Characterisation of the Novel Apoptotic and Therapeutic Activities of the Histone Deacetylase Inhibitor Romidepsin (vol 7, pg 1066, 2008)

Newbold A.; Lindmann R. K.; Cluse L. A.; Whitecross K. F.; Dear A. E.; Johnstone R. W.

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Characterisation of the Novel Apoptotic and Therapeutic Activities of the Histone Deacetylase Inhibitor Romidepsin (vol 7, pg 1066, 2008)

机译：组蛋白脱乙酰基酶抑制剂罗米地辛的新型凋亡和治疗活性的表征（第7卷，第1066页，2008年）

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《Molecular cancer therapeutics》 |2014年第6期|共1页
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Newbold A.; Lindmann R. K.; Cluse L. A.; Whitecross K. F.; Dear A. E.; Johnstone R. W.;
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正文语种 eng
中图分类肿瘤学;
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1. 人源化PD-1单抗联合组蛋白去乙酰化酶抑制剂罗米地辛治疗T细胞淋巴瘤的临床前研究 [J] . 温霆宇, 刘鹏癌症（英文版） . 2021,第003期
2. Characterisation of the Novel Apoptotic and Therapeutic Activities of the Histone Deacetylase Inhibitor Romidepsin (vol 7, pg 1066, 2008) [J] . Newbold A., Lindmann R. K., Cluse L. A., Molecular cancer therapeutics . 2014,第6期

机译：组蛋白脱乙酰基酶抑制剂罗米地辛的新型凋亡和治疗活性的表征（第7卷，第1066页，2008年）
3. Romidepsin reduces histone deacetylase activity, induces acetylation of histones, inhibits proliferation, and activates apoptosis in immortalized epithelial endometriotic cells. [J] . Imesch P, Fink D, Fedier A Fertility and Sterility: Official Journal of the American Fertility Society, Pacific Coast Fertility Society, and the Canadian Fertility and Andrology Society . 2010,第7期

机译：罗米地辛降低了组蛋白去乙酰化酶的活性，诱导组蛋白的乙酰化，抑制了增殖，并激活了永生化的上皮子宫内膜异位细胞的凋亡。
4. Romidepsin (FK228) and its analogs directly inhibit phosphatidylinositol 3‐kinase activity and potently induce apoptosis as histone deacetylase/phosphatidylinositol 3‐kinase dual inhibitors [J] . Akifumi Oda, Hideki Shimodaira, Ken Saijo, Cancer science. . 2012,第11期

机译：罗米地辛（FK228）及其类似物作为组蛋白脱乙酰酶/磷脂酰肌醇3激酶双重抑制剂直接抑制磷脂酰肌醇3激酶活性并有效诱导凋亡
5. Synthesis of Histone Deacetylases Inhibitor and Activity in Vitro [C] . Baoping KUANG, Hui ZHANG, Zhihang SHANG International Conference on Information Engineering for Mechanics and Materials . 2015

机译：组合组蛋白脱乙酰酶的合成体外抑制剂和活性
6. P27 as a molecular target for cancer therapeutics: Discovering small molecule inhibitors of p27 proteolysis and structure-activity relationship and mechanistic studies of largazole, a potent inhibitor of histone deacetylase . [D] . Ungermannova, Dana. 2010

机译：P27作为癌症治疗的分子靶标：发现p27蛋白水解和结构活性关系的小分子抑制剂以及组蛋白脱乙酰基酶的有效抑制剂largazole的机理研究。
7. Romidepsin (FK228) and its analogs directly inhibit phosphatidylinositol 3‐kinase activity and potently induce apoptosis as histone deacetylase/phosphatidylinositol 3‐kinase dual inhibitors [O] . Ken Saijo, Tadashi Katoh, Hideki Shimodaira, 2012

机译：ROMIDESIN（FK228）及其类似物直接抑制磷脂酰肌醇3-激酶活性并易于诱导凋亡作为组蛋白脱乙酰酶/磷脂酰肌醇3-激酶双抑制剂
8. Analysis of the apoptotic and therapeutic activities of histone deacetylase inhibitors by using a mouse model of B cell lymphoma [O] . Lindemann R. K., Newbold A., Whitecross K. F., 2007

机译：使用B细胞淋巴瘤小鼠模型分析组蛋白脱乙酰基酶抑制剂的凋亡和治疗活性

Characterisation of the Novel Apoptotic and Therapeutic Activities of the Histone Deacetylase Inhibitor Romidepsin (vol 7, pg 1066, 2008)

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