ライフサイエンスコーパス: lymphotropic

1 icating that the BASE prion is intrinsically lymphotropic.

2 ain is a more virulent BSE strain and likely lymphotropic.

3 A lymphotropic agent frequently reactivated in HIV-infecte

4 ed (KS-associated) herpesvirus (KSHV) is a B-lymphotropic agent linked to AIDS-related lymphoprolifer

5 Marek's disease virus (MDV), a lymphotropic alphaherpesvirus, causes Marek's disease (M

6 Here we investigated incunabular events in lymphotropic and intranodal prion trafficking by followi

7 Human herpesvirus 6 (HHV-6), a latent lymphotropic and neurotropic virus, has been suspected a

8 rated that the virus was epitheliotropic and lymphotropic and that infection was systemic in the majo

9 These results demonstrate that lymphotropic B. burgdorferi is infectious in mice and su

10 uman herpesvirus 6 (HHV-6) is a ubiquitous T-lymphotropic betaherpesvirus that encodes two G protein-

11 The vector was packaged into an MVM lymphotropic capsid and inoculated into naive C3H/HeNcr

12 Because the lymphotropic cytokine IL-7 plays crucial roles in both d

13 this approach for tumor-localized as well as lymphotropic delivery.

14 ibit exacerbated neurovirulence and atypical lymphotropic dissemination of HSV-1 following ocular inf

15 s sarcoma-associated herpesvirus (KSHV) is a lymphotropic DNA tumor virus that induces Kaposi's sarco

16 The B lymphotropic EBV is a major risk factor in multiple scle

17 The lymphotropic Epstein-Barr virus (EBV) seems to avoid rec

18 phoma (PEL), are closely associated with the lymphotropic gamma herpes virus Kaposi's sarcoma-associa

19 th murine gammaherpesvirus 68 (gammaHV68), a lymphotropic gamma-2-herpesvirus that establishes latent

20 HHV-8 is a B-lymphotropic gamma-herpesvirus closely related to the Ep

21 Epstein-Barr virus (EBV) is a lymphotropic gamma-herpesvirus that has co-evolved with

22 Two other T-lymphotropic gamma-herpesviruses, AlHV-1 and OvHV-2, do

23 ular CD21 and CD23a are common targets for B lymphotropic gammaherpesviruses and that KSHV RTA regula

24 alizing anti-E2 or anti-E1 antibodies with a lymphotropic HCV (SB strain).

25 e viral envelope and 5'-UTR sequences of the lymphotropic HCV strain were responsible for the lymphot

26 clone and chimeric virus of hepatotropic and lymphotropic HCV strains derived from an HCV-positive B-

27 Together, a co-receptor B7.2 enabled lymphotropic HCV to infect memory B cells, leading to in

28 a co-receptor specific for the infection by lymphotropic HCV, we established an infectious clone and

29 ory receptor B7.2 (CD86) as a co-receptor of lymphotropic HCV.

30 A lymphotropic hepatitis C virus strain (HCV, SB strain, h

31 porcine cytomegalovirus (PCMV), and porcine lymphotropic herpesvirus (PLHV) are common porcine virus

32 Porcine lymphotropic herpesvirus (PLHV)-1 is associated with B c

33 Here we show that the human lymphotropic herpesvirus Epstein-Barr virus (EBV) transc

34 Epstein-Barr virus (EBV), a B lymphotropic herpesvirus etiologically linked to several

35 These results demonstrate that a lymphotropic herpesvirus has evolved a novel mechanism t

36 Thus, lymphotropic herpesvirus has evolved an elaborate mechan

37 The lymphotropic Herpesvirus saimiri (HVS) causes acute leuk

38 ne kinase-interacting protein (Tip) of the T lymphotropic Herpesvirus saimiri (HVS) is constitutively

39 Using the conserved snRNAs encoded by the lymphotropic Herpesvirus saimiri (HVS), we determined th

40 sarcoma-associated herpesvirus (KSHV) is a B-lymphotropic herpesvirus strongly linked to both lymphop

41 iruses, porcine cytomegalovirus, and porcine lymphotropic herpesvirus type 1 are all concerns that mu

42 Epstein-Barr virus (EBV), a B-lymphotropic herpesvirus widespread in the human populat

43 Porcine lymphotropic herpesvirus-1 (PLHV-1) is a gamma-herpesvir

44 ical features of PTLD were increased porcine lymphotropic herpesvirus-1 viral loads in blood and tiss

45 oma-associated herpesvirus (KSHV) is a human lymphotropic herpesvirus.

