Search alternatives:
teer decrease » mean decrease (Expand Search), greater decrease (Expand Search)
fold decrease » fold increase (Expand Search), fold increased (Expand Search)
nn decrease » _ decrease (Expand Search), mean decrease (Expand Search), gy decreased (Expand Search)
a decrease » _ decrease (Expand Search), _ decreased (Expand Search), _ decreases (Expand Search)
teer decrease » mean decrease (Expand Search), greater decrease (Expand Search)
fold decrease » fold increase (Expand Search), fold increased (Expand Search)
nn decrease » _ decrease (Expand Search), mean decrease (Expand Search), gy decreased (Expand Search)
a decrease » _ decrease (Expand Search), _ decreased (Expand Search), _ decreases (Expand Search)
-
601
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). …”
-
602
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). …”
-
603
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). …”
-
604
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). …”
-
605
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). …”
-
606
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). …”
-
607
-
608
-
609
-
610
-
611
-
612
Genes showing ≥3-fold differences in expression level in IgG4-RD patients and healthy controls.
Published 2015“…<p>We identified 21 genes showing a ≥3-fold increase (16 genes) or decrease (5genes) in expression level among 4 samples from 4 healthy controls and 2 IgG4-RD patients before and after therapy.…”
-
613
Inhibition and assessment of the biophysical gating properties of GluA2 and GluA2/A3 AMPA receptors using curcumin derivatives
Published 2019“…The biophysical parameter (i.e., desensitization, deactivation, and peak currents) were measured by using whole-cell patch clamp electrophysiology with and without the administration of the derivatives onto HEK293 cells. CR-NN, CR-NNPh, CR-MeNH, and CR-NO of the tested derivatives showed inhibition on all AMPA receptors up to 6 folds. …”
-
614
-
615
-
616
-
617
-
618
-
619
Sequence of <i>DpAP2</i> promoter.
Published 2024“…Carotenoid biosynthesis was enhanced by <i>DpAP2</i> overexpression (1.4930 fold of control) and exogenous substances such as GA3 (1.5889 fold of control), which laid a foundation for massive accumulation of carotenoids in microalgae. …”
-
620