ライフサイエンスコーパス: somatotopy

1 tivity to account for observed adult RFs and somatotopy.

2 e dorsal locus, consistent with motor cortex somatotopy.

3 stic pattern, from tonotopy to retinotopy to somatotopy [1].

4 ncluding the following: a rough, overlapping somatotopy; a posterior strip in which simpler movements

5 tigate the intersubject variability of digit somatotopy across participants and the stability of this

6 the concept of a segregated "point-to-point" somatotopy and instead resembles the complex patterns th

7 sed model of development of dorsal horn cell somatotopy and RF geometries must be revised to take var

8 he processing of information related to both somatotopy and sensory modality.

9 ) the reorganized map maintained a fractured somatotopy, and (3) the denervated area was predominantl

10 osensory area (S1) by its relative position, somatotopy, architecture, and connections.

11 ostrocaudal segregation and trigeminal tract somatotopy are similar to mouse.

12 improvements in primary somatosensory cortex somatotopy can predict long-term clinical outcomes for c

13 here we reveal the existence of fine-grained somatotopy for nociceptive inputs to the digits in human

14 ovement zone reflected an overall pattern of somatotopy, from eye and face movements most ventrally t

15 traced into the hindbrain, where a distinct somatotopy has been previously described, we find that t

16 However, in most previous studies somatotopy has not been examined in detail and brief, se

17 s unclear if this descending pathway retains somatotopy, i.e., body map organization, a hallmark of t

18 nnectivity of these homunculi, such that the somatotopy in one hemisphere could have been found given

19 substantial reorganization of the body part somatotopy in primary sensory cortex (S1 complex, hereaf

20 contradictory and partial results regarding somatotopy in the caudal-cingulate zone and rostral-cing

21 n in children depends on this restoration of somatotopy in the central sensory maps.

22 e complete description of the dorsal-ventral somatotopy in the lateral striatum of the rat, which as

23 nctional magnetic resonance imaging assessed somatotopy in the primary somatosensory cortex using vib

24 e properties and the recovery of near-normal somatotopy likely supported the recovery of hand use.

25 rtical organization differs significantly in somatotopy, number, and position of fields from that of

26 mary afferent terminations and corresponding somatotopy of cytochrome oxidase (CO) blotches.

27 caudal to the obex, characterized by precise somatotopy of primary afferent terminations and correspo

28 e also interested in determining whether the somatotopy of rDAO is the result of a point-to-point pro

29 trate the presence of very stable fine-grain somatotopy of the digits in human S1 and raise the issue

30 We determined the somatotopy of the face and the oral cavity representatio

31 n other species of monkey shows a consistent somatotopy of the face between species; size variations

32 The somatotopy of the other, satellite maxima in the field o

33 were 6-8 months old, the responsiveness and somatotopy of the primary somatosensory cortex (S1) cont

34 The effects followed the somatotopy of the rostral IO: a loss of cells in medial

35 The general somatotopy of the trigeminal representation in monkeys i

36 Thus, somatotopy of trigeminal ganglion and nerve organization

37 s provided, demonstrating that the ratio and somatotopy of types A and C sensory fibers at the site o

38 perience-dependent changes in cortical digit somatotopy, relatively little work has considered the va

39 The well-known subthalamic somatotopy showed a large overlap of feet and hand repre

40 nite foot-dorsal, hand-ventral basal ganglia somatotopy, similar to prior data from primates.

41 vestigated whether CBI changes in humans are somatotopy specific and how they relate to motor adaptat

42 nges in cerebellar-M1 connectivity reflect a somatotopy-specific interaction.

43 simple hand or leg movement would produce a somatotopy-specific modulation of CBI.

44 ection map that was systematically linked to somatotopy, such that neurons were tuned for motion towa

45 Somatotopy (upper versus lower limb: 93% accuracy for bo

46 nar organization of direction preference and somatotopy using a new omni-directional, multi-vibrissa

47 ments examining this projection to cingulate somatotopy using combined neural tracing strategies and

48 segmental movements were represented and the somatotopy was less segregated; a clustering of differen

49 that we found followed known corticostriatal somatotopy, was dose-dependent, and was selectively sens

50 aphy of alpha ERD more resembled traditional somatotopy when its temporal profile approximated that o

51 ary motor area (SMA) showed more integrative somatotopy with higher sharing for within-limb represent

52 ng pre- and postsynaptic embryonic and adult somatotopies, with a progressive transformation of RF an