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1 lution of influenza virus, dengue virus, and cytomegalovirus.
2 dones showed mild activity against the human cytomegalovirus.
3 us and the 310 "Delta"-shaped CATCs in human cytomegalovirus.
4 berculosis, Salmonella, Cryptosporidium, and cytomegalovirus.
5 with varicella-zoster virus (4.9%), 27 with cytomegalovirus (26.5%), and 1 with Epstein-Barr virus (
6 s pneumoniae (54 [20%]), HIV (40 [15%]), and cytomegalovirus (34 [12%]), and multiple infections were
7 , including Aspergillus fumigatus (1.4%) and cytomegalovirus (6%), were rare, scattering over 12 mont
8 of virus-employed countermeasures.IMPORTANCE Cytomegalovirus (a betaherpesvirus) is a master at manip
12 to prior infections, and higher incidence of cytomegalovirus and herpes simplex virus 1, possibly inf
13 d hypersusceptibility to infection by murine cytomegalovirus and multiple defects of lymphoid develop
14 bda"-shaped dimeric CATCs observed in murine cytomegalovirus and the 310 "Delta"-shaped CATCs in huma
15 ite of persistence for both human and murine cytomegaloviruses, and salivary secretions appear to pla
17 is virus (LCMV) vectors expressing the human cytomegalovirus antigens glycoprotein B (gB) and the 65-
18 tivation states in animals infected by mouse cytomegalovirus by combining Ifnb1 reporter mice with fl
19 and specific for the detection of congenital cytomegalovirus (cCMV) in universal screening studies.
22 paucity of data on the burden of congenital cytomegalovirus (cCMV) infections in low- and middle-inc
24 en seronegative before pregnancy, congenital cytomegalovirus (cCMV)-related sequelae are exclusively
28 exhibit memory-like recall responses against cytomegalovirus (CMV) and human immunodeficiency/virus s
39 ork model can accurately diagnose the latent cytomegalovirus (CMV) in healthy individuals, even when
40 The antimalarial agents artemisinins inhibit cytomegalovirus (CMV) in vitro and in vivo, but their ta
41 umoral immunity on the prevention of primary cytomegalovirus (CMV) infection after hematopoietic cell
43 Previous studies on the association between cytomegalovirus (CMV) infection and cardiac allograft va
44 Previous studies on the association between cytomegalovirus (CMV) infection and cardiac allograft va
46 This work provides specific tools to combat cytomegalovirus (CMV) infection and helps illuminate a g
47 munosuppression, leading to a higher risk of cytomegalovirus (CMV) infection compared with anti-inter
50 trials, 120 patients received maribavir for cytomegalovirus (CMV) infection failing conventional the
51 tor, has been approved for the prevention of cytomegalovirus (CMV) infection in hematopoietic stem ce
59 between posttransplant PCP and 3 variables: cytomegalovirus (CMV) infection, allograft rejection, an
68 ach against human cCMV attractive.IMPORTANCE Cytomegalovirus (CMV) is a leading cause of congenital d
75 ntary DNA genome copy under the control of a cytomegalovirus (CMV) promoter confirms autonomous genom
76 Adenoviral firefly luciferase vector with a cytomegalovirus (CMV) promotor to porcine donor hearts p
83 individual virions of the human herpesvirus cytomegalovirus (CMV) showed that virion-to-virion level
85 The considerable public health burden due to cytomegalovirus (CMV) supports current interest in vacci
93 th AD while other related viruses, including cytomegalovirus (CMV), Epstein-Bar virus and human herpe
95 iruses, such as Epstein-Barr virus (EBV) and cytomegalovirus (CMV), were detected at comparable level
99 .26), study heterogeneity index (I)= 23.4%), cytomegalovirus (CMV)-related illnesses (pOR = 3.14 (2.3
102 antiviral prophylaxis (AP) on development of cytomegalovirus (CMV)-specific neutralizing antibody (nA
103 Triplex vaccine was developed to enhance cytomegalovirus (CMV)-specific T cells and prevent CMV r
109 The most frequently detected targets were cytomegalovirus (CMV, n = 139, 41%), Mycobacterium tuber
110 ose of other chronic viral infections (i.e., cytomegalovirus [CMV] and Epstein-Barr virus [EBV]).
111 C virus [HCV], Epstein-Barr virus [EBV], and cytomegalovirus [CMV]) have limited breadth and diversit
112 ) viruses (adenovirus [ADV], BK virus [BKV], cytomegalovirus [CMV], Epstein-Barr virus [EBV], human h
113 a composite outcome of infection (including cytomegalovirus [CMV], herpes simplex I/II or varicella
118 l response of neurons to infection, as human cytomegalovirus did not downregulate DBH expression.
