ライフサイエンスコーパス: mechanoreceptor

1 ceptor neurons (which include high-threshold mechanoreceptors).

2 nance and sensory function of the piloneural mechanoreceptor.

3 alpha5beta1 integrin acting as a predominant mechanoreceptor.

4 t a requirement for a conventional molecular mechanoreceptor.

5 osensing without the need for a conventional mechanoreceptor.

6 hanical signaling pathway in fly campaniform mechanoreceptor.

7 a critical role in craniofacial growth as a mechanoreceptor.

8 lanceolate nerve endings of rapidly adapting mechanoreceptors.

9 criminating functional subtypes of cutaneous mechanoreceptors.

10 ng signals from multiple types of peripheral mechanoreceptors.

11 ng is essential for the development of these mechanoreceptors.

12 e esophagus activated from different sets of mechanoreceptors.

13 , and allodynia involves TrkB(+) light-touch mechanoreceptors.

14 d utilizes variables easily sensed by insect mechanoreceptors.

15 umber and function of regenerated fibers and mechanoreceptors.

16 that these fibers function as low-threshold mechanoreceptors.

17 agus with nociceptors in addition to tension mechanoreceptors.

18 ears use chordotonal organs as the auditory mechanoreceptors.

19 f cutaneous (SSEA4) and muscle (parvalbumin) mechanoreceptors.

20 ent with an origin from cutaneous and muscle mechanoreceptors.

21 ng information from slow- and rapid-adapting mechanoreceptors.

22 sensory organs, ganglion cells and hair cell mechanoreceptors.

23 anosensation: low-threshold rapidly adapting mechanoreceptors.

24 of the DEG/ENaC cation channel family may be mechanoreceptors.

25 Mechano-gated ion channels are cardiac mechanoreceptors.

26 , suggesting a limited contribution from the mechanoreceptors.

27 lly composed of cell bodies of low threshold mechanoreceptors.

28 dback from stretch-sensitive cardiopulmonary mechanoreceptors.

29 force stimuli that mimics slow-adapting skin mechanoreceptors.

30 neighboring DRG neurons activates RET in RA mechanoreceptors.

31 termination and the specification of lingual mechanoreceptors.

32 that larger fingers have more widely spaced mechanoreceptors.

33 al fibers innervating the lamina propria and mechanoreceptors.

34 initiated when fast conducting low-threshold mechanoreceptors (Abeta-LTMRs) generate impulses at thei

35 l reflexes may be caused by left ventricular mechanoreceptor activation.

36 e mechanical ventilation (hence, respiratory mechanoreceptor activity remained constant).

37 ans in the absence of changes in respiratory mechanoreceptor activity.

38 ), central respiratory drive, or respiratory mechanoreceptor activity.

39 Zymosan produced sensitization of colon mechanoreceptors acutely in vitro and chronic (>or=7 wee

40 ry somatosensory cortex (SI and SII) to skin mechanoreceptor afferent drive.

41 REM increases V A possibly via activation of mechanoreceptor-afferent pathways rather than by respira

42 We conclude that spike-timing precision of mechanoreceptor afferents in response to dynamic stimula

43 sensory terminals, suggesting innervation by mechanoreceptor afferents.

44 riate sensory information from low-threshold mechanoreceptor after sciatic nerve neuroma formation.

45 iceptors was apparent both in high threshold mechanoreceptor and polymodal nociceptors and also in un

46 between touch threshold, tactile gnosis, and mechanoreceptor and sensory fiber function after nerve r

47 and painful stimuli, perhaps contributing to mechanoreceptor and/or H+ -gated nociceptor function.

48 The hypothesis that polymodal mechanoreceptors and capsaicin-sensitive afferent nerves

49 convergence and divergence between cutaneous mechanoreceptors and dorsal horn cell are constant was e

50 ns to integrate information from neighboring mechanoreceptors and generate somatosensory perception.

51 Sensory information from mechanoreceptors and nociceptors in the skin plays key r

52 ctional classes (nociceptors/pruritoceptors, mechanoreceptors and proprioceptors) that are distinguis

53 Thus, the early Ret(+) neurons are RA mechanoreceptors and Ret signaling is required for the a

54 n, but they have been proposed to constitute mechanoreceptors and/or nociceptors.

55 Local mechanoreceptors are a leading possibility.

56 rmation coded by the different low-threshold mechanoreceptors are carried by anatomically and electro

57 The non-nociceptive vagal tension mechanoreceptors are distinguished from nociceptors by t

58 hances the pressor response seen when muscle mechanoreceptors are engaged by muscle stretch.

