ライフサイエンスコーパス: human herpesvirus

1 hogenic state investigated is infection by a human herpesvirus.

2 ous cycle of varicella-zoster virus (VZV), a human herpesvirus.

3 nse to infection with this common pathogenic human herpesvirus.

4 Human cytomegalovirus (HCMV) is a ubiquitous human herpesvirus.

5 to a small genomic region, as seen in other human herpesviruses.

6 ach of the alpha, beta, and gamma classes of human herpesviruses.

7 gG do not have orthologs in HSV-2 or 8 other human herpesviruses.

8 and gG) do not have orthologs in all 40 non-human herpesviruses.

9 d that have undetectable levels of the eight human herpesviruses.

10 he nucleoside kinase activity of coinfecting human herpesviruses.

11 of novel entry inhibitors of EBV and related human herpesviruses.

12 ey mechanism appears to be common to several human herpesviruses.

13 ciated tegument proteins compared with other human herpesviruses.

14 the circulating diversity of all classes of human herpesviruses.

15 n varicella-zoster virus (VZV; also known as human herpesvirus 3 [HHV-3]).

16 hat varicella-zoster virus (VZV; also called human herpesvirus 3 [HHV3]), the human alphaherpesvirus

17 s Prevotella spp., Streptococcus mutans, and Human herpesvirus 4 (Epstein-Barr virus [EBV]) were more

18 coma herpesvirus (KSHV), formally designated human herpesvirus 4 (HHV-4) and 8 (HHV-8), respectively,

19 n gammaherpesvirus Epstein-Barr virus (EBV) (human herpesvirus 4 [HHV4]) infects most adults and is a

20 Human cytomegalovirus (HCMV, or human herpesvirus 5 [HHV-5]) is a large DNA-containing v

21 n distinct strains of human cytomegalovirus (human herpesvirus 5) and show that gene drive viruses ca

22 receptor encoded by CMV (also referred to as human herpesvirus 5), a highly prevalent human virus tha

23 inherits a chromosomally integrated copy of human herpesvirus 6 (CI-HHV-6), but the consequences of

24 esence of inherited chromosomally integrated human herpesvirus 6 (ciHHV-6) in hematopoietic cell tran

25 Cytomegalovirus (CMV) (18.3%), human herpesvirus 6 (HHV-6) (34.2%), human herpesvirus 7

26 targets detected were enterovirus (n = 38), human herpesvirus 6 (HHV-6) (n = 30), and Streptococcus

27 Human herpesvirus 6 (HHV-6) and cytomegalovirus (CMV) ar

28 Human herpesvirus 6 (HHV-6) and oncogenic Marek's diseas

29 The majority of human herpesvirus 6 (HHV-6) congenital infections (86%)

30 This review evaluates publications on human herpesvirus 6 (HHV-6) encephalitis recognizing fir

31 Following primary infection, human herpesvirus 6 (HHV-6) establishes a persistent inf

32 mory subsets of CD4(+) and CD8(+) T cells to human herpesvirus 6 (HHV-6) have not been previously inv

33 te concerning the role of herpesviruses, and human herpesvirus 6 (HHV-6) in particular, in AD.

34 Higher incidence of human herpesvirus 6 (HHV-6) infection has been documente

35 Congenital human herpesvirus 6 (HHV-6) infection results from germl

36 bella, 309 cases of dengue, and 260 cases of human herpesvirus 6 (HHV-6) infection.

37 Human herpesvirus 6 (HHV-6) is an important cause of men

38 Human herpesvirus 6 (HHV-6) is detected in the plasma of

39 Human herpesvirus 6 (HHV-6) is susceptible to latency an

40 Human herpesvirus 6 (HHV-6) may be associated with LFUE,

41 Human herpesvirus 6 (HHV-6) species have a unique abilit

42 megalovirus (CMV), Epstein-Barr virus (EBV), human herpesvirus 6 (HHV-6), herpes simplex virus types

43 uses such as Marek's disease virus (MDV) and human herpesvirus 6 (HHV-6), integrate their DNA into ho

44 , cytomegalovirus (CMV), BK virus (BKV), and human herpesvirus 6 (HHV-6).

