Search alternatives:
akt decrease » awd decreased (Expand Search), ash decreased (Expand Search), a decreased (Expand Search)
a decrease » _ decreased (Expand Search), _ decreases (Expand Search)
m decrease » _ decreased (Expand Search), _ decreases (Expand Search), a decreased (Expand Search)
_ akt » _ art (Expand Search)
12 m » 12 mm (Expand Search), 12 mg (Expand Search), 12 _ (Expand Search)
akt decrease » awd decreased (Expand Search), ash decreased (Expand Search), a decreased (Expand Search)
a decrease » _ decreased (Expand Search), _ decreases (Expand Search)
m decrease » _ decreased (Expand Search), _ decreases (Expand Search), a decreased (Expand Search)
_ akt » _ art (Expand Search)
12 m » 12 mm (Expand Search), 12 mg (Expand Search), 12 _ (Expand Search)
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AKT inhibition decreases neuroblast populations.
Published 2012“…<p>(<b>A</b>) SOX2 expression upon PI3K-AKT inhibition. …”
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Loss of Trib2 decreases disease latency of Notch-driven T-ALL.
Published 2016“…Mice with a body condition score of ≤2 and decreased mobility were euthanized (n = 8 Trib2<sup>+/+</sup> and n = 12 Trib2<sup>-/-</sup> recipients. …”
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Activation of AKT, decrease in FOXO and activation of glycolytic genes in CERT heterozygous mice.
Published 2013“…A simple graphical model depicting metabolic reprogramming in <i>dcerk<sup>1</sup></i> due to increased AKT activation and decreased FOXO to maintain energy balance. …”
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Curcumin induces phosphorylation of p38 MAPK and decreases phosphorylation of Akt in RPE cells.
Published 2013Subjects: -
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mGluR5 receptor decreased glycinergic currents.
Published 2019“…CHPG, α-amino-2-chloro-5-hydroxybenzeneacetic acid; DHPG, (S)-3,5-Dihydroxyphenylglycine; GABA<sub>A</sub> receptor, γ-Aminobutyric acid type A receptor; GDP-β-S, Guanosine 5ʹ-O-(2-Thiodiphosphate); GlyR, glycine receptor; IPSC, inhibitory postsynaptic current; mGluR5, metabotropic glutamate receptor 5; MPEP, 6-Methyl-2-(phenylethynyl) pyridine; PD98059, 2ʹ-Amino-3ʹ-methoxyflavone; Ro-32-0432, 2-{8-[(Dimethylamino)methyl]-6,7,8,9-tetrahydropyrido[1,2-a]indol-3-yl}-3-(1-methyl-1H-indol-3-yl)maleimide.…”