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1 ibratory sensation, ankle reflexes, or light touch).
2 imaging and electrophysiology during active touch.
3 ly brief volleys of activity associated with touch.
4 cuits dedicated to the spatial processing of touch.
5 to judge the speed of an object's motion by touch.
6 adaptation-aftereffect paradigm with passive touch.
7 could be tactile, involving direct physical touch.
8 iscrimination and hypersensitivity to gentle touch.
9 perceive sights, sounds, smells, tastes, and touch.
10 powerful insights into population coding in touch.
11 were or were not accompanied by simultaneous touch.
12 pressed, which could facilitate detection of touch.
13 lower than those that occurred during active touch.
14 t, L4 excitatory neurons responded mainly to touch.
15 pace, where the valence and conduction bands touch.
16 the antenna due to sound, wind, gravity, and touch.
17 T-optimal) vs. neutral (fast; CT-suboptimal) touch.
18 ng literature showing postural modulation of touch.
19 by multi-whisker interactions during active touch.
20 mice respond to both self-motion and active touch.
21 nto an independent sensory modality, namely, touch.
22 r confidence in what we have seen, heard, or touched.
23 H-bonded complexes has been only marginally touched.
24 f the hand on the perceived distance between touches.
25 hich has been shown to host a quadratic band touching.
26 st detection of single-point and multi-point touching.
31 ection, and even the ability to habituate to touch, a simple form of learning usually seen in higher
33 r clinicians to conduct remote palpation, or touching, a key component of the physical exam, remains
36 both visual and haptic exploration; however, touch also recruits high-acuity central representation w
37 e horizontal angle at which a vibrissa first touches an object, and we therefore asked whether this p
38 igm focusing on the anticipation of actively touching an animate (human hand) versus an inanimate tar
46 information about both innocuous and painful touch and inhibitory populations that serve as a gate to
47 locally to the skin can be used to modulate touch and may represent peripherally available drugs to
48 anical stimulations, namely, proprioception, touch and nociception were delivered to the limb and the
49 inal circuit that mediates crosstalk between touch and pain pathways and suggest that some early RET+
50 al descending serotonergic control of spinal touch and pain processing emerges in late postnatal life
55 go external mechanical loads such as wind or touch and respond to these stimuli by acclimating their
58 ation-related behaviours such as locomotion, touch and sound sensation across different species inclu
59 nals arising from the whisker movements with touch and stimulation by the littermates, support: (1) a
60 ty of nociceptive stimuli, including noxious touch and temperature, with stereotyped escape responses
63 tic domain and BECN1:ATG14 subcomplex do not touch, and it is unclear how allosteric signals are tran
65 tic sensation (pain localization, fine/crude touch, and proprioceptive sensing) in multiple dermatome
66 integrates it with information about sound, touch, and state of the animal that is relayed from othe
69 d S1 process signals related to movement and touch are enabled by targeted muscle and sensory reinner
70 The sensations of sound, acceleration and touch are mediated by mechanotransduction channels, whic
73 hat body posture modulates the perception of touch, as well as somatosensory processing more widely.
