ライフサイエンスコーパス: pseudorabies

1 rabies virus (PRV) is the causative agent of pseudorabies, a disease of great economic and welfare im

2 Control viruses, including pseudorabies, adeno-associated, or replication-deficient

3 In addition, UL11 homologs from pseudorabies and Marek's disease herpesviruses were also

4 neurons were revealed using Cre-conditional pseudorabies and rabies viruses.

5 two isogenic strains of a neurotropic virus (pseudorabies, Bartha) tagged with either green or red fl

6 s, which caused the recent devastating swine pseudorabies outbreak in China.

7 y in pigs and the promise to control current pseudorabies outbreak.

8 Using pseudorabies (PRV) viral transneuronal tracing, we repor

9 The alpha-herpes virus (pseudorabies, PRV) was used to observe central nervous s

10 of the advantages and limitations of herpes, pseudorabies, rabies, adeno-associated, lentivirus, and

11 d using green fluorescent protein expressing pseudorabies virus (GFP-PRV) to (1) characterize age-dep

12 A strain of pseudorabies virus (PRV 152) isogenic with the Bartha st

13 itreal injection of the attenuated strain of pseudorabies virus (PRV Bartha) results in transneuronal

14 ntraocular injection of the Bartha strain of pseudorabies virus (PRV Bartha) results in transsynaptic

15 rus (HSV), varicella-zoster virus (VZV), and pseudorabies virus (PRV) all utilize a complex of two gl

16 well as for the animal herpesviruses porcine pseudorabies virus (PRV) and bovine herpesvirus 1 (BHV-1

17 entified by immunohistochemical detection of pseudorabies virus (PRV) and corticotropin-releasing fac

18 ative to the model alphaherpesvirus pathogen pseudorabies virus (PRV) and demonstrate that this criti

19 are the most widely used method to visualize pseudorabies virus (PRV) and herpes simplex virus (HSV)

20 he gD glycoprotein of the alphaherpesviruses pseudorabies virus (PRV) and herpes simplex virus 2 (HSV

21 Pseudorabies virus (PRV) and herpes simplex virus type 1

22 9p and the glycoprotein heterodimer gE/gI of pseudorabies virus (PRV) and herpes simplex virus type 1

23 Both Pseudorabies virus (PRV) and human Herpes simplex virus

24 3 in herpes simplex virus type 1 (HSV-1) and pseudorabies virus (PRV) and ORF66 in varicella-zoster v

25 ane proteins encoded by the alphaherpesvirus pseudorabies virus (PRV) are internalized after reaching

26 The membrane proteins gI and gE of Pseudorabies virus (PRV) are required for viral invasion

27 Using pseudorabies virus (PRV) as model virus, we performed ch

28 The structure of pseudorabies virus (PRV) capsids isolated from the nucle

29 the viral transcriptional activator, VP16 on pseudorabies virus (PRV) escape from genome silencing.

30 The alphaherpesvirus pseudorabies virus (PrV) establishes latency primarily i

31 Like other alphaherpesviruses, pseudorabies virus (PrV) exhibits restricted gene expres

32 d PSPMNs by using recombinant strains of the pseudorabies virus (PRV) for trans-synaptic tract tracin

33 d PSPMNs by using recombinant strains of the pseudorabies virus (PRV) for transsynaptic tract-tracing

34 pothesis, we used recombinant strains of the pseudorabies virus (PRV) for transsynaptic tract-tracing

35 rograde transport of an attenuated strain of pseudorabies virus (PRV) from the nucleus accumbens was

36 endent retrograde transneuronal transport of pseudorabies virus (PRV) from the stomach wall.

37 determine the role of internalization of the pseudorabies virus (PRV) gE and gI proteins, we construc

38 The pseudorabies virus (PRV) gE gene encodes a multifunction

39 A full-length clone of the 142-kb pseudorabies virus (PRV) genome was constructed as a sta

40 nabled the escape from silencing of incoming pseudorabies virus (PRV) genomes.

41 Pseudorabies virus (PRV) glycoprotein E (gE) is a type I

42 ynaptic tracing with peripheral injection of pseudorabies virus (PRV) has been extensively characteri

43 K in herpes simplex virus type 1 (HSV-1) and pseudorabies virus (PRV) have been well studied.

44 using transneuronal retrograde transport of pseudorabies virus (PRV) in normal animals and in animal

45 ction of the transneuronal retrograde tracer pseudorabies virus (PRV) in rats, we previously localize

46 s, was mapped using the transneuronal tracer pseudorabies virus (PRV) in the ferret.

