ライフサイエンスコーパス: Saimiri

1 Barr virus and the ORF65 gene of herpesvirus saimiri.

2 rcoma-associated herpesvirus and herpesvirus saimiri.

3 om a rhesus monkey infected with herpesvirus saimiri.

4 rved with Epstein-Barr virus and herpesvirus saimiri.

5 tion in T cell transformation by herpesvirus saimiri.

6 rmation by subgroup A strains of herpesvirus saimiri.

7 t, point mutant, and recombinant herpesvirus saimiri.

8 porter gene from the recombinant herpesvirus saimiri.

9 f rhesus monkey rhadinovirus and herpesvirus saimiri.

10 transcripts encoded by KSHV and herpesvirus saimiri.

11 l name, human herpesvirus 8) and herpesvirus saimiri.

12 nscriptional regulating genes in 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 Though similar to those of herpesvirus saimiri and Epstein-Barr virus (EBV), the Kaposi's sarco

18 mma herpesvirus with homology to herpesvirus Saimiri and Epstein-Barr virus, both of which can transf

19 to human gammaherpesviruses and herpesvirus saimiri and has been reported to be associated with lymp

20 ee species diverged, L1 has amplified in the Saimiri and Saguinus lineages but L1 activity seems to h

21 the active L1 lineage has evolved rapidly in Saimiri and Saguinus, generating species-specific subfam

22 tein-coupled receptor encoded by herpesvirus Saimiri and to human interleukin-8 receptors.

23 sviruses, Epstein-Barr virus and Herpesvirus saimiri, and are present in the lesions of more than 95%

24 RF45s of rhesus rhadinovirus and herpesvirus saimiri are found exclusively in the nucleus.

25 cy virus type 1 (HIV-1) by using herpesvirus saimiri as described recently.

26 Tip of herpesvirus saimiri associates with Lck and down-regulates Lck-media

27 Tip of herpesvirus saimiri associates with Lck and downregulates Lck functi

28 pvdhfr), we transfected blood specimens from Saimiri boliviensis monkeys infected with the pyrimetham

29 tire blue opsin gene in the squirrel monkey (Saimiri boliviensis) and the five introns of the human b

30 ing KSbcl-2, BHRF1, and ORF16 of herpesvirus saimiri contain poorly conserved Bcl-2 homology 3 (BH3)

31 The Bcl-2 homologs encoded by herpesvirus saimiri, Epstein-Barr virus, and BHV4 were not cleaved b

32 T cells transformed by Herpesvirus saimiri express seven viral U-rich noncoding RNAs of unk

33 were investigated in four squirrel monkeys (Saimiri) following extracellular injections of the trace

34 Herpesvirus Saimiri gene 13 (HVS13) exhibits 57% identity with the p

35 K-3beta also interacted with the herpesvirus saimiri homolog ORF73.

36 al gammaherpesviruses, including herpesvirus saimiri, human herpesvirus 8, and MHV68, encode proteins

37 ase interacting protein (Tip) of Herpesvirus saimiri (HVS) activates the lymphoid-specific member of

38 rus-encoded cyclin (v-cyclin) of herpesvirus saimiri (HVS) and 31% identity and 53% similarity to hum

39 formation by the DNA tumor virus herpesvirus saimiri (HVS) and designated tyrosine kinase interacting

40 ri transforming protein (STP) of herpesvirus saimiri (HVS) and of K1 of KSHV, other members of the ga

41 The lymphotropic Herpesvirus saimiri (HVS) causes acute leukemia, T-cell lymphoma, an

42 Herpesvirus saimiri (HVS) encodes seven Sm-class small nuclear RNAs,

43 open reading frame 14 (orf14) of herpesvirus saimiri (HVS) exhibits significant homology with mouse m

44 ently infected marmoset T cells, Herpesvirus saimiri (HVS) expresses six microRNAs (known as miR-HSUR

45 earity with the right end of the herpesvirus saimiri (HVS) genome and more limited homology to the le

46 The herpesvirus saimiri (HVS) immediate-early gene product encoded by op

47 Herpesvirus saimiri (HVS) infects a range of human cell types with h

48 Herpesvirus saimiri (HVS) is a gamma-herpesvirus that expresses Sm c

49 Herpesvirus saimiri (HVS) is a T-cell-specific transforming and onco

50 Herpesvirus saimiri (HVS) is an oncogenic gamma-herpesvirus that pro

51 Herpesvirus saimiri (HVS) is an oncogenic, lymphotropic, gamma-herpe

52 tein (Tip) of the T lymphotropic Herpesvirus saimiri (HVS) is constitutively present in lipid rafts a

53 Herpesvirus saimiri (HVS) is divided into three subgroups, A, B, and

54 ase-interacting protein (Tip) of herpesvirus saimiri (HVS) is required for binding to the cellular Sr

55 rpesvirus, including the gamma-2 herpesvirus saimiri (HVS) of New World squirrel monkeys.

