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1 tion outside the AFP (e.g., within the vocal motor pathway).
2 triatum, all of which converge onto the same motor pathway.
3 by the overall number of neurons in the song motor pathway.
4 tive signal that improves performance in the motor pathway.
5 oration and instruct synaptic changes in the motor pathway.
6 terns that have been observed throughout the motor pathway.
7 a basal ganglia circuit and its target vocal motor pathway.
8 AR contribution to synaptic responses in the motor pathway.
9 associated with hyperactivity in the flight motor pathway.
10 one guidance decisions along the ISN and SNb motor pathways.
11 ed that song perception involved sensory and motor pathways.
12 spike timing-dependent plasticity in spared motor pathways.
13 es of CST anatomy in experimental studies of motor pathways.
14 egrate their inputs and influence downstream motor pathways.
15 m neck afferents projecting onto ipsilateral motor pathways.
16 rent combinations of a small number of basic motor pathways.
17 rmalities in cerebellothalamocortical (CbTC) motor pathways.
18 eraction between the basal ganglia and vocal motor pathways.
19 phy efforts to localize descending orofacial motor pathways.
20 cies in the organization and function of the motor pathways.
21 nation of separate laryngeal and respiratory motor pathways.
22 NaCh6 was present in both sensory and motor pathways.
23 ence of functionally related corticostriatal motor pathways.
24 TX, but the ICc does not project directly to motor pathways.
25 d brain nuclei organized into a direct vocal motor pathway and an anterior forebrain (pallium-basal g
26 hanism of GABAergic dysfunction in the major motor pathway and potential targets for pharmacotherapy
27 (RA) is a key nucleus in the forebrain song motor pathway and receives glutamatergic input from the
28 h by targeting the interaction of descending motor pathways and large diameter afferents in the spina
29 increased dysfunction in the primary central motor pathways and no evidence that FDCB is the pathophy
30 he combined effects of excessive activity in motor pathways and reduced activation in control portion
32 develop in response to damage to descending motor pathways and to motor neurons and interneurons in
33 ent in human M1 after the loss of descending motor pathways, and that M1 spiking activities share man
34 irect connections between auditory and vocal motor pathways, and two newly identified centers for aud
35 scious motor code, based on a direct sensory-motor pathway; and a slower conscious intention code tha
36 y control ventilator VT using nonrespiratory motor pathways; and (2) Do subjects obtain more relief w
37 However, the extent to which ipsilateral motor pathways are engaged in voluntary activity in inta
39 idge motoneurons could be used by descending motor pathways as premotor interneurons to transmit neur
40 these changes may reflect the plasticity of motor pathways associated with cortical reorganisation.
41 al sclerosis (ALS), which extends beyond the motor pathways, can be visualised by diffusion tensor im
43 of PD with RBD emphasizes the complexity of motor pathway control during wakefulness and REM sleep.
49 b (SNb) motor axons normally exit the common motor pathway, enter the ventral target region, and then
52 accumulation of neuronal signals in sensory-motor pathways, favoring one alternative over others.
57 , allows us to more easily determine how CNS motor pathways function to produce sex-specific songs.
58 malian pre-motor and motor cortex (the vocal motor pathway) generates the patterned structure of lear
64 ison subjects throughout all portions of the motor pathway, including the sensorimotor cortex, putame
65 ith sympathetic outflow to blood vessels and motor pathways, including the intermediolateral nucleus
66 eticulospinal tract is one of the descending motor pathways involved in recovery of hand function aft
68 a principle component of the mammalian vocal motor pathway, making it a likely site for vocal-respira
69 in addition, new neuron survival in the song motor pathway may be regulated by the quality of song-ge
70 ave documented two points at which the vocal motor pathway may pick up auditory signals: the HVC-shel
71 roadly, hierarchical organization of sensory-motor pathways may develop through a cascade of CPs indu
73 as, and the relationship between sensory and motor pathways of the brain, including cognitive aspects
74 trograde transport along specific descending motor pathways of the spinal cord and, as a result, can
75 brain and then shared between perceptual and motor pathways or is centrally represented sensory activ
76 visual and parietal WM pathways, but not to motor pathways or the corpus callosum indicates that ind
77 same auditory stimulus activates sensory and motor pathways, perception and production of song are ac
79 to axial, but not distal, musculature by the motor pathways responsible for this oscillatory input.
80 hese results collectively delineate multiple motor pathways subserving distinct aspects of the OKR in
81 The present study focuses on the trigeminal motor pathway that controls Schnauzenorgan movement and
82 tal gray (PAG) form a crucial segment of the motor pathway that produces the lordosis posture, the ha
83 spinal cord contains segregated sensory and motor pathways that have been difficult to quantify usin
84 tinct pattern of acute injury to subcortical motor pathways that involved the basal ganglia and thala
85 3A loss on dopamine signaling in subcortical motor pathways that may inform ongoing clinical trials o
86 lude genes whose products act in two spindle motor pathways that overlap in function with Cin8p, the
88 al circuits that exert top-down control over motor pathways (the caudate and anterior cingulate corte
89 overlap in early visual areas and the final motor pathways, the pursuit and saccadic systems share p
92 ion, conscious decisions, and nonrespiratory motor pathways to achieve an appropriate respiratory res
93 vestibular system and descending brain stem motor pathways to the erectores spinae muscles in the co
94 Here we ask whether the excitability of the motor pathways to the real (disembodied) hand are affect
98 uction block (FDCB) in the patients' central motor pathways was sought by measuring the EMG responses
99 s of defined components of the corticospinal motor pathway were made in adult rats in the rostral cer
100 upregulated in either denervated sensory or motor pathways were identified and two secreted factors
101 onal dissociation extended to the descending motor pathway, where recordings from a premotor cortex a
102 complete lesions of the dorsal corticospinal motor pathway, which contains more than 95% of all corti
103 s induce a premature maturation of the vocal motor pathway, which may lead to a loss of behavioral pl
104 d electrophysiological changes in descending motor pathways with motor-evoked potentials recorded dur
106 omic relationships between somatosensory and motor pathways within ventrolateral (VL) thalamic nuclei
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