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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
4                                  Baclofen, a GABAB receptor agonist, activated G-protein gated inward
5 ]CGP54626 was inhibited by several mammalian GABA(B) receptor agonists and antagonists.
6      To explore this possibility a number of GABAB receptor agonists and antagonists were examined fo
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
10             Application of either GABA(A) or GABA(B) receptor agonists attenuated the colonic afferen
11      Effects of spinal administration of the GABA(B) receptor agonist baclofen (0.1-10 microg/50 micr
12                                          The GABA(B) receptor agonist baclofen (20 mum) enhanced GABA
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.
15           In C57BL/6 mice, pretreatment with GABA(B) receptor agonist baclofen blocked the rewarding
16 ent with a subthreshold concentration of the GABA(B) receptor agonist baclofen blocks ethanol but not
17                                          The GABA(B) receptor agonist baclofen decreased the rate of
18                                          The GABA(B) receptor agonist baclofen facilitates the extinc
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
24  values and a GIRK-dependent response to the GABA(B) receptor agonist baclofen, but not DAMGO.
25 mitter release from POMC neurons, as did the GABA(B) receptor agonist baclofen.
26                             In contrast, the GABAB receptor agonist baclofen (1-100 microM) exerted a
27                                 GABA and the GABAB receptor agonist baclofen activated a potassium co
28                                          The GABAB receptor agonist baclofen also inhibited inward cu
29                Simultaneous injection of the GABAB receptor agonist baclofen at doses of 2.5, 5.0 and
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
34                              The orthosteric GABAB receptor agonist baclofen has been shown to suppre
35        E2 reduced rapidly the potency of the GABAB receptor agonist baclofen to activate G-protein-co
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
38 eed, the calcium influx was inhibited by the GABAB receptor agonist baclofen.
39 sitivity of SOM-IPSCs, but not PV-IPSCs to a GABAb receptor agonist baclofen.
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
43                                          The GABA(B) receptor agonist (-)-baclofen (5-10 microM) depr
44               Systemic administration of the GABA(B) receptor agonist, baclofen (10 mg/kg, i.p.), sig
45                        In young animals, the GABA(B) receptor agonist, baclofen, inhibited the amplit
46                                Baclofen is a GABAB receptor agonist commonly used to relief spasticit
47 lcium Green-1 dextran revealed that 5HT1 and GABA(B) receptor agonists decreased presynaptic calcium
48                                      Whereas GABAB receptor agonists exert a significant effect on ci
49                           The application of GABAB receptor agonists failed to affect the membrane pr
50 ivity marker Fos, muscimol-baclofen (GABAa + GABAb receptor agonists) global inactivation, Daun02-sel
51          Application of baclofen, a specific GABA(B) receptor agonist, inhibited significantly neuron
52           Using microinjections of GABA(A) + GABA(B) receptor agonists (muscimol + baclofen) in media
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
57                                The selective GABAB receptor agonist R-baclofen previously reversed so
58                                          The GABAB receptor agonist (R)-baclofen (10 microM) reduced
59                                              GABA(B) receptor agonists reduce receptor phosphorylatio
60                                  GABA(A) and GABA(B) receptor agonists stimulate feeding following mi
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
64            Inhibition of calcium currents by GABAB receptor agonists was accompanied by an apparent c
65 rminals can be readily modulated, opioid and GABA(B) receptor agonists were applied.
66 of GHB was mimicked by baclofen, a selective GABAB receptor agonist, whereas the high affinity GHB re