Search alternatives:
026 decrease » _ decrease (Expand Search)
nn decrease » _ decrease (Expand Search), mean decrease (Expand Search), gy decreased (Expand Search)
c decrease » c decreased (Expand Search), _ decrease (Expand Search), rc decreased (Expand Search)
a decrease » _ decrease (Expand Search), _ decreased (Expand Search), _ decreases (Expand Search)
026 decrease » _ decrease (Expand Search)
nn decrease » _ decrease (Expand Search), mean decrease (Expand Search), gy decreased (Expand Search)
c decrease » c decreased (Expand Search), _ decrease (Expand Search), rc decreased (Expand Search)
a decrease » _ decrease (Expand Search), _ decreased (Expand Search), _ decreases (Expand Search)
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781
<i>dVMAT</i> mutants show decreased histamine labeling in subretinal glia.
Published 2013“…Tangential views are shown in (A,C,D,F,G); the surface of the lamina is shown in (B) and (E). …”
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782
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783
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784
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785
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786
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787
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788
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789
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790
Aspirin decreases expression of NFκB and β-catenin in colon cancer cells.
Published 2013“…<p>Decreased p65/p50 in RKO (A) and SW480 (B) cells. Cells were treated for 48 hr with 5 or 10 mM, and whole cell, nuclear and cytosolic extracts were analyzed by western blot analysis as described in the <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0048208#s3" target="_blank">Experimental Procedures</a>. …”
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791
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792
Simultaneous ablation of Syt1 and Syt7 decreases the RRP size at excitatory synapses.
Published 2015“…<p><b>A & B.</b> Ablation of both Syt1 and Syt7 in hippocampal neurons decreases the RRP size at excitatory synapses in a manner that is rescued by WT Syt7 (Syt7<sup>WT</sup>) or Syt1 (Syt1<sup>WT</sup>) but not by mutant Syt7 (Syt7<sup>C2A</sup>*<sup>B</sup>*) or Syt1 (Syt1<sup>C2A</sup>*<sup>B</sup>*) with altered top-loop sequences containing the Ca<sup>2+</sup>-binding sequences (A, Syt7 rescue; B, Syt1 rescue). …”
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793
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794
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795
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796
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797
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798
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799
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800
Desmosomal Cadherins Are Decreased in Explanted Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy Patient Hearts
Published 2013“…Genetic studies have demonstrated the central role of desmosomal proteins in this disease, where 50% of patients harbor a mutation in a desmosmal gene. …”