dox

TRAIL gene expression before and after combination with DOX was measured by RT-PCR .

通过MTT比色法与流式细胞仪研究分析其对RKO细胞的作用效果，并以RT&PCR检测联合应用阿霉素前后TRAIL基因的表达水平。

RT-PCR exams whether there was any change of the TRAIL gene expression after combination with DOX .

以RT－PCR分析经联合应用阿霉素后，TRAIL基因的表达是否有所增加。

The average drug concentration in K562 / DOX cells was evaluated by flow cytometry .

流式细胞术检测细胞内药物浓度；

Cellular accumulation of Dox was measured by fluorescence spectrophotometry .

荧光分光光度法检测细胞内多柔比星（Dox）的积蓄；

Activity of TRAIL Gene Modification Combined with DOX on Human Colon Cancer Cell Line RKO

TRAIL基因修饰联合阿霉素对大肠癌细胞株RKO作用的研究

DOX niosomes were prepared by film dispersion method .

采用薄膜分散法制备了DOX非离子型表面活性剂囊泡（DOX-N）。

Multidrug resistance was the main mechanism of drug resistance in BGC 823 / DOX .

多药耐药是BGC－823／DOX主要的耐药机理。

The composite indicator of using DOX to characterize the disinfection by-product has been one hot international research issue .

以DOX表征的消毒副产物的综合指标已成为目前国际上研究的热点问题。

BGC 823 / DOX with doxorubicin resistance has many characteristics of gastrointestinal tumors .

作者认为，BGC－823／DOX是比较符合临床消化道肿瘤特点的阿霉素耐药细胞系。

Establishment and characterization of doxorubicin resistant BGC 823 / DOX of human gastric cancer cell line

人胃腺癌阿霉素耐药细胞系BGC-823/DOX建立

Effect of Caveolin-1 on growth and apoptosis of human breast carcinoma cell line Hs578T / Dox

Caveolin-1蛋白对乳腺癌耐药细胞株Hs578T/Dox生长凋亡的影响

To investigate the mechanism of growth inhibition induced by Doxorubicin ( DOX ) in human endometrial carcinoma cells .

为探讨阿霉素（DOX）抑制人子宫内膜癌细胞生长的分子机制。

Classic Logic BF , is one of the most widely applied logic system which however contains para - dox .

经典逻辑BF是应用最广的一种系统，但存在悖理。

DOX magnetization vector at PBS in the stability of red blood cells stored up to 4 days .

磁化DOX载体红细胞在PBS中稳定贮存可达4天。

The virus supernatant was used to infect the BEL 7402 / DOX cell .

经PA317包装后，病毒上清感染BEL－7402／DOX细胞株。

Doxorubicin ( Dox ), an anticancer drug , was used as a model drug for controlled release experiments .

以抗癌药物阿霉素（DOX）为模型药物，研究了嵌段聚合物胶束对DOX的控制释放行为。

The synthetic method , structure . conductivity and reversibility . electrochemical n dox reaction of polyaniline were introduced .

本文介绍了作为锂二次电池阴极材料的聚苯胺的合成方法、结构，导电性和氧化还原可逆性。

Overexpression of S3 ribosomal protein gene is involved in drug resistance in K562 / DOX cells

S3核糖体蛋白基因的过表达与K562/DOX细胞耐药性的关系

The in vitro drug release behavior of anticancer drug DOX in the polymeric micelles was investigated .

以抗癌药DOX作为模型药研究了胶束的载药能力及体外释药行为。

The apoptosis rate of K562 / DOX cells exposed to Artesunate and Doxorubicin was increased .

Zug/m1阿霉素联合3ug/ml青篙玻酷作用K562/D0X细胞48h可以增加K562/DOX细胞的凋亡率。

Effect of cyclosporin A on intracellular accumulation and efflux of drug in K562 / DOX cells

环孢霉素A对K562/DOX细胞药物积聚和外排的影响

Reversal of Drug Sensitivity in Multidrug resistant Human Liver Carcinoma Cells BEL 7402 / DOX by Ribozyme

核酶对肝癌耐药细胞株BEL-7402/DOX耐药性的逆转作用

Objective To study the fluorescence spectrometry method for determining doxorubicin ( Dox ) concentration in nude mice xenograft tissues .

目的建立裸鼠移植瘤组织中阿霉（Dox）素浓度的荧光分光光度法检测方法。

Study of the Schisandra Chinensis Extract for Reversing Adriamycin Resistance Cell Strain K562 / DOX 's Drug Tolerance

五味子提取物逆转阿霉素耐药细胞株K562/DOX耐药性的研究

So micelles which were used for oral chemotherapy could improve the intestinal permeability and increase the oral bioavailability of DOX .

这样阿霉素纳米胶束可显著提高药物的肠渗透性，进而提高阿霉素的口服生物利用度。

In the rat carotid artery injury model , we examined the effects of Dox on neointimal hyperplasia and .

目的：初步探讨瑞舒伐他汀对大鼠颈动脉球囊损伤后新生内膜增生的影响及其作用机制。

The cellular Dox accumulation was markedly increased in the presence of bepridil in MDR cells .

苄丙洛能显著地增加MDR细胞内Dox的积累。

The expression of HSVtk gene was controlled by Tet-On regulation system under the inducement of Dox .

该基因的表达受到Tet－On基因调控系统的调控，由强力霉素调节HSVtk基因表达。

In vitro DOX release profiles from DOX-CSO-SA / DOX micelles showed excellent characteristic of drug controlled release .

体外释放结果表明，DOX-CSO-SA/DOX载药胶团呈现良好的药物缓控释特征。

Reversal effect of haloperidol on doxorubicin resistance and chloride channel inhibition in erythroleukemic cell K562 / Dox

氟哌啶醇在K562/Dox细胞中对P-糖蛋白及氯离子通道的影响