1)  MDR1 gene
多药耐药基因MDR1
2)  multidrug resistance gene (MDR1)
多药耐药基因(MDR1)
3)  multidrug resistance gene1/P-glycoprotein(MDR1/ P-gp)
多药耐药基因MDR1(P-gp)
4)  multiple
多药
1.
Chemoprotective role of multiple drug resistance gene over expression in human bone marrow CD34~+ cells;
多药耐药基因在人骨髓CD34~+细胞中的表达及对化疗药物的耐受性
2.
Relationship between expression of pS2, ER, PR, c-erbB-2 and multiple drug resistance in breast cancer;
乳腺浸润性导管癌pS2基因、ER、PR、c-erbB-2与多药耐药基因表达及临床指标的相关性
3.
Objective: To evaluate the feasibility of gene therapy using Zinc ribbon domaincontaining 1 (ZNRD1) as target for multiple drug resistance of leukemia.
目的:探讨转录相关锌带蛋白基因(zincribbondomaincontaining1protein,ZNRD1)作为靶分子进行白血病多药耐药基因治疗的可行性。
5)  Multidrug
多药
1.
Reversal of multidrug resistance of K562/A02 cell line by mdr1 and GSTπ gene silence;
mdr1和GSTπ基因缄默逆转K562/A02细胞多药耐药性的研究
2.
Progress in the study for mechanisms of multidrug resistance in breast cancer;
乳腺癌多药耐药机制研究进展
3.
OBJECTIVE: To evaluate the relationship between the clinical stages of nasopharyngeal carcinoma (NPC) and the expression of multidrug resistance-associated protein (MRP).
目的:探讨多药耐药相关蛋白(mul-tidrugresistance-associatedprotein,MRP)在鼻咽癌中的表达及与临床分期的关系。
6)  multidrug resistance
多药耐药
1.
Function and mechanism of Baihua Sheshecao Injection reversing multidrug resistance of K562/ADM cells;
白花蛇舌草注射液逆转K562/ADM细胞多药耐药的作用和机制
2.
In Vitro study of the effect of cyclosporine A,tetrandrine and their combination on the reversion of multidrug resistance in leukemia cell line;
环孢菌素A、汉防己甲素及两者联合逆转K562/A02细胞的多药耐药
3.
Reversal of multidrug resistance of hepatocellular carcinoma by siRNA/mdr1;
RNA干扰逆转肝细胞癌多药耐药
参考词条
补充资料:安眠药、镇静药


安眠药、镇静药
HyPnoties,Sedatives

an而anyao、Zhenjingyao安眠药、镇静药Hypnotics,SedativeS蔡月刚上海医药工业研究院L概述··············……2.主要的安眠、镇静药2.1.醇类·········.··..……2.2.环状酞胺类·····……2.3.酸脉类···········……2.4.氨基甲酸醋类·”一2.5.苯二氮草类····……2.6.吩唯嗦类·······································……312.7.乙醇胺类·······································……312.8.二苯甲烷类······················,····……,··……312.9.叱咯酮类·······································……312.10.巴比妥类·······································……31参考文献················································……咒墓本参考文献··········································……33q八成J gJ广n占亡户nt了0‘2,﹄Q乙2,︺21.概述 安眠药又称催眠药,是一类对中枢神经系统产生抑制作用的药物,在应用适当剂量时,这种抑制作用能导致睡眠(见神经调节荆)。在较小剂量时可使紧张、焦虑和兴奋不安的患者安静下来,有思睡状态,但又不致入睡,这时就称为镇静药。大剂量的安眠药还可产生麻醉。实际上安眠药和镇静药并无明显的界限,而只有量的差别。有些类别的安眠药如使用特大剂量时还可引起昏迷和可能死亡。 失眠是一种不能得到良好睡眠的生理现象,表现为入睡困难、早醒、夜不成寐,即使暂时入睡,但醒后常感头晕脑胀、腰酸背痛,并无正常睡眠醒后的清新之感等等,总之,失眠患者常不能从睡眠中完全消除疲劳。失眠常与下列原因有关;如焦虑、心理障碍、精神上的打击、噪声(见噪声)和工作过度等等。长期失眠可造成中枢神经细胞功能失调,适当应用安眠药是必要的。 理想的安眠药应能使病人安然入睡,而在醒后不遗留任何不适感,并有正常工作的能力。一般患有失眠症的人,服用安眠药后即能获得类似生理性的睡眠,但多数醒后有精神萎靡不振等不良反应。如由于某些躯体疾病,如关节炎、神经痛和心绞痛等引起的失眠,则需首先进行病因性治疗口长期应用安眠药可产生依赖性和成瘾性。 目前对于睡眠发生的机理尚不清楚,但经过多年的努力,已经深入了一步。
说明:补充资料仅用于学习参考,请勿用于其它任何用途。