46 Epstein-Barr virus (EBV) is a lymphotropic herpesvirus.

47 rable to the reactivation and replication of lymphotropic herpesviruses.

48 Epstein-Barr virus, a B-lymphotropic human herpesvirus, persists in vivo by ente

49 GB virus C (GBV-C) is a lymphotropic human virus discovered in 1995 that is rela

50 ptor, in contrast to coreceptors used by the lymphotropic immunodeficiency lentiviruses.

51 The structure of virus-like particles of the lymphotropic, immunosuppressive strain of minute virus o

52 Infections of a lymphotropic nature are caused by cytomegalovirus, HSV-6

53 caused by Marek's disease virus (MDV), is a lymphotropic neoplastic disease.

54 A lymphotropic papovavirus (LPV) archetypal regulatory reg

55 lyomaviruses, simian virus (SV)40 and B-cell lymphotropic polyomavirus (LPV) are also present in huma

56 simian virus 40, simian agent 12 [Sa12], and lymphotropic polyomavirus) and rodent (hamster polyomavi

57 by the viral vector coupled with the innate lymphotropic properties of adenovirus.

58 The human T-lymphotropic retrovirus type-I trans-activator, Tax, has

59 virus type 1 (HTLV-1) is a persistent CD4+ T-lymphotropic retrovirus.

60 tant translation regulatory axis of multiple lymphotropic retroviruses.

61 o that of other pathogenic and nonpathogenic lymphotropic SIVs.

62 ptible to infection with a macrophage than a lymphotropic strain of human immunodeficiency virus type

63 wing transfection of murine fibroblasts, the lymphotropic strain of minute virus of mice (MVMi) does

64 ours after the intravenous administration of lymphotropic superparamagnetic nanoparticles (2.6 mg of

65 MRI with lymphotropic superparamagnetic nanoparticles correctly i

66 We investigated whether highly lymphotropic superparamagnetic nanoparticles, which gain

67 We detected biphasic lymphotropic transport of prions from the initial entry

68 of a small signaling protein, ORF5, of the T-lymphotropic tumor virus herpesvirus saimiri (HVS).

69 n of herpesvirus saimiri (HVS), which is a T-lymphotropic tumor virus, interacts with cellular Lck ty

70 p of herpesvirus saimiri (HVS), which is a T-lymphotropic tumor virus, is constitutively targeted to

71 Lymphotropic viral dissemination was commensurate with a

72 an immunodeficiency virus (HIV), and human T-lymphotropic virus (HTLV) among tissue donors.

73 rom the consequences associated with human T lymphotropic virus (HTLV) infection.

74 cells in patients infected with human T cell lymphotropic virus (HTLV) is associated with expression

75 nding the immunopathogenesis of human T cell lymphotropic virus (HTLV) type I-associated myelopathy/t

76 for susceptibility to infection with human T lymphotropic virus (HTLV) type I.

77 ple from Central Africa identified 2 human T-lymphotropic virus (HTLV)-4-infected individuals.

78 The human T lymphotropic virus (HTLV)-I or -II proviral load (VL) ma

79 High human T lymphotropic virus (HTLV)-I provirus load (VL) has been

80 udies support sexual transmission of human T lymphotropic virus (HTLV)-I/II; however, prospective inc

81 for the study of vaccination against human T lymphotropic virus (HTLV).

82 ), human papilloma virus (HPV), human T-cell lymphotropic virus (HTLV-1) and Kaposi's associated sarc

83 hal hepatitis C virus (HCV) and human T-cell lymphotropic virus (HTLV-1) can be used to investigate p

84 while hunting, 7 were infected with human T lymphotropic virus (HTLV-1).

