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1 ions of the cerebellum are organized in poly-somatotopic "action maps" to reduce dimensionality and s
2                           This sound-related somatotopic activation in precentral gyrus shows that, d
3                      The abilities to detect somatotopic activation within the ganglion and to segreg
4 oxious thermal forearm stimulation generated somatotopic-activation of dorsal horn (DH) whose activit
5 both verbs and nouns produced characteristic somatotopic activations in the motor strip, with words r
6                 Genital representations were somatotopic and bilaterally symmetric, and their relativ
7                          When inspecting the somatotopic and nonsomatotopic connectivity patterns, a
8       Gradient continuity may be crucial for somatotopic and other topographical organization, and it
9 results challenge the prevalent dichotomy of somatotopic and spatiotopic selectivity and suggest that
10 ese high-level representations are basically somatotopic and that area 3b neurons amplify some featur
11  visual polar-angle representations in these somatotopic areas gradually shifts from near the horizon
12 ull-body air-puff stimulation suits revealed somatotopic areas of the face and multiple body parts fo
13 ive orexin A hypothalamic innervation with a somatotopic arrangement of the projections in the nucleu
14 or sagittal sinus suggest a highly organised somatotopic arrangement of the trigeminal innervation of
15             Next, we review the modality and somatotopic arrangements of the remaining constituents o
16 regation of thalamocortical afferents into a somatotopic barrel pattern in developing rodent primary
17 lateral visual system, revealing an array of somatotopic body maps that tile the cortical surface.
18 f the body model have been attributed to the somatotopic cerebral representation.
19 ational distances during BCI control without somatotopic changes.
20 , we demonstrate interhemispheric functional somatotopic connectivity of these homunculi, such that t
21 matosensory areas, and that the rehearsal of somatotopic coordinates in memory is accomplished by mod
22  thalamus was used to indicate the degree of somatotopic correspondence at the SI and SII injection s
23 rlap appeared to be related to the degree of somatotopic correspondence.
24 nt to induce task-relevant plasticity in the somatotopic cortical motor map.
25 results in significant reorganization of the somatotopic cortical motor map; however, the mechanisms
26  results, however, present an alternative to somatotopic cortical reorganization, namely, cortical pl
27  hemispheres of owl monkeys, focusing on the somatotopic distribution of evoked movements, thresholds
28 sses underlying negative BOLD participate in somatotopic encoding in M1 but not in the SMA.
29 ld facilitate texture discrimination through somatotopic encoding of frequency content.
30 nsity of [3H]KA sites at all ages was low, a somatotopic expression of [3H]KA sites was missing, and
31 n of peripheral receptors, thus generating a somatotopic facial map during development.
32 ifferent motoneuron pools are organized in a somatotopic fashion in the motor column related to the t
33 he inferior olive, where they terminate in a somatotopic fashion.
34 aken together, our results elucidate a novel somatotopic functional organization of the mammalian pai
35 posterior, dorsal-to-ventral, toes-to-tongue somatotopic gradient in a mirror orientation to the SMA.
36  in tetraplegic patients to characterise the somatotopic hand layout in primary somatosensory cortex.
37 ion somatotopy deteriorated, suggesting that somatotopic hand representations are more easily targete
38                                We found that somatotopic hand representations can be activated throug
39 ients who presented with a lesion at or near somatotopic hand representations performed significantly
40 x (M1) has been thought to form a continuous somatotopic homunculus extending down the precentral gyr
41 n M1 and SMA and negative BOLD in M1 contain somatotopic information, enabling prediction of the movi
42 homunculi, thus confirming that they contain somatotopic information.
43 ose, upper lip, lower lip, and chin caused a somatotopic lateral-to-medial, ipsilateral response patt
44       Here, we challenge the assumption that somatotopic layout restricts remapping, by comparing pat
45 nals of the sensorimotor network show varied somatotopic layouts, in which the relative position, dis
46 bellum, cerebrum, putamen) contain different somatotopic layouts, the parallel remapping they undergo
47  Sensorimotor representation was found to be somatotopic, localized in stereotactic space to rolandic
48 ttern was neither located at the ipsilateral somatotopic location nor randomly distributed.