56 f the terminal repeats (TR) from herpesvirus saimiri (HVS) renders it unable to produce infectious vi

57 formation by the DNA tumor virus herpesvirus saimiri (HVS) strain 484, designated tyrosine kinase-int

58 otein oncogene, called STP-A, of herpesvirus saimiri (HVS) subgroup A is not required for viral repli

59 The STP oncoproteins of the herpesvirus saimiri (HVS) subgroup A strain 11 and subgroup C strain

60 Mutant forms of herpesvirus saimiri (HVS) subgroup C strain 488 with deletions in ei

61 The herpesvirus saimiri (HVS) tyrosine kinase-interacting protein (Tip),

62 ns encoded by two herpesviruses, herpesvirus saimiri (HVS) which can transform blood lymphocytes and

63 s of the Sm class are encoded by Herpesvirus saimiri (HVS), a gamma Herpesvirus that causes aggressiv

64 marmoset T cells transformed by Herpesvirus saimiri (HVS), a viral U-rich noncoding (nc) RNA, HSUR 1

65 o known as human herpesvirus 8), herpesvirus saimiri (HVS), and Epstein-Barr virus (EBV).

66 Herpesvirus saimiri (HVS), another gamma-2-herpesvirus, primarily in

67 nd of the genome in RRV26-95 and herpesvirus saimiri (HVS), but in KSHV the DHFR gene is displaced 16

68 ssociated herpesvirus (KSHV) and herpesvirus saimiri (HVS), has been shown to encode a latency-associ

69 ri transforming protein (STP) of herpesvirus saimiri (HVS), Kaposi's sarcoma-associated herpesvirus (

70 normal donors by infection with Herpesvirus saimiri (HVS), to evaluate functional properties of thes

71 RNAs encoded by the lymphotropic Herpesvirus saimiri (HVS), we determined the specific sequence and s

72 The Tip protein of herpesvirus saimiri (HVS), which is a T-lymphotropic tumor virus, in

73 es have demonstrated that Tip of herpesvirus saimiri (HVS), which is a T-lymphotropic tumor virus, is

74 -defensin-1 and CAF derived from herpesvirus saimiri (HVS)-transformed CD8(+) cells inhibited HIV-1 i

75 ding frame 6 (ORF6) and ORF31 of herpesvirus saimiri (HVS).

76 an open reading frame (ORF) from herpesvirus saimiri (HVS).

77 by the related gammaherpesvirus herpesvirus saimiri (HVS).

78 f the T-lymphotropic tumor virus herpesvirus saimiri (HVS).

79 STP-C488 (STP of herpesvirus saimiri [HVS] group C strain 488 [C488]) is the only vir

80 lymphocyte clones established by herpesvirus saimiri immortalization.

81 ects on TCR signal transduction, herpesvirus saimiri-immortalized CD4 Th cells from XLP patients and

82 ystander apoptosis was tested in herpesvirus saimiri-immortalized primary CD4(+) T cells (CD4/HVS), w

83 H. saimiri-induced transformation of T cells is becoming an

84 Herpesvirus saimiri is a lymphotropic herpesvirus capable of immorta

85 he role of StpC in cell transformation by H. saimiri may be mediated by signaling that results in NF-

86 We report here an immunization study of Saimiri monkeys with a yeast-expressed recombinant prote

87 hat, unlike the ORF57 homolog in herpesvirus saimiri, nucleolar trafficking is not required for ORF57

88 s, including 66 with homology to herpesvirus saimiri ORFs, and 5 internal repeat regions are present

89 rame 16 (ORF16) of the oncogenic herpesvirus saimiri protects cells from heterologous virus-induced a

90 at the X-linked locus among three species of Saimiri representing a wide range of geographical and be

91 Herpesvirus saimiri (Saimiriine herpesvirus-2) causes lethal T lymph

92 halamus was re-examined in squirrel monkeys (Saimiri sciureus) and macaques (Macaca mulatta).