45 Here, we show that human herpesvirus 6 (HHV-6, A or B) RNA was detected in

46 (EBV), BK virus (BKV), adenovirus (ADV), and human herpesvirus 6 (HHV6) were evaluated to determine o

47 cytomegalovirus (CMV), Epstein-Bar virus and human herpesvirus 6 (HHV6), are known to infect neurons.

48 omes of interest were VR of adenovirus, EBV, human herpesvirus 6 (HHV6), cytomegalovirus (CMV), and B

49 Coreactivation of both human herpesvirus 6 and cytomegalovirus in ICU patients

50 The association of human herpesvirus 6 and cytomegalovirus reactivation wit

51 ilation and ICU type, only coreactivation of human herpesvirus 6 and cytomegalovirus was significantl

52 CMV, herpes simplex virus type 1, and human herpesvirus 6 infection were independently associa

53 Human herpesvirus 6 is associated with a variety of comp

54 expanded panel of HHV-6B antigens.IMPORTANCE Human herpesvirus 6 is highly prevalent and maintains ch

55 n Results: First-onset viral infections with human herpesvirus 6 or Epstein-Barr virus within 100 day

56 Most patients with human herpesvirus 6 reactivation also reactivated cytome

57 ical ventilation, burn ICU, major infection, human herpesvirus 6 reactivation, and cytomegalovirus re

58 y and comprehensively assessed the impact of human herpesvirus 6 reactivation, and its interaction wi

59 Human herpesvirus 6 viremia occurred in 23% of patients

60 and the thymus, kidneys, and adrenal glands (human herpesvirus 6).

61 uding BK virus, cytomegalovirus, adenovirus, human herpesvirus 6, and Epstein-Barr virus.

62 Murine roseolovirus, a homolog of human herpesvirus 6, can also be reactivated in the lung

63 Viruses (human herpesvirus 6, Epstein-Barr virus, and cytomegalov

64 , enterovirus, herpes simplex virus 1 and 2, human herpesvirus 6, human parechovirus, varicella-zoste

65 positive by qPCR for Epstein-Barr virus and human herpesvirus 6, including the brain cortex (Epstein

66 9; p = 0.005) compared to patients with only human herpesvirus 6, only cytomegalovirus, or no viral r

67 30 febrile children positive for adenovirus, human herpesvirus 6, or enterovirus infection or with ac

68 galovirus, EBV, adenovirus, BK virus, and/or human herpesvirus 6.

69 new and conserved features in the genome of human herpesvirus 6.

70 d: 11 with infectious causes (2 influenza; 2 human herpesvirus 6; 2 group B Streptococcus; 2 Streptoc

71 inical relevance of chromosomally integrated human herpesvirus-6 (CIHHV-6) after transplantation is n

72 zoster virus 6% in saliva and 3% in GCF; of human herpesvirus-6 (HHV-6) 6% in saliva and 2% in GCF;

73 Human herpesvirus-6 (HHV-6) A and B are ubiquitous betah

74 In addition, viral copy number of human herpesvirus-6 (HHV-6) and human herpesvirus-7 (HHV

75 To investigate whether human herpesvirus-6 (HHV-6) is a causative agent of ence

76 Human herpesvirus-6 (HHV-6) is a neurotropic virus that

77 Human herpesvirus-6 (HHV-6) is known to reactivate after

78 Previous research has suggested that human herpesvirus-6 (HHV-6) may integrate into host cell

79 A real-time quantitative human herpesvirus-6 (HHV-6) polymerase chain reaction as

80 Inherited chromosomally integrated human herpesvirus-6 (iciHHV-6) results in the germ-line

81 ations in ATRX and CTNNB1 and integration of human herpesvirus-6 in chromosome 11p.

82 cytomegalovirus (genus Cytomegalovirus) and human herpesvirus 6A (genus Roseolovirus).

