ライフサイエンスコーパス: sensory neuron

1 human cell line that has the properties of a sensory neuron.

2 ntity aspects of a terminally differentiated sensory neuron.

3 ry-related genes, suggesting a novel type of sensory neuron.

4 of ion channels/exchangers expressed in each sensory neuron.

5 factors in the calcium transients of the ASH sensory neuron.

6 s (miRs) occurs in dorsal root ganglia (DRG) sensory neurons.

7 ystem, including the spinal cord and primary sensory neurons.

8 saicin-induced calcium influx in a subset of sensory neurons.

9 gh activation of receptors on mast cells and sensory neurons.

10 ch development of dorsal root ganglion (DRG) sensory neurons.

11 ne pathogen, establishes lifelong latency in sensory neurons.

12 ing expression of the channel selectively in sensory neurons.

13 tors expressed in the cilia of the olfactory sensory neurons.

14 tes the D1-like dopamine receptor on primary sensory neurons.

15 rs mitochondrial trafficking and function in sensory neurons.

16 rapidly differentiate hPSCs into peripheral sensory neurons.

17 ain DOR analgesic incompetence in peripheral sensory neurons.

18 ith sensory epithelia that are innervated by sensory neurons.

19 receptors and channels expressed by primary sensory neurons.

20 mutants show abnormal axonal connections of sensory neurons.

21 s been extensively studied in nociception of sensory neurons.

22 DAF-7/TGF-beta ligand that is secreted from sensory neurons.

23 e with alphaII spectrin-deficient peripheral sensory neurons.

24 43, two markers of regenerative activity, in sensory neurons.

25 ed for the formation of functional olfactory sensory neurons.

26 ne B4 receptors were expressed in peripheral sensory neurons.

27 level by a cessation of ectopic activity in sensory neurons.

28 fection and for reactivation from latency in sensory neurons.

29 ng to changes in the functional responses of sensory neurons.

30 hts into how the brain uses information from sensory neurons.

31 that AIA enhanced the excitability of joint sensory neurons.

32 es, altogether recording from half a million sensory neurons.

33 n of NC derivatives, including autonomic and sensory neurons.

34 ations that primarily affect sympathetic and sensory neurons.

35 naptic input from both pain and itch primary sensory neurons.

36 ury on the regenerative state of the primary sensory neurons.

37 tion, BoHV-1 establishes lifelong latency in sensory neurons.

38 hibiting the basal spike firing in olfactory sensory neurons.

39 model to support ciliogenesis in a subset of sensory neurons.

40 esponses reflects distinct subpopulations of sensory neurons.

41 is abundantly expressed in latently infected sensory neurons.

42 ted protein 7 (MAP7) in dorsal root ganglion sensory neurons.

43 ies additional populations of itch-dedicated sensory neurons.

44 f interneuronal "noise" correlations between sensory neurons.

45 d decreases surface delivery in rat and mice sensory neurons.

46 agonist treatment and transient silencing of sensory neurons.

47 I in L7, or PKM Apl II or PKM Apl III in the sensory neuron 2 d after 5-hydroxytryptamine (5-HT) trea

48 I or PKM Apl III in L7, or PKM Apl II in the sensory neuron 2 d after paired stimuli reversed persist

49 Sensory neurons activated by either dry or moist air ('d

50 Temporally targeted deletion of Cdc42 in sensory neurons after sensory-motor circuit establishmen

51 Exogenous in vivo expression of zTrpa1b in sensory neurons allowed subcellular photo-activation, en

52 f PKCs generated by calpain cleavage, in the sensory neuron and L7 are required to maintain each form

53 ous expression, in both Drosophila olfactory sensory neurones and in human embryonic kidney cells, to

54 osensory neurons in prothoracic tarsi and in sensory neurons and accessory cells of long labellar sen

55 both expressed in glial cells that surround sensory neurons and also in muscle tissue, probably arou

56 nherited allele in myelinated large-diameter sensory neurons and biallelically expressed in unmyelina

57 LPS-induced calcium changes in a majority of sensory neurons and decreased LPS-dependent neuronal exc

58 Here, we examined Drosophila olfactory sensory neurons and found that inhibitory odors triggere

59 erative PKC-2-mediated signaling in both AFD sensory neurons and intestinal cells.

60 results show that Drosophila TZ assembly in sensory neurons and male germ cells involves cooperative

61 esting a causal link between the activity of sensory neurons and perceptual judgments.