47 esviruses herpes simplex virus 1 (HSV-1) and pseudorabies virus (PRV) in the infected cell cytoplasm

48 cellular virions and axonal assemblies after pseudorabies virus (PRV) infection of cultured neurons.

49 After pseudorabies virus (PRV) infection of murine L929 cells,

50 the host gene expression profile after acute pseudorabies virus (PRV) infection of the CNS using Affy

51 models of viral egress from neurons by using pseudorabies virus (PRV) infection of the rat retina: do

52 nal spread of herpes simplex virus (HSV) and pseudorabies virus (PRV) infection, a culture system con

53 nduced after herpes simplex virus type 1 and pseudorabies virus (PRV) infections of rat embryonic fib

54 When the swine alphaherpesvirus pseudorabies virus (PRV) infects the rat retina, it repl

55 ed by retrograde trans-synaptic migration of pseudorabies virus (PRV) injected into the adrenal gland

56 Using the retrograde, transsynaptic tracer pseudorabies virus (PRV) injected into the BAT of mice,

57 astric nerves transected, were infected with pseudorabies virus (PRV) injected into the external uret

58 ia the transsynaptic retrograde transport of pseudorabies virus (PRV) injected into the kidneys of ra

59 ted neurons in the preoptic region following pseudorabies virus (PRV) injections into either the supe

60 Pseudorabies virus (PRV) injections were made into the l

61 sneuronal tracing studies using injection of pseudorabies virus (PRV) into either the diaphragm or re

62 studied after injecting the Bartha strain of pseudorabies virus (PRV) into the sciatic nerve to provi

63 epithelial cells, alphaherpesviruses such as pseudorabies virus (PRV) invade axons of peripheral nerv

64 Pseudorabies virus (PRV) is a broad host range, swine al

65 Transneuronal spread of pseudorabies virus (PRV) is a multistep process that req

66 Pseudorabies virus (PRV) is a porcine alphaherpesvirus t

67 Pseudorabies virus (PRV) is a useful tracer that is retr

68 Pseudorabies virus (PRV) is an alphaherpesvirus related

69 mal degradation of KIF1A in axons.IMPORTANCE Pseudorabies virus (PRV) is an alphaherpesvirus related

70 Glycoprotein E (gE) gene of pseudorabies virus (PRV) is conserved among diverse alph

71 The alphaherpesvirus pseudorabies virus (PRV) is the causative agent of pseud

72 Pseudorabies virus (PRV) mutants lacking the Us9 gene ca

73 Retrograde infection by pseudorabies virus (PRV) of neuronal populations neighbo

74 by inoculating the ventral stomach wall with pseudorabies virus (PRV) on postnatal day 1 (P1), P4, or

75 simplex virus (HSV) entry activity, but not pseudorabies virus (PRV) or bovine herpesvirus 1 (BHV-1)

76 d the retrograde transneuronal tracer Bartha-pseudorabies virus (PRV) or the retrograde marker choler

77 ane protein present in the lipid envelope of pseudorabies virus (PRV) particles in a unique tail-anch

78 Toward this end, we generated a novel pseudorabies virus (PrV) recombinant in which a 282-bp r

79 In this report, we describe construction of pseudorabies virus (PRV) recombinants that efficiently e

80 escape from latency by the alphaherpesvirus pseudorabies virus (PRV) relies on a structural viral te

81 ial cells infected with the alphaherpesvirus pseudorabies virus (PRV) results in activation of the ha

82 Here, we refine this map using pseudorabies virus (PRV) retrograde tracing, indicating

83 Notably, retrograde tracing using pseudorabies virus (PRV) revealed that both dorsal and v

84 rted methods we solved the structures of (i) Pseudorabies virus (PRV) RNA G-quadruplex and ligand com

85 stem, we have discovered a novel role of the pseudorabies virus (PRV) serine/threonine kinase US3 in

86 The attenuated pseudorabies virus (PRV) strain Bartha contains several

87 After intraocular injection of the virulent pseudorabies virus (PRV) strain Becker into late-stage c

88 To accomplish this, we have constructed pseudorabies virus (PRV) strains in which viral propagat

89 , but partial deletions generated in HSV and pseudorabies virus (PrV) suggest an additional function

90 egulates interferon (IFN) induction and that pseudorabies virus (PRV) targets PRDX1 to evade IFN indu

91 axonally delivered genomes is facilitated by pseudorabies virus (PRV) tegument proteins.

