Myasthenia gravis is an autoimmune disease mediated by auto-antibodies most often directed against the nicotinic acetylcholine receptor.
重癥肌无力是因自体抗体攻击乙醯胆堿的尼古丁受器所造成的自体免疫疾病。
To investigate the role of cytokines, we blocked cytokine release by using GTS-21, a selective agonist of the 7 nicotinic acetylcholine receptor.
为研究细胞因子的作用,我们使用GTS - 21(烟堿乙酰胆堿受体7的一种选择性激动剂)来阻断细胞因子的释放。
Novel 1, 2, 3-triazole derivatives useful as modulators of nicotinic acetylcholine receptors.
用作烟堿型乙酰胆堿受体的调节剂的新颖的1,2,3 -三唑衍生物。
Blockade of cytokine production by 7 nicotinic acetylcholine receptor agonists is a novel therapeutic option to treat stroke in a proinflammatory context.
通过烟堿乙酰胆堿受体7激动剂阻断细胞因子生成是在炎癥发生前治疗中风的一种新疗法。
Neuronal nicotinic acetylcholine receptors (nAChRs) are widely distributed in the central nervous system, and they participate in complex neuronal signal transduction and regulation in the brain.
神经元烟堿受体广泛地分布于中枢神经系统并参与脑内信号传导系统的调节过程。
Objective:To elucidate the effect of strain on nicotinic acetylcholine receptor (nAChR) mRNA expression in maxillofacial skeletal myocytes.
目的评价张应力作用后面颌肌细胞烟堿样乙酰胆堿受体基因表达变化。
The compounds of the invention are found to be cholinergic ligands at the nicotinic acetylcholine receptors and modulators of the monoamine receptors and transporters.
发现本发明化合物是烟堿样乙酰胆堿受体的胆堿能配体和单胺受体和转运蛋白的调节剂。
Objective to investigate the influence of fluorosis on nicotinic acetylcholine receptors (nAChRs) in protein and gene levels in SH-SY5Y cells and the mechanism of the receptor modification.
目的观察氟中毒对神经细胞中尼古丁受体亚单位蛋白和基因表达水平的影响及氟中毒引起尼古丁受体功能改变的发生机制。