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1 ctions with HIV, hepatitis C virus, or human cytomegalovirus).
2 ex, HLA type, or previous exposure to EBV or cytomegalovirus.
3 efforts to decrease the effect of congenital cytomegalovirus.
4 rget for antiviral development against human cytomegalovirus.
5 are always serologically positive for human cytomegalovirus.
6 oth inflammasome and IFN-I to control murine cytomegalovirus.
7 virus, but dispensable in the case of mouse cytomegalovirus.
8 dependent after viral challenge with murine cytomegalovirus.
9 vented necroptosis upon infection with mouse cytomegalovirus.
10 nt of opportunistic infections (OI), such as cytomegalovirus.
11 hallmark of the cytopathic effect induced by cytomegaloviruses.
12 on, we have analyzed an infection with mouse cytomegalovirus, a persistent-latent virus that elicits
13 ange of viral infections including BK virus, cytomegalovirus, adenovirus, human herpesvirus 6, and Ep
14 circuits in HIV-1 and the human herpesvirus cytomegalovirus along with potential circuit-disruption
16 AIM2 activators Francisella novicida, mouse cytomegalovirus and DNA, and the infectious agents Liste
18 ings help explain the broad tropism of human cytomegalovirus and indicate that PDGFRalpha and the vir
20 latter indicates the involvement of HSV1 and cytomegalovirus (and the necessity of taking into accoun
24 virus, HIV, varicella zoster virus, Rubella, Cytomegalovirus, and Herpesviruses are a major cause of
28 ytokine IL-12 was added, which also affected cytomegalovirus- and Epstein-Barr virus-specific T cells
29 c substitutions did not confer resistance to cytomegalovirus antivirals in vitro, suggesting that the
31 ificantly lower rates of avascular necrosis, cytomegalovirus, cataracts, new-onset diabetes after tra
34 knowledge of the epidemiology of congenital cytomegalovirus (cCMV) with the type of maternal infecti
37 thesized that the presence of replication of cytomegalovirus (CMV) and Epstein-Barr virus (EBV) (the
41 y, we investigated the effect of subclinical cytomegalovirus (CMV) and Epstein-Barr virus (EBV) repli
45 unmasking of cryptotopes by unfolding whole cytomegalovirus (CMV) antigen preparations with the chao
46 oliferate when exposed to superantigen or to cytomegalovirus (CMV) antigen using matched T cells and
48 nstructing an rMVA encoding 3 immunodominant cytomegalovirus (CMV) antigens, which stimulates a host
51 nous ganciclovir and oral valganciclovir for cytomegalovirus (CMV) disease in solid organ transplant
60 s is exacerbated in patients with concurrent cytomegalovirus (CMV) infection and inflammatory bowel d
61 es in a comparison group) revealed prevalent cytomegalovirus (CMV) infection at diagnosis in childhoo
69 Persistent herpesvirus infections including cytomegalovirus (CMV) infection may be particularly impo
72 pathways contribute to the control of early cytomegalovirus (CMV) infection, leading to a multiphasi
73 ifferentiated NK cell subsets in response to cytomegalovirus (CMV) infection, paralleling antigen-spe
76 ization or passive administration.IMPORTANCE Cytomegalovirus (CMV) is a significant cause of birth de
87 n association between early (before day 100) cytomegalovirus (CMV) reactivation and decreased inciden
88 transplant (allo-HCT) recipients at risk for cytomegalovirus (CMV) reactivation from those who are no
94 T cell repertoire of 666 subjects with known cytomegalovirus (CMV) serostatus by immunosequencing.
96 sus, Streptococcus viridians bacteremia, and cytomegalovirus (CMV) viremia and identified mutations i
98 minister long courses of prophylaxis against cytomegalovirus (CMV) without evidence of benefit and wi
99 ection for each herpesvirus were as follows: cytomegalovirus (CMV), 44%; human herpesvirus [HHV] 6, 1
100 adenovirus, EBV, human herpesvirus 6 (HHV6), cytomegalovirus (CMV), and BK virus screened weekly.
