Search alternatives:
μ decrease » _ decrease (Expand Search), _ decreased (Expand Search), _ decreases (Expand Search)
ng decrease » _ decrease (Expand Search), we decrease (Expand Search), gy decreased (Expand Search)
nn decrease » _ decrease (Expand Search), mean decrease (Expand Search), gy decreased (Expand Search)
a decrease » _ decrease (Expand Search), _ decreased (Expand Search), _ decreases (Expand Search)
50 μ » 10 μ (Expand Search), 5 μ (Expand Search)
50 a » 50 _ (Expand Search), 50 c (Expand Search), 5 a (Expand Search)
μ decrease » _ decrease (Expand Search), _ decreased (Expand Search), _ decreases (Expand Search)
ng decrease » _ decrease (Expand Search), we decrease (Expand Search), gy decreased (Expand Search)
nn decrease » _ decrease (Expand Search), mean decrease (Expand Search), gy decreased (Expand Search)
a decrease » _ decrease (Expand Search), _ decreased (Expand Search), _ decreases (Expand Search)
50 μ » 10 μ (Expand Search), 5 μ (Expand Search)
50 a » 50 _ (Expand Search), 50 c (Expand Search), 5 a (Expand Search)
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Intermediate architecture can form despite decreased cell-substrate adhesion.
Published 2024“…Chi-squared test <i>p</i>-value < 0.0001. Scale bar = 50 μm. E and F) Plating cells on a PDMS membrane leads to islands of primarily Disorganized architecture but Intermediate architectures are still found (E). …”
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Synthesis, Biological Evaluation, Structure–Activity Relationship, and Mechanism of Action Studies of Quinoline–Metronidazole Derivatives Against Experimental Visceral Leishmaniasi...
Published 2019“…Among all synthesized derivatives, <b>15b</b> and <b>15i</b> showed significant antileishmanial efficacy against both extracellular promastigote (IC<sub>50</sub> 9.54 and 5.42 μM, respectively) and intracellular amastigote (IC<sub>50</sub> 9.81 and 3.75 μM, respectively) forms of Leishmania donovani with negligible cytotoxicity toward the host (J774 macrophages, Vero cells). …”
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Medium-Ring Keto Bislactams with Antischistosomal Activity
Published 2024“…Aryl substitution with EWG functional groups decreased the chemical stability. These compounds were relatively polar with the measured LogD<sub>7.4</sub> values ranging from <0 to 2.4, had kinetic aqueous solubilities between 40 and >320 μM, and had relatively low cytotoxicities with IC<sub>50s</sub> ranging from 52 to >390 μM. …”
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