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1 nvulsant against seizures induced by maximal electroshock.
2 eased threshold to tonic seizures induced by electroshock.
4 nic stimulation in Fring's mice, and maximal electroshock and subcutaneous pentylenetetrazol (Metrazo
5 pe can be measured in larval stages using an electroshock assay, and this behavior in bs mutants is d
6 vulsants against seizures induced by maximal electroshock (ED50 = 41, 55, and 74 mg/kg, respectively)
8 d in mice for their ability to block maximal electroshock-induced convulsions and ATPA-induced rigidi
9 t anticonvulsant activity in a mouse maximum electroshock-induced seizure (MES) assay: the ED50 was 2
11 th potent anticonvulsants in a mouse maximal electroshock-induced seizure (MES) study (ED(50) (iv) =
14 ntraperitoneal (i.p.) dosing for the maximal electroshock-induced seizure test for 18 and 19 were 8.3
15 osemide suppressed the occurrence of maximal electroshock-induced seizures in a dose-dependent manner
19 oral anticonvulsant activity against maximal electroshock (MES) and subcutaneous metrazol (scMET) mod
20 s comparatively evaluated in the rat maximal electroshock (MES) and subcutaneous metrazol (scMet) sei
21 rogram for seizure protection in the maximal electroshock (MES) and subcutaneous Metrazol models.
24 jected to acute seizure induction by maximal electroshock (MES) or pilocarpine, variably including el
26 pronounced seizure protection in the maximal electroshock (MES) seizure test with activities similar
27 d animal seizure models, namely, the maximal electroshock (MES) test and the psychomotor 6 Hz (32 mA)
29 clinical seizure models, namely, the maximal electroshock (MES) test, the subcutaneous pentylenetetra
30 y in the pentylenetetrazol (PTZ) and maximal electroshock (MES) tests following ip administration in
34 nd quinoxalin-4-ones were active in an acute electroshock physical dependence side effect assay in mi
35 otent anticonvulsant activity in the maximal electroshock seizure (MES) test (ca. 8 times greater tha
36 ivities in animal models, and in the maximal electroshock seizure test the activity of (3'-trifluorom
37 dissect the multifactorial nature of maximal electroshock seizure threshold (MEST) in C57BL/6 (B6) an
40 nds were active in the mouse and rat maximal electroshock tests but not in the mouse metrazole test.
42 lsive shock (ECS) was used to assess maximal electroshock threshold (MET) in B6, D2 and hybrid mice.
43 s in freely moving rats subjected to maximal electroshock to simultaneously measure glucose, lactate,
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