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1 manipulation and cutaneous stimulation of 14 body parts).
2 rs, the trident is not located on an exposed body part.
3 omes not only a tool, but also an integrated body part.
4 injected bilaterally, and into more than one body part.
5 ession of afferent sensation from the moving body part.
6 y was not affected by viewing the stimulated body part.
7 striatal neurons that have switched to that body part.
8 as of cortex after amputation of an adjacent body part.
9 present the location of the arm or any other body part.
10 suggest a representation anchored to another body part.
11 , establishing the healthy baseline for this body part.
12 y part into something that resembles another body part.
13 sms and/or aberrant postures of the affected body part.
14 regenerate limbs, brains, and other complex body parts.
15 duced somatosensation in the stroke-affected body parts.
16 s, in some animals, the regeneration of lost body parts.
17 ) or laterality judgment (left/right) of the body parts.
18 sue necessary for the replacement of missing body parts.
19 y asymmetric fragments to regenerate missing body parts.
20 kernels, which underlie development of major body parts.
21 n their natural abilities to regenerate lost body parts.
22 rrespond to the representations of different body parts.
23 dify developmental pathways to sculpt animal body parts.
24 ted bilaterally responding preferentially to body parts.
25 ng goal-directed movements of the observer's body parts.
26 ons that innervate homologous right and left body parts.
27 BA) has been implicated in the perception of body parts.
28 from one body part to one or more different body parts.
29 omotoneuronal excitability to the stimulated body parts.
30 it its intents to replacement or reactivated body parts.
31 regeneration (with organogenesis) of missing body parts.
32 ces, with overlapping patterns for different body parts.
33 the brain encodes the relative positions of body parts.
34 ale allocates the received PA quickly to all body parts.
35 o touch or taps on the stump and neighboring body parts.
36 fold in adult head (brain) relative to other body parts.
37 y excessive, unintended motion of contiguous body parts.
38 omains and dachsous mutations cause deformed body parts.
39 tween Hox proteins cause differences between body parts.
40 interspersed with clusters related to other body parts.
41 d no evidence of overlap, or convergence, of body parts.
42 light septa that formed isomorphs with some body parts.
43 retention in the tumor, the liver and other body parts.
44 lity among vertebrates to regenerate complex body parts.
45 by the real-time physical distances between body parts.
46 related to functional-semantic properties of body parts.
47 oportions, eclipsing in size the surrounding body parts.
48 ammatory papules and ulcers, located in >/=2 body parts.
49 hilst social anointing targets hard-to-reach body parts.
50 high, for instance when grooming vulnerable body parts.
51 vements, and movements coordinating multiple body parts.
52 ol of voluntary movement involving different body parts.
53 re pronounced species differences than other body parts.
54 istinct motor programs that clean individual body parts.
55 duals showed global differentiation of adult body parts.
56 ns are flatworms capable of regenerating all body parts.
58 rganization, sensory activity in a localized body part activates striatal neurons that have switched
59 motor strip, with words related to different body parts activating the corresponding body representat
60 uch as external cause, intent, location, and body part affected were reported for all injury outcomes
61 7 [95% CI, 1.71-2.75; P<.001]) and number of body parts affected with vitiligo (P</=.009) but not lat
64 hin anthropology and, second, what defines a body "part." After exploring these initial questions, th
65 phila wing imaginal disc gives rise to three body parts along the proximo-distal (P-D) axis: the wing
66 vity for motion, intact objects, bodies, and body parts, although only the peak voxel of each region
67 ians are capable of regenerating any missing body part and present an attractive system for molecular
68 Oral representation was most ventral of all body parts and extended to the ventral boundary of the l
70 ion between faces and nonface objects (i.e., body parts and inanimate objects), and (2) the regionall
71 rate aging mostly utilized the whole body or body parts and limited age-points, and failed to address
73 cally on how multisensory representations of body parts and of the 'peripersonal' space immediately a
74 ide new markers that address the homology of body parts and provide clues as to how body plans have e
75 age underwater face challenges because their body parts and senses are adapted for land--for example,
78 ative genetic correlation among the involved body parts and, therefore, constitutes a developmental s
79 atosensory responses to both face (congruent body part) and finger (control site) tactile stimulation
80 or cut with a bloody object, pierced ears or body parts, and immunoglobulin injection must be interpr
81 ctivated by natural categories (e.g., faces, body parts, and places), artificial categories (numerals
83 bly they depend on the patterns of growth of body parts, and simple analyses have shown that exponent
84 clear selectivity to static images of human body parts, and upper limbs in particular, with respect
85 ttempts at individuated movements of a given body part are accompanied by excessive, unintended motio
95 A preferential fetal blood flow to the upper body parts at the expense of the intra-abdominal organs
96 f preferential fetal blood flow to the upper body parts at the expense of the intra-abdominal organs.
