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1 S, multicentric Castleman disease (MCD), and primary effusion lymphoma.
2 suppression, including Kaposi's sarcoma and primary effusion lymphoma.
3 open reading frames shown to be expressed in primary effusion lymphoma.
4 1 protein is expressed in Kaposi sarcoma and primary effusion lymphoma.
5 rus) has been linked to Kaposi's sarcoma and primary effusion lymphoma.
6 at induces Kaposi's sarcoma and AIDS-related primary effusion lymphoma.
7 activity and contribute to the phenotype of primary effusion lymphoma.
8 ric Castleman's disease, and AIDS-associated primary effusion lymphoma.
9 lex virus ICP27 genes, from an HHV8-infected primary effusion lymphoma.
10 ly etiological agent of Kaposi's sarcoma and primary effusion lymphoma.
11 iated with HHV8 include Kaposi's sarcoma and primary effusion lymphoma.
12 Kaposi's sarcoma and a rare B cell lymphoma, primary effusion lymphoma.
13 orders, multicentric Castleman's disease and primary effusion lymphoma.
14 rpesvirus (KSHV) causes Kaposi's sarcoma and primary effusion lymphoma.
15 ng AIDS-associated neoplasms, such as KS and primary-effusion lymphoma.
16 umors, multicentric Castleman's disease, and primary effusion lymphomas.
17 hogenesis of Kaposi's sarcoma, as well as in primary effusion lymphomas.
18 lymphoma subtypes such as plasmablastic and primary effusion lymphomas.
19 to the pathogenesis of Kaposi's sarcoma and primary effusion lymphomas.
20 (KS), multicentric Castleman's disease, and primary effusion lymphomas.
21 pathogenesis of Kaposi's sarcoma and B cell primary effusion lymphomas.
22 in the pathogenesis of Kaposi's sarcoma and primary effusion lymphomas.
23 ; 4 of 11 AIDS-Burkitt lymphoma; 4 of 6 AIDS-primary effusion lymphoma; 1 of 4 AIDS-primary central n
24 with KS, multicentric Castleman disease, or primary effusion lymphoma and 8 HIV-uninfected men recei
25 ifest with Kaposi's sarcoma or less commonly primary effusion lymphoma and Castleman's disease; these
27 k6 complex exists in cell lines derived from primary effusion lymphoma and in Kaposi's sarcoma, this
28 present in all cases of Kaposi's sarcoma and primary effusion lymphoma and in some cases of multicent
29 t is implicated in B cell neoplasias such as primary effusion lymphoma and multicentric Castleman dis
30 ther lymphoproliferative diseases, including primary effusion lymphoma and multicentric Castleman's d
31 might also contribute to the pathogenesis of primary effusion lymphoma and multicentric Castleman's d
32 , and to hematologic malignancies, including primary effusion lymphoma and multicentric Castleman's d
33 cal factor of this malignancy, as well as of primary effusion lymphoma and multicentric Castleman's d
34 mplicated in Kaposi's sarcoma, as well as in primary effusion lymphoma and multicentric Castleman's d
35 a and with two lymphoproliferatve disorders, primary effusion lymphoma and multicentric Castleman's d
36 mmaherpesvirus that has been associated with primary effusion lymphoma and multicentric Castleman's d
37 ved in the pathogenesis of Kaposi's sarcoma, primary effusion lymphoma and some cases of multicentric
38 ith two B-cell lymphoproliferative diseases, primary effusion lymphoma and the plasmablastic form of
39 ays showed consistent expression of vIL-6 in primary effusion lymphomas and in a case of human immuno
41 h multicentric Castleman disease, and 1 with primary effusion lymphoma) and 1 asymptomatic PrEP user
42 B-cell lymphomas, such as Hodgkin lymphoma, primary effusion lymphoma, and a diffuse large B-cell ly
43 to the development of Kaposi's sarcoma (KS), primary effusion lymphoma, and a proportion of Castleman