85 Baboons naturally infected with simian T lymphotropic virus (STLV) are a potentially useful model

86 he prevalence and diversity of simian T-cell lymphotropic virus (STLV) isolates within the long-estab

87 vide fundamental information on the simian T lymphotropic virus (STLV) naturally transmitted in a col

88 immunodeficiency virus (SIV), simian T-cell lymphotropic virus (STLV), simian type D retrovirus (SRV

89 ain that was closely related to the simian T lymphotropic virus (STLV-1) that infects this monkey spe

90 retroviruses are common in animals, human T-lymphotropic virus 1 (HTLV-1) is the only transmissible

91 studies suggest that infection with human T-lymphotropic virus 1 (HTLV-1) might be associated with b

92 genic activation of NF-kappaB by the human T-lymphotropic virus 1 (HTLV-1) oncoprotein Tax immediatel

93 progressive myelopathies, including human T-lymphotropic virus 1 (HTLV-1)-associated myelopathy/trop

94 n several cell types, including human T-cell lymphotropic virus 1 (HTLV-1)-infected cell lines.

95 all known viral genomes and discover human T-lymphotropic virus 1 integrations in six samples in a re

96 e human immunodeficiency virus, human T-cell lymphotropic virus and murine leukaemia virus are believ

97 GBV-C is a lymphotropic virus capable of persistent infection.

98 two of 2,831 (0.07%) were positive for human lymphotropic virus enzyme immunoassay, and none of 2,831

99 ell leukemia (ATL) is caused by human T-cell lymphotropic virus I (HTLV-1) and is an aggressive malig

100 ntributes to the persistence of human T cell lymphotropic virus I viral-specific CD8 cells.

101 eta1 in groups of patients with human T cell lymphotropic virus I-associated myelopathy/tropical spas

102 the neurological disease termed human T cell lymphotropic virus I-associated myelopathy/tropical spas

103 of HLA molecules improves human immunity to lymphotropic virus infections in humanized mice.

104 KSHV is a lymphotropic virus that has pirated many mammalian genes

105 that can be productively infected by human T-lymphotropic virus type 1 (HTLV-1) and can spread HTLV-1

106 The prevalence of human T-cell lymphotropic virus type 1 (HTLV-1) and hepatitis B virus

107 Human T-lymphotropic virus type 1 (HTLV-1) and HTLV-2 are preval

108 Human T lymphotropic virus type 1 (HTLV-1) and HTLV-2 are relate

109 Human T-cell lymphotropic virus type 1 (HTLV-1) and HTLV-2 encode aux

110 individual integration sites of human T-cell lymphotropic virus type 1 (HTLV-1) and human immunodefic

111 Human T lymphotropic virus type 1 (HTLV-1) appears to persist in

112 Human T-lymphotropic virus type 1 (HTLV-1) causes adult T-cell l

113 Human T-cell lymphotropic virus type 1 (HTLV-1) causes adult T-cell l

114 Human T-cell lymphotropic virus type 1 (HTLV-1) causes adult T-cell l

115 Human T-lymphotropic virus type 1 (HTLV-1) encodes a transcripti

116 Human T-lymphotropic virus type 1 (HTLV-1) encodes the viral pro

117 teract with a TG-rich element in the human T-lymphotropic virus type 1 (HTLV-1) enhancer thought to m

118 Human T-lymphotropic virus type 1 (HTLV-1) envelope (Env) glycop

119 Human T-cell lymphotropic virus type 1 (HTLV-1) establishes persisten

120 tivation, rather than repression, of human T lymphotropic virus type 1 (HTLV-1) expression, while YY1

121 For example, human T-cell lymphotropic virus type 1 (HTLV-1) has been reported to

122 ity of dendritic cells (DCs) to human T-cell lymphotropic virus type 1 (HTLV-1) infection and the def

123 the past 25 years, animal models of human T-lymphotropic virus type 1 (HTLV-1) infection and transfo

124 Human T-lymphotropic virus type 1 (HTLV-1) infection causes adul

125 Human T-lymphotropic virus type 1 (HTLV-1) infection causes adul

126 We recently reported that human T-lymphotropic virus type 1 (HTLV-1) infection is accompan

127 Human T-cell lymphotropic virus type 1 (HTLV-1) infection is endemic

128 The proviral load in human T cell lymphotropic virus type 1 (HTLV-1) infection is typicall

129 ding puzzle on progression from Human T-cell Lymphotropic Virus Type 1 (HTLV-1) infection to lethal A

