ライフサイエンスコーパス: sensory neuron

1 ssed, leading to transduction in an internal sensory neuron.

2 ntly reduced migration of PDAC cells towards sensory neurons.

3 ience arises from the cellular properties of sensory neurons.

4 brain can extract from the noisy dynamics of sensory neurons.

5 migration of pancreatic cancer cells toward sensory neurons.

6 are heavily populated with primary afferent sensory neurons.

7 l sensilla to receptors present in olfactory sensory neurons.

8 light of population-wide correlations among sensory neurons.

9 ne pathogen, establishes lifelong latency in sensory neurons.

10 urial glia and endothelial cells, but not in sensory neurons.

11 racterized the mechanosensitivity of corneal sensory neurons.

12 onnectivity and neuronal function of phasmid sensory neurons.

13 omy that shapes the functional properties of sensory neurons.

14 ors, T (touch) neurons, but not P (pressure) sensory neurons.

15 ritic scaffold protein, ARCP-1, expressed in sensory neurons.

16 t critical for differential sensitization of sensory neurons.

17 ion factor 3, showing active regeneration in sensory neurons.

18 in cocultures of epidermal keratinocytes and sensory neurons.

19 r interaction between non-neuronal cells and sensory neurons.

20 as a regulator of dendritic arborization in sensory neurons.

21 sory communication between keratinocytes and sensory neurons.

22 the brain, suboesophageal ganglion (SOG) and sensory neurons.

23 on is a key component of efficient coding in sensory neurons.

24 t local searches can be initiated by diverse sensory neurons.

25 organization that occurs in mouse olfactory sensory neurons.

26 s well as direct input from vagal and spinal sensory neurons.

27 ibutes to deficient replacement of olfactory sensory neurons.

28 the importance of immune cell regulation by sensory neurons.

29 responses, as well as from vagal and spinal sensory neurons.

30 sed the firing rate of medium but not small, sensory neurons.

31 he morphogenesis and function of nociceptive sensory neurons.

32 tryptase) and the pattern of activated itch-sensory neurons.

33 r determinant of the excitability of primary sensory neurons.

34 eurons, myenteric interneurons, and putative sensory neurons.

35 ed central nervous system (CNS) and isogenic sensory neurons.

36 rial functions in cultured adult rat primary sensory neurons.

37 rength of the signal transmission out of the sensory neurons.

38 involved in nociceptive pathways, including sensory neurons.

39 However, the USH2A protein was not found in sensory neurons.

40 roposed to generate mechanical strain within sensory neurons.

41 ing epithelial cells of the gut, pharynx and sensory neurons.

42 both the bladder urothelium and innervating sensory neurons.

43 induced paralysis via the cilia of nematode sensory neurons.

44 Thus, sensory neurons act as primary sensors of allergens, lin

45 e systems, the immunological consequences of sensory neuron activation can be either host adaptive or

46 tional protein C2C was tested for control of sensory neuron activity by targeted G-actin modification

47 Remarkably, sensory neurons also adopted this transcriptomic state f

48 Sensory neurons also express TLRs and other PRRs that di

49 pproaches, we observed that loss of LXR from sensory neurons altered genes in non-neuronal cells loca

50 ult peripheral nerves and highlight that the sensory neuron and its surrounding glial coat form a fun

51 of different PKM isoforms in the presynaptic sensory neuron and postsynaptic motor neuron.

52 udies in isolated rat vagal bronchopulmonary sensory neurones and also in the cough response to SO(2)

53 processes governing the interactions between sensory neurons and both target and non-target motor neu

54 transient receptor potential melastatin 8 in sensory neurons and causes mechanical hypersensitivity a

55 milar microfluorimetric calcium responses of sensory neurons and expression of itch-related TRP chann

56 calization of subunit C2I with CGRP-positive sensory neurons and fibers but not with ChAT-positive mo

57 Sensory neurons and immune cells share a common microenv

58 tion and on protein expression/activation in sensory neurons and in target and non-target motor neuro

59 rate molecular cross-talk between axotomized sensory neurons and macrophages, revealing potential per

60 that most pharyngeal neurons are also likely sensory neurons and most, if not all, pharyngeal neurons

61 al regulation of molecular signaling between sensory neurons and non-target motor neurons.

62 main Ca(2+)-extrusion mechanism in olfactory sensory neurons and photoreceptor cells.

