receptor tyrosine kinases.

抑制BCR-ABL酪氨酸激酶可有效抑制肿瘤生长。Inhibiting BCR-ABL tyrosine kinases can impede the growing progress of tumors.

是生长受体酪氨酸蛋白激酶抑制剂。Genistein, which is an inhibitor of the growth receptor, tyrosine protein-kinase.

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酪氨酸脱羧酶与发酵食品中酪胺的产生密切相关。Tyrosine decarboxylase is closely related to tyramine production of fermented food.

应用免疫沉淀法检测瘦素受体的酪氨酸磷酸化程度。The tyrosine phosphorylation of leptin receptor was revealed by immunoprecipitation.

厄洛替尼是一种小分子的酪氨酸激酶抑制剂，它能有效地阻断EGFR的作用。Erlotinib is a small molecule tyrosine kinase inhibitor that efficiently blocks EGFR.

本文介绍了第一、二代以及新近开发的BCR-ABL酪氨酸激酶抑制剂。This paper introduces the first, second and some new BCR-ABL tyrosine kinases inhibitors.

NR2B酪氨酸磷酸化通过免疫沉淀和免疫印渍分析。The tyrosine phosphorylation of NR2B was analyzed by immunoprecipitation and immunoblot assay.

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因此，在深入模拟计算过程中，我们重点考虑了酪氨酸磷酸化修饰的作用。Thus, in the following studies, we pay much attention on the role of phosphorylation of tyrosine.

②诱导不同时间的大鼠神经干细胞分化成酪氨酸羟化酶阳性细胞的比值。The percentage of tyrosine hydroxylase positive neurons in differentiated cells derived from NSCs.

鉴定了分子量为130000酪氨酸磷酸化的蛋白质为JAK2，一种非受体型酪氨酸激酶。The tyrosine phosphorylated 130000 protein was identified as JAK2, a non receptor tyrosine kinase.

继发性FLT3-TKD突变与酪氨酸激酶抑制剂治疗失败有关。Secondary FLT3-TKD mutations are associated with treatment failure with tyrosine kinase inhibitors.

用L-酪氨酸作底物，测定了牛磺酸对酪氨酸酶的非竞争性抑制。The noncompetitive inhibition of taurine on tyrosinase was determined with L- Tyrosine as substrate.

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曲妥单抗是一种直接针对HER2酪氨酸激酶受体的单抗。Trastuzumab is a monoclonal antibody that directly targets part of the HER2 tyrosine kinase receptor.

它对裂开诸如酪氨酸这类氨基酸的羧基末端的侧肽链最为有效。It is most efficient in clearing the peptide bonds on the C-terminal side of such amino acids tyrosine.

胰岛素受体自身酪氨酸磷酸化抑制剂一一HNMPA一AM3可以阻断胰岛素的抗凋亡作用。HNMPA-AM3 -the insulin receptor tyrosine kinase inhibitor could block the anti-apoptosis effect of insulin.