Search alternatives:
nn decrease » mean decrease (Expand Search), gy decreased (Expand Search), b1 decreased (Expand Search)
wt decrease » we decrease (Expand Search), awd decreased (Expand Search), step decrease (Expand Search)
_ decrease » _ decreased (Expand Search)
a decrease » _ decreased (Expand Search), _ decreases (Expand Search)
30 a » 30 _ (Expand Search), 30 c (Expand Search), 3 a (Expand Search)
nn decrease » mean decrease (Expand Search), gy decreased (Expand Search), b1 decreased (Expand Search)
wt decrease » we decrease (Expand Search), awd decreased (Expand Search), step decrease (Expand Search)
_ decrease » _ decreased (Expand Search)
a decrease » _ decreased (Expand Search), _ decreases (Expand Search)
30 a » 30 _ (Expand Search), 30 c (Expand Search), 3 a (Expand Search)
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TMD residues decrease sensitivity.
Published 2017“…Glu residues are color coded based upon effect, with residues in red producing a significant decrease in pH<sub>50</sub>, and in yellow, an insignificant or weak effect, whereas the dark purple and magenta for His residues are synonymous to the red of Glu residues. …”
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Developmental Defects Observed among WT Strains after Decreasing Hsp90 Function at 30% Epiboly
Published 2007Subjects: -
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Decreased dendritic spine density and mEPSC amplitude in the DG of Arf4<sup>+/−</sup> mice compared to WT mice.
Published 2013“…(<i>C</i>) Spine densities for specific spine subtypes in the DG of WT and Arf4<sup>+/−</sup> mice. (<i>D–F</i>) Electrophysiological recordings reveal a decrease in amplitude of mEPSCs in Arf4<sup>+/−</sup> (n = 9 cells) compared to WT controls (n = 6 cells) at 2 months of age. …”
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Simultaneous ablation of Syt1 and Syt7 decreases the RRP size at inhibitory synapses: Rescue by WT but not mutant Syt1 or Syt7.
Published 2015“…Recordings were performed in the presence of 1 μM tetrodotoxin, 20 μM CNQX, and 50 μM AP5 to isolate inhibitory currents. <b>B.</b> Simultaneous ablation of Syt1 and Syt7 decreases the RRP size of inhibitory synapses in a manner that is rescued by WT Syt7 (Syt1<sup>WT</sup>) but not Syt7 with mutations in the top C2 domain sequences containing the Syt7 Ca<sup>2+</sup> binding sites (Syt7<sup>C2A</sup>*<sup>B</sup>*). …”
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