受体

The results showed that during oogenesis there was no distribution of the UEA-I receptor.

结果表明，在卵子发生的各期滤泡细胞和卵母细胞中没有UEA-I受体的表达， SBA和PNA受体以不同的分布模式呈阶段性表达。

Severe inflammatory reaction can in- jury the body. Thereflore, retarding synthesis of PAF, increasing catabolism of PAF or blocking the combination of PAF and its re- ceptor might be the appropriate treatment. Hitherto, antagonists of PAF have been studied extensively. More than a hundred of such antagonists have been reported, some of them having even been used in clinic and having presented an optimistical prospects, especially natural antagonists BN series and kadsurenone, which have shown sound effects in both basic and clinical experiments.

因此通过阻止PAF合成，增加PAF分解和阻止PAF与其受体结合发挥生物效应可以作为一种适宜的治疗手段，PAF受体拮抗剂研究已成为热点，天然及人工合成的PAF拮抗剂种类很多，已报道有一百种以上，有些已进入临床应用，具有较好的前景，尤其是天然拮抗剂BN系列（以BN52021为代表）及海风藤酮巳在基础及临床研究中取得了可喜成果。

When the pollen density of pollen donor exceeded the critical density, the gene flow frequency did not increased any longer, and the maximum gene flow frequency detected was equal to the outcrossing rate of pollen receiver in theory.

在其他因素都固定的情况下，如果花粉受体的异交率较高，那么到该花粉受体的基因漂移频率也相对较高。

Excitotoxicity resulting from overstimulation of NMDA-type glutamate receptors may contribute to AD, providing a rationale for blocking these receptors.

对NMDA型谷氨酸受体的过度刺激引起的兴奋性中毒可能与AD也有关系，这是阻断这些受体以治疗AD的原理所在。

Because nicotine is so similar to acetylcholine, and binds to cholinergic receptors, nicotine in excess produces the same overstimulation and toxicity.

绑定到烟碱性的胆碱能受体的尼古丁越多，随后乙酰胆碱就释放的越多，更加自由地激活其他部分的胆碱能受体。

Results Expression levels of the three lectin receptors in the epithelium of palatal shelves in the experimental group were significantly lower than in the control group. But they were not differently significant in the mesenchyma between the test and control groups.

结果 3种凝集素受体在实验组不同发育阶段的小鼠胚胎腭突上皮内的表达量显著低于相应对照组。3种凝集素受体在小鼠胚胎腭板间充质中的表达量在实验组及对照组之间差异无统计学意义。

There is a parallel shift of the dose-response curve of the ligand to left. Present study suggests that there may be an internal molecular/chemistry interaction between quinolones and BPAA, producing a new structure which has a high affinity on the GABAA receptor sites.

本研究直接反映了联苯丁酮酸和BPAA与喹诺酮类药物在体内与GABAA受体的相互作用，其作用机制可能是两种药物发生了化学/分子作用，形成一种与GABAA受体有着极高亲和力的新结构。

We examined the effects and mechanisms of methyl pentyl 1,4-dihydro-2,6-dimethyl-4-(3-notrophenyl)-3,5-pyridinedicarboxylate (Mn9202), a novel DHPs calcium antagonist and lacidipine on the 5-HT2B receptor in cultured rat stomach fundus smooth muscle cells.

本研究以富含5-HT_(2B)受体的大鼠胃底平滑肌细胞为模板，观察了二氢吡啶类钙拮抗剂2，6-二甲基-4-（3-硝基苯基）-1，4-二氢-3，5-吡啶二羧酸-3-甲酯-5-正戊酯（Mn9202）、拉西地平对 5-HT_(2B)受体功能的影响，并对其影响机制进行了较为深入的研究。

According to the present research, this process includes the deactivation of certain suppress cancer genes , like p53, Rb, p16, BRAC1, BRAC2 , PETN and so on. It also includes the abnormal expression of certain acceptor proteins, like estrogen acceptor and so on.

据目前的研究，这一过程包括某些抑癌基因的失活，如p53、Rb、p16、BRAC1、BRAC2和PETN等，也包括某些受体蛋白的异常表达，如雌激素受体等。

The receptor binding experiment agreed to the result of Pettit's experiment, which suggested that Asp〓 and Gln〓were essential to receptor binding.

上述结果表明这二株突变体均保留了与受体结合的活性，这与Pettit等分析Asp〓、Gln〓对受体结合很重要的结论是一致的。

She gently rebuff ed him, but agreed that they could be friends

她婉言拒绝了，但同意作为朋友相处。

If in the penal farm, you were sure to be criticized.

要是在劳改农场，你等着挨绳子吧！