83 The genomes of human herpesvirus 6A (HHV-6A) and HHV-6B have the capaci

84 ous human diseases have been correlated with human herpesvirus 6A (HHV-6A) and HHV-6B, the lack of an

85 ity of the human population is infected with human herpesvirus 6A (HHV-6A), a betaherpesvirus family

86 Human herpesvirus 6A (HHV-6A), a member of the betaherpe

87 Human herpesvirus 6A (HHV-6A), HHV-6B, and HHV-7 are cla

88 Human herpesvirus 6A (HHV-6A), HHV-6B, and HHV-7 are cla

89 The human roseoloviruses human herpesvirus 6A (HHV-6A), HHV-6B, and HHV-7 compris

90 We show that in T cells infected with human herpesvirus 6A (HHV-6A), the E2F1 protein and its

91 megalovirus [CMV], Epstein-Barr virus [EBV], human herpesvirus 6A [HHV-6A], HHV-6B, herpes simplex vi

92 Human herpesvirus 6A and 6B (HHV-6A and HHV-6B) are clos

93 y 1% of people worldwide carry a copy of the human herpesvirus 6A or 6B (HHV-6A/B) in every cell of t

94 The U24 protein expressed by human herpesvirus 6A, a ubiquitous human pathogen, has b

95 red to as inherited chromosomally integrated human herpesvirus 6A/B (iciHHV-6A/B).

96 Human herpesviruses 6A and 6B (HHV-6A and HHV-6B) are hu

97 most closely related to the roseoloviruses, human herpesviruses 6A, 6B, and 7.

98 Human herpesviruses 6A/B (HHV-6A/B) can integrate their

99 ier of an inherited-chromosomally-integrated human herpesvirus-6A (iciHHV-6A) genome in one 19q telom

100 The roseoloviruses, human herpesvirus-6A -6B and -7 (HHV-6A, HHV-6B and HHV-

101 Human herpesvirus 6B (HHV-6B) belongs to the beta-herpes

102 Human herpesvirus 6B (HHV-6B) commonly reactivates after

103 Human herpesvirus 6B (HHV-6B) DNA is frequently detected

104 Human herpesvirus 6B (HHV-6B) DNA is frequently detected

105 Human herpesvirus 6B (HHV-6B) frequently reactivates aft

106 tomic analyses for HCT recipients.IMPORTANCE Human herpesvirus 6B (HHV-6B) is a DNA virus that infect

107 is positive for Epstein-Barr virus (EBV) or human herpesvirus 6B (HHV-6B), with one coinfection.

108 Human herpesvirus 6B was the species detected in eight s

109 o test for cytomegalovirus, BK polyomavirus, human herpesvirus 6B, HHV-6A, adenovirus, and Epstein-Ba

110 y CD4(+) T cells were enriched with DNA from human herpesvirus 6b.

111 18.3%), human herpesvirus 6 (HHV-6) (34.2%), human herpesvirus 7 (HHV-7) (20.5%) and Epstein-Barr vir

112 including the closely related human viruses human herpesvirus 7 (HHV-7) and human cytomegalovirus (H

113 In this report, we show that the human herpesvirus 7 (HHV-7) immunoevasin U21, itself a c

114 Here, we show that human herpesvirus 7 (HHV-7) U21 binds to and downregulat

115 The U21 gene product from human herpesvirus 7 binds to and redirects class I major

116 of HBV, parvovirus B19, cytomegalovirus, and human herpesvirus 7).

117 tial pathogens reported included bunyavirus, human herpesvirus 7, and enterovirus D-68, ultimately im

118 The human herpesvirus-7 (HHV-7) U21 glycoprotein binds to cl

119 py number of human herpesvirus-6 (HHV-6) and human herpesvirus-7 (HHV-7) were measured in both saliva

120 The U21 open reading frame from human herpesvirus-7 encodes a membrane protein that asso

121 ypothesized that they could be infected with human herpesvirus 8 (HHV-8) (Kaposi's sarcoma [KS]-assoc

122 We have developed a human herpesvirus 8 (HHV-8) 50% tissue culture infective

123 oma (cKS) is an inflammatory tumor caused by human herpesvirus 8 (HHV-8) commonly observed in elderly

124 posi's sarcoma-associated herpesvirus (KSHV)/human herpesvirus 8 (HHV-8) displays two distinct life s

125 Human herpesvirus 8 (HHV-8) encodes four viral interfero

126 Here, we report that human herpesvirus 8 (HHV-8) gene product viral interfero

127 Human herpesvirus 8 (HHV-8) infection is associated with

128 Human herpesvirus 8 (HHV-8) infection is endemic in sub-

129 Human herpesvirus 8 (HHV-8) infection occurs in early ch

130 plantation through reactivation of recipient human herpesvirus 8 (HHV-8) infection or through donor-d

