ライフサイエンスコーパス: proprioceptive

1 ar central pattern generator and/or hindlimb proprioceptive activity.

2 ng proprioception can a) effectively enhance proprioceptive acuity and b) improve the accuracy of unt

3 p, there were no strong associations between proprioceptive acuity and development of adverse OA outc

4 Proprioceptive acuity as assessed by the accuracy of rep

5 We hypothesized that proprioceptive acuity in both planes of movement will be

6 oss-sectional studies have reported impaired proprioceptive acuity in people with osteoarthritis (OA)

7 We examined the relation of baseline proprioceptive acuity in quartiles with baseline knee pa

8 The aim of this study was to assess knee proprioceptive acuity in the frontal and sagittal planes

9 Proprioceptive acuity was assessed in varus, valgus, fle

10 At baseline, proprioceptive acuity was associated with the presence a

11 Due to discrepancies in proprioceptive acuity, overlap in motor cortex represent

12 int scale) compared with those with the best proprioceptive acuity, whose pain and physical function

13 or all directions tested, indicating reduced proprioceptive acuity.

14 sening was not significantly associated with proprioceptive acuity.

15 leg and used a person's worst score as their proprioceptive acuity.

16 Compared to proprioceptive afferent collateral projections, less is

17 We show that the development of proprioceptive afferent input to motoneurons (MNs) and R

18 pinal axons in response to two complementary proprioceptive afferent manipulations: (1) enhancing pro

19 Knowledge of proprioceptive afferent responses after loss of the CST

20 Electrical stimulation produced proprioceptive afferent sprouting that was accompanied b

21 eptive afferent manipulations: (1) enhancing proprioceptive afferents activity by electrical stimulat

22 The reaction of proprioceptive afferents after this CST injury, however,

23 ons, indicating that the recruitment of limb proprioceptive afferents could participate in the locomo

24 pinal cord, while the projections of TrkC(+) proprioceptive afferents into the ventral horn are also

25 l spinal cord projections that converge with proprioceptive afferents on common spinal targets.

26 We found that 10 d after PTx, proprioceptive afferents sprout into cervical gray matte

27 dings suggest a novel structural reaction of proprioceptive afferents to the loss of CST terminations

28 r Math1 (Atoh1) lack multiple neurons of the proprioceptive and arousal systems and die shortly after

29 y schema processing (tactile discrimination, proprioceptive and body part illusions and self/non-self

30 showed that competitive interactions between proprioceptive and corticospinal axons are an important

31 view of somatosensory processing holds that proprioceptive and cutaneous inputs are conveyed to cort

32 However, proprioceptive and cutaneous maps have traditionally bee

33 The summed weighting of neck proprioceptive and efference copy information was suffic

34 l populations that contribute to cerebellar, proprioceptive and interoceptive networks.

35 generating the directional signal, but motor/proprioceptive and landmark information are important fo

36 ed from optic flow and run speed gauged from proprioceptive and locomotor systems.

37 We found that most large-diameter proprioceptive and mechanosensitive DRG neurons expresse

38 When self-motion is voluntarily generated, proprioceptive and motor efference copy information is a

39 odal information during self-motion, such as proprioceptive and motor efference copy signals, includi

40 ut instead by extravestibular inputs such as proprioceptive and motor efference copy signals.

41 ay interneurons that serve to integrate both proprioceptive and nociceptive afferent information.

42 Chordotonal organs perform proprioceptive and other mechanosensory functions in ins

43 y of higher-order sensorimotor coordination, proprioceptive and tactile feedback, and modulation of l

44 of participants' reaching was measured when proprioceptive and visual cues to the location of the ri

45 hese data suggest that despite an absence of proprioceptive and visual information regarding hand loc

46 he course of an erroneous reaching movement, proprioceptive and visual sensory pathways not only sens

47 convergence of separate sensory (upper body proprioceptive) and basilar pontine pathways onto indivi

48 brain neuronal networks serving respiratory, proprioceptive, and arousal functions share a developmen

49 Thus, motor, proprioceptive, and even some interneuron inputs are bia

50 ough the (Bayesian) fusion of exteroceptive, proprioceptive, and interoceptive signals, the precision

51 imals reached to visual, combined visual and proprioceptive, and proprioceptive targets while fixing

52 low-threshold mechanoreceptive neurons, two proprioceptive, and six principal types of thermosensiti

53 of three sensory feedback streams (auditory, proprioceptive, and vagal) did not alter the frequency o

54 postural control system to integrate visual, proprioceptive, and vestibular sensory information.