120 d during treatment of symptomatic congenital cytomegalovirus disease, but their predictive value is u
121 munosuppression may be at increased risk for Cytomegalovirus disease, notably Cytomegalovirus retinit
124 3 accurately detects BK polyomavirus DNA and cytomegalovirus DNA from patient-derived blood and urine
128 rospinal fluid is warranted in subjects with cytomegalovirus encephalitis, owing to the low penetrati
132 s frequent than T cells with specificity for cytomegalovirus, Epstein-Barr virus, or influenza virus.
134 s a decreased proportion of viral (including cytomegalovirus), fungal (including Aspergillus spp. and
135 es, which revealed the extent to which human cytomegalovirus generates nuclear polarity through a vir
138 ) viral vaccine strain based on a guinea pig cytomegalovirus (GPCMV) capsid mutant was evaluated.
139 rr virus 36% in saliva and 39% in GCF; human cytomegalovirus (HCMV) 11% in GCF; varicella zoster viru
141 herpes simplex virus 1 (HSV-1), HSV-2, human cytomegalovirus (HCMV) and Epstein-Barr virus (EBV) entr
142 hannel inhibitors for activity against human cytomegalovirus (HCMV) and identified the voltage-gated
144 spase-8 activation (vICA) conserved in human cytomegalovirus (HCMV) and murine CMV (MCMV) prevents th
146 widely held that clinical isolates of human cytomegalovirus (HCMV) are highly cell associated, and m
152 to restrict HCMV infections.IMPORTANCE Human cytomegalovirus (HCMV) continues to cause serious and of
153 jor immediate early promoter (MIEP) of human cytomegalovirus (HCMV) drives the expression of crucial
154 ine to prevent maternal acquisition of human cytomegalovirus (HCMV) during pregnancy is a primary str
157 ditionally, we report that GA inhibits human cytomegalovirus (HCMV) genome replication and Zika virus
158 ncing efforts have led to estimates of human cytomegalovirus (HCMV) genome-wide intrahost diversity t
161 hich showed antiviral activity against Human Cytomegalovirus (HCMV) in our previous work, could restr
165 ividuals, immune control of persistent human cytomegalovirus (HCMV) infection is effectively mediated
166 ltimately viral persistence.IMPORTANCE Human cytomegalovirus (HCMV) infection is endemic throughout t
167 ssemination within the host.IMPORTANCE Human cytomegalovirus (HCMV) infection is endemic throughout t
175 that occur during infection.IMPORTANCE Human cytomegalovirus (HCMV) is a common pathogen that asympto
176 may be a therapeutic target.IMPORTANCE Human cytomegalovirus (HCMV) is a herpesvirus present in up to
177 efficiency of virus spread.IMPORTANCE Human cytomegalovirus (HCMV) is a herpesvirus that leads to se
179 HCMV-induced birth defects.IMPORTANCE Human cytomegalovirus (HCMV) is a leading cause of central ner
192 s II transactivator (CIITA).IMPORTANCE Human cytomegalovirus (HCMV) is an opportunistic herpesvirus t
193 irect engagement of virions.IMPORTANCE Human cytomegalovirus (HCMV) is major pathogen of nonimmunocom
194 to the viral dissemination strategy of human cytomegalovirus (HCMV) is the induction of monocyte surv
196 uated in preclinical models.IMPORTANCE Human cytomegalovirus (HCMV) is the most common infectious cau
198 Human progenitor cells (HPCs) support human cytomegalovirus (HCMV) latency, and their differentiatio
206 egulation in infected cells.IMPORTANCE Human cytomegalovirus (HCMV) replicates in several cell types
208 ricting ribosome biogenesis stimulated human cytomegalovirus (HCMV) replication without suppressing t
210 istinctly regulate the activity of the human cytomegalovirus (HCMV) transactivator immediate early 2
213 e of human-restricted viruses, such as human cytomegalovirus (HCMV), a leading cause of congenital in
214 scripts of hepatitis B virus (HBV) and human cytomegalovirus (HCMV), generated via a similar mechanis
217 poor prognosis in colon cancer, and in human cytomegalovirus (HCMV)-infected fibroblasts, where the R
219 unger than 1 month diagnosed with-congenital cytomegalovirus, herpes simplex virus (HSV), varicella z
220 ouble weight compared to class B infections (cytomegalovirus, herpes simplex virus-1/2, human herpesv
221 -4.85]) and opportunistic infections such as cytomegalovirus (HR, 3.98 [95% CI, 1.40-11.26]), varicel
223 e sequence between distinct strains of human cytomegalovirus (human herpesvirus 5) and show that gene
225 rocally, several unrelated viruses including cytomegalovirus, human immunodeficiency virus, influenza
227 tional divergence between homologous primate cytomegalovirus immunevasins and suggest that the capaci
228 iterature on the diagnosis and management of cytomegalovirus in patients after HSCT and in patients r
229 ommendations of the ECIL 7 for management of cytomegalovirus in patients with haematological malignan
230 .IMPORTANCE Varicella-zoster virus and human cytomegalovirus infect a majority of the global populati
232 liver disease (HR, 2.18; 95% CI, 1.29-3.67), cytomegalovirus infection (HR, 1.89; 95% CI, 1.08-3.3),
233 in 46 [30%] and 42 [28%], respectively), and cytomegalovirus infection (in 39 [26%] and 31 [21%]).
