您要查找的是不是:
- Vincristine could affect the activity of p38 MAPK in gastric cancer cell SGC7901 and multidrug resistant cell SGC7901/VCR. p38MAPK信号转导途径可能与长春新碱的抗肿瘤活性相关 ,肿瘤细胞内 p38MAPK对长春新碱刺激的反应速度可能与胃癌长春新碱耐药相关
- The chemosensitivity of multidrug resistant cell MCF-7Adr and drug sensitive cell MCF-7WTto doxorubicin,vincristine and colchicine was tested by MTT assay. 用MTT方法测定了多药抗药细胞MCF-7Adr及其敏感细胞MCF-7WT对阿霉素、长春新碱、秋水仙碱的化学敏感性。
- Flow cytometry was used to detect theexpression of HLA-l, HLA-2, B7-l, B7-2 in parent cell lines (COC1 andSKOV3 ) and multidrug resistant cell sublines (COCI/DDP andSKOV3/Adr). 运用流式细胞仪技术检测了各种不同细胞亚株的HLA-1、HLA-2、B7-1、B7-2的表达。 结果:耐药亚株COC1/DDP、SKOV_3/Adr和亲本株COC1、SKOV_3的N-GSLs表达有差异,COC1/DDP、SKOV_3/Adr的CMH表达较COC1、SKOV_3强。
- Objective To investigate the restoration of the subcellular distribution of daunorubicin in the P glycoprotein mediated multidrug resistant cell line K562/ADR by quercetin. 目的研究槲皮素处理前后柔红霉素(DNR)在耐药细胞株K562/ADR亚细胞结构的不同分布。
- Objective: To investigate the inhibitory effect of ampelopsin (AMP) combined with adriamycin (ADR) on growth of human leukemia multidrug resistant cell line K562/ADR. 目的:研究蛇葡萄素与阿霉素合用对人白血病多药耐药细胞株K562/ADR增殖的抑制作用及其机制。
- Objective To explore the reversal effect of cyclosporin A(CsA) in combination with cytokines on multidrug resistant cell line K562/A02. Method The cytotoxicities of daunorubicin(DNR) were assayed by MTT method. 目的探讨环孢菌素A(CsA)联合细胞因子对耐药细胞系K562/A02的逆转作用。 方法以甲基四唑蓝法测定柔红霉素(DNR)的细胞毒性;
- Tetrandrine, neferine and dauricine showed obvious potenitiation of vincristine induced apoptosis in the human mammary MCF 7 multidrug resistant cells. 粉防己碱、甲基莲心碱和蝙蝠葛碱均有明显的增强长春新碱诱导人乳腺癌MCF 7多药耐药细胞的凋亡作用
- Conclusion A multidrug resistance cell line (SPC-A-1/CDDP) from human lung adenocarcinoma is established.It can be used to downstream experiment. 结论本研究建立了稳定的人肺腺癌多药耐药细胞系(SPC-A-1/CDDP),可应用于下游实验。
- AIM and METHODS: Matrine (50mg/L) potentiated the cytotoxicity of daunorubicin (DNR) in human leukemia multidrug resistance cell line K562/A02 by MTT assay. 方法和结果:经MTT法发现苦参碱50mg/L能增加K562/A02对柔红霉素的敏感性,使柔红霉素半数抑制浓度(IC50)由14?92mg/L降至8?29mg/L,部分逆转了K562/A02对柔红霉素耐药性,逆转倍数为1?80倍。
- Reversal Effect of Verapamil on Multidrug Resistant Cell Line HL-60/ADR 异搏定逆转HL-60/ADR细胞株耐药机理的初步探讨
- KBV200 multidrug resistance cell line KBV200细胞株
- THE CHARACTERIZATION IN MULTIDRUG RESISTANT MECHANISMS OF A HUMAN OVARIAN CARCINOMA DRUG RESISTANT CELL LINE COC_1/DDP 人卵巢癌多药耐药细胞系COC_1/DDP的耐药机制探讨
- STUDIES WITH FLOW CYTOMETRY ON THE REGULATION OF PKC AND REVERSAL EFFECTS OF VRP,CsA ON MULTIDRUG RESISTANT CELL LINES 用流式细胞术研究PKC及VRP,CsA对多药抗性细胞的调制与逆转
- Altered subcellular distribution of daunorubicin in the non P-glycoprotein mediated multidrug resistant cell line HL-60/ADR 柔红霉素在HL-60ADR细胞内的异常分布
- Establishment of Multidrug Resistant Cell Line (HepG2/mrp1) Transfected the Mrp1 cDNA into HepG2 and the Study of Reversing MRP1 with Hepatocellular Carcinoma by RNA Interference 单基因转入人肝癌耐药细胞株的建立及RNA干扰靶向MRP1逆转多药耐药的实验研究
- The study of effects on accumulation and efflux of intracellular adrimycine with FFTLG for multidrug resistant cell lines K562/ADR and K562/VCR in vitro 复方藤梨根制剂体外对MDR细胞株K562/ADR和K562/VCR细胞积聚和外排阿霉素(ADR)的影响研究
- Methods We induced human lung adenocarcinoma cell line A549 into multidrug resistant cell line A549/ADM through step-wise selection with adriamycin,establishing a MDR cell model; 方法 采用浓度递增法经阿霉素(ADM)诱导A549细胞系成为MDR细胞系A549/ADM,建立MDR细胞模型;
- EFFECT OF PIC-BE ON THE EXPRESSION OF MDR-1 AND BCL-2 GENES IN A MULTIDRUG RESISTANCE CELL VARIANT K562/ADM PIC-BE对K_(562)/ADM多药耐药细胞mdr-1和bcl-2基因表达的影响
- Obsjective:To observe the reversal effect of Sangen Mixture(SGM) in multidrug resistant(MDR) cell lines K562/ADR and K562/VCR. 目的:研究三根制剂对多药耐药(MDR)细胞株的逆转作用。
- Reversal of adriamycin resistance by matrine in leukemia multidrug resistance cell line K562/ADM 苦参碱逆转人白血病K562/ADM细胞对阿霉素耐药性的研究