55 ssive upper motor neuron spastic and general proprioceptive ataxia in the pelvic limbs occurs at 8 ye

56 f, affected DRG neuron maturation as well as proprioceptive axon projection toward the ventral horn i

57 ve axons project to the ventral spinal cord, proprioceptive axons and their associated oligodendrocyt

58 esults in ectopic placement of the shafts of proprioceptive axons and their associated oligodendrocyt

59 sensory neurons into the spinal cord, where proprioceptive axons avoid the superficial dorsal horn-t

60 Whereas most proprioceptive axons enter the spinal cord medially, cut

61 Lastly, we detect guidance errors of proprioceptive axons in ADAM knockouts that are consiste

62 Because heavily myelinated proprioceptive axons project to the ventral spinal cord,

63 veals that ectopic oligodendrocytes, but not proprioceptive axons, inhibit synapse formation in Sema6

64 The signal is proprioceptive, because it can be obliterated by anesthe

65 Last, heat, mechanical, and proprioceptive behaviors were normal in ablated mice, de

66 Late-born ELs contribute to a proprioceptive body posture circuit, whereas early-born

67 lly expand the diversity of known vertebrate proprioceptive capabilities, and suggest that the pector

68 facial mucosa and skin and transmit tactile, proprioceptive, chemical, and nociceptive sensations.

69 odes eye position and that this signal has a proprioceptive component.

70 m as a new model for studying vestibular and proprioceptive contributions to the acquisition of senso

71 significant advances in our understanding of proprioceptive control of locomotion, and more abstract

72 c release, thereby providing a mechanism for proprioceptive control of locomotion.

73 e results of modelling provide insights into proprioceptive control of locomotion.

74 ately predicted the complete gravitropic and proprioceptive control over the movement of different or

75 tself, the connectivity of which facilitates proprioceptive control.

76 the macaque monkey, cebus monkeys possess a proprioceptive cortical area 2 and a well developed area

77 Proprioceptive coupling between adjacent body regions tr

78 in the 'Hold' condition, which suggests that proprioceptive cues apparently solidify spatial informat

79 We investigated whether proprioceptive cues interact with auditory attention to

80 contrast, when targets are defined by unseen proprioceptive cues, activity in these areas switches to

81 execution of movements based on sensory and proprioceptive cues.

82 and on self-generated (e.g., vestibular and proprioceptive) cues that signal the organism's own move

83 lude that cerebellar patients have an active proprioceptive deficit consistent with disrupted movemen

84 We did not observe any motor or proprioceptive deficits and noted no reduction in cutane

85 we show that human cerebellar patients have proprioceptive deficits compared with controls during ac

86 ce of JDY, a woman with severe, longstanding proprioceptive deficits from a sensory peripheral neurop

87 ignals during action and suggest that active proprioceptive deficits should be considered a fundament

88 ith unpredictable dynamics, they have active proprioceptive deficits similar to cerebellar patients.

89 difficulty ambulating, ataxia, hypermetria, proprioceptive deficits, and respiratory abnormalities.

90 tus provides the instructive cues to pattern proprioceptive dendrites.

91 actor (TF), BARHL2, regulates this choice in proprioceptive dI1 interneurons by selectively suppressi

92 t indirect effect of implicit racial bias on proprioceptive drift and magnitude of illusion through o

93 ed lower RH illusion magnitude and a smaller proprioceptive drift for the black RH.

94 ejudice and magnitude of the RH illusion and proprioceptive drift.

95 training to clinical populations with known proprioceptive dysfunction to enhance sensorimotor perfo

96 isorder, showing an increased sensitivity to proprioceptive error and a decreased sensitivity to visu

97 ents only occurred in the face of unexpected proprioceptive error.

98 d by the pattern of learning from visual and proprioceptive errors.

99 Whereas in the monkey, proprioceptive eye position signals have been recorded i

100 of the tibia and provides the main source of proprioceptive feedback about tibial kinematics.

