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1 ase of infection in Vero cells infected with pseudorabies virus.
2 c recombinant strains (PRV-152 and BaBlu) of pseudorabies virus.
3 sport of two recombinant isogenic strains of pseudorabies virus.
4 scles, were injected with Bartha's strain of pseudorabies virus.
5 to infer the proximity of several strains of pseudorabies virus.
6 imilar to the phenotype previously shown for pseudorabies virus.
7 o infections by unrelated pathogens, such as pseudorabies virus.
8 ique long region similar to that observed in pseudorabies virus.
9 g after inoculation of the stomach wall with pseudorabies virus 152, a viral label that reports enhan
10 rebral injections of an attenuated strain of pseudorabies virus, a neurotropic alpha herpesvirus that
11 s in the spinal cord, was characterized with pseudorabies virus, a retrograde transynaptic tracer.
12                                        Using pseudorabies virus, a transsynaptic tracer, in anestheti
13 e poliovirus, herpesvirus, rabies virus, and pseudorabies virus all utilize neuronal retrograde trans
14                                              Pseudorabies virus, an alpha-herpesvirus, is capable of
15 tructure of the N-terminal half of UL37 from pseudorabies virus, an alphaherpesvirus closely related
16 following infection with the closely related pseudorabies virus and observed similar perimeters of gl
17 ynaptically labeled from the distal colon by pseudorabies virus and several of these were also retrog
18 a subunit, Fluoro-Gold, the Bartha strain of pseudorabies virus, and biotinylated dextran amine.
19  simplex virus types 1 and 2 (HSV-1 and -2), pseudorabies virus, and bovine herpesvirus 1.
20 phaherpesviruses herpes simplex virus (HSV), pseudorabies virus, and bovine herpesvirus type 1.
21 ctures of gH/gL from herpes simplex virus 2, pseudorabies virus, and Epstein-Barr virus revealed dist
22                             Cytomegalovirus, pseudorabies virus, and Sindbis virus all evoked a 2-log
23 ilar mutant of the related alphaherpesvirus, pseudorabies virus, and suggests that the glycoprotein r
24 lycoproteins of herpes simplex virus type 1, pseudorabies virus, and varicella-zoster virus, BHV-1 gI
25  fork movement in vivo during replication of pseudorabies virus, another herpesvirus.
26                 The glycoproteins I and E of pseudorabies virus are important mediators of cell-to-ce
27 s simplex virus, varicella zoster virus, and pseudorabies virus are neurotropic pathogens of the Alph
28                                        Using pseudorabies virus as a model, we infected neuron cell b
29                 In this report, we have used pseudorabies virus as a neuroanatomical tract tracer in
30 ame animals by injection of a recombinant of pseudorabies virus Bartha (PRV) into the contralateral v
31 he transsynaptic retrograde transport of the pseudorabies virus Bartha (PRV-Bartha) strain has become
32                                              Pseudorabies virus, Bartha's K strain, was injected into
33 ry associated with the hippocampus using the pseudorabies virus-Bartha strain (PRV-Bartha) tracer in
34 virus 1 (EHV-1), varicella-zoster virus, and pseudorabies virus, but very little is known about the p
35 labeling of the phrenic motoneuron pool with pseudorabies virus demonstrated a substantial number of
36                                              Pseudorabies virus encodes a membrane protein (Us9) that
37                                     By using pseudorabies virus expressing green fluorescence protein
38 rions, epithelial cells infected by HSV-1 or pseudorabies virus following ADS express fewer than two
39 milarities and differences between HSV-1 and pseudorabies virus gE.
40 icial chromosome (BAC) containing the 142-kb pseudorabies virus genome was constructed such that the
41 d using green fluorescent protein expressing pseudorabies virus (GFP-PRV) to (1) characterize age-dep
42 sons with homologous HSV-2 gH/gL and partial pseudorabies virus gH structures support the domain boun
43                                  Recently, a pseudorabies virus glycoprotein D (gD)-green fluorescent
44                         The Bartha strain of pseudorabies virus has several recognized mutations, inc
45 naptic labeling from the adrenal gland using pseudorabies virus identified presympathetic GABAergic n
46 ficking, we analyzed the axonal transport of pseudorabies virus in the presence and absence of pUS9.
47 tween HSV1 and the related alphaherpesvirus, pseudorabies virus, in which the homologues of all three
48 al afferent pathways can be identified after pseudorabies virus infection of the kidney.
