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1 tibular system about ongoing head movements (vestibulo-ocular reflex).
2 es, pursuit, convergence, accommodation, and vestibulo-ocular reflex.
3 n, (3) gaze-holding deficits, and (4) normal vestibulo-ocular reflex.
4 e movements of, for example, the eyes in the vestibulo-ocular reflex.
5 serving cerebellar-dependent learning in the vestibulo-ocular reflex.
6 rive motor learning during adaptation of the vestibulo-ocular reflex.
7  explained by retinal slip due to a residual vestibulo-ocular reflex.
8 yer interneurons regulates adaptation of the vestibulo-ocular reflex.
9 g and memory in a quantifiable behavior, the vestibulo-ocular reflex.
10  and may contribute to motor learning in the vestibulo-ocular reflex.
11 at could contribute to motor learning in the vestibulo-ocular reflex.
12 ontal and vertical nystagmus and an abnormal vestibulo-ocular reflex.
13 g in cross-axis adaptation of the horizontal vestibulo-ocular reflex.
14 ed a model of phase-reversal learning of the vestibulo-ocular reflex, a well-established, cerebellar-
15                             Here, we use the vestibulo-ocular reflex-a simple behavior that stabilize
16 tive motor learning--eyelid conditioning and vestibulo-ocular reflex adaptation--and implicates prima
17         Reduced visual inputs may weaken the vestibulo-ocular reflex, an important system that mainta
18 velocity with the eye velocity output of the vestibulo-ocular reflex and (ii) to study vestibular fun
19 assess the effect of hyperventilation on the vestibulo-ocular reflex and its visual suppression, the
20 ays, including analysis of motor learning in vestibulo-ocular reflex and rotarod tests, we find that
21 lts and the growing evidence from studies of vestibulo-ocular reflex and saccadic adaptation, we conc
22  mild, the ability to adapt the phase of the vestibulo-ocular reflex and to consolidate gain adaptati
23 ted to the dysfunction of semicircular canal vestibulo-ocular reflexes, as they have been shown to st
24 ant target during head rotation, the angular vestibulo-ocular reflex (aVOR) should rotate the eyes at
25 s showed decreased gains for optokinetic and vestibulo-ocular reflexes, confirming an effect of dark
26 tion signals within the afferent arms of the vestibulo-ocular reflex consisting of the otic vesicle,
27                              Learning in the vestibulo-ocular reflex depends initially on the activit
28 motor systems a simulation of the horizontal Vestibulo-Ocular Reflex (hVOR) system is presented.
29 hat govern smooth pursuit, saccades, and the vestibulo-ocular reflex in normal humans and patients wi
30 tially and temporally specific activation of vestibulo-ocular reflexes in distinct planes.
31 ibular dysfunction was apparent from altered vestibulo-ocular reflexes in Kcnq4(-/-)/Kcnq5(dn/dn) and
32 nificant reduction in the horizontal angular vestibulo-ocular reflex, indicating that detection of bo
33 efore, at least for frequencies in which the vestibulo-ocular reflex is important for gaze stabilizat
34 reversal adaptation and consolidation of the vestibulo-ocular reflex is significantly impaired in Ts6
35 irrelevant visual background both influenced vestibulo-ocular reflex learning in rhesus monkeys.
36 he generation of the otolith-mediated linear vestibulo-ocular reflex (LVOR).
37 t the interaction between the cerebellum and vestibulo-ocular reflexes mediated by the semicircular c
38  nerves can improve vision by augmenting the vestibulo-ocular reflex, no information is available reg
39  robust and consistent motor learning in the vestibulo-ocular reflex of rhesus monkeys.
40  to perturbations with reflexes, such as the vestibulo-ocular reflex or stretch reflex, whose gains a
41          Indeed, subjecting the KO mice to a vestibulo-ocular reflex phase reversal test reveals impa
42 e gaze at the level of single neurons in the vestibulo-ocular reflex premotor circuitry.
