ライフサイエンスコーパス: vestibulo-ocular reflex

1 tibular system about ongoing head movements (vestibulo-ocular reflex).

2 mature neuromuscular junctions, had a strong vestibulo-ocular reflex.

3 R postural instability or maladaption of the vestibulo-ocular reflex.

4 es, pursuit, convergence, accommodation, and vestibulo-ocular reflex.

5 n, (3) gaze-holding deficits, and (4) normal vestibulo-ocular reflex.

6 e movements of, for example, the eyes in the vestibulo-ocular reflex.

7 serving cerebellar-dependent learning in the vestibulo-ocular reflex.

8 rive motor learning during adaptation of the vestibulo-ocular reflex.

9 explained by retinal slip due to a residual vestibulo-ocular reflex.

10 yer interneurons regulates adaptation of the vestibulo-ocular reflex.

11 g and memory in a quantifiable behavior, the vestibulo-ocular reflex.

12 and may contribute to motor learning in the vestibulo-ocular reflex.

13 at could contribute to motor learning in the vestibulo-ocular reflex.

14 ontal and vertical nystagmus and an abnormal vestibulo-ocular reflex.

15 g in cross-axis adaptation of the horizontal vestibulo-ocular reflex.

16 etion of GC NMDARs affects adaptation of the vestibulo-ocular reflex.

17 drift beyond the brainstem circuitry of the vestibulo-ocular reflex.(9)(,)(10) Here, we investigated

18 ed a model of phase-reversal learning of the vestibulo-ocular reflex, a well-established, cerebellar-

19 Here, we use the vestibulo-ocular reflex-a simple behavior that stabilize

20 tive motor learning--eyelid conditioning and vestibulo-ocular reflex adaptation--and implicates prima

21 Reduced visual inputs may weaken the vestibulo-ocular reflex, an important system that mainta

22 velocity with the eye velocity output of the vestibulo-ocular reflex and (ii) to study vestibular fun

23 assess the effect of hyperventilation on the vestibulo-ocular reflex and its visual suppression, the

24 ays, including analysis of motor learning in vestibulo-ocular reflex and rotarod tests, we find that

25 lts and the growing evidence from studies of vestibulo-ocular reflex and saccadic adaptation, we conc

26 mild, the ability to adapt the phase of the vestibulo-ocular reflex and to consolidate gain adaptati

27 t with abnormal vestibular input, but normal vestibulo-ocular reflexes and apparently normal motor pe

28 e cyclic structure coexists with the classic vestibulo-ocular reflex arc for horizontal eye movements

29 ted to the dysfunction of semicircular canal vestibulo-ocular reflexes, as they have been shown to st

30 ant target during head rotation, the angular vestibulo-ocular reflex (aVOR) should rotate the eyes at

31 We studied the functional development of vestibulo-ocular reflex circuit components in the larval

32 s showed decreased gains for optokinetic and vestibulo-ocular reflexes, confirming an effect of dark

33 tion signals within the afferent arms of the vestibulo-ocular reflex consisting of the otic vesicle,

34 Learning in the vestibulo-ocular reflex depends initially on the activit

35 ll activation drives an adaptive decrease in vestibulo-ocular reflex gain when vestibular stimuli are

36 h large-magnitude Ca(2+) responses increases vestibulo-ocular reflex gain.

37 motor systems a simulation of the horizontal Vestibulo-Ocular Reflex (hVOR) system is presented.

38 hat govern smooth pursuit, saccades, and the vestibulo-ocular reflex in normal humans and patients wi

39 tially and temporally specific activation of vestibulo-ocular reflexes in distinct planes.

40 ibular dysfunction was apparent from altered vestibulo-ocular reflexes in Kcnq4(-/-)/Kcnq5(dn/dn) and

41 nificant reduction in the horizontal angular vestibulo-ocular reflex, indicating that detection of bo

42 efore, at least for frequencies in which the vestibulo-ocular reflex is important for gaze stabilizat

43 reversal adaptation and consolidation of the vestibulo-ocular reflex is significantly impaired in Ts6

44 irrelevant visual background both influenced vestibulo-ocular reflex learning in rhesus monkeys.

45 about the loci and directions of plasticity: vestibulo-ocular reflex learning.

46 he generation of the otolith-mediated linear vestibulo-ocular reflex (LVOR).

47 t the interaction between the cerebellum and vestibulo-ocular reflexes mediated by the semicircular c

48 cify the fate, function, and organization of vestibulo-ocular reflex neurons.

49 nerves can improve vision by augmenting the vestibulo-ocular reflex, no information is available reg

50 robust and consistent motor learning in the vestibulo-ocular reflex of rhesus monkeys.

51 to perturbations with reflexes, such as the vestibulo-ocular reflex or stretch reflex, whose gains a

52 Indeed, subjecting the KO mice to a vestibulo-ocular reflex phase reversal test reveals impa

53 e gaze at the level of single neurons in the vestibulo-ocular reflex premotor circuitry.

54 The vestibulo-ocular reflex produces eye movements that comp

55 trast to the phylogenetically old rotational vestibulo-ocular reflex (RVOR), it has been proposed tha

56 Rotational and translational vestibulo-ocular reflexes (RVOR and TrVOR) function to m

57 e been proposed to explain adaptation of the vestibulo-ocular reflex so similar mechanisms may also u

58 The vestibulo-ocular reflexes stabilize retinal images durin

59 he eyelid response and motor learning in the vestibulo-ocular reflex suggests that (i) plasticity is

60 r positional downbeat nystagmus and impaired vestibulo-ocular reflex suppression.