59 In rodent hairy skin these mechanoreceptors are excited by hair movement.

60 These tension mechanoreceptors are exclusively A-fibres arising from t

61 Ventricular mechanoreceptors are known to exist and can when stimula

62 s and mechanisms of development of RA and SA mechanoreceptors are largely unknown.

63 These results show that coronary mechanoreceptors are likely to play an important role in

64 at MSNA responses to isolated stimulation of mechanoreceptors are measurable.

65 When mechanoreceptors are stimulated, mechanically sensitive

66 currently it is not known how impulses in C-mechanoreceptors are transmitted to higher centres.

67 peripheral mechanoreceptor types, as well as mechanoreceptors at different sites in the body.

68 regions is affected by loading low pressure mechanoreceptors at the SVC-RAJ, a manipulation that als

69 d isolectin B4 binding, suggesting that some mechanoreceptors became CGRP-IR.

70 PCs are classified as primary mechanoreceptors because there is no synapse between the

71 mmunohistochemistry and possible alternative mechanoreceptors by real-time quantitative polymerase ch

72 , suggesting the functional reinnervation of mechanoreceptors by the reinnervating afferents.

73 VGLUT3-expressing unmyelinated low-threshold mechanoreceptors (C-LTMRs) are proposed to mediate pleas

74 od population of unmyelinated, low threshold mechanoreceptors (C-LTMRs).

75 Indeed, some mechanoreceptors can detect even nanometer-scale movemen

76 verified whether isolated stimulation of the mechanoreceptors can induce responses in muscle sympathe

77 udies demonstrate that modulation of surface mechanoreceptors can regulate the sensitivity to mechani

78 Interestingly, the body touch mechanoreceptors can themselves excite the dopamine neur

79 The identity of mechanoreceptor candidates is approached, with considera

80 Mechanoreceptor cells of the somatosensory system initia

81 Mechanoreceptor cells respond to a vast span of stimulus

82 Hair cells in the inner ear are specialized mechanoreceptor cells that detect sound and head movemen

83 pose that md-L neurons are long sought after mechanoreceptor cells through which food mechanics are p

84 cochlear sensory epithelium to replace lost mechanoreceptor cells, or hair cells.

85 he incapacity of the cochlea to replace lost mechanoreceptor cells, or hair cells.

86 fruit fly larvae and that it is a bona fide mechanoreceptor channel for nematode feeding behavior.

87 een made towards identifying the elusive AHC mechanoreceptor channel.

88 that the response was mediated primarily by mechanoreceptors close to the mucosal surface; whereas t

89 e pathway requires a conserved DEG/ENaC/ASIC mechanoreceptor complex in the FLP neuron pair.

90 This mechanoreceptor complex was recognized to have an essent

91 The two-receptor system could provide this mechanoreceptor complex with a tuning mechanism to achie

92 stimulation in the tiny population of leech mechanoreceptors, consisting of only 10 cells of two typ

93 These papillae show the hallmarks of a mechanoreceptor, containing nerves and encapsulated nerv

94 to sympathetic outflow is attenuated and the mechanoreceptor contribution is accentuated.

95 Signals from cutaneous mechanoreceptors convey the information necessary for bo

96 imb increases HR suggesting that small fibre mechanoreceptors could also have a role.

97 ity and a modest decrease in the size of the mechanoreceptor current (MRC).

98 Touching e1605 animals produces a reduced mechanoreceptor current that inactivates more rapidly th

99 cesses of ALM neurons and, consequently, the mechanoreceptor current.

100 hat external force evokes rapidly activating mechanoreceptor currents (MRCs) carried mostly by Na(+)

101 onses to noxious stimuli, we found that both mechanoreceptor currents and potentials were essentially

102 entified which is required for production of mechanoreceptor currents by insect bristles, and seems l

103 ation at the central terminals of myelinated mechanoreceptors depresses synaptic input to the spinal

104 The star has the densest concentration of mechanoreceptors described for any mammal, with a centra

105 gically distinct, myelinated, nodose-derived mechanoreceptors described in animals are poorly charact

106 Loss of DRASIC increased the sensitivity of mechanoreceptors detecting light touch, but it reduced t

107 mice the majority of putative low threshold mechanoreceptors did not exhibit ASIC-like currents but

108 sed the threshold pressure for initiation of mechanoreceptor discharge.

