Search alternatives:
non decrease » point decrease (Expand Search), note decreased (Expand Search), fold decrease (Expand Search)
nn decrease » _ decrease (Expand Search), gy decreased (Expand Search), b1 decreased (Expand Search)
a decrease » _ decrease (Expand Search), _ decreased (Expand Search), _ decreases (Expand Search)
non decrease » point decrease (Expand Search), note decreased (Expand Search), fold decrease (Expand Search)
nn decrease » _ decrease (Expand Search), gy decreased (Expand Search), b1 decreased (Expand Search)
a decrease » _ decrease (Expand Search), _ decreased (Expand Search), _ decreases (Expand Search)
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1701
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1703
Nitric Oxide Oxidatively Nitrosylates Ni(I) and Cu(I) <i>C</i>-Organonitroso Adducts
Published 2009“…The addition of ArNO to 2 equiv of [Me<sub>2</sub>NN]Ni(2,4-lutidine) {[Me<sub>2</sub>NN]<sup>−</sup> = 2,4-bis(2,6-dimethylphenylimido)pentyl} gives {[Me<sub>2</sub>NN]Ni}<sub>2</sub>(μ-η<sup>2</sup>:η<sup>2</sup>-ONAr) (<b>1a</b> and <b>1b</b>), which exhibit symmetrical bonding of the ArNO moiety between two [Me<sub>2</sub>NN]Ni fragments, with a N−O bond distance of 1.440(4) Å in <b>1a</b> that is significantly longer than those in free <i>C</i>-organonitroso compounds (1.13−1.29 Å). …”
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1704
Nitric Oxide Oxidatively Nitrosylates Ni(I) and Cu(I) <i>C</i>-Organonitroso Adducts
Published 2009“…The addition of ArNO to 2 equiv of [Me<sub>2</sub>NN]Ni(2,4-lutidine) {[Me<sub>2</sub>NN]<sup>−</sup> = 2,4-bis(2,6-dimethylphenylimido)pentyl} gives {[Me<sub>2</sub>NN]Ni}<sub>2</sub>(μ-η<sup>2</sup>:η<sup>2</sup>-ONAr) (<b>1a</b> and <b>1b</b>), which exhibit symmetrical bonding of the ArNO moiety between two [Me<sub>2</sub>NN]Ni fragments, with a N−O bond distance of 1.440(4) Å in <b>1a</b> that is significantly longer than those in free <i>C</i>-organonitroso compounds (1.13−1.29 Å). …”
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1705
Nitric Oxide Oxidatively Nitrosylates Ni(I) and Cu(I) <i>C</i>-Organonitroso Adducts
Published 2009“…The addition of ArNO to 2 equiv of [Me<sub>2</sub>NN]Ni(2,4-lutidine) {[Me<sub>2</sub>NN]<sup>−</sup> = 2,4-bis(2,6-dimethylphenylimido)pentyl} gives {[Me<sub>2</sub>NN]Ni}<sub>2</sub>(μ-η<sup>2</sup>:η<sup>2</sup>-ONAr) (<b>1a</b> and <b>1b</b>), which exhibit symmetrical bonding of the ArNO moiety between two [Me<sub>2</sub>NN]Ni fragments, with a N−O bond distance of 1.440(4) Å in <b>1a</b> that is significantly longer than those in free <i>C</i>-organonitroso compounds (1.13−1.29 Å). …”
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1706
Nitric Oxide Oxidatively Nitrosylates Ni(I) and Cu(I) <i>C</i>-Organonitroso Adducts
Published 2009“…The addition of ArNO to 2 equiv of [Me<sub>2</sub>NN]Ni(2,4-lutidine) {[Me<sub>2</sub>NN]<sup>−</sup> = 2,4-bis(2,6-dimethylphenylimido)pentyl} gives {[Me<sub>2</sub>NN]Ni}<sub>2</sub>(μ-η<sup>2</sup>:η<sup>2</sup>-ONAr) (<b>1a</b> and <b>1b</b>), which exhibit symmetrical bonding of the ArNO moiety between two [Me<sub>2</sub>NN]Ni fragments, with a N−O bond distance of 1.440(4) Å in <b>1a</b> that is significantly longer than those in free <i>C</i>-organonitroso compounds (1.13−1.29 Å). …”
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1707