49 sitive neurones in the LH were labelled with pseudorabies virus injected into the liver of parasympat
50 erebral cortex were identified in rats after pseudorabies virus injections were made in functionally
51                                              Pseudorabies virus inoculated into the distal femoral me
52                                 Injection of pseudorabies virus into different regions of the MD or r
53 nsneuronally infected following injection of pseudorabies virus into rectus abdominis or transversus
54  injected the retrograde transynaptic tracer pseudorabies virus into single tensor tympani (TT) muscl
55                     Injection of conditional pseudorabies virus into the brain of an LHRH::CRE mouse
56 injected a retrograde-specific strain of the pseudorabies virus into the rat OB and piriform cortex.
57              Fluorogold or green fluorescent pseudorabies virus labeled postganglionic neurons in the
58            We used transsynaptic anterograde pseudorabies virus labeling of fungiform taste papillae
59               The stability of interneuronal pseudorabies virus labeling patterns following lateral c
60                                              Pseudorabies virus-labelled cells were also seen in the
61 and bladder body injections, the majority of pseudorabies virus-labelled cells were found in the late
62                                     Very few pseudorabies virus-labelled cells were found rostral to
63  resembles in many respects the phenotype of pseudorabies virus lacking glycoproteins gM, gE, and gI.
64                                       Mutant pseudorabies virus lacking U(L)3.5 is deficient in viral
65  demonstrate that the pUL31 component of the pseudorabies virus nuclear egress complex is a condition
66 remotor interneurons with the trans-synaptic pseudorabies virus PRV-152 revealed the presence of burs
67                                  A strain of pseudorabies virus (PRV 152) isogenic with the Bartha st
68 itreal injection of the attenuated strain of pseudorabies virus (PRV Bartha) results in transneuronal
69 ntraocular injection of the Bartha strain of pseudorabies virus (PRV Bartha) results in transsynaptic
70 rus (HSV), varicella-zoster virus (VZV), and pseudorabies virus (PRV) all utilize a complex of two gl
71 well as for the animal herpesviruses porcine pseudorabies virus (PRV) and bovine herpesvirus 1 (BHV-1
72 entified by immunohistochemical detection of pseudorabies virus (PRV) and corticotropin-releasing fac
73 are the most widely used method to visualize pseudorabies virus (PRV) and herpes simplex virus (HSV)
74 he gD glycoprotein of the alphaherpesviruses pseudorabies virus (PRV) and herpes simplex virus 2 (HSV
75                                              Pseudorabies virus (PRV) and herpes simplex virus type 1
76                                         Both Pseudorabies virus (PRV) and human Herpes simplex virus
77 3 in herpes simplex virus type 1 (HSV-1) and pseudorabies virus (PRV) and ORF66 in varicella-zoster v
78 ane proteins encoded by the alphaherpesvirus pseudorabies virus (PRV) are internalized after reaching
79           The membrane proteins gI and gE of Pseudorabies virus (PRV) are required for viral invasion
80                             The structure of pseudorabies virus (PRV) capsids isolated from the nucle
81                         The alphaherpesvirus pseudorabies virus (PrV) establishes latency primarily i
82               Like other alphaherpesviruses, pseudorabies virus (PrV) exhibits restricted gene expres
83 d PSPMNs by using recombinant strains of the pseudorabies virus (PRV) for trans-synaptic tract tracin
84 d PSPMNs by using recombinant strains of the pseudorabies virus (PRV) for transsynaptic tract-tracing
85 pothesis, we used recombinant strains of the pseudorabies virus (PRV) for transsynaptic tract-tracing
86 rograde transport of an attenuated strain of pseudorabies virus (PRV) from the nucleus accumbens was
87 endent retrograde transneuronal transport of pseudorabies virus (PRV) from the stomach wall.
88 determine the role of internalization of the pseudorabies virus (PRV) gE and gI proteins, we construc
89                                          The pseudorabies virus (PRV) gE gene encodes a multifunction
90            A full-length clone of the 142-kb pseudorabies virus (PRV) genome was constructed as a sta
91                                              Pseudorabies virus (PRV) glycoprotein E (gE) is a type I
92 ynaptic tracing with peripheral injection of pseudorabies virus (PRV) has been extensively characteri
93 K in herpes simplex virus type 1 (HSV-1) and pseudorabies virus (PRV) have been well studied.
94  using transneuronal retrograde transport of pseudorabies virus (PRV) in normal animals and in animal
95 ction of the transneuronal retrograde tracer pseudorabies virus (PRV) in rats, we previously localize
96 s, was mapped using the transneuronal tracer pseudorabies virus (PRV) in the ferret.
