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- Aim To investigate the cytotoxic activity of HDAC inhibitor Trichostatin A (TSA)combined with anticancer drugs targeting DNA on T24 bladder cancer cell line. 目的观察HDAC抑制剂曲古霉素A(TSA)和针对DNA的抗癌药物联用对膀胱癌T24细胞的杀伤作用。
- Keywords leukemia;differentiation;apotosis;AML1;AML1-ETO;HDAC inhibitor;PB;MDK;gene;target gene;promoter/enhancer; 白血病;分化;凋亡;AML1;AML1-ETO;脱乙酰基酶抑制剂;苯丁酸钠;基因;靶基因;MDK;启动子/增强子;
- HDAC inhibitor 组蛋白去乙酰化酶抑制剂
- CL was a potent inhibitor of Ca 2+ ,Mg 2+ ATPase. 马桑内酯是Ca2＋，Mg2＋?ATP酶的强力抑制剂。
- Usually, Clr is binding to C1INH (Cl inhibitor). 补体组分C1r含有两个CUB结构域，一个EGF结构域和一个丝氨酸蛋白酶结构域，是一种丝氨酸蛋白酶原。
- Mouldproof wall paper, join mould inhibitor. 防霉墙纸，加入防霉剂。
- Rat Tissue factor pathway inhibitor,TFPI ... 大鼠组织因子途径抑制物(TFPI)ELISA Kit；
- Rabbit Tissue factor pathway inhibitor，TFPI... 兔组织因子途径抑制物（TFPI）试剂盒；
- Human Tissue factor pathway inhibitor，TFPI ... 人组织因子途径抑制物（TFPI）试剂盒；
- Argatroban is a new direct thrombin inhibitor. 阿加曲班是一种新型的直接凝血酶抑制药。
- Objective:To investigate the influence of trichostatin A(TSA),a histone deacetylase(HDAC) inhibitor,on the growth of human bladder cancer cells and on the expression of related genes,and to explore the mechanism involved. 目的:观察组蛋白去乙酰化酶(HDAC)抑制剂曲古霉素A(TSA)对体外培养膀胱癌细胞生长情况及相关基因表达的影响,并探讨其可能的作用机制。
- Lurgiuses have used undisclosed promoter and corrosion inhibitor. 鲁奈公司采用了未公开的活性剂和防蚀剂。
- Lurgiuses has used undisclosed promoter and corrosion inhibitor. 鲁奈公司采用了未公开的活性剂和防蚀剂。
- Therefore, DOC - 1R gene may be an CDK2 inhibitor specifically. 因此DOC-1R可能为CDK2专一性的CDK抑制因子(CDK inhibitor，CK1)。
- Inhibitor of protein kinase C (PKC). Aglycone of staurosporine. PKC抑制剂。星胞菌素的糖苷配基。
- The link between tumorigenic processes and misregulated or mistargeted HAT and HDAC activities has been reported. HAT和HDAC的异常与肿瘤发生有密切的关系。
- Cystatin C is the most abundant protease inhibitor in the plasma. 在血清中Cystatin C是最丰富的蛋白酶抑制剂。
- Highly active inhibitor of fibrinolysin and chymotrypsin. 溶纤维蛋白酶和胰凝乳蛋白酶的高活性抑制剂。
- Foam inhibitor additives are either silicones or polyacrylates. 泡沫抑制剂添加剂都是有机硅或聚丙烯酸酯。
- Irinotecan is the specific inhibitor of topoismerase I. 伊立替康是拓扑异构酶I的特异性抑制剂。