131 Human herpesvirus 8 (HHV-8) interleukin-6 (vIL-6) is dis

132 Human herpesvirus 8 (HHV-8) interleukin-6 (vIL-6) promot

133 Human herpesvirus 8 (HHV-8) is an oncogenic virus causal

134 Viral interleukin-6 (vIL-6) encoded by human herpesvirus 8 (HHV-8) is believed to contribute vi

135 Human herpesvirus 8 (HHV-8) is endemic in Uganda and tra

136 Human herpesvirus 8 (HHV-8) is the causative agent of Ka

137 The human herpesvirus 8 (HHV-8) viral G protein-coupled rece

138 Human herpesvirus 8 (HHV-8) viral interleukin-6 (vIL-6)

139 The contributions of human herpesvirus 8 (HHV-8) viral interleukin-6 (vIL-6)

140 Human herpesvirus 8 (HHV-8) viral interleukin-6 (vIL-6)

141 Human herpesvirus 8 (HHV-8) viral interleukin-6 (vIL-6),

142 -1, HSV-2), varicella-zoster virus (VZV) and human herpesvirus 8 (HHV-8) were not or rarely detected

143 epithelial cells persistently infected with human herpesvirus 8 (HHV-8), an oncogenic herpesvirus th

144 Other viruses, such as hepatitis B virus or human herpesvirus 8 (HHV-8), establish persistent infect

145 associated herpesvirus (KSHV), also known as human herpesvirus 8 (HHV-8), is a cancer-related human v

146 0-CD200R pathway during infection, including human herpesvirus 8 (HHV-8), the causative agent of Kapo

147 erent efficiencies and with the exception of human herpesvirus 8 (HHV-8), these chimeric variants res

148 evious analyses of vIL-6 activity.IMPORTANCE Human herpesvirus 8 (HHV-8)-encoded viral interleukin-6

149 Kaposi sarcoma is the most common human herpesvirus 8 (HHV-8)-related disease described af

150 Ebola virus (EBOV), Tacaribe arenavirus, and human herpesvirus 8 (HHV-8).

151 most always multicentric (MCD) and linked to human herpesvirus 8 (HHV-8).

152 aque (RM) monkeys that is closely related to human herpesvirus 8 (HHV-8)/Kaposi's Sarcoma-associated

153 Human herpesvirus 8 (HHV8) causes multicentric Castleman

154 central Italy and a surveillance program for human herpesvirus 8 (HHV8) infection after transplant, a

155 ly improved survival and reduced the risk of human herpesvirus 8 (HHV8)-associated lymphoma.

156 nsfection replication assay identified eight human herpesvirus 8 (HHV8)-encoded proteins required for

157 irus Kaposi's sarcoma-associated herpesvirus/human herpesvirus 8 (KSHV/HHV8), exploit microtubule (MT

158 -associated herpesvirus (KSHV; also known as human herpesvirus 8 [HHV-8]) is the etiologic agent of K

159 -associated herpesvirus (KSHV; also known as human herpesvirus 8 [HHV-8]), Epstein-Barr virus (EBV),

160 ma-associated herpesvirus (KSHV; also called human herpesvirus 8 [HHV-8]), upon being reactivated, ca

161 i's sarcoma-associated herpesvirus (KSHV; or human herpesvirus 8 [HHV8]) is implicated in the pathoge

162 ma-associated herpesvirus (KSHV; also called human herpesvirus 8 [HHV8]), the switch from latency to

163 ain at increased KS risk, likely due to high human herpesvirus 8 coinfection rates.