62 , the virus establishes latent reservoirs in sensory neurons and persists for life.

63 glutamate) is highly effective in silencing sensory neurons and reversing neuropathic pain-related h

64 ensitivity of mechanically gated currents in sensory neurons and silence mechanoreceptors in vivo.

65 ell body and axon compartments of peripheral sensory neurons and the 3' untranslated region (3'UTR) l

66 xamined the changes in the activity of joint sensory neurons and the associated ionic mechanisms usin

67 ion of the arc is composed of proprioceptive sensory neurons and the muscle spindle, which is embedde

68 ized monosynaptic connection between cranial sensory neurons and the PBL-nociceptive neurons.

69 has included connections between peripheral sensory neurons and their spinal targets.

70 1-sensitization and the hyperexcitability of sensory neurons and thereby to reduce pain in patients t

71 o analyze the IL-31-related transcriptome in sensory neurons and to investigate whether IL-31 promote

72 ermis, intestine, body wall muscle, ciliated sensory neurons and touch receptor neurons - where it re

73 The CsnAChalpha subunit was not expressed in sensory neurons and was expressed at extremely low level

74 intracellular calcium flux and excitation in sensory neurons, and behavioral changes due to TLR4 acti

75 otein localizes to ciliated endings of these sensory neurons, and is transcribed at different levels

76 at increases TRPA1 sensitivity in peripheral sensory neurons, and likely contributes to persistent me

77 ions regulate pain through direct actions on sensory neurons, and specific receptors are present in n

78 y abilities likely originates in the primary sensory neurons, and suggest that hormonal modulation of

79 creted protein signal, is expressed in these sensory neurons, and that experimental ablation of neuro

80 ur samples of larval Drosophila melanogaster sensory neurons, and used three trimming algorithms--Sol

81 Sensory neurons are activated by a range of stimuli to w

82 r potential (TRP) ion channels in peripheral sensory neurons are functionally regulated by hydrolysis

83 Our results demonstrated that peripheral sensory neurons are required for normal contractions tha

84 influence the tuning parameters of cortical sensory neurons as selectivity emerges, or rather whethe

85 d establish latency in different subtypes of sensory neurons, as well as in neurons of the autonomic

86 G protein-coupled receptor, functions in the sensory neurons ASH and ASI to suppress innate immune re

87 e to exhibit neuronal morphology and express sensory neuron-associated markers such as neurotrophin r

88 We show that the glutamatergic sensory neurons AWC(ON) and ASH have distinct synaptic d

89 show that there exists a critical balance in sensory neurons between the rates of anterograde and ret

90 naptic connectivity similar to that of other sensory neurons, but in males PHC differentiates into a

91 rom collateral damage to peripheral afferent sensory neurons by anticancer pharmacotherapy, leading t

92 lowing the activation of nociceptive primary sensory neurons by burn injury, capsaicin application or

93 We demonstrated activation of sensory neurons by microbes, correlating with RORg(+) Tr

94 f Cut expression are diversified in distinct sensory neurons by selective expression of Scalloped and

95 ransducing mechanical inputs and stimulating sensory neurons by using a host of known and as yet unkn

96 human induced pluripotent stem cell-derived sensory neurons can be cultured with rat Schwann cells,

97 We show that choice-related activity in sensory neurons can be highly variable across observers

98 uggest that regulation of gene expression in sensory neurons can function in the integration of a wid

99 Responses of individual task-relevant sensory neurons can predict monkeys' trial-by-trial choi

100 choice-correlated activity in task-relevant sensory neurons can reflect postdecision modulatory sign

101 Optogenetic activation of Piezo2(+) vagal sensory neurons causes apnoea in adult mice.

102 Olfactory sensory neurons chemosensory cilia are elongated, mucus

103 cribed the three-dimensional morphologies of sensory neuron cilia in adult C. elegans hermaphrodites

104 matopoietic sites are in direct contact with sensory neuron clusters of the peripheral nervous system

105 , as well as in both MOR flox and MOR-Nav1.8 sensory neuron conditional KO mice.

106 whether intracellular retention of deltaR in sensory neurons contributes to this low deltaR agonist e

107 cal signals transduced by airway-innervating sensory neurons control respiration; however, the physio

108 This mechanism of local sensory neurons controlling blood cell adaptation invite

109 In vitro primary sensory neuron culture systems were subjected to whole-t

110 egeneration after axotomy in sympathetic and sensory neurons cultured in microfluidic devices.

