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Aromatase inhibiton 芳香化酶抑制剂
Genistein, the tyrosine kinase inhibitors, plays the effect by an inhibiton of tyrosine phosphorlation. Genistein是酪氨酸激酶的非特异性抑制剂，通过抑制酪氨酸的磷酸化而发挥作用。
To see if they could block this growth, the team started with the enzyme aromatase. 为了了解它们能否阻断这种生长，小组开始用芳香酶作研究。
If Dex and RU_(38486) were given together, the inhibiton of DEx on PMNS adhesion was reduced gradually till reversed completely. 若同时给予Dex和RU_(38486),则Dex抑制PMNS粘附的作用逐渐减小,直至完全逆转。
As the third generation of aromatase inhibitor,letrozole has been used widely in the sphere of tumor. 来曲唑作为第3代芳香酶抑制剂,已被广泛应用于肿瘤领域。
Aromatase inhibitors, such as aminoglutethimide and anastrozole, work in a different way to lower estrogen leels. 氨鲁米特和阿那曲唑作为芳香酶抑制剂是通过另一途径来降低雌激素。
Aromatase immunoreactive material was distributed in the cytoplasm with negative nuclei. 芳香化酶免疫活性物质分布在胞质，核为阴性。
The musculoskeletal complaints common to aromatase inhibitors can be addressed with NSAID pain relievers. 芳香酶抑制剂常见的肌和骨骼的主诉能够通过非甾体抗炎药来处理。
Unlike tamoxifen, aromatase inhibitors do not cause menopausal symptoms, but they may increase risk of osteoporosis. 与三苯氧胺不同的是，芳香抑制剂不会引起绝经期症状，但可增加骨质疏松症危险。
CONCLUSION:Aceclofenac exerted marked therapeutic activity against adjuvant-induced arthritis,associated with its inhibiton to inflammatory response and DTH. 结论：醋氯芬酸对大鼠佐剂关节炎具有治疗作用，其作用机制可能与其抗炎作用及对迟发型超敏反应的抑制作用有关。
Objective To improve the synthetic procedure of aromatase inhibitor-anastrozole. 目的改进芳香化酶抑制剂阿那曲唑的合成工艺。
Several large-scale clinical trials about aromatase inhibitors and medical ovarian ablation are ongoing and attract attention widely. 芳香化酶抑制剂及药物去势等多个大型的临床研究还正在进行并备受关注。
The results of ongoing studies "should inform us whether bisphosphonates can be used to preent bone loss due to aromatase inhibitors," he added. 他还补充说，目前研究尚未结束，其最终结果“将会告诉我们二膦酸盐类药物是否能够用于预防芳香酶抑制剂引起的骨盐丢失。”
Objective:To compare the difference between conventional drug abortion protocol and the same protocol combined with aromatase inhibitor. 目的:比较常规药物流产方案配伍芳香化酶抑制剂与常规药物流产方案的差异性。
Aromatase inhibitors are superior to tamoxifen in postmenopausal patients, and preclinical data suggest that zoledronic acid has antitumor properties. 芳香酶抑制剂在绝经后患者中优于他莫昔芬，且临床前数据表明唑来膦酸具有抗肿瘤特性。
Aromatase inhibitors (anastrozole, exemestane, letrozole) block peripheral production of estrogen in postmenopausal women. 芳香酶抑制剂（阿那曲唑、依西美坦、来曲唑）阻断绝经后妇女周围雌激素的产生。
Concern has been raised that phytoestrogens may interfere with selective estrogen receptor modulators and aromatase inhibitors. 植物性雌激素可能和选择性的雌激素受体调节剂及芳香酶抑制剂相互作用，从而引起人们的关注。
The third-gene ration aromatase inhibitors have become one of the first-line therapies of post menopausal breast cancer. 第3代芳香化酶抑制剂已成为绝经后乳腺癌的一线药物选择之一。
The preparation of Flavonoid-N-Meglumine salts, the structures, the solubility, the scavenging effects on free radicals and inhibiton on tyrosinase were primarily studied in this thesis . 本课题主要研究了黄酮化合物葡甲胺盐的制备,结构分析,溶解度实验,清除自由基性能及对酪氨酸酶的抑制作用研究。
This study was designed to induce sex-reversed male phenotype chickens with letrozole, an aromatase inhibitor, and dihydrotesterone. 本论文用来曲唑、二氢睾酮、来曲唑与二氢睾酮联合处理性别分化前的鸡胚胎，观察对鸡性别分化的影响，探索低剂量来曲唑诱导雄性表型性反转鸡的可行性，探讨二氢睾酮及其与低剂量来曲唑联合处理鸡胚诱导雄性表型性反转鸡的效果，为禽类的性别控制提供参考数据。