63 ulated in the nuclei of dorsal root ganglion sensory neurons and prevented neuronal cell death follow

64 Abnormalities in interactions between sensory neurons and Schwann cells (SCs) may result in he

65 A network of sensory neurons and Schwann cells form nerve-like bundle

66 C2C treatment of sensory neurons and SH-SY5Y cells in vitro remodeled act

67 C), is expressed in a subpopulation of joint sensory neurons and that, under naive conditions, Fcgamm

68 er of the contacts between keratinocytes and sensory neurons and their involvement in sensory communi

69 ng to its functional inactivation in primary sensory neurons and to an efficacious attenuation of the

70 is the capacity to establish latency in the sensory neurons and to reactivate from latency and then

71 d a co-culture system of trigeminal ganglion sensory neurons and vascular endothelial cells (VEC) and

72 ked inward currents (current density ~10% of sensory neurons) and raised intracellular Ca(2+) levels

73 in by the collective population responses of sensory neurons, and an object presented under varying c

74 cell types, including resident immune cells, sensory neurons, and arrector pili muscles.

75 Bone cancer upregulated CCR2 in primary sensory neurons, and CCR2 antagonism effectively reduced

76 ouse PDAC cells (K8484) and mouse peripheral sensory neurons, and confirmed findings in studies of DT

77 er identify how different sub-populations of sensory neurons, and their peripheral nerve terminal end

78 were each innervated by myelinated (NF200+) sensory neurons, and unmyelinated (NF200-) sensory neuro

79 eceptor that promotes itch via activation of sensory neurons, and we find that that CXCR3 antagonism

80 16:0 can induce Ca(2+) transients in primary sensory neurons, and we identify LPC 18:1 as a previousl

81 f a statocyst cell and projecting excitatory sensory neurons (antenna cells).

82 Sensory neurons are activated by physical and chemical s

83 Cortical sensory neurons are characterized by selectivity to stim

84 neurons for non-histaminergic itch, and GRP sensory neurons are dedicated to itch transmission.

85 Intrinsic mechanisms operating in sensory neurons are known to regulate nerve repair, but

86 esterol sensor, LXR alpha/beta, expressed in sensory neurons are necessary for proper peripheral nerv

87 Responses of sensory neurons are often modeled using a weighted combi

88 el predicts that in mammals, where olfactory sensory neurons are replaced regularly, receptor abundan

89 survival; however, the receptors, olfactory sensory neurons, are directly exposed to the environment

90 or potential (TRP) A1 but, unlike multimodal sensory neurons, are inert to hyperoxia and other TRPA1

91 ity in primary nociceptors (injury-detecting sensory neurons), associated with a decrease in the sens

92 that broadly cover a vagal/glossopharyngeal sensory neuron atlas to map, ablate, and control specifi

93 e specialized glia associated with olfactory sensory neuron axons.

94 ied synaptic transmission between an Aplysia sensory neuron (B21) and its postsynaptic follower, the

95 Ringer is expressed in sensory neurons before and after injury, and is cell-aut

96 d selective in vitro C2I delivery to primary sensory neurons but not motor neurons.

97 Activation of nociceptor sensory neurons by noxious stimuli both triggers pain an

98 ropose that cutaneous activation of TRPV1(+) sensory neurons by protease allergens stimulates release

99 ermatitis in a way that is unique from other sensory neurons by regulating a combination of transcrip

100 We next isolated a subset of sensory neurons by sorting DRG neurons back-labeled from

101 show that trophic deprivation (TD) of mouse sensory neurons causes a rapid disassembly of the axonal

102 m central terminals and/or signalling in the sensory neuron cell body.

103 In sensory neurons, cell-specific alternative splicing of t

104 states leading to the generation of the main sensory neuron classes.

105 erative ability of dorsal root ganglia (DRG) sensory neurons compared to EE or a conditioning injury

106 human intrafusal muscle fibers, DRG organoid sensory neurons contact their peripheral targets and rec

107 resulting abnormal interactions of SGCs with sensory neurons could provide a mechanistic approach tha

108 rs, which are critical in the development of sensory neurons, could be binding HSV-1 genome directly

109 nglia (DRG) contain the somas of first-order sensory neurons critical for somatosensation.

