Search alternatives:
non decrease » nn decrease (Expand Search), point decrease (Expand Search), note decreased (Expand Search)
ht decrease » nn decrease (Expand Search), we decrease (Expand Search), step decrease (Expand Search)
a decrease » _ decreased (Expand Search), _ decreases (Expand Search)
_ decrease » _ decreased (Expand Search)
a non » _ non (Expand Search)
5 ht » 5 h (Expand Search)
non decrease » nn decrease (Expand Search), point decrease (Expand Search), note decreased (Expand Search)
ht decrease » nn decrease (Expand Search), we decrease (Expand Search), step decrease (Expand Search)
a decrease » _ decreased (Expand Search), _ decreases (Expand Search)
_ decrease » _ decreased (Expand Search)
a non » _ non (Expand Search)
5 ht » 5 h (Expand Search)
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Changes in neural activity were decreased in animals pre-exposed to 5-HT and <i>mod-1</i> mutants when the worms switched their locomotive direction.
Published 2019“…(F) Decreasing levels of RID neural activity during the transition periods from forward to backward locomotion in mock, 5-HT pre-exposed (p = 1.3 × 10<sup>−3</sup>), and <i>mod-1</i> mutant (p = 5.4 × 10<sup>−4</sup>) animals. …”
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Demographic of the study participants, urinary arsenic species and IL-17A cytokine.
Published 2022Subjects: -
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PBA decreases ER stress induced apoptosis.
Published 2010“…With the addition of 1 mM PBA, the number of detached cells decreased to non-statistically significant levels in the tunicamycin and thapsigargin treated cells, while the numbers remained statistically different in the BFA treated cells. …”
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Pharmacological Mechanism of the Non-hallucinogenic 5‑HT<sub>2A</sub> Agonist Ariadne and Analogs
Published 2022“…Ariadne emerges as a prototype of a new drug class, non-hallucinogenic 5-HT<sub>2A</sub> agonists, with considerable therapeutic potential across psychiatric and neurological indications.…”
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Pharmacological Mechanism of the Non-hallucinogenic 5‑HT<sub>2A</sub> Agonist Ariadne and Analogs
Published 2022“…Ariadne emerges as a prototype of a new drug class, non-hallucinogenic 5-HT<sub>2A</sub> agonists, with considerable therapeutic potential across psychiatric and neurological indications.…”
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