ライフサイエンスコーパス: unmyelinated

1 e percentage of the SGNs in this strain were unmyelinated.

2 missive neuronal somata and dendrites remain unmyelinated.

3 are immunopositive for VR1 are predominantly unmyelinated.

4 on postnatal day 1 (P1) when WM tracts were unmyelinated.

5 ent for NRG1 type III are disproportionately unmyelinated, aberrantly ensheathed, and hypomyelinated,

6 pha3 expression is similar in myelinated and unmyelinated adult sensory neurons, suggesting that ARTN

7 We conclude that unmyelinated AEN terminal projections are involved in th

8 ehavioral responses and neuronal activity in unmyelinated afferent fibers were assessed in monkey aft

9 eceptor within skeletal muscle (localized to unmyelinated afferent fibres) elicits increases in MAP a

10 the thermal pain sensitivity by depletion of unmyelinated afferent neurons.

11 that correspondingly identify myelinated and unmyelinated afferent pathways at the NTS.

12 ta-methylene ATP suggest that myelinated and unmyelinated afferent pathways engage both mGluR-GABA me

13 of the sciatic nerve to trace myelinated and unmyelinated afferent terminations, respectively, in the

14 an with a tracer that labels non-peptidergic unmyelinated afferents (Griffonia simplicifolia isolecti

15 eA neurons received inputs derived from only unmyelinated afferents [transient receptor potential cat

16 nts is particularly surprising because these unmyelinated afferents are thought to respond to the gra

17 activates a subpopulation of myelinated and unmyelinated afferents in monkey, (4) the time course of

18 elated peptide and isolectin B4, and injured unmyelinated afferents labeled with vasoactive intestina

19 additional and separate phenotypic marker of unmyelinated afferents rather than operated by TRPV1.

20 l ganglion neurons (SGNs) are small caliber, unmyelinated afferents that extend dendritic arbors hund

21 sly uncharacterized subset of myelinated and unmyelinated afferents, few of which express the proinfl

22 ae I and IIo and in terminals of peptidergic unmyelinated afferents, it is suggested that presynaptic

23 expressed the IB4 marker of non-peptidergic unmyelinated afferents.

24 ccount for heat and capsaicin sensitivity in unmyelinated afferents.

25 in medial NTS, whereas IB4 was found only in unmyelinated afferents.

26 By contrast, olfactory nerve axons are unmyelinated and arranged in tightly packed bundles, fea

27 maining spiral ganglion cells (type IIs) are unmyelinated and contact OHCs [2-4].

28 Increased numbers of small, unmyelinated and degenerated optic nerves as well as los

29 imb movement; most lack an AIS, and some are unmyelinated and have no nodes.

30 npruned collaterals in adult mutant mice are unmyelinated and maintain their synaptic contacts.

31 ic itch is mediated through activity in both unmyelinated and myelinated afferents.

32 s used to evaluate morphological features of unmyelinated and myelinated axons.

33 tively excited neural activity in endogenous unmyelinated and myelinated axons.

34 r PNS myelination driving axonal wrapping by unmyelinated and myelinated Schwann cells and enhancing

35 s of function in modalities mediated by both unmyelinated and myelinated sensory axons.

36 istinct sodium channel alpha subunits to the unmyelinated and myelinated zones of the same retinal ga

37 morphometrically evaluated at intraorbital (unmyelinated and myelinated) and intracranial sections.

