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1200字范文 > Mu阿片受体 Mu opioid receptor英语短句 例句大全

Mu阿片受体 Mu opioid receptor英语短句 例句大全

时间:2023-12-16 08:30:48

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Mu阿片受体 Mu opioid receptor英语短句 例句大全

Mu阿片受体,Mu opioid receptor

1)Mu opioid receptorMu阿片受体

1.Mu opioid receptor is a member of G protein-coupled receptor family.Mu阿片受体属于G蛋白偶联受体,分布在痛觉传导区以及与情绪和行为有关的区域,影响动物的神经反应和行为表现。

英文短句/例句

1.Polymorphism Analysis of MOR Gene in Different Horse;不同品种马Mu阿片受体基因多态性研究

2.Studies on the Expression of Endomorphins and Mu-opioid Receptors on Murine Dendritic Cells and Their Functions内吗啡肽和Mu阿片受体在小鼠树突状细胞的表达及其相关功能的研究

3.Changes of mu Opioid Receptor in Brain Regions of Morphine Dependent Rats;吗啡成瘾大鼠部分脑区mu阿片受体的变化

4.To determine the function of new opioid receptor ligands and onδ opioid receptor.研究新合成的阿片受体配基对δ阿片受体的激动作用。

5.A G Protein-coupled Receptor Heterodimer between Mu-opioid Receptor and Oxytocin Receptor;μ型阿片受体与催产素受体二聚化的研究

6.Effects of κ-Agonists on Dependece of Opioidκ-受体激动剂在阿片依赖中的作用

7.Study of the Coexistence of TrkB Receptor, NMDA Receptor and Opiate μ Receptor in Spinal Cord Following Peripheral Inflammatory Hyperalgesia in Rats;炎性痛大鼠脊髓TrkB受体、NMDA受体、阿片μ受体共存的研究

8.Mechanism Underlying the Cardioprotection of κ-opioid Receptor in Ischemic Preconditioning and Receptor Tolerance in the Rat Cardiomyocytes;κ-阿片受体参与心肌缺血预处理保护作用及阿片受体耐受机制的研究

9.Objective To determine the affinity of new opioid receptor ligands to clonedμ opioid receptors stably expressed in CHO cell.目的研究新合成的阿片受体配基对稳定表达于CHO细胞的μ阿片受体的结合特性。

10.Agmatine-I1 Imidazoline Receptor Mediates the Modulation to Compensatory Adaptation of μ-opioid Receptor by Long-term Treatment of Opioids;胍丁胺-I1咪唑啉受体系统对阿片长期处理导致的μ-阿片受体代偿性适应的调节

11.The Study on Expression of κ-Opioid Receptor in Human Atria of Congestive Heart Failure Cases;心力衰竭患者心房κ-阿片肽受体表达的研究

12.Effects of Electro-acupuncture on Opioid Peptides Receptors in Inflamed Location in Inflammatory-Pain Rats;电针对炎症痛大鼠炎症局部阿片受体的影响

13.Detection of Opioid Receptors on Cells from Immune System;免疫系统来源的细胞中阿片肽受体的检测

14.The anti-hypertension effects of cardiac κopioid rector and its mechanism;心脏κ阿片受体在抗高血压中的作用及其机制

15.κ-Opioid Receptor Stimulation Induced Delayed Cardioprotection;刺激κ-阿片受体诱导的延迟性心肌保护作用

16.Advances in Effects of Opioids and Opioid Receptors on Immune System阿片及其受体对免疫系统影响的研究进展

17.Homology Modeling of Human μ Opioid Receptor and Analysis of its Active Siteμ阿片受体的三维结构预测及活性位点分析

18.Opioid Receptor Mediates the Cardioprotective Effect of Ischemic Postconditioning;阿片受体介导缺血后处理的心肌保护作用及其受体后机制

相关短句/例句

Mu opioid receptor geneMu阿片受体基因

1.This study was designed to investigate the Single Nucleotide Polymorphism (SNP) ofMu opioid receptor gene in various breeds,including duroc,landrace and Yorkshire.该研究以长白猪、大白猪和杜洛克猪为试验材料,用8对引物对Mu阿片受体基因的5′UTR区域、整个编码区和3′UTR区域用PCR SSCP方法进行了扫描,发现5处突变基因座(GenBank登录号:AF521309)。

3)Opiate receptor阿片受体

1.Effect of methionine-enkephalin on proliferationand mechanism involved by opiate receptor of peripheral bloodlymphocyte from patients with systemic lupus erythematosus;甲硫氨酸脑啡肽对系统性红斑狼疮患者外周血淋巴细胞增殖反应的影响及阿片受体介导机制的研究

4)opioid receptor阿片受体

1.The function of C-terminal tail ofopioid receptors and the proteins interaction with C-terminal tail ofopioid receptors;阿片受体C-末端的功能及与其相互作用蛋白的研究进展

2.Role ofopioid receptors in cerebral ischemic tolerance induced by electroacupuncture preconditioning in rats;阿片受体在电针预处理诱导大鼠脑缺血耐受效应中的作用

3.Role ofopioid receptor in nucleus submedius in mediating electroacupuncture analgesia in rats;丘脑中央下核内的阿片受体在介导大鼠电针镇痛中的作用

5)Opioid receptors阿片受体

1.The new development of the research on cloning of the opioid receptors;阿片受体克隆研究新进展

2.Aim: To investigate the effect on myocardial apoptosis and Bcl-2/Bax induced by remote preconditioning(RP) and to discuss the hypothesis from opioid receptors in pigs.目的:确定骨骼肌缺血预适应对猪心肌凋亡及其调控基因Bcl-2/Bax的影响,并探讨阿片受体在此机制中可能的作用。

3.It binds to μ-、δ-and κ-opioid receptors with a high affinity,and this binding is naloxone-displaceable.BAM22神经肽能够与μ、-δ-和κ-阿片受体特异性地结合,具有阿片样生物活性。

6)human opioid receptor-like 1阿片受体样受体

1.Stable expression ofhuman opioid receptor-like 1 in Chinese hamster ovary cells人重组阿片受体样受体在CHO细胞稳定表达系统的建立

延伸阅读

阿片受体分子式:CAS号:性质:为介导阿片类镇痛药及内源性阿片肽作用的受体。药理学实验已证明至少存在着μ、K、δ三种阿片受体,属于G蛋白偶联受体;并认为每种阿片受体仍具有多个亚型。目前已知μ、K、δ受体均可介导镇痛。

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