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1 esult that was positive for varicella-zoster virus DNA.
2 than the representation of dGMP in vaccinia virus DNA.
3 ved peptide pools and absence of torque teno virus DNA.
4 tion PCR were performed to screen for herpes virus DNA.
5 patient's lesion tested positive for cowpox virus DNA.
6 nged lowering of serum levels of hepatitis B virus DNA.
7 h conventional measures of serum hepatitis B virus DNA.
8 ed onto unintegrated Moloney murine leukemia virus DNAs.
9 assays that can detect as low as 16 pM Ebola Virus DNA, 0.01ng/mL carcinoembryonic antigen (CEA), and
10 the 328 patients with data for Epstein-Barr virus DNA, a detectable viral DNA titre was an independe
11 polymerase chain reaction (PCR) assay for BK virus DNA, a retrospective analysis was done of sequenti
14 s autointegration of Moloney murine leukemia virus DNA, also plays an indirect role in generating the
15 erived from the terminal regions of vaccinia virus DNA and contained in a superhelical plasmid, into
16 sed on restriction enzyme digest patterns of virus DNA and growth rates both in vitro and in vivo.
19 10(4) cellular genomes, whereas Epstein-Barr virus DNA and HIV-1 DNA were detected in 16 and 22 sampl
20 patitis B virus infection, serum hepatitis B virus DNA and liver biochemical test levels should be or
21 (v) Despite the reduced recoveries of LAT- virus DNA and productive-cycle transcripts in reactivati
23 d capsid has formed, it is packaged with the virus DNA and transported to the cytoplasm where further
24 ems, in which an immune response eliminating virus DNA and/or RNA is launched first, but then, if it
25 mutation was transferred into wild-type (wt) virus DNA, and the UL25 mutant ts1249 was isolated and c
26 wide variety of antigens including bacteria, viruses, DNA, and proteins due to the simplicity of thei
27 sease has been made using cloned hepatitis B virus DNA as a transgene in a severe combined immunodefi
29 ransactivator IE62, ORF 29 encodes the major virus DNA binding protein, and ORF 21 encodes a protein
30 iation with sorting nexin 17, to ensure that virus DNA bound to L2 is recycled through the trans-Golg
31 igned specifically for detection of smallpox virus DNA, but all viruses of the genus Orthopoxvirus te
35 e host range among haloarchaea, and purified virus DNA can cause an infection after transformation in
37 There were doses of 01/PEME for which the virus DNA concentration in the tumor increased over time
40 tem lymphoma, and monitoring of Epstein-Barr virus DNA copy number in spinal fluid may be useful in a
42 infected cell cultures and tissues, smallpox virus DNA could be detected in a background of human DNA
45 d pretreatment levels of plasma Epstein Barr virus DNA (EBV-DNA), as determined by quantitative real-
46 linical presentation and demonstration of JC virus DNA either in the CSF or by histopathology, is an
47 9 which binds to integrated murine leukaemia virus DNA elements and recruits KAP1 to repress them.
48 A binding through specific contacts with the virus DNA ends in the 3'-processing and ST reactions.
53 rase chain reaction [PCR] for herpes simplex virus DNA in cerebrospinal fluid) were randomized to rec
54 chain reaction amplification of Epstein-Barr virus DNA in cerebrospinal fluid, 18F-fluoro-deoxyglucos
55 demonstrated 2.75 times less herpes simplex virus DNA in cyclic-AMP treated BeWo cells, but 2.0 to 7
57 n plants that did become infected, levels of virus DNA in mutants and wild-type did not differ signif
58 on magnetic resonance imaging regressed; JC virus DNA in plasma, likely originating from the brain b
59 It is concluded that quantitative PCR for BK virus DNA in serum is useful both for identifying transp
61 association of the presence of Epstein-Barr virus DNA in systemic lupus erythematosus patients compa
63 rospinal fluid positivity for herpes simplex virus DNA in the polymerase chain reaction analysis.
64 ticle reporting the presence of Epstein-Barr virus DNA in the vitreous of a patient with Vogt-Koyanag
70 s study, we investigated whether hepatitis B virus DNA integration occurs preferentially at sites of
71 enetics and biochemistry of avian and murine virus DNA integration, but the pace of discovery increas
73 frequent integration of mouse mammary tumor virus DNA into chromosomes, implicating the gene in the
78 not catalyze base changes in murine leukemia virus DNA, it can be recovered from these virus particle
79 ot on treatment but with a serum hepatitis B virus DNA level >200,000 IU/mL during the third trimeste
83 containing only the 298-amino acid Chlorella virus DNA ligase (a 'minimal' eukaryotic ATP-dependent l
87 the conformational dynamics of the Chlorella virus DNA ligase (ChVLig), a minimized eukaryal ATP-depe
92 roles of conserved amino acids of Chlorella virus DNA ligase during the third step of the ligation p
95 ion analysis of the 298 amino acid Chlorella virus DNA ligase indicates that motif VI plays a critica
99 )) in the nick joining reaction of Chlorella virus DNA ligase, an exemplary ATP-dependent enzyme.
