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point decrease » point increase (Expand Search)
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a decrease » _ decrease (Expand Search), _ decreased (Expand Search), _ decreases (Expand Search)
point decrease » point increase (Expand Search)
fold decrease » fold increase (Expand Search), fold increased (Expand Search)
n decrease » nn decrease (Expand Search), _ decrease (Expand Search), _ decreased (Expand Search)
a decrease » _ decrease (Expand Search), _ decreased (Expand Search), _ decreases (Expand Search)
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1181
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1182
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1183
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1184
Decreased diaphragm muscle lateral bifurcations in GAD67-deficient (−/−) E15.5 mice.
Published 2013“…<b>D</b> shows a significantly decreased lateral bifurcation number but not medial bifurcation (mean ± SEM) in GAD67-deficient mice compared to wild type (<i>n</i> = 5, *<i>P</i><0.05, unpaired <i>t</i> test). …”
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1185
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1186
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1187
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1188
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1189
The GluN2B-C456Y mutation decreases recombinant NMDAR currents and alters receptor properties.
Published 2020“…<p>(A) The GluN2B-C456Y mutation strongly decreases diheteromeric GluN1/GluN2B NMDAR currents in <i>Xenopus</i> oocytes. …”
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1190
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1191
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1192
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1193
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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1194
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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1195
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1196
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1197
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1198
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1199
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1200