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a decrease » _ decrease (Expand Search), _ decreased (Expand Search), _ decreases (Expand Search)
point decrease » point increase (Expand Search)
teer decrease » greater decrease (Expand Search)
a decrease » _ decrease (Expand Search), _ decreased (Expand Search), _ decreases (Expand Search)
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8401
Table_5_Tramadol’s Inhibitory Effects on Sexual Behavior: Pharmacological Studies in Serotonin Transporter Knockout Rats.PDF
Published 2018“…To investigate whether other mechanisms contribute to the inhibitory effects, WAY100,635, a 5-HT<sub>1A</sub> receptor antagonist and naloxone, a μ-opioid receptor antagonist, were tested on sexual behavior together with tramadol. …”
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8402
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8403
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8404
Expression of pro-fibrotic genes: TGFβ1, COL1A1, DNMT1 and RASAL1 in GTM cells in response to the methylation inhibitor 5-azacytidine.
Published 2016“…Further, the pro-fibrotic genes COL1A1 and TGFβ1 were also significantly (P<0.01) decreased by 5-azacytidine. …”
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8405
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8406
Syntheses, Characterization, and Ethylene (Co-)Polymerization Screening of Amidate Half-Titanocene Dichlorides
Published 2010“…A series of amidate half-titanocene dichlorides, Cp′Ti<b>L</b>Cl<sub>2</sub> [Cp′ = Cp (as η<sup>5</sup>-C<sub>5</sub>H<sub>5</sub>) or Cp* (as η<sup>5</sup>-C<sub>5</sub>Me<sub>5</sub>), <b>L</b> = <i>N</i>-(2-methylquinolin-8-yl)-<i>p</i>-R-benzamides; <b>C1</b>: Cp′ = Cp, R = OMe; <b>C2</b>: Cp′ = Cp, R = Me; <b>C3</b>: Cp′ = Cp, R = H; <b>C4</b>: Cp′ = Cp, R = F; <b>C5</b>: Cp′ = Cp, R = Cl; <b>C6</b>: Cp′ = Cp*, R = OMe; <b>C7</b>: Cp′ = Cp*, R = Me], have been synthesized by the stoichiometric reaction of Cp′TiCl<sub>3</sub> with the corresponding potassium amidates. …”
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8407
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8408
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8409
Decreased ubiquitination in the dTAK1<sup>K156R</sup> mutant.
Published 2014“…<p>(A) Mutant dTAK1<sup>K156R</sup> showed decreased polyubiquitination when compared with dTAK1. …”
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8410
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8411
Casein kinase 1.2 depletion decreases ZC3H11 phosphorylation.
Published 2016“…Procyclic cells expressing in situ tagged V5-CK1.2, with a tetracycline-inducible stem-loop RNAi construct, were induced with tetracycline (200g/ml). …”
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8412
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8413
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8414
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8415
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8416
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8417
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8418
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8419
A Practical, Fast, and High-Yielding Aziridination Procedure Using Simple Cu(II) Complexes Containing N-Donor Pyridine-Based Ligands
Published 2005“…<i>Four-coordinate</i> dichlorocopper(II) complexes derived from di(2-pyridyl)methanes or pyridine itself exhibit high catalytic activity in aziridination of regular olefins with PhINTs in weakly coordinating chloroform in the presence of 1−2 equiv of NaBAr<sup>F</sup><sub>4</sub> (BAr<sup>F</sup><sub>4</sub><sup>-</sup> = tetra[3,5-di(trifluoromethyl)phenyl]borate). High yields of aziridines exceeding 90% can be obtained with a 1:1 olefin/PhINTs ratio and 1−5 mol % catalyst loading for such reactive olefins as styrene, tri- and tetramethylethylene. …”
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8420
A Practical, Fast, and High-Yielding Aziridination Procedure Using Simple Cu(II) Complexes Containing N-Donor Pyridine-Based Ligands
Published 2005“…<i>Four-coordinate</i> dichlorocopper(II) complexes derived from di(2-pyridyl)methanes or pyridine itself exhibit high catalytic activity in aziridination of regular olefins with PhINTs in weakly coordinating chloroform in the presence of 1−2 equiv of NaBAr<sup>F</sup><sub>4</sub> (BAr<sup>F</sup><sub>4</sub><sup>-</sup> = tetra[3,5-di(trifluoromethyl)phenyl]borate). High yields of aziridines exceeding 90% can be obtained with a 1:1 olefin/PhINTs ratio and 1−5 mol % catalyst loading for such reactive olefins as styrene, tri- and tetramethylethylene. …”