ライフサイエンスコーパス: turning behavior

1 are also required for inhibiting repetitive turning behavior.

2 or the sensory transduction involved in male turning behavior.

3 red preferred patterns of motor activity and turning behavior.

4 of movements, from locomotion to posture and turning behavior.

5 ly gate motor activity but inversely control turning behavior.

6 persisted during cAMP-dependent switching of turning behaviors.

7 located hindbrain SPNs (vSPNs) in generating turning behaviors.

8 iversal role of these neurons in controlling turning behaviors.

9 eated mice exhibited significant ipsilateral turning behavior after d-amphetamine challenge, indicati

10 n motor deficits without eliciting any vivid turning behavior and abolishes electrophysiological abno

11 re assessed for their preferred direction of turning behavior and for high vs. low levels of spontane

12 o) granule cells exhibit the highest rate of turning behavior and have multiple short processes.

13 eurons through the p38 MAPK PMK-1 to promote turning behavior and limit foraging when food is abundan

14 Spontaneous turning behavior and locomotor activity were evaluated f

15 ted using motor cortex stimulation to induce turning behaviors) and wireless optogenetics in arenas o

16 ry have shown that individual differences in turning behavior are accompanied by different asymmetrie

17 r regions, we show that action sequences and turning behavior are regulated by dopamine D1-like recep

18 Turning behaviors are affected in people with Parkinson'

19 Instead, the different rheotactic turning behaviors are linked to a broken mirror symmetry

20 ole of striatal cholinergic interneurons for turning behavior as well as for traversing dynamic surfa

21 is achieved by modulating the probability of turning behavior, as in C. elegans chemotaxis.

22 s elegans larvae, sleep is associated with a turning behavior, called flipping, in which animals rota

23 block the amphetamine-induced, ipsiversive, turning-behavior caused by the lesion in the pTR-UF4 gro

24 icantly increase repetition of substep(s) of turning behavior compared with wild-type males.

25 These results show that Drosophila optomotor turning behaviors contain rich, stimulus-dependent dynam

26 spond to the same guidance cue with opposite turning behavior, dependent on other coincident signals

27 e brain can result in attractive or aversive turning behaviors depending on the cell type.

28 ient of D1 receptor signaling present normal turning behavior despite decreased activity, restoring D

29 thereby modulating patterns of activity and turning behavior for goal-directed locomotion.

30 in Kir6.2 expression on apomorphine-induced turning behavior in rats with unilateral 6-hydroxydopami

31 aight swimming larvae of C. natans increased turning behavior in regions with high concentrations of

32 new task to demonstrate impairments in cued turning behavior in rodents modeling the cholinergic-dop

33 lated in a manner consistent with a role for turning behavior in thermal migration.

34 locomotor activity and increased measures of turning behaviors in zebrafish, suggesting that alloster

35 part of the neural circuitry regulating male turning behavior, indicating the existence of functional

36 d with local searching, while they decreased turning behavior near high concentrations of [Formula: s

37 ults, a mechanical model is proposed for the turning behavior of keratocytes in response to photorele

38 tagonists in that the locomotor activity and turning behavior of SIB-1663 were partially sensitive to

39 e (MLCK) were responsible for the intriguing turning behavior of T cells climbing the ramp-like struc

40 ramp-like structures, indicating intriguing turning behavior of T cells mediated by lamellipodia for

41 larger environment and the left versus right turning behavior of the animal.

42 ence of the vimentin meshwork influenced the turning behavior of the bacteria; in the vimentin-null c

43 ERT-/- mice consistently displayed increased turning behavior, potentially representing a perseveranc

44 well as to observe effects on locomotor and turning behaviors relative to other mAChR PAMs.

45 d temporal organization of motor actions and turning behavior, reminiscent of indecisiveness.

46 ticular the food-no food interface, controls turning behavior, stimulating turns toward the food when

47 d that timing encodes more information about turning behavior than spike count in every motor unit, e

48 alphao-/- mice are hyperactive and exhibit a turning behavior that has them running in circles for ho

49 irectional memory can arise from contrasting turning behaviors, therefore increasing the likelihood o

50 istinct swimming states that entail opposite turning behaviors under flow reversal.

51 Significant turning behavior was also observed in free-3NT-treated m

52 Turning behavior was correlated with striatal TH ratio (

53 the number of neurons with Fos expression to turning behavior was stronger for contralateral versus i