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1  are also required for inhibiting repetitive turning behavior.
2 or the sensory transduction involved in male turning behavior.
3 iversal role of these neurons in controlling turning behaviors.
4 persisted during cAMP-dependent switching of turning behaviors.
5 located hindbrain SPNs (vSPNs) in generating turning behaviors.
6 eated mice exhibited significant ipsilateral turning behavior after d-amphetamine challenge, indicati
7 n motor deficits without eliciting any vivid turning behavior and abolishes electrophysiological abno
8 re assessed for their preferred direction of turning behavior and for high vs. low levels of spontane
9 o) granule cells exhibit the highest rate of turning behavior and have multiple short processes.
10                                  Spontaneous turning behavior and locomotor activity were evaluated f
11 ry have shown that individual differences in turning behavior are accompanied by different asymmetrie
12            Instead, the different rheotactic turning behaviors are linked to a broken mirror symmetry
13 is achieved by modulating the probability of turning behavior, as in C. elegans chemotaxis.
14 s elegans larvae, sleep is associated with a turning behavior, called flipping, in which animals rota
15  block the amphetamine-induced, ipsiversive, turning-behavior caused by the lesion in the pTR-UF4 gro
16 icantly increase repetition of substep(s) of turning behavior compared with wild-type males.
17 spond to the same guidance cue with opposite turning behavior, dependent on other coincident signals
18 e brain can result in attractive or aversive turning behaviors depending on the cell type.
19  in Kir6.2 expression on apomorphine-induced turning behavior in rats with unilateral 6-hydroxydopami
20 lated in a manner consistent with a role for turning behavior in thermal migration.
21 part of the neural circuitry regulating male turning behavior, indicating the existence of functional
22 ults, a mechanical model is proposed for the turning behavior of keratocytes in response to photorele
23 tagonists in that the locomotor activity and turning behavior of SIB-1663 were partially sensitive to
24 e (MLCK) were responsible for the intriguing turning behavior of T cells climbing the ramp-like struc
25  ramp-like structures, indicating intriguing turning behavior of T cells mediated by lamellipodia for
26 larger environment and the left versus right turning behavior of the animal.
27 ence of the vimentin meshwork influenced the turning behavior of the bacteria; in the vimentin-null c
28 ERT-/- mice consistently displayed increased turning behavior, potentially representing a perseveranc
29 alphao-/- mice are hyperactive and exhibit a turning behavior that has them running in circles for ho
30 irectional memory can arise from contrasting turning behaviors, therefore increasing the likelihood o
31 istinct swimming states that entail opposite turning behaviors under flow reversal.
32                                  Significant turning behavior was also observed in free-3NT-treated m
33                                              Turning behavior was correlated with striatal TH ratio (
34 the number of neurons with Fos expression to turning behavior was stronger for contralateral versus i

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