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1 reverse transcription-PCR detection of HSV-1 latency-associated transcripts).
2 encoded within the second exon of the HSV-1 latency-associated transcript.
3 ined expression of four previously described latency-associated transcripts.
4 latently infected neurons is limited to the latency-associated transcripts.
5 res of latent infection, including classical latency-associated transcripts, a punctate pattern of LA
7 aracterized by the expression of a noncoding latency-associated transcript and a set of microRNAs.
8 similar to those of WT virus, the levels of latency-associated transcript and micro-RNAs were 50- to
9 egalovirus is accompanied by the presence of latency-associated transcripts and expression of immunog
11 me loads and exhibited reduced expression of latency-associated transcripts and reduced reactivation
12 d to support latency and expression of viral latency-associated transcripts and to undergo reactivati
13 nsory neurons in which only noncoding (e.g., latency-associated transcript) and micro-RNAs are expres
14 hich do not accumulate significant levels of latency-associated transcripts, and (iii) the activation
15 pes simplex virus, which is characterized by latency-associated transcripts, and from lytic VZV repli
16 n used as a model for latency; viral DNA and latency-associated transcripts are expressed in dorsal r
17 ome, corresponding to the 5' end of the LAT (latency-associated transcript) coding region, is respons
19 e percentage of neurons expressing the major latency-associated transcript during the latent infectio
20 genitors is characterized by the presence of latency-associated transcripts encoded in the ie1/ie2 re
21 root ganglia were positive for HSV-2 DNA and latency-associated transcripts for 5/8 animals in the gC
22 utilized by the herpes simplex virus type 1 latency-associated transcript in latently infected mice
24 alternative promoter usage by LMP2 and other latency-associated transcripts, intergenic splicing at t
25 tion of sensory ganglia of mice, in that HSV latency-associated transcript is expressed, but to be de
26 d to inoculate rabbit corneas: 17deltaPst, a latency associated transcript (LAT) negative, low-reacti
29 ese, miR-H7 and miR-H9, are derived from the latency-associated transcript (LAT) and are located anti
31 in the HSV-1 genome, specifically around the latency-associated transcript (LAT) and ICP0 and ICP4 re
33 ation of herpes simplex virus type 1 (HSV-1) latency-associated transcript (LAT) expression and proce
34 stitution of a 2.8-kbp region from the HSV-1 latency-associated transcript (LAT) for native HSV-2 seq
35 s study, a chimeric HSV-2 that expressed the latency-associated transcript (LAT) from HSV-1 reactivat
36 s of deletions in the promoter region of the latency-associated transcript (LAT) gene in impairing he
42 productive ("lytic") infection, but only the latency-associated transcript (LAT) gene is expressed at
45 t of the herpes simplex virus type 1 (HSV-1) latency-associated transcript (LAT) gene to analyze its
49 the amount of CS and the level of the HSV-1 latency-associated transcript (LAT) in trigeminal gangli
51 indicated that the unusual stability of the latency-associated transcript (LAT) intron was due to it
53 The herpes simplex virus type 1 (HSV-1) 2-kb latency-associated transcript (LAT) is a stable intron,
60 l ganglia when only the transcription of the latency-associated transcript (LAT) locus is detected.
61 er cassette, when placed in the context of a latency-associated transcript (LAT) null mutant, resulte
65 ER and dlsptk expressed higher levels of the latency-associated transcript (LAT) per genome earlier i
66 fluence latency-associated transcription and latency-associated transcript (LAT) phenotypes, we studi
68 and HSV-2) establish latency and express the latency-associated transcript (LAT) preferentially in di
69 udies have demonstrated that histones in the latency-associated transcript (LAT) promoter and intron
71 ownstream of the herpes simplex virus type 2 latency-associated transcript (LAT) promoter and upstrea
73 e herpes simplex virus type 1 (HSV-1) or the latency-associated transcript (LAT) promoter deletion mu
74 primary herpes simplex virus type 2 (HSV-2) latency-associated transcript (LAT) promoter influences
76 he murine IL-2 gene under the control of the latency-associated transcript (LAT) promoter of HSV-1 in
77 designated miR-H6 is located upstream of the latency-associated transcript (LAT) promoter region on t
78 acted from whole ganglia, (ii) the number of latency-associated transcript (LAT) promoter-positive ne
79 HSV, we have shown previously that the viral latency-associated transcript (LAT) promotes lytic gene
81 k the meq oncogene and three that map to the latency-associated transcript (LAT) region of the genome
82 ganglia (DRG), chromatin associated with the latency-associated transcript (LAT) region of the viral
87 I, encoded by herpes simplex virus 2 (HSV-2) latency-associated transcript (LAT) through small RNA cl
88 Further analysis confirmed that this SVV latency-associated transcript (LAT) was oriented antisen
91 addition, we show that in the absence of the latency-associated transcript (LAT), the latent genome s
94 ross talk appears to occur between the HSV-1 latency-associated transcript (LAT), the only viral gene
95 tream of the transcription start site of the latency-associated transcript (LAT), were detected durin
96 anglia, HSVs express a long noncoding RNA, a latency-associated transcript (LAT), which plays a key r
97 a harvested during HSV latency, 25% of HSV-1 latency-associated transcript (LAT)- and 4% of HSV-2 LAT
98 sed to examine the role of the cornea in the latency-associated transcript (LAT)-mediated reactivatio
100 ular inoculation with HSV strain KOS, 81% of latency-associated transcript (LAT)-positive trigeminal
107 herpes simplex virus type 1 (HSV-1) DNA and latency-associated transcripts (LAT) in the latently inf
108 ive by in situ hybridization (ISH) for HSV-1 latency-associated transcripts (LAT), the classical surr
109 erized by the constitutive expression of the latency-associated transcripts (LAT), which originate fr
113 latently infected ganglia is reduced by the latency-associated transcripts (LATs) and whether splici
115 e expression is severely repressed; only the latency-associated transcripts (LATs) are expressed abun
116 and HSV-2 also preferentially express their latency-associated transcripts (LATs) in different senso
117 s type 1 is required to generate a series of latency-associated transcripts (LATs) in sensory neurons
118 sly, we documented the focal presence of the latency-associated transcripts (LATs) in the hippocampi
119 detectable viral proteins, expression of the latency-associated transcripts (LATs) is likely regulate
121 of HSV genes and accumulation of the stable latency-associated transcripts (LATs), as occurs in neur
122 1 and -2 to establish latency and to express latency-associated transcripts (LATs), virulent strains
133 In this study, we tested whether the LAT (latency-associated transcript) locus regulates the frequ
137 ICP4, thymidine kinase, glycoprotein C, and latency-associated transcript RNA by in situ hybridizati
140 iral genome became relatively quiescent, the latency-associated transcript was specifically upregulat
142 : sense and antisense meq, ORF L1, ICP4, and latency-associated transcripts, which are antisense to I
143 ve (NgK) form of the gK gene in place of the latency-associated transcript with a myc epitope tag to
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