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1 nscriptional regulating genes in herpesvirus saimiri.
2 Barr virus and the ORF65 gene of herpesvirus saimiri.
3 rcoma-associated herpesvirus and herpesvirus saimiri.
4 om a rhesus monkey infected with herpesvirus saimiri.
5 rved with Epstein-Barr virus and herpesvirus saimiri.
6 tion in T cell transformation by herpesvirus saimiri.
7 rmation by subgroup A strains of herpesvirus saimiri.
8 t, point mutant, and recombinant herpesvirus saimiri.
9 porter gene from the recombinant herpesvirus saimiri.
10 f rhesus monkey rhadinovirus and herpesvirus saimiri.
11  transcripts encoded by KSHV and herpesvirus saimiri.
12 l name, human herpesvirus 8) and herpesvirus saimiri.
13               The Tip protein of herpesvirus saimiri 484 binds to the Lck tyrosine-protein kinase at
14 er known human herpesviruses and herpesvirus saimiri, a closely related gammaherpesvirus of nonhuman
15                                  Herpesvirus saimiri, a gamma-herpesvirus that establishes latency in
16 sformed to permanent growth with Herpesvirus saimiri, an oncogenic virus of nonhuman primates.
17 g (RNAseq) data for late-stage infections in Saimiri and Aotus erythrocytes when invasion ligands are
18 nds, we compared parasite gene expression in Saimiri and Aotus monkey erythrocytes infected with P. v
19       Though similar to those of herpesvirus saimiri and Epstein-Barr virus (EBV), the Kaposi's sarco
20 mma herpesvirus with homology to herpesvirus Saimiri and Epstein-Barr virus, both of which can transf
21  to human gammaherpesviruses and herpesvirus saimiri and has been reported to be associated with lymp
22 akes it an attractive cytogenetic marker for Saimiri and other New World monkeys.
23 ee species diverged, L1 has amplified in the Saimiri and Saguinus lineages but L1 activity seems to h
24 the active L1 lineage has evolved rapidly in Saimiri and Saguinus, generating species-specific subfam
25 tein-coupled receptor encoded by herpesvirus Saimiri and to human interleukin-8 receptors.
26 sviruses, Epstein-Barr virus and Herpesvirus saimiri, and are present in the lesions of more than 95%
27 RF45s of rhesus rhadinovirus and herpesvirus saimiri are found exclusively in the nucleus.
28 cy virus type 1 (HIV-1) by using herpesvirus saimiri as described recently.
29                           Tip of herpesvirus saimiri associates with Lck and down-regulates Lck-media
30                           Tip of herpesvirus saimiri associates with Lck and downregulates Lck functi
31  RNAs expressed by the oncogenic Herpesvirus saimiri, bind host microRNAs miR-142-3p, miR-16, and miR
32 pvdhfr), we transfected blood specimens from Saimiri boliviensis monkeys infected with the pyrimetham
33 tire blue opsin gene in the squirrel monkey (Saimiri boliviensis) and the five introns of the human b
34 oma, we elevated IOP in the squirrel monkey (Saimiri boliviensis) using intracameral injection of 35
35 thrix jacchus), Humboldt's squirrel monkeys (Saimiri cassiquiarensis), and yellow-breasted capuchins
36 ing KSbcl-2, BHRF1, and ORF16 of herpesvirus saimiri contain poorly conserved Bcl-2 homology 3 (BH3)
37    The Bcl-2 homologs encoded by herpesvirus saimiri, Epstein-Barr virus, and BHV4 were not cleaved b
38 ythrocytes; thus, P. vivax Sal I must invade Saimiri erythrocytes independent of DBP1.
39        DBP1 binds Aotus but does not bind to Saimiri erythrocytes; thus, P. vivax Sal I must invade S
40           T cells transformed by Herpesvirus saimiri express seven viral U-rich noncoding RNAs of unk
41  were investigated in four squirrel monkeys (Saimiri) following extracellular injections of the trace
42                                  Herpesvirus Saimiri gene 13 (HVS13) exhibits 57% identity with the p
43 haracterizing satellite DNA sequences in the Saimiri genus.
