Showing 741 - 760 results of 76,154 for search '(( 20 a decrease ) OR ( 5 ((((wt decrease) OR (nn decrease))) OR (we decrease)) ))', query time: 1.31s Refine Results
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    WT and Δpbp4 SACs in placebo and vancomycin treated tibiae. by Elysia A. Masters (9553742)

    Published 2020
    “…<i>aureus</i> IHC as described in <a href="http://www.plospathogens.org/article/info:doi/10.1371/journal.ppat.1008988#ppat.1008988.g007" target="_blank">Fig 7</a>, and representative micrographs of SACs in the tibial marrow space are shown at 20x. …”
  5. 745

    The effects of thioperamide and alpha-FMH on the amount of sleep/wake in WT and W/W<sup>v</sup> mice. by Sachiko Chikahisa (417256)

    Published 2013
    “…<p>(A) Injection of thioperamide (ip), a H3 antagonist, at a high dose (10 mg/kg) increased wakefulness in both WT and W/W<sup>v</sup> mice for 3 hours. (B) In contrast, injection of alpha-FMH (ip), a HDC blocker, at medium (50 mg/kg) and high (100 mg/kg) doses decreased the amount of wakefulness in WT mice. …”
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    Resveratrol decreases proliferation of Cisplatin-sensitive A2780 cells but not Cisplatin-resistant A2780CP cells. by Sébastien Baribeau (512869)

    Published 2014
    “…A2780 cells proliferation was increased by Resveratrol at 20 µM and decreased at 60 µM while all doses suggest an increase in proliferation in A2780CP cells. …”
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    Image 5_Exploration of the diagnostic and prognostic roles of decreased autoantibodies in lung cancer.tif by Ying Ye (72583)

    Published 2025
    “…Moreover, 5 of the decreased autoantibodies can also be applied for supervising bone metastasis in lung adenocarcinoma. …”
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    Downregulation of DOM decreases the abundance of PER and TIM. by Zhenxing Liu (399809)

    Published 2019
    “…<p><b>A.</b> Quantitative RT-PCR showing the expression of <i>clk</i>, <i>per</i> and <i>tim</i>. …”
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    Inhibition of Fatty Acid Synthase Decreases Expression of Stemness Markers in Glioma Stem Cells by Yuki Yasumoto (685821)

    Published 2016
    “…When GSCs were treated with 20 μM cerulenin, a pharmacological inhibitor of FASN, their proliferation and migration were significantly suppressed and <i>de novo</i> lipogenesis decreased. …”
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