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de decrease » we decrease (Expand Search), _ decrease (Expand Search), nn decrease (Expand Search)
ms decrease » _ decrease (Expand Search), nn decrease (Expand Search), use decreased (Expand Search)
a decrease » _ decrease (Expand Search), _ decreased (Expand Search), _ decreases (Expand Search)
a de » _ de (Expand Search), a d (Expand Search), i de (Expand Search)
de decrease » we decrease (Expand Search), _ decrease (Expand Search), nn decrease (Expand Search)
ms decrease » _ decrease (Expand Search), nn decrease (Expand Search), use decreased (Expand Search)
a decrease » _ decrease (Expand Search), _ decreased (Expand Search), _ decreases (Expand Search)
a de » _ de (Expand Search), a d (Expand Search), i de (Expand Search)
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1321
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1324
Activation of Wnt/β-catenin signaling decreases mRNA expressions of <i>Scx</i>, <i>Mkx</i> and <i>Tnmd</i> in rat TDCs.
Published 2017“…<p>Relative expressions of <i>Axin2</i>, <i>Scx</i>, <i>Mkx</i>, and <i>Tnmd</i> in TDCs treated with 50 ng/ml Wnt3a with or without 5 μM IWR (an inhibitor of β-catenin) <b>(A)</b>, 0 to 4 μM BIO (an activator of β-catenin) <b>(B)</b>, or 0 to 20 μM IWR <b>(C)</b> for 72 hrs. …”
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1325
MiR-24 is required for blood development from mouse embryonic stem cells.
Published 2015“…Error bars represent the standard error of the mean (SEM).</p>…”
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1326
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1327
2-DE gels of <i>A. brasilense</i> Sp7 and Sp7-flcAΔ under flocculation conditions.
Published 2014“…<p>Blue silver stained 2-DE gel of proteins extracted from <i>Azospirillum</i> Sp7 (A) and Sp7-flcAΔ mutant (B) under flocculation conditions. …”
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1328
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1329
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1330
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1331
Decreased proliferation in <i>Csf1r<sup>−/−</sup></i> and <i>Csf1<sup>op/op</sup></i> mouse colonic epithelium.
Published 2013“…Bar = 50 µm. Means are depicted by horizontal bars, n = 3 per group, *<b>*</b>P<0.01, *P<0.05, using unpaired two-tailed t-test. …”
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1332
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1333
Multiple Organ System Defects and Transcriptional Dysregulation in the <em>Nipbl</em><sup>+/−</sup> Mouse, a Model of Cornelia de Lange Syndrome
Published 2009“…<div><p>Cornelia de Lange Syndrome (CdLS) is a multi-organ system birth defects disorder linked, in at least half of cases, to heterozygous mutations in the <em>NIPBL</em> gene. …”
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1334
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1335
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1336
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1337
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1338
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1339
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1340