130 s that analyzed the effect of A3G on human T-lymphotropic virus type 1 (HTLV-1) infectivity resulted

131 Human T-lymphotropic virus type 1 (HTLV-1) is a causative agent

132 Human T-lymphotropic virus type 1 (HTLV-1) is a complex retrovir

133 Human T-cell lymphotropic virus type 1 (HTLV-1) is a deltaretrovirus

134 Human T-lymphotropic virus type 1 (HTLV-1) is a pathogenic retro

135 Human T-lymphotropic virus type 1 (HTLV-1) is a persistent CD4+

136 Human T-lymphotropic virus type 1 (HTLV-1) is an exogenous retro

137 Infection with human T lymphotropic virus type 1 (HTLV-1) is associated with th

138 Human T-lymphotropic virus type 1 (HTLV-1) is etiologically asso

139 Human T-lymphotropic virus type 1 (HTLV-1) is linked to multiple

140 Human T-lymphotropic virus type 1 (HTLV-1) is the agent of an ag

141 Human T-cell lymphotropic virus type 1 (HTLV-1) is the agent of HTLV-

142 Human T-lymphotropic virus type 1 (HTLV-1) is the causative agen

143 Human T-lymphotropic virus type 1 (HTLV-1) is the causative agen

144 Human T-lymphotropic virus type 1 (HTLV-1) is the causative agen

145 Human T-lymphotropic virus type 1 (HTLV-1) is the etiologic agen

146 Human T-cell lymphotropic virus type 1 (HTLV-1) is the etiologic agen

147 Human T lymphotropic virus type 1 (HTLV-1) is the etiologic agen

148 Human T-lymphotropic virus type 1 (HTLV-1) is the etiological ag

149 Human T-lymphotropic virus type 1 (HTLV-1) is the etiological ag

150 ased Tax transactivation of the human T-cell lymphotropic virus type 1 (HTLV-1) long terminal repeat

151 Human T lymphotropic virus type 1 (HTLV-1) mainly causes adult T

152 ctroscopy was used to study the human T-cell lymphotropic virus type 1 (HTLV-1) nucleocapsid protein

153 The human T-cell lymphotropic virus type 1 (HTLV-1) oncoprotein Tax is im

154 Serological screening for human T-lymphotropic virus type 1 (HTLV-1) parallels the standar

155 Human T-lymphotropic virus type 1 (HTLV-1) persists by driving c

156 Human T-cell lymphotropic virus type 1 (HTLV-1) screening of blood an

157 The human T-lymphotropic virus type 1 (HTLV-1) Tax binds the anaphas

158 reviously demonstrated that the human T-cell lymphotropic virus type 1 (HTLV-1) Tax can inactivate p5

159 Human T-lymphotropic virus type 1 (HTLV-1) Tax exerts pleiotropi

160 We report here that human T-lymphotropic virus type 1 (HTLV-1) Tax interacts with th

161 In our studies of the human T-cell lymphotropic virus type 1 (HTLV-1) Tax oncoprotein, we h

162 Human T-lymphotropic virus type 1 (HTLV-1) transcription is cont

163 y, we analyzed the effect of Brd4 on human T-lymphotropic virus type 1 (HTLV-1) transcription.

164 Cell-free human T-lymphotropic virus type 1 (HTLV-1) virions are poorly in

165 aggressive subtype) associated with human T-lymphotropic virus type 1 (HTLV-1) were analyzed using c

166 Virus (BLV) and humans infected with Human T Lymphotropic Virus type 1 (HTLV-1) which together with e

167 on in individuals infected with human T-cell lymphotropic virus type 1 (HTLV-1), a real-time quantita

168 The Tax protein of human T-lymphotropic virus type 1 (HTLV-1), an oncoprotein that

169 y the pX open reading frame I of the human T-lymphotropic virus type 1 (HTLV-1), is a hydrophobic pro

170 ransmission of retroviruses, such as human T lymphotropic virus type 1 (HTLV-1), is well documented,

171 Human T-lymphotropic virus type 1 (HTLV-1), the etiological agen

172 mbinant strain had been observed for human T-lymphotropic virus type 1 (HTLV-1), the first isolated h

173 evaluated for the treatment of human T cell lymphotropic virus type 1 (HTLV-1)-associated disease.