49 moving body part from inside and outside its somatotopic location.
50 d passive movements were calculated for each somatotopic location.
51 ngue were also differentially activated in a somatotopic manner when subjects listened to the lip- or
52 both maps of the ELL terminate in a detailed somatotopic manner within the midbrain NL.
53 whisker touch excites vS1 and later vM1 in a somatotopic manner.
54 nsory, also projected in a similar, strictly somatotopic, manner, and the arbors from these neurons o
55 the structure of the salt-and-pepper whisker somatotopic map among L2/3 pyramidal neurons in somatose
56  the complex link between an activation in a somatotopic map and the associated touch location on the
57 Taken together, these data indicate that the somatotopic map in S1 is transformed into a value-based
58 rly, cutaneous nerves established a "normal" somatotopic map in the dorsal horn, but in more rostral
59  tactile hairs form a complete 3-dimensional somatotopic map in the mesothoracic ganglion.
60 ociceptors project to a spatially-organised, somatotopic map in the primary somatosensory cortex.
61 tecto-thalamic subnetworks, and identify the somatotopic map in the SC that displays distinguishable
62  innervating the cortex) and at P6 (when the somatotopic map is well established) resulted in a marke
63  This provides the first synaptic resolution somatotopic map of a head, and defines the parallel-proj
64                          Further, a putative somatotopic map of frequency selectivity was observed in
65 lly arrayed subtypes, establishing a central somatotopic map of peripheral target innervation.
66 pic maps of these cerebellar nuclei with the somatotopic map of projections to RTP from primary motor
67 on appears to be embedded within the classic somatotopic map of skeletomotor representation.
68         These competing requisites include a somatotopic map of the body, a map of hand location in s
69 sory cortical area 3b in macaques contains a somatotopic map of the hand, encompassing representation
70                      Each VC cluster forms a somatotopic map of the ipsilateral body, a "sensory aplu
71       Sensory input from the tailfan forms a somatotopic map on the projecting LG dendrites, which to
72                 Here, we present a disrupted somatotopic map phenotype in cortex, in clear contrast t
73 als that the somatosensory system can form a somatotopic map to integrate bilateral sensory inputs, b
74 os in the horizontal plane (the plane of the somatotopic map).
75 y to monitor axons, identified a spinal cord somatotopic map, performed months-long imaging in freely
76 l signal reduction or disorganization of the somatotopic map, such as disturbed continuity.
77 sal accessory olive, however, formed a clear somatotopic map.
78 hted towards either stimulus, in line with a somatotopic map.
79 en a key contributor to our understanding of somatotopic maps and developmental plasticity.
80 respect to the detailed electrophysiological somatotopic maps and histologically determined hand-face
81 jects scanned, four, mirrored, within-finger somatotopic maps defining the extent of the Brodmann are
82                                        These somatotopic maps differed from those in the cat in that
83          During this period, we found stable somatotopic maps in both the anesthetized and awake stat
84                                              Somatotopic maps in the cortex and the thalamus of adult
85  distinguishable spatial properties from the somatotopic maps in the neocortex and basal ganglia.
86 be a powerful influence on reorganization of somatotopic maps in the somatosensory cortex.
87     Injury-induced reorganization of central somatotopic maps is a phenomenon that has proven to be u
88 onance imaging analysis methods, we observed somatotopic maps of the digits in contralateral SI.
89 entral to ventrolateral RTP appears to match somatotopic maps of these cerebellar nuclei with the som
90 rangement of cell aggregates to form precise somatotopic maps.
91 y system as culturally universal categorical somatotopic maps.
92 ntribute to the formation of retinotopic and somatotopic maps.
93 ant mice (AC1-/-) have disordered visual and somatotopic maps.
94 d4 signaling in the formation of the whisker somatotopic maps.
95                                              Somatotopic memory load effects of arm- and leg-related
96 avioural research, such as demonstrations of somatotopic motor cortex activations following the prese
97 icks is not mutually exclusive, discarding a somatotopic muscle-level representation of movement in t
98 f body-part tuning in the brain's endogenous somatotopic network.