38 tive (NET-ir) axonal profiles were typically unmyelinated and occasionally were observed to form symm

39 Nociception is produced by stimulation of unmyelinated and small myelinated fibers in the joint an

40 ents from these neurons can be myelinated or unmyelinated and their terminals in these laminae can be

41 early overlapped in laminae I-II with normal unmyelinated and thin myelinated afferents labeled with

42 odulate afferent transmission by myelinated, unmyelinated, and peptidergic afferents in the dorsal ho

43 tigate its effect on the morphology of small unmyelinated as well as myelinated sensory axons and rel

44 , neocortical auditory fields are relatively unmyelinated at birth and only attain adult-like MFLD va

45 apses; (ii) postsynaptic disorders affecting unmyelinated auditory nerve dendrites; (iii) postsynapti

46 s in which the small, lightly myelinated and unmyelinated autonomic nerve fibres are selectively targ

47 We confirmed the presence of unmyelinated axon bundles within the P3 CC, but failed t

48 that TRIF-dependent microglial clearance of unmyelinated axon debris facilitates axon outgrowth.

49 conduction delays of action potentials in an unmyelinated axon depended on the history of activity an

50 region that corresponded most closely to the unmyelinated axon initial segment, as defined by Golgi a

51 an orientation consistent with granule cell unmyelinated axon labeling.

52 ssociated with microstructural WM injury and unmyelinated axon loss at P1, diagnosed by diffusion ten

53 The model replicates activity in the unmyelinated axon of the crustacean stomatogastric pylor

54 be explained in one of two ways: either the unmyelinated axon of the immature cerebral hemispheres i

55 no systematic observations directed towards unmyelinated axon pathophysiology.

56 odelling emphasises uncertainties about fine unmyelinated axon physiology but, when informed by biolo

57 Thus, unmyelinated axon tracts are critical for patterning the

58 ing 12% were associated with glial and small unmyelinated axon-like structures.

59 daily to adult rats to examine its effect on unmyelinated axon-Schwann cell units in intact periphera

60 oform, Na(v)1.2, is found in the neighboring unmyelinated axon.

61 properties of the cerebellar granule cell's unmyelinated axon.

62 unusually long (approximately 20-40 microm) unmyelinated axonal heminode.

63 function of slow-conducting, small-diameter unmyelinated axons (C fibers) during aglycemia.

64 generated by myelinated axons (N1 wave) and unmyelinated axons (N2 wave).

65 y to TAI, the present study examines whether unmyelinated axons also respond differentially to FK506,

66 ic level demonstrate that 32.4+/-2.9% of the unmyelinated axons and 21.6+/-4.7% of the myelinated axo

67 nfirmed the localization of endomorphin-2 to unmyelinated axons and axon terminals in the trigeminal

68 VAChT immunoreactivity was in unmyelinated axons and axon terminals, and was most ofte

69 eurotrophins and tyrosine phosphorylation in unmyelinated axons and dendrites, where Na(V)1.2 channel

70 Moreover, GPER1-IR was found in unmyelinated axons and glial profiles.

71 c profiles, but it was also present in small unmyelinated axons and in a few axon terminals and glia,

72 chwann cell proliferation and death, loss of unmyelinated axons and marked heat and cold pain insensi

73 DAT and TH were localized primarily in small unmyelinated axons and morphologically heterogeneous axo

74 omy) of the rat is highly selective, sparing unmyelinated axons and myelinated sensory axons; Walleri

75 rbB-family receptors in interactions between unmyelinated axons and non-myelinating Schwann cells in

76 rm cortex layers, which are characterized by unmyelinated axons and perisynaptic astroglial envelopes

77 athway, we increased the caliber of normally unmyelinated axons and the expression of numerous genes

78 siological evidence, however, indicates that unmyelinated axons are more vulnerable than myelinated a

79 Unmyelinated axons are not protected by glycogen and are

80 hough GLT1 is present on developing OLs when unmyelinated axons are prevalent in the developing rat c

81 all population of type II neurons with their unmyelinated axons are undetectable with most recording

82 oexpression, we studied large populations of unmyelinated axons by using quantitative single-label EM

83 Gap junctions between fine unmyelinated axons can electrically couple groups of bra

84 Regenerated unmyelinated axons expressing calcitonin gene-related pe

85 Most craniosensory afferents have unmyelinated axons expressing TRP Vanilloid 1 (TRPV1) re

86 ed a significantly higher density of labeled unmyelinated axons for both receptor subtypes.