76 nsduction for senses such as proprioception, touch, balance, acceleration, hearing and pain relies on
78 the extent to which brain responses to light touch (but not sham) are attenuated at the time of disch
80 t only activate "visual" areas during object touch, but also that this information appears to be used
81 the somatosensory thalamus (VPM), respond to touch, but have low spike rates and low sensitivity to t
82 ins, a display that emits light from regions touched by human fingers (or painted upon using a mixtur
83 onmental stimuli (such as humidity, light or touch) by varying internal turgor, which leads to dynami
84 ess, no study has examined whether affective touch can also modulate psychological identification wit
85 injury or diabetic neuropathy, the slightest touch can produce pain, and here STOML3 inhibitors can r
86 , it remains unknown whether slow, affective touch, can also reduce feelings of social exclusion, a f
87 ives rise to feelings of pleasant, affective touch, can enhance the experience of body ownership duri
88 e developed and report for the first time a "touch-capable" mHealth technology that enables a patient
89 rovides computational solutions for tracking touching cells in confluent samples, handles various cel
90 eceptor types, the transient responses of T (touch) cells and the sustained responses of P (pressure)
91 experiment (N = 38) spatial incongruence of touch (cheek vs. forehead) was used as a control conditi
96 This spatial pattern selectivity requires touch-dependent dopamine signaling, including the mechan
101 wever, have cast doubt on the segregation of touch discrimination and affect, suggesting that S1 also
103 ulation to demonstrate the representation of touch discrimination and intensity in S1, but the repres
107 population coding is a general mechanism of touch encoding common to species as different as man and
108 skin revealed striking similarities between touch encoding in the primate and the leech: summed spik
109 our data suggest that CT-optimal, affective touch enhances subjective (but not behavioural) self-fac
110 ypersensitivity (aversion to certain sounds, touch, etc., or increased ability to make sensory discri
111 ith disorganized lens, microcephaly, reduced touch-evoked motility, and highly disorganized myofibers
112 legans nematodes deprived of a sense of body touch exhibit various changes in behavior, associated wi
113 e number of unstimulated fingers between two touched fingers or a localization task in which particip
114 agement of sensory aspects such as sight and touch for materials and structures that are otherwise in
115 al rewards, indexed by a lower proportion of touches for the button associated with the social reward
119 uced haptoelectric stimulation activates the touch hormone jasmonate (JA) signaling pathway, which in
121 TEMENT In daily life, we seamlessly localize touch in external space for action planning toward a sti
123 the neural implementation of the location of touch in space.SIGNIFICANCE STATEMENT In daily life, we
124 aradigm to investigate the role of affective touch in the modulation of self-face recognition during
129 duce thigmomorphogenesis - the phenomenon of touch-induced changes in plant growth and development.
132 y abolished by MEC-10 mutations encoded by a touch-insensitive mec-10 allele, providing a correlation
133 ies spike count and response latency to both touch intensity and location, leading to ambiguous respo
135 the sustained responses of P cells indicate touch intensity by summed spike counts and stimulus dura
137 experiences (e.g., supportive versus painful touch) interact to shape the development of the somatose
138 rns of vibration to vary systematically with touch interactions and determined that it is possible to
146 slow-affective, as compared to fast-neutral, touch led to a specific decrease in feelings of social e
147 underlying temperature sensation and gentle touch, less is known about the neurons specific for mech
149 hether the administration of slow, affective touch may reduce the negative feelings of ostracism indu
150 recovery of object attributes during active touch, may guide the development of approaches to roboti
152 ion channel that plays a major role in light-touch mechanosensation and has recently been identified
153 trochemical microscopy, operated in molecule touching mode (Mt/AFM-SECM), and of dense nanodot arrays
155 in 108 consecutive patients treated with no-touch multibipolar radiofrequency ablation (RFA) for hep
157 that met Milan criteria were treated with no-touch multibipolar RFA, which consisted of activating, i
158 I) ensures that this essential micronutrient touches nearly every major metabolic process or pathway
159 phb-2 partially phenocopied loss of mec-2 in touch neurons of the nematode, resulting in impaired gen
164 patterns, but direct interactions involving touch occurred at a rate two orders of magnitude higher
165 The most commonly used maneuver was the touching of facial areas (35 of 64 patients [54.7%]); ot
168 their diverse and essential functions, which touch on nearly all aspects of RNA metabolism, the roles
169 tional network analysis of these papers, and touch on some of the important discoveries in plant biol
172 llusion, the temporal window for integrating touch on the physical body with touch seen on a virtual
173 on basal bud (tiller) formation but scarcely touched on aerial buds, which may lead to aerial branch
176 Larvae escape by backward locomotion when touched on the head, while they crawl forward when touch
178 terminants of endurance performance but also touches on some historical and sociological factors rele
179 hand modulate the perceived distance between touches on the hand, and add to a growing literature sho
180 to come into contact with the body, evoking touch or pain sensations and possibly triggering an appr
184 ntial in applications such as photovoltaics, touch panels, liquid crystal displays, and organic light
186 to the soothing function of slow, affective touch, particularly in the context of social separation
188 dition, they negatively regulate DH pain and touch pathways through both pre- and postsynaptic inhibi
189 each had a selective loss of discriminative touch perception but nevertheless responded to specific
192 anically activated ion channels that mediate touch perception, proprioception and vascular developmen
196 re two sets of Weyl points (, ) exist at the touching points of electron and hole pockets and are loc
199 (ROI) from the background, and then separate touching RBCs in the ROI images by applying an improved
201 indicate that under normal function, ongoing touch receptor neuron activation evokes FLP-20 release,
204 dy wall muscle, ciliated sensory neurons and touch receptor neurons - where it recapitulates expected
206 echanotransduction in Caenorhabditis elegans touch receptor neurons is mediated by an ion channel for
210 xcitatory neurons, enhancing selectivity for touch-related information during active tactile sensatio
218 odel hand felt like one's own (illusory self-touch); reversely, the attenuation that was expected to
220 gger the activation of a visual display on a touch screen as part of an operant conditioning task.
