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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 reported that hepatitis C virus (HCV) may be lymphotropic in the setting of human immunodeficiency vi
53                              Infections of a lymphotropic nature are caused by cytomegalovirus, HSV-6
54  caused by Marek's disease virus (MDV), is a lymphotropic neoplastic disease.
55                                            A lymphotropic papovavirus (LPV) archetypal regulatory reg
56 lyomaviruses, simian virus (SV)40 and B-cell lymphotropic polyomavirus (LPV) are also present in huma
57 simian virus 40, simian agent 12 [Sa12], and lymphotropic polyomavirus) and rodent (hamster polyomavi
58  by the viral vector coupled with the innate lymphotropic properties of adenovirus.
59                                  The human T-lymphotropic retrovirus type-I trans-activator, Tax, has
60 virus type 1 (HTLV-1) is a persistent CD4+ T-lymphotropic retrovirus.
61 tant translation regulatory axis of multiple lymphotropic retroviruses.
62 o that of other pathogenic and nonpathogenic lymphotropic SIVs.
63 ptible to infection with a macrophage than a lymphotropic strain of human immunodeficiency virus type
64 wing transfection of murine fibroblasts, the lymphotropic strain of minute virus of mice (MVMi) does
65 ours after the intravenous administration of lymphotropic superparamagnetic nanoparticles (2.6 mg of
66                                     MRI with lymphotropic superparamagnetic nanoparticles correctly i
67               We investigated whether highly lymphotropic superparamagnetic nanoparticles, which gain
68                         We detected biphasic lymphotropic transport of prions from the initial entry
69 of a small signaling protein, ORF5, of the T-lymphotropic tumor virus herpesvirus saimiri (HVS).
70 n of herpesvirus saimiri (HVS), which is a T-lymphotropic tumor virus, interacts with cellular Lck ty
71 p of herpesvirus saimiri (HVS), which is a T-lymphotropic tumor virus, is constitutively targeted to
72                                              Lymphotropic viral dissemination was commensurate with a
73 an immunodeficiency virus (HIV), and human T-lymphotropic virus (HTLV) among tissue donors.
74 rom the consequences associated with human T lymphotropic virus (HTLV) infection.
75 cells in patients infected with human T cell lymphotropic virus (HTLV) is associated with expression
76 nding the immunopathogenesis of human T cell lymphotropic virus (HTLV) type I-associated myelopathy/t
77 for susceptibility to infection with human T lymphotropic virus (HTLV) type I.
78 ple from Central Africa identified 2 human T-lymphotropic virus (HTLV)-4-infected individuals.
79                                  The human T lymphotropic virus (HTLV)-I or -II proviral load (VL) ma
80                                 High human T lymphotropic virus (HTLV)-I provirus load (VL) has been
81 udies support sexual transmission of human T lymphotropic virus (HTLV)-I/II; however, prospective inc
82 for the study of vaccination against human T lymphotropic virus (HTLV).
83 ), human papilloma virus (HPV), human T-cell lymphotropic virus (HTLV-1) and Kaposi's associated sarc
84 hal hepatitis C virus (HCV) and human T-cell lymphotropic virus (HTLV-1) can be used to investigate p
85  while hunting, 7 were infected with human T lymphotropic virus (HTLV-1).
86     Baboons naturally infected with simian T lymphotropic virus (STLV) are a potentially useful model
87 he prevalence and diversity of simian T-cell lymphotropic virus (STLV) isolates within the long-estab
88 vide fundamental information on the simian T lymphotropic virus (STLV) naturally transmitted in a col
89  immunodeficiency virus (SIV), simian T-cell lymphotropic virus (STLV), simian type D retrovirus (SRV
90 ain that was closely related to the simian T lymphotropic virus (STLV-1) that infects this monkey spe
91  retroviruses are common in animals, human T-lymphotropic virus 1 (HTLV-1) is the only transmissible
92  studies suggest that infection with human T-lymphotropic virus 1 (HTLV-1) might be associated with b
93 genic activation of NF-kappaB by the human T-lymphotropic virus 1 (HTLV-1) oncoprotein Tax immediatel
94  progressive myelopathies, including human T-lymphotropic virus 1 (HTLV-1)-associated myelopathy/trop
95 n several cell types, including human T-cell lymphotropic virus 1 (HTLV-1)-infected cell lines.
96 all known viral genomes and discover human T-lymphotropic virus 1 integrations in six samples in a re
97 e human immunodeficiency virus, human T-cell lymphotropic virus and murine leukaemia virus are believ
98                                   GBV-C is a lymphotropic virus capable of persistent infection.
99 two of 2,831 (0.07%) were positive for human lymphotropic virus enzyme immunoassay, and none of 2,831
100 ell leukemia (ATL) is caused by human T-cell lymphotropic virus I (HTLV-1) and is an aggressive malig
101 ntributes to the persistence of human T cell lymphotropic virus I viral-specific CD8 cells.