92 ly(A) fraction of the lytic transcriptome of pseudorabies virus (PRV) throughout a 12-hour interval o

93 This study used the transneuronal tracer pseudorabies virus (PRV) to investigate the CNS network

94 ns were identified by immunogold labeling of pseudorabies virus (PRV) transported retrogradely and tr

95 UL13 protein kinase of the alphaherpesvirus pseudorabies virus (PRV) triggers phosphorylation of FTO

96 The subcellular distribution of the pseudorabies virus (PRV) UL28 protein was examined by in

97 The pseudorabies virus (PRV) UL54 homologs are important mul

98 We demonstrate here that the pseudorabies virus (PRV) Us2 protein is synthesized earl

99 The pseudorabies virus (PRV) Us3 gene is conserved among the

100 The protein product of the pseudorabies virus (PRV) Us9 gene is a phosphorylated, t

101 Pseudorabies virus (PRV) Us9 is a small, tail-anchored (

102 In this report, we demonstrate that the pseudorabies virus (PRV) Us9 protein is present in infec

103 s simplex virus (HSV) and, as reported here, pseudorabies virus (PRV) utilize the ESCRT apparatus to

104 nal sorting and transport of fully assembled pseudorabies virus (PRV) virions is dependent on the vir

105 e provide an initial characterization of the pseudorabies virus (PRV) VP22 homologue.

106 ingly, entry of the porcine alphaherpesvirus pseudorabies virus (PRV) was inhibited by sphingomyelin-

107 Pseudorabies virus (PRV) was injected into the pancreas

108 tracing experiments were performed in which pseudorabies virus (PRV) was injected into the stellate

109 riments, the retrograde transneuronal tracer pseudorabies virus (PRV) was microinjected into the CEAm

110 A replication-competent gL-null pseudorabies virus (PrV) was shown to express a gDgH hyb

111 ade tract tracing, using isogenic strains of pseudorabies virus (PRV) with distinct fluorescent repor

112 dies, we compared gH of the alphaherpesvirus pseudorabies virus (PrV) with gH of the gammaherpesvirus

113 Pseudorabies virus (PRV), a broad host range alphaherpes

114 Pseudorabies virus (PRV), a member of the Alphaherpesvir

115 Pseudorabies virus (PRV), a neurotropic swine alpha herp

116 brane glycoproteins gE and gI are encoded by pseudorabies virus (PRV), a neurotropic, broad-host-rang

117 lenic function was accomplished by injecting pseudorabies virus (PRV), a retrograde transynaptic trac

118 that the amino-terminal one-third of gC from pseudorabies virus (PRV), a swine herpesvirus, includes

119 Pseudorabies virus (PRV), a swine neurotropic alphaherpe

120 g vesicular stomatitis (VSV), Sindbis virus, pseudorabies virus (PRV), adeno-associated virus (AAV),

121 Using pseudorabies virus (PRV), an alphaherpesvirus capable of

122 Pseudorabies virus (PRV), an alphaherpesvirus related to

123 Previous studies showed that proteins from pseudorabies virus (PRV), an alphaherpesvirus, localize

124 work reports that the UL13 protein kinase of pseudorabies virus (PRV), an alphaherpesvirus, mediates

125 erpes simplex viruses (HSV) 1 and 2, porcine pseudorabies virus (PRV), and bovine herpesvirus 1 (BHV-

126 (BHV-1), equine herpesvirus type 1 (EHV-1), pseudorabies virus (PRV), and varicella-zoster virus (VZ

127 pesviruses, such as herpes simplex virus and pseudorabies virus (PRV), are neuroinvasive dsDNA viruse

128 Alphaherpesviruses, including pseudorabies virus (PRV), are neuroinvasive pathogens th

129 including herpes simplex virus 1 (HSV-1) and pseudorabies virus (PRV), are pathogens of the nervous s

130 U(S)11c119.3 cells are fully susceptible to pseudorabies virus (PRV), as shown by single-step growth

131 The related animal herpesvirus, pseudorabies virus (PRV), encodes a homologous set of gl

132 sviruses, herpes simplex virus 1 (HSV-1) and pseudorabies virus (PRV), have suggested that UL37 plays

133 pes viruses: herpes simplex virus (HSV1) and pseudorabies virus (PrV), human immunodeficiency virus t

