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"law p y"的相關文件
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| 國立成功大學 |
2022 |
Selective and antagonist-dependent �-opioid receptor activation by the combination of 2-{[2-(6-chloro-3,4-dihydro-1(2H)-quinolinyl)-2-oxoethyl]sulfanyl}-5-phenyl-4,6-(1H,5H)-pyrimidinedione and naloxone/naltrexone
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Lin, S.-Y.;Tien, Y.-W.;Ke, Y.-Y.;Chang, Y.-C.;Chang, H.-F.;Ou, L.-C.;Law, P.-Y.;Xi, J.-H.;Tao, P.-L.;Loh, H.H.;Chao, Y.-S.;Shih, C.;Chen, Chen C.-T.;Yeh, S.-H.;Ueng, S.-H. |
| 臺大學術典藏 |
2021-09-04T06:12:20Z |
Intrathecal delivery of a mutant μ-opioid receptor activated by naloxone as a possible antinociceptive paradigm
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JIA-HORNG KAO; Chen S.L.; Ma H.I.; Law P.Y.; Tao P.L.; Loh H.H. |
| 國立成功大學 |
2019 |
The in vivo antinociceptive and μ-opioid receptor activating effects of the combination of N-phenyl-2′,4′-dimethyl-4,5′-bi-1,3-thiazol-2-amines and naloxone
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Lin, S.-Y.;Kuo, Y.-H.;Tien, Y.-W.;Ke, Y.-Y.;Chang, W.-T.;Chang, H.-F.;Ou, L.-C.;Law, P.-Y.;Xi, J.-H.;Tao, P.-L.;Loh, H.H.;Chao, Y.-S.;Shih, C.;Chen, Chen C.-T.;Yeh, S.-H.;Ueng, S.-H. |
| 臺大學術典藏 |
2018-09-10T08:16:49Z |
Intrathecal delivery of a mutant μ-opioid receptor activated by naloxone as a possible antinociceptive paradigm
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Kao, J.H.;Chen, S.L.;Ma, H.I.;Law, P.Y.;Tao, P.L.;Loh, H.H.; JIA-HORNG KAO |
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