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As a journalist, you can create a free Muck Rack account to customize your profile, list your contact preferences, and upload a portfolio of your best work.Articles
Carbon Dots-Biomembrane Interactions and Their Implications for Cellular Drug Delivery
This is an early access version, the complete PDF, HTML, and XML versions will be available soon.
Inorganics | Free Full-Text | A Tridentate Cu(II) Complex with a 2-(4′-Aminophenyl)benzothiazole Derivative: Crystal Structure and Biological Evaluation for Anticancer Activity
This is an early access version, the complete PDF, HTML, and XML versions will be available soon. Open AccessArticle by Barbara Mavroidi 1,2,*, Marina Sagnou 2,†, Eleftherios Halevas 2,†, George Mitrikas 3, Fotis Kapiris 4, Penelope Bouziotis 4, Antonios G.
Monocarbonyl Curcumin Analogues as Potent Inhibitors against Human Glutathione Transferase P1-1
3. Results and Discussion 3.1. Screening of the Curcuminoids and Curcumin Analogues and Selection of the Most Potent Inhibitors Recombinant hGSTP1-1 was expressed in E. coli BL21 cells and was purified to apparent homogeneity with a 38% yield using affinity chromatography on the GSH–Sepharose column [3,9]. The inhibitory potency of the curcumin analogues () against hGSTP1-1 was assessed at a final concentration of 100 μM, using enzyme activity assays [9].
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