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1 pic glutamate receptors, mGluR1a, mGluR2, or mGluR8.
2 at, except for the mouse cDNA clone encoding mGluR8.
3 pha-methyl-amino-phosphonobutyrate inhibited mGluR8.
4 ng either mGluR4, mGluR8, or both mGluR4 and mGluR8.
5 xpress either group II mGluR2/3 or group III mGluR8.
7 analyzed the mechanism of action underlying mGluR8 activity and modulation of the cytosolic Ca2+ con
8 ated the biological effects of the selective mGluR8 agonist (S)-3,4-dicarboxyphenylglycine ((S)-3,4-D
9 rents in Xenopus laevis oocytes coexpressing mGluR8 and G protein-coupled inwardly rectifying potassi
12 gh percentage of single-labeled mGluR2/3 and mGluR8 cells, there is a considerable population of doub
14 pression, with 75.0% of DRG cells expressing mGluR8, followed by group II, with 51.6% expressing mGlu
15 ic glutamate receptor (mGluR), type 8 mGluR (mGluR8), has been identified functionally as a presynapt
20 localization of the group III mGluR subtype, mGluR8, in the human body and investigated the biologica
23 role for mGluR8 in anxiety and suggest that mGluR8 may not be a therapeutic target for schizophrenia
26 These results suggest that the function of mGluR8 of modulating the cytosolic Ca2+ concentration an
29 glutamate activates presynaptic mGluR2/3 and mGluR8 receptors but not mGluR4, although this receptor
31 bands, corresponding to sublaminae 1-4; and mGluR8 was localized in two broad bands, one each in the
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