101 layed-state manipulations between visual and proprioceptive feedback during a tracking task, we show

102 own), creating a conflict between visual and proprioceptive feedback for the hand behind the mirror.

103 comotor pattern degrades upon elimination of proprioceptive feedback from muscle spindles and Golgi t

104 Furthermore, proprioceptive feedback from ongoing movements provides

105 oprioception was introduced, indicating that proprioceptive feedback from the arm also affected size

106 ocess also hypothesized to be underpinned by proprioceptive feedback from the face.

107 mechanosensory inputs from the antennae and proprioceptive feedback from the ipsilateral but not the

108 elective visual neurons could reflect either proprioceptive feedback from the turn or internally gene

109 To demonstrate the role of proprioceptive feedback in aimed limb movements, we indu

110 These findings establish a role for proprioceptive feedback in the control of fundamental as

111 locomotor pattern under conditions in which proprioceptive feedback is attenuated genetically and bi

112 is elegans connectome dynamics, we show that proprioceptive feedback is necessary for sustained dynam

113 In the bony fishes it is unclear what proprioceptive feedback is provided from the paired fins

114 Our data demonstrate that proprioceptive feedback provides a graded signal that is

115 ormyrid fish--to directly examine how CD and proprioceptive feedback signals are transformed into neg

116 When visual and proprioceptive feedback were congruent, both the time to

117 Animal locomotion depends on proprioceptive feedback, which is generated by mechanose

118 be explained by an effect of diversion from proprioceptive feedback.

119 eurones in the absence of rhythmic input and proprioceptive feedback.

120 commands based on the <3 Hz fluctuations of proprioceptive feedback.

121 using sensory prediction errors detected by proprioceptive feedback.

122 on between self-generated motor commands and proprioceptive feedback; furthermore, the greater the re

123 rceptual regulation processes disambiguating proprioceptive first-person information (touch) from ext

124 Proprioceptive function can become enhanced during motor

125 we have incomplete knowledge to what extent proprioceptive function is trainable and how a training

126 These findings call into doubt the proposed proprioceptive function of palisade endings.

127 d circuit completely abolishes the recovered proprioceptive function of the hindlimb.

128 ecific Nf1 mutant mice spontaneously recover proprioceptive function.

129 These connections support proprioceptive functional recovery in a conditioning les

130 We hypothesize that the proprioceptive gaze signal in S1, although playing only

131 t resistance, and had an increased number of proprioceptive glutamatergic and calbindin-labeled putat

132 Nerve injury provokes the loss of many proprioceptive IA afferent synapses (VGLUT1-IR boutons)

133 ing (fMRI) revealed that matching visual and proprioceptive information about arm position engaged th

134 ontributed by the integration of tactile and proprioceptive information about current body posture wi

135 s of DSZ facilitate a modular integration of proprioceptive information along its major axis and diss

136 human brain dynamically handles the flow of proprioceptive information and converts it into appropri

137 es cortical processing of both cutaneous and proprioceptive information and their integration into mo

138 reflex arc is the system that integrates the proprioceptive information for muscle length and activit

139 mall, manipulable objects, where tactile and proprioceptive information form part of the multimodal p

140 brain areas thus likely integrate visual and proprioceptive information into a flexible multisensory

141 s could be achieved either by means of motor/proprioceptive information or by inferring eye movements

142 lated with CoG, TA may be a better source of proprioceptive information than the active agonists (sol

143 s for the relative role played by visual and proprioceptive information to be quantified.

144 stances from the mirror), and also when only proprioceptive information was available (i.e., when the

145 nd enhancing transmission of nociceptive and proprioceptive information, respectively; (2) by alterat

146 ition of the upper limbs based on visual and proprioceptive information.

147 estions: (1) Which ankle muscles provide the proprioceptive information?