111 e to epinephrine and corticosterone than are sensory neurons, demonstrating that the autonomic nervou

112 Pure sensory neuron-derived exosomes released by capsaicin ar

113 Nociceptor sensory neurons detect immune mediators to produce pain,

114 lfactory chemosensory neurons and nociceptor sensory neurons-detect bacterial toxins, formyl peptides

115 is an important constituent of KARs early in sensory neuron development and suggest that Neto2 assemb

116 ion of Trk signaling, which is essential for sensory neuron differentiation and development.

117 Sensory neurons downstream of primary receptors are sele

118 rrelates with variability in the activity of sensory neurons driven by the stimulus.

119 ly, this odor-evoked inhibition of olfactory sensory neurons elicited by itself a full range of olfac

120 To this end, "efficient coding" posits that sensory neurons encode maximal information about their i

121 cules responsible for this change in primary sensory neuron excitability are still not well defined.

122 the bacterial strains capable of suppressing sensory neuron excitability, and their mechanisms of act

123 n to avoidance, as did odor-evoked olfactory sensory neuron excitation.

124 heterologous expression systems and cultured sensory neurons, exposure to blue light activated TRPA1

125 ing the Nrp1 ligand Sema3A and in mice whose sensory neurons express an Nrp1 mutant unable to bind Se

126 We found that sensory neurons express major proteins necessary for GAB

127 ponse; i.e., the probability distribution of sensory neuron firing rates across the population of odo

128 Membrane fractions from cultured rat sensory neurons following AKAP siRNA transfection and fr

129 vectors are suitable for gene delivery to TG sensory neurons following intradermal whiskerpad injecti

130 Group Ia proprioceptive sensory neurons form direct synapses with motor neurons,

131 Primary sensory neurons form the interface between world and bra

132 ing roles in the sensitization of peripheral sensory neurons forming a self-restricting system.

133 of CXCL12-induced Ca(2+) response in primary sensory neurons from CCD mice was significantly increase

134 nce is to predict the response properties of sensory neurons from first principles.

135 Sensory neurons from mice lacking the muscarinic ACh typ

136 y generate cells expressing markers of human sensory neurons from neural crest cells and established

137 dulation of ASIC currents by endomorphins in sensory neurons from rats with freely perfused and ligat

138 lecules implicated in memory induction using sensory neurons from the marine mollusk Aplysia californ

139 timuli was also reduced by pre-incubation of sensory neurons from untreated BALB/c mice with 0.0001%

140 Sensory neurons give highly variable responses to stimul

141 ANCE STATEMENT Injury of peripheral axons of sensory neurons has been known to strongly enhance the r

142 Sensory neurons have the capacity to produce, release, a

143 importance of O-GlcNAc transferase (OGT) for sensory neuron health and survival in vivo This study is

144 independently promote fasciculation between sensory neuron HOA and its postsynaptic target interneur

145 at birth and nonprogressive, indicating that sensory neuron identity is prenatally perturbed and that

146 C. elegans CHE-1, a terminal selector of ASE sensory neuron identity.

147 1 and HSV-2 infections in autonomic, but not sensory, neurons.IMPORTANCE Stress exacerbates acute dis

148 e equilibrium between functional subtypes of sensory neuron in dorsal root ganglia is distorted by Ga

149 tion of eIF2alpha phosphorylation in primary sensory neurons in a chronic inflammation pain model con

150 of rabies virus-based retrograde tracing of sensory neurons in adult mice, and may help to better un

151 l recordings revealed that Dil-labeled joint sensory neurons in AIA mice exhibited a greater incidenc

152 d transgenes within cell bodies and axons of sensory neurons in all three branches of the TG.

153 show that type 2 cytokines directly activate sensory neurons in both mice and humans.

154 expressed on nerve fibers in human skin and sensory neurons in dorsal root ganglia.

155 fferents converged onto NTS-CeA second-order sensory neurons in greater numbers, as well as indirectl

156 modulation (SM) is a fundamental property of sensory neurons in many species and sensory modalities.

157 Peripheral sensory neurons in particular are subject to degeneratio

158 ted substantially in chemoreceptive petrosal sensory neurons in rats with hypertension.

