Showing 121 - 140 results of 1,867 for search '(( 5 ppm decrease ) OR ((( 5 nn decrease ) OR ( 5 nm decrease ))))', query time: 0.50s Refine Results
  1. 121

    Data_Sheet_1_Hepcidin Decreases Rotenone-Induced α-Synuclein Accumulation via Autophagy in SH-SY5Y Cells.PDF by Meiqi Li (4169182)

    Published 2020
    “…We demonstrated that SH-SY5Y cell viability was impaired after rotenone treatment in a dose-dependent manner. α-syn expression and iron content increased under a low concentration rotenone (25 nM for 3 days) treatment in SH-SY5Y cells. …”
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    Electrically Controlled Lasing in Supercooled Liquid Crystal Blue Phase I Microdroplets by Gia Petriashvili (8920925)

    Published 2020
    “…When the electric field intensity is increased, the lasing intensity is increased too along with the linewidth that decreases from 6 to 2.5 nm. Besides, the laser lines were shifted toward the shorter wavelength by 11 nm. …”
  16. 136

    Phosphomimetic mutations impair the export of GRA16 from the parasitophorous vacuole. by Joshua Mayoral (9922544)

    Published 2020
    “…Kruskal-Wallis and Dunn’s multiple comparisons tests were performed to calculate p-values. Scale bars indicate 5μm in <b>B</b> and 10μm in <b>C</b>. <b>(C)</b> Violin plots and representative images of GRA16 intensity in host nuclei as described in <b>(B)</b>, except that all experiments were conducted in the ΔTgPPM3C strain. …”
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    Structure-Based Design of a Chemical Probe Set for the 5‑HT<sub>5A</sub> Serotonin Receptor by Anat Levit Kaplan (12126567)

    Published 2022
    “…Docking over 6 million molecules against a 5-HT<sub>5A</sub>R homology model identified 5 mid-μM ligands, one of which was optimized to <b>UCSF678</b>, a 42 nM arrestin-biased partial agonist at the 5-HT<sub>5A</sub>R with a more restricted off-target profile and decreased assay liabilities versus SB-699551. …”
  20. 140

    Structure-Based Design of a Chemical Probe Set for the 5‑HT<sub>5A</sub> Serotonin Receptor by Anat Levit Kaplan (12126567)

    Published 2022
    “…Docking over 6 million molecules against a 5-HT<sub>5A</sub>R homology model identified 5 mid-μM ligands, one of which was optimized to <b>UCSF678</b>, a 42 nM arrestin-biased partial agonist at the 5-HT<sub>5A</sub>R with a more restricted off-target profile and decreased assay liabilities versus SB-699551. …”