Showing 1,081 - 1,100 results of 101,130 for search '(( 5 ((nn decrease) OR (a decrease)) ) OR ( 5 ((nm decrease) OR (mean decrease)) ))', query time: 1.47s Refine Results
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    Inclusion of TPP side chains result in decreased melanoma cell mitochondria membrane potential, oxygen consumption, and increased DHE oxidation. by Kyle C. Kloepping (9928265)

    Published 2020
    “…<p>(A) A375 melanoma cells were treated with 0.5 μM, 1.0 μM, or 2.0 μM 5-, 10-, or 16-TPP for 1 h and analyzed for mitochondria membrane potential by the JC-1 method (* significant relative to control; p<0.05; n = 2 from 2 separate experiments; N = 4). …”
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    Retinoic acid alleviates decrease of phospho-Bad and 14-3-3 interaction caused by MCAO damage. by Ju-Bin Kang (16021324)

    Published 2024
    “…Molecular weights (kDa) are depicted at right. Data (<i>n</i> = 5) are represented as mean ± S.E.M. *<i>p</i> < 0.001, **<i>p</i> < 0.01, ***<i>p</i> < 0.05 vs. vehicle + sham animals, #<i>p</i> < 0.01, ##<i>p</i> < 0.05 vs. vehicle + MCAO animals.…”
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    Housing conditions specifically impaired long-term SRM (mean±SEM): A) Rats in group housing displayed a significant decrease in SIT during the second 5 min encounter (A2, empty bars) compared to the first (A1, gray bars), regardless of the time interval between the encounters. by Hadar Shahar-Gold (283031)

    Published 2013
    “…D) Rats from group housing (gray bars, n<i> = </i>10) and socially isolated rats (empty bars, n = 10) similarly retained object recognition memory for 120 min following a single 5 min exposure. Both groups showed a significant decrease in investigation time during the second exposure to an object (A2), compared with the first exposure (A1) 120 min earlier and compared with exposure to a novel object (B) 30 min later. …”
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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. …”