receptor造句
OBJECTIVE: Progress and clinical application of leukotrienes ( LTs )
receptor antagonists in the treatment of asthma were summarized.
目的: 评价 白三烯 受体拮抗剂在治疗哮喘中的进展和临床应用.
Receptor protein kinase ( RPK ) is an important kinase in protein kinase family.
受体蛋白激酶是蛋白激酶家族中的重要一类.
The liver not only is the
receptor of dietary fat.
肝脏是日粮脂肪的接受者.
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.
Astemizole is H 1 -
receptor antagonist, which is used to treat allergic disorder and allergic rhinitis etc.
阿司咪唑为H1受体拮抗剂, 主要用于荨麻疹、过敏性鼻炎等变态反应性疾病的治疗.
This antibody agonistic effect on the CD 40
receptor.
这种抗体CD40的受体激动施加一对.
Amiodarone also acts as a thyroid hormone
receptor antagonist.
胺碘酮也可作为甲状腺激素受体拮抗剂.
The majority of AMPA
receptor is a GluR 2 - containing heterotetramer in hippocampus.
在海马中大部分AMPA受体是以含 GluR2 的异四聚体的形式存在.
The team estimates that the kakapo has 667 functional olfactory
receptor genes.
据估计鸮鹉有667个起作用的嗅觉感受器.
These may bind to
receptor molecules on the surfaces of cells.
这些可能会在细胞表面和受体分子结合在一起。
a
receptor organ
接收器官
Role of Soluble Tumor Necrosis Factor
Receptor Type I in Alopecia Areata.
可溶性肿瘤坏死因子型受体在斑秃发病中的作用.
They are in key
receptor areas of the brain.
它们位于大脑关键的接收区域。
Objective To synthesize raloxifene hydrochloride, which is a selective estrogen
receptor modulator.
目的合成选择性雌激素受体调节剂盐酸雷洛昔芬.
Conclusion: Burned serum may up - regulate ETB
receptor.
结论: 烧伤血清可上调亚型B内 皮素受体.
AIM : To study the functional α _ 1 - adrenergic
receptor ( α _ 1 - AR ) subtypes in human right gastroepiploic artery ( RGA ).
目的: 研究人右胃网膜动脉 ( RGA ) 中介导收缩的功能性α_ 1- 肾上腺素受体 ( α_1-AR ) 亚型.
Age - related alteration in hepatic acyl - CoA: cholesterol acyltransferase and its relation to LDL
receptor and MAPK.
(与年龄相关的肝酰基辅酶A的改变: 胆固醇酰基转移酶及其与LDL受体和MAPK的关系).
These may bind to
receptor molecules on the surfaces of cells...
这些可能会在细胞表面和受体分子结合在一起。
Definitive determination of the benefit of angiotensin - converting angiotensin -
receptor blockade.
而血管紧张素转化酶抑制剂疗法获益的确切结果则需要像血管紧张素受体拮抗剂一样的确定性临床试验研究.
A noncompetitive antagonist prevents the agonist from producing any effect at a given
receptor site.
非竞争性拮抗剂可阻止激动剂在特定受体部位产生任何效应.