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1)  anti-multidrug resistance
抗多药耐药
2)  anti-MDR-tumour
抗肿瘤多药耐药
3)  multidrug resistance
多药耐药
1.
Function and mechanism of Baihua Sheshecao Injection reversing multidrug resistance of K562/ADM cells;
白花蛇舌草注射液逆转K562/ADM细胞多药耐药的作用和机制
2.
In Vitro study of the effect of cyclosporine A,tetrandrine and their combination on the reversion of multidrug resistance in leukemia cell line;
环孢菌素A、汉防己甲素及两者联合逆转K562/A02细胞的多药耐药
3.
Reversal of multidrug resistance of hepatocellular carcinoma by siRNA/mdr1;
RNA干扰逆转肝细胞癌多药耐药
4)  Multi-drug resistance
多药耐药
1.
The research of CIK cells reverse multi-drug resistance in vitro;
CIK细胞体外逆转多药耐药性的研究
2.
Relation between multi-drug resistance and apoptosis of HepG2/5-Fu;
人肝癌HepG2/5-Fu耐药细胞株多药耐药与凋亡关系的研究
3.
Expression of glutathione S-transferase π and multi-drug resistance associated protein in squamous cell carcinoma tissue;
皮肤鳞状细胞癌组织中谷胱甘肽-S-转移酶和多药耐药相关蛋白的表达
5)  Multidrug-resistance
多药耐药
1.
Expression of N-methylpurine-DNA-glycosylase in lung cancer H446/CDDP multidrug-resistance cell line;
N-甲基化嘌呤-DNA-糖基化酶在肺癌H446多药耐药细胞中的表达
2.
Study on the mechanisms of multidrug-resistance reversed by quercetin in HL-60/ADR;
槲皮素逆转HL-60/ADR多药耐药机制的研究
3.
Methods Myelodysplastic syndrome cell line(MUTZ-1) and a multidrug-resistance(MDR) erythroleukemia cell line(K562/A02) were cultured in medium of RPMI 1640 with 0.
L-1阿霉素的RPM I 1640分别培养MDS细胞株MUTZ-1和多药耐药(MDR)红白血病细胞株K562/A02。
6)  MDR
多药耐药
1.
The Mechanism on Reversion of MDR in Human Carcinoma Line with HCFU-SLNs;
卡莫氟固脂纳米粒对人大肠癌细胞多药耐药的逆转的机制研究
2.
Research on Inhibition of Cell Apoptosis and Multidrug Resistance (MDR);
细胞凋亡抑制与肿瘤多药耐药的研究进展
3.
Study on Effect Reversing MDR of Ligustrazine Liposomes on Human Erythroleukemia cell line K _(562) /ADM;
川芎嗪脂质体对人白血病细胞株K_(562)多药耐药逆转作用的研究
补充资料:节后抗胆碱药
分子式:
CAS号:

性质:又称节后抗胆碱药,M胆碱受体阻断药。代表药是阿托品,能阻断节后胆碱能神经支配效应器上的M胆碱受体,从而对抗乙酰胆碱和拟胆碱药的毒蕈碱样作用,引起平滑肌松弛、腺体分泌抑制、心率加速、瞳孔扩大等。临床应用广泛,主要用于内脏平滑肌绞痛。常见副作用是口干、乏汗、心悸、视力模糊等。青光眼和前列腺肥大者禁用。合成解痉药包括季铵类(如溴丙胺太林)和叔胺类(如贝那替嗪)两大类,主要用于溃疡病。

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