101 ontrol viruses, Epstein-Barr virus (EBV) and cytomegalovirus (CMV), and compared to bulk memory CD8 T
102 Epstein-Barr virus (EBV), adenovirus (AdV), cytomegalovirus (CMV), BK virus (BKV), and human herpesv
104 sting surveys for quantitative PCR assays of cytomegalovirus (CMV), Epstein-Barr virus (EBV), BK viru
106 d 5 herpesviruses (Epstein Barr virus (EBV), cytomegalovirus (CMV), herpes simplex virus types 1 and
107 -15, and IL-18 or in response to antigens or cytomegalovirus (CMV), human and mouse NK cells exhibit
108 , and in some cases exclusively, detected in cytomegalovirus (CMV)- and Epstein-Barr virus (EBV)-resp
112 en we measured the CD4(+) T cell response to cytomegalovirus (CMV)-infected dendritic cells in vitro,
113 tudies, we demonstrate that the frequency of cytomegalovirus (CMV)-pp65-specific T-cell responses in
116 C virus [HCV], Epstein-Barr virus [EBV], or cytomegalovirus [CMV]) in KTR on sirolimus (SRL) + mycop
120 disease; death was directly attributable to cytomegalovirus disease in three (1%) of 263 patients wh
121 was poor, including increased incidences of cytomegalovirus disease, herpes zoster, BK virus, and ne
129 and Drug Administration-approved anti-human cytomegalovirus drugs mainly target the viral polymerase
130 tion with nonintegrin receptors (i.e., human cytomegalovirus EGFR), to dictate species-specific entry
136 coccus pneumoniae, Streptococcus agalactiae, cytomegalovirus, enterovirus, herpes simplex virus 1 and
137 alysis for Herpes simplex, varicella zoster, cytomegalovirus, Epstein-Barr virus and Toxoplasma gondi
138 onotherapy with autologous VSTs specific for cytomegalovirus, Epstein-Barr virus, or adenovirus and g
139 differences in organism density, except with cytomegalovirus, for which there was a higher quantity i
143 0 (vIL-10) ortholog of both human and rhesus cytomegalovirus (HCMV and RhCMV, respectively) suppresse
146 f infection of certain cell types with human cytomegalovirus (HCMV) and that THY-1 is important for H
147 The genomes of DNA viruses such as human cytomegalovirus (HCMV) are devoid of histones within vir
150 n the central nervous system caused by human cytomegalovirus (HCMV) congenital infection, the mechani
152 In lung transplant recipients (LTRs), human cytomegalovirus (HCMV) DNA detection in the bronchoalveo
155 8 locus present in clinical strains of human cytomegalovirus (HCMV) encodes proteins required for lat
156 alizing antibodies (NAb) targeting the human cytomegalovirus (HCMV) envelope pentamer complex (PC) ar
157 for the hematogenous dissemination of human cytomegalovirus (HCMV) following a primary infection.
158 vidence is provided demonstrating that human cytomegalovirus (HCMV) gB depends on the S-palmitoylatio
163 -stranded RNAs (dsRNA) produced during human cytomegalovirus (HCMV) infection activate the antiviral
169 and are directly antiviral.IMPORTANCE Human cytomegalovirus (HCMV) infection is carried for a lifeti
171 the biological impact in patients with human cytomegalovirus (hCMV) infection is not well defined in
172 developing brain.IMPORTANCE Congenital human cytomegalovirus (HCMV) infection is the most common vira
176 based on dense bodies (DB) produced by human cytomegalovirus (HCMV) infections, we evaluated scalable
194 osphatases for their importance during human cytomegalovirus (HCMV) replication and identified the cl
196 pacity to block HAdV and, in addition, human cytomegalovirus (HCMV) replications at low micromolar co
202 oses (60, 120, and 240 mg/day) against human cytomegalovirus (HCMV) was evaluated in a recent phase 2
203 others show that microRNAs encoded by human cytomegalovirus (HCMV) were readily detected in human se
204 ic diversity over the entire genome of human cytomegalovirus (HCMV), a significant pathogen for immun
207 aboratory strains (AD169 and Towne) of human cytomegalovirus (HCMV), which are known to use cell memb
210 or and inhibits viral DNA replication (human cytomegalovirus [HCMV] and human papillomavirus [HPV]) a
211 nfections that cause substantial impairment: cytomegalovirus, herpes simplex virus, rubella virus, To
212 l diagnosis included toxoplasmosis, rubella, cytomegalovirus, herpes simplex virus, syphilis, and hum
213 al infections, including rubella, congenital cytomegalovirus, human immunodeficiency virus, hepatitis
214 vities to HSV-1 IgG, cytomegalovirus IgM, or cytomegalovirus IgG did not appear to increase gastrosch
216 expression cassette under the control of the cytomegalovirus immediate early promoter into the VC2 ve
218 screening of mothers and the routine use of cytomegalovirus immunoglobulin for prophylaxis or treatm
219 immunological presentation, the presence of cytomegalovirus in some glioblastomas may impact progres
220 nfluenza A virus, herpes simplex virus 1, or cytomegalovirus induced a strong antiviral response meas
224 d in 47% of patients, with 4 presenting with cytomegalovirus infection and 4 (age, 42-59 years) diagn
226 cidofovir to placebo for prophylaxis against cytomegalovirus infection in hematopoietic cell transpla
