• The magnitude and duration of T-cell immune response are critically regulated by the interaction of interleukin-2 (IL-2) and its high-affinity receptor (IL-2R) on the surface of the cell.

    白细胞介素2 (IL - 2)与其高亲和力受体(IL - 2r)的相互作用在调节T细胞免疫反应的强度和持续时间方面起着关键作用。

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  • While receptor affinity determines the amount of opioid needed to occupy a given percentage of receptors, it is the intrinsic activity of the opioid that determines its analgesic efficacy.

    受体亲和力决定了占据一定百分比的受体所需阿片类药物的量,而内在活性决定了阿片类药物的镇痛效果。

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  • Numbers of fasting insulin receptor of high and low affinity in erythrocyte membrane were lower than post-prandial insulin receptor.

    红细胞膜高、低亲和力胰岛素受体数目餐前、餐后自身对照均明显下降。

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  • Its analgesic effects are associated with not only the affinity between itself and its receptors but also the factors influencing the process of reaching its receptor.

    其镇痛效果不仅与其受体的亲和力有关,还与影响其到达受体的过程等因素有关。

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  • Experiments showed that berberine neither affected insulin secretion or release, nor affected the capacity and affinity of insulin receptor of liver membrane.

    实验表明,小檗碱未影响胰岛素的分泌与释放,也未影响肝细胞膜胰岛素受体的数目与亲和力,小檗碱的作用可能为受体后效应。

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  • The binding ability of new peptide ligand GE11 and epidermal growth factor receptor (EGFR) was analyzed by affinity capillary electrophoresis (ACE) method.

    应用亲和毛细管电泳(ace)分析方法,对表皮生长因子受体(EGFR)和新多肽配体GE11之间的结合能力进行分析。

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  • Insulin receptor affinity and insulin binding were lower, too.

    受体与胰岛素的高亲和力及结合率亦明显降低。

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  • In the past, the Affinity Labeling and Site-Directed Mutagenesis are the primary methods to study amine receptor.

    过去主要是通过亲和标记和点突变等实验方法进行研究。

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  • The compounds show a high and selective binding affinity for the histamine H3 receptor, indicating histamine H3 receptor antagonistic, inverse agonistic or agonistic activity.

    这些化合物表现出对组胺h 3受体的高度和选择性亲和力,从而表现出组胺h3受体的拮抗、反激动剂或激动剂活性。

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  • The compounds show a high and selective binding affinity for the histamine H3 receptor, indicating histamine H3 receptor antagonistic, inverse agonistic or agonistic activity.

    这些化合物表现出对组胺h 3受体的高度和选择性亲和力,从而表现出组胺h3受体的拮抗、反激动剂或激动剂活性。

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