109 Thus, gastric vagal mechanoreceptors display circadian rhythm, which may act

110 and to compare this with the contribution of mechanoreceptors.Eighteen heart failure patients and 12

111 e relative timing of the first spikes of two mechanoreceptors encodes stimulus location, whereas summ

112 Vagal afferent input from cardiac mechanoreceptors excites neurones in the nucleus tractus

113 eflex is also demonstrated in the leg, while mechanoreceptors exhibited a non-significant contributio

114 Putative low threshold mechanoreceptors exhibited rapidly adapting mechanically

115 d, respiratory activity is modulated by lung mechanoreceptor feedback: transient lung inflation trigg

116 clude that after nerve injury, low threshold mechanoreceptor fibers may play a major role in producin

117 sts that PECAM-1 may not function as a major mechanoreceptor for activation of MAPK and AKT in ECs an

118 ein-3 (STOML3), which is required for normal mechanoreceptor function.

119 dependent on this information serve similar mechanoreceptor functions.

120 latory circuit downstream of the MK-specific mechanoreceptor GPIb to coordinate polarized transendoth

121 sensory-related genes such as TRPs, PPKs and mechanoreceptors had consistent levels of expression in

122 Receptors innervating long mechanoreceptor hairs (>1000 microm) are most sensitive

123 at IHCs are compartmentalized into an apical mechanoreceptor half and a basal half that affects neuro

124 a suggest that if paradoxic activation of LV mechanoreceptors has a role in mediating neurally mediat

125 pe similar to that of IVD cells, a number of mechanoreceptors have been identified, with alpha5beta1

126 cal activation of pressure-sensitive cardiac mechanoreceptors have not been studied in vivo.

127 sation is normally suppressed by inputs from mechanoreceptors; however, in many forms of chronic itch

128 might be true for myelinated high-threshold mechanoreceptors (HTMRs).

129 Esophageal mechanoreceptors, i.e. muscular slowly adapting tension

130 these data show for the first time that the mechanoreceptor ICAM-1 is negatively regulated by an act

131 muscle spindles, which are stretch-sensitive mechanoreceptors important for proprioception.

132 The DGC likely represents a mechanoreceptor in skeletal muscle-regulating muscle gro

133 acutely, zymosan sensitized muscular/mucosal mechanoreceptors in both naive and hypersensitive mice.

134 Rapidly adapting (RA) mechanoreceptors in dorsal root ganglia (DRGs) express R

135 in ECs and that there are likely to be other mechanoreceptors in ECs functioning to detect shear stre

136 tified as candidates for a spring that gates mechanoreceptors in hair cells as well as in Drosophila

137 in the primary cilia, which also function as mechanoreceptors in many cells that influence multiple b

138 It is suggested that mechanoreceptors in muscle play an important role in the

139 e whisker deformations, which in turn excite mechanoreceptors in the follicle.

140 s reveal MC4R expression in nerve fibers and mechanoreceptors in the glans of the penis.

141 or laryngeal nerve (SLN) or by deflection of mechanoreceptors in the laryngeal mucosa.

142 ecific vibrotactile stimulation of different mechanoreceptors in the skin.

143 hal ganglion and receive input from antennal mechanoreceptors in this lower region of the CNS.

144 From hair cells and skin mechanoreceptors in vertebrates, to bristle receptors in

145 ated currents in sensory neurons and silence mechanoreceptors in vivo.

146 two types of vagal afferents (both putative mechanoreceptors) in the muscle of the gastrointestinal

147 of the somatic afferent paths from forelimb mechanoreceptors (including low threshold cutaneous rece

148 ical properties with those of intrapulmonary mechanoreceptors indicates that the afferent neurones me

149 ndicated that the stimulation of ventricular mechanoreceptors induces significant reflex responses ca

150 t also revealed new sites of expression: PNS mechanoreceptors (inner ear hair cells and Merkel cells)

151 The central projections of these RA mechanoreceptors innervate layers III through V of the s

152 Mechanoreceptors innervated by the internal branch of th

153 Monitoring the responses of all four mechanoreceptors innervating a patch of skin revealed st

154 ng stimuli to identify whether low-threshold mechanoreceptor input to these neurons arises from myeli

155 -126 cm s(-1)) were used to characterize the mechanoreceptor inputs to 'wide dynamic range' neurons i

156 es, but not A-fibres, conveyed low-threshold mechanoreceptor inputs to lamina I projection neurons.

157 nsic structure, likely integrates visual and mechanoreceptor inputs.