148 nt condition, when only afferent (visual and proprioceptive) information can be used to estimate the

149 f different modalities of sensory, including proprioceptive, information forwarded to a major supsras

150 sis and show that a 15 min intervention with proprioceptive input (proprioceptive training) restored

151 Here, we show in humans that attention to proprioceptive input during a purely sensory task can in

152 the end of the saccade was not derived from proprioceptive input from eye muscles, and was not alter

153 learning gain: increasing the integration of proprioceptive input from the APB increased the rate of

154 ibed previously, which removed cutaneous and proprioceptive input from the thumb, index finger, and m

155 The effect of proprioceptive input from the trained muscle on SMO was

156 icant correlation between the integration of proprioceptive input in the motor cortex and the motor l

157 sly found an expanded spatial integration of proprioceptive input into the hand motor cortex [sensori

158 nsory attention tasks transiently change how proprioceptive input is integrated into the motor cortex

159 necessary for roughness perception and that proprioceptive input resulting from hand movement-rather

160 neurons with convergent vestibular and neck proprioceptive input those inputs functionally canceled

161 the motor cortex by testing the efficacy of proprioceptive input to reduce GABA(A)ergic intracortica

162 presumed, given the recently identified eye proprioceptive input to S1 and the established links bet

163 rimination task increased the interaction of proprioceptive input with motor cortex excitability in t

164 f the motor command to the moving hand or by proprioceptive input.

165 e scanning, which stresses the importance of proprioceptive input.

166 nding while providing bilateral load-bearing proprioceptive input.

167 th the capacity to mark or modulate incoming proprioceptive input.

168 tions revealed that cervical and lumbosacral proprioceptive inputs are more effective in this entrain

169 consequences of tail bending are opposed by proprioceptive inputs conveyed by parallel fibers and th

170 t with a disturbed integration of visual and proprioceptive inputs in the posterior parietal cortex.

171 properties and synaptic inputs, for example proprioceptive inputs preferentially target IaINs, while

172 d by parallel fibers and that the effects of proprioceptive inputs to efferent cells are plastic.

173 scending coupling influences of distant limb proprioceptive inputs to the cervical and lumbar generat

174 ous (early-born) and unconscious (late-born) proprioceptive inputs to the cortex and cerebellum, resp

175 on information from vestibular, visual, and proprioceptive inputs, degrades with aging, and falls ar

176 vestibular balance by minimizing visual and proprioceptive inputs.

177 w cells receive motor axon synapses and lack proprioceptive inputs.

178 ed performance variability, while decreasing proprioceptive integration had opposite effects.

179 tile interactions, they cannot isolate visuo-proprioceptive integration.

180 ral interneurons, which comprise a subset of proprioceptive interneurons.

181 None of the probes gave signals in proprioceptive joint receptors, suggesting that efferent

182 ely returning to the level expected based on proprioceptive learning alone.

183 astic process of state estimation underlying proprioceptive localization of the hand.

184 Drosophila larvae-which plays a key role in proprioceptive locomotion control.

185 Proprioceptive mechanoreceptors reside in skeletal muscl

186 g cutaneous low-threshold mechanosensory and proprioceptive mechanosensory neurons.

187 , and trochlear motor nuclei, as well as the proprioceptive mesencephalic trigeminal nucleus.

188 cally removed vision to eliminate the visual-proprioceptive mismatch that is a salient cue specific t

189 All participants showed evidence of proprioceptive-motor learning.

190 We next asked whether proprioceptive nerve endings are similarly affected in t

191 d early and significant alterations at Ia/II proprioceptive nerve endings in muscle spindles before t

192 However, analysis of proprioceptive nerve endings in muscles revealed early a

193 The proprioceptive neuron PVD in C. elegans extends regular

194 in the uterus defined by coexpression of the proprioceptive neuronal marker pickpocket (ppk) and the

195 x-determination gene fruitless (fru) and the proprioceptive neuronal marker pickpocket (ppk) in the f

196 , Cbln2 is expressed by mechanoreceptive and proprioceptive neurons and in regions of the spinal cord

197 Instead, SMN must be expressed in proprioceptive neurons and interneurons in the motor cir

198 corded comprised 14 cutaneous neurons and 28 proprioceptive neurons at 400 mum in the dorsal horn, 13

199 Proprioceptive neurons characterized by the expression o

200 ciated with the Johnston's organ, peripheral proprioceptive neurons in the legs, neurons in the larva

201 independent mouse lines that lack Piezo2 in proprioceptive neurons showed severely uncoordinated bod

202 li in a specific subpopulation of Drosophila proprioceptive neurons that sense joint angles.