174 Human T-lymphotropic virus type 1 (HTLV-1)-associated myelopathy

175 ar mimicry, we studied patients with human T-lymphotropic virus type 1 (HTLV-1)-associated myelopathy

176 Human T-cell lymphotropic virus type 1 (HTLV-1)-associated myelopathy

177 ive neurologic diseases such as human T-cell lymphotropic virus type 1 (HTLV-1)-associated myelopathy

178 nts over a 10-year period, in a human T-cell lymphotropic virus type 1 (HTLV-1)-endemic area of Centr

179 Treatment of HIV-1- and human T-cell lymphotropic virus type 1 (HTLV-1)-infected cells with 2

180 Most human T-lymphotropic virus type 1 (HTLV-1)-infected HeLa and Sup

181 re currently 5 million to 10 million human T-lymphotropic virus type 1 (HTLV-1)-infected people, and

182 odeficiency virus type 1 (HIV-1) and human T-lymphotropic virus type 1 (HTLV-1).

183 mbrane binding of a deltaretrovirus, human T-lymphotropic virus type 1 (HTLV-1).

184 , Rous sarcoma virus (RSV), and human T-cell lymphotropic virus type 1 (HTLV-1).

185 omaleukemia (ATLL) is caused by human T-cell lymphotropic virus type 1 (HTLV-1).

186 e etiological agent of which is human T-cell lymphotropic virus type 1 (HTLV-1).

187 ciency virus type 1 (HIV-1) and human T cell lymphotropic virus type 1 (HTLV-1).

188 si's sarcoma herpesvirus (KSHV), and human T-lymphotropic virus type 1 (HTLV-1).

189 tive dermatitis associated with human T-cell lymphotropic virus type 1 (HTLV-1; IDH) is a chronic rec

190 ncy syndrome (AIDS) and infection with human lymphotropic virus type 1 (HTLV-I) causing HTLV-I-associ

191 and CD4(+) T cell response against simian T-lymphotropic virus type 1 (STLV-1), a virus closely rela

192 o delta-retroviruses, including human T cell lymphotropic virus type 1 and 2 (HTLV-1 and HTLV-2) and

193 osi's sarcoma herpesvirus (KSHV) and human T-lymphotropic virus type 1 are major contributors to onco

194 proteins, adenovirus type 9 E4-ORF1, human T-lymphotropic virus type 1 Tax, and high-risk human papil

195 ssociated myelopathy (HAM; HTLV-1 is human T-lymphotropic virus type 1) is a chronic debilitating neu

196 gh breastmilk: cytomegalovirus, human T-cell lymphotropic virus type 1, and HIV.

197 virus type 1 (HTLV-1), also known as human T lymphotropic virus type 1, was the first exogenous human

198 binding for the Gag matrix domain of human T-lymphotropic virus type 1, which provides insight into e

199 ure demonstrating high expression of human T-lymphotropic virus type 1-induced genes.

200 rization of the Gag matrix domain of Human T-lymphotropic virus Type 1.

201 +)CD25(+) lymphocytes caused by human T-cell lymphotropic virus type 1.

202 ulations from subjects infected with human T-lymphotropic virus type 1; (ii) T cell antigen receptor

203 Coinfection with human T-cell lymphotropic virus type 2 (HTLV-2) and human immunodefic

204 Human T-lymphotropic virus type 3 (HTLV-3) is a new virus recent

205 ly discovered human retrovirus, human T-cell lymphotropic virus type 3 (HTLV-3).

206 cterization of the newly described primate T-lymphotropic virus type 3 (PTLV-3).

207 Simian T-cell lymphotropic virus type 3 (STLV-3) is almost identical t

208 TLV-2 but is genetically similar to simian T-lymphotropic virus type 3 (STLV-3).

209 Human T-cell lymphotropic virus type I (HTLV-1) is an oncogenic retro

210 The human T-cell lymphotropic virus type I (HTLV-1) Tax transactivator in

211 The human T-lymphotropic virus type I (HTLV-I) causes a chronic infl

212 Human T-lymphotropic virus type I (HTLV-I) causes chronic infect

213 ne, hepatitis B virus (HBV) gene and human T-lymphotropic virus type I (HTLV-I) gene.