44 K-3beta also interacted with the herpesvirus saimiri homolog ORF73.
45 al gammaherpesviruses, including herpesvirus saimiri, human herpesvirus 8, and MHV68, encode proteins
46 ase interacting protein (Tip) of Herpesvirus saimiri (HVS) activates the lymphoid-specific member of
47 rus-encoded cyclin (v-cyclin) of herpesvirus saimiri (HVS) and 31% identity and 53% similarity to hum
48 formation by the DNA tumor virus herpesvirus saimiri (HVS) and designated tyrosine kinase interacting
49 ri transforming protein (STP) of herpesvirus saimiri (HVS) and of K1 of KSHV, other members of the ga
50                 The lymphotropic Herpesvirus saimiri (HVS) causes acute leukemia, T-cell lymphoma, an
51                                  Herpesvirus saimiri (HVS) encodes seven Sm-class small nuclear RNAs,
52 open reading frame 14 (orf14) of herpesvirus saimiri (HVS) exhibits significant homology with mouse m
53 ently infected marmoset T cells, Herpesvirus saimiri (HVS) expresses six microRNAs (known as miR-HSUR
54 earity with the right end of the herpesvirus saimiri (HVS) genome and more limited homology to the le
55                              The herpesvirus saimiri (HVS) immediate-early gene product encoded by op
56                                  Herpesvirus saimiri (HVS) infects a range of human cell types with h
57                                  Herpesvirus saimiri (HVS) is a gamma-herpesvirus that expresses Sm c
58                                  Herpesvirus saimiri (HVS) is a T-cell-specific transforming and onco
59                                  Herpesvirus saimiri (HVS) is an oncogenic gamma-herpesvirus that pro
60                                  Herpesvirus saimiri (HVS) is an oncogenic, lymphotropic, gamma-herpe
61 tein (Tip) of the T lymphotropic Herpesvirus saimiri (HVS) is constitutively present in lipid rafts a
62                                  Herpesvirus saimiri (HVS) is divided into three subgroups, A, B, and
63 ase-interacting protein (Tip) of herpesvirus saimiri (HVS) is required for binding to the cellular Sr
64 rpesvirus, including the gamma-2 herpesvirus saimiri (HVS) of New World squirrel monkeys.
65 f the terminal repeats (TR) from herpesvirus saimiri (HVS) renders it unable to produce infectious vi
66 formation by the DNA tumor virus herpesvirus saimiri (HVS) strain 484, designated tyrosine kinase-int
67 otein oncogene, called STP-A, of herpesvirus saimiri (HVS) subgroup A is not required for viral repli
68      The STP oncoproteins of the herpesvirus saimiri (HVS) subgroup A strain 11 and subgroup C strain
69                  Mutant forms of herpesvirus saimiri (HVS) subgroup C strain 488 with deletions in ei
70                              The herpesvirus saimiri (HVS) tyrosine kinase-interacting protein (Tip),
71 ns encoded by two herpesviruses, herpesvirus saimiri (HVS) which can transform blood lymphocytes and
72 s of the Sm class are encoded by Herpesvirus saimiri (HVS), a gamma Herpesvirus that causes aggressiv
73  marmoset T cells transformed by Herpesvirus saimiri (HVS), a viral U-rich noncoding (nc) RNA, HSUR 1
74 o known as human herpesvirus 8), herpesvirus saimiri (HVS), and Epstein-Barr virus (EBV).