203 eurons, as well as defects of spinal sensory proprioceptive neurons, but cranial nerve nuclei have re

204 Large, mainly proprioceptive neurons, had very low or negative stainin

205 e majority of nociceptive, pruriceptive, and proprioceptive neurons.

206 ccurately to their central targets to convey proprioceptive, nociceptive and mechanoreceptive informa

207 gs suggest that the application of a tactile-proprioceptive noise can improve the stability in sensor

208 ation and predator detection by transforming proprioceptive organs into ears.

209 piders have a variety of mechanosensilla and proprioceptive organs that are innervated by efferents i

210 TRPgamma is expressed in proprioceptive organs, and is required in both neurons a

211 tor control through mechanical activation in proprioceptive organs, thereby promoting Ca(2+) influx,

212 fine motor control, both of which depend on proprioceptive organs.

213 edback from mechanosensory-and particularly, proprioceptive-organs may help an animal to keep its cir

214 specifies distinct neuronal subtypes of the proprioceptive pathway in mammals including the dI1 (dor

215 nucleus, suggesting a monosynaptic, possibly proprioceptive, pathway.

216 human PPC, PMv, and EBA evaluate visual and proprioceptive position information and, under sufficien

217 primary visual cortex during congruent visuo-proprioceptive position information.

218 ce, in which subjects try to minimise their (proprioceptive) prediction error based upon posterior be

219 They also suggest that effective cortical proprioceptive processing operates at <3 Hz frequencies,

220 ical circuits are organized for higher order proprioceptive processing.

221 information from joints has been attributed proprioceptive properties similar to those of muscle spi

222 d, or sighted) were briefly presented with a proprioceptive reach target while facing it.

223 guided reaches and a body-centered frame for proprioceptive reaches.

224 Muscle spindle proprioceptive receptors play a primary role in encoding

225 SMA motor neurons show reduced proprioceptive reflexes that correlate with decreased nu

226 orticocortical circuits arising in the major proprioceptive region of the primary somatosensory corte

227 vidence accumulation signal was expressed in proprioceptive regions (bilateral posterior insula).

228 Proprioceptive reinforcement of fundus pattern recogniti

229 In contrast, proprioceptive-related neurons and ventral horn neurons

230 We aimed to disrupt the proprioceptive representation of the right eye in the le

231 tcentral gyrus that overlapped the human eye proprioceptive representation.

232 Neurons (29/44) had proprioceptive responses; the majority (21/29) were acti

233 be perceived as a diversion from unpleasant proprioceptive sensations that go along with exhaustion.

234 Proprioceptive sensing is thus as important as gravisens

235 on (pain localization, fine/crude touch, and proprioceptive sensing) in multiple dermatomes.

236 reflects the ratio between graviceptive and proprioceptive sensitivities.

237 toral fins need to be considered as possible proprioceptive sensors in studies of their functional mo

238 ing Cdc42 in sensory neurons does not affect proprioceptive sensory axon targeting because axons reac

239 acking Cdc42 in presynaptic sensory neurons, proprioceptive sensory axons appropriately reach the ven

240 ant dynein-mediated postnatal loss of lumbar proprioceptive sensory axons, accompanied by decreased e

241 on signal was only gated in conditions where proprioceptive sensory feedback matched the motor-based

242 ral pattern generators." The contribution of proprioceptive sensory feedback to the coordination of l

243 Furthermore, we show that a simple form of proprioceptive sensory feedback, wherein local muscle ac

244 ity that spinocerebellar neurons that convey proprioceptive sensory information also integrate inform

245 o difference in the total number and size of proprioceptive sensory neuron soma between symptomatic S

246 on the specification of distinct classes of proprioceptive sensory neurons (pSN), but the factors th

247 hair cell transduction, is also expressed by proprioceptive sensory neurons (pSNs) in dorsal root gan

248 sponse of motoneurons, intermediate gray and proprioceptive sensory neurons after spinal cord injury

249 ABApre, forms synapses with the terminals of proprioceptive sensory neurons and controls information

250 Pdm1 and Pdm2 are expressed in a subset of proprioceptive sensory neurons and function to inhibit d

251 nderlying synapse formation between group Ia proprioceptive sensory neurons and motor neurons is the