46 aherpesvirus implicated in Kaposi's sarcoma, primary effusion lymphoma, and Castleman's disease, enco
49 ributing to development of Kaposi's sarcoma, primary effusion lymphoma, and multicentric Castleman de
50 ent human malignancies: Kaposi sarcoma (KS), primary effusion lymphoma, and multicentric Castleman di
51 an malignancies, including Kaposi's sarcoma, primary effusion lymphoma, and multicentric Castleman's
52 erpesvirus (KSHV) is tightly linked with KS, primary effusion lymphoma, and multicentric Castleman's
53 lignancies, including Kaposi's sarcoma (KS), primary effusion lymphoma, and multicentric Castleman's
54 an malignancies, including Kaposi's sarcoma, primary effusion lymphoma, and multicentric Castleman's
55 ogic agent associated with Kaposi's sarcoma, primary effusion lymphoma, and multicentric Castleman's
56 is the etiologic agent of Kaposi's sarcoma, primary effusion lymphoma, and multicentric Castleman's
57 e different human cancers: Kaposi's sarcoma, primary effusion lymphoma, and multicentric Castleman's
58 s the etiological agent of Kaposi's sarcoma, primary effusion lymphoma, and multicentric Castleman's
59 ssociated with three human malignancies, KS, primary effusion lymphoma, and multicentric Castleman's
60 /HHV-8) has been linked to Kaposi's sarcoma, primary effusion lymphoma, and multicentric Castleman's
61 ) has been associated with Kaposi's sarcoma, primary effusion lymphoma, and multicentric Castleman's
62 (KSHV) is associated with Kaposi's sarcoma, primary effusion lymphoma, and multicentric Castleman's
63 (HHV-8) is associated with Kaposi's sarcoma, primary effusion lymphoma, and multicentric Castleman's
64 d with the pathogenesis of Kaposi's sarcoma, primary effusion lymphoma, and multicentric Castleman's
65 stently identified in Kaposi's sarcoma (KS), primary effusion lymphoma, and multicentric Castleman's
66 e etiologic agent underlying Kaposi sarcoma, primary effusion lymphoma, and multicentric Castleman's
67 nked to the development of Kaposi's sarcoma, primary effusion lymphoma, and multicentric Castleman's
68 ed with the development of Kaposi's sarcoma, primary effusion lymphoma, and multicentric Castleman's
69 us is the etiologic agent of Kaposi sarcoma, primary effusion lymphoma, and plasma cell-type multicen
70 is the infectious cause of Kaposi's sarcoma, primary effusion lymphoma, and plasmablastic multicentri
71 induction and maintenance of Kaposi sarcoma, primary effusion lymphoma, and some cases of Castleman d
72 s the etiological agent of Kaposi's sarcoma, primary effusion lymphoma, and some forms of multicentri
73 is etiologically linked to Kaposi's sarcoma, primary effusion lymphomas, and multicentric Castleman's
74 ted Kaposi's sarcoma (KS), body cavity-based primary effusion lymphomas, and multicentric Castleman's
75 tion using antagomirs in KSHV-infected human primary effusion lymphoma B cells resulted in derepressi
76 ion was explored by studying 2 KSHV-infected primary effusion lymphoma B-cell lines (BC-3 and BCBL-1)
77 ctor activity was expressed in KSHV-infected primary effusion lymphoma BCBL1 cells (TRExBCBL1-hNIC) i
78 rly, transient expression of siRNAs into the primary effusion lymphoma cell line BCBL-1 caused a subs
81 by diluting KSHV DNA from the KS-1 cells (a primary effusion lymphoma cell line which is estimated t
82 lytic KSHV replication in two KSHV-infected primary effusion lymphoma cell lines (BC-3 and BC-1) and
83 K3+1 expression in a subset of KSHV-infected primary effusion lymphoma cell lines as a consequence of
84 SHV mature microRNA expression in a panel of primary effusion lymphoma cell lines by real-time RT-PCR
