柔红霉素
- Daunorubicin;Daunoblastina
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柔红霉素与DNA作用的序列特异性研究
Studies on the Interaction of Daunomycin and the Specific Sequence of DNA
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紫杉醇对柔红霉素与DNA作用影响的研究
Influence of Paclitaxel on the Interaction between Daunorubicin and DNA
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柔红霉素修饰的纳米金电极的制备及其对DNA检测
Preparation of Daunomycin Modified Nano Gold Electrode and Its Application to Detection of DNA
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用钴离子注入修饰电极研究了柔红霉素与DNA的相互作用。
With Co / GCE as the working electrode , an interaction between daunorubicin and DNA was studied .
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盐酸柔红霉素能嵌入DNA双螺旋中与DNA结合,使其模板发生改变,抑制DNA和RNA聚合酶,阻止DNA和RNA的合成。
It has characters of binding of daunomycin to DNA and the inhibition of RNA and DNA synthesis .
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汉防己甲素联合柔红霉素对K562/A02细胞株P21蛋白和P糖蛋白表达的影响
Effect of Tetrandrine Combined with Daunorubicin on Expressions of P21 and P-gp in K562 / A02 Cells
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柔红霉素联合bax基因转染对兔实验性增生性玻璃体视网膜病变的影响
Combined effects of daunorubicin and bax gene transfection on rabbit proliferative vitreoretinopathy
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乌索酸诱导K562细胞与耐柔红霉素的K562细胞凋亡及其机制的初步研究
Study on Ursolic Acid-Induced Apoptosis in K562 and K562 / DNR Cells
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Caspase-3在柔红霉素诱导的人视网膜色素上皮细胞凋亡中作用
Caspase-3 activity during daunorubicin induced human retinal pigment epithelium cell apoptosis
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转染反义Bcl-2对柔红霉素诱导人视网膜色素上皮细胞凋亡的影响
Effect of transfection with anti-sense Bcl-2 on daunomycin induced apoptosis of human retinal pigment epithelial cells
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建立脂质体中柔红霉素含量测定的可见分光光度法和HPLC方法;
Visible spectrophotometry and the HPLC method were established for determination of the daunorubicin in the long circulating liposomes .
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柔红霉素对K562细胞凋亡的影响
Influence of daunorubicin on apoptosis factor of K562 cells
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小剂量柔红霉素对HL-60细胞增殖分化的影响
Effects of Low-dose Daunorubicin on Proliferation and Differentiation of HL-60 cells
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去甲氧基柔红霉素在一定范围内对HL-60细胞的杀伤作用呈剂量、时间依赖性。
The effect of IDA was dosage and time - dependency .
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柔红霉素体外对HL-60细胞的凋亡作用
The apoptosis effect of daunorubicin on HL-60 cells in vitro
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重组变构人TRAIL联合柔红霉素对白血病细胞诱导凋亡作用及其机制的研究
Combined Effect of Recombinant Mutant Human TRAIL and Daunorubicin in Inducing Apoptosis of Leukemia Cell and Its Mechanism
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银盘电极盐酸柔红霉素电化学行为及其与BSA的相互作用
The Electrochemical Behavior of Daunorubicin Hydrochloride on Galactic Disk Electrode and its Reaction with BSA
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NF-κB与柔红霉素对HL-60细胞凋亡作用关系的探讨
In vitro study on the relationship between nf - κ b and the apoptosis effect of daunorubicin ( dnr ) on HL-60 cells
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蒽环类抗生素柔红霉素(DNR)、表柔比星(EPI)、米托葸醌(MXT)与刚果红(CR)相互作用的反应体系;
Anthracycline antibiotics such as daunomycin , epirubicin , mitoxantrone and congo red systems ;
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柔红霉素作用后G2期细胞由9.9%增加至30.4%;
The percentage of cells in G2 increased from 9.9 % to 30.4 % ;
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铁剥夺对柔红霉素诱导K562细胞多药耐药基因1表达及NFκB活化的影响
Effects of iron-deprivation on the activation of NF κ B and the expression of multidrug resistance gene 1 of K562 cells induced by daunorubicin
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方法采用甲基四唑蓝法(MTT)测定柔红霉素(DNR)的细胞毒性;
Methods The cytotoxicity of daunorubicin ( DNR ) was assayed by MTT method .
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柔红霉素在人敏感和抗三尖杉酯碱的HL-60细胞中分布和积聚变化
Changes of the distribution and accumulation of daunorubicin in the sensitive and harringtonine-resistant HL-60 cells
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另外,以柔红霉素为指示剂,检测DNA电化学探针对目标DNA的识别能力,柔红霉素响应信号明显。
In addition , we use daunomycin as indicator to test the recognition of DNA electrochemical probe on the target DNA . As a result , response signal is significant and satisfactory .
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目的探讨天冬酰胺特异酶切的半胱氨酸蛋白酶(caspase)成员caspase-3在柔红霉素诱导的人视网膜色素上皮(RPE)细胞凋亡中的变化。
AIM To study the function of caspase-3 activity during daunorubicin induced human retinal pigment epithelium cell apoptosis .
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柔红霉素C-14羟化酶基因在E.coli中的克隆、融合表达及酶的纯化
Cloning and Expression of doxA Gene Encoding Daunorubicin C-14 Hydroxylase in E.coli and Its Purification
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结论Caspase-3参与了柔红霉素诱导的人视网膜色素上皮细胞的凋亡,柔红霉素可使其活性增加。
CONCLUSION Caspase-3 is involved in daunorubicin induced human retinal pigment epithelium cell apoptosis , and daunorubicin could raise the activity of caspase-3 .
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去甲氧柔红霉素联合Ara-C治疗难治性白血病
The idarubicin in combination with ara C treatment of refractory leukemia
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结果K562/ADM细胞对阿霉素呈高度耐药性,并与柔红霉素和鬼臼乙叉甙交叉耐药,但与CsA无交叉耐药。
Results K562 / ADM cells were highly resistant to adriamycin , and cross-resistant to daunorubicin and etoposide , but uncross-resistant to CsA .
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诱导治疗主要采用全反式维A酸诱导分化,继以柔红霉素-阿糖胞苷(DA)、三尖杉酯碱-阿糖胞苷(HA)、柏林-法兰克福-慕尼黑(BFM)方案巩固治疗。
The patients were treated with protocol including induction of differentiation with ATRA followed by consolidation therapy with DA , HA or BFM protocol .