159 e functional expression of IKD is reduced in sensory neurons in response to peripheral nerve damage.

160 Additionally, AAVrh10 has tropism towards sensory neurons in skeletal tissue, such as bone marrow

161 Peripheral sensory neurons in the dorsal root ganglia (DRG) are the

162 Primary sensory neurons in the DRG play an essential role in ini

163 n achieve a transduction rate of >90% of the sensory neurons in the DRG that innervate the footpad.

164 e and function of the axonal arbor in mature sensory neurons in the main olfactory system but not in

165 nical origin of tactile information, primary sensory neurons in the trigeminal ganglion (Vg) have oft

166 human induced pluripotent stem cell-derived sensory neurons in vitro potently inhibited their respon

167 ype, but not Cdc42-deficient, proprioceptive sensory neurons in vitro Together, our findings demonstr

168 e channel was successfully targeted to mouse sensory neurons in vivo, resulting in high level and lon

169 opioid receptor (MOP) mediated inhibition in sensory neurons in which beta-arrestin2 (beta-arr2) is i

170 several markers for regenerative activity in sensory neurons, including phospho-STAT3 and GAP43.

171 nhibition and excitation in single olfactory sensory neurons increases the odor-coding capacity, prov

172 e to acetophenone, a ligand of M72 olfactory sensory neurons, increases the strength of M72-mediated

173 hectomy greatly reduced hyperexcitability of sensory neurons induced by local DRG inflammation observ

174 Some sensory neurons innervate the ventral brain directly to

175 The selectivity with which proprioceptive sensory neurons innervate their central and peripheral t

176 d, in part because little is known about why sensory neurons innervating muscle appear more capable o

177 differentiates into a densely connected hub sensory neuron/interneuron, integrating a large number o

178 iring rates across the population of odorant sensory neurons is an exponential for nearly all odors a

179 ansduction within various airway-innervating sensory neurons is critical for establishing efficient r

180 umber of TLR signaling cascades, its role in sensory neurons is poorly understood.

181 t of ORs is regulated in mammalian olfactory sensory neurons is poorly understood.

182 sensory input from innocuous and nociceptive sensory neurons is required for robust mechanonociceptiv

183 A common way to assess the function of sensory neurons is to measure the number of spikes produ

184 st abundant neuropeptide in primary afferent sensory neurons, is strongly implicated in the pathophys

185 Cultured sensory neurons lacking OGT also exhibit decreased axona

186 Ion channels expressed by peripheral sensory neurons largely contribute to mechanical hyperse

187 und that in these mice, the mature olfactory sensory neuron layer is reduced, and that olfactory sens

188 The sensory neurons lie outside of the blood-brain barrier a

189 gulation and release of miR-21 contribute to sensory neuron-macrophage communication after damage to

190 Here we show that adaptation in cortical sensory neurons maximizes information about visual motio

191 erleukin-1 Receptor (TIR) domains present in sensory neurons may modulate neuropathic pain states.

192 SP was released from the sensory neurons, MNECs, and HNECs within 15 minutes of l

193 y to specific features of their environment, sensory neurons need to integrate multiple incoming nois

194 re we identified two classes of unmyelinated sensory neurons (nonpeptidergic and C-fiber low-threshol

195 activity modifies the thickness of myelin in sensory neurons, not only in development but also in mat

196 Moreover, induced ablation of Piezo2 in sensory neurons of adult mice causes decreased neuronal

197 esses, because inducing OGT knock-out in the sensory neurons of adult mice results in a similar decre

198 mulates lytic cycle viral gene expression in sensory neurons of calves latently infected with BoHV-1,

199 Sensory neurons of the "necklace" subsystem are nestled

200 ICANCE STATEMENT Pain-transducing peripheral sensory neurons of the dorsal root ganglia (DRG) express

201 Here, we screened the olfactory sensory neurons of the maxillary palp (MP-OSNs) using a

202 ls of olfactory sensory neurons (the primary sensory neurons of the olfactory system, which provide t

203 a, a TGF-beta family ligand, is expressed by sensory neurons of the PNS and regulates the proliferati

204 rus 1 (HSV-1) establishes latency within the sensory neurons of the trigeminal ganglia (TG).