97 cellular virions and axonal assemblies after pseudorabies virus (PRV) infection of cultured neurons.
98                                        After pseudorabies virus (PRV) infection of murine L929 cells,
99 the host gene expression profile after acute pseudorabies virus (PRV) infection of the CNS using Affy
100 models of viral egress from neurons by using pseudorabies virus (PRV) infection of the rat retina: do
101 nal spread of herpes simplex virus (HSV) and pseudorabies virus (PRV) infection, a culture system con
102 nduced after herpes simplex virus type 1 and pseudorabies virus (PRV) infections of rat embryonic fib
103              When the swine alphaherpesvirus pseudorabies virus (PRV) infects the rat retina, it repl
104 ed by retrograde trans-synaptic migration of pseudorabies virus (PRV) injected into the adrenal gland
105   Using the retrograde, transsynaptic tracer pseudorabies virus (PRV) injected into the BAT of mice,
106 astric nerves transected, were infected with pseudorabies virus (PRV) injected into the external uret
107 ia the transsynaptic retrograde transport of pseudorabies virus (PRV) injected into the kidneys of ra
108 ted neurons in the preoptic region following pseudorabies virus (PRV) injections into either the supe
109                                              Pseudorabies virus (PRV) injections were made into the l
110 sneuronal tracing studies using injection of pseudorabies virus (PRV) into either the diaphragm or re
111 studied after injecting the Bartha strain of pseudorabies virus (PRV) into the sciatic nerve to provi
112 epithelial cells, alphaherpesviruses such as pseudorabies virus (PRV) invade axons of peripheral nerv
113                                              Pseudorabies virus (PRV) is a broad host range, swine al
114                      Transneuronal spread of pseudorabies virus (PRV) is a multistep process that req
115                                              Pseudorabies virus (PRV) is a useful tracer that is retr
116                                              Pseudorabies virus (PRV) is an alphaherpesvirus related
117                  Glycoprotein E (gE) gene of pseudorabies virus (PRV) is conserved among diverse alph
118                                              Pseudorabies virus (PRV) mutants lacking the Us9 gene ca
119                      Retrograde infection by pseudorabies virus (PRV) of neuronal populations neighbo
120 by inoculating the ventral stomach wall with pseudorabies virus (PRV) on postnatal day 1 (P1), P4, or
121  simplex virus (HSV) entry activity, but not pseudorabies virus (PRV) or bovine herpesvirus 1 (BHV-1)
122 d the retrograde transneuronal tracer Bartha-pseudorabies virus (PRV) or the retrograde marker choler
123 ane protein present in the lipid envelope of pseudorabies virus (PRV) particles in a unique tail-anch
124        Toward this end, we generated a novel pseudorabies virus (PrV) recombinant in which a 282-bp r
125  In this report, we describe construction of pseudorabies virus (PRV) recombinants that efficiently e
126               Here, we refine this map using pseudorabies virus (PRV) retrograde tracing, indicating
127                               The attenuated pseudorabies virus (PRV) strain Bartha contains several
128  After intraocular injection of the virulent pseudorabies virus (PRV) strain Becker into late-stage c
129      To accomplish this, we have constructed pseudorabies virus (PRV) strains in which viral propagat
130 , but partial deletions generated in HSV and pseudorabies virus (PrV) suggest an additional function
131 ly(A) fraction of the lytic transcriptome of pseudorabies virus (PRV) throughout a 12-hour interval o
132     This study used the transneuronal tracer pseudorabies virus (PRV) to investigate the CNS network
133 ns were identified by immunogold labeling of pseudorabies virus (PRV) transported retrogradely and tr
134          The subcellular distribution of the pseudorabies virus (PRV) UL28 protein was examined by in
135                                          The pseudorabies virus (PRV) UL54 homologs are important mul
136                 We demonstrate here that the pseudorabies virus (PRV) Us2 protein is synthesized earl
137                                          The pseudorabies virus (PRV) Us3 gene is conserved among the
138                   The protein product of the pseudorabies virus (PRV) Us9 gene is a phosphorylated, t
139                                              Pseudorabies virus (PRV) Us9 is a small, tail-anchored (
140      In this report, we demonstrate that the pseudorabies virus (PRV) Us9 protein is present in infec
141 s simplex virus (HSV) and, as reported here, pseudorabies virus (PRV) utilize the ESCRT apparatus to
142 nal sorting and transport of fully assembled pseudorabies virus (PRV) virions is dependent on the vir
143 e provide an initial characterization of the pseudorabies virus (PRV) VP22 homologue.
