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1 astric distension that could be rescued with GABA(B) receptor agonist.
2 30 mg of arbaclofen (STX209), a GABA type B (GABA(B)) receptor agonist.
3 thing medium or mimicked by adding baclofen (GABA(B) receptor agonist; 100 microM) to normally-record
7 and DMS with muscimol+baclofen (GABA(a) and GABA(b) receptor agonists) and then tested them for rela
8 promoted by 4-aminopyridine and inhibited by GABA(B) receptor agonists, and appears far more sensitiv
9 quantify the relative binding affinities of GABA(B) receptor agonists, antagonists and the effect of
13 u-opioid receptor agonist DAMGO (93%) or the GABA(B) receptor agonist baclofen (83%) with a membrane
14 arizing response of GABAergic neurons to the GABA(B) receptor agonist baclofen 24 hr after treatment.
16 ent with a subthreshold concentration of the GABA(B) receptor agonist baclofen blocks ethanol but not
19 L-type Ca(2+) channel current induced by the GABA(B) receptor agonist baclofen or by guanosine 5'-3-O
20 of VDCCs nor their inhibition by either the GABA(B) receptor agonist baclofen or intracellular guano
21 With G-protein inhibition induced by the GABA(B) receptor agonist baclofen or the adenosine A1 re
22 -estradiol (E(2)) reduced the potency of the GABA(B) receptor agonist baclofen to activate G protein-
23 crease in intracellular calcium, whereas the GABA(B) receptor agonist baclofen was ineffective, sugge
30 ong-term ( approximately 5 years) use of the GABAb receptor agonist baclofen by SCI patients reduced
31 used by a lack of GIRK activity, because the GABAB receptor agonist baclofen continued to elicit thes
32 ne methiodide had little effect, whereas the GABAB receptor agonist baclofen dramatically attenuated
33 f the GABAA receptor agonist muscimol or the GABAB receptor agonist baclofen elicited intense, dose-r
36 ve activation, are minimally affected by the GABAB receptor agonist baclofen, and express NMDA recept
37 ted the effects of estrogen on DAMGO- or the GABAB receptor agonist baclofen-stimulated [35S]GTPgamma
40 ulation of astrocytes, or application of the GABAB-receptor agonist baclofen, potentiated miniature i
41 a 5-HT2C receptor antagonist (SB242084) or a GABAB receptor agonist (baclofen), but not a GABAA recep
42 s were reversibly inhibited by the selective GABA(B) receptor agonists (+/-)-baclofen or CGP 27492 (1
47 lcium Green-1 dextran revealed that 5HT1 and GABA(B) receptor agonists decreased presynaptic calcium
50 ivity marker Fos, muscimol-baclofen (GABAa + GABAb receptor agonists) global inactivation, Daun02-sel
53 nally, we used local infusion of GABA(A) and GABA(B) receptor agonists (muscimol + baclofen) to show
54 ect of LH reversible inactivation by GABAA + GABAB receptor agonists (muscimol + baclofen) on this ef
55 versible inactivation of CeA or BLA by GABAA+GABAB receptor agonists (muscimol+baclofen, 0.03+0.3 nmo
56 e protective effect of baclofen, a selective GABA(B) receptor agonist, on the induced Fos protein inc
61 odification generates a potent and selective GABA(B) receptor agonist that inhibits Ca(v)2.2 channels
62 e prevention, we examined whether baclofen-a GABAB receptor agonist that reduces mesolimbic dopamine
63 as attenuated in the presence of GABA(A) and GABA(B) receptor agonists, the VMR was only consistently
66 of GHB was mimicked by baclofen, a selective GABAB receptor agonist, whereas the high affinity GHB re