87 ittle is known about repolarization in thin, unmyelinated axons forming en passant synapses, which re

88 the passage of action potential spikes along unmyelinated axons in a simple nervous system.

89 s further substantiate a distinctive role of unmyelinated axons in TAI, and suggest a highly efficaci

90 studies to assess large myelinated and small unmyelinated axons in the db/db type II diabetes mouse m

91 radish peroxidase, labeled as many as 52% of unmyelinated axons in the dorsal root.

92 rily on the plasma membrane of dendrites and unmyelinated axons in the hippocampus and cerebellum, wi

93 ecently, vesicular release of glutamate from unmyelinated axons in the rat corpus callosum has been s

94 PRV infection induce electrical coupling in unmyelinated axons in vivo.

95 s, which resulted in the segregation of many unmyelinated axons into a 1:1 relationship with Schwann

96 In the unmyelinated axons of hippocampus, the conduction speed

97 The small, unmyelinated axons of olfactory sensory neurons project

98 ve fibre layer (RNFL) is composed largely of unmyelinated axons of retinal ganglion cells, and is acc

99 Expression also converts the normally unmyelinated axons of sympathetic neurons to myelination

100 n whether adult-born OLs ensheath previously unmyelinated axons or remodel existing myelin.

101 ce were smaller than wild-type mice, whereas unmyelinated axons showed no difference.

102 nce of the large number of thin-diameter and unmyelinated axons that connect different cortical areas

103 slow-conducting, and energetically expensive unmyelinated axons to large, fast-conducting, and energe

104 s showed that regeneration of myelinated and unmyelinated axons was inhibited.

105 etwork of 30 multicompartmental neurons with unmyelinated axons was used to infer that: axon-axon gap

106 ure myelinating Schwann cells (SCs), whereas unmyelinated axons were aberrantly ensheathed in Remak b

107 Two phases of increase in the number of unmyelinated axons were observed at C7, while only one s

108 he area occupied by glial cell processes and unmyelinated axons which significantly increased followi

109 We find for example that for mammalian unmyelinated axons with 0.2 microm diameter (matching ce

110 In dendrites, spines, and unmyelinated axons, a significantly larger proportion of

111 small- and medium-sized myelinated and small unmyelinated axons, although sensory nerve action potent

112 N2D is predominantly expressed in dendrites, unmyelinated axons, and axon terminals within the STN.

113 abeling was seen in small axon terminals and unmyelinated axons, and the postsynaptic density (PSD) f

114 labeling was also present in numerous small unmyelinated axons, axon terminals, and glial processes.

115 EM-1 immunoreactivity was identified in unmyelinated axons, axon terminals, and occasionally in

116 ium channels are uniformly distributed along unmyelinated axons, but are highly concentrated at nodes

117 in this model may be the less myelinated or unmyelinated axons, extracellular matrix, or synaptic fi

118 noreactive (KOR-ir) neuronal structures were unmyelinated axons, followed by axon terminals, dendrite

119 sults are specific to signal transmission in unmyelinated axons, I suggest that the conclusions are l

120 es of partially denervated Schwann cells and unmyelinated axons, or the byproducts of Wallerian degen

121 harmacological stimulation of myelinated and unmyelinated axons, respectively.

122 and dendrites, but the proportion of labeled unmyelinated axons, terminals, and glia was higher than

123 Unmyelinated axons, the most prominent CST element durin

124 cross the CC, presumably in conjunction with unmyelinated axons, to colonize the contralateral hemisp

125 ial afferents is exclusively associated with unmyelinated axons, VR1 identifies C-fiber afferent path

126 ain conduction times are especially great in unmyelinated axons, which may transmit information via f

127 odium channel density and gating in proximal unmyelinated axons.

128 about 15% of PR-immunoreactive profiles were unmyelinated axons.

