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101.
Povarova K. B. Bazyleva O. A. Drozdov A. A. Morozov A. E. Arginbaeva E. G. Antonova A. V. 《Metal Science and Heat Treatment》2019,60(9-10):594-601
Metal Science and Heat Treatment - The nature of stability of dendritic microsegregation of rhenium in single crystals of intermetallic (γ′ + γ) alloys based on γ′-Ni3Al... 相似文献
102.
103.
Nikiforova T. E. Kozlov V. A. Sionikhina A. N. 《Protection of Metals and Physical Chemistry of Surfaces》2019,55(5):849-857
Protection of Metals and Physical Chemistry of Surfaces - The results of studying the equilibrium and kinetics of Cu2+ ions’ sorption from aqueous solutions by the initial and modified wool... 相似文献
104.
Drozdov V. A. Pyanova L. G. Lavrenov A. V. Likholobov V. A. Kudrya E. N. Luzyanina L. S. 《Protection of Metals and Physical Chemistry of Surfaces》2019,55(6):1035-1043
Protection of Metals and Physical Chemistry of Surfaces - A method for introducing small amounts of betulin (up to 1 wt %) into a mesoporous carbon material with a preset specific surface area of... 相似文献
105.
Emel’yanov A. S. Rodin A. V. Belova E. V. Vidanov V. L. 《Protection of Metals and Physical Chemistry of Surfaces》2019,55(6):1044-1049
Protection of Metals and Physical Chemistry of Surfaces - The thermal stability of KU-2*8 cation exchanger mixed with 4 and 12 mol/L nitric acids is studied via differential scanning calorimetry... 相似文献
106.
Solovtsova O. V. Shkolin A. V. Men’shchikov I. E. Knyazeva M. K. Fomkin A. A. Tsivadze A. Yu. Aksyutin O. E. Ishkov A. G. Khozina E. V. 《Protection of Metals and Physical Chemistry of Surfaces》2019,55(6):1080-1084
Protection of Metals and Physical Chemistry of Surfaces - In the present work, a method for producing new shaped composite materials by introducing a metal-organic framework structure Cu-BTC110... 相似文献
107.
Spiridonova E. A. Khrylova E. D. Samonin V. V. Podvyaznikov M. L. Yakovleva A. V. Kicha M. A. 《Protection of Metals and Physical Chemistry of Surfaces》2019,55(2):335-340
Protection of Metals and Physical Chemistry of Surfaces - Comparison of methods for modification of active carbon by fullerenes with and without a stabilizer is presented. The possibility of... 相似文献
108.
109.
Stefania Cuzzubbo Benoit Roch Guillaume Darrasse-Jze Benoit Hosten Manon Leclercq Nicolas Vignal Claire Banissi Eric Tartour Antoine F. Carpentier 《International journal of molecular sciences》2022,23(23)
We previously reported that a novel peptide vaccine platform, based on synthetic melanin nanoaggregates, triggers strong cytotoxic immune responses and significantly suppresses tumor growth in mice. However, the mechanisms underlying such an efficacy remained poorly described. Herein, we investigated the role of dendritic cells (DCs) in presenting the antigen embedded in the vaccine formulation, as well as the potential stimulatory effect of melanin upon these cells, in vitro by coculture experiments and ELISA/flow cytometry analysis. The vaccine efficiency was evaluated in FLT3-L−/− mice constitutively deficient in DC1, DC2, and pDCs, in Zbtb46DTR chimera mice deficient in DC1 and DC2, and in LangerinDTR mice deficient in dermal DC1 and Langerhans cells. We concluded that DCs, and especially migratory conventional type 1 dendritic cells, seem crucial for mounting the immune response after melanin-based vaccination. We also assessed the protective effect of L-DOPA melanin on peptides from enzymatic digestion, as well as the biodistribution of melanin–peptide nanoaggregates, after subcutaneous injection using [18F]MEL050 PET imaging in mice. L-DOPA melanin proved to act as an efficient carrier for peptides by fully protecting them from enzymatic degradation. L-DOPA melanin did not display any direct stimulatory effects on dendritic cells in vitro. Using PET imaging, we detected melanin–peptide nanoaggregates up to three weeks after subcutaneous injections within the secondary lymphoid tissues, which could explain the sustained immune response observed (up to 4 months) with this vaccine technology. 相似文献
110.
Vijay H. Masand Sami A. Al-Hussain Mithilesh M. Rathore Sumer D. Thakur Siddhartha Akasapu Abdul Samad Aamal A. Al-Mutairi Magdi E. A. Zaki 《International journal of molecular sciences》2022,23(23)
Aurora kinase B (AKB) is a crucial signaling kinase with an important role in cell division. Therefore, inhibition of AKB is an attractive approach to the treatment of cancer. In the present work, extensive quantitative structure–activity relationships (QSAR) analysis has been performed using a set of 561 structurally diverse aurora kinase B inhibitors. The Organization for Economic Cooperation and Development (OECD) guidelines were used to develop a QSAR model that has high statistical performance (R2tr = 0.815, Q2LMO = 0.808, R2ex = 0.814, CCCex = 0.899). The seven-variable-based newly developed QSAR model has an excellent balance of external predictive ability (Predictive QSAR) and mechanistic interpretation (Mechanistic QSAR). The QSAR analysis successfully identifies not only the visible pharmacophoric features but also the hidden features. The analysis indicates that the lipophilic and polar groups—especially the H-bond capable groups—must be present at a specific distance from each other. Moreover, the ring nitrogen and ring carbon atoms play important roles in determining the inhibitory activity for AKB. The analysis effectively captures reported as well as unreported pharmacophoric features. The results of the present analysis are also supported by the reported crystal structures of inhibitors bound to AKB. 相似文献