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1 icating that the BASE prion is intrinsically lymphotropic.
2 ain is a more virulent BSE strain and likely lymphotropic.
4 ed (KS-associated) herpesvirus (KSHV) is a B-lymphotropic agent linked to AIDS-related lymphoprolifer
6 Here we investigated incunabular events in lymphotropic and intranodal prion trafficking by followi
8 rated that the virus was epitheliotropic and lymphotropic and that infection was systemic in the majo
10 uman herpesvirus 6 (HHV-6) is a ubiquitous T-lymphotropic betaherpesvirus that encodes two G protein-
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
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
23 ular CD21 and CD23a are common targets for B lymphotropic gammaherpesviruses and that KSHV RTA regula
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-
28 a co-receptor specific for the infection by lymphotropic HCV, we established an infectious clone and
31 porcine cytomegalovirus (PCMV), and porcine lymphotropic herpesvirus (PLHV) are common porcine virus
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
44 ical features of PTLD were increased porcine lymphotropic herpesvirus-1 viral loads in blood and tiss
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
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
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
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
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
81 udies support sexual transmission of human T lymphotropic virus (HTLV)-I/II; however, prospective inc
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
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
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
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
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
106 that can be productively infected by human T-lymphotropic virus type 1 (HTLV-1) and can spread HTLV-1
110 individual integration sites of human T-cell lymphotropic virus type 1 (HTLV-1) and human immunodefic
117 teract with a TG-rich element in the human T-lymphotropic virus type 1 (HTLV-1) enhancer thought to m
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
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
150 ased Tax transactivation of the human T-cell lymphotropic virus type 1 (HTLV-1) long terminal repeat
152 ctroscopy was used to study the human T-cell lymphotropic virus type 1 (HTLV-1) nucleocapsid protein
158 reviously demonstrated that the human T-cell lymphotropic virus type 1 (HTLV-1) Tax can inactivate p5
162 CBP)/p300-binding domain of the human T-cell lymphotropic virus type 1 (HTLV-1) transactivator, Tax,
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
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,
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
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
181 re currently 5 million to 10 million human T-lymphotropic virus type 1 (HTLV-1)-infected people, and
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
202 ulations from subjects infected with human T-lymphotropic virus type 1; (ii) T cell antigen receptor
204 of the p53 tumor suppressor in human T-cell lymphotropic virus type 2 (HTLV-2)-transformed cells.
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
224 We quantitatively identified human T-cell lymphotropic virus type I (HTLV-I) Tax(11-19) peptide-sp
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
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
242 lear cells, and a high ratio of 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
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
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
259 NILR protein was detected on human T cell lymphotropic virus type I-transformed T cell lines, Raji
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
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
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
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
291 are related to distinct lineages of simian T-lymphotropic viruses (STLV-1 and STLV-2, respectively).
297 log, murine gammaherpesvirus 68 (MHV68), are lymphotropic viruses that establish latent infection in
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