129 nd spines, with rare presynaptic labeling in unmyelinated axons.

130 ons, we investigated channel-noise limits in unmyelinated axons.

131 antly the presence of functional channels in unmyelinated axons.

132 nals forming symmetric synapses and in small unmyelinated axons.

133 f a few axon initial segments and many small unmyelinated axons.

134 ibers, despite a loss in both myelinated and unmyelinated axons.

135 mitochondrial traffic in both myelinated and unmyelinated axons.

136 axonal excitability and synaptic function in unmyelinated axons.SIGNIFICANCE STATEMENT Voltage-gated

137 es several new features of AP propagation in unmyelinated axons: (1) branches of a single axonal arbo

138 f other structures, including myelinated and unmyelinated, axons were also labeled.

139 segments of both of the axons that flank the unmyelinated bipolar ganglion cell bodies.

140 elinated A fibers and isolectin B4 (IB4) for unmyelinated C fibers and both labels were quantified in

141 Yet, both unmyelinated C fibers and particularly the morphological

142 These results further support the role of unmyelinated C fibers in injury-induced modulation of sp

143 t involved large Abeta myelinated fibers and unmyelinated C fibers were most affected by chemotherapy

144 ted with altered nerve function, we measured unmyelinated C-fiber conduction velocities (CV) in nerve

145 G neurons, whereas it was decreased in small unmyelinated C-fiber neurons as a result of diabetes.

146 with peripherin and isolectin B4 markers of unmyelinated C-fiber neurons; 68% colabeled with antibod

147 developing and adult DRGs that give rise to unmyelinated C-fibers (neurofilament 200 negative).

148 We show that mGlu4 are located both on unmyelinated C-fibers and spinal neurons terminals in th

149 asodilation via antidromic activation of the unmyelinated C-fibers and/or the small myelinated fibers

150 xons and, additionally, is distributed along unmyelinated C-fibers of sensory neurons.

151 In mammalian peripheral nerves, unmyelinated C-fibers usually outnumber myelinated A-fib

152 myelinated dorsal root axons, but rarely in unmyelinated C-fibers, and heavily expressed in the dors

153 ry bladder consist of myelinated Adelta- and unmyelinated C-fibers, the neuronal cell bodies of which

154 f action potentials in myelinated A, but not unmyelinated C-fibers.

155 dder consist of myelinated Adelta-fibers and unmyelinated C-fibers.

156 y also involve antidromic activation of some unmyelinated C-fibers.

157 bserve pruriceptive itch which includes both unmyelinated C-fibres and thinly myelinated Adelta nerve

158 ffecting thinly myelinated Adelta-fibres and unmyelinated C-fibres.

159 to assess the changes in myelinated (A) and unmyelinated (C) cutaneous nociceptors after transection

160 inosa (SG) is a major termination region for unmyelinated (C) primary afferent fibers; however, how t

161 (SG; lamina II) is a major synaptic zone for unmyelinated (C) primary afferents.

162 us (NTS) neurons via myelinated (A-type) and unmyelinated (C-type) axons in the solitary tract (ST).

163 taining glutamate homeostasis at a time when unmyelinated callosal axons are engaging in glutamatergi

164 of sensory neurons, including small-diameter unmyelinated cells that respond to capsaicin (but not mu

165 primary afferents but are also expressed in unmyelinated cranial visceral primary afferents linked t

166 Previous studies using reporter proteins in unmyelinated cultured neurons suggest that an ankyrinG-b

167 Unmyelinated cutaneous axons are vulnerable to physical

168 ng electrophysiological recordings of single unmyelinated cutaneous fibres and their compound action

169 ber tactile afferents are a subpopulation of unmyelinated cutaneous sensory neurons activated by gent

170 capable of firing at high frequencies, small unmyelinated DRG neurons typically display much lower ma

171 ation of myelinated fibers without affecting unmyelinated DRG neurons.

