Showing 1,001 - 1,020 results of 153,210 for search '(( 10 ((we decrease) OR (nn decrease)) ) OR ( 5 ((nm decrease) OR (a decrease)) ))', query time: 1.73s Refine Results
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    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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  7. 1007

    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. …”
  8. 1008

    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. …”
  9. 1009

    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. …”
  10. 1010

    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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    Decreased MMP-9 protein expression induced by STIP1 knockdown is independent of common signaling pathways. by Hsin-Shih Wang (8802)

    Published 2018
    “…(B) Decreased MMP-9 protein expression induced by siRNA knockdown of STIP1 was unaffected by exposure either to the DNA methylation inhibitor 5-aza-2’-deoxycytidine (AZA; 10 μM) or the histone deacetylase inhibitor trichostatin A (TSA; 20 nM). …”
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    datasheet1_Allopregnanolone Decreases Evoked Dopamine Release Differently in Rats by Sex and Estrous Stage.docx by Ana Paula S. Dornellas (9983996)

    Published 2021
    “…Previous studies found that the endogenous GABAergic steroid (3α,5α)-3-hydroxy-5-pregnan-20-one (allopregnanolone) modulates dopamine levels in the nucleus accumbens and prefrontal cortex. …”
  17. 1017

    DataSheet_1_microRNA-144/451 decreases dendritic cell bioactivity via targeting interferon-regulatory factor 5 to limit DSS-induced colitis.pdf by Zhijie Lin (173992)

    Published 2022
    “…Thus, our results reveal a novel miR144/451-IRF5 pathway in DCs that protects experimental colitis. …”
  18. 1018

    Data Sheet 1_Probiotic Limosilactobacillus reuteri KUB-AC5 decreases urothelial cell invasion and enhances macrophage killing of uropathogenic Escherichia coli in vitro study.pdf by Arishabhas Tantibhadrasapa (13929639)

    Published 2024
    “…The human bladder epithelial cell line UM-UC-3 was used to assess the adhesion and pathogen-attachment inhibition properties of AC5 on UPEC.</p>Results and discussion<p>Our data showed that AC5 can attach to UM-UC-3 and decrease UPEC attachment in a dose-dependent manner. …”
  19. 1019

    Length-Dependent Convergence and Saturation Behavior of Electrochemical, Linear Optical, Quadratic Nonlinear Optical, and Cubic Nonlinear Optical Properties of Dipolar Alkynylruthe... by Bandar Babgi (2360545)

    Published 2009
    “…The syntheses of <i>trans</i>-[Ru{4,4′-CCC<sub>6</sub>H<sub>2</sub>[2,5-(OEt)<sub>2</sub>]CCC<sub>6</sub>H<sub>4</sub>NO<sub>2</sub>}Cl(dppm)<sub>2</sub>] (<b>19</b>), <i>trans</i>-[Ru{4,4′,4′′-CCC<sub>6</sub>H<sub>4</sub>CCC<sub>6</sub>H<sub>2</sub>[2,5-(OEt)<sub>2</sub>]CCC<sub>6</sub>H<sub>4</sub>NO<sub>2</sub>}Cl(dppm)<sub>2</sub>] (<b>20</b>), <i>trans</i>-[Ru{4,4′,4′′,4′′′-CCC<sub>6</sub>H<sub>4</sub>CCC<sub>6</sub>H<sub>2</sub>[2,5-(OEt)<sub>2</sub>]CCC<sub>6</sub>H<sub>2</sub>[2,5-(OEt)<sub>2</sub>]CCC<sub>6</sub>H<sub>4</sub>NO<sub>2</sub>}Cl(dppe)<sub>2</sub>] (<b>21</b>), <i>trans</i>-[Ru{4,4′,4′′,4′′′-CCC<sub>6</sub>H<sub>4</sub>CCC<sub>6</sub>H<sub>2</sub>[2,5-(OEt)<sub>2</sub>]CCC<sub>6</sub>H<sub>2</sub>[2,5-(OEt)<sub>2</sub>]CCC<sub>6</sub>H<sub>4</sub>NO<sub>2</sub>}Cl(dppm)<sub>2</sub>] (<b>22</b>), <i>trans</i>-[Ru{4,4′,4′′,4′′′-CCC<sub>6</sub>H<sub>4</sub>CCC<sub>6</sub>H<sub>4</sub>CCC<sub>6</sub>H<sub>2</sub>[2,5-(OEt)<sub>2</sub>]CCC<sub>6</sub>H<sub>4</sub>NO<sub>2</sub>}Cl(dppm)<sub>2</sub>] (<b>23</b>), and <i>trans</i>-[Ru{4,4′,4′′,4′′′,4′′′′-CCC<sub>6</sub>H<sub>4</sub>CCC<sub>6</sub>H<sub>4</sub>CCC<sub>6</sub>H<sub>2</sub>[2,5-(OEt)<sub>2</sub>]CCC<sub>6</sub>H<sub>2</sub>[2,5-(OEt)<sub>2</sub>]CCC<sub>6</sub>H<sub>4</sub>NO<sub>2</sub>}Cl(dppm)<sub>2</sub>] (<b>24</b>) are reported, together with those of precursor alkynes, complexes with the donor−π-bridge−acceptor formulation that affords efficient quadratic and cubic NLO compounds; the identity of <b>19</b> was confirmed by a structural study. …”
  20. 1020

    Bee Venom for the Treatment of Parkinson Disease – A Randomized Controlled Clinical Trial by Andreas Hartmann (241073)

    Published 2016
    “…<div><p>In the present study, we examined the potential symptomatic and/or disease-modifying effects of monthly bee venom injections compared to placebo in moderatly affected Parkinson disease patients. We conducted a prospective, randomized double-blind study in 40 Parkinson disease patients at Hoehn & Yahr stages 1.5 to 3 who were either assigned to monthly bee venom injections or equivalent volumes of saline (treatment/placebo group: n = 20/20). …”