2,5- and 2,6-disubstituted benzazole analogues are used as protein kinase inhibitors.
2，5和2，6双取代氮茚类似物被用作蛋白激酶抑制剂。
Overall, the results from oral kinase inhibitors are very exciting, says Robinson.
整体而言，口服激酶抑制剂的结果已经非常令人兴奋了，罗宾逊说。
The scientists successfully identified the small enzyme molecule responsible, a gene called focal adhesion kinase.
科学家成功分离出这种小小的酶分子，基因学上称之为局部粘着激酶。
However, the involvement of tyrosine kinase either directly or through the prostaglandins and nitric oxide synthase in response to inflammation during diabetes is not completely understood.
不过，酪氨酸激酶是直接参与还是通过前列腺素和一氧化氮合酶对糖尿病炎症产生反应的，我们目前还不知道。
HHMI researchers have now learned that this pairing causes a physical change in the shape of the kinase domain.
霍华德·休斯医学研究所的研究人员现已经得知，这种配对导致了激酶结构域形状上的物理变化。
Kinase Buffer can be used to assay protein kinase activity.
激酶缓冲液用来分析蛋白激酶的活性。
The kinetic property of glycerol kinase from debaryomyces sp.
甘油激酶基本动力学性质研究。
Objective To purify and recombine the creatine kinase (CK) isoenzyme.
目的对肌酸激酶(CK)同工酶进行纯化和重组。
Protein kinase assay was used to detect the activity of MKK6 in cells.
使用激酶活性测定法检测细胞内mkk6的激酶活性。
The soft-tissue injury was assessed by measuring serum creatine kinase.
软组织损伤通过检测血清肌酸磷酸激酶评价；
The inhibitor of VEGF receptor tyrosine kinase was introduced in detail.
详细介绍了VEGF受体酪氨酸激酶抑制剂的研究进展。
In the past we relied on creatine kinase or the MB fragment of creatine kinase.
过去我们依靠肌酸激酶或肌酸激酶MB片段进行诊断。
Objective:To search for natural substrates of protein kinase CK2 in pig platelets.
目的：寻找猪血小板中蛋白激酶CK2可能的天然底物。
Objective: to study the expression of mitochondrial creatine kinase in lung cancers.
目的：研究线粒体肌酸激酶在肺癌中的表达及意义。
Objective: to review the progress in the research of tyrosine kinase inhibitors in recent years.
目的：对近年来酪氨酸激酶抑制剂的研究进展作以综述。
The small molecule tyrosine kinase inhibitors may bring hope in the future for patient with EMS.
小分子酪氨酸激酶抑制剂为治疗EMS带来新的希望。
It binds and activates protein kinase c, causing a wide range of effects in cells and tissues (1, 2).
它结合并激活蛋白激酶c，对很多细胞和组织产生影响(1,2)。
Insulin receptor substrate 2 (IRS-2) is one of the major substrates of the insulin receptor kinase (1).
胰岛素受体底物2 (IRS - 2)是胰岛素受体激酶的主要底物之一(1)。
The changes of fluorescence and UV differential spectra are the same as those of rabbit creatine kinase.
而紫外差吸收光谱和荧光光谱的变化与兔肌肌酸激酶的结果相似。
But ERBB3 is a pseudo-kinase; it functions only by binding with other proteins that have kinase activity.
但ERBB3是一种假激酶，它仅通过与其他有激酶活动的蛋白相互作用才能发挥功能。
AIM To explore if nucleoside diphosphate kinase a (NDPK-A) can potentiate the antitumor action of cisplatin.
目的了解核苷二磷酸激酶a亚基(NDPK A)能否提高顺铂的抗癌效果。
Objective:To evaluate the degree of the injuries and necrosis of muscle based on serum creatine kinase values.
目的：根据骨折伴软组织损伤患者的肌酸激酶测定值，判别肌肉损伤及坏死的程度。
ObjectiveTo study the abnormity and clinical value of tyrosine kinase signaling pathway in lung adenocarcinoma.
目的探讨肺腺癌患者酪氨酸激酶传导通路的异常和临床预后的关系。
Objective: to establish a method of detecting insulin receptor tyrosine kinase (IRTK) activity from erythrocytes.
目的：建立红细胞胰岛素受体酪氨酸蛋白激酶(IRTK)的活性测定法。
AIM To analyze the expression and significance of cyclin dependent kinase 4 (CDK4) in chondrosarcoma of the jaws.
目的分析细胞周期素依赖激酶4 (CDK4)在颌骨软骨肉瘤的表达及意义。
Conclusion Genistein and daidzein were two effective inhibitors of recombinant human protein kinase CK2 in vitro.
结论染料木黄酮和大豆甙元是两种有效的重组人CK2全酶的抑制剂。
The extracellular signal-regulated kinase(ERK) is an important member of mitogen-activated protein kinase(MAPK) family.
细胞外信号调节激酶是丝裂原激活蛋白激酶家族的重要成员。
Stimulation of this receptor in vitro results in up-regulation of activated extracellular signal–regulated kinase (ERK).
体外实验中对相应受体进行刺激后导致对细胞外信号调节酶（ERK）的激活有促进作用。
Stimulation of this receptor in vitro results in up-regulation of activated extracellular signal–regulated kinase (ERK).
体外实验中对相应受体进行刺激后导致对细胞外信号调节酶（ERK）的激活有促进作用。
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