97 a discussion of demarcation of an invisible body part, before concluding that images of phantom limb
98 rs, tactile processing but not auditory, and body-part bisection tasks but not line bisection tasks.
99 to the painful side for visual processing of body parts but not letters, tactile processing but not a
100 only during the perception of other people's body parts, but also during goal-directed movements of t
101 h show great interdependence: the sight of a body part can reduce tactile target detection times [1],
104 ts that the primate brain constructs various body-part-centred representations of space, based on the
105 ands, feet, arms, and legs), (2) noneffector body parts (chests and waists), and (3) face parts (uppe
106 ifferent functions associated with the three body part clusters, reflecting the unique processing and
107 e test how three motor variables (body side, body part, cognitive strategy) are coded in the human an
110 etrieval of limbs, faces, and possibly other body parts demands algorithms for the sequence of steps
111 ng images to reveal an absent though sensate body part, depictions of phantom limbs are discussed fro
119 es on the representation of the deafferented body parts (feet, but not hands) and (ii) regardless of
120 d somatotopic areas of the face and multiple body parts forming a higher-level homunculus in the supe
121 formation, enabling prediction of the moving body part from inside and outside its somatotopic locati
122 y simulating one's action and discriminating body part handedness both depend on lateralized sensorim
123 pictures of whole persons, chairs, and eight body parts (hands, arms, legs, feet, chests, waists, upp
124 ence that: taking ownership of an artificial body part has consequences for the real body part; that
125 cern about the proprietary rights over human body parts has had a dramatic recent impact in some Euro
126 The task involved choosing between using a body part (i.e. crows: beak; humans: hand) or a tool for
127 on in order to generate the desired cells or body parts; identification and appropriate manipulation
128 (tactile discrimination, proprioceptive and body part illusions and self/non-self differentiation).
131 magnification of the representation of that body part in the somatosensory cortex, so that the repre
132 might not be predictive for the actual plant body part in which a transcript exerts its function.
133 ow a fruit fly's brain tells it to groom its body parts in a stereotyped order might help us understa
136 e findings illustrate that interaction among body parts in development is part of the mechanism of si
138 take into account the movements of multiple body parts in haptic perception, and they show that the
139 We suggest that the semantic organization of body parts in high-level visual cortex relates to the di
141 eater numbers of differentiated segments and body parts in insects, compared with the simpler body pl
142 model best captured the neural similarity of body parts in lateral and ventral OTC, which followed an
145 nts viewed color photographs depicting human body parts in painful or nonpainful situations and perfo
150 is, we could predict movements of individual body parts in these homunculi, thus confirming that they
151 tes that it is a vertebrate; considering its body parts in this new light suggests it was an anatomic
152 sh have the remarkable ability to regenerate body parts including the heart and fins by a process ref
153 ry bristles and pegs distributed on multiple body parts including the proboscis, wing margins, legs,
154 capacity to regenerate their arms and other body parts, including central and peripheral nervous sys
155 ans possess the capacity to regenerate their body parts, including the limbs and the lens of the eye.