110 nvier and other myelinated axonal domains in sensory neurons cultured alone or together with Schwann

111 We identified a subpopulation of olfactory sensory neurons, defined by receptor expression, whose a

112 Sensory neuron-derived CCL21 and CXCL10 promoted migrati

113 gesting that Tao/Taok2 mutations can disrupt sensory neuron development and function.

114 vivo time-lapse imaging of Drosophila adult sensory neuron differentiation, integrating machine-lear

115 Taken together, our data suggested that sensory neurons directly promote angiogenesis via SP sig

116 3.3 emerging as one potential contributor to sensory neuron dysfunction.

117 s consists of 40 scolopidia comprising three sensory neurons each.

118 asticity in mammals, be extended by blocking sensory neurons early in life.

119 ontrol, but how distinct MS and GTO afferent sensory neurons emerge during development remains poorly

120 However, many sensory neurons encode multiple stimulus dimensions simu

121 Fingertip mechanoreceptors comprise sensory neuron endings together with specialized skin ce

122 e-domain K+ channels, to increase trigeminal sensory neuron excitability, leading to a migraine-like

123 Diverse sensory neurons exhibit distinct neuronal morphologies w

124 Mouse DRG sensory neurons express GluK2, and GluK2 knockdown in th

125 Peripheral sensory neurons express multiple voltage-gated sodium ch

126 human induced pluripotent stem cell-derived sensory neurons expressed the receptor for PACAP and tha

127 e found that the DEG/ENaC channel ppk301 and sensory neurons expressing ppk301 control egg-laying ini

128 data indicate that GRP is a neuropeptide in sensory neurons for non-histaminergic itch, and GRP sens

129 t that increased GDNF/GFRalpha1 signaling to sensory neurons from ischemia/reperfusion-affected muscl

130 ivation of PKC was substantially impaired in sensory neurons from KI mice.

131 Single-cell transcriptomic analyses of sensory neurons from mutant mice lacking transcription f

132 nical signaling pathways to alter peripheral sensory neuron function in a nociceptive modality-specif

133 or such fundamental qualities in relation to sensory neurons' functional organizations, because of th

134 ons in Nav1.8 associated with hypersensitive sensory neurons: G1662S reported in painful SFN; and T79

135 but how islet endocrine cells interact with sensory neurons has not been studied.

136 MrgprA3(+) sensory neurons have been identified as one of the major

137 a (DRG), which contain the somata of primary sensory neurons, have increasingly been considered as no

138 ot clear how Nav1.8 disease mutations induce sensory neuron hyperexcitability.

139 dition, knock down of RSK by RNAi in Aplysia sensory neurons impairs LTF, suggesting that this may be

140 rs of colon can arise from the same axon and sensory neuron in DRG.

141 proliferation of macrophages around injured sensory neurons in dorsal root ganglia (DRG).

142 uggest single peptidergic and nonpeptidergic sensory neurons in DRG are potentially capable of detect

143 actory epithelium, imaging ~10,000 olfactory sensory neurons in parallel.

144 odor of ethanol potentiates the activity of sensory neurons in response to an aggression-promoting p

145 have seen studies demonstrating the role of sensory neurons in sleep apnea-related atrial fibrillati

146 to TRPV channels causing overstimulation of sensory neurons in the aphid feeding apparatus.

147 Nociceptors, sensory neurons in the DRG that detect damaging or poten

148 Sensory neurons in the mouse eye and nose have unusual c

149 both regeneration-competent and -incompetent sensory neurons in the peripheral nervous system but als

150 ponse magnitude of whisker-sensitive primary sensory neurons in the trigeminal ganglion.

151 Sex peptide is detected by sensory neurons in the uterus(2-4), and silences these n

152 ing status information is mediated by ppk(+) sensory neurons in the uterus, which are activated upon

153 dritic arbor, as well as the activity of the sensory neuron, in response to sensory stimuli.

154 Sensory neurons initiate defensive reflexes that ensure

155 -activated TRP channels (TRPV1 and TRPA1) in sensory neurons innervating the ipsilateral and contrala

156 Peripheral sensory neurons interact intimately with glial cells.

157 Overall, the early diversity of sensory neurons is generated through successive bi-poten

158 ry neuronal population, we show that Prlr in sensory neurons is necessary for the development of hype

159 dendrites, and synapses from motoneurons and sensory neurons is strongly inhibited.