85 ma-associated herpesvirus (KSHV)-transformed primary effusion lymphoma cell lines contain ~70 to 150
87 as well as cocultivation with HHV-8-positive primary effusion lymphoma cell lines, activated the lacZ
88 rcoma-associated herpesvirus (KSHV)-infected primary effusion lymphoma cell lines, and its expression
91 tetradecanoyl phorbol acetate-treated JSC-1 primary effusion lymphoma cell lysate, the levels of ass
92 VEC) infected through coculture with induced primary effusion lymphoma cells and telomerase-immortali
93 virus (KSHV) maintains a latent infection in primary effusion lymphoma cells but can be induced to en
94 in vitro and in vivo, and Kaposi sarcoma and primary effusion lymphoma cells demonstrate high levels
95 nvasiveness, as well as colony formation, by primary effusion lymphoma cells derived from human tumor
96 shown to be important for the maintenance of primary effusion lymphoma cells in culture and is chroni
98 esolution ChIP/deep sequencing from infected primary effusion lymphoma cells revealed that RBP-Jkappa
99 tic replication of KSHV in latently infected primary effusion lymphoma cells via beta-adrenergic acti
100 nd to LANA in transfected cells and in BCBL1 primary effusion lymphoma cells was found to be enriched
101 -I expression on EC and MHC-II expression on primary effusion lymphoma cells, but its effects on EC M
112 , and we administered them directly to human primary-effusion lymphoma cells infected with KSHV.
113 issues of patients with Kaposi's sarcoma and primary effusion lymphomas, contains a gene that encodes
115 containing the remaining 2 microRNAs from 5 primary effusion lymphoma-derived cell lines and from 17
116 NAs, we cloned small RNAs from KSHV-positive primary effusion lymphoma-derived cells and endothelial
117 in the pathogenesis of Kaposi's sarcoma and primary effusion lymphomas, encodes a G protein-coupled
118 he etiological agent of Kaposi's sarcoma and primary effusion lymphoma, has developed a unique mechan
120 es Kaposi's sarcoma, Castleman's disease and primary effusion lymphomas in transplant recipients.
121 ymphocytes, and human herpesvirus 8-positive primary effusion lymphoma, inhibitors of Syk, MEK, and,
124 L; n = 61), plasmablastic lymphoma (n = 15), primary effusion lymphoma (n = 7), unclassifiable B-cell
126 bly range from Kaposi sarcoma (KS) to either primary effusion lymphoma or multicentric Castleman dise
127 context of reactivated lytic replication in primary effusion lymphoma (PEL) and endothelial cells an
128 family) were significantly down-regulated in primary effusion lymphoma (PEL) and in Kaposi sarcoma (K
129 of immunocompromised individuals, including primary effusion lymphoma (PEL) and Kaposi's sarcoma (KS
130 B cell lymphoproliferative diseases, namely primary effusion lymphoma (PEL) and multicentric Castlem
131 ontribute to B-cell disorders, which include primary effusion lymphoma (PEL) and multicentric Castlem
132 ifferent human cancers, Kaposi sarcoma (KS), primary effusion lymphoma (PEL) and multicentric Castlem
133 tive disorders of these cells manifesting as primary effusion lymphoma (PEL) and multicentric Castlem
134 and two other lymphoproliferative disorders, primary effusion lymphoma (PEL) and multicentric Castlem
136 is associated with two B cell malignancies, primary effusion lymphoma (PEL) and the plasmablastic va
137 h KS, in 6 (85.7%) of 7 HIV(+) patients with primary effusion lymphoma (PEL) and/or multicentric Cast
139 ells of classical Hodgkin lymphoma (cHL) and primary effusion lymphoma (PEL) are derived from germina
141 wn of miR-K1 in latently KSHV-infected human primary effusion lymphoma (PEL) B cells revealed a derep