99 m the mechanosensory lateral line organize a somatotopic neural map.
100                             Importantly, the somatotopic neural organization of pain systems can shed
101                             However, neither somatotopic nor external-spatial representations can acc
102                     Recognition of a precise somatotopic onset of nigrostriatal denervation may help
103 nts, significantly outperforming alternative somatotopic or muscle-based models.
104 iceptively mediated sensation depends on the somatotopic or spatiotopic configuration of thermal inpu
105 generate "warm-cold-warm" patterns in either somatotopic or spatiotopic coordinates.
106                                A reversal of somatotopic order and an enlargement of receptive fields
107 was observed that proved consistent with the somatotopic organisation of the ventral intermediate nuc
108 e three facial stimulation sites exhibited a somatotopic organization along the longitudinal (rostroc
109                            The revelation of somatotopic organization and intensity dependency in dri
110                   This study aims to explore somatotopic organization and neural coding in the telenc
111 ts treated with MAM on E33 demonstrated that somatotopic organization and receptive field size are no
112 a preservation of tactile responsiveness and somatotopic organization but, in addition, involves tran
113 erminals in the neostriatum followed a crude somatotopic organization in which the amount of overlap
114            The neuroanatomical basis of this somatotopic organization is, however, unknown.
115 iological recording techniques to assess the somatotopic organization of brainstem and thalamic areas
116 rpinned by maladaptive neural changes to the somatotopic organization of finger representations withi
117 admill locomotion, 3 min/d, 5 d/week) on the somatotopic organization of forelimb and hindlimb somato
118 ges, surprisingly, we found that there is no somatotopic organization of motor units.
119                                          The somatotopic organization of somatosensory cortex of the
120 nnections, which appear to be woven into the somatotopic organization of the forelimb representation.
121                       In order to reveal the somatotopic organization of the gracile nucleus of the d
122                                          The somatotopic organization of the lateral striatum has bee
123 exact location of the neck motor area in the somatotopic organization of the motor homunculus is stil
124 s in the nodose MEA to determine if there is somatotopic organization of the neurons in that ganglion
125 rtially fits into the traditional concept of somatotopic organization of the nucleus.
126 nfirm the previously postulated ipsilateral, somatotopic organization of the sheep's sensory cortex.
127 ed a qualitatively and quantitatively normal somatotopic organization of vibrissae follicle input to
128 ed sagittal orientation, in keeping with the somatotopic organization present in the pattern of prima
129 two fields that corresponded in location and somatotopic organization to the second somatosensory are
130 e responsiveness, receptive field locations, somatotopic organization, and spatial properties of repr
131                        In the present study, somatotopic organization, architectonic features, and pa
132           Because of the spinal motoneuronal somatotopic organization, motor coordination implies int
133               To investigate conservation of somatotopic organization, we compared trigeminal nerve o
134                                   To examine somatotopic organization, we separately stimulated the l
135  dorsal horn cell receptive fields (RFs) and somatotopic organization.
136  part of the ipsilateral pRN, reflecting its somatotopic organization.
137 e primary motor cortex and to its underlying somatotopic organization.
138 isual processes, but no work was done on its somatotopic organization.
139 iveness to cutaneous stimuli and patterns of somatotopic organization.
140 ties of coherence indicate a differentiated, somatotopic organization; so far, however, little attent
141                              Retinotopic and somatotopic organizations have been described in the cla
142  trigeminal nerve, a major relay station for somatotopic pattern formation in the trigeminal system.
143 ntrast, mGluR1alpha was never localized in a somatotopic pattern in barrel field cortex.
144                                            A somatotopic pattern of AMPA receptors with fewer [3H]AMP
145                                    At P60, a somatotopic pattern of binding was not apparent.
146                        After that point, the somatotopic pattern of GluR6,7 subunit expression was lo
147                                            A somatotopic pattern of mGluR5 immunoreactivity persisted
148     With repetitive recordings of SEPs, this somatotopic pattern was reliably recorded for up to 16 w
149 e binding to mGluRs was not distributed in a somatotopic pattern.
