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9篇 您的检索式:作者名="Xiukun Lin"
    题名 作者 年代 出处 被引量
1Silencing myostatin gene by RNAi in sheep embryos显示文摘Dayun Tang Huabin Zhu Jianmin Wu Hanzhong Chen Yan Zhang Xueming Zhao Xiaoliang Chen Weihua Du Dong Wang Xiukun Lin 2012Journal of Biotechnology2012,,3:2
2Bromophenols from Marine Algae with Potential Anti-Diabetic Activities显示文摘Marine algae contain various bromophenols with a variety of biological activities,including antimicrobial,anticancer,and anti-diabetic effects.Here,we briefly review the recent progress in researches on the biomaterials from marine algae,emphasizing the relationship between the structure and the potential anti-diabetic applications.Bromophenols from marine algae display their hyperglycemic effects by inhibiting the activities of protein tyrosine phosphatase 1B,α-glucosidase,as well as other mechanisms.LIN Xiukun LIU Ming 2012Journal of Ocean University of China2012,11,4:1
3Silencing myostatin gene by RNAi in sheep embryos显示文摘Dayun Tang Huabin Zhu Jianmin Wu Hanzhong Chen Yan Zhang Xueming Zhao Xiaoliang Chen Weihua Du Dong Wang Xiukun Lin 2012Journal of Biotechnology2012,,3:1
4In vitro studies of polyethyleneimine coated miRNA microspheres as anticancer agents显示文摘RNA 作为一个基因沉默代理人起重要作用,为临床的处理的一个治疗学的代理人,并且在房间的区别,增长,和发展。然而, RNA 是很困难的工作与由于它的敏感和脆弱。在为基因交货 / 沉默使用 RNA 的另一个障碍是它的否定费用,它由房间膜引起它的排斥,它否定地也被控告。我们的最近的学习证明 miR-125b 是在 glioblastoma (GMB ) 的 upregulated 并且由支持房间增长并且禁止 apoptosis 在 GMB 房间起一个 oncogenic 作用。内长的 miR-125b 能被它的 antisense RNA 分子的 transfection 堵住, miR-125b antisense (miR-125b-AS ) 。因此,米尔 -- 125b-AS 能为癌症治疗作为一个基于 RNA 的代理人被开发。然而,不稳定性远这样在在进房间的交货的存储和困难期间限制了基于 RNA 的治疗的使用。在当前的工作,我们为断然控告的 RNA nanospheres (miR-125b-RNS 和 miR-125b-AS-RNS ) 的准备表明一种短、简单的一步舞技术与 bioavailable 聚合物涂, polyethylenimine (PEI ) 。这些 RNA nanospheres 能没有 liposomes 的使用,直接渗透房间。我们的学习证实进 nanospheres 的那变换 miR-125b 和 miR-125b-AS 是为存储 RNA 的一条可行途径。另外,这研究提供证据那 PEI 涂的 RNA nanospheres 有潜力被用作 anticancer 代理人的一个新奇的班。Irena Rytblat Ning Wu Huangli Xu Aharon Gedanken Xiukun Lin 2016Nano Research2016,9,6:1
5Chaotic behavior in fractional-order memristor-based simplest chaotic circuit using fourth degree polynomial显示文摘Lin Teng Herbert H. C. Iu Xingyuan Wang Xiukun Wang 2014Nonlinear Dynamics . 2014 (1-2)2014,,:1
6Chaotic behavior in fractional-order memristor-based simplest chaotic circuit using fourth degree polynomial显示文摘Lin Teng Herbert H. C. Iu Xingyuan Wang Xiukun Wang 2014Nonlinear Dynamics2014,,1:1
7Oleanolic acid induces protective autophagy in cancer cells throughthe JNK and mTOR pathways显示文摘Jia Liu Lanhong Zheng Jiateng Zhong Ning Wu Ge Liu Xiukun Lin 2014Oncology Reports2014,,2:1
8Oleanolic acid potentiates the antitumor activity of 5-fluorouracilin pancreatic cancer cells显示文摘Jianteng Wei Haizhou Liu Ming Liu Ning Wu Jin Zhao Lin Xiao Lijun Han Edward Chu Xiukun Lin 2012Oncology Reports2012,,4:1
9PI3K/Akt/mTOR Signaling as Targets for Developing Anticancer Agents from Marine Organisms显示文摘The PI3K/Akt/mTOR signaling pathway is one of the most frequently dysregulated pathways in cancer.Targeting the PI3K-mediated pathway has been an important strategy for developing novel anticancer agents.In the past decades,more than 40 inhibitors of the PI3K/Akt/mTOR pathway have been developed at different clinical stages.Temsirolimus,everolimus,idelalisib,and copanlisib have been approved for clinical use by the Food and Drug Administration of the United States(FDA).However,the toxic-ity and drug resistance limit their efficiency in the treatment.Novel compounds with greater potency and selectivity,as well as im-proved therapeutic indices with reduced toxicity,are clearly required.Over the past three decades,a lot of bioactive ingredients with anticancer effects by affecting the PI3K-mediated pathways have been found from marine organisms.In the present mini-review,anticancer compounds from marine source that target the PI3K/Akt/mTOR signaling were reviewed.The molecular entities and their modes of action were presented.The marine compounds targeting special factors of the PI3K/Akt/mTOR were highlighted.GUO Mingyue ZUO Ling QIAO Gan LIU Minghua CAO Shousong LIN Xiukun 2021Journal of Ocean University of China2021,20,3:0
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