100 to the mitochondria or expressing Chlorella virus DNA ligase, the minimal eukaryal nick-sealing enzy
101 progressive decrease in the median plasma BK virus-DNA load, and undetectable levels at the last foll
103 according to the VR definition (hepatitis B virus DNA <200, < 2000, < 20,000 IU/mL) or duration of o
105 ion inhibitor, partially reversed the helper virus DNA methylation and restored a portion of vector p
107 each containing >/=105 copies herpes simplex virus DNA/ml collected a median of 5 months apart (IQR:
108 tained within those 322 samples were variola virus DNA, obtained from purified viral preparations, at
109 ic assay for the rapid detection of smallpox virus DNA on both the Smart Cycler and LightCycler platf
111 varicella (by detection of varicella zoster virus DNA or epidemiological link) from 42 days after th
112 in cells transgenomic for EBV (Epstein Barr Virus) DNA or for the telomerase gene, the large number
113 y been described which use inactivated whole virus, DNA or RNA that express the virus' Envelope (E) g
114 Since this assembly step is unique to the virus, DNA packaging is a novel target for the developme
115 f exonuclease activity of the herpes simplex virus DNA polymerase (Pol) on DNA replication fidelity w
116 The catalytic subunit of herpes simplex virus DNA polymerase (Pol), a member of the B family pol
117 to the role of D4 as a co-factor of vaccinia virus DNA polymerase and allows a better understanding o
121 seen even in the presence of herpes simplex virus DNA polymerase inhibitors, but not in the absence
122 he catalytic subunit, Pol, of herpes simplex virus DNA polymerase interacts via its extreme C terminu
127 n of the catalytic subunit of herpes simplex virus DNA polymerase with the processivity subunit, UL42
128 rase beta (Pol beta) and African swine fever virus DNA polymerase X (ASFV Pol X) with one-nucleotide
129 cently demonstrated that African swine fever virus DNA polymerase X (Pol X) is extremely error-prone
131 low-fidelity polymerase, African swine fever virus DNA polymerase X (Pol X), and showed that they fol
133 yields of interleukin-12 p40, herpes simplex virus DNA polymerase, and interferon-gamma PCR products
134 e processivity subunit of the herpes simplex virus DNA polymerase, interacts with DNA and promotes pr
135 e processivity subunit of the herpes simplex virus DNA polymerase, UL42, is a monomer and has an intr
136 e processivity subunit of the herpes simplex virus DNA polymerase, UL42, is a monomer in solution.
137 e processivity subunit of the herpes simplex virus DNA polymerase, UL42, is essential for viral repli
138 The processivity factor of herpes simplex virus DNA polymerase, UL42, unlike "sliding clamp" proce
139 f the processivity subunit of herpes simplex virus DNA polymerase, UL42, which is crucial for interac
140 critical for horizontal transmission of the virus, DNA priming/MVA boosting was evaluated for the ab
142 containing packaging signals from these two viruses, DNA proviruses containing genetic information f
143 e 43 samples that contained purified variola virus DNA ranging in concentration from 1 fg/ microl to
144 Of the 206 samples that contained variola virus DNA ranging in concentrations from 100 fg/ microl
145 a indicated that a host pathway initiated by virus DNA replication and acting through instability mot
146 tiviral role for ANKLE2 in limiting vaccinia virus DNA replication and progeny release through regula
147 s origin-binding domain in the initiation of virus DNA replication by analyzing the biochemical activ
148 Thus, the activity of replicative lefs or virus DNA replication is sufficient to trigger apoptosis
149 The identification of BocaSR and its role in virus DNA replication reveals potential avenues for deve
151 n of host protein synthesis, suggesting that virus DNA replication triggers inhibition of host biosyn
152 TNF-alpha is shown to suppress hepatitis B virus DNA replication without cell killing by disrupting
153 virus uracil DNA glycosylase is required for virus DNA replication, coupled with an inability to isol
161 s to interact with naked mouse mammary tumor virus DNA somewhat differently than with chromatin and A
162 substrates typically utilized the end of the virus DNA substrate as the point of integration, whereas
163 anscripts disappeared prior to initiation of virus DNA synthesis (considered early), and 100 transcri
164 enome allowed gamma-H2AX accumulation during virus DNA synthesis and impaired both very late viral ge
165 lef-11, p143, dnapol, and ie-1/ie-0) blocked virus DNA synthesis and late gene expression in permissi
166 ocalization of EAP and ICP4 did not occur if virus DNA synthesis and late gene expression were preven
167 nd 100 transcripts were still detected after virus DNA synthesis begins (considered early/late); (v)
168 ) 133 (36%) of the CDSs were expressed after virus DNA synthesis begins (considered late); and (vi) e
169 227 (62%) of the CDSs were expressed before virus DNA synthesis begins; (iv) these 227 CDSs were gro
170 he effect of the HIV-2IN(IN(2)) mutations on virus DNA synthesis was analyzed by packaging IN(2) muta
173 ine aminotransferase and 44% had hepatitis B virus DNA testing; hepatitis B e antigen and hepatitis B
174 ition to packing the approximately 103 kb of virus DNA, the PhicrAss001 virion has extensive storage
179 article (LNP)-formulated Andes virus or Zika virus DNA vaccines are elevated over unformulated vaccin
186 patitis C virus, West Nile virus, and dengue virus), DNA viruses (vaccinia virus and human adenovirus
195 revealed a normal cell count, herpes simplex virus DNA was detected in all samples by polymerase chai
196 this increased to 20 patients (71.4%) as JC virus DNA was detected in cerebrospinal fluid of two add
199 eim, Germany) PCR identification of smallpox virus DNA was developed and compiled in a kit system und
202 ents without toxoplasmosis, and Epstein-Barr virus DNA was found in 9 of 14 patients with central ner
207 ght hemispheric and brainstem lesions and JC virus DNA was undetectable in his cerebrospinal fluid.
208 short (<10 min) circulating half-life of the virus DNA, we could monitor virus distribution to the tu
210 Serum qHBcrAg, qAnti-HBc, and hepatitis B virus DNA were obtained at TDF initiation and every 6-12
211 mit of detection of 50 aM toward hepatitis B virus DNA with the capability of discriminating a single