221 gger the activation of a visual display on a touch screen as part of an operant conditioning task.
226 integrating touch on the physical body with touch seen on a virtual body representation, increases w
227 cold (38 of 51 patients [75%]), loss of fine touch sensation (17 of 35 patients [49%]), and epidermal
229 raphy activity from reinnervated muscles and touch sensation on the missing limb is enabled by stimul
231 cal signals for critical processes including touch sensation, balance, and cardiovascular regulation.
234 theory (GCT) of pain proposes that pain- and touch-sensing neurons antagonize each other through spin
237 athic pain transduction in a specific, light-touch-sensitive neuronal type recruited during mechanica
239 to make two mutually exclusive actions on a touch-sensitive screen: "tap" and "hold." Taps led to th
240 udy, we employed smart tablet computers with touch-sensitive screens and embedded inertial movement s
250 ctive when blind individuals read Braille by touch, suggesting that vision is not required for the de
251 tor behavior was paired with whisker-texture touches, suggesting that direct S1-S2 interactions are s
252 role of the activity in dl-FC before target touch; suppression of activity in pyramidal neurons with
253 In less than two to three hours, most high-touch surfaces in the cabin are contaminated, and within
255 utes to growing delineation of the affective touch system, a crucial step in understanding its dysreg
258 aracteristics of cortical responses to light touch that differentiate them from sham stimuli in full-
261 hen a mite (a parasitic pest for Drosophila) touches the wing margin, the fly initiates a swift and a
262 ) and specific healthcare worker activities (touching the bed rail [odds ratio, 2.19; 95% CI, 1.00-4.
264 total of 1000 patients with TT, with lashes touching the eye or evidence of epilation, in associatio
265 matous trichiasis with one or more eyelashes touching the eye or evidence of epilation, in associatio
269 is stabilized in the TAR complex despite not touching the RNA, explaining how it enhances TAR binding
271 iscovered, from the people whose lives she'd touched, the ways in which Deborah had been a gift.
274 ests were performed to measure the cutaneous touch threshold and perceptual threshold of force pertur
275 have investigated the relationships between touch threshold, tactile gnosis, and mechanoreceptor and
280 t use single senses alone (vision to vision; touch to touch) to perform this recognition until the fo
281 gle senses alone (vision to vision; touch to touch) to perform this recognition until the following d
288 i-proliferative transcriptional program that touches upon a bewildering array of biological responses
295 scrimination thresholds obtained for passive touch were significantly lower than those that occurred
296 compared to when they were close together or touching, whereas judgements were unaltered when adjacen
297 Recent studies suggest that slow, affective touch, which is mediated by a separate, specific C tacti
299 hat was expected to occur during actual self-touch with the real hands was reduced when the participa
300 ormance characteristics of the FibroScan 502 Touch with two probes, medium (M+) and extra large (XL+)
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