164 Kaposi sarcoma-associated herpesvirus/human herpesvirus 8 is associated with multicentric Cast

165 6 homologue (viral interleukin-6 [vIL-6]) of human herpesvirus 8 is implicated in viral pathogenesis

166 Viral interleukin-6 (vIL-6) specified by human herpesvirus 8 is, unlike its cellular counterpart,

167 Human herpesvirus 8 seroprevalence was 4% (10/249) in do

168 CMV, herpes simplex virus types 1 and 2, and human herpesvirus 8 was 99.4%, 74.9%, 26.2%, 8.0%, and 1

169 s sarcoma-associated herpesvirus (also named human herpesvirus 8) is a gamma-herpesvirus that undergo

170 persistent gamma-herpesvirus infection (EBV, human herpesvirus 8) is a significant problem in AIDS pa

171 posi's sarcoma-associated herpesvirus (KSHV; human herpesvirus 8) is an oncogenic gammaherpesvirus th

172 ma-associated herpesvirus (KSHV, also called human herpesvirus 8) is linked to the development of Kap

173 s (CMV), herpes simplex virus types 1 and 2, human herpesvirus 8) using multiplex serology on blood s

174 aposi's sarcoma-associated herpesvirus (KSHV/human herpesvirus 8).

175 (cytomegalovirus, herpes simplex virus-1/2, human herpesvirus 8, hepatitis E virus, parvovirus B19).

176 associated herpesvirus (KSHV), also known as human herpesvirus 8, is the etiologic agent of Kaposi sa

177 associated herpesvirus (KSHV), also known as human herpesvirus 8, is the etiologic agent underlying K

178 The rhadinovirus 1 (RV1) lineage consists of human herpesvirus 8, Kaposi's sarcoma-associated herpesv

179 Human herpesvirus 8, which causes Kaposi sarcoma, expres

180 Human herpesvirus 8-DNA was detected in 6.8% and 2.9% of

181 in HHV-8 latent and lytic biology.IMPORTANCE Human herpesvirus 8-encoded IRF homologues were the firs

182 Because human herpesvirus 8-encoded K13 selectively activates th

183 Epstein-Barr virus-infected lymphocytes, and human herpesvirus 8-positive primary effusion lymphoma,

184 ted to rhesus macaque rhadinovirus (RRV) and human herpesvirus 8.

185 e of Kaposi's sarcoma-associated herpesvirus/human herpesvirus 8.

186 gammaherpesviruses, Epstein-Barr virus, and human herpesvirus 8/Kaposi's sarcoma-associated herpesvi

187 posi's sarcoma-associated herpesvirus (KSHV [human herpesvirus 8; HHV-8]) open reading frame 57 (ORF5

188 onsequence of dysregulated expression of the human herpesvirus-8 (HHV-8 or KSHV)-encoded G protein-co

189 effusion lymphomas (PEL) are associated with human herpesvirus-8 (HHV-8) and usually occur in immunoc

190 ranean Basin, despite the high prevalence of human herpesvirus-8 (HHV-8) infection in this region.

191 s led to a dramatic rise in the incidence of human herpesvirus-8 (HHV-8)-associated Kaposi's sarcoma

192 S), a multifocal vascular neoplasm linked to human herpesvirus-8 (HHV-8/KS-associated herpesvirus [KS

193 Posttransplantation human herpesvirus-8 (HHV8)/Kaposi sarcoma herpesvirus (K

194 i's sarcoma-associated herpesvirus (KSHV, or human herpesvirus-8 [HHV-8]) has another, alternative em

195 sociation was observed with plasma levels of human herpesvirus-8 DNA.

196 of KS is KS herpesvirus (KSHV; also known as human herpesvirus-8), and viral proteins can induce KS-a

197 osi sarcoma-associated herpesvirus (KSHV; or human herpesvirus-8)-encoded protein called K-bZIP (also

198 mely Kaposi's sarcoma-associated herpesvirus/human herpesvirus-8, has been confirmed to be a direct c

199 nflammatory protein-II (vMIP-II), encoded by human herpesvirus-8, has garnered interest because of it

200 We enrolled HIV-negative and human herpesvirus-8-seronegative patients with symptomat

201 liferative disorder caused by infection with human herpesvirus-8.

202 esvirus family including cytomegalovirus and human herpesvirus-8.

203 n shown to be associated with infection with human herpesvirus-8.

204 ) and HSV-2, two closely related neurotropic human herpesviruses, achieve neurotropism through ICP34.

205 onors to seropositive recipients for several human herpesviruses and adenoviruses.