142 NA-1) protein, and in KSHV latently infected primary effusion lymphoma (PEL) BCBL-1 and BC-3 cells.
143 is pathway.IMPORTANCE One hundred percent of primary effusion lymphoma (PEL) cases are associated wit
147 latency-associated nuclear antigen (LANA) in primary effusion lymphoma (PEL) cell lines and also incr
148 induction of lytic viral replication in both primary effusion lymphoma (PEL) cell lines and KS tumors
150 quences revealed that c-Myc in KSHV-positive primary effusion lymphoma (PEL) cell lines is wild type
151 d the expression of vGCR mRNA and protein in primary effusion lymphoma (PEL) cell lines, PEL and mult
152 cle can be induced in rare latently infected primary effusion lymphoma (PEL) cell lines, the ability
155 negatively impacting HHV-8 latently infected primary effusion lymphoma (PEL) cell viability and react
156 ibutes to the viability of latently infected primary effusion lymphoma (PEL) cells and to HHV-8 produ
159 e from all ~100 copies of the KSHV genome in primary effusion lymphoma (PEL) cells by coexpressing tw
160 nce-based knockdown of KAP1 in KSHV-infected primary effusion lymphoma (PEL) cells disrupted viral ep
165 e that vFLIP in BCBL-1 endogenously infected primary effusion lymphoma (PEL) cells mediates JNK/AP1 a
166 tance of iASPP to KSHV-infected-cell growth, primary effusion lymphoma (PEL) cells were treated with
167 epetitive region of LNA, detected antigen in primary effusion lymphoma (PEL) cells, and precipitated
168 , and 3 are also expressed during latency in primary effusion lymphoma (PEL) cells, and vIRF-1 and vI
169 rantly accumulated in KSHV latently infected primary effusion lymphoma (PEL) cells, as well as HEK293
170 ation of these proteins was also detected in primary effusion lymphoma (PEL) cells, as well as in a c
171 virus (KSHV) maintains a latent infection in primary effusion lymphoma (PEL) cells, but treatment wit
181 ts low-level expression in latently infected primary effusion lymphoma (PEL) cultures, in the absence
182 this we investigated whether KSHV associated primary effusion lymphoma (PEL) derived cell lines are r
185 man herpesvirus 8) has been linked to KS and primary effusion lymphoma (PEL) in immunocompromised ind
186 rus) has been linked to Kaposi's sarcoma and primary effusion lymphoma (PEL) in immunocompromised ind
187 e (RNAi) to inhibit the growth of a model of primary effusion lymphoma (PEL) in vitro and in vivo.
202 human B-cell non-Hodgkin lymphomas (B-NHL), primary effusion lymphoma (PEL) is a unique subset that
212 ations, the vIRF3-expressing KSHV-associated primary effusion lymphoma (PEL) lines are generally resi
213 ads in molecular pathogenesis, AIDS-defining primary effusion lymphoma (PEL) remains a fatal malignan
214 -related human herpesvirus type 8-associated primary effusion lymphoma (PEL) responds poorly to chemo
215 cell lines and 6 Kaposi's sarcoma (KS) and 4 primary effusion lymphoma (PEL) tumor samples from the U
216 vital for the survival and proliferation of primary effusion lymphoma (PEL), an aggressive malignanc
218 (KSHV) is the cause of Kaposi sarcoma (KS), primary effusion lymphoma (PEL), and a form of Castleman
219 the causative agent for Kaposi sarcoma (KS), primary effusion lymphoma (PEL), and a subset of multice
220 s the etiological agent of Kaposi's sarcoma, primary effusion lymphoma (PEL), and multicentric Castle
221 V) is associated with Kaposi's sarcoma (KS), primary effusion lymphoma (PEL), and multicentric Castle
222 etiologically linked to Kaposi sarcoma (KS), primary effusion lymphoma (PEL), and multicentric Castle
223 herpesvirus 8, is an etiologic agent of KS, primary effusion lymphoma (PEL), and multicentric Castle
224 pesvirus is linked to Kaposi's sarcoma (KS), primary effusion lymphoma (PEL), and multicentric Castle