134 peroxidase conjugated to colloidal gold, or pseudorabies virus (PRV), into the nuclear core of the r

135 st commonly varicella-zoster virus (VZV) and pseudorabies virus (PRV), may cause cranial nerve disord

136 In the swine pathogen pseudorabies virus (PRV), mutant viruses with internal d

137 ls also showed enhanced fusion activity with pseudorabies virus (PRV), paramyxovirus, and rhabdovirus

138 Alphaherpesviruses, including pseudorabies virus (PRV), spread directionally within th

139 Live attenuated vaccine strains of pseudorabies virus (PRV), such as PRV Bartha, are among

140 lex virus 1 (HSV-1), HSV-2, and veterinarian pseudorabies virus (PRV), that infect the peripheral ner

141 In pseudorabies virus (PRV), the Us9 protein is a 98-amino-

142 ished retrograde transneuronal viral tracer, pseudorabies virus (PRV), was injected into the ventral

143 The transneuronal tracer, pseudorabies virus (PRV), was used to identify pathways

144 Using a viral transneuronal tract tracer, pseudorabies virus (PRV), we also tested whether the com

145 Using pseudorabies virus (PRV), we have previously shown that

146 Using the neuroinvasive herpesvirus, pseudorabies virus (PRV), we show that the viral protein

147 cle-specific injection of an mRFP-expressing pseudorabies virus (PRV), which acts as a transsynaptic

148 including herpes simplex virus 1 (HSV-1) and pseudorabies virus (PRV), within neurons is poorly under

149 Pseudorabies virus (PRV)-a retrograde transneuronal trac

150 s study were to identify the mechanism(s) of pseudorabies virus (PrV)-induced down-regulation of porc

151 nervous system, alphaherpesviruses-including pseudorabies virus (PRV)-use retrograde axonal transport

152 tion with virulent and attenuated strains of pseudorabies virus (PRV).

153 athways in rats using recombinant strains of pseudorabies virus (PRV).

154 te entry of herpes simplex viruses (HSV) and pseudorabies virus (PRV).

155 of gD (for example, HSV-1/Rid), and porcine pseudorabies virus (PRV).

156 following infection of the left kidney with pseudorabies virus (PRV).

157 a receptor for the porcine alphaherpesvirus pseudorabies virus (PRV).

158 es, such as herpes simplex virus 1 (HSV1) or pseudorabies virus (PRV).

159 el to study neuronal spread and virulence of pseudorabies virus (PRV).

160 -1), HSV-2, and the related alphaherpesvirus pseudorabies virus (PRV).

161 an alpha-herpes virus, the Bartha strain of pseudorabies virus (PRV).

162 DMV neurons projecting to the stomach using pseudorabies virus (PRV).

163 DA), and retrograde tracing with fluorescent pseudorabies virus (PRV).

164 onserved in varicella-zoster virus (VZV) and pseudorabies virus (PRV).

165 of two neurotropic herpesviruses: HSV-1 and pseudorabies virus (PRV).

166 emale Sprague-Dawley rats were infected with pseudorabies virus (PRV, Bartha's K-strain) by injection

167 nstructing a replication-competent strain of pseudorabies virus (PRV-263) that changes the profile of

168 were transsynaptically labeled by injecting pseudorabies virus (PRV-614) into the kidney, indicating

169 train of the retrograde transneuronal tracer pseudorabies virus (PRV-Ba) was injected into rat choroi

170 e transneuronal tracer, the Bartha strain of pseudorabies virus (PRV-Ba), were injected into the uppe

171 tract tracing using an attenuated strain of pseudorabies virus (PRV-Bartha) was combined with immuno

172 S-specific transneuronal viral tract tracer, pseudorabies virus (PRV152) and demonstrated the sensory

173 , to identify GG premotoneurons, we injected pseudorabies virus (PRV152) into the GG muscle.