206 the structure of region IX is present in all human herpesviruses and thus represents a potential stru

207 Human cytomegalovirus (CMV) is a human herpesvirus, and infection is widespread in the hu

208 Human herpesviruses are among the most prevalent pathoge

209 e against Epstein-Barr virus (EBV) and other human herpesviruses are limited to those targeting viral

210 Human herpesviruses are responsible for a range of debil

211 Infections with human herpesviruses are ubiquitous and a public health c

212 logues of pUL7 and pUL51 is conserved across human herpesviruses, as is their association with trans-

213 Epstein-Barr virus is a ubiquitous human herpesvirus associated with epithelial and lymphoi

214 Because KSBcl-2 and BHRF1 are from human herpesviruses associated with malignancies, we scr

215 Human herpesviruses-associated vasculitis can cause vasc

216 de analog, is thought to be specific for the human herpesviruses because it requires a virally encode

217 ched the genome-wide level for CMV and other human herpesviruses, but study of HHV-6 is at an earlier

218 This study examined the association of 4 human herpesviruses (CMV, herpes simplex virus type 1, h

219 olution imaging of individual virions of the human herpesvirus cytomegalovirus (CMV) showed that viri

220 -regulating master circuits in HIV-1 and the human herpesvirus cytomegalovirus along with potential c

221 more differentiated T cells specific for the human herpesviruses cytomegalovirus and Epstein-Barr vir

222 By simulating infection of the human herpesvirus, cytomegalovirus, we hypothesize that

223 Of the human herpesviruses, cytomegalovirus (HCMV) and Epstein-

224 The ORF54-related proteins of other human herpesviruses do not possess this activity, sugges

225 Currently, there are approximately 150 known human herpesvirus-encoded miRNAs, although an miRNA(s) e

226 Our results show VZV, like other human herpesviruses, encodes several sncRNAs and miRNAs,

227 genic latency gene expression program of the human herpesvirus Epstein-Barr virus (EBV).

228 Human herpesviruses establish life-long latency in the h

229 sized that HHV-6A, like other members of the human herpesvirus family, encodes miRNAs, which function

230 l mechanism by which HHV-6A, a member of the human herpesvirus family, may contribute to inadequate m

231 g 3 HSV-1 genomes, one HSV-2 genome, 8 other human herpesvirus genomes, and 40 non-human herpesvirus

232 other human herpesvirus genomes, and 40 non-human herpesvirus genomes.

233 All eight human herpesviruses have a conserved herpesvirus protein

234 Since all eight human herpesviruses have UL25 orthologs, this discovery

235 Human herpesvirus (HHV) 6 causes substantial morbidity a

236 nd that certain infectious pathogens such as human herpesvirus (HHV) 6, HHV-7, and adenovirus, which

237 immunological tools available to detect both human herpesvirus (HHV) and immune control of replicatio

238 d men have at least one actively replicating human herpesvirus (HHV) in their mucosal secretions at a

239 Human herpesvirus (HHV) infections are common during inf

240 Both human immunodeficiency virus (HIV) and human herpesvirus (HHV) infections persist lifelong, and

241 Reactivation of human herpesvirus (HHV)-6 and HHV-7 has been linked to v

242 ced hypersensitivity syndrome (DIHS), latent human herpesvirus (HHV)-6 is frequently reactivated in a

243 identification of suitable animal models for human herpesvirus (HHV)-6A and HHV-6B infections has bee

244 for a single virus: Epstein-Barr virus (23), human herpesvirus (HHV)-6B (10), human parainfluenza vir

245 KS) is a rare vascular tumor associated with human herpesvirus (HHV)-8 infection.

246 nt studies have found evidence of occasional human herpesvirus (HHV)-8 transmission via blood transfu

247 Human herpesviruses (HHV) 6 and 7 are ubiquitous infecti

248 Infections due to the eight human herpesviruses (HHV) are exacerbated by immunosuppr

249 Human herpesviruses (HHV) establish lifelong latent infe

250 Asymptomatic replication of human herpesviruses (HHV) is frequent in HIV-infected me

251 were as follows: cytomegalovirus (CMV), 44%; human herpesvirus [HHV] 6, 18%; HHV8, 6%; Epstein-Barr v

252 Reactivations of human herpesviruses (HHVs) contribute to the development

253 Seminal HIV RNA and DNA from 7 human herpesviruses (HHVs) were measured by real-time po

254 , acts as a DNA chain terminator for several human herpesviruses (HHVs), including HHV-2 (HSV-2), a c

255 lly occurring genetic variants of persistent human herpesviruses imprints on the evolution of the ant

256 us (EBV), known as an oncovirus, is the only human herpesvirus in the genus Lymphocryptovirus (LCV).

