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1 idue with N-(2-bromoethyl)-3-oxidopyridinium hydrobromide.
2 ce microscope tip coated with poly-dl-lysine hydrobromide.
3 on with 6-(bromomethyl)-2,4-pteridinediamine hydrobromide.
4 ethoxyphenyl)-1(6H)-p yridazinebutanoic acid hydrobromide]).
5 nd tested under the influence of scopolamine hydrobromide (0.2 or 0.5 mg/kg, intraperitoneal) after a
6 t with the muscarinic antagonist scopolamine hydrobromide (1.5-6 mg/kg) potentiated the response to A
10 ation of the antimuscarinic drug scopolamine hydrobromide (4 microg/kg intravenously) compared with p
12 +/-)-8-hydroxy-2-di-(n-propylamino) tetralin hydrobromide; 5-HT(1A) agonist; in vivo] reduced respira
13 injection of 25 microg of 6-hydroxydopamine hydrobromide (6-OHDA) midway between the two implant sit
14 mino-8-hydroxy-1,2,3,4-tetrahydronaphthalene hydrobromide (8-OH-DPAT) (10 nmol), when microinjected b
15 onist 8-hydroxy-N,N-dipropyl-2-aminotetralin hydrobromide (8-OH-DPAT) was inhibited completely by per
17 agonist, (+)-8-hydroxy-dipropylaminotetralin hydrobromide (8-OHDPAT) (50 pmol, 2.0 and 3.0 nmol), int
19 withdrawal and concomitant use of citalopram hydrobromide, a phenomenon that has been rarely reported
20 fied with (2-aminoethyl)methanethiosulfonate hydrobromide, a reagent that restores positive charge at
22 ate nasal spray and zolmitriptan, eletriptan hydrobromide, almotriptan malate, and rizatriptan benzoa
23 3-hydroxy-5-methylisoxazole-4-propionic acid hydrobromide (AMPA) interact additively to evoke [3H]ACh
24 3-hydroxy-5-methylisoxazole-4-propionic acid hydrobromide (AMPA) receptor function at endogenously ac
25 MMP-13 expression was inhibited by CCT031374 hydrobromide, an inhibitor of the canonical Wnt/beta-cat
26 ass were synthesized starting from arecoline hydrobromide and obtained in optically pure form through
27 mino-7-hydroxy-1,2,3,4-tetrahydronaphthalene hydrobromide and PD 168,077 maleate did not produce such
28 loro-7,8-dihydroxy-1-phenyl-1H-3-benzazepine hydrobromide) and the D2-like agonist quinelorane both f
29 the linker bromoacetyl hydrazinonicotinamide hydrobromide (BAHNH) conjugated site specifically at pro
30 ,6-dimethoxybenzocyclobuten-1-yl)methylamine hydrobromide, binds less to the mGlu2 promoter in fronta
31 c interneurons via dihydro-beta-erythroidine hydrobromide (DHbetaE)-insensitive nicotinic receptors.
32 ino-8-hydroxy-1,2,3, 4-tetrahydronaphthalene hydrobromide (DPAT), with an EC(50) of approximately 10
33 +/-)-8-hydroxy-2-(di-n-propylamino)tetralin) hydrobromide] (DPAT), which acts on autoreceptors and in
34 hloride, bupropion hydrochloride, citalopram hydrobromide, duloxetine hydrochloride, escitalopram oxa
35 ed by solvent precipitation of triethylamine hydrobromide, enabled their regiospecific ring-opening a
36 NTS: Randomized clinical trial of citalopram hydrobromide for children and adolescents with autism sp
38 oxetine hydrochloride initiation: citalopram hydrobromide, hazard ratio = 1.00 (95% confidence interv
39 or cells (hNPCs) and found that hippeastrine hydrobromide (HH) and amodiaquine dihydrochloride dihydr
40 of this series were prepared from arecoline hydrobromide in optically pure form and were evaluated f
41 ivatives ((2-aminoethyl)methanethiosulfonate hydrobromide (MTSEA) and [(2-(trimethylammonium)ethyl]me
43 d inside 2-(aminoethyl)-methanethiosulfonate hydrobromide (MTSEA) Further study of those mutants show
44 e reagent 2-(aminoethyl)methanethiosulfonate hydrobromide (MTSEA) in membrane preparations from trans
45 of 2.5 mM 2-aminoethyl methanethiosulfonate hydrobromide (MTSEA) or 1 mM [2-(trimethylammonium) ethy
47 AT), 25 ng (5-aminomethyl-3-hydroxyisoxazole)hydrobromide (muscimol), 10 ng bicuculline or a combinat
48 (-)-2,10,11-trihydroxy-N-propyl-noraporphine hydrobromide (NPA) also causes translocation of delta an
49 st 2,10,11-trihydroxy-N-propylnorapomorphine hydrobromide (NPA) involve both epsilon protein kinase C
51 mino-7-hydroxy-1,2,3,4-tetrahydronaphthalene hydrobromide, or PD 168,077 maleate (D(2)-like, D(2), D(
52 onsisting of the polypeptide, poly(l-lysine) hydrobromide, poly(l-lysine) and the polymeric dipeptide
53 (+/-)-8-hydroxy-2-(di-N-propylamino)tetralin hydrobromide rapidly stimulated proton efflux that was b
54 l-phenyl-2,3,4,5-tetrahydro-1H-3-benzazepine hydrobromide] reversed AMPAR responsiveness in cocaine w
57 n efficient synthesis of S-allyl thioimidate hydrobromide salts via coupling of thioamides with allyl
58 ubcutaneous injections of either scopolamine hydrobromide (SCOP; 0.5 mg/0.2 mL) or saline (SAL) four
59 hydrate-resistant, dihydro-beta-erythroidine hydrobromide-sensitive nicotinic currents elicited by 3-
60 3,4,5-tetrahydro-(1H)-3-benzazepine-7,8-diol hydrobromide] significantly increased EPSC amplitude, wh
62 2,3,4,5-tetrahydro-1-phenyl-1H-3-benzazepine hydrobromide (SKF81297) (1-10 microm) nor the D2-like ag
63 1-phenyl-2,3,4,5-tetrahydro-1H-3-benzazepine hydrobromide (SKF81297) altered EphA5, EphrinA1, EphrinA
64 4-methoxyphenyl)pyridazin-1-yl]butanoic acid hydrobromide (SR-95531; antagonist), pentobarbital (allo
65 ,6-dimethoxybenzocyclobuten-1-yl)methylamine hydrobromide (TCB-2) enhanced C-fiber-evoked dorsal horn
67 The mean (SD) maximum dosage of citalopram hydrobromide was 16.5 (6.5) mg/d by mouth (maximum, 20 m
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