144                                              Pseudorabies virus (PRV) was injected into the pancreas
145  tracing experiments were performed in which pseudorabies virus (PRV) was injected into the stellate
146 riments, the retrograde transneuronal tracer pseudorabies virus (PRV) was microinjected into the CEAm
147              A replication-competent gL-null pseudorabies virus (PrV) was shown to express a gDgH hyb
148 dies, we compared gH of the alphaherpesvirus pseudorabies virus (PrV) with gH of the gammaherpesvirus
149                                              Pseudorabies virus (PRV), a broad host range alphaherpes
150                                              Pseudorabies virus (PRV), a member of the Alphaherpesvir
151                                              Pseudorabies virus (PRV), a neurotropic swine alpha herp
152 brane glycoproteins gE and gI are encoded by pseudorabies virus (PRV), a neurotropic, broad-host-rang
153 lenic function was accomplished by injecting pseudorabies virus (PRV), a retrograde transynaptic trac
154 that the amino-terminal one-third of gC from pseudorabies virus (PRV), a swine herpesvirus, includes
155                                              Pseudorabies virus (PRV), a swine neurotropic alphaherpe
156 g vesicular stomatitis (VSV), Sindbis virus, pseudorabies virus (PRV), adeno-associated virus (AAV),
157                                        Using pseudorabies virus (PRV), an alphaherpesvirus capable of
158                                              Pseudorabies virus (PRV), an alphaherpesvirus related to
159   Previous studies showed that proteins from pseudorabies virus (PRV), an alphaherpesvirus, localize
160 erpes simplex viruses (HSV) 1 and 2, porcine pseudorabies virus (PRV), and bovine herpesvirus 1 (BHV-
161  (BHV-1), equine herpesvirus type 1 (EHV-1), pseudorabies virus (PRV), and varicella-zoster virus (VZ
162 pesviruses, such as herpes simplex virus and pseudorabies virus (PRV), are neuroinvasive dsDNA viruse
163  U(S)11c119.3 cells are fully susceptible to pseudorabies virus (PRV), as shown by single-step growth
164              The related animal herpesvirus, pseudorabies virus (PRV), encodes a homologous set of gl
165 sviruses, herpes simplex virus 1 (HSV-1) and pseudorabies virus (PRV), have suggested that UL37 plays
166 pes viruses: herpes simplex virus (HSV1) and pseudorabies virus (PrV), human immunodeficiency virus t
167  peroxidase conjugated to colloidal gold, or pseudorabies virus (PRV), into the nuclear core of the r
168                        In the swine pathogen pseudorabies virus (PRV), mutant viruses with internal d
169                Alphaherpesviruses, including pseudorabies virus (PRV), spread directionally within th
170           Live attenuated vaccine strains of pseudorabies virus (PRV), such as PRV Bartha, are among
171 lex virus 1 (HSV-1), HSV-2, and veterinarian pseudorabies virus (PRV), that infect the peripheral ner
172                                           In pseudorabies virus (PRV), the Us9 protein is a 98-amino-
173 ished retrograde transneuronal viral tracer, pseudorabies virus (PRV), was injected into the ventral
174                    The transneuronal tracer, pseudorabies virus (PRV), was used to identify pathways
175    Using a viral transneuronal tract tracer, pseudorabies virus (PRV), we also tested whether the com
176                                        Using pseudorabies virus (PRV), we have previously shown that
177         Using the neuroinvasive herpesvirus, pseudorabies virus (PRV), we show that the viral protein
178 cle-specific injection of an mRFP-expressing pseudorabies virus (PRV), which acts as a transsynaptic
179                                              Pseudorabies virus (PRV)-a retrograde transneuronal trac
180 s study were to identify the mechanism(s) of pseudorabies virus (PrV)-induced down-regulation of porc
181 nervous system, alphaherpesviruses-including pseudorabies virus (PRV)-use retrograde axonal transport
182 tion with virulent and attenuated strains of pseudorabies virus (PRV).
