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1 tivity to account for observed adult RFs and somatotopy.
2 e dorsal locus, consistent with motor cortex somatotopy.
3 o behaviorally relevant whiskers, overriding somatotopy.
4 ects with detailed tonotopy, retinotopy, and somatotopy.
5 lateral corticospinal tract, arguing against somatotopy.
7 ncluding the following: a rough, overlapping somatotopy; a posterior strip in which simpler movements
8 tigate the intersubject variability of digit somatotopy across participants and the stability of this
10 the concept of a segregated "point-to-point" somatotopy and instead resembles the complex patterns th
11 dystonia is associated with a distorted hand somatotopy and lend weight to an alternative hypothesis
13 sed model of development of dorsal horn cell somatotopy and RF geometries must be revised to take var
15 e, we characterize the spatial organization (somatotopy) and stability of the bilateral sensorimotor
16 ) the reorganized map maintained a fractured somatotopy, and (3) the denervated area was predominantl
20 ndicate that S1 and M1 independently develop somatotopy before establishing the interactive relations
22 improvements in primary somatosensory cortex somatotopy can predict long-term clinical outcomes for c
24 over years since SCI the hand representation somatotopy deteriorated, suggesting that somatotopic han
26 here we reveal the existence of fine-grained somatotopy for nociceptive inputs to the digits in human
27 ovement zone reflected an overall pattern of somatotopy, from eye and face movements most ventrally t
28 traced into the hindbrain, where a distinct somatotopy has been previously described, we find that t
31 cording to current understanding of striatal somatotopy (i.e. the lower limb is dorsal to the upper l
32 s unclear if this descending pathway retains somatotopy, i.e., body map organization, a hallmark of t
35 nnectivity of these homunculi, such that the somatotopy in one hemisphere could have been found given
36 substantial reorganization of the body part somatotopy in primary sensory cortex (S1 complex, hereaf
37 contradictory and partial results regarding somatotopy in the caudal-cingulate zone and rostral-cing
39 e complete description of the dorsal-ventral somatotopy in the lateral striatum of the rat, which as
40 nctional magnetic resonance imaging assessed somatotopy in the primary somatosensory cortex using vib
41 ncle, there is accumulating evidence against somatotopy in the pyramidal tract in the lower brainstem
43 e properties and the recovery of near-normal somatotopy likely supported the recovery of hand use.
44 rtical organization differs significantly in somatotopy, number, and position of fields from that of
45 ivity throughout several sessions, comparing somatotopy of active electrodes, as well as neural signa
47 caudal to the obex, characterized by precise somatotopy of primary afferent terminations and correspo
48 e also interested in determining whether the somatotopy of rDAO is the result of a point-to-point pro
49 trate the presence of very stable fine-grain somatotopy of the digits in human S1 and raise the issue
51 n other species of monkey shows a consistent somatotopy of the face between species; size variations
53 were 6-8 months old, the responsiveness and somatotopy of the primary somatosensory cortex (S1) cont
54 -paced motor task were used to represent the somatotopy of the putamen and were then used to characte
58 s provided, demonstrating that the ratio and somatotopy of types A and C sensory fibers at the site o
60 are still based on a supposed corticospinal somatotopy or 'lamination', with greater vulnerability o
61 eurobiological model to study development of somatotopy, patterning, and plasticity at both the morph
62 perience-dependent changes in cortical digit somatotopy, relatively little work has considered the va
63 on fMRI tasks documented concentric effector somatotopies, separated by the CON-linked inter-effector
67 vestigated whether CBI changes in humans are somatotopy specific and how they relate to motor adaptat
70 to be driven by the layout of the underlying somatotopy, such that neighboring body-part representati
71 ection map that was systematically linked to somatotopy, such that neurons were tuned for motion towa
73 nar organization of direction preference and somatotopy using a new omni-directional, multi-vibrissa
74 ments examining this projection to cingulate somatotopy using combined neural tracing strategies and
75 segmental movements were represented and the somatotopy was less segregated; a clustering of differen
76 that we found followed known corticostriatal somatotopy, was dose-dependent, and was selectively sens
77 aphy of alpha ERD more resembled traditional somatotopy when its temporal profile approximated that o
78 le in the somatosensory and motor systems is somatotopy, where specific body parts are represented se
79 ary motor area (SMA) showed more integrative somatotopy with higher sharing for within-limb represent
80 ng pre- and postsynaptic embryonic and adult somatotopies, with a progressive transformation of RF an