205 dents, these receptors are also expressed by sensory neurons of the vomeronasal organ, an olfactory s

206 HSV-1 establishes latency within sensory neurons of trigeminal ganglia (TG), and TG-resid

207 Sensory neurons often possess cilia with elaborate membr

208 Second, peripheral sensory neurons-olfactory chemosensory neurons and nocic

209 ures, we found that only a small fraction of sensory neurons optimally encoded natural stimuli throug

210 It is not known which PKC isoforms in the sensory neuron or motor neuron L7 are required to sustai

211 own whether Ube3a is expressed in peripheral sensory neurons or whether maternal deletion of Ube3a af

212 Cilia on dendritic endings of sensory neurons organize distinct types of sensory machi

213 The mouse olfactory sensory neuron (OSN) repertoire is composed of 10 millio

214 show that, whereas TCs respond to olfactory sensory neuron (OSN) stimulation with short latencies re

215 um is mostly populated by ciliated olfactory sensory neurons (OSNs) and surrounding sustentacular cel

216 Olfactory sensory neurons (OSNs) are chemoreceptors that establish

217 In Drosophila melanogaster olfactory sensory neurons (OSNs) establish synapses with projectio

218 h more sensitive to stimulation of olfactory sensory neurons (OSNs) in bulb slices.

219 ral biosensor since its peripheral olfactory sensory neurons (OSNs) respond to the external stimuli a

220 rous chemicals through specialized olfactory sensory neurons (OSNs) that transduce odorants into neur

221 ithelium continues to generate new olfactory sensory neurons (OSNs) throughout life, we investigated

222 perate to provide individual mouse olfactory sensory neurons (OSNs) with the cell surface diversity r

223 In vertebrate olfactory sensory neurons (OSNs), Ca(2+) plays key roles in both m

224 rphic neural coding of odorants by olfactory sensory neurons (OSNs), primary sensory neurons that phy

225 ory epithelium (OE) is composed of olfactory sensory neurons (OSNs), sustentacular supporting cells,

226 that appears to specifically label olfactory sensory neurons (OSNs), which are essential for olfactio

227 Quantification of the olfactory sensory neurons (OSNs), which detect odors within the na

228 Iba-1-positive cells, and loss of olfactory sensory neurons (OSNs).

229 V and WEEV enter the brain through olfactory sensory neurons (OSNs).

230 cific expression pattern of daf-7 in the ASJ sensory neuron pair with the onset of reproductive matur

231 Surprisingly, a large fraction of sensory neurons performed little if no filtering of stim

232 to CASY-1/calsyntenin in AVG; SAX-7/L1CAM in sensory neuron PHC binds to RIG-6/contactin in AVG.

233 Our findings suggest that MyD88 in primary sensory neurons plays an active role in regulating IL-1b

234 orant receptors on the membrane of olfactory sensory neurons, plays a vital role in their host seekin

235 report that deletion of Ric-8b in olfactory sensory neurons prevents stable expression of Galphaolf.

236 tion, HSV establishes latency in innervating sensory neurons, primarily located in the trigeminal gan

237 , is known to mediate targeting of olfactory sensory neurons (primary neurons), to the posteroventral

238 Using organoid culture, we demonstrated that sensory neurons promoted the proliferation of PanIN orga

239 In mice lacking Cdc42 in presynaptic sensory neurons, proprioceptive sensory axons appropriat

240 Nociceptor sensory neurons protect organisms from danger by eliciti

241 We deduce that SP activates MrgprA1 on sensory neurons rather than NK-1R to induce itch.

242 agomir and conditional deletion of miR-21 in sensory neurons reduce neuropathic hypersensitivity as w

243 ministration increased the rate of motor and sensory neuron regeneration and the number of proliferat

244 sary for GABA synthesis and release and that sensory neurons released GABA in response to depolarizat

245 oteins are combined to modulate how strongly sensory neurons respond to mechanical force.

