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1 a2-adrenergic (alpha2AR), cannabinoid 1, and serotonin 1A receptors.
2 anophenylthio) benzylamine ([(11)C]DASB) and serotonin 1A receptor ([(18)F]MPPF) levels between four
8 lines of evidence demonstrate involvement of serotonin 1A receptors (5-HT1ARs) in the pathophysiology
11 ng to investigate modulations of the DMN via serotonin-1A receptors (5-HT(1A)), separated for 5-HT au
13 cohort also underwent (11)C-WAY100635 scans (serotonin-1A receptor [5-HT1A]), we examined whether usi
19 he daytime regulation of core temperature by serotonin 1A receptors appears normal in seasonal affect
25 he 5'-flanking region of the mouse and human serotonin 1a receptor gene have been analyzed by RNA 5'
26 articipate in regulating expression from the serotonin 1a receptor gene promoter, and it raises the p
31 pyl)aminotetralin (8-OH-DPAT), an agonist at serotonin-1A receptors, is altered in the midbrain of su
32 ompartments of each arena and were larger in serotonin 1A receptor knockout mice, a genetic model of
33 During neonatal hippocampal development, serotonin 1A receptor-mediated signaling initially emplo
35 and (3) the core hypothermic response to the serotonin 1A receptor partial agonist ipsapirone hydroch
36 an emphasis on the contribution of different serotonin 1A receptor populations to mood and behavior.
37 e of serotonin, which in turn impacts on the serotonin 1A receptor system, by modulating its availabi
38 increase in the binding of [3H]8-OH-DPAT to serotonin-1A receptors was detected in the entire DR and
41 ist activation of muscarinic m2 receptors or serotonin 1A receptors were dramatically accelerated by
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