102 eta1 in groups of patients with human T cell lymphotropic virus I-associated myelopathy/tropical spas
103 the neurological disease termed human T cell lymphotropic virus I-associated myelopathy/tropical spas
104  of HLA molecules improves human immunity to lymphotropic virus infections in humanized mice.
105                                    KSHV is a lymphotropic virus that has pirated many mammalian genes
106 that can be productively infected by human T-lymphotropic virus type 1 (HTLV-1) and can spread HTLV-1
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-cell 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-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                    For example, human T-cell lymphotropic virus type 1 (HTLV-1) has been reported to
121 ity of dendritic cells (DCs) to human T-cell lymphotropic virus type 1 (HTLV-1) infection and the def
122  the past 25 years, animal models of human T-lymphotropic virus type 1 (HTLV-1) infection and transfo
123                                      Human T-lymphotropic virus type 1 (HTLV-1) infection causes adul
124                                      Human T-lymphotropic virus type 1 (HTLV-1) infection causes adul
125            We recently reported that human T-lymphotropic virus type 1 (HTLV-1) infection is accompan
126                                 Human T-cell lymphotropic virus type 1 (HTLV-1) infection is endemic
127            The proviral load in human T cell lymphotropic virus type 1 (HTLV-1) infection is typicall
128 ding puzzle on progression from Human T-cell Lymphotropic Virus Type 1 (HTLV-1) infection to lethal A
129 s that analyzed the effect of A3G on human T-lymphotropic virus type 1 (HTLV-1) infectivity resulted
130                                      Human T-lymphotropic virus type 1 (HTLV-1) is a causative agent
131                                      Human T-lymphotropic virus type 1 (HTLV-1) is a complex retrovir
132                                      Human T-lymphotropic virus type 1 (HTLV-1) is a complex retrovir
133                                      Human T-lymphotropic virus type 1 (HTLV-1) is a pathogenic retro
134                                      Human T-lymphotropic virus type 1 (HTLV-1) is a persistent CD4+
135                                      Human T-lymphotropic virus type 1 (HTLV-1) is an exogenous retro
136                                 Human T-cell lymphotropic virus type 1 (HTLV-1) is associated with ad
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 CBP)/p300-binding domain of the human T-cell lymphotropic virus type 1 (HTLV-1) transactivator, Tax,
163                                      Human T-lymphotropic virus type 1 (HTLV-1) transcription is cont
164 y, we analyzed the effect of Brd4 on human T-lymphotropic virus type 1 (HTLV-1) transcription.
165                            Cell-free human T-lymphotropic virus type 1 (HTLV-1) virions are poorly in
166  aggressive subtype) associated with human T-lymphotropic virus type 1 (HTLV-1) were analyzed using c
167 Virus (BLV) and humans infected with Human T Lymphotropic Virus type 1 (HTLV-1) which together with e
168 on in individuals infected with human T-cell lymphotropic virus type 1 (HTLV-1), a real-time quantita
169                   The Tax protein of human T-lymphotropic virus type 1 (HTLV-1), an oncoprotein that
170 y the pX open reading frame I of the human T-lymphotropic virus type 1 (HTLV-1), is a hydrophobic pro
171 ransmission of retroviruses, such as human T lymphotropic virus type 1 (HTLV-1), is well documented,
172                                      Human T-lymphotropic virus type 1 (HTLV-1), the etiological agen
173 mbinant strain had been observed for human T-lymphotropic virus type 1 (HTLV-1), the first isolated h
174  evaluated for the treatment of human T cell lymphotropic virus type 1 (HTLV-1)-associated disease.
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 , Rous sarcoma virus (RSV), and human T-cell lymphotropic virus type 1 (HTLV-1).
183 omaleukemia (ATLL) is caused by human T-cell lymphotropic virus type 1 (HTLV-1).
184 e etiological agent of which is human T-cell lymphotropic virus type 1 (HTLV-1).
185 ciency virus type 1 (HIV-1) and human T cell lymphotropic virus type 1 (HTLV-1).
186 si's sarcoma herpesvirus (KSHV), and human T-lymphotropic virus type 1 (HTLV-1).
187 odeficiency virus type 1 (HIV-1) and human T-lymphotropic virus type 1 (HTLV-1).