75                                  Herpesvirus saimiri (HVS), another gamma-2-herpesvirus, primarily in
76 nd of the genome in RRV26-95 and herpesvirus saimiri (HVS), but in KSHV the DHFR gene is displaced 16
77 ssociated herpesvirus (KSHV) and herpesvirus saimiri (HVS), has been shown to encode a latency-associ
78 ri transforming protein (STP) of herpesvirus saimiri (HVS), Kaposi's sarcoma-associated herpesvirus (
79  normal donors by infection with Herpesvirus saimiri (HVS), to evaluate functional properties of thes
80 close homolog of KSHV ORF57 from herpesvirus saimiri (HVS), we determined the crystal structure of th
81 RNAs encoded by the lymphotropic Herpesvirus saimiri (HVS), we determined the specific sequence and s
82               The Tip protein of herpesvirus saimiri (HVS), which is a T-lymphotropic tumor virus, in
83 es have demonstrated that Tip of herpesvirus saimiri (HVS), which is a T-lymphotropic tumor virus, is
84 -defensin-1 and CAF derived from herpesvirus saimiri (HVS)-transformed CD8(+) cells inhibited HIV-1 i
85 ding frame 6 (ORF6) and ORF31 of herpesvirus saimiri (HVS).
86 an open reading frame (ORF) from herpesvirus saimiri (HVS).
87  by the related gammaherpesvirus herpesvirus saimiri (HVS).
88 f the T-lymphotropic tumor virus herpesvirus saimiri (HVS).
89                 STP-C488 (STP of herpesvirus saimiri [HVS] group C strain 488 [C488]) is the only vir
90 lymphocyte clones established by herpesvirus saimiri immortalization.
91 ects on TCR signal transduction, herpesvirus saimiri-immortalized CD4 Th cells from XLP patients and
92 ystander apoptosis was tested in herpesvirus saimiri-immortalized primary CD4(+) T cells (CD4/HVS), w
93                        Moreover, Herpesvirus saimiri-immortalized T cells from the patient produced a
94                                           H. saimiri-induced transformation of T cells is becoming an
95 ilies that were more abundantly expressed in Saimiri infections compared with Aotus infections.
96                                    The genus Saimiri is a decades-long taxonomic and phylogenetic puz
97                                  Herpesvirus saimiri is a lymphotropic herpesvirus capable of immorta
98 he role of StpC in cell transformation by H. saimiri may be mediated by signaling that results in NF-
99      We report here an immunization study of Saimiri monkeys with a yeast-expressed recombinant prote
100                    We describe infections of Saimiri monkeys with two strains of P. vivax and the ana
101 tes from bloodstream infections of Aotus and Saimiri monkeys.
102 hat, unlike the ORF57 homolog in herpesvirus saimiri, nucleolar trafficking is not required for ORF57
103 L as a restriction target of the herpesvirus saimiri ORF3 protein, implying a role for Sp140L in immu
104 s, including 66 with homology to herpesvirus saimiri ORFs, and 5 internal repeat regions are present
105 rame 16 (ORF16) of the oncogenic herpesvirus saimiri protects cells from heterologous virus-induced a
106 at the X-linked locus among three species of Saimiri representing a wide range of geographical and be
107                                  Herpesvirus saimiri (Saimiriine herpesvirus-2) causes lethal T lymph
108 halamus was re-examined in squirrel monkeys (Saimiri sciureus) and macaques (Macaca mulatta).
109 World monkeys - the diurnal squirrel monkey (Saimiri sciureus) and the nocturnal owl monkey (Aotus tr
110 type II hair cells (HCs) in squirrel monkey (Saimiri sciureus) cristae by a nearly 3:1 ratio.
111 e report that infection of squirrel monkeys (Saimiri sciureus) fulfills these requirements.
112                      Three squirrel monkeys (Saimiri sciureus) learned to reach toward a container th
113 nomolgus (Macaca fascicularis) and squirrel (Saimiri sciureus) monkey eyes (n = 20), matrix placement
114 utans (Pongo pygmaeus) and squirrel monkeys (Saimiri sciureus) on object permanence tasks.
