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1 red to control groups (measured with the BBB open field test).
2 c knock-out (Hdc KO) mice was assessed in an open field test.
3 vated plus maze, the light/dark box, and the open field test.
4 ted to the tail suspension test (TST) and an open field test.
5 ion, locomotor activity was studied using an open field test.
6 avioral testing, including a protocol for an open field test.
7 lso was demonstrated to be anxiolytic in the open field test.
8 bic areas signal movement during the TST and open field test.
9 -GABAARs increased time in the center in the open-field test.
10 s, 60 min before the tail suspension test or open-field test.
11 e animals were tested in the forced swim and open field tests.
12 tified in all cohorts using the cylinder and open field tests.
13 ted with mouse hyperactivity in homecage and open field tests.
14 d place preference, pre-pulse inhibition and open-field tests.
15 less exploratory activity during Y-maze and open-field tests.
16 behaviors, tested by elevated plus-maze and open-field tests.
17 like behaviors in the elevated plus maze and open-field tests.
18 rcles for hours on end, both in cages and in open-field tests.
19 eference and increased locomotor activity in open-field testing.
20 assessed via 1) neurologic testing and 2) an open-field test 24 hours after subarachnoid hemorrhage,
21 We discovered significant alterations in an open field test, a novel object recognition test and in
22 e behaved similarly as wild-type mice in the open field test and in the elevated plus maze test of an
24 ime, ambulatory behavior, and rearing in the open-field test and decreased the number of entrances an
27 eg, posture, bradykinesia) and behaviorally (open field test), and their brains were processed for im
28 reezing time and time spent in the center in open field test, and entries and duration in the novel a
30 phenotype in both the elevated plus maze and open field tests, and increased the startle response.
31 ogenic profile in the elevated plus-maze and open field tests, and reduced social exploration of unfa
32 e showed behavioral avoidance of light in an open-field test, and they could discriminate a light sti
34 sures of spontaneous movement and gait in an open-field test declined as expected in control lesioned
37 exhibited fewer stereotypic movements in the open field test, higher baseline startle responses in th
39 normalities including hyperlocomotion in the open field test, impaired coordination and balance in th
40 comparable to that of wild-type mice in the open-field test, in which, however mSOD1 exhibited incre
41 tant mice had a hyperactive phenotype in the open field test, independent of sex, and were more sensi
42 No psychostimulant effect was shown in the open-field test, indicating that the effects in the tail
44 mphetamine-stimulated hyperlocomotion in the open field test, it restored d-amphetamine-disrupted pre
46 re conducted to assess exploratory activity (open field test, light-dark box test) and cognitive func
52 he elevated plus maze and thigmotaxis in the open field test revealed increased anxiety-like behavior
57 he rats exhibited improved motor function as open-field tests showed higher activity scores for runne
58 poactive in a test for exploratory behavior (open-field test), showing markedly reduced locomotion an
60 ed locomotion in both elevated plus-maze and open field tests, suggesting heightened novelty-induced
61 mice developed greater locomotor deficits in open-field tests than wild-type mice following low oral
62 manifested by 4.5-mo-old Naglu-/- mice in an open field test; the hyperactivity that is characteristi
64 aze which provides a measure of anxiety, the open field test which provides a measure of anxiety and
65 est phenotypic differences were found in the open field test, which maximizes avoidance behavior.
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