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1 l drug ecstasy, is a potent serotonin (5-HT) releaser.
2 of the DAT to other uptake blockers, but not releasers.
3  in BAT had lower basophil count compared to releasers (249 vs 630 counts/min).
4 nd phentermine, as well as a non-amphetamine releaser, 4-benzylpiperidine, were all unaffected.
5 as a rich pharmacology including inhibitors, releasers (amphetamines, which promote the exchange mode
6 ur 4-year long study and cycling between the releaser and nonreleaser phenotypes occurred at least on
7                In addition, MDMA is a potent releaser and reuptake inhibitor of presynaptic serotonin
8         D-Fenfluramine, a putative serotonin releaser and reuptake inhibitor, is commonly prescribed
9 e is a serotonin (5-hydroxytryptamine, 5-HT) releaser and reuptake inhibitor.
10                    Fenfluramine, a serotonin releaser and uptake inhibitor, has been widely prescribe
11 brid' activity as a SERT substrate (ie, 5-HT releaser) and DAT blocker, whereas 4-MePPP is a blocker
12 trosoglutathione (GSNO, widely used as an NO releaser) and sodium nitroprusside (SNP, which is a NO+
13 ethyl 4-MA was an efficacious substrate-type releaser at DAT that evoked an inward depolarizing curre
14 n uptake blocker at low concentrations and a releaser at high concentrations.
15 Methylone, MDC, and HHMC were substrate-type releasers at monoamine transporters as determined in vit
16 sion was generally lower in nonreleaser than releaser basophils.
17                                           In releaser cells, FcepsilonRI cross-linking up-regulated >
18 tions of a newly identified water-soluble CO releaser (CORM-A1) that, unlike the first prototypic mol
19 Apis mellifera, possess unrelated primer and releaser functions for the workers and act as a sex attr
20 mine, an indirect presynaptic norepinephrine releaser, into dorsal hand veins of 49 normotensive men
21      We report that exposure to the dopamine releaser methamphetamine for 10 days elicits a long-last
22 creased stereotypic response to the dopamine releaser, methamphetamine, and an insensitivity to the a
23                       Finally, although a DA releaser, muscimol was neither self-administered in drug
24 pase A2alpha (cPLA2alpha), the rate-limiting releaser of arachidonic acid used for pro-inflammatory e
25  (HYCOs) that combine an Nrf2 inducer with a releaser of carbon monoxide (CO), an anti-inflammatory p
26 LHRH and AA, whereas sodium nitroprusside, a releaser of NO, stimulated LH and FSH release.
27 ethamphetamine (MDMA, Ecstasy) is a powerful releaser of serotonin.
28         The toil of 3 billion years by these releasers of molecular oxygen finally triggered the Camb
29  These consumers of carbon dioxide were also releasers of molecular oxygen.
30 igated the effect of FK409, a spontaneous NO releaser, on the development of allograft vasculopathy,
31 inhibitor and as a prodrug for the monoamine-releaser phenmetrazine (PM), and it may serve as a clini
32         The main component, 9-ODA, acts as a releaser pheromone by attracting workers to the queen an
33 nteraction with the DAT as a pure blocker or releaser rather than their structural similarity to coca
34 given these compounds function as primer and releaser signals that regulate the social organization o
35  dilation in the piglet, responses to the NO releasers SNP and SNAP are unchanged by the Kca channel
36   The potencies of amphetamine-like dopamine releasers such as 3,4-methylenedioxymethamphetamine, met
37                                    Monoamine releasers such as d-amphetamine constitute one class of
38 methamphetamine (MDMA) is a potent monoamine releaser that produces an acute euphoria in most individ
39 ty of different dopamine uptake blockers and releasers to inhibit dopamine uptake, measured using fas
40 ed c-fos induction by the specific serotonin releaser-uptake inhibitor dexfenfluramine and alteration
41 (via the parent drug PDM) and as a monoamine releaser (via the active metabolite PM).
42                         PCA is a potent 5-HT releaser which can induce gliosis in the rodent brain.
43  intrinsic biochemical behavior of a slow CO releaser, which may be advantageous in the treatment of
44                     MDMA, a potent monoamine-releaser with particularly pronounced serotonin- releasi

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