93 World monkeys - the diurnal squirrel monkey (Saimiri sciureus) and the nocturnal owl monkey (Aotus tr

94 type II hair cells (HCs) in squirrel monkey (Saimiri sciureus) cristae by a nearly 3:1 ratio.

95 e report that infection of squirrel monkeys (Saimiri sciureus) fulfills these requirements.

96 Three squirrel monkeys (Saimiri sciureus) learned to reach toward a container th

97 nomolgus (Macaca fascicularis) and squirrel (Saimiri sciureus) monkey eyes (n = 20), matrix placement

98 utans (Pongo pygmaeus) and squirrel monkeys (Saimiri sciureus) on object permanence tasks.

99 Squirrel monkeys (Saimiri sciureus) that had learned to reach toward 1 pie

100 oon (Papio hamadryas) and 1 squirrel monkey (Saimiri sciureus) to respond to stimuli representing the

101 ys (Cebus apella) and four squirrel monkeys (Saimiri sciureus) were given demonstration trials in whi

102 characterised (humans and squirrel monkeys (Saimiri sciureus)), the aVOR response to roll head rotat

103 nkeys (Aotus trivirgatus), squirrel monkeys (Saimiri sciureus), and macaque monkeys (Macaca fascicula

104 s in three NWM species, the squirrel monkey (Saimiri sciureus), the tamarin (Saguinus oedipus), and t

105 To investigate if squirrel monkeys (Saimiri sciureus), which are reported to develop a cours

106 ysiological study employed squirrel monkeys (Saimiri sciureus), which moved freely on the walls and f

107 e-consolidating animal, the squirrel monkey (Saimiri sciureus).

108 erimental WNV infection of squirrel monkeys (Saimiri sciureus).

109 mitochondrial genomes from Aotus lemurinus, Saimiri sciureus, Saguinus oedipus, Ateles belzebuth, an

110 red reporter genes cloned within herpesvirus saimiri sequences, recombinant viruses were readily iden

111 quencies were approximately the same for all Saimiri species, with a slight but significant differenc

112 The Tip protein from Herpesvirus saimiri specifically binds to and activates the protein

113 Herpesvirus saimiri strain 11 of subgroup A contains a gene called t

114 orming protein (STP) oncogene of Herpesvirus saimiri subgroup A strain 11 (STP-A11) is not required f

115 Two proteins of H. saimiri subgroup C, Tip and StpC, are essential for T ce

116 d by transformation of PBMC with herpesvirus saimiri, suggesting that this phenomenon is an intrinsic

117 he mouse mammary tumor virus and herpesvirus saimiri superantigens.

118 Herpesvirus saimiri Tip associates with Lck and downregulates Lck si

119 11 of subgroup A contains a gene called the saimiri transformation-associated protein, STP, which is

120 n the cell culture medium of the herpesvirus saimiri-transformed CD8(+) T-cell line, K#1 50K, has pot

121 2-kDa viral protein expressed by herpesvirus saimiri-transformed lymphocytes, is essential for transf

122 llular protein in untransformed, herpesvirus saimiri-transformed, and Jurkat lymphocytes.

123 of the R1 gene is equivalent to that of the saimiri transforming protein (STP) of herpesvirus saimir

124 position equivalent to the gene encoding the saimiri transforming protein (STP) of herpesvirus saimir

125 The saimiri transforming protein (STP) oncogene of Herpesvir

126 at the left end of genomic DNA in which the saimiri transforming protein (STP) resides.

127 The saimiri transforming protein oncogene, called STP-A, of

128 viral small nuclear RNA (snRNA) Herpesvirus saimiri U RNA 1 (HSUR 1) also contains an AUUUA-rich seq

129 The Herpesvirus saimiri U RNAs (HSURs) are the most abundant viral trans

130 nuclear RNAs, called HSURs (for Herpesvirus saimiri U RNAs), that are abundantly expressed in HVS-tr

131 resses six microRNAs (known as miR-HSURs [H. saimiri U-rich RNAs]).

132 lex of six New World primates (Cebus apella, Saimiri ustius, Saguinus midas niger, Alouatta caraya, A

133 ve cells were cotransfected with herpesvirus saimiri virion DNA and one of the engineered reporter ge

134 because they are specifically well-tuned to Saimiri visual ecology.

135 nucleolar localization signal in herpesvirus saimiri was constructed.

136 sm modulating gene expression in herpesvirus saimiri, whereby ORF 50a transcription is downregulated

137 uses, the Epstein-Barr virus and herpesvirus saimiri, which are known to be associated with lymphomas