Nitric Oxide Oxidatively Nitrosylates Ni(I) and Cu(I) <i>C</i>-Organonitroso Adducts
Published 2009“…The addition of ArNO to 2 equiv of [Me<sub>2</sub>NN]Ni(2,4-lutidine) {[Me<sub>2</sub>NN]<sup>−</sup> = 2,4-bis(2,6-dimethylphenylimido)pentyl} gives {[Me<sub>2</sub>NN]Ni}<sub>2</sub>(μ-η<sup>2</sup>:η<sup>2</sup>-ONAr) (<b>1a</b> and <b>1b</b>), which exhibit symmetrical bonding of the ArNO moiety between two [Me<sub>2</sub>NN]Ni fragments, with a N−O bond distance of 1.440(4) Å in <b>1a</b> that is significantly longer than those in free <i>C</i>-organonitroso compounds (1.13−1.29 Å). …”
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1708
Nitric Oxide Oxidatively Nitrosylates Ni(I) and Cu(I) <i>C</i>-Organonitroso Adducts
Published 2009“…The addition of ArNO to 2 equiv of [Me<sub>2</sub>NN]Ni(2,4-lutidine) {[Me<sub>2</sub>NN]<sup>−</sup> = 2,4-bis(2,6-dimethylphenylimido)pentyl} gives {[Me<sub>2</sub>NN]Ni}<sub>2</sub>(μ-η<sup>2</sup>:η<sup>2</sup>-ONAr) (<b>1a</b> and <b>1b</b>), which exhibit symmetrical bonding of the ArNO moiety between two [Me<sub>2</sub>NN]Ni fragments, with a N−O bond distance of 1.440(4) Å in <b>1a</b> that is significantly longer than those in free <i>C</i>-organonitroso compounds (1.13−1.29 Å). …”
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1709
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1710
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1711
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1712
Inhibition and assessment of the biophysical gating properties of GluA2 and GluA2/A3 AMPA receptors using curcumin derivatives
Published 2019“…Hence, to potentially serve as a new AMPAR inhibitor with therapeutic potential, the current study provides compounds that are non-selective and non-competitive antagonist, which also effect the desensitization and deactivation rates of the receptor.…”
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1713
Data_Sheet_1_A de novo Mutation in the MTUS1 Gene Decreases the Risk of Non-compaction of Ventricular Myocardium via the Rac1/Cdc42 Pathway.pdf
Published 2019“…</p><p>Aims: To investigate the association between a de novo c. 2617A->C mutation in MTUS1 (NM_001001924.2) and non-compaction of ventricular myocardium (NVM) and explore the potential mechanisms.…”
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1714
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1715
Expression of cytokines by CD3+ infiltration in PDAC.
Published 2024“…<p>(A) Heatmap of 41 analytes in PDAC (n = 55) and non-PDAC tissue (Pancreatitis (n = 12), IPMN (n = 3), Other (n = 6)), expression levels were normalized to protein concentration (B, C): Spearman correlation analysis of IL-1B (r = -0.3704, p = 0.0187) and IL-2 (r = -0.4275, p = 0.0074) show decreased concentrations were significantly associated with increased CD3+ infiltration. …”
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1716
Expression of cytokines by CD8+ infiltration in PDAC.
Published 2024“…<p>(A) Expression of 41 analytes in PDAC (n = 58) and non-PDAC (Pancreatitis (n = 13), IPMN (n = 4), Other (n = 7)) expression is normalized to protein concentration (B) Spearman correlation analyses showing increased expression of IL-1B significantly associated with decreased CD8+ infiltration (r = -0.4299, p = 0.0045). …”
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1720