246 hanges in sound level.SIGNIFICANCE STATEMENT Sensory neurons' responses are typically modulated simul

247 ability to distinguish between elements of a sensory neuron's activity that are stimulus independent

248 ed Ca(2+) influx in a subpopulation of mouse sensory neurons sensitive to the TRPA1 agonist, mustard

249 whose variance scales with the mean signal, sensory neurons should selectively divide their input si

250 neuron layer is reduced, and that olfactory sensory neurons show increased rate of cell death compar

251 phery and the overall health and survival of sensory neurons.SIGNIFICANCE STATEMENT We show the impor

252 POMT transgenic expression limited to sensory neurons significantly rescued the torsion phenot

253 nistically, GABA depolarized the majority of sensory neuron somata, yet produced a net inhibitory eff

254 Here we show that global and sensory neuron-specific ablation of the mechanically act

255 Sensory neuron-specific knock-out of OGT results in beha

256 in (Arch) was expressed under control of the sensory neuron-specific sodium channel (sns) gene to sel

257 muli were enhanced following global, but not sensory neuron-specific, deletion of maternal Ube3a in m

258 G1) in induced pluripotent stem cell-derived sensory neurons strongly enhances myelination, while con

259 Injury to the peripheral axons of sensory neurons strongly enhances the regeneration of th

260 omises, sensory behavior and the function of sensory neurons such as ASH.

261 nt noise accounts for ubiquitous features of sensory neurons such as divisive normalization, gain con

262 Our findings in mouse olfactory sensory neurons suggest that mechanisms that are primari

263 be required for proper axon connectivity of sensory neurons, suggesting that O-mannosylation regulat

264 vivo Here, we show that OGT is essential for sensory neuron survival and maintenance in mice.

265 equires that significant numbers of infected sensory neurons survive infection and maintain normal fu

266 ualization of synaptic output from olfactory sensory neuron terminals into the olfactory bulb of the

267 ly mediated by local inhibition of olfactory sensory neuron terminals.

268 LP) expressed specifically in the paired ASI sensory neurons that are required for dauer bypass.

269 nal imaging to identify a class of cutaneous sensory neurons that are selectively activated by high-t

270 SIGNIFICANCE STATEMENT: Activity in sensory neurons that correlates with an animal's decisio

271 contrast to C4da neurons, non-space-filling sensory neurons that develop in the same microenvironmen

272 ion to identify and optogenetically activate sensory neurons that elicit specific grooming movements.

273 eptors regulate Galpha pathways in gustatory sensory neurons that extend cilia through the male nose.

274 ty to large myelinated and small peptidergic sensory neurons that innervate bone, compared to small n

275 ns rely on the interactions between LPFC and sensory neurons that not only supply sensory signals but

276 by olfactory sensory neurons (OSNs), primary sensory neurons that physically contact odor molecules i

277 vate bone, compared to small non-peptidergic sensory neurons that rarely innervate bone.

278 e reported that neurite outgrowth from adult sensory neurons that were maintained under subsaturating

279 urons and of synaptic terminals of olfactory sensory neurons (the primary sensory neurons of the olfa

280 ic pain arises as a consequence of injury to sensory neurons; the development of ectopic activity in

281 Achieving transduction of hair cells, or sensory neurons, throughout the cochlea has proven diffi

282 human induced pluripotent stem cell-derived sensory neurons thus provide insights into the cellular

283 and aversive responses through modulation of sensory neuron to interneuron synapses.

284 Organisms rely on nociceptive sensory neurons to detect and avoid potentially tissue-d

285 gnaling is necessary and sufficient in these sensory neurons to influence sperm motility parameters.

286 cas#9 receptor that acts in the ASI class of sensory neurons to suppress exploration.

287 anism.SIGNIFICANCE STATEMENT The response of sensory neurons to their preferred stimulus is often mod

288 In afferent sensory neurons, trains of action potentials (spikes) en

289 ns lead to prestimulus baseline increases in sensory neurons tuned to the expected stimulus, which in

290 itizes the ligand-gated ion channel TRPV1 in sensory neurons via activation of PKC.

291 Here we show that BomoTx excites a cohort of sensory neurons via ATP release and consequent activatio

292 Acting from the ASG and BAG sensory neurons, we show that ETS-5 functions in a compl

293 of motoneurons, inhibitory interneurons, and sensory neurons, we uncover a mechanism for generating a

294 changes, mice expressing GCaMP3 in cutaneous sensory neurons were generated and neuronal responses to

295 demonstrate that two classes of unmyelinated sensory neurons, which account for >40% of dorsal root g

296 behaviors are mediated primarily by the AFD sensory neurons, which are extraordinarily thermosensiti

297 nt to action potential generation in certain sensory neurons, which possess myelinated distal dendrit

298 Ultimately, these sensory neurons will successfully integrate into appropr

299 the genetically labeled murine M72 olfactory sensory neurons with the green fluorescent protein (GFP)

300 e and consequently increases DOR activity in sensory neurons without a priming event.