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1 thing medium or mimicked by adding baclofen (GABA(B) receptor agonist; 100 microM) to normally-record
5 quantify the relative binding affinities of GABA(B) receptor agonists, antagonists and the effect of
8 u-opioid receptor agonist DAMGO (93%) or the GABA(B) receptor agonist baclofen (83%) with a membrane
9 arizing response of GABAergic neurons to the GABA(B) receptor agonist baclofen 24 hr after treatment.
11 ent with a subthreshold concentration of the GABA(B) receptor agonist baclofen blocks ethanol but not
14 L-type Ca(2+) channel current induced by the GABA(B) receptor agonist baclofen or by guanosine 5'-3-O
15 of VDCCs nor their inhibition by either the GABA(B) receptor agonist baclofen or intracellular guano
16 With G-protein inhibition induced by the GABA(B) receptor agonist baclofen or the adenosine A1 re
17 -estradiol (E(2)) reduced the potency of the GABA(B) receptor agonist baclofen to activate G protein-
18 crease in intracellular calcium, whereas the GABA(B) receptor agonist baclofen was ineffective, sugge
25 ong-term ( approximately 5 years) use of the GABAb receptor agonist baclofen by SCI patients reduced
26 used by a lack of GIRK activity, because the GABAB receptor agonist baclofen continued to elicit thes
27 ne methiodide had little effect, whereas the GABAB receptor agonist baclofen dramatically attenuated
28 f the GABAA receptor agonist muscimol or the GABAB receptor agonist baclofen elicited intense, dose-r
31 ve activation, are minimally affected by the GABAB receptor agonist baclofen, and express NMDA recept
32 ted the effects of estrogen on DAMGO- or the GABAB receptor agonist baclofen-stimulated [35S]GTPgamma
35 ulation of astrocytes, or application of the GABAB-receptor agonist baclofen, potentiated miniature i
36 a 5-HT2C receptor antagonist (SB242084) or a GABAB receptor agonist (baclofen), but not a GABAA recep
37 s were reversibly inhibited by the selective GABA(B) receptor agonists (+/-)-baclofen or CGP 27492 (1
42 lcium Green-1 dextran revealed that 5HT1 and GABA(B) receptor agonists decreased presynaptic calcium
46 ect of LH reversible inactivation by GABAA + GABAB receptor agonists (muscimol + baclofen) on this ef
47 versible inactivation of CeA or BLA by GABAA+GABAB receptor agonists (muscimol+baclofen, 0.03+0.3 nmo
48 e protective effect of baclofen, a selective GABA(B) receptor agonist, on the induced Fos protein inc
53 e prevention, we examined whether baclofen-a GABAB receptor agonist that reduces mesolimbic dopamine
56 of GHB was mimicked by baclofen, a selective GABAB receptor agonist, whereas the high affinity GHB re
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