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1 mGluR1alpha orthosteric antagonist (S)-alpha-methyl-4-carboxyphenylglycine.
2 he group I mGluR antagonist MCPG [(RS)-alpha-methyl-4-carboxyphenylglycine, 50-500 mum] on persistent
3 e group I/II-specific antagonist (R,S)-alpha-methyl-4-carboxyphenylglycine and the group III-specific
4                                          (S)-Methyl-4-carboxyphenylglycine, L-(+)-2-amino-3-phosphono
5  the metabotropic receptors 1 (mGluR1), +/-2-methyl-4-carboxyphenylglycine (LY367385), and mGluR5, 2-
6 nylglycine (4CPG) or mGluR1 antagonist (+)-2-methyl-4-carboxyphenylglycine (LY367385).
7 ibited by the metabotropic antagonists alpha-methyl-4-carboxyphenylglycine (MCPG) and 1-aminoindan-1,
8          The broad-spectrum antagonist alpha-methyl-4-carboxyphenylglycine (MCPG) and/or (RS)-alpha-c
9  antagonism of group 1 mGluRs with (S)-alpha-methyl-4-carboxyphenylglycine (MCPG) did not result in s
10 he APB-insensitive receptor antagonist alpha-methyl-4-carboxyphenylglycine (MCPG) does not block the
11  Over the past few years, the compound alpha-methyl-4-carboxyphenylglycine (MCPG) has been widely use
12  glutamate receptor (mGluR) antagonist alpha-methyl-4-carboxyphenylglycine (MCPG) strongly attenuated
13            The mGluR antagonist (R, S)-alpha-methyl-4-carboxyphenylglycine (MCPG) was infused into th
14 ulfamoylbenzo[f]quinoxaline (NBQX) and alpha-methyl-4-carboxyphenylglycine (MCPG) were evaluated agai
15 ed the effect of the infusion of (+/-)-alpha-methyl-4-carboxyphenylglycine (MCPG), a metabotropic glu
16  a non-selective mGluR antagonist, (S)-alpha-methyl-4-carboxyphenylglycine (MCPG), into the dorsal st
17 botropic glutamate receptor antagonist alpha-methyl-4-carboxyphenylglycine (MCPG).
18 d by the broad spectrum mGluR antagonist (S)-Methyl-4-carboxyphenylglycine (MCPG).
19 liminated by the mGluR antagonist (RS)-alpha-methyl-4-carboxyphenylglycine (MCPG; 500 microM) and by
20 on of the mGlu receptor antagonist (+)-alpha-methyl-4-carboxyphenylglycine (MCPG; 500 microM).
21 opic glutamate receptor antagonist (+)-alpha-methyl-4-carboxyphenylglycine ((+)-MCPG; 1000 microM) bu
22  the broadly acting mGluR antagonist S-alpha-methyl-4-carboxyphenylglycine (S-MCPG).

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