257 ass A infections, the high seroprevalence of human herpesviruses in lr-MSM warrants further investiga

258 of this study was to analyse the presence of human herpesviruses in saliva and gingival crevicular fl

259 Nineteen proteins are conserved in all human herpesviruses, including capsid scaffold protein U

260 we found that HDAC inhibiting proteins from human herpesviruses induce human NKG2D ligand ULBP-1.

261 t as additional therapeutic options to treat human herpesvirus infections.

262 vide additional therapeutic options to treat human herpesvirus infections.

263 s sarcoma-associated herpesvirus (KSHV) is a human herpesvirus involved in the causation of several h

264 The most recently identified human herpesvirus is Kaposi's sarcoma-associated herpesv

265 The epidemiology and essential biology of human herpesvirus is reviewed.

266 EBV, a human herpesvirus, is commonly acquired during childhood

267 nding recruiting p53 to Zp.IMPORTANCE EBV, a human herpesvirus, is latently present in most nasophary

268 llular protein and has homologs in all other human herpesviruses, it has potential importance as a th

269 the data suggest that HHV-6 is unique among human herpesviruses: it specifically and efficiently int

270 Kaposi sarcoma (KS) to infection by a novel human herpesvirus (Kaposi sarcoma-associated herpesvirus

271 Human herpesviruses may cause severe complications after

272 is to investigate the effect of any of eight human herpesviruses on development of dementia or mild c

273 All members of the human herpesvirus protease (HHV Pr) family are active as

274 yzed the incidence of infection of the eight human herpesviruses simultaneously in 1 045 peripheral b

275 pUL47 may have a similar function in human herpesviruses such as varicella-zoster virus or he

276 Human cytomegalovirus (HCMV) is a ubiquitous human herpesvirus that can cause life-threatening diseas

277 Epstein-Barr virus (EBV) is a human herpesvirus that can cause lymphomas, epithelial c

278 -zoster virus (VZV) is a medically important human herpesvirus that causes chickenpox and shingles, b

279 Epstein-Barr virus (EBV) is an oncogenic human herpesvirus that dramatically reorganizes host gen

280 Epstein-Barr Virus (EBV) is a human herpesvirus that efficiently establishes latent in

281 EBV is an oncogenic human herpesvirus that has the ability to infect and tra

282 EBV is a ubiquitous human herpesvirus that is associated with various lympho

283 Epstein-Barr virus (EBV) is a ubiquitous human herpesvirus that is causally implicated in the dev

284 , the replication of herpes simplex virus, a human herpesvirus that is closely related to HCMV, was n

285 pstein-Barr virus, one of the most prevalent human herpesviruses that also causes cancer, we have dis

286 ibody response.IMPORTANCE HHV-6A and -6B are human herpesviruses that have the unique property of bei

287 Epstein-Barr virus (EBV) is one of nine human herpesviruses that persist latently to establish p

288 genomes, combined with the inability of most human herpesviruses to replicate in animals, has until r

289 Enterovirus and human herpesvirus type 6 had agreements of 95.7% and 85.

290 esviruses (CMV, herpes simplex virus type 1, human herpesvirus type 6, and Epstein-Barr virus) with c

291 afamilial dynamics of endemic infection with human herpesvirus type 8 (HHV-8) in Amerindian populatio

292 quently Epstein-Barr virus (EBV) positive or human herpesvirus type-8 (HHV-8) positive.

293 Strikingly, as all human herpesviruses use conserved mRNA processing pathwa

294 that the hexon-capping SCP-the largest among human herpesviruses-uses its N-terminal half to bridge h

295 is substantially smaller than those of other human herpesviruses, VZV has a similarly sized capsid, c

296 Levels of HIV and 7 human herpesviruses were measured by real-time polymeras

297 Compared to blood donors, human herpesviruses were more prevalent in all MSM group

298 we address this issue for EBV, a widespread human herpesvirus with oncogenic potential.

299 Epstein-Barr virus (EBV), a human herpesvirus with potent B cell growth transforming

300 We focus on human herpesviruses, with key insights drawn from veteri