ライフサイエンスコーパス: lymphocryptovirus

1 the capsid have not been determined for this lymphocryptovirus.

2 es of chimeras with the gH homolog of rhesus lymphocryptovirus.

3 olutionary transition from rhadinoviruses to lymphocryptoviruses.

4 cted (n = 143/332) with a specific strain of lymphocryptovirus 1 (GbbLCV-1).

5 orilla was incorrectly referred to as Gibbon lymphocryptovirus 1 in Table 1.

6 The correct aetiology is Gbb lymphocryptovirus 1.

7 nal role(s) of EBV TK and to uncover how the lymphocryptovirus and rhadinovirus enzymes differ, the s

8 appreciation for circRNA repertoires in the Lymphocryptovirus and Rhadinovirus genera of gammaherpes

9 pression by a BHRF1 miRNA is conserved among lymphocryptoviruses, and further reveal virally-encoded

10 targets for testing in vivo with the rhesus lymphocryptovirus animal model for EBV infection.

11 ction is not possessed by New World marmoset lymphocryptovirus BILF1.

12 tion will facilitate investigations of human lymphocryptovirus biology.

13 A) and the orthologous pre-miRNA from Rhesus lymphocryptovirus contribute to reducing IFN signaling.

14 encephalomyelitis model that an EBV-related lymphocryptovirus enables B cells to protect a proteolys

15 scription initiation site) from the EBV-like lymphocryptoviruses found in baboons (herpesvirus papio;

16 pression are conserved among the EBV-related lymphocryptoviruses found in nonhuman primates.

17 ng the immune-evasion strategies used by the lymphocryptovirus (gamma(1)-herpesvirus) EBV is the down

18 gene of HV(MNE) placed this virus within the Lymphocryptovirus genus and demonstrated that HV(MNE) is

19 evolution of immunoevasive functions by the lymphocryptovirus genus of herpesviruses.

20 we explore the evolution of BILF1 within the lymphocryptovirus genus.

21 have studied its conservation in the simian lymphocryptovirus herpesvirus papio (HVP) by cloning HVP

22 er AdC-rhEBNA-1 immunizations in chronically lymphocryptovirus-infected rhesus macaques, an EBV infec

23 Although the homolog of BILF1 encoded by the lymphocryptovirus infecting Old World rhesus primates sh

24 An animal model of lymphocryptovirus infection will facilitate investigatio

25 eport that B cells infected with EBV-related lymphocryptovirus (LCV) are requisite APCs for MHC-E-res

26 tic EBV vaccines that target the rhesus (rh) lymphocryptovirus (LCV) EBNA-1 to determine if ongoing T

27 A closely related herpesvirus in the same lymphocryptovirus (LCV) genera as EBV naturally infects

28 We sequenced the rhesus lymphocryptovirus (LCV) genome in order to determine its

29 mber of the Epstein-Barr virus (EBV)-related lymphocryptovirus (LCV) genus and extended the known hos

30 with a gammaherpesvirus which is in the same lymphocryptovirus (LCV) genus as and closely related to

31 ilar to other gammaherpesviruses in the same lymphocryptovirus (LCV) genus that naturally infect Old

32 The rhesus lymphocryptovirus (LCV) is an EBV-related herpesvirus th

33 overy of an Epstein-Barr virus (EBV)-related lymphocryptovirus (LCV) naturally infecting common marmo

34 ree EBNA-3 homologues from a closely related lymphocryptovirus (LCV) which naturally infects rhesus m

35 stein-Barr virus (EBV), the only known human lymphocryptovirus (LCV), displays a remarkable degree of

36 , is the only human herpesvirus in the genus Lymphocryptovirus (LCV).

37 rhesus macaques with the EBV-related rhesus lymphocryptovirus (LCV).

38 homologue is conserved in the rhesus monkey lymphocryptovirus (LCV).

39 ne sequences from EBV and the related herpes lymphocryptoviruses (LCV) infecting baboons and rhesus m

40 d World primates are naturally infected with lymphocryptoviruses (LCV) that are closely related to Ep

41 Epstein-Barr-related herpesviruses, or lymphocryptoviruses (LCV), naturally infect humans and n

42 LP homologues from baboon and rhesus macaque lymphocryptoviruses (LCVs) (baboon LCV and rhesus LCV).

43 Lymphocryptoviruses (LCVs) naturally infecting Old World

44 the homologous proteins of nonhuman primate lymphocryptoviruses (LCVs), which bear a strong genetic

45 ously uncharacterized nonhuman primate (NHP) lymphocryptoviruses (LCVs).

46 f LMP1 expression is a conserved function of lymphocryptovirus miRNAs.

47 A highly similar rhesus lymphocryptovirus naturally endemic in rhesus monkeys wa

48 on, chimeric proteins were made using rhesus lymphocryptovirus (Rh-LCV) gL (Rh gL), which shares a hi

49 une response using the EBV-homologous rhesus lymphocryptovirus (rhLCV) infection in rhesus macaques.

50 t recombinant 72A1 did not neutralize rhesus lymphocryptovirus (rhLCV) infection of macaque B cells.

51 Rhesus lymphocryptovirus (rhLCV) is a gamma-herpesvirus closely

52 ed with the Epstein-Barr virus (EBV)-related lymphocryptovirus (rhLCV).

53 Rhesus lymphocryptovirus (rLCV) and Epstein-Barr virus (EBV) ar

54 Epstein-Barr virus (EBV) and rhesus lymphocryptovirus (rLCV) are closely related gammaherpes

55 of the interspecies homologue rhesus macaque lymphocryptovirus (rLCV) in a naturally occurring lympho

56 an primate (NHP) gamma-herpesviruses (rhesus lymphocryptovirus [rLCV], rhesus rhadinovirus [RRV], and

57 The epidemiology of herpesvirus papio, a lymphocryptovirus similar to Epstein-Barr virus (EBV), w

58 re closely related gammaherpesviruses in the lymphocryptovirus subgroup that express viral microRNAs

59 Epstein-Barr virus (EBV) is a human lymphocryptovirus that causes infectious mononucleosis,

60 ated a higher risk of reactivation of rhesus lymphocryptovirus (the rhesus macaque Epstein-Barr virus

61 Cross-sectional measurement of lymphocryptovirus, the rhesus monkey EBV, demonstrated e

62 rL1-17, and IE transcripts encoded by rhesus lymphocryptovirus were further identified.

63 us (EBV) is a highly prevalent human gamma 1 lymphocryptovirus which infects both B lymphocytes and e