150                                 By contrast, somatotopic patterns exist in the spinal trigeminal subn
151 ent of connectivity and the establishment of somatotopic patterns in the three main relay stations of
152 uR expression coincide with the emergence of somatotopic patterns in this region.
153 ncidences and sizes of receptive fields, (3) somatotopic progressions, (4) properties of representati
154        Fibers from one whisker had precisely somatotopic projections but highly varied morphologies.
155 neuronal aggregates in layer IV that receive somatotopic projections from whiskers on the rodent's sn
156 organization of the trigeminal ganglion, its somatotopic projections upon the principal sensory nucle
157 M representations in this task were based on somatotopic rather than allocentric spatial coordinates.
158 mation of tactile stimuli from a skin-based, somatotopic reference frame into an external one.
159              Similarly, inputs from distinct somatotopic regions of the somatosensory cortex are inte
160 nals have been the main focus of research on somatotopic remapping following loss of sensory input (e
161                   There was evidence both of somatotopic reorganization and of anatomic reorganizatio
162 cord in adult primates result in large-scale somatotopic reorganization due to which chin inputs expa
163 distributed more widely and covered a larger somatotopic representation including more proximal parts
164    However, under those conditions where the somatotopic representation is given priority over the ac
165 umn in cyprinid fish, ideally suited for the somatotopic representation of oropharyngeal and bodily s
166 insular cortex that provides the basis for a somatotopic representation of selectively nociceptive la
167 t even maintained by a reorganization of the somatotopic representation of the affected limb in prima
168 -1 antigen distribution was localized to the somatotopic representation of the footpad dermatome with
169 rn classification analysis revealed that the somatotopic representation of the right palm in contrala
170 s anatomical data indicate that the detailed somatotopic representation present in the ELL is lost in
171 road, rather than focal, sensorimotor cortex somatotopic representation.
172  epileptic seizures he developed the idea of somatotopic representation.
173 tional MRI study, we demonstrate overlapping somatotopic representations between the larynx and the j
174 llenge the treatment rationale for restoring somatotopic representations in complex regional pain syn
175 ve convergent projections from corresponding somatotopic representations in SI and SII, but also sugg
176                We agree with others that the somatotopic representations of different body parts over
177 aking, responses were distributed throughout somatotopic representations of speech articulators in mo
178  are organized in a pattern corresponding to somatotopic representations of the body (e.g., whiskers,
179 ghly overlapped and fuzzy borders, as do the somatotopic representations of the sensorimotor cortex i
180 nale for interventions that aim to "restore" somatotopic representations to treat pain.SIGNIFICANCE S
181                                              Somatotopic representations, assessed with two 7 tesla f
182  pre- and post-central area corresponding to somatotopic representations.
183 imates, the motor areas contain independent, somatotopic, representations of the forelimb (i.e., moto
184 dibular trigeminal nerve branches maintain a somatotopic segregation and generate spatially organized
185  simpler movements were represented and more somatotopic segregation was observed, and an anterior st
186              This design distinguished among somatotopic selectivity for locations on the skin and sp
187 ea 1 and area 3a, respectively, have similar somatotopic sequences.
188 wing electrical forepaw stimulation revealed somatotopic signal enhancement in the primary and second
189       This article discusses the fundamental somatotopic signals controlling immunity and the two aut
190  of everyday movements and understanding the somatotopic specificity of this pathway in the context o
191  the cortex, red nucleus and cerebellum with somatotopic spinal terminations suitable for point-to-po
192 of optimal stimulation sites that map to the somatotopic structure of the internal pallidum.
193 ary motor cortex (M1) possesses a functional somatotopic structure-representations of adjacent within
194 s was integral to illustrating comprehensive somatotopic structure; complex tasks can potentially hel
195           The observed pattern suggests that somatotopic subcortical remapping, projected to the cort
196                       During video watching, somatotopic tuning explains responses throughout the ent
197 first 3 weeks of postnatal development, when somatotopic whisker representations are sequentially est
198                             VIP cells showed somatotopic whisker tuning that was spatially organized

 
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