172 Therefore, in unmyelinated Drosophila motoneurons different functions

173 onal L-type channels enhance firing rates in unmyelinated Drosophila motoraxons.

174 2 in the organ of Corti was localized to the unmyelinated efferent axons and their endings on the inn

175 Unmyelinated epidermal nerve fiber and myelinated dermal

176 ined the effects of C-peptide replacement on unmyelinated fiber function in the hind paw, sural nerve

177 III, and IV are now known and there is clear unmyelinated fiber loss.

178 d restored the diabetes-induced reduction of unmyelinated fiber number (P < 0.01) and mean axonal siz

179 tion of the sciatic nerve revealed a loss of unmyelinated fibers and extensive ultrastructural damage

180 ites that serve local high-energy demands of unmyelinated fibers and signal transmission.

181 ated axons in the dorsal roots, although the unmyelinated fibers are preserved.

182 ements of conduction velocity indicated that unmyelinated fibers are responsible for glutamatergic si

183 es revealed early preferential loss of small unmyelinated fibers followed by prominent demyelination

184 old reduction in the density of regenerating unmyelinated fibers in LAR-/- nerves distal to the crush

185 l sprouting occurs, producing an increase in unmyelinated fibers in the corpus callosum.

186 1.2 channels were predominately localized in unmyelinated fibers in the cortex, hippocampus, spinal c

187 vier along adult CNS and PNS axons and along unmyelinated fibers in the PNS.

188 otion that altered potassium homeostasis and unmyelinated fibers may represent a potential vehicle fo

189 Myelinated and unmyelinated fibers of the lingual nerve were increased

190 n of the labeling patterns suggests that AEN unmyelinated fibers project primarily to the ventral tip

191 eripherin (a marker of thinly myelinated and unmyelinated fibers) or calcitonin gene-related peptide

192 se to cowhage is different in myelinated and unmyelinated fibers, (5) the time of peak itch sensation

193 ngs in hypertonic P18 kits decreased only in unmyelinated fibers, despite a loss in both myelinated a

194 ever, although 65% of the AEN is composed of unmyelinated fibers, it has not been determined whether

195 he role of degeneration of myelinated versus unmyelinated fibers, we investigated the effects of an L

196 amatic proliferation in the Schwann cells of unmyelinated fibers, which resulted in the segregation o

197 ch matches the time for the peak response in unmyelinated fibers.

198 in receptor terminals of both myelinated and unmyelinated fibers.

199 i-GluR4 or anti-GluR2/4 stains predominantly unmyelinated fibers.

200 Myelin thickness and unmyelinated fibre diameter were not affected.

201 Moreover, SARM1 knockout mice do not lose unmyelinated fibres in the skin or myelinated axons in t

202 ity is a functional signature of a subset of unmyelinated fibres innervating the urinary bladder.

203 e activity from different sets of peripheral unmyelinated fibres through neural circuitry that includ

204 ondary to anatomical (high frequency of long unmyelinated fibres) and biomechanics factors.

205 ns of propagating action potentials in small unmyelinated fibres, such as the axons within mammalian

206 r ablation of high-threshold, small-diameter unmyelinated group C nerve fibers (C-fibers) has limited

207 y the mechanisms underlying AP initiation in unmyelinated hippocampal mossy fibers of adult mice, we

208 ns are myelinated in the optic nerve but are unmyelinated in the retina.

209 positive for TRPV1 and CGRP and most likely unmyelinated, in that most colonic afferents were not po

210 VGLUT3-expressing unmyelinated low-threshold mechanoreceptors (C-LTMRs) ar

211 es them as a poorly understood population of unmyelinated, low threshold mechanoreceptors (C-LTMRs).

212 terneurons suggests that myelinated, but not unmyelinated, LTMRs play a critical role in the expressi

213 Low threshold unmyelinated mechanoafferents (C tactile, CT) in the hum

214 Thus, sodium channel gating and density in unmyelinated mossy fiber axons appear to be specialized

215 chwann cell proliferation, the morphology of unmyelinated nerve (Remak) bundles was static.

