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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 nal role(s) of EBV TK and to uncover how the lymphocryptovirus and rhadinovirus enzymes differ, the s
6  targets for testing in vivo with the rhesus lymphocryptovirus animal model for EBV infection.
7 ction is not possessed by New World marmoset lymphocryptovirus BILF1.
8 tion will facilitate investigations of human lymphocryptovirus biology.
9 A) and the orthologous pre-miRNA from Rhesus lymphocryptovirus contribute to reducing IFN signaling.
10  encephalomyelitis model that an EBV-related lymphocryptovirus enables B cells to protect a proteolys
11 scription initiation site) from the EBV-like lymphocryptoviruses found in baboons (herpesvirus papio;
12 pression are conserved among the EBV-related lymphocryptoviruses found in nonhuman primates.
13 ng the immune-evasion strategies used by the lymphocryptovirus (gamma(1)-herpesvirus) EBV is the down
14 gene of HV(MNE) placed this virus within the Lymphocryptovirus genus and demonstrated that HV(MNE) is
15  evolution of immunoevasive functions by the lymphocryptovirus genus of herpesviruses.
16 we explore the evolution of BILF1 within the lymphocryptovirus genus.
17  have studied its conservation in the simian lymphocryptovirus herpesvirus papio (HVP) by cloning HVP
18 er AdC-rhEBNA-1 immunizations in chronically lymphocryptovirus-infected rhesus macaques, an EBV infec
19 Although the homolog of BILF1 encoded by the lymphocryptovirus infecting Old World rhesus primates sh
20                           An animal model of lymphocryptovirus infection will facilitate investigatio
21 eport that B cells infected with EBV-related lymphocryptovirus (LCV) are requisite APCs for MHC-E-res
22 tic EBV vaccines that target the rhesus (rh) lymphocryptovirus (LCV) EBNA-1 to determine if ongoing T
23    A closely related herpesvirus in the same lymphocryptovirus (LCV) genera as EBV naturally infects
24                      We sequenced the rhesus lymphocryptovirus (LCV) genome in order to determine its
25 mber of the Epstein-Barr virus (EBV)-related lymphocryptovirus (LCV) genus and extended the known hos
26 with a gammaherpesvirus which is in the same lymphocryptovirus (LCV) genus as and closely related to
27 ilar to other gammaherpesviruses in the same lymphocryptovirus (LCV) genus that naturally infect Old
28                                   The rhesus lymphocryptovirus (LCV) is an EBV-related herpesvirus th
29 overy of an Epstein-Barr virus (EBV)-related lymphocryptovirus (LCV) naturally infecting common marmo
30 ree EBNA-3 homologues from a closely related lymphocryptovirus (LCV) which naturally infects rhesus m
31 stein-Barr virus (EBV), the only known human lymphocryptovirus (LCV), displays a remarkable degree of
32  rhesus macaques with the EBV-related rhesus lymphocryptovirus (LCV).
33  homologue is conserved in the rhesus monkey lymphocryptovirus (LCV).
34 , is the only human herpesvirus in the genus Lymphocryptovirus (LCV).
35 ne sequences from EBV and the related herpes lymphocryptoviruses (LCV) infecting baboons and rhesus m
36 d World primates are naturally infected with lymphocryptoviruses (LCV) that are closely related to Ep
37       Epstein-Barr-related herpesviruses, or lymphocryptoviruses (LCV), naturally infect humans and n
38 LP homologues from baboon and rhesus macaque lymphocryptoviruses (LCVs) (baboon LCV and rhesus LCV).
39                                              Lymphocryptoviruses (LCVs) naturally infecting Old World
40  the homologous proteins of nonhuman primate lymphocryptoviruses (LCVs), which bear a strong genetic
41 ously uncharacterized nonhuman primate (NHP) lymphocryptoviruses (LCVs).
42 f LMP1 expression is a conserved function of lymphocryptovirus miRNAs.
43                      A highly similar rhesus lymphocryptovirus naturally endemic in rhesus monkeys wa
44 on, chimeric proteins were made using rhesus lymphocryptovirus (Rh-LCV) gL (Rh gL), which shares a hi
45 une response using the EBV-homologous rhesus lymphocryptovirus (rhLCV) infection in rhesus macaques.
46 t recombinant 72A1 did not neutralize rhesus lymphocryptovirus (rhLCV) infection of macaque B cells.
47                                       Rhesus lymphocryptovirus (rhLCV) is a gamma-herpesvirus closely
48 ed with the Epstein-Barr virus (EBV)-related lymphocryptovirus (rhLCV).
49                                       Rhesus lymphocryptovirus (rLCV) and Epstein-Barr virus (EBV) ar
50          Epstein-Barr virus (EBV) and rhesus lymphocryptovirus (rLCV) are closely related gammaherpes
51     The epidemiology of herpesvirus papio, a lymphocryptovirus similar to Epstein-Barr virus (EBV), w
52 re closely related gammaherpesviruses in the lymphocryptovirus subgroup that express viral microRNAs
53          Epstein-Barr virus (EBV) is a human lymphocryptovirus that causes infectious mononucleosis,
54               Cross-sectional measurement of lymphocryptovirus, the rhesus monkey EBV, demonstrated e
55 us (EBV) is a highly prevalent human gamma 1 lymphocryptovirus which infects both B lymphocytes and e

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