1)  MDR1 C3435T
MDR1C3435T
1.
Aim:To investigate the effects of CYP3A5*3 and MDR1 C3435T polymorphism on azithromycin pharmacokinetics in Chinese healthy volunteers.
结论:CYP3A5*3和MDR1C3435T基因多态性是影。
2)  MDR1(C3435T)
MDR1 C3435T
1.
Detection of MDR1(C3435T) polymorphism in the Hans of Chinese;
汉族人MDR1 C3435T基因的多态性
3)  mdr1
mdr1
1.
Meta-analysis of the effect of MDR1 C3435T polymorphism on cyclosporine pharmacokinetics;
MDR1 C3435T基因多态性对环孢素体内代谢影响的荟萃分析
2.
Construction and expression of recombinant retroviral vectors expressing siRNA for MDR1 gene;
MDR1基因RNAi逆转录病毒载体的构建及表达
3.
The effects of resveratrol on apoptosis of K562/AO_2 and its relationship with mdr1 mRNA;
白藜芦醇诱导K562/AO_2凋亡与mdr1基因表达的关系
4)  MDR1
多药耐药基因1
1.
CYP3A5 and MDR1 gene polymorphisms is associated with pharmacokinetic variation of tacrolimus in renal transplant patients;
细胞色素P450 3A5和多药耐药基因1基因多态性在肾移植患者他克莫司血药浓度监测中的应用
5)  MDR1
多药耐药基因
1.
Association of a polymorphism in MDR1 C3435T with response to antiepileptic drug treatment in ethic Han Chinese children with epilepsy;
儿童癫癎对药物反应性与多药耐药基因MDR1C3435T多态性的相关性研究
2.
Resistance of Cord Blood Nucleate Cells Transfected with Adenovirus-MDR1 Gene to Chemotherapeutic Drug;
导入以腺病毒为载体多药耐药基因的脐血有核细胞对化疗药物的耐受性
3.
Effects of genetic polymorphisms of CYP2C19,CYP3A5 and MDR1 on the pharmacokinetics of lansoprazole;
细胞色素P450 2C19、3A5和多药耐药基因多态性对兰索拉唑代谢的影响
6)  MDR1
MDRl
1.
AIM: To explore the feasibility of using vector-based small interfereing RNA(siRNA) to inhibit the expression of MDR1 mRNA and P-glycoprotein and to reverse the multidrug resistance of drug-resistant ovarian cancer cell line.
脂质体介导将MDR1特异性siRNA的表达载体(pSN/mdr1a和pSN/mdr1b)转染耐药细胞,实时定量RT-PCR方法检测MDRl mRNA的表达,流式细胞术检测P-gp的表达,MTT法检测耐药细胞对化疗药的抵抗性。
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。