Showing 941 - 960 results of 132,805 for search '(( 5 ((((nm decrease) OR (nn decrease))) OR (a decrease)) ) OR ( 2 we decrease ))', query time: 2.01s Refine Results
  1. 941

    Rat tickling: A systematic review of applications, outcomes, and moderators by Megan R. LaFollette (3911140)

    Published 2017
    “…The most common method used for tickling was cycling through 15 seconds of tickling and 15 seconds of rest for 2 minutes for 3 to 5 days. Experiments with a control for tickling (N = 22) showed that tickling increases positive vocalization, approach behavior, decreases anxiety measures, improves handling, and in some cases decreases stress hormones. …”
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    AMPK activators reverse the decreased expression of GR induced by DEX in cultured prefrontal cortical astrocytes. by Shi-Ying Yuan (2937669)

    Published 2016
    “…<p>(A) Representative western blot images (upper) and summarized data (lower) showing the effects of AICAR (n = 5 for each group) (A), ASP (n = 4 for each group) (B), and MET (n = 7 for each group) (C) on DEX-induced decreases of GR and pAMPK in cultured astrocytes. …”
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    Meta data to Fig 2. by Xiaowen Jiang (8291814)

    Published 2024
    “…Thus, we provide a mechanism for how retinoic acid via <i>rcan2</i> can regulate K<sup>+</sup>-channel activity to scale a vertebrate appendage via intercellular Ca<sup>2+</sup> signaling.…”
  12. 952

    Meta data to S2 Fig. by Xiaowen Jiang (8291814)

    Published 2024
    “…Thus, we provide a mechanism for how retinoic acid via <i>rcan2</i> can regulate K<sup>+</sup>-channel activity to scale a vertebrate appendage via intercellular Ca<sup>2+</sup> signaling.…”
  13. 953

    Repurposing of a Nucleoside Scaffold from Adenosine Receptor Agonists to Opioid Receptor Antagonists by Dilip K. Tosh (1668115)

    Published 2018
    “…In an effort to increase OR and decrease AR affinity by structure activity analysis of this series, antagonist activity at κ-(K)­OR appeared in 5′-esters (ethyl <b>24</b> and propyl <b>30</b>), which retained TSPO interaction (μM). 7-Deaza modification of C2-(arylethynyl)-5′-esters but not 4′-truncation enhanced KOR affinity (MRS7299 <b>28</b> and <b>29</b>, <i>K</i><sub>i</sub> ≈ 40 nM), revealed μ-OR and DOR binding, and reduced AR affinity. …”
  14. 954

    Repurposing of a Nucleoside Scaffold from Adenosine Receptor Agonists to Opioid Receptor Antagonists by Dilip K. Tosh (1668115)

    Published 2018
    “…In an effort to increase OR and decrease AR affinity by structure activity analysis of this series, antagonist activity at κ-(K)­OR appeared in 5′-esters (ethyl <b>24</b> and propyl <b>30</b>), which retained TSPO interaction (μM). 7-Deaza modification of C2-(arylethynyl)-5′-esters but not 4′-truncation enhanced KOR affinity (MRS7299 <b>28</b> and <b>29</b>, <i>K</i><sub>i</sub> ≈ 40 nM), revealed μ-OR and DOR binding, and reduced AR affinity. …”
  15. 955

    Repurposing of a Nucleoside Scaffold from Adenosine Receptor Agonists to Opioid Receptor Antagonists by Dilip K. Tosh (1668115)

    Published 2018
    “…In an effort to increase OR and decrease AR affinity by structure activity analysis of this series, antagonist activity at κ-(K)­OR appeared in 5′-esters (ethyl <b>24</b> and propyl <b>30</b>), which retained TSPO interaction (μM). 7-Deaza modification of C2-(arylethynyl)-5′-esters but not 4′-truncation enhanced KOR affinity (MRS7299 <b>28</b> and <b>29</b>, <i>K</i><sub>i</sub> ≈ 40 nM), revealed μ-OR and DOR binding, and reduced AR affinity. …”
  16. 956

    Repurposing of a Nucleoside Scaffold from Adenosine Receptor Agonists to Opioid Receptor Antagonists by Dilip K. Tosh (1668115)

    Published 2018
    “…In an effort to increase OR and decrease AR affinity by structure activity analysis of this series, antagonist activity at κ-(K)­OR appeared in 5′-esters (ethyl <b>24</b> and propyl <b>30</b>), which retained TSPO interaction (μM). 7-Deaza modification of C2-(arylethynyl)-5′-esters but not 4′-truncation enhanced KOR affinity (MRS7299 <b>28</b> and <b>29</b>, <i>K</i><sub>i</sub> ≈ 40 nM), revealed μ-OR and DOR binding, and reduced AR affinity. …”
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