ライフサイエンスコーパス: human herpesvirus

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

2 nse to infection with this common pathogenic human herpesvirus.

3 The Epstein-Barr virus (EBV) is an oncogenic human herpesvirus.

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

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

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

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

8 he nucleoside kinase activity of coinfecting human herpesviruses.

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

10 ause of the species-specific tropism of many human herpesviruses.

11 rticularly murine cytomegalovirus (MCMV) and human herpesviruses.

12 n compared to T-cell responses against other human herpesviruses.

13 to a small genomic region, as seen in 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 coma herpesvirus (KSHV), formally designated human herpesvirus 4 (HHV-4) and 8 (HHV-8), respectively,

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

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

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

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

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

22 Six immunocompetent patients with human herpesvirus 6 (HHV-6) chromosomal integration had

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

24 The prevalence and concentration of human herpesvirus 6 (HHV-6) DNA in the cerebrospinal flu

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

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

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

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

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

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

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

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

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

34 Human herpesvirus 6 (HHV-6) was detected in specimens fr

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

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

37 have performed a screen aimed at identifying human herpesvirus 6 (HHV-6)-encoded proteins that modula

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

39 Here, we describe a human herpesvirus 6 (HHV-6A) chemokine, U83A, which bind

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

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

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

43 The association of human herpesvirus 6 and cytomegalovirus reactivation wit

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

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

46 Human herpesvirus 6 is associated with a variety of comp

47 Most patients with human herpesvirus 6 reactivation also reactivated cytome

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

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

50 Human herpesvirus 6 viremia occurred in 23% of patients

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

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

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

54 9; p = 0.005) compared to patients with only human herpesvirus 6, only cytomegalovirus, or no viral r

55 30 febrile children positive for adenovirus, human herpesvirus 6, or enterovirus infection or with ac

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

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

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

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

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

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

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

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

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

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

66 ncluding adenovirus, bocavirus, coronavirus, human herpesvirus-6, lymphocytic choriomeningitis virus,

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

87 Here, we identified another virus, human herpesvirus 7 (HHV-7) that interferes with HIV typ

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

89 T cell function, deduced from levels of human herpesvirus 7 and response to hepatitis B immuniza

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

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

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

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

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

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

96 posi's sarcoma-associated herpesvirus (KSHV)/human herpesvirus 8 (HHV-8) and causes KSHV-like disease

97 o investigate a possible association between human herpesvirus 8 (HHV-8) and prostate cancer, we eval

98 Human herpesvirus 8 (HHV-8) causes Kaposi sarcoma.

99 Human herpesvirus 8 (HHV-8) causes Kaposi's sarcoma and

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

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

102 Human herpesvirus 8 (HHV-8) encodes a viral FLICE inhibi

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

104 children, but there is a paucity of data on human herpesvirus 8 (HHV-8) incidence and routes of infe

105 pulations are associated with the control of human herpesvirus 8 (HHV-8) infection in vivo.

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

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

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

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

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

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

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

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

114 Human herpesvirus 8 (HHV-8) is the etiological agent of

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

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

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

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

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

120 infected patients, Epstein-Barr virus (EBV), human herpesvirus 8 (HHV-8), cytomegalovirus (CMV), and

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

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

123 (RRV), a gammaherpesvirus closely related to human herpesvirus 8 (HHV-8), is described here.

124 0-CD200R pathway during infection, including human herpesvirus 8 (HHV-8), the causative agent of Kapo

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

126 Human herpesvirus 8 (HHV-8), which is associated with th

127 Human herpesvirus 8 (HHV-8)-encoded viral interleukin-6

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

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

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

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

132 iologically linked to the infection with the human herpesvirus 8 (HHV-8/KSHV).

133 Human herpesvirus 8 (HHV8) causes multicentric Castleman

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

135 Kaposi's sarcoma-associated herpesvirus/human herpesvirus 8 (HHV8) ORF50 encodes a transactivato

136 Human herpesvirus 8 (HHV8), also known as Kaposi's sarco

137 The lytic origins of DNA replication for human herpesvirus 8 (HHV8), oriLyt-L and oriLyt-R, are l

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

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

140 utively active chemokine receptor encoded by human herpesvirus 8 (HHV8, also known as Kaposi sarcoma

141 Kaposi's sarcoma-associated herpesvirus/human herpesvirus 8 (KSHV/HHV-8) interacts with cell sur

142 Kaposi's sarcoma-associated herpesvirus/human herpesvirus 8 (KSHV/HHV-8) RTA is an important pro

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

144 osi's sarcoma-associated herpesvirus (KSHV) (human herpesvirus 8 [HHV-8]) induces the host cell's pre

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

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

147 aposi's sarcoma-associated herpesvirus (KSHV/human herpesvirus 8 [HHV8]) and Epstein-Barr virus (EBV/

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

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

150 Expression of the K1 gene of human herpesvirus 8 activates nuclear factor-kappaB and

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

152 requently in saliva and buffy coats than was human herpesvirus 8 DNA.