214 no et al., who demonstrate that human T cell lymphotropic virus type I (HTLV-I) infection of CD4(+)CD

215 l analysis of 308 Jamaican children, human T lymphotropic virus type I (HTLV-I) infection was found t

216 luding HAM/TSP, associated with human T-cell lymphotropic virus type I (HTLV-I) infection, and multip

217 le associated with susceptibility to human T lymphotropic virus type I (HTLV-I) infection, we examine

218 Human T lymphotropic virus type I (HTLV-I) is endemic in souther

219 Human T cell lymphotropic virus type I (HTLV-I) is sexually transmitt

220 Human T-cell lymphotropic virus type I (HTLV-I) is the etiologic agen

221 It is thought that human T-cell lymphotropic virus type I (HTLV-I) preferentially infect

222 We quantitatively identified human T-cell lymphotropic virus type I (HTLV-I) Tax(11-19) peptide-sp

223 Expression of the human T lymphotropic virus type I (HTLV-I) transactivator/oncopr

224 ciation between mother-to-child human T cell lymphotropic virus type I (HTLV-I) transmission and huma

225 conducted a longitudinal analysis of human T lymphotropic virus type I (HTLV-I) viral markers in 28 J

226 toimmune disease, from patients with human T lymphotropic virus type I (HTLV-I)-associated myelopathy

227 nervous system inflammation in human T-cell lymphotropic virus type I (HTLV-I)-associated myelopathy

228 Human T-lymphotropic virus type I (HTLV-I)-associated myelopathy

229 Human T lymphotropic virus type I (HTLV-I)-associated myelopathy

230 ells (PBMCs) from patients with human T-cell lymphotropic virus type I (HTLV-I)-associated myelopathy

231 Adult T-cell leukemia (ATL) and human T-cell lymphotropic virus type I (HTLV-I)-associated myelopathy

232 adult T-cell leukemia (ATL) is human T cell lymphotropic virus type I (HTLV-I).

233 increased in diseases caused by human T cell lymphotropic virus type I (HTLV-I).

234 Aspects of human T cell lymphotropic virus type I biology, host genetic suscepti

235 s illustrated in this report using a human T-lymphotropic virus type I gene fragment.

236 is the exclusive target of the human T-cell lymphotropic virus type I oncoprotein Tax.

237 The human T-cell lymphotropic virus type I protein, Tax, which is critica

238 Human T-cell lymphotropic virus type I proviral load in cerebrospinal

239 lear cells, and a high ratio of human T-cell lymphotropic virus type I proviral load in cerebrospinal

240 We measured human T-cell lymphotropic virus type I proviral load in cerebrospinal

241 reduced HIV-1 plasma viral load and human T-lymphotropic virus type I proviral load in infected pati

242 To date, high human T-cell lymphotropic virus type I proviral load in patients with

243 ultinucleated cells, similar to human T-cell lymphotropic virus type I Tax-expressing cells.

244 Human T-cell lymphotropic virus type I Tax-specific CD8+ T cells, as

245 agnosis include infections with HIV, human T-lymphotropic virus type I, or hepatitis C virus.

246 ell population in patients with human T cell lymphotropic virus type I-associated (HTLV-I-associated)

247 y a role in the pathogenesis of human T-cell lymphotropic virus type I-associated myelopathy/tropical

248 proviral load in patients with human T-cell lymphotropic virus type I-associated myelopathy/tropical

249 related to the pathogenesis of human T-cell lymphotropic virus type I-associated myelopathy/tropical

250 cerebrospinal fluid cells from human T-cell lymphotropic virus type I-associated myelopathy/tropical

251 Human T cell lymphotropic virus type I-associated myelopathy/tropical

252 echanisms that are operative in human T cell lymphotropic virus type I-associated myelopathy/tropical

253 ggest that accumulation of both human T-cell lymphotropic virus type I-infected cells and preferentia

254 s and preferential expansion of human T-cell lymphotropic virus type I-specific CD8+ cells in cerebro

255 r-536 in the presence of Tax in human T-cell lymphotropic virus type I-transformed cells.

256 k of mother-to-child transmission of human T lymphotropic virus type I.