158 are minimal, or are not simply summated with mechanoreceptor inputs.

159 rsor cells intended to become BDNF-dependent mechanoreceptors instead differentiate into NT-3-depende

160 cellular signaling systems on-line after the mechanoreceptor is activated are reviewed, including tho

161 ng role of the lipid membrane across various mechanoreceptors is now an accepted hypothesis.

162 essure-sensitive afferent input from cardiac mechanoreceptors is transmitted primarily by left vagal

163 of the dorsal root ganglion and in cutaneous mechanoreceptors known as Merkel-cell-neurite complexes.

164 th the hypothesis that the stimulation of LV mechanoreceptors leads to reflex hypotension and/or brad

165 The Pacinian corpuscle (PC), a cutaneous mechanoreceptor located deep within the dermis of the sk

166 s: arterial wall deformation, stimulation of mechanoreceptors located in the BR nerve-endings, and mo

167 that it receives substantial input from skin mechanoreceptors located on both sides of the body.

168 egion implicated in processing low-threshold mechanoreceptor (LTMR) information.

169 Low-threshold mechanoreceptors (LTMRs) are believed to project extensi

170 ition and that A- and C-fibers low threshold mechanoreceptors (LTMRs) terminate in lamina IIi raise t

171 hanosensory end organs and the low-threshold mechanoreceptors (LTMRs) that innervate them.

172 rmed by unique combinations of low-threshold mechanoreceptors (LTMRs), Abeta RA-LTMRs, Adelta-LTMRs,

173 ct populations of neurons, the low-threshold mechanoreceptors (LTMRs), which are classified as Abeta-

174 ialized sensory neurons termed low-threshold mechanoreceptors (LTMRs).

175 taneous sensory neurons called low-threshold mechanoreceptors (LTMRs).

176 sifying them as nociceptive or low-threshold-mechanoreceptors (LTMs) and as having C-, Adelta- or Aal

177 tively innervated by cutaneous low threshold mechanoreceptors (LTMs).

178 of large-diameter GG neurons expressing the mechanoreceptor marker NF200 and the GDNF coreceptor GFR

179 lly related suggests that all these ciliated mechanoreceptors may be derived from the same ancestral

180 ted peripheral nerve fibers and reinnervated mechanoreceptors may differentially influence recovery o

181 structural specializations, the two putative mechanoreceptors may have different functions: IGLEs app

182 In mechanoreceptors, mechanical stimulation by external for

183 Each mechanoreceptor neuron of the leech varies spike count a

184 r contribute indirectly by maintaining basic mechanoreceptor neuron physiology.

185 in amplitude than responses of low threshold mechanoreceptor neurones.

186 in control by studying responses from single mechanoreceptor neurons in Drosophila.

187 ead and nose touch using multiple classes of mechanoreceptor neurons that are electrically coupled th

188 l for survival and relies on the function of mechanoreceptor neurons that vary in their size, shape,

189 ns (nonpeptidergic and C-fiber low-threshold mechanoreceptor neurons) resistant to direct and trans-s

190 n the environment may impact the function of mechanoreceptor neurons.

191 conduct electrophysiological recording from mechanoreceptor neurons.

192 and encoding of mechanical forces by primary mechanoreceptor neurons.

193 stigating the cell-surface activation of two mechanoreceptors: Notch and E-cadherin.

194 Moreover, in the duck, the expansion of mechanoreceptors occurs at the expense of thermosensors.

195 nsitivity and assessed the function of colon mechanoreceptors of hypersensitive mice.

196 Sensory hair cells are mechanoreceptors of the auditory and vestibular systems

197 In vertebrates, hair cells are well-known mechanoreceptors of the inner ear and lateral line, typi

198 es share expression in the neuromasts, known mechanoreceptors of the lateral line peripheral nervous

199 y of ion channel proteins coexpressed in the mechanoreceptors of worms, flies, and mice.

200 ditionally, obesity loads may be detected by mechanoreceptors on chondrocyte surfaces triggering intr

201 m a variety of sensory modalities, including mechanoreceptors on their antennae, to stabilize the dir

202 sociating the sensory epithelia of the three mechanoreceptor organs, the utricle/saccule, cristae, an

203 cific role of KCNQ4 in rapidly adapting skin mechanoreceptors, our results show that different KCNQ i

204 cratica (Salpida)--to verify the presence of mechanoreceptors, particularly hair cells.