229 Gaps remain in understanding the role that cytomegalovirus infection plays in HIV-exposed infants.
230 than groups A (37%) or B (23%) (P < 0.001); cytomegalovirus infection rates were 35%, 20% and 23%, r
231 ta in the literature suggest that congenital cytomegalovirus infection remains a research priority, b
232 the mother increases the rate of congenital cytomegalovirus infection, while maternal antiretroviral
236 rleukin 10 (cmvIL-10) and Latency-associated cytomegalovirus interleukin 10 (LAcmvIL-10) (collectivel
237 ere also obtained that indicated that rhesus cytomegalovirus is able to persist due to upregulation o
239 reening a panel of deletion mutants of mouse cytomegalovirus (MCMV) a mutant was identified that did
241 y contrast, systemic infection with a murine cytomegalovirus (MCMV) engineered to express HEL induced
245 ls were able to respond to a specific murine cytomegalovirus (MCMV) protein and that in the absence o
250 opositive donor, and underwent weekly plasma cytomegalovirus monitoring by PCR through to day 100 pos
253 says also revealed positive test results for cytomegalovirus or Epstein-Barr virus, indicating possib
254 Neutrophils pulsed with the cognate antigens cytomegalovirus pp65 or influenza hemagglutinin were abl
255 , as opposed to the conventional approach of cytomegalovirus promoter-driven expression from an episo
258 post-HCT dasatinib use increased the risk of cytomegalovirus reactivation (adjusted hazard ratio, 7.6
260 s pUL89 endonuclease inhibitor blocked human cytomegalovirus replication at a relatively late time po
262 n, which have received FDA approval to treat cytomegalovirus retinitis and high blood cholesterol, re
263 ve been reported with dasatinib use, but its cytomegalovirus risk after hematopoietic-cell transplant
265 between Jan 1, 2007, and Feb 28, 2013, were cytomegalovirus seropositive or had a seropositive donor
266 an 50 years, performance of a kidney biopsy, cytomegalovirus seropositive status, donation after card
267 ted with higher mortality included recipient cytomegalovirus seropositivity (HR 1.40, 95% CI 1.13-1.7
269 nor characteristics such as sex, parity, and cytomegalovirus serostatus were not associated with surv
270 year overall survival adjusted for recipient cytomegalovirus serostatus, conditioning regimen intensi
271 een donor characteristics (age, sex, parity, cytomegalovirus serostatus, HLA match, and blood group A
272 We have previously shown that the human cytomegalovirus signal-anchored protein known as viral m
273 higher frequencies of regulatory T cells and cytomegalovirus-specific CD4(+) T cells correlated negat
277 ic testing ruled out toxoplasmosis, rubella, cytomegalovirus, syphilis, and human immunodeficiency vi
280 %) patients were excluded because of missing cytomegalovirus testing and 24 (2%) were excluded becaus
282 be given to universal neonatal screening for cytomegalovirus to facilitate early detection and interv
288 that vaccinating rhesus macaques with rhesus cytomegalovirus vectors in which genes Rh157.5 and Rh157
289 e antileukemic responses than UV-inactivated cytomegalovirus, vesicular stomatitis virus, reovirus, o
291 erefore investigated the association between cytomegalovirus viral load and mortality in the first ye
292 els were used to estimate the association of cytomegalovirus viral load at different thresholds with
296 tract infection (cystitis) (34.9% vs 25.2%), cytomegalovirus viremia (17.8% vs 24.2%), flu-like syndr
298 iller cells among donors infected with human cytomegalovirus with one or two copies of the allele.
299 flationary effector responses against latent cytomegalovirus with only limited evidence of exhaustion
300 ently reported a replication-defective human cytomegalovirus with restored pentameric complex glycopr
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