43                                          The vestibulo-ocular reflex produces eye movements that comp
44 trast to the phylogenetically old rotational vestibulo-ocular reflex (RVOR), it has been proposed tha
45                 Rotational and translational vestibulo-ocular reflexes (RVOR and TrVOR) function to m
46 e been proposed to explain adaptation of the vestibulo-ocular reflex so similar mechanisms may also u
47                                          The vestibulo-ocular reflexes stabilize retinal images durin
48 he eyelid response and motor learning in the vestibulo-ocular reflex suggests that (i) plasticity is
49 r positional downbeat nystagmus and impaired vestibulo-ocular reflex suppression.
50          In the circuitry that subserves the vestibulo-ocular reflex, the postsynaptic targets of Pur
51  it has been proposed that the translational vestibulo-ocular reflex (TVOR) represents a newly develo
52 or learning was induced in the translational vestibulo-ocular reflex (TVOR) when monkeys were repeate
53 l and vestibular information and control the vestibulo-ocular reflex, vestibulo-collic reflex, smooth
54                    During head rotation, the vestibulo-ocular reflex violates LL by driving ocular to
55                  The horizontal and vertical vestibulo ocular reflex (VOR) of head tilted (het) mutan
56 ivity have both been postulated to influence vestibulo-ocular reflex (VOR) axis direction.
57                      Here we investigate the vestibulo-ocular reflex (VOR) circuitry by applying temp
58                                          The vestibulo-ocular reflex (VOR) comprises an outstanding s
59 nt neurons in modulating the dynamics of the vestibulo-ocular reflex (VOR) during normal and adaptive
60 bular nucleus (MVN) neurons in vitro, and on vestibulo-ocular reflex (VOR) function in vivo, were inv
61                               While an ideal vestibulo-ocular reflex (VOR) generates ocular rotations
62 gate vertical saccade behavior after the yaw vestibulo-ocular reflex (VOR) had driven eye torsion out
63 lar function was assessed by quantifying the vestibulo-ocular reflex (VOR) in alert mice.
64  in the dark was opposite to that during the vestibulo-ocular reflex (VOR) in the light.
65 cent studies of simple behaviors such as the vestibulo-ocular reflex (VOR) indicate that multiple pla
66 gh memory for an increase in the gain of the vestibulo-ocular reflex (VOR) induced with high-frequenc
67 ence is accumulating that the high-frequency vestibulo-ocular reflex (VOR) is not affected by transit
68     Previous experiments have shown that the vestibulo-ocular reflex (VOR) is partially suppressed du
69  PKCgamma-/- mice are profoundly impaired in vestibulo-ocular reflex (VOR) motor learning.
70 learned changes in the gain and phase of the vestibulo-ocular reflex (VOR) of mice.
71 e dependence of motor learning in the monkey vestibulo-ocular reflex (VOR) on the duration, frequency
72          Here, using the cerebellar-specific vestibulo-ocular reflex (VOR) paradigm, we determined th
73                                              Vestibulo-ocular reflex (VOR) suppression was also norma
74 nked to chromosome 19p by using a battery of vestibulo-ocular reflex (VOR) tests.
75 d that larval zebrafish perform an effective vestibulo-ocular reflex (VOR) that serves to stabilize g
76 neurons putatively involved in producing the vestibulo-ocular reflex (VOR) was studied during active
77 s for the induction of motor learning in the vestibulo-ocular reflex (VOR) were evaluated by recordin
78 , we consider phase-reversal training of the vestibulo-ocular reflex (VOR), a simple form of motor le
79 suit, saccades, optokinetic nystagmus (OKN), vestibulo-ocular reflex (VOR), and vergence using video-
80 innovative methods to change the gain of the vestibulo-ocular reflex (VOR).
81 d increases and decreases in the gain of the vestibulo-ocular reflex (VOR).
82 h evokes ocular counter-rolling, a torsional vestibulo-ocular reflex (VOR).
83 d-free pursuit and how it interacts with the vestibulo-ocular reflex (VOR).
84 pendent learning task, motor learning in the vestibulo-ocular reflex (VOR).
85                                              Vestibulo-ocular reflexes (VORs) are the dominating cont
86 on depends critically on the contribution of vestibulo-ocular reflexes (VORs) to gaze stabilization.
87     This activated the torsional, rotational vestibulo-ocular reflex, which exhibits a zero-angle or
88 controlled by the cerebellum, the horizontal vestibulo-ocular reflex, which involves only two eye mus
89                                          The vestibulo-ocular reflex, with or without visual enhancem

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