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1 dation, catalepsy, or learning impairment in passive avoidance.
2 NT-3 did not influence locomotor activity or passive avoidance.
3 findings bridge rodent and human research on passive avoidance and behavioral inhibition and furnish
4 sponses to learn aversive situations (in the passive avoidance and fear conditioning tests) and an im
5 rotein mice worsened the memory retention in passive avoidance and novel object recognition tests, an
6 n memory retention for temporal dissociative passive avoidance and object recognition memory.
7 , in two different learning paradigms, mouse passive avoidance and rat spatial memory.
8 sions of the nucleus basalis interfered with passive avoidance and spatial memory-related behaviors.
9 tor subtypes in Xenopus oocytes; (2) improve passive avoidance and spatial Morris water task performa
10         Weight gain, fertility, habituation, passive avoidance, and locomotor activities are similar
11 anagement of food allergy has shifted from a passive avoidance approach to active interventions that
12                                       In the passive avoidance assay, tropicamide treatment resulted
13 easured in the same cohort of mice using the passive avoidance assay.
14 s showed analogous behavior by adapting both passive avoidance behavior and behavioral inhibition to
15 he hippocampus with patients showing reduced passive avoidance behavior and inhibition across all thr
16              DMXB (0.5 mg/kg, i.p.) improved passive avoidance behavior in lesioned animals in a meca
17  the emergence of cold hypersensitivity, and passive avoidance behavior.
18 and attenuated nicotine-dependent changes in passive avoidance behavior.
19 diated alterations of neuronal structure and passive avoidance behavior.
20 hology was correlated with improvements in a passive avoidance behavioral task in Tg2576 mice.
21 n System, which controls "anxiety" (conflict/passive avoidance) but not "fear" (withdrawal/active avo
22 tion specifically when it is punished, as in passive avoidance, but act when it is beneficial, as in
23 changes in associative memory by employing a passive avoidance conditioning task.
24                               No deficits in passive avoidance conditioning were measured among the 4
25  and on an associative/contextual task using passive avoidance conditioning.
26 the open field and enhanced performance in a passive-avoidance fear conditioning task, which were bot
27                                    One-trial passive avoidance learning can be established by coating
28 ce training, but castration did not modulate passive avoidance learning or memory.
29 ferences in conditioned place preference and passive avoidance learning seen in Kal7(KO) mice are abr
30 n of recall of a weak version of the 1-trial passive avoidance learning task could be achieved by beh
31 l-induced deficits in spatial navigation and passive avoidance learning were investigated with a rat
32 contextual fear learning and enhances future passive avoidance learning, which may model certain beha
33                       Rats were trained on a passive-avoidance learning (PAL) protocol that was follo
34      Training for contextual conditioning or passive avoidance led to significant increases in CRE-de
35 rse scopolamine induced amnesia in rats in a passive avoidance memory paradigm.
36 showed that 6-OHDA significantly reduced the passive avoidance memory performance, non-enzymatic (tot
37 in the hidden sessions of the water maze and passive avoidance memory retention.
38 nistration of GA significantly increased the passive avoidance memory, total thiol and GPx contents a
39  exhibited normal learning and memory in the passive avoidance, Morris water maze, and fear condition
40  (i.e., decreased burying behavior), but not passive avoidance of aversive stimuli (i.e., exploration
41   In these, a key behavioral assay comprises passive avoidance of potential threat and inhibition, bo
42 ChRs) contain the beta2 subunit and modulate passive avoidance (PA) learning in mice.
43 ing electrical footshocks exhibited enhanced passive avoidance (PA) learning when trained 24 h after
44 dor delayed nonmatch-to-sample (DNMS) tasks, passive avoidance (PA), and locomotor activity.
45 ormed similarly to wild-type controls in the passive avoidance paradigm, a test of aversive learning.
46                            In a single trial passive avoidance paradigm, SHR again displayed signific
47 generation-associated memory impairment in a passive avoidance paradigm.
48 e exhibit normal learning and retention of a passive avoidance paradigm; however, they do not master
49 holinergic drugs have been shown to regulate passive avoidance performance via the amygdala, the neur
50                                              Passive avoidance performance was not affected.
51 ined in radial arm maze, but not inhibitory (passive) avoidance, performance.
52 r blockade on retention in a mildly aversive passive-avoidance procedure was investigated.
53 munity were able to learn active, as well as passive, avoidance protocols with shock as reinforcement
54                           In a single-trial, passive-avoidance response (PAR) paradigm, young rats at
55 ts typically learn to respond with active or passive avoidance responses that circumvent the threat.
56 ng impairment and nesting behaviors based on passive avoidance, T-Maze, and nesting behavior tests.
57 maze, novel objective recognition, step-down passive avoidance, tail suspension, and sucrose preferen
58 , they performed significantly better in the passive avoidance task (255 +/- 36 s and 145 +/- 18 s in
59 ated with behavioral analysis, including the passive avoidance task and elevated plus maze.
60 ound impairment in acquisition of a standard passive avoidance task but failed to impair place learni
61                       Long-term memory for a passive avoidance task in day-old chicks has proved to d
62 of impaired performance of fmr1 KO mice on a passive avoidance task is suggestive of a deficit in lea
63 ehavior in a novel open field and learning a passive avoidance task were assessed during nicotine tre
64 p-matched on IQ, gender, and age performed a passive avoidance task while undergoing functional MRI.
65 p-matched on IQ, gender, and age performed a passive avoidance task while undergoing functional MRI.
66 ated zero maze and impaired acquisition of a passive avoidance task, but normal behavior in open fiel
67 xhibited impaired performance in a long-term passive avoidance task, providing additional evidence fo
68 and shortened retention (79 +/- 26 s) of the passive avoidance task.
69 ater maze training and in chicks following a passive avoidance task.
70 nd memory events associated with a one-trial passive avoidance task.
71 te the formation of memory for the one-trial passive avoidance task.
72 k and a significant memory impairment on the passive avoidance task.
73 en greater impairments in performance on the passive avoidance task.
74  functional magnetic resonance imaging-based passive avoidance task.
75  likely source of NO involved in learning of passive avoidance tasks in hatchling chicks.
76 sion Test (TST), Morris Water Maze (MWM) and Passive Avoidance Test (PAT).
77                    Novel object recognition, passive avoidance test and Morris water maze were used t
78 ce have no memory 21 d after training in the passive avoidance test, suggesting a pivotal role for ad
79 mice in emotional learning and memory in the passive avoidance test.
80 scopolamine-induced amnesia as measured by a passive avoidance test.
81 E3 or Apoe-/- mice to reach criterion during passive avoidance training, but castration did not modul
82                              Rats were given passive-avoidance training--1 trial per day for 4 days-a
83  8-OH-DPAT at training on 72-hr retention of passive avoidance was investigated in rats.
84 ale DISC1(D453G) mice displayed a deficit in passive avoidance, while neither males nor females exhib
85      In contrast, nicotine exposure enhanced passive avoidance, with the effect intensifying and pers