160 rexpression in the motor neuron, but not the sensory neuron, is sufficient to increase synaptic stren

161 Itch, initiated by the activation of sensory neurons, is associated frequently with dermatolo

162 ly for direct signaling between microbes and sensory neurons, is lacking.

163 etrieval of aversive memories, stored within sensory neurons, is sufficient to induce a protective sy

164 Deletion of LXR alpha/beta from sensory neurons lead to pain-like behaviors.

165 w that allergens directly activated TRPV1(+) sensory neurons leading to itch and pain behaviors.

166 upregulation of sialyltransferase St3gal2 in sensory neurons leads to an increase in expression of th

167 Overexpression of TRPV1 in TRPM8(+) sensory neurons leads to cold allodynia in both corneal

168 pancreatic beta-cells communicate with vagal sensory neurons, likely using serotonin signaling as a t

169 Nervous systems contain sensory neurons, local neurons, projection neurons, and

170 r stimulates CYP26B1 expression in olfactory sensory neurons mainly located in the dorsomedial OE, wh

171 Thus, a unique population of sensory neurons monitors peripheral LNs and may locally

172 Sensory neuron numbers and positions are precisely organ

173 changes of pain-associated genes in primary sensory neurons of DRG are critical for neuropathic pain

174 The TRPV1 expression pattern in sensory neurons of S801A knock-in (KI) mice was comparab

175 background potassium current in the primary sensory neurons of the dorsal root and trigeminal gangli

176 nly specific cell types, primarily the large sensory neurons of the dorsal root ganglia and cardiomyo

177 lopment of the peripheral taste system, oral sensory neurons of the geniculate ganglion project via t

178 digm that drives the regenerative ability of sensory neurons offering a potential redox-dependent reg

179 Eliminating NMDARs in primary sensory neurons or alpha2delta-1 KO also attenuates calc

180 ated considerable heterogeneity of olfactory sensory neuron (OSN) cell populations in wild-type (WT)

181 starvation-dependent modulation of olfactory sensory neuron (OSN) function in the Drosophila larva.

182 h is known about the activation of olfactory sensory neuron (OSN) glomerular responses in the dorsal

183 Here, we examine olfactory sensory neuron (OSN) innervation of the Drosophila anten

184 nd 48 h if EB- or CO(2)-responsive olfactory sensory neurons (OSNs) are silenced after eclosion; thus

185 ses of the olfactory system, where olfactory sensory neurons (OSNs) contact second-order projection n

186 then are switched out, and/or the olfactory sensory neurons (OSNs) expressing them die.

187 n hillock spiking mechanism of the olfactory sensory neurons (OSNs) have yet to be fully determined.

188 Olfactory sensory neurons (OSNs) in chordates usually have multipl

189 Olfactory sensory neurons (OSNs) located in the dorsomedial and ve

190 orant receptors (ORs) expressed in olfactory sensory neurons (OSNs) of the nose.

191 Primary olfactory sensory neurons (OSNs) project their axons directly to t

192 TCs receive direct input from the olfactory sensory neurons (OSNs).

193 unique, overlapping populations of olfactory sensory neurons (OSNs).

194 -wide inversion is not observed in olfactory sensory neurons (OSNs).

195 MORs in primary sensory neurons, particularly those expressed presynapti

196 ls, this study demonstrates the diversity of sensory neuron pathophysiology is due in part to subtype

197 Furthermore, in isolated rat vagal pulmonary sensory neurones, perfusion of an aqueous solution of SO

198 we deleted p75 specifically in Phox2b + oral sensory neurons (Phox2b-Cre; p75(fx/fx)) or in neural cr

199 considered as targets for indications where sensory neurons play a fundamental role, such as pain, i

200 Sensory neurons play a key role in encoding by selective

201 Sensory neurons play a role in apnea-induced AF.

202 observed that PSI can be evoked by different sensory neuron populations and mediated through at least

203 her increased expression of SIRT1 protein in sensory neurons prevents and reverses experimental diabe

204 ng network that receives input from about 90 sensory neurons, processes that information through a hi

205 Sensory neurons provide organisms with data about the wo

206 ics of behavior induced by the activation of sensory neurons, providing simple transformations that q

207 on of motor behavior, but how proprioceptive sensory neurons (pSNs) establish functionally appropriat

208 Sensory neuron purification increased numbers of sex-dep

209 Peripheral sensory neurons regenerate their axon after nerve injury

210 identified that LXR alpha/beta expressed in sensory neurons regulates neuronal Neuregulin 1 (Nrg1),

211 Female-predominant DEGs in sensory neurons relate to inflammatory, synaptic transmi

212 Allergen-activated sensory neurons released the neuropeptide Substance P, w

213 pment, as well as the basic biology of these sensory neurons, remains rudimentary.