205 ciliary-associated proteins polycystin-1 (a mechanoreceptor), polycystin-2 (a Ca2+ channel), and the

206 no mechanoreceptor potential (nomp) mutations have been iso

207 The reduced mechanoreceptor potential A (rempA) locus of Drosophila

208 Loss-of-function mutations in the no mechanoreceptor potential C (nompC) gene virtually aboli

209 For example, no mechanoreceptor potential C (NOMPC), a member of transie

210 nnels, we identified Ripped Pocket (rpk), No Mechanoreceptor Potential C (nompC), and NMDA Receptors

211 We further identify NOMPC (No mechanoreceptor potential C), a member of the transient

212 Mutations in the no-mechanoreceptor-potential A (nompA) gene, which eliminat

213 d vagal axon bundles, single axons, putative mechanoreceptor precursors (intraganglionic laminar endi

214 cles and exhibit a dramatic disruption of RA mechanoreceptor projections to both the spinal cord and

215 the response to cocaine through ventricular mechanoreceptors rather than mediating the responses.

216 Pelvic nerve mechanoreceptors recorded from zymosan-treated or naive

217 l projection deficits, but Gfralpha2 null RA mechanoreceptors recover later.

218 activated throughout inspiration via ongoing mechanoreceptor reflexes.

219 known, however, whether integrins, acting as mechanoreceptors, regulate cell survival via the PI3K/Ak

220 in the transmission of this putative cardiac mechanoreceptor-related activity to NTS neurones.

221 present report, centered on rapidly adapting mechanoreceptors, represents the first study of the cent

222 Proprioceptive mechanoreceptors reside in skeletal muscle and inform th

223 he primary afferent neurons of the haltere's mechanoreceptors respond selectively with high temporal

224 The rapidly adapting (RA) low-threshold mechanoreceptors respond to movement of the skin and vib

225 t touch, but it reduced the sensitivity of a mechanoreceptor responding to noxious pinch and decrease

226 We conclude that in man small fibre muscle mechanoreceptors responding to stretch, inhibit cardiac

227 standardized mechanical stimulus to compare mechanoreceptor response before and after treatment.

228 a control preparation, suppression of type I mechanoreceptor response during 2-min, arterial infusion

229 Metaboreceptor and mechanoreceptor responses were measured in the leg by bi

230 riments have shown an increase in rat type I mechanoreceptor responsiveness during arterial serotonin

231 from outside the type I complex, influences mechanoreceptor responsiveness.

232 The identity of the mechanoreceptor(s) is approached, with consideration of

233 of four slowly adapting type I low-threshold mechanoreceptors (SAIs) that innervated the back skin of

234 The beta(1) integrin, functioning as a mechanoreceptor, senses a mechanical stimulus generated

235 ceptors, sensitive to metabolic changes, and mechanoreceptors, sensitive to mechanical changes) in th

236 diverse etiologies, presumably as part of a mechanoreceptor signaling complex.

237 ever, chondrocyte cilia were not the initial mechanoreceptors, since both WT and ORPK cells showed me

238 antitative activation of genetically encoded mechanoreceptors) stems from the fact that many mechanic

239 responses to both tooth pulp and facial hair mechanoreceptor stimulation are significantly attenuated

240 The mechanoreceptor stimulation model, uses circumferential

241 components produced by contralateral tactile mechanoreceptor stimulation of the tip of the index fing

242 dify reflex bronchospasm initiated by airway mechanoreceptor stimulation.

243 Within-breath phasic changes in airway mechanoreceptor stimuli (negative pressure or flow) were

244 that the mechanosensitivity of low-threshold mechanoreceptors strongly depends on Piezo2.

245 the mechanosensitivity of most low-threshold mechanoreceptor subtypes involved in innocuous touch sen

246 cell types formed include neurons, hair-cell mechanoreceptors, supporting cells, secretory cells that

247 Mechanoreceptors surrounding each whisker encode and tra

248 anchored proteoglycan dystroglycan (DG) is a mechanoreceptor that transmits mechanical stretch forces

249 The skin is equipped with specialized mechanoreceptors that allow the perception of the slight

250 air cells of the mammalian inner ear are the mechanoreceptors that convert sound-induced vibrations i

251 atosensory system contains multiple types of mechanoreceptors that detect different mechanical stimul

252 the majority of duck trigeminal neurons are mechanoreceptors that express the Piezo2 ion channel and

253 ptor (DOR), which is expressed by myelinated mechanoreceptors that form Meissner corpuscles, Merkel c

