张成梅高级实验师
暂无内容
- [1] 徐国鹏. Electron Lock Manipulates the Catalytic Selectivity of Nanozyme. ACS nano, 18, 3814-3825, 2024.
- [2] 王纯真. Donkey-Hide Gelatin-Derived Carbon Dots Activate Erythropoiesis and Eliminate Oxidative Stress for Aplastic Anemia Treatment. ACS nano, 2025.
- [3] Yan, Ning. Design, synthesis and biological evaluation of thieno[3,2-c]pyrazol-urea derivatives as potent glycogen synthase kinase 3β inhibitors based on the DFG-out conformation. Biorganic & Medicinal Chemistry Letter, 112, 2024.
- [4] 田文坦. 在生物医药创新升级背景下模式动物研究中心的发展. 医学动物防制, 2024.
- [5] 田文坦. 在生物医药创新升级背景下模式动物研究中心的发展. 医学动物防制, 40, 2024.
- [6] 张成梅. 吲哚布芬对血小板聚集及血栓形成的影响. 山东大学学报（医学版）., 48, 2006.
- [7] 张成梅. 泛酸钠 对 Ｂ ｅ ａ ｇｌ ｅ 犬 心 血 管指标 的 影 响. 实验动物与比较医学, 37, 2017.
- [8] 刘莲莲. 浅析高校动物尸体规范化管理及生物安全管控. 前沿科学, 422, 2023.
- [9] 耿旭东. Confined cascade metabolic reprogramming nanoreactor for targeted alcohol detoxification and alcoholic liver injury management. ACS nano, 17, 7443, 2023.
- [10] 饶雨晴. Coupling doping and localized surface plasmon resonance toward acidic pH-preferential catalase-like nanozyme for oxygen-dominated synergistic cancer therapy. Chemical Engineering Journal, 465, 142961, 2023.
- [11] 杜炫呈. Decoy nanozymes enable multitarget blockade of proinflammatory cascades for the treatment of multi-drug-resistant bacterial sepsis. Research, 2022, 9767643, 2022.
- [12] Du, Xuancheng. pH-switchable nanozyme cascade catalysis: a strategy for spatial–temporal modulation of pathological wound microenvironment to rescue stalled healing in diabetic ulcer. JOURNAL OF NANOBIOTECHNOLOGY, 20, 12, 2022.
- [13] 刘兆鹏. A branched small molecule-drug conjugate nanomedicine strategy for the targeted HCC chemotherapy. EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 228, 104037, 2022.
- [14] 杜炫呈. pH-switchable nanozyme cascade catalysis: a strategy for spatial-temporal modulation of pathological wound microenvironment to rescue stalled healing in diabetic ulcer. Journal of Nanobiotechnology, 20, 12, 2022.
- [15] 崔英杰. SAR Investigation and Discovery of Water-Soluble 1-Methyl-1,4-dihydroindeno[1,2-c]pyrazoles as Potent Tubulin Polymerization Inhibitors. 《Journal of Medicinal Chemistry》, 63, 14840, 2020.
- [16] 崔英杰. SAR Investigation and Discovery of Water-Soluble 1-Methyl-1,4-dihydroindeno[1,2-c]pyrazoles as Potent Tubulin Polymerization Inhibitors. Journal of Medicinal Chemistry, 63, 14840, 2020.
- [17] 吴敬德. Tubulin colchicine site binding agent LL01 displays potent antitumor efficiency both in vitro and in vivo with suitable drug-like properties. Investigational New Drugs, 38, 29, 2020.
- [18] 崔英杰. The discovery of novel indazole derivatives as tubulin colchicine site binding agents that displayed potent antitumor activity both in vitro and in vivo. EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 187, 111968, 2020.
- [19] 刘莲莲. 高校动物房屏障系统高效管理初探. 医学动物防制, 2020.
- [20] Wu, Chun. A transformable gold nanocluster aggregate-based synergistic strategy for potentiated radiation/gene cancer therapy. Journal of Materials Chemistry B, 9, 2314, 2021.