156 study population, physical injuries to other body parts, including the trunk, arms, or legs, were not
158 ntation involves subdivision of a developing body part into multiple repetitive units during embryoge
159 sically defined as the transformation of one body part into something that resembles another body par
160 nt (spastic or athetoid) or according to the body parts involved (hemiplegia, diplegia, or quadripleg
163 rodele amphibians to regenerate a variety of body parts is providing insight into mechanisms of tissu
166 by an uncontrollable shaking of the affected body part, is often professed to be the most common move
167 s a rhythmic and involuntary movement of any body part, is the most prevalent movement disorder, affe
171 n gene expression have been observed between body parts made of similar cell types, how regulatory in
172 ure - Matrix Generation pipeline to generate body part measurement matrices from a set of 188 spider
173 The tools produced two corresponding spider body part measurement matrices, and the matrix from the
174 ming its validity, 96.7% reported right-left body part mislabeling during examination or biopsy, and
176 lecular basis for segmentation of individual body parts occurring at later developmental stages.
177 bitants of Sulawesi fashioned ornaments from body parts of endemic animals, suggesting modern humans
181 (OR = 2.1; 95% CI: 1.1-4.1), pierced ears or body parts (OR = 2.0; 95% CI: 1.1-3.7), and immunoglobul
182 to a portion of the SI cortex representing a body part other than the hand, suggesting that multisens
185 rity of multivoxel activity patterns for all body part pairs was established in whole person-selectiv
186 dieter obsesses about reduction of different body parts, permanent reduction of many structures seems
190 nd vice versa, led to a greater reduction in body part priming than compatible training, in which sub
191 presentation of (i) the intact hand and (ii) body parts proximal to the deafferented hand (upper arm)
194 fferentiation, which allow complex organ and body part regeneration, are discussed and common molecul
195 r representations of monkey faces and monkey body parts relative to man-made objects using functional
199 ficance statement: While the organization of body part representations in motor and somatosensory cor
201 ell characterized, the principles underlying body part representations in visual cortex have not yet
202 ear to be both matched and mismatched to the body part representations injected in the opposite hemis
203 l body, and that the general organization of body part representations mirrors that of the primary so
204 died the effects of rTMS delivered to nearby body part representations on the motor output from the u
205 the absence of excitability changes in other body part representations such as thorax or leg muscles.
206 significant differences in averaged area of body-part representations for body/chest and head/neck w
207 jacent to the border of lateral S1 and other body-part representations progressing more caudally towa
211 ortical genital neurons showed unusual multi-body-part responses and sexually dimorphic receptive fie
214 on induces substantial reorganization of the body part somatotopy in primary sensory cortex (S1 compl
215 motor system more than truthful actions in a body-part-specific manner, suggesting that motor resonan
217 uggesting the main tissues or cells in these body parts, such as brain, neurons and muscles, which ha
220 resent the hand per se, but rather any other body part that shares the functionality of the missing h
221 Individual anointing targets hard-to-see body parts that are harder to groom, whilst social anoin
222 y behaviors may involve utilization of other body parts that do not cortically neighbor the hand terr
224 cial body part has consequences for the real body part; that the awareness of our physical self and t
229 o multisensorially determined perceptions of body parts, to action execution, and even to attribution
230 d isometric muscle contractions in different body parts (tongue protrusion, fist-clenching or foot do
232 lowed an organization in three clusters: (1) body parts used as action effectors (hands, feet, arms,
236 ibians and teleost fish regenerate amputated body parts via a process called epimorphic regeneration.
237 creen and told to imagine that the displayed body part was part of a standing mirror image of themsel
238 porating the bilateral/axial movements of 20 body parts, we report detailed mototopic imaging maps in
239 eurons related functionally to an individual body part were interspersed with clusters related to oth
240 ntral area resulting from stimulation of all body parts were considered, this region appeared to cont
244 ity resulted in largely orthogonal coding of body parts, which "functionally segregate" the effector
245 new experimental procedures on virtual human body parts, which are generated and visualised three-dim
246 ensory illusions and ownership of artificial body parts, which has important implications for patient
250 al responses to motion, objects, bodies, and body parts with whole-brain group-average analyses and w
251 visual processing of hands as highly salient body parts, with distortions engaging neural resources t
252 ion, the relative independence of moving one body part without others is lost; attempts at individuat
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