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1 le compared with the prototypic hallucinogen lysergic acid diethylamide.
2 telet membrane 5-HT2A receptors by using [3H]lysergic acid diethylamide.
3 etanserin (100 nM), mesulergine (100 nM) and lysergic acid diethylamide (1 microM) significantly redu
5 inding affinities were determined using [3H]-lysergic acid diethylamide ([3H]-LSD) binding to cell me
6 ted by 33% of the sample, most commonly LSD (lysergic acid diethylamide), amphetamines, Ecstasy (meth
9 ed the PLC-IP pathway, whereas others (e.g., lysergic acid diethylamide) favored the PLA2-AA pathway.
10 emical studies showing that the hallucinogen lysergic acid diethylamide, its precursor ergotamine (ER
12 uestions were asked about: use of ayahuasca, lysergic acid diethylamide (LSD) and magic mushrooms; de
13 ng method for quantitation of (3)H-labeled d-lysergic acid diethylamide (LSD) binding to recombinant
14 40 years, there is renewed interest in using lysergic acid diethylamide (LSD) in clinical psychiatric
17 ies have started to elucidate the effects of lysergic acid diethylamide (LSD) on the human brain but
18 -)-2,5-dimethoxy-4-iodoamphetamine (DOI) and lysergic acid diethylamide (LSD) stimulated a head-twitc
20 However, other 5-HT2A receptor ligands like lysergic acid diethylamide (LSD), in which the amine nit
21 nogens, including mescaline, psilocybin, and lysergic acid diethylamide (LSD), profoundly affect perc
23 ds of recent other drug use (eg, cocaine and lysergic acid diethylamide; odds ratio [OR], 1.73; 95% C
25 hallucinogenic drugs, such as psilocybin and lysergic acid diethylamide, require the 2AR and resemble
26 ne (selective for the 5-HT2C receptor) and d-lysergic acid diethylamide (selective for the 5-HT2A rec
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