61 In the circuitry that subserves the vestibulo-ocular reflex, the postsynaptic targets of Pur

62 Sensory feedback tunes this vestibulo-ocular reflex throughout life.

63 it has been proposed that the translational vestibulo-ocular reflex (TVOR) represents a newly develo

64 or learning was induced in the translational vestibulo-ocular reflex (TVOR) when monkeys were repeate

65 Visual-vestibulo-ocular reflex (V-VOR) adaptation was also test

66 r different types of eye movement (saccades, vestibulo-ocular reflex, vergence) and gaze-holding.

67 l and vestibular information and control the vestibulo-ocular reflex, vestibulo-collic reflex, smooth

68 During head rotation, the vestibulo-ocular reflex violates LL by driving ocular to

69 The horizontal and vertical vestibulo ocular reflex (VOR) of head tilted (het) mutan

70 culus of both sexes of mice before and after vestibulo-ocular reflex (VOR) adaptation.

71 that mediate essential functions such as the vestibulo-ocular reflex (VOR) and its adaptation.

72 The functional complementarity of the vestibulo-ocular reflex (VOR) and optokinetic reflex (OK

73 d control subjects and by characterizing the vestibulo-ocular reflex (VOR) and vestibular and headach

74 ivity have both been postulated to influence vestibulo-ocular reflex (VOR) axis direction.

75 Here we investigate the vestibulo-ocular reflex (VOR) circuitry by applying temp

76 The vestibulo-ocular reflex (VOR) comprises an outstanding s

77 nt neurons in modulating the dynamics of the vestibulo-ocular reflex (VOR) during normal and adaptive

78 bular nucleus (MVN) neurons in vitro, and on vestibulo-ocular reflex (VOR) function in vivo, were inv

79 ctivated K+ channel SK2 (L7-SK2) show intact vestibulo-ocular reflex (VOR) gain adaptation but impair

80 While an ideal vestibulo-ocular reflex (VOR) generates ocular rotations

81 gate vertical saccade behavior after the yaw vestibulo-ocular reflex (VOR) had driven eye torsion out

82 lar function was assessed by quantifying the vestibulo-ocular reflex (VOR) in alert mice.

83 in the dark was opposite to that during the vestibulo-ocular reflex (VOR) in the light.

84 cent studies of simple behaviors such as the vestibulo-ocular reflex (VOR) indicate that multiple pla

85 gh memory for an increase in the gain of the vestibulo-ocular reflex (VOR) induced with high-frequenc

86 ence is accumulating that the high-frequency vestibulo-ocular reflex (VOR) is not affected by transit

87 Previous experiments have shown that the vestibulo-ocular reflex (VOR) is partially suppressed du

88 are essential for eyeblink conditioning and vestibulo-ocular reflex (VOR) learning.

89 PKCgamma-/- mice are profoundly impaired in vestibulo-ocular reflex (VOR) motor learning.

90 learned changes in the gain and phase of the vestibulo-ocular reflex (VOR) of mice.

91 e dependence of motor learning in the monkey vestibulo-ocular reflex (VOR) on the duration, frequency

92 Here, using the cerebellar-specific vestibulo-ocular reflex (VOR) paradigm, we determined th

93 oked potential (VsEP) responses and abnormal vestibulo-ocular reflex (VOR) responses demonstrated tha

94 Quantitative assessment of the vestibulo-ocular reflex (VOR) revealed a reduction in VO

95 Vestibulo-ocular reflex (VOR) suppression was also norma

96 nked to chromosome 19p by using a battery of vestibulo-ocular reflex (VOR) tests.

97 d that larval zebrafish perform an effective vestibulo-ocular reflex (VOR) that serves to stabilize g

98 neurons putatively involved in producing the vestibulo-ocular reflex (VOR) was studied during active

99 s for the induction of motor learning in the vestibulo-ocular reflex (VOR) were evaluated by recordin

100 , we consider phase-reversal training of the vestibulo-ocular reflex (VOR), a simple form of motor le

101 suit, saccades, optokinetic nystagmus (OKN), vestibulo-ocular reflex (VOR), and vergence using video-

102 The cerebellum-dependent vestibulo-ocular reflex (VOR), which helps maintain one'

103 The eye movements produced by the vestibulo-ocular reflex (VOR), which plays an essential

104 innovative methods to change the gain of the vestibulo-ocular reflex (VOR).

105 d increases and decreases in the gain of the vestibulo-ocular reflex (VOR).

106 h evokes ocular counter-rolling, a torsional vestibulo-ocular reflex (VOR).

107 d-free pursuit and how it interacts with the vestibulo-ocular reflex (VOR).

108 pendent learning task, motor learning in the vestibulo-ocular reflex (VOR).

109 Vestibulo-ocular reflexes (VORs) are the dominating cont

110 on depends critically on the contribution of vestibulo-ocular reflexes (VORs) to gaze stabilization.

111 little as 10 ms-a delay similar to the human vestibulo-ocular reflex-whereas wing steering responses

112 This activated the torsional, rotational vestibulo-ocular reflex, which exhibits a zero-angle or

113 controlled by the cerebellum, the horizontal vestibulo-ocular reflex, which involves only two eye mus

114 The vestibulo-ocular reflex, with or without visual enhancem