183 athways in rats using recombinant strains of pseudorabies virus (PRV).
184 te entry of herpes simplex viruses (HSV) and pseudorabies virus (PRV).
185  of gD (for example, HSV-1/Rid), and porcine pseudorabies virus (PRV).
186  following infection of the left kidney with pseudorabies virus (PRV).
187  a receptor for the porcine alphaherpesvirus pseudorabies virus (PRV).
188 el to study neuronal spread and virulence of pseudorabies virus (PRV).
189 -1), HSV-2, and the related alphaherpesvirus pseudorabies virus (PRV).
190  an alpha-herpes virus, the Bartha strain of pseudorabies virus (PRV).
191  DMV neurons projecting to the stomach using pseudorabies virus (PRV).
192 DA), and retrograde tracing with fluorescent pseudorabies virus (PRV).
193 onserved in varicella-zoster virus (VZV) and pseudorabies virus (PRV).
194  of two neurotropic herpesviruses: HSV-1 and pseudorabies virus (PRV).
195 emale Sprague-Dawley rats were infected with pseudorabies virus (PRV, Bartha's K-strain) by injection
196 nstructing a replication-competent strain of pseudorabies virus (PRV-263) that changes the profile of
197 train of the retrograde transneuronal tracer pseudorabies virus (PRV-Ba) was injected into rat choroi
198 e transneuronal tracer, the Bartha strain of pseudorabies virus (PRV-Ba), were injected into the uppe
199  tract tracing using an attenuated strain of pseudorabies virus (PRV-Bartha) was combined with immuno
200 ions of the SCN using the swine herpesvirus (pseudorabies virus, PRV) as a tool for transynaptic anal
201 S-specific transneuronal viral tract tracer, pseudorabies virus (PRV152) and demonstrated the sensory
202 , to identify GG premotoneurons, we injected pseudorabies virus (PRV152) into the GG muscle.
203 ed fluorophore expression from a recombinant pseudorabies virus (PRV263) carrying a Brainbow cassette
204 tructed a panel of Cre recombinase-activated pseudorabies viruses (PRVs) that enabled retrograde trac
205    Specifically, we injected the conditional pseudorabies virus recombinant (BA2001) that can replica
206                   Dual-labeling studies with pseudorabies virus recombinants also showed prephrenic i
207              The first method uses HSV-1 and pseudorabies virus recombinants that express one of thre
208 ransneuronal retrograde pathway tracing with pseudorabies virus revealed connectivity between MnPO VG
209                             We constructed a pseudorabies virus strain that expressed Us9-GFP and tes
210 liver and epididymal white fat in mice using pseudorabies virus strains expressing different reporter
211           Two immunohistochemically distinct pseudorabies virus strains were injected into male Sprag
212 riments with ICP4 homologs revealed that the pseudorabies virus TAD is a potent activator of the gD p
213       Despite being a major component of the pseudorabies virus tegument, VP22 is not required for PR
214               We report the development of a pseudorabies virus that can be used for retrograde traci
215                 Starting with derivatives of pseudorabies virus that encode a fluorescent protein fus
216 ell imaging, we made a series of recombinant pseudorabies viruses that encoded green fluorescent prot
217                          Here, the spread of pseudorabies virus through renal sensory pathways was ex
218  vulgaris leucoagglutinin (anterograde), and pseudorabies virus (transneuronal retrograde) tract-trac
219 n subunit b retrograde tracing from rRPa and pseudorabies virus transynaptic retrograde tracing from
220    The large DNA viruses, herpes simplex and pseudorabies viruses, use ubiquitous nectins 1 and 2.
221                            The resistance to pseudorabies virus was CD4(+) T cell dependent, because
222                                              Pseudorabies virus was injected into the wall of the ven
223  pathway, a retrograde transsynaptic tracer (pseudorabies virus) was injected into the orbicularis oc
224 r the retrograde transneuronal viral tracer, pseudorabies virus, was injected into the stellate sympa
225  an infectious clone of the alphaherpesvirus pseudorabies virus, we have made a collection of truncat
226 ntral nervous system neurons infected with a pseudorabies virus were examined in vitro by using whole
227 /Cas9 and Cre/Lox system against re-emerging Pseudorabies virus, which caused the recent devastating

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