216 but significantly improved measures of small unmyelinated nerve fiber architecture and function.

217 by the preprotachykinin A (PPT-A) gene, from unmyelinated nerve fibers (C-fibers) following noxious s

218 Unmyelinated nerve fibers (Remak bundles) in the rodent

219 d objective measures of small myelinated and unmyelinated nerve fibers can improve in these diabetic

220 usor overactivity, there is up-regulation of unmyelinated nerve fibers expressing both the vanilloid

221 receptors are present on both myelinated and unmyelinated nerve fibers in human dental pulp and may p

222 d macrophages-preceded altered conduction of unmyelinated nerve fibers in SIV-infected macaques, sugg

223 and interweaving reported in humans and had unmyelinated nerve fibers within micrometers of the endo

224 ated peptide (CGRP; a marker more typical of unmyelinated nerve fibers).

225 By contrast, Pik3c3-deficient small-diameter unmyelinated neurons accumulated excessive numbers of ly

226 VGLUT3-persistent neurons are small-diameter unmyelinated neurons that are further divided into two s

227 mmetrical junction-like contacts between the unmyelinated neurons, 3) abnormal expression patterns fo

228 n RUNX1(+)/TrkA(+) neurons that develop into unmyelinated neurons.

229 ed sensory neurons, but is absent from small unmyelinated neurons.

230 sitivity accompanied by marked neuropathy of unmyelinated nociceptive sensory axons terminating in th

231 ptic glomeruli, assumed to be the endings of unmyelinated nociceptive terminals, were found on these

232 ss MOR mRNA below this level, whereas small, unmyelinated nociceptors are likely to express above it.

233 Approximately half of unmyelinated nociceptors express the NGF receptor TrkA,

234 (IIo), where they intermingled with those of unmyelinated nociceptors.

235 h, after sciatic nerve injection, labels all unmyelinated nociceptors.

236 growth takes place, but not in the smaller, unmyelinated nodes.

237 ed receptor B4 marks a rare subpopulation of unmyelinated, nonpeptidergic sensory fibers that exclusi

238 le sources of the PERG bioelectric field are unmyelinated optic nerve axons adjacent to the sclera.

239 a clustering in the inner central retina and unmyelinated optic nerve regions, with microglia activat

240 logy as measured by assays such as amount of unmyelinated or disorganized axons.

241 d whether this afferent signal is carried by unmyelinated or myelinated fibers.

242 e detected in adults are likely to be either unmyelinated or sprouting axons.

243 oriented along and across, respectively, the unmyelinated parallel fibers.

244 iously reported findings, we also found that unmyelinated pathways contain only CB, whereas myelinate

245 , the vast majority of 5-HT1D-IR neurons are unmyelinated peptidergic afferents that distribute perip

246 sory neurons, slowing conduction velocity in unmyelinated peripheral nerve fibers, and stimulating re

247 on along the axonal membrane of nociceptive, unmyelinated peripheral nerve fibers, but clarifying the

248 ation is due to altered function of terminal unmyelinated portions of auditory nerve.

249 Using an experimentally tractable unmyelinated preparation for detailed investigation and

250 scopic level, opsin labeling was confined to unmyelinated preterminal axons and small terminals that

251 Numerous fibers, presumably of unmyelinated primary afferent (C fiber) origin, stained

252 mmunoelectron microscopy results, imply that unmyelinated primary afferent fibers terminating in the

253 mplicifolia (IB4) is selectively taken up by unmyelinated primary afferent fibers that terminate in t

254 L5 DRG that were labeled by IB4, a marker of unmyelinated primary afferent neurons, were largely abse

255 ocal circuit neurons, but it does not act on unmyelinated primary afferent terminals via sGC.