174 ed fluorophore expression from a recombinant pseudorabies virus (PRV263) carrying a Brainbow cassette

175 vulgaris leucoagglutinin (anterograde), and pseudorabies virus (transneuronal retrograde) tract-trac

176 g after inoculation of the stomach wall with pseudorabies virus 152, a viral label that reports enhan

177 hway with those of other alphaherpesviruses (pseudorabies virus [PRV] and herpes simplex virus 1 [HSV

178 e poliovirus, herpesvirus, rabies virus, and pseudorabies virus all utilize neuronal retrograde trans

179 following infection with the closely related pseudorabies virus and observed similar perimeters of gl

180 ynaptically labeled from the distal colon by pseudorabies virus and several of these were also retrog

181 The glycoproteins I and E of pseudorabies virus are important mediators of cell-to-ce

182 s simplex virus, varicella zoster virus, and pseudorabies virus are neurotropic pathogens of the Alph

183 Using pseudorabies virus as a model, we infected neuron cell b

184 In this report, we have used pseudorabies virus as a neuroanatomical tract tracer in

185 Here, using herpes simplex virus type I and pseudorabies virus as model alphaherpesviruses, we show

186 ame animals by injection of a recombinant of pseudorabies virus Bartha (PRV) into the contralateral v

187 he transsynaptic retrograde transport of the pseudorabies virus Bartha (PRV-Bartha) strain has become

188 labeling of the phrenic motoneuron pool with pseudorabies virus demonstrated a substantial number of

189 Pseudorabies virus encodes a membrane protein (Us9) that

190 By using pseudorabies virus expressing green fluorescence protein

191 rions, epithelial cells infected by HSV-1 or pseudorabies virus following ADS express fewer than two

192 milarities and differences between HSV-1 and pseudorabies virus gE.

193 icial chromosome (BAC) containing the 142-kb pseudorabies virus genome was constructed such that the

194 sons with homologous HSV-2 gH/gL and partial pseudorabies virus gH structures support the domain boun

195 Recently, a pseudorabies virus glycoprotein D (gD)-green fluorescent

196 The Bartha strain of pseudorabies virus has several recognized mutations, inc

197 naptic labeling from the adrenal gland using pseudorabies virus identified presympathetic GABAergic n

198 ficking, we analyzed the axonal transport of pseudorabies virus in the presence and absence of pUS9.

199 al afferent pathways can be identified after pseudorabies virus infection of the kidney.

200 sitive neurones in the LH were labelled with pseudorabies virus injected into the liver of parasympat

201 erebral cortex were identified in rats after pseudorabies virus injections were made in functionally

202 Pseudorabies virus inoculated into the distal femoral me

203 Injection of pseudorabies virus into different regions of the MD or r

204 nsneuronally infected following injection of pseudorabies virus into rectus abdominis or transversus

205 injected the retrograde transynaptic tracer pseudorabies virus into single tensor tympani (TT) muscl

206 Injection of conditional pseudorabies virus into the brain of an LHRH::CRE mouse

207 By injecting pseudorabies virus into the diaphragm and using c-Fos ac

208 injected a retrograde-specific strain of the pseudorabies virus into the rat OB and piriform cortex.

209 Fluorogold or green fluorescent pseudorabies virus labeled postganglionic neurons in the

210 We used transsynaptic anterograde pseudorabies virus labeling of fungiform taste papillae

211 The stability of interneuronal pseudorabies virus labeling patterns following lateral c

212 resembles in many respects the phenotype of pseudorabies virus lacking glycoproteins gM, gE, and gI.

213 Mutant pseudorabies virus lacking U(L)3.5 is deficient in viral

214 demonstrate that the pUL31 component of the pseudorabies virus nuclear egress complex is a condition

215 remotor interneurons with the trans-synaptic pseudorabies virus PRV-152 revealed the presence of burs

216 re retrogradely labelled (prior injection of pseudorabies virus PRV-152) and whole-cell, patch clamp

217 Specifically, we injected the conditional pseudorabies virus recombinant (BA2001) that can replica

218 Dual-labeling studies with pseudorabies virus recombinants also showed prephrenic i

219 The first method uses HSV-1 and pseudorabies virus recombinants that express one of thre

220 Combined with pseudorabies virus retrograde tracing from the iWAT, we

221 ransneuronal retrograde pathway tracing with pseudorabies virus revealed connectivity between MnPO VG

222 We constructed a pseudorabies virus strain that expressed Us9-GFP and tes

223 liver and epididymal white fat in mice using pseudorabies virus strains expressing different reporter

224 Two immunohistochemically distinct pseudorabies virus strains were injected into male Sprag

225 omplemented prior herpes simplex virus 1 and pseudorabies virus studies investigating two other inhib

226 riments with ICP4 homologs revealed that the pseudorabies virus TAD is a potent activator of the gD p

