查询词典 inhibitors

John's wort for four to 12 weeks with either placebo or tri- or tetracyclic antidepressants and selective serotonin reuptake inhibitors.

审稿相比，治疗抑郁症患者与提取物的圣约翰麦汁4至12周与安慰剂或任何三或四环抗抑郁药和羟色胺再摄取抑制剂。

These efforts aimed at the discovery of therapeutically useful inhibitors of antitumor have resulted in many attractive targets.

这些研究导致了许多有吸引力的癌症药物研究靶点。

A number of inhibitors have been studied; however, it is apparent from research results to date that N- thiophosphoric triamide is the most effective compound on non-flooded soils.

开发延缓无处不在的脲酶作用的高活性化合物已经使利用生物抑制剂成为可能。

Background Selectie cyclooxygenase inhibitors may retard the progression of cancer, but they hae enhanced thrombotic potential.

背景选择性环氧化酶抑制剂能够延缓癌症的进展，但是它们也有更强的致血栓作用。

According to Towner the ongoing study known as "DUET-2" is the pivotal test of effectiveness for etravirine which is in a class of drugs called non-nucleoside reverse transcriptase inhibitors.

据城镇居民目前正在研究被称为&二重奏-2&是关键性的考验效能etravirine这是一类药物称为非核苷逆转录酶抑制剂。

Suicide genes can convert the drug into toxical metabolic product, cytokines can enhance the antineoplastic and immunologic responses, angiogenesis inhibitors can inhibit the development of new vessels, and apoptosis related factors can induce the apoptosis of tumor cells.

自杀基因能将药物转化为毒性代谢产物，细胞因子能增强抗肿瘤免疫效应，血管生成抑制因子能抑制血管生成，凋亡相关分子能诱导细胞凋亡，这些基因在前列腺癌的基础和临床研究中均表现出一定的肿瘤生长抑制作用。

Both results indicate that SF-1 is transcriptionally down-regulated by these inhibitors.

表示HDAC 抑制剂是透过SF-1启动子来控制基因转录的表现。

In a pot experiment with spring wheat and buckwheat as test crops and with thiophosphric triamide and dicyandiamide as test inhibitors, the transformation, regulation and residual effect of 〓N-labelled urea were studied.

采用〓N标记的尿素，以N-丁基硫代磷酰三胺和双氰胺为供试抑制剂，春小麦和荞麦分别为供试作物进行尿素N转化的调节及其残效盆栽试验。

In addition, this system can also be used for compound optimization, as well as IC50 testing. Using this system a series of compounds are identified that are effective Trypanosoma inhibitors without toxicity to human cells. Therefore, targeting tbLeuRS may represent a new venue for the development of anti-Trypanosoma drugs.

使用这一系统筛选到了对锥虫有较好抑制作用，但对人类细胞毒性较小的一系列新型化合物，因而锥虫亮氨酰tRNA合成酶很可能成为开发有效抗锥虫药物的新靶标。

METHODS: Collaborative meta-analyses were undertaken of 194 unconfounded randomised trials of adjuvant chemotherapy or hormonal therapy that began by 1995. Many trials involved CMF (cyclophosphamide, methotrexate, fluorouracil), anthracycline-based combinations such as FAC (fluorouracil, doxorubicin, cyclophosphamide) or FEC (fluorouracil, epirubicin, cyclophosphamide), tamoxifen, or ovarian suppression: none involved taxanes, trastuzumab, raloxifene, or modern aromatase inhibitors.

对194个开始于1995年的关于辅助化疗或激素治疗的随机试验进行meta分析，许多试验包含了CMF(环磷酰胺、氨甲喋呤、氟尿嘧啶)，蒽环药物为基础的联合化疗比如FAC(氟尿嘧啶、阿霉素、环磷酰胺)或FEC（氟尿嘧啶、表阿霉素、环磷酰胺）及他莫昔芬或卵巢去势；无一包含紫杉烷类、赫赛汀、雷洛昔芬及芳香化酶抑制剂。

The split between the two groups can hardly be papered over.

这两个团体间的分歧难以掩饰。

This approach not only encourages a greater number of responses, but minimizes the likelihood of stale groupthink.

这种做法不仅鼓励了更多的反应，而且减少跟风的可能性。