153 s sarcoma (KS)-associated herpesvirus (KSHV)/human herpesvirus 8 functions as the key regulator to in

154 Human herpesvirus 8 interleukin-6 (vIL-6) displays 25% a

155 6 homologue (viral interleukin-6 [vIL-6]) of human herpesvirus 8 is implicated in viral pathogenesis

156 Human herpesvirus 8 is the etiologic agent associated wi

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

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

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

160 osi's sarcoma-associated herpesvirus (KSHV) (human herpesvirus 8) binds to adherent target cell surfa

161 i's sarcoma-associated herpesvirus (KSHV, or human herpesvirus 8) infection in individuals remains a

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

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

164 i's sarcoma-associated herpesvirus (KSHV, or human herpesvirus 8) is etiologically linked to KS, and

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

166 oma-associated herpesvirus (KSHV; also named human herpesvirus 8) is necessary but not sufficient for

167 posi's sarcoma-associated herpesvirus (KSHV, human herpesvirus 8) is the causative agent of Kaposi's

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

169 -associated herpesvirus (KSHV, also known as human herpesvirus 8) with the development of the disease

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

171 a-associated herpesvirus, also identified as human herpesvirus 8, contains genes producing proteins t

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

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

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

175 Similar to its close relative human herpesvirus 8, rhesus monkey rhadinovirus (RRV) pe

176 Human herpesvirus 8, which causes Kaposi sarcoma, expres

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

178 Because human herpesvirus 8-encoded K13 selectively activates th

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

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

181 herpesviruses such as Epstein-Barr virus and human herpesvirus 8.

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

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

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

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

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

187 Human herpesvirus-8 (HHV-8) replication is critical in t

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

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

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

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

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

193 eries regarding Kaposi's sarcoma herpesvirus/human herpesvirus-8 infection and its activation of sign

194 t findings show Kaposi's sarcoma herpesvirus/human herpesvirus-8 specific signaling pathways and pira

195 si's sarcoma-associated herpesvirus (KSHV or human herpesvirus-8) is frequently tumorigenic in immuno

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

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

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

199 rize major recent findings on the biology of human herpesvirus-8, i.e. Kaposi's sarcoma-associated he

200 on with HIV and Kaposi's sarcoma herpesvirus/human herpesvirus-8, which leads to the development of a

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

202 ma is driven by Kaposi's sarcoma herpesvirus/human herpesvirus-8-specific pathways, which include vir

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

204 esvirus family including cytomegalovirus and human herpesvirus-8.

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

206 ction by Kaposi's sarcoma herpesvirus (KSHV)/human herpesvirus-8.

207 re 'pirated' by Kaposi's sarcoma herpesvirus/human herpesvirus-8.

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

209 An ORF57 homolog is present in all known human herpesviruses and many animal herpesviruses.

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

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

212 Human herpesviruses are among the most prevalent pathoge

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

214 Human herpesviruses are responsible for a range of debil

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

216 Epstein-Barr virus (EBV) is a ubiquitous human herpesvirus associated with many malignant and non

217 Epstein-Barr virus (EBV) is a ubiquitous human herpesvirus associated with the development of bot

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

219 Human herpesviruses-associated vasculitis can cause vasc

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

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

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

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

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 a model our current understanding of how the human herpesvirus Epstein-Barr virus establishes and mai

229 Human herpesviruses establish life-long latency in the h

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

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

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

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

234 All eight human herpesviruses have a conserved herpesvirus protein

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

236 Although both human herpesvirus (HHV) 6 and HHV-7 infections are ubiqu

237 Human herpesvirus (HHV) 6 causes substantial morbidity a

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

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

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

241 Human herpesvirus (HHV) infections are common during inf

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

243 plant recipients have reactivation of latent human herpesvirus (HHV)-6 2-4 weeks after transplant.

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

245 Both intrauterine and sexual transmission of human herpesvirus (HHV)-6 and HHV-7 have been suggested,

246 tem cell donor with chromosomally integrated human herpesvirus (HHV)-6 and monitored the recipient fo

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

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

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

250 Kaposi sarcoma (KS) is associated with human herpesvirus (HHV)-8 and is dependent on the induct

251 the clinical and virologic manifestations of human herpesvirus (HHV)-8 infection in immunocompetent p

252 Kaposi sarcoma (KS) is primarily caused by human herpesvirus (HHV)-8 infection, and the risk is inc

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

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

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

256 Human herpesviruses (HHV) establish lifelong latent infe

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

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

259 ion is associated with an increased risk for human herpesviruses (HHVs) and their related diseases.

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

261 We investigated the hypothetical role of human herpesviruses (HHVs) in tumour formation of the ce

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

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

264 The virion of the largest human herpesvirus, human cytomegalovirus (HCMV), contain

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

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

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

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

269 vide additional therapeutic options to treat human herpesvirus infections.

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

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

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

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

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

275 EBV, a ubiquitous human herpesvirus, is the causative agent of infectious

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

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

278 ecently, 11 miRNAs encoded by the pathogenic human herpesvirus Kaposi's sarcoma-associated herpesviru

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

280 Human herpesviruses may cause severe complications after

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

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

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

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

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

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

287 Epstein-Barr virus is an orally transmitted human herpesvirus that infects epithelial cells and esta

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

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

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

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

292 Epstein-Barr virus (EBV), a human herpesvirus, transforms B cell growth in vitro thr

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

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

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

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

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

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