Showing 5,621 - 5,640 results of 80,896 for search '(( 50 ((teer decrease) OR (((nn decrease) OR (a decrease)))) ) OR ( 2 we decrease ))', query time: 1.18s Refine Results
  1. 5621
  2. 5622
  3. 5623
  4. 5624

    Iridium Dihydroxybipyridine Complexes Show That Ligand Deprotonation Dramatically Speeds Rates of Catalytic Water Oxidation by Joseph DePasquale (1922713)

    Published 2013
    “…With NaIO<sub>4</sub> as the oxidant at pH 5.6, water oxidation occurred most rapidly with (N,N) = 4,4′-dhbp, and activity decreased in the order 4,4′-dhbp (<b>3</b>) > 6,6′-dhbp (<b>2</b>) ≫ 4,4′-dimethoxybipyridine (<b>4</b>) > bipy (<b>1</b>). …”
  5. 5625

    Double Mutant of Chymotrypsin Inhibitor 2 Stabilized through Increased Conformational Entropy by Yulian Gavrilov (1365888)

    Published 2022
    “…Here, we have examined whether changed native-state dynamics, and resulting entropy changes, can explain the stability changes in the double mutant protein, as well as the two single mutant forms. …”
  6. 5626
  7. 5627

    EBNA3C down-regulated RASSF1A mRNA expression by enhancing RASSF1A promoter methylation. by Shengwei Zhang (321384)

    Published 2019
    “…<p>(A-D) RASSF1A mRNA expression was decreased in A-B) EBV positive cell lines and C-D) BJAB7, BJAB10, LCL1, and LCL2 cells. 5 million B-cells were collected and total RNA extracted via Trizol reagent. cDNAs were generated by reverse transcriptase kit and RASSF1A mRNA expression level was detected by real-time PCR. …”
  8. 5628
  9. 5629

    Addressing a Trapped High-Energy Water: Design and Synthesis of Highly Potent Pyrimidoindole-Based Glycogen Synthase Kinase-3β Inhibitors by Stanislav Andreev (11067165)

    Published 2021
    “…Here, by addressing a high-energy water, we improved the IC<sub>50</sub> value of our co-crystallized glycogen synthase kinase-3β (GSK-3β) inhibitor by nearly two orders of magnitude. …”
  10. 5630

    Addressing a Trapped High-Energy Water: Design and Synthesis of Highly Potent Pyrimidoindole-Based Glycogen Synthase Kinase-3β Inhibitors by Stanislav Andreev (11067165)

    Published 2021
    “…Here, by addressing a high-energy water, we improved the IC<sub>50</sub> value of our co-crystallized glycogen synthase kinase-3β (GSK-3β) inhibitor by nearly two orders of magnitude. …”
  11. 5631

    Optimal conditions for vigor indexes A and B. by Ahad Asghari (20615202)

    Published 2025
    “…The results revealed that increasing PAW levels up to 0.18 min/mL led to an increase in seed germination percentage, seedling weight (both fresh and dry), seedling length, vigor indexes A and B, and water uptake and decreasing mean germination time. …”
  12. 5632
  13. 5633

    Scattering Properties of MoS<sub>2</sub> Edges and Folds Using Darkfield Hyperspectral Microscopy by Sungmin Bong (14013295)

    Published 2024
    “…In this study, we utilize dark-field hyperspectral microscopy (DFHM) to investigate the optical properties of individual edges and folds in MoS<sub>2</sub> synthesized by chemical vapor deposition. …”
  14. 5634
  15. 5635

    Multifunctional Hybrid Compounds Derived from 2‑(2,5-Dioxopyrrolidin-1-yl)-3-methoxypropanamides with Anticonvulsant and Antinociceptive Properties by Michał Abram (4490902)

    Published 2017
    “…Such hybrids demonstrated effectiveness in two of the most widely used animal seizure models, namely, the maximal electroshock (MES) test and the psychomotor 6 Hz (32 mA) seizure models. Compound <b>33</b> showed the highest anticonvulsant activity in these models (ED<sub>50</sub> MES = 79.5 mg/kg, ED<sub>50</sub> 6 Hz = 22.4 mg/kg). …”
  16. 5636

    Table of flow cytometry experiments. by Xinwen Zhu (14709669)

    Published 2023
    “…Here, we screen the most commonly used 2A peptides, porcine teschovirus-1 2A (P2A), <i>Thosea asigna</i> virus 2A (T2A), equine rhinitis A virus 2A (E2A), and foot-and-mouth disease virus 2A (F2A), for activity in <i>D. discoideum</i> and find that all the screened 2A sequences are effective. …”
  17. 5637
  18. 5638

    Development of <i>N</i>‑(1-Adamantyl)benzamides as Novel Anti-Inflammatory Multitarget Agents Acting as Dual Modulators of the Cannabinoid CB2 Receptor and Fatty Acid Amide Hydrola... by Francesca Intranuovo (2231401)

    Published 2022
    “…Encouraged by principal component analysis (PCA) data identifying a wide chemical space shared by CB2R and FAAH ligands, we designed a small library of adamantyl-benzamides, as potential dual agents, CB2R agonists, and FAAH inhibitors. …”
  19. 5639

    Development of <i>N</i>‑(1-Adamantyl)benzamides as Novel Anti-Inflammatory Multitarget Agents Acting as Dual Modulators of the Cannabinoid CB2 Receptor and Fatty Acid Amide Hydrola... by Francesca Intranuovo (2231401)

    Published 2022
    “…Encouraged by principal component analysis (PCA) data identifying a wide chemical space shared by CB2R and FAAH ligands, we designed a small library of adamantyl-benzamides, as potential dual agents, CB2R agonists, and FAAH inhibitors. …”
  20. 5640

    Development of <i>N</i>‑(1-Adamantyl)benzamides as Novel Anti-Inflammatory Multitarget Agents Acting as Dual Modulators of the Cannabinoid CB2 Receptor and Fatty Acid Amide Hydrola... by Francesca Intranuovo (2231401)

    Published 2022
    “…Encouraged by principal component analysis (PCA) data identifying a wide chemical space shared by CB2R and FAAH ligands, we designed a small library of adamantyl-benzamides, as potential dual agents, CB2R agonists, and FAAH inhibitors. …”