214 th large-fiber nerve bundles and small-fiber sensory neurons; report that muscle mSCs transcribe an a

215 ndritic arborisation (c1vpda) proprioceptive sensory neurons respond to contractions in the Drosophil

216 Gut-innervating nociceptor sensory neurons respond to noxious stimuli by initiating

217 tumor cells to secrete factors that augment sensory neuron responsiveness, and thus identify a poten

218 We found that conditional knockout of Grp in sensory neurons results in attenuated non-histaminergic

219 Activation of TRPV1 channels in sensory neurons results in opening of a cation permeatio

220 mplexity of cold-sensing mechanisms in mouse sensory neurons, revealing a principal role for Na(V)1.8

221 DC2s) recruited to wounds and increased itch sensory neuron sensitivity.

222 ontrol the frequency of firing in peripheral sensory neurons signalling pain.

223 formation of intracellular lipid droplets in sensory neurons.SIGNIFICANCE STATEMENT There is a global

224 channels in these injured trigeminal primary sensory neurons.SIGNIFICANCE STATEMENT We unveil a key r

225 und to be widely expressed in all classes of sensory neurons (small, medium, large) where it contribu

226 blunted phosphorylation of c-Jun in primary sensory neurons subjected to trophic deprivation, a well

227 scriptomics profiling revealed that multiple sensory neuron subsets, predominantly peptidergic nocice

228 ue for defining ion channel contributions to sensory neuron subtype-specific intrinsic physiological

229 Unique features of sensory neuron subtypes are manifest by their distinct p

230 Dorsal root ganglion (DRG) sensory neuron subtypes defined by their in vivo propert

231 spatial patterning of neurites from multiple sensory neuron subtypes.

232 hannels showing high levels of expression in sensory neurons such as TRPV1, TRPA1, and TRPM8, have be

233 ase in dendritic development and function of sensory neurons, suggesting that aberrant sensory functi

234 The discovery of keratinocyte-sensory neuron synaptic-like contacts may call for a rea

235 tive communication between keratinocytes and sensory neurons, synaptic-like contacts are the hubs of

236 The significance of sensory neuron targeting was pursued subsequently by tes

237 Sensory neurons, termed nociceptors, are derived from do

238 and energy homeostasis roles map to a set of sensory neurons that act upstream of fat regulation as w

239 reafference is specifically targeted at the sensory neurons that are affected by the movements; and

240 termined the transcriptomic diversity of the sensory neurons that can be retrogradely labeled from mo

241 he interactions between urothelial cells and sensory neurons that control urination.

242 s are heavily innervated by nociceptors, the sensory neurons that detect noxious stimuli, leading to

243 which are neuropeptide-producing nociceptive sensory neurons that express the ion channel TRPV1 and T

244 It is mediated by nociceptor sensory neurons that innervate the skin, joints, bones,

245 Further, although many of the sensory neurons that mediate taxis have been described,

246 n-perceptual nociceptors (PPN) are essential sensory neurons that recognize harmful stimuli and can e

247 f HbSS-BERK mice and sensitizes nociceptors (sensory neurons that respond to noxious stimuli), and th

248 lamina I of the spinal cord, which contains sensory neurons that transmit pain and itch information

249 ) sensory neurons, and unmyelinated (NF200-) sensory neurons that were either peptidergic (CGRP+) or

250 ation of early differentiating LgDel cranial sensory neurons, those in CNgV, a major source of innerv

251 Epidermal keratinocytes dialogue with sensory neurons through en passant synaptic-like contact

252 produce inflammatory mediators that activate sensory neurons through neuro-immune interactions.

253 cal TLR signaling, TLRs function uniquely in sensory neurons through non-canonical coupling to ion ch

254 nformation transmitted from keratinocytes to sensory neurons through SNARE-mediated (syntaxin1) vesic

255 tion channel subfamily V member 1 (TRPV1) on sensory neurons to alter their membrane potential and in

256 that processes information perceived by two sensory neurons to control the induction of hydrogen per

257 , transcriptionally silent latency states in sensory neurons to escape host detection.