115                            Squirrel monkeys (Saimiri sciureus) that had learned to reach toward 1 pie
116 oon (Papio hamadryas) and 1 squirrel monkey (Saimiri sciureus) to respond to stimuli representing the
117 ys (Cebus apella) and four squirrel monkeys (Saimiri sciureus) were given demonstration trials in whi
118  characterised (humans and squirrel monkeys (Saimiri sciureus)), the aVOR response to roll head rotat
119 nkeys (Aotus trivirgatus), squirrel monkeys (Saimiri sciureus), and macaque monkeys (Macaca fascicula
120 s in three NWM species, the squirrel monkey (Saimiri sciureus), the tamarin (Saguinus oedipus), and t
121          To investigate if squirrel monkeys (Saimiri sciureus), which are reported to develop a cours
122 ysiological study employed squirrel monkeys (Saimiri sciureus), which moved freely on the walls and f
123 e in a colony of 15 female squirrel monkeys (Saimiri sciureus).
124 revents measles disease in squirrel monkeys (Saimiri sciureus).
125 erimental WNV infection of squirrel monkeys (Saimiri sciureus).
126 e-consolidating animal, the squirrel monkey (Saimiri sciureus).
127  mitochondrial genomes from Aotus lemurinus, Saimiri sciureus, Saguinus oedipus, Ateles belzebuth, an
128 red reporter genes cloned within herpesvirus saimiri sequences, recombinant viruses were readily iden
129                                          All Saimiri species apparently have a diploid number of 2n =
130 quencies were approximately the same for all Saimiri species, with a slight but significant differenc
131 ochromatin and its distribution varies among Saimiri species.
132             The Tip protein from Herpesvirus saimiri specifically binds to and activates the protein
133                                  Herpesvirus saimiri strain 11 of subgroup A contains a gene called t
134 orming protein (STP) oncogene of Herpesvirus saimiri subgroup A strain 11 (STP-A11) is not required f
135                           Two proteins of H. saimiri subgroup C, Tip and StpC, are essential for T ce
136 d by transformation of PBMC with herpesvirus saimiri, suggesting that this phenomenon is an intrinsic
137 he mouse mammary tumor virus and herpesvirus saimiri superantigens.
138                                  Herpesvirus saimiri Tip associates with Lck and downregulates Lck si
139  11 of subgroup A contains a gene called the saimiri transformation-associated protein, STP, which is
140 n the cell culture medium of the herpesvirus saimiri-transformed CD8(+) T-cell line, K#1 50K, has pot
141 2-kDa viral protein expressed by herpesvirus saimiri-transformed lymphocytes, is essential for transf
142 llular protein in untransformed, herpesvirus saimiri-transformed, and Jurkat lymphocytes.
143 position equivalent to the gene encoding the saimiri transforming protein (STP) of herpesvirus saimir
144  of the R1 gene is equivalent to that of the saimiri transforming protein (STP) of herpesvirus saimir
145                                          The saimiri transforming protein (STP) oncogene of Herpesvir
146  at the left end of genomic DNA in which the saimiri transforming protein (STP) resides.
147                                          The saimiri transforming protein oncogene, called STP-A, of
148  viral small nuclear RNA (snRNA) Herpesvirus saimiri U RNA 1 (HSUR 1) also contains an AUUUA-rich seq
149                              The Herpesvirus saimiri U RNAs (HSURs) are the most abundant viral trans
150  nuclear RNAs, called HSURs (for Herpesvirus saimiri U RNAs), that are abundantly expressed in HVS-tr
151 resses six microRNAs (known as miR-HSURs [H. saimiri U-rich RNAs]).
152 lex of six New World primates (Cebus apella, Saimiri ustius, Saguinus midas niger, Alouatta caraya, A
153 ve cells were cotransfected with herpesvirus saimiri virion DNA and one of the engineered reporter ge
154  because they are specifically well-tuned to Saimiri visual ecology.
155 nucleolar localization signal in herpesvirus saimiri was constructed.
156 sm modulating gene expression in herpesvirus saimiri, whereby ORF 50a transcription is downregulated
157 uses, the Epstein-Barr virus and herpesvirus saimiri, which are known to be associated with lymphomas

 
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