252 he sensory portion of the arc is composed of proprioceptive sensory neurons and the muscle spindle, w

253 ssion and/or activity of Runx3 in individual proprioceptive sensory neurons appears to specify whethe

254 Overall, we show that Ia/II proprioceptive sensory neurons are affected by ALS-causi

255 Immunohistochemical analyses reveal that proprioceptive sensory neurons are severely compromised

256 In both transgenic lines, we found fewer proprioceptive sensory neurons containing fluorescently

257 Group Ia proprioceptive sensory neurons form direct synapses with

258 This study examines proprioceptive sensory neurons in mice harboring mutatio

259 gin-dependent presynaptic differentiation of proprioceptive sensory neurons in vitro These data sugge

260 ation of wild-type, but not Cdc42-deficient, proprioceptive sensory neurons in vitro Together, our fi

261 The selectivity with which proprioceptive sensory neurons innervate their central a

262 ll autonomous, excitotoxic contribution from proprioceptive sensory neurons that modestly accelerates

263 l cells, little is known about its effect on proprioceptive sensory neurons.

264 oss, also present with a severe, early-onset proprioceptive sensory neuropathy.

265 Proprioceptive sensory signals inform the CNS of the con

266 c neurons exhibits an absolute dependence on proprioceptive sensory terminals, yet the molecular unde

267 type cholinergic motor neurons transduce the proprioceptive signal.

268 hways (nociceptive signals are reduced while proprioceptive signals are enhanced); (2) alterations in

269 one's hand changes according to tactile and proprioceptive signals conveying hand position.

270 projected on one's hand changes according to proprioceptive signals conveying hand position.

271 an inability to generally enhance peripheral proprioceptive signals during action and suggest that ac

272 Large sensory neurons of the Me5 receive proprioceptive signals from periodontal ligaments and ma

273 y and absence of body-weight-supporting limb proprioceptive signals in amphibian tadpoles as a potent

274 esentations are used to represent visual and proprioceptive signals in both area 5 and MIP.

275 n combine motor commands with vestibular and proprioceptive signals optimally.

276 onstrated precise matching of vestibular and proprioceptive signals, even for complicated stimuli, wh

277 s traditional for vestibular signals without proprioceptive signals.

278 upon the integration of visual, tactile, and proprioceptive signals.

279 left limbs, and the third compares touch and proprioceptive signals.

280 y/vestibular, somatosensory (lemniscal), and proprioceptive (spinocerebellar) systems.

281 integrating changes in visual, tactile, and proprioceptive stimulation from self-motion and discrimi

282 alert squirrel monkeys during vestibular and proprioceptive stimulation produced during (1) yaw head-

283 bject-comparison task, concurrent tactile or proprioceptive stimulation to the hands facilitates conc

284 that most neurons responded to cutaneous and proprioceptive stimuli, including cells in areas 3a and

285 rived IaINs and RCs are competent to receive proprioceptive synapses, these synapses preferentially t

286 pinal muscular atrophy (SMA), a reduction in proprioceptive synaptic drive leads to motor neuron dysf

287 In SMA mice or after the blockade of proprioceptive synaptic transmission, we observed a decr

288 r ear hair cells, and several neurons of the proprioceptive system, as well as diverse nonneuronal ce

289 hat Math1 is also required for the conscious proprioceptive system, including excitatory projection n

290 ord, including the vestibular, auditory, and proprioceptive systems.

291 ual, combined visual and proprioceptive, and proprioceptive targets while fixing their gaze on anothe

292 tegration through self-touch, which provides proprioceptive, thermal, and tactile input forming a coh

293 Proprioceptive training restored this balance in musicia

294 min intervention with proprioceptive input (proprioceptive training) restored SMO in pianists with m

295 otion-related interoceptive representations (proprioceptive, vestibular, and motor efference copy) co

296 ace, and trunk), based on the integration of proprioceptive, vestibular, and visual bodily inputs, an

297 nd provides a novel method for investigating proprioceptive-vestibular interactions during stance.

298 Proprioceptive-vestibular interactions, coupled with cor

299 Cs in neonates, raising the possibility that proprioceptive (VGLUT1-positive) and motor axon synapses

300 imotor area whose sensory input is primarily proprioceptive, while sPOS is a visuomotor area that rec