258 sophila describes a circuit mechanism - from sensory neurons to higher brain centers - that encodes a

259 Here, we uncover a specialized circuit, from sensory neurons to higher brain centers, that processes

260 on the feedforward flow of information from sensory neurons to motor neurons, and apply a recently d

261 The molecular mechanisms that enable sensory neurons to remain flexible and adapt to a partic

262 confer the cellular plasticity required for sensory neurons to transform into a regenerative state.

263 d mice lacking nodal spectrins in peripheral sensory neurons to uncouple their nodal functions from t

264 al progression from the early involvement of sensory neurons, to the later appearance of vestibular a

265 sodium channels are critical for peripheral sensory neuron transduction and have been implicated in

266 receptor potential melastatin 8) in primary sensory neurons using both pharmacological inhibition an

267 We discuss how sensory neurons utilize TLRs and other PRR pathways to d

268 n vesicular glutamate transporter 1 (Vglut1) sensory neurons (Vglut1-ChR2), which is a heterogeneous

269 riggers SARM1-dependent axon degeneration in sensory neurons via a noncanonical necroptotic signaling

270 -histaminergic itch, but its site of action (sensory neurons vs spinal cord) remains controversial.

271 or (Fpr) family are expressed by vomeronasal sensory neurons (VSNs) in the accessory olfactory system

272 (VNO) contains two main types of vomeronasal sensory neurons (VSNs) that express distinct vomeronasal

273 This subpopulation of olfactory sensory neurons was over-represented in sex-separated mi

274 In trigeminal primary sensory neurons, we detected single-channel activity wit

275 mones and is female-selectively activated in sensory neurons, we evaluated whether Prlr signaling con

276 sent at much lower levels than in peripheral sensory neurons, we found cells expressing TRPM8 in rest

277 To determine the role of GRP in sensory neurons, we generated a floxed Grp mouse line.

278 cells that may interact with LN-innervating sensory neurons, we generated a LN single-cell transcrip

279 tional interactions of beta-cells with vagal sensory neurons, we recorded Ca(2+) responses in individ

280 Historically, epidermal-innervating sensory neurons were thought to be the exclusive detecto

281 t Wnt5a is released spinally from peripheral sensory neurons, where it recruits the tyrosine kinase r

282 T-type Ca(2+) channels that are expressed in sensory neurons, where they play a role in the regulatio

283 Pvr is expressed and functions in class IV sensory neurons, whereas Pvf2 and Pvf3 are produced by m

284 22%, respectively) of airway-specific vagal sensory neurons; whereas S1PR4 and S1PR5 were rarely exp

285 hogenetic protein signaling in proprioceptor sensory neurons which are critical for the relay of the

286 ncestral chordates) contrast with vertebrate sensory neurons, which arise from placodes and neural cr

287 potentiates temperature responses in the AWC sensory neurons, which inhibit the postsynaptic AIA inte

288 onditions induce physiological regulation of sensory neurons, which is critical for the maintenance o

289 cally increased in Rtca-deficient Drosophila sensory neurons, which is dependent on Xbp1.

290 deletion of colony-stimulating factor 1 from sensory neurons, which prevents nerve injury-induced mic

291 dependent DEGs in estrous female versus male sensory neurons, which were prepared by using different

292 od signals are detected by a small number of sensory neurons whose activity non-autonomously regulate

293 STATEMENT Visceral organs are innervated by sensory neurons whose cell bodies are located in multipl

294 Jugular vagal airway sensory neurons wire into a brainstem circuit with ascen

295 is a heterogeneous population of large-sized sensory neurons with features consistent with Abeta-LTMR

296 anscriptomes of cancer-associated trigeminal sensory neurons with those of endogenous neurons in mous

297 d by the existence of a diversity of primary sensory neurons with unique biological features and resp

298 Photoreceptors are highly specialized sensory neurons with unique metabolic and physiological

299 nfection of ocular, oral, or nasal cavities, sensory neurons within trigeminal ganglia (TG) are an im

300 for bovine herpesvirus 1 (BoHV-1) latency is sensory neurons within trigeminal ganglia (TG).