234 re features were not observed during chronic cytomegalovirus infection in an independent cohort.
235 ent of patients with resistant or refractory cytomegalovirus infection or cytomegalovirus disease is
236 infection (OR = 7.75; 95% CI = 1.60-37.57), cytomegalovirus infection or disease (OR = 2.67; 95% CI
238 d in natural killer (NK) cells responding to cytomegalovirus infection, and consider the requirements
240 as discussed at the 2018 workshop entitled "Cytomegalovirus Infection: Advancing Strategies for Prev
241 l, letermovir reduced clinically significant cytomegalovirus infections (CS-CMVi) and all-cause morta
243 n increasing number of reports indicate that cytomegalovirus is also a potentially important pathogen
244 he way to a successful vaccine against human cytomegalovirus is hampered by the peculiar biology of t
245 in hospital discharges coded with congenital cytomegalovirus is most likely due to the introduction o
247 nfection of Zbtb32(-/-) chimeras with murine cytomegalovirus led to nearly 20-fold higher antigen-spe
248 nce status, donor age, HLA match, sex match, cytomegalovirus match, conditioning intensity, type of T
249 lytic activity, and mice infected with mouse cytomegalovirus (MCMV) displayed elevated titers in the
255 rticipated in KPD for the following reasons: cytomegalovirus mismatch (18.5% [10/54]), Epstein-Barr v
256 rs and chronic graft dysfunction (5 points); cytomegalovirus mismatch (4 points); and CD8+ T-cell cou
257 ovirus [n = 2]), hepatitis B virus (n = 10), cytomegalovirus (n = 9), Epstein-Barr virus (n = 5), and
261 cells or in cells infected with either human cytomegalovirus or Kaposi's sarcoma-associated herpesvir
263 HR, 2.97 [95% CI, 1.51-5.83]; P = .002), and cytomegalovirus pneumonitis (HR, 3.76 [95% CI, 1.23-11.4
264 % confidence interval [CI], 26.7-204) and in cytomegalovirus-positive recipients (OR = 3.70; 95% CI,
265 strain Paraiba/2015 under the control of the cytomegalovirus promoter was complexed with a commercial
266 trial of twice-weekly oral brincidofovir for cytomegalovirus prophylaxis after allogeneic HCT to stud
267 The patient had had several episodes of Cytomegalovirus reactivation subsequent to the introduct
268 ed VDJ segments to generate invariant/public cytomegalovirus-reactive CDR3 sequences (TRGV8-TRJP1-CAT
270 of belatacept-associated multidrug-resistant Cytomegalovirus retinitis in a kidney transplant recipie
276 terleukin-10 (IL-10) manifest delayed rhesus cytomegalovirus (RhCMV) acquisition and altered immune r
278 raft, - mismatch, comorbidity index >=3, and cytomegalovirus seropositivity (P < .001 for all variabl
280 betes stratified by HIV status, adjusted for cytomegalovirus serostatus and traditional risk factors.
283 ssed the safety and therapeutic potential of cytomegalovirus-specific (CMV-specific) ACT in an adjuva
285 hritidis mitogen, on influenza virus- and/or cytomegalovirus-specific memory TCD8 could be monitored.
287 ses were lost after transplantation, whereas cytomegalovirus-specific responses were detectable.
288 quencing and structural affinity analyses of cytomegalovirus-specific T cells, and through the genera
289 al insight into the mechanism by which human cytomegalovirus subverts viperin; they also provide a bi
290 ossible to infect model organisms with human cytomegalovirus, the aim of this study was to develop a
291 we review the diverse strategies adopted by cytomegaloviruses to target immune pathways and outline
292 Additionally, we found that the chimpanzee cytomegalovirus UL148 homolog suppresses surface present
293 nd, possibly, by evolution, since chimpanzee cytomegalovirus UL148 retains CD58 but does not remodel
294 ficiency, mechanical ventilation, high-level cytomegalovirus viremia, gram-negative bacteremia, invas
297 mulating infection of the human herpesvirus, cytomegalovirus, we hypothesize that virus-mediated disr
298 a from the prototypic betaherpesvirus, human cytomegalovirus, we uncover numerous uORFs and iORFs con
299 By contrast, receptors for Zika virus and cytomegalovirus, which cause congenital infections, are
300 affinity during the course of infection with cytomegalovirus, which elicits large T cell populations