225 and -unrelated cases of Kaposi sarcoma (KS), primary effusion lymphoma (PEL), and multicentric Castle
226 ed herpesvirus (KSHV) is associated with KS, primary effusion lymphoma (PEL), and multicentric Castle
227 ed in the etiology of Kaposi's sarcoma (KS), primary effusion lymphoma (PEL), and multicentric Castle
228 vities to HHV-8-associated Kaposi's sarcoma, primary effusion lymphoma (PEL), and multicentric Castle
229 the causative agent for Kaposi sarcoma (KS), primary effusion lymphoma (PEL), and multicentric Castle
230 cally associated with Kaposi's sarcoma (KS), primary effusion lymphoma (PEL), and multicentric Castle
231 teins, in HHV-8-associated Kaposi's sarcoma, primary effusion lymphoma (PEL), and multicentric Castle
232 ibutor to virus-associated Kaposi's sarcoma, primary effusion lymphoma (PEL), and multicentric Castle
233 to the development of Kaposi's sarcoma (KS), primary effusion lymphoma (PEL), and multicentric Castle
234 oliferative diseases: Kaposi's sarcoma (KS), primary effusion lymphoma (PEL), and multicentric Castle
235 fection is associated with Kaposi's sarcoma, primary effusion lymphoma (PEL), and multicentric Castle
236 veral neoplastic diseases: Kaposi's sarcoma, primary effusion lymphoma (PEL), and multicentric Castle
237 ing region of KSHV from Kaposi sarcoma (KS), primary effusion lymphoma (PEL), and multicentric Castle
238 uding diffuse large B-cell lymphoma (DLBCL), primary effusion lymphoma (PEL), and multiple myeloma (M
239 Certain lymphomas in AIDS patients, such as primary effusion lymphoma (PEL), are closely associated
240 ed tumors, such as Kaposi's sarcoma (KS) and primary effusion lymphoma (PEL), are of endothelial and
241 ly associated with Kaposi's sarcoma (KS) and primary effusion lymphoma (PEL), defective KSHV has not
242 V), a virus linked to malignancies including primary effusion lymphoma (PEL), encodes 12 miRNA genes,
243 th 3 distinct lymphoproliferative disorders: primary effusion lymphoma (PEL), multicentric Castleman
244 herpesvirus (KSHV) is the etiologic agent of primary effusion lymphoma (PEL), multicentric Castleman'
245 regulated and important for cell survival in primary effusion lymphoma (PEL), which is a viral lympho
246 ammatory protein 1A (vMIP-1A) and vMIP-1B in primary effusion lymphoma (PEL)-derived cell lines and e
275 th two additional AIDS-related malignancies: primary effusion lymphomas (PEL) and multicentric Castle
278 human immunodeficiency virus (HIV)- related primary effusion lymphomas (PEL), a sensitive enzyme-lin
279 sociated herpesvirus (KSHV) is linked to KS, primary effusion lymphomas (PEL), and a subset of multic
280 lines, a type III latency line, three EBV(+) primary effusion lymphomas (PEL), and three AIDS-related
281 ) are found together in approximately 80% of primary effusion lymphomas (PEL), but their contribution
291 of Kaposi's sarcoma (KS), body-cavity-based, primary effusion lymphomas (PELs), and a subset of Castl
292 rpesvirus (KSHV) latently infects KS tumors, primary effusion lymphomas (PELs), and PEL cell lines.
293 n herpesvirus 8) latently infects KS tumors, primary effusion lymphomas (PELs), and PEL cell lines.
296 , as well as a rare form of B cell lymphoma (primary effusion lymphoma) primarily observed in HIV-inf
297 present in all cases of Kaposi's sarcoma and primary effusion lymphoma, provide opportunities for sel
298 n Kaposi sarcoma herpesvirus (KSHV)-infected primary effusion lymphoma through down-regulation of the
299 gher in latently infected cells derived from primary effusion lymphomas; thus, it appears that HHV-8
300 ly associated with Kaposi's sarcoma (KS) and primary effusion lymphoma, with viral genomes present in