257 Infection with human T lymphotropic virus type II (HTLV-II) has been linked to

258 immunodeficiency virus (HIV) and/or human T-lymphotropic virus type II (HTLV-II) is common among dru

259 whom may be coinfected with HIV and human T-lymphotropic virus type II (HTLV-II), are at high risk f

260 sociated polymerase activity of human T-cell lymphotropic virus type-1 (HTLV-1) are due to the quanti

261 a/lymphoma (ATL) resulting from human T-cell lymphotropic virus type-1 (HTLV-1) infection develop hum

262 Human T-lymphotropic virus type-1 (HTLV-1) persists within hosts

263 cular and genetic factors induced by human T-lymphotropic virus type-1 (HTLV-1) that initiate adult T

264 te (DIS) of the deltaretrovirus human T-cell lymphotropic virus type-I (HTLV-I) has been previously l

265 egulated during transmission of human T-cell lymphotropic virus type-I (HTLV-I) to primary T cells in

266 aggressive malignancy caused by human T cell lymphotropic virus type-I (HTLV-I) without curative trea

267 protein levels are increased in human T cell lymphotropic virus type-I (HTLV-I)-associated adult T ce

268 s virus, Orientia tsutsugamushi, and human T lymphotropic virus types 1 and 2.

269 Human T lymphotropic virus types I and II (HTLV-I/II) Western bl

270 ; hepatitis B virus [HBV], HIV, human T-cell lymphotropic virus types I and II, hepatitis C virus [HC

271 sarcoma-associated herpesvirus (KSHV) is a B-lymphotropic virus whose primary site of replication is

272 , human immunodeficiency virus, human T-cell lymphotropic virus, and bacterial contamination, stratif

273 Though first described as a lymphotropic virus, human herpesvirus 6 (HHV-6) is highl

274 The human T-cell lymphotropic virus, type (HTLV)-1 trans-activator, Tax,

275 We showed recently that the human T-lymphotropic virus, type 1 (HTLV-1), spreads directly fr

276 we examined the response of the human T cell lymphotropic virus-1 (HTLV-1) Tax-specific T cell recept

277 es (HBV and HCV, respectively), human T cell lymphotropic virus-1 (HTLV-1), and Kaposi's sarcoma herp

278 cription from DNA constructs of human T-cell lymphotropic virus-1 (HTLV-1), which use the same primer

279 al T-cell malignancy due to the human T-cell lymphotropic virus-1 (HTLV-1).

280 , human immunodeficiency virus, human T-cell lymphotropic virus-1, Helicobacter pylori, hepatitis C,

281 ies of the molecular biology of human T cell lymphotropic virus-1-induced T cell leukemia/lymphoma ha

282 tis B virus, hepatitis C virus, human T-cell lymphotropic virus-1/2, syphilis) given double weight co

283 rent pathophysiologic basis for human T cell lymphotropic virus-associated leukemia/lymphoma as well

284 show that DUB-2 is expressed in human T-cell lymphotropic virus-I (HTLV-1)-transformed T cells that e

285 urface antigen, hepatitis C virus, and human lymphotropic virus.

286 titis B and C viruses, HIV, and human T-cell lymphotropic virus.

287 sed by EBV, hepatitis B, C, and human T cell lymphotropic virus.

288 cts of Ikaros on the life cycle of any human lymphotropic virus.

289 The human T-lymphotropic viruses (HTLVs) types 1 and 2 originated in

290 are related to distinct lineages of simian T-lymphotropic viruses (STLV-1 and STLV-2, respectively).

291 One possibility is that KSHV, like the lymphotropic viruses Epstein-Barr virus (EBV) and human

292 ure that facilitates the transfer of certain lymphotropic viruses into uninfected T cells.

293 Some herpesviruses, particularly lymphotropic viruses such as Marek's disease virus (MDV)

294 For lymphotropic viruses such as the human immunodeficiency

295 Gammaherpesviruses are lymphotropic viruses that are associated with the develo

296 log, murine gammaherpesvirus 68 (MHV68), are lymphotropic viruses that establish latent infection in

297 Human T-lymphotropic viruses type 1 and 2 (HTLV-1/2) are prevale

298 Human T-lymphotropic viruses types I and II (HTLV-I and HTLV-II)

299 Other lymphotropic viruses, such as HIV-1, may similarly subve

300 imian counterparts, HTLVs form the primate T-lymphotropic viruses.