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10 μ » 10 _ (Expand Search)
mean decrease » a decrease (Expand Search)
nn decrease » _ decrease (Expand Search), a decrease (Expand Search), gy decreased (Expand Search)
we decrease » _ decrease (Expand Search), a decrease (Expand Search), teer decrease (Expand Search)
μ decrease » _ decrease (Expand Search), a decrease (Expand Search), _ decreased (Expand Search)
10 μ » 10 _ (Expand Search)
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Datasheet1_Impact of lockdown on children with type-1 diabetes: returning to the community was associated with a decrease in HbA1c.pdf
Published 2023“…No significant difference was observed between medians of HbA1c_mean and HbA1c_after values (8.37% [7.88; 9.32%] vs. 8.50% [7.70; 9.50%], respectively; p = 0.391). …”
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Datasheet2_Impact of lockdown on children with type-1 diabetes: returning to the community was associated with a decrease in HbA1c.pdf
Published 2023“…No significant difference was observed between medians of HbA1c_mean and HbA1c_after values (8.37% [7.88; 9.32%] vs. 8.50% [7.70; 9.50%], respectively; p = 0.391). …”
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246
Extracellular vesicles isolated from patients undergoing remote ischemic preconditioning decrease hypoxia-evoked apoptosis of cardiomyoblasts after isoflurane but not propofol expo...
Published 2020“…Prior isoflurane exposure <i>in vitro</i> even increased protection (RIPC-EVs/control, apoptotic ratio: 0.79; p = 0.0035; Sham-EVs/control, apoptotic ratio:1.04) while propofol (50μM) abrogated protection by RIPC-EVs (RIPC-EVs/control, Apoptotic ratio: 1.01; Sham-EVs/control, apoptotic ratio: 0.94; p = 0.602). …”
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DataSheet_1_Decreased TCF1 and BCL11B expression predicts poor prognosis for patients with chronic lymphocytic leukemia.docx
Published 2022“…Intriguingly, BCL11B was highly consistent with TCF1 in its decreased expression and prediction of poor prognosis. …”
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<i>In vitro</i> activity of aryl-thiazole derivatives against <i>Schistosoma mansoni</i> schistosomula and adult worms
Published 2019“…Adult worms’ treatment with 50 μM NJ05, NJ07 or NJ05 + NJ07 showed decreased motility to 30–50% compared with controls. …”
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Nanodomains and Their Temperature Dependence in a Phosphonium-Based Ionic Liquid: A Single-Molecule Tracking Study
Published 2024“…., nanodomains) characterized by their organization into distinct domains. We present evidence of nanodomains in trihexyl(tetradecyl)phosphonium chloride, [P<sub>66614</sub>][Cl], using single-molecule tracking (SMT) and the maximum entropy method (MEM) to analyze single-molecule trajectories. …”
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254
Nanodomains and Their Temperature Dependence in a Phosphonium-Based Ionic Liquid: A Single-Molecule Tracking Study
Published 2024“…., nanodomains) characterized by their organization into distinct domains. We present evidence of nanodomains in trihexyl(tetradecyl)phosphonium chloride, [P<sub>66614</sub>][Cl], using single-molecule tracking (SMT) and the maximum entropy method (MEM) to analyze single-molecule trajectories. …”
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255
Nanodomains and Their Temperature Dependence in a Phosphonium-Based Ionic Liquid: A Single-Molecule Tracking Study
Published 2024“…., nanodomains) characterized by their organization into distinct domains. We present evidence of nanodomains in trihexyl(tetradecyl)phosphonium chloride, [P<sub>66614</sub>][Cl], using single-molecule tracking (SMT) and the maximum entropy method (MEM) to analyze single-molecule trajectories. …”
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256
Nanodomains and Their Temperature Dependence in a Phosphonium-Based Ionic Liquid: A Single-Molecule Tracking Study
Published 2024“…., nanodomains) characterized by their organization into distinct domains. We present evidence of nanodomains in trihexyl(tetradecyl)phosphonium chloride, [P<sub>66614</sub>][Cl], using single-molecule tracking (SMT) and the maximum entropy method (MEM) to analyze single-molecule trajectories. …”
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Identification, Synthesis, and Biological Evaluations of Potent Inhibitors Targeting Type I Protein Arginine Methyltransferases
Published 2022“…CARM1 (coactivator-associated arginine methyltransferase 1), which belongs to type I PRMTs (protein arginine methyltransferases), is a potential therapeutic target for treatment of multiple cancers. In this study, we first identified several hit compounds against CARM1 by structure-based virtual screening (IC<sub>50</sub> = 35.51 ± 6.68 to 68.70 ± 8.12 μM) and then carried out chemical structural optimizations, leading to six compounds with significantly improved activities targeting CARM1 (IC<sub>50</sub> = 18 ± 2 to 107 ± 6 nM). …”