227 Despite being a major component of the pseudorabies virus tegument, VP22 is not required for PR

228 We report the development of a pseudorabies virus that can be used for retrograde traci

229 Starting with derivatives of pseudorabies virus that encode a fluorescent protein fus

230 Here, the spread of pseudorabies virus through renal sensory pathways was ex

231 n subunit b retrograde tracing from rRPa and pseudorabies virus transynaptic retrograde tracing from

232 The resistance to pseudorabies virus was CD4(+) T cell dependent, because

233 Pseudorabies virus was injected into the wall of the ven

234 ntral nervous system neurons infected with a pseudorabies virus were examined in vitro by using whole

235 pathway, a retrograde transsynaptic tracer (pseudorabies virus) was injected into the orbicularis oc

236 rebral injections of an attenuated strain of pseudorabies virus, a neurotropic alpha herpesvirus that

237 s in the spinal cord, was characterized with pseudorabies virus, a retrograde transynaptic tracer.

238 Using pseudorabies virus, a transsynaptic tracer, in anestheti

239 Pseudorabies virus, an alpha-herpesvirus, is capable of

240 tructure of the N-terminal half of UL37 from pseudorabies virus, an alphaherpesvirus closely related

241 a subunit, Fluoro-Gold, the Bartha strain of pseudorabies virus, and biotinylated dextran amine.

242 simplex virus types 1 and 2 (HSV-1 and -2), pseudorabies virus, and bovine herpesvirus 1.

243 phaherpesviruses herpes simplex virus (HSV), pseudorabies virus, and bovine herpesvirus type 1.

244 ctures of gH/gL from herpes simplex virus 2, pseudorabies virus, and Epstein-Barr virus revealed dist

245 Cytomegalovirus, pseudorabies virus, and Sindbis virus all evoked a 2-log

246 ilar mutant of the related alphaherpesvirus, pseudorabies virus, and suggests that the glycoprotein r

247 lycoproteins of herpes simplex virus type 1, pseudorabies virus, and varicella-zoster virus, BHV-1 gI

248 fork movement in vivo during replication of pseudorabies virus, another herpesvirus.

249 Pseudorabies virus, Bartha's K strain, was injected into

250 virus 1 (EHV-1), varicella-zoster virus, and pseudorabies virus, but very little is known about the p

251 pesviruses, such as herpes simplex virus and pseudorabies virus, cause a broad range of diseases in h

252 ine herpesvirus 1, equine herpesvirus 4, and pseudorabies virus, establish a quiescent/latent infecti

253 tween HSV1 and the related alphaherpesvirus, pseudorabies virus, in which the homologues of all three

254 ions of the SCN using the swine herpesvirus (pseudorabies virus, PRV) as a tool for transynaptic anal

255 n tracing using a sympathetic nerve-specific pseudorabies virus, PRV152.

256 r the retrograde transneuronal viral tracer, pseudorabies virus, was injected into the stellate sympa

257 an infectious clone of the alphaherpesvirus pseudorabies virus, we have made a collection of truncat

258 paring HSV-1 to a related alpha herpesvirus, pseudorabies virus, we show that this preferential exocy

259 /Cas9 and Cre/Lox system against re-emerging Pseudorabies virus, which caused the recent devastating

260 ry associated with the hippocampus using the pseudorabies virus-Bartha strain (PRV-Bartha) tracer in

261 Pseudorabies virus-labelled cells were also seen in the

262 and bladder body injections, the majority of pseudorabies virus-labelled cells were found in the late

263 Very few pseudorabies virus-labelled cells were found rostral to

264 ique long region similar to that observed in pseudorabies virus.

265 ase of infection in Vero cells infected with pseudorabies virus.

266 c recombinant strains (PRV-152 and BaBlu) of pseudorabies virus.

267 sport of two recombinant isogenic strains of pseudorabies virus.

268 o infections by unrelated pathogens, such as pseudorabies virus.

269 scles, were injected with Bartha's strain of pseudorabies virus.

270 to infer the proximity of several strains of pseudorabies virus.

271 hed from studies of herpes simplex virus and pseudorabies virus.

272 imilar to the phenotype previously shown for pseudorabies virus.

273 tructed a panel of Cre recombinase-activated pseudorabies viruses (PRVs) that enabled retrograde trac

274 ell imaging, we made a series of recombinant pseudorabies viruses that encoded green fluorescent prot

275 The large DNA viruses, herpes simplex and pseudorabies viruses, use ubiquitous nectins 1 and 2.

276 the cervical spinal cord in which c-Fos and pseudorabies were co-localized, and these neurons expres