188 mbrane binding of a deltaretrovirus, 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 ible macaques were seropositive for simian T-lymphotropic virus type 1 may suggests a role for this v
195 proteins, adenovirus type 9 E4-ORF1, human T-lymphotropic virus type 1 Tax, and high-risk human papil
196 ssociated myelopathy (HAM; HTLV-1 is human T-lymphotropic virus type 1) is a chronic debilitating neu
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  of the p53 tumor suppressor in human T-cell lymphotropic virus type 2 (HTLV-2)-transformed cells.
205                                      Human T-lymphotropic virus type 3 (HTLV-3) is a new virus recent
206 ly discovered human retrovirus, human T-cell lymphotropic virus type 3 (HTLV-3).
207 cterization of the newly described primate T-lymphotropic virus type 3 (PTLV-3).
208                                Simian T-cell lymphotropic virus type 3 (STLV-3) is almost identical t
209 TLV-2 but is genetically similar to simian T-lymphotropic virus type 3 (STLV-3).
210                                 Human T-cell lymphotropic virus type I (HTLV-1) is an oncogenic retro
211                             The human T-cell lymphotropic virus type I (HTLV-1) Tax transactivator in
212                                  The human T-lymphotropic virus type I (HTLV-I) causes a chronic infl
213                                      Human T-lymphotropic virus type I (HTLV-I) causes chronic infect
214 ne, hepatitis B virus (HBV) gene and human T-lymphotropic virus type I (HTLV-I) gene.
215 no et al., who demonstrate that human T cell lymphotropic virus type I (HTLV-I) infection of CD4(+)CD
216 l analysis of 308 Jamaican children, human T lymphotropic virus type I (HTLV-I) infection was found t
217 le associated with susceptibility to human T lymphotropic virus type I (HTLV-I) infection, we examine
218                                 Human T cell lymphotropic virus type I (HTLV-I) is associated with a
219                                      Human T lymphotropic virus type I (HTLV-I) is endemic in souther
220                                 Human T cell lymphotropic virus type I (HTLV-I) is sexually transmitt
221                                 Human T-cell lymphotropic virus type I (HTLV-I) is the etiologic agen
222                                      Human T lymphotropic virus type I (HTLV-I) is the etiological ag
223              It is thought that human T-cell lymphotropic virus type I (HTLV-I) preferentially infect
224    We quantitatively identified human T-cell lymphotropic virus type I (HTLV-I) Tax(11-19) peptide-sp
225                    Expression of the human T lymphotropic virus type I (HTLV-I) transactivator/oncopr
226                                 Human T-cell lymphotropic virus type I (HTLV-I) transforms T cells in
227 ciation between mother-to-child human T cell lymphotropic virus type I (HTLV-I) transmission and huma
228 conducted a longitudinal analysis of human T lymphotropic virus type I (HTLV-I) viral markers in 28 J
229 toimmune disease, from patients with human T lymphotropic virus type I (HTLV-I)-associated myelopathy
230  nervous system inflammation in human T-cell lymphotropic virus type I (HTLV-I)-associated myelopathy
231                                      Human T-lymphotropic virus type I (HTLV-I)-associated myelopathy
232                                      Human T lymphotropic virus type I (HTLV-I)-associated myelopathy
233 ells (PBMCs) from patients with human T-cell lymphotropic virus type I (HTLV-I)-associated myelopathy
234 Adult T-cell leukemia (ATL) and human T-cell lymphotropic virus type I (HTLV-I)-associated myelopathy
235  adult T-cell leukemia (ATL) is human T cell lymphotropic virus type I (HTLV-I).
236 increased in diseases caused by human T cell lymphotropic virus type I (HTLV-I).
237                      Aspects of human T cell lymphotropic virus type I biology, host genetic suscepti
238 s illustrated in this report using a human T-lymphotropic virus type I gene fragment.
239  is the exclusive target of the human T-cell lymphotropic virus type I oncoprotein Tax.
240                             The human T-cell lymphotropic virus type I protein, Tax, which is critica
241                                 Human T-cell lymphotropic virus type I proviral load in cerebrospinal
242 lear cells, and a high ratio of human T-cell lymphotropic virus type I proviral load in cerebrospinal
243                     We measured human T-cell lymphotropic virus type I proviral load in cerebrospinal
244  reduced HIV-1 plasma viral load and human T-lymphotropic virus type I proviral load in infected pati
245                   To date, high human T-cell lymphotropic virus type I proviral load in patients with
246 ultinucleated cells, similar to human T-cell lymphotropic virus type I Tax-expressing cells.
247                                 Human T-cell lymphotropic virus type I Tax-specific CD8+ T cells, as
248 agnosis include infections with HIV, human T-lymphotropic virus type I, or hepatitis C virus.
