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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.
13 e poliovirus, herpesvirus, rabies virus, and pseudorabies virus all utilize neuronal retrograde trans
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
21 ctures of gH/gL from herpes simplex virus 2, pseudorabies virus, and Epstein-Barr virus revealed dist
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
27 s simplex virus, varicella zoster virus, and pseudorabies virus are neurotropic pathogens of the Alph
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
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
38 rions, epithelial cells infected by HSV-1 or pseudorabies virus following ADS express fewer than two
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
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
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
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
56 injected a retrograde-specific strain of the pseudorabies virus into the rat OB and piriform cortex.
61 and bladder body injections, the majority of pseudorabies virus-labelled cells were found in the late
63 resembles in many respects the phenotype of pseudorabies virus lacking glycoproteins gM, gE, and gI.
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
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
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
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
88 determine the role of internalization of the pseudorabies virus (PRV) gE and gI proteins, we construc
92 ynaptic tracing with peripheral injection of pseudorabies virus (PRV) has been extensively characteri
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
97 cellular virions and axonal assemblies after pseudorabies virus (PRV) infection of cultured neurons.
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
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
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
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
125 In this report, we describe construction of pseudorabies virus (PRV) recombinants that efficiently e
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
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
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
148 dies, we compared gH of the alphaherpesvirus pseudorabies virus (PrV) with gH of the gammaherpesvirus
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
156 g vesicular stomatitis (VSV), Sindbis virus, pseudorabies virus (PRV), adeno-associated virus (AAV),
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
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
171 lex virus 1 (HSV-1), HSV-2, and veterinarian pseudorabies virus (PRV), that infect the peripheral ner
173 ished retrograde transneuronal viral tracer, pseudorabies virus (PRV), was injected into the ventral
175 Using a viral transneuronal tract tracer, pseudorabies virus (PRV), we also tested whether the com
178 cle-specific injection of an mRFP-expressing pseudorabies virus (PRV), which acts as a transsynaptic
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
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
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
208 ransneuronal retrograde pathway tracing with pseudorabies virus revealed connectivity between MnPO VG
210 liver and epididymal white fat in mice using pseudorabies virus strains expressing different reporter
212 riments with ICP4 homologs revealed that the pseudorabies virus TAD is a potent activator of the gD p
216 ell imaging, we made a series of recombinant pseudorabies viruses that encoded green fluorescent prot
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
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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