256 receive monosynaptic input from a subset of unmyelinated primary afferents and connect to other lami

257 release by terminals of both myelinated and unmyelinated primary afferents.

258 The principle by which unmyelinated primary sensory neurons transducing thermal

259 Other unmyelinated projections were to the ventral paratrigemi

260 of Wallerian and retrograde degeneration of unmyelinated retinal ganglion cell axons in living rats

261 de RGC dendrites, cell bodies and axons, the unmyelinated retinal nerve fiber layer and the myelinate

262 Unmyelinated sections of axon are very diverse structure

263 ted with improperly formed paranodes, and in unmyelinated segments between internodes.

264 In unmyelinated segments bordered by myelin sheaths, these

265 ament transport in contiguous myelinated and unmyelinated segments of axons in long-term myelinating

266 not appear to be diffusely localized in the unmyelinated segments themselves.

267 ger cross-sectional area than the contiguous unmyelinated segments, and this correlated with a local

268 d gray matter of the dorsal spinal cord, but unmyelinated sensory afferents do not regenerate.

269 ide the central nervous system on peripheral unmyelinated sensory afferents.

270 pic analysis further revealed hypertrophy of unmyelinated sensory axons and a subset of myelinated ax

271 (>25 mm) regeneration of both myelinated and unmyelinated sensory axons with topographically correct

272 s is characterized by distal degeneration of unmyelinated sensory axons, similar to the "dying back"

273 turn modulates the structure and function of unmyelinated sensory axons.

274 anosensitive terminals of myelinated but not unmyelinated sensory fibers, whereas HCN2 and HCN4 were

275 ns between non-myelinating Schwann cells and unmyelinated sensory neuron axons that are critical for

276 Here we identified two classes of unmyelinated sensory neurons (nonpeptidergic and C-fiber

277 Small unmyelinated sensory neurons classified as nociceptors a

278 Genetic ablation in adulthood of unmyelinated sensory neurons expressing the G protein-co

279 n of the spinal cord is a recipient zone for unmyelinated sensory neurons in adults.

280 eviously, we identified a rare population of unmyelinated sensory neurons in mice that express the G-

281 xpresser mice had increased numbers of small unmyelinated sensory neurons that express the tyrosine k

282 Here we demonstrate that two classes of unmyelinated sensory neurons, which account for >40% of

283 cteristics, including 1) large aggregates of unmyelinated SGNs in the apical and middle turns, 2) sym

284 a high degree of the "human-like" feature of unmyelinated SGNs that aggregate into neural clusters.

285 th Schwann cells and myelination of normally unmyelinated small axons.

286 f axons in LKB1 mutants was most dramatic in unmyelinated small sensory fibers, whereas motor axons w

287 nitial myelinated part gives rise to several unmyelinated small-diameter branches that have a high nu

288 nsory neurons and biallelically expressed in unmyelinated small-diameter neurons.

289 large-diameter neurons and biallelically in unmyelinated small-diameter neurons.

290 Nociceptive nerve function, unmyelinated sural nerve fiber and dorsal root ganglion

291 7.3 at heminodes, nodes, internodes, and the unmyelinated synaptic terminal segments beneath IHCs in

292 an change the phenotype of nerve fibers from unmyelinated to myelinated.

293 linated segments are interspersed with long, unmyelinated tracts.

294 The remaining thin, unmyelinated type II afferents extend hundreds of micron

295 the possibility that glutamate release from unmyelinated vagal afferents may be regulated by a disti

296 CTb was found in both myelinated and unmyelinated vagal axons and terminals in medial NTS, wh

297 provides excellent contrast visualization of unmyelinated white matter in the immature mouse brain.

298 is to functional electrical connectivity in unmyelinated WM fibers by conducting a longitudinal stud

299 cerebral palsy were associated with loss of unmyelinated WM tracts.

300 In adult axons, Na(v)1.2 is localized to the unmyelinated zone, whereas Na(v)1.6 is specifically targ