254 ons are large- or medium-diameter myelinated mechanoreceptors that form the Merkel cell-neurite compl

255 al endings of a broad range of low-threshold mechanoreceptors that innervate both hairy and glabrous

256 d the TRPV family of cation channels as osmo-mechanoreceptors that may mediate the neuronal responses

257 r cells are exquisitely sensitive vertebrate mechanoreceptors that mediate the senses of hearing and

258 endowed with low-threshold, slowly adapting mechanoreceptors that respond to self-generated movement

259 However, the mechanoreceptors that respond to tissue stretch are poor

260 amuscular arrays (IMAs) are the two putative mechanoreceptors that the vagus nerve supplies to gastro

261 ntramuscular arrays (IMAs), the two putative mechanoreceptors that the vagus nerve supplies to the ga

262 Merkel cells form slowly adapting cutaneous mechanoreceptors that transduce steady indentation in ha

263 arying stretches of two different crustacean mechanoreceptors, the gastropyloric receptor 2 in the cr

264 In fly campaniform mechanoreceptors, the mechanotransduction channels are g

265 ans and other mammals implicate one of these mechanoreceptors, the Merkel cell/neurite complex, in tw

266 ing the touch responses of the anterior-body mechanoreceptors; this modulation involves a D1-like dop

267 estimate of the sensitivity of an individual mechanoreceptor to an applied stimulus (parameterised as

268 Many arthropods use filiform hairs as mechanoreceptors to detect air motion.

269 ays relaying inputs from low-threshold Abeta mechanoreceptors to lamina I output neurons.

270 ity; and (4) SRIF reduces responses of joint mechanoreceptors to noxious rotation of the knee joint.

271 o generate shearing forces essential for the mechanoreceptors to sense gravity and linear acceleratio

272 y organs contain hair cells that function as mechanoreceptors to transduce sound and head motion.

273 nner ear contain hair cells that function as mechanoreceptors to transduce sound and motion signals.

274 peripheral mechanical nociceptors and Abeta mechanoreceptors, together with spinal SOM(+) excitatory

275 Cutaneous mechanoreceptors transduce different tactile stimuli int

276 biological receptors like photoreceptors and mechanoreceptors transduce physical energy into a neural

277 Mutations disrupting the DVA mechanoreceptor (TRP-4) decreased aldicarb-induced NLP-1

278 ust combine signals from multiple peripheral mechanoreceptor types, as well as mechanoreceptors at di

279 For the two mechanoreceptor types, the transient responses of T (tou

280 ical and optogenetic stimulation of specific mechanoreceptor types.

281 l and cisplatin administration on the type I mechanoreceptor using a skin-nerve preparation in rat an

282 , the only effective stimulus to ventricular mechanoreceptors was an increase in filling.

283 te the origin of firing patterns in branched mechanoreceptors, we combined neuroanatomy, electrophysi

284 ing the leech body wall while recording from mechanoreceptors, we show that pairs of leech sensory ne

285 Recently, Merkel cell mechanoreceptors were identified as a fourth lineage der

286 urons to air puff stimulation of facial hair mechanoreceptors were significantly increased by 96% dur

287 tro single-fiber recordings of gastric vagal mechanoreceptors were taken at all time points.

288 technique, including tactile stimulation of mechanoreceptors, were followed for 2 years, and results

289 rst reconstructs the stresses experienced by mechanoreceptors when the skin is deformed and then simu

290 oural data to estimate the minimum number of mechanoreceptors which must be activated to elicit a beh

291 In addition to these mechanoreceptors, which are found in most teleost fishes

292 equire facilitation by additional nose touch mechanoreceptors, which couple electrically to the nocic

293 d that the "early Ret(+)" DRG neurons are RA mechanoreceptors, which form Meissner corpuscles, Pacini

294 pressed in muscle spindles-stretch-sensitive mechanoreceptors, while muscle denervation induces exten

295 that early-born Ret+ sensory neurons are RA mechanoreceptors, whose peripheral nerve terminals are a

296 We present a power-efficient skin-inspired mechanoreceptor with a flexible organic transistor circu

297 ion (control), during stimulation of forearm mechanoreceptors with venous congestion, and during isch

298 receiving inputs from nociceptors and Abeta mechanoreceptors, with Abeta inputs gated through feed-f

299 Sensory hair cells (HCs) are the mechanoreceptors within the inner ear responsible for ou

300 inly in TrkB-expressing (TrkB(+)) and Ret(+) mechanoreceptors within the TG during embryogenesis.