249 ell population in patients with human T cell lymphotropic virus type I-associated (HTLV-I-associated)
250 y a role in the pathogenesis of human T-cell lymphotropic virus type I-associated myelopathy/tropical
251  proviral load in patients with human T-cell lymphotropic virus type I-associated myelopathy/tropical
252  related to the pathogenesis of human T-cell lymphotropic virus type I-associated myelopathy/tropical
253  cerebrospinal fluid cells from human T-cell lymphotropic virus type I-associated myelopathy/tropical
254                                 Human T cell lymphotropic virus type I-associated myelopathy/tropical
255 echanisms that are operative in human T cell lymphotropic virus type I-associated myelopathy/tropical
256 ggest that accumulation of both human T-cell lymphotropic virus type I-infected cells and preferentia
257 s and preferential expansion of human T-cell lymphotropic virus type I-specific CD8+ cells in cerebro
258 r-536 in the presence of Tax in human T-cell lymphotropic virus type I-transformed cells.
259    NILR protein was detected on human T cell lymphotropic virus type I-transformed T cell lines, Raji
260 k of mother-to-child transmission of human T lymphotropic virus type I.
261                       Infection with human T lymphotropic virus type II (HTLV-II) has been linked to
262  immunodeficiency virus (HIV) and/or human T-lymphotropic virus type II (HTLV-II) is common among dru
263  whom may be coinfected with HIV and human T-lymphotropic virus type II (HTLV-II), are at high risk f
264 sociated polymerase activity of human T-cell lymphotropic virus type-1 (HTLV-1) are due to the quanti
265 a/lymphoma (ATL) resulting from human T-cell lymphotropic virus type-1 (HTLV-1) infection develop hum
266 cular and genetic factors induced by human T-lymphotropic virus type-1 (HTLV-1) that initiate adult T
267 te (DIS) of the deltaretrovirus human T-cell lymphotropic virus type-I (HTLV-I) has been previously l
268 egulated during transmission of human T-cell lymphotropic virus type-I (HTLV-I) to primary T cells in
269 aggressive malignancy caused by human T cell lymphotropic virus type-I (HTLV-I) without curative trea
270 protein levels are increased in human T cell lymphotropic virus type-I (HTLV-I)-associated adult T ce
271 s virus, Orientia tsutsugamushi, and human T lymphotropic virus types 1 and 2.
272                                      Human T lymphotropic virus types I and II (HTLV-I/II) Western bl
273 sarcoma-associated herpesvirus (KSHV) is a B-lymphotropic virus whose primary site of replication is
274 , human immunodeficiency virus, human T-cell lymphotropic virus, and bacterial contamination, stratif
275                  Though first described as a lymphotropic virus, human herpesvirus 6 (HHV-6) is highl
276                             The human T-cell lymphotropic virus, type (HTLV)-1 trans-activator, Tax,
277          We showed recently that the human T-lymphotropic virus, type 1 (HTLV-1), spreads directly fr
278 we examined the response of the human T cell lymphotropic virus-1 (HTLV-1) Tax-specific T cell recept
279 es (HBV and HCV, respectively), human T cell lymphotropic virus-1 (HTLV-1), and Kaposi's sarcoma herp
280 cription from DNA constructs of human T-cell lymphotropic virus-1 (HTLV-1), which use the same primer
281 al T-cell malignancy due to the human T-cell lymphotropic virus-1 (HTLV-1).
282 , human immunodeficiency virus, human T-cell lymphotropic virus-1, Helicobacter pylori, hepatitis C,
283 ies of the molecular biology of human T cell lymphotropic virus-1-induced T cell leukemia/lymphoma ha
284 rent pathophysiologic basis for human T cell lymphotropic virus-associated leukemia/lymphoma as well
285 show that DUB-2 is expressed in human T-cell lymphotropic virus-I (HTLV-1)-transformed T cells that e
286 urface antigen, hepatitis C virus, and human lymphotropic virus.
287 titis B and C viruses, HIV, and human T-cell lymphotropic virus.
288 sed by EBV, hepatitis B, C, and human T cell lymphotropic virus.
289 cts of Ikaros on the life cycle of any human lymphotropic virus.
290                                  The human T-lymphotropic viruses (HTLVs) types 1 and 2 originated in
291 are related to distinct lineages of simian T-lymphotropic viruses (STLV-1 and STLV-2, respectively).
292       One possibility is that KSHV, like the lymphotropic viruses Epstein-Barr virus (EBV) and human
293 ure that facilitates the transfer of certain lymphotropic viruses into uninfected T cells.
294             Some herpesviruses, particularly lymphotropic viruses such as Marek's disease virus (MDV)
295                                          For lymphotropic viruses such as the human immunodeficiency
296                       Gammaherpesviruses are lymphotropic viruses that are associated with the develo
297 log, murine gammaherpesvirus 68 (MHV68), are lymphotropic viruses that establish latent infection in
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.

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