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1 s with members of the genera Hepacivirus and Pegivirus.
2 of HCV genotype 6, and a co-infecting human pegivirus.
3 pread natural infection of horses by a novel pegivirus.
4 s, which sheds lights on the pathobiology of pegivirus.
5 ns included hepatitis B virus (n = 2), human pegivirus 1 (n = 2), Epstein-Barr virus (n = 9), and Oru
6 uences corresponding to anelloviruses, human pegivirus 1, herpesviruses, and papillomaviruses were de
7 d virus, salivirus, cyclovirus-VN, and human pegivirus 2 [HPgV2] [n, 1 each]), adding to the growing
8 the E1E2 glycoproteins of the hepaciviruses, pegiviruses and pestiviruses are structurally distinct,
9 natural reservoir for both hepaciviruses and pegiviruses and provide insights into the evolutionary h
10 demonstrate that in addition to SIV, simian pegiviruses and simian arteriviruses are widespread and
17 confirmed that the tentatively named equine pegivirus (EPgV) represents a novel species within the P
18 of these animals were coinfected with equine pegivirus (EPgV), also a flavivirus, EPgV viral loads we
19 ery and characterization of two novel simian pegiviruses (family Flaviviridae) and two novel simian a
20 ted flaviviruses hepatitis C virus and human pegivirus (formerly named GBV-C) interfere with T-cell r
23 s and then in horses prompted us to look for pegiviruses (GB virus-like viruses) in these species.
24 DAV with GB viruses of the recently proposed Pegivirus genus, although it shares only 35.3% amino aci
26 ported pegiviruses.IMPORTANCE Members of the Pegivirus genus, family Flaviviridae, widely infect huma
29 we report a phylogenetically distinct goose pegivirus (GPgV) that should be classified as a new spec
30 uses, we expanded the previously mammal-only pegivirus-hepacivirus group to include a virus from the
36 hat is characteristic of previously reported pegiviruses.IMPORTANCE Members of the Pegivirus genus, f
37 ote, the NS2 virus replicated better than WT pegivirus in astrocytes, with both viruses being able to
38 Here, we report a new, genetically distinct pegivirus in goose (Anser cygnoides), the first identifi
39 es revealed that all known hepaciviruses and pegiviruses, including those previously documented in hu
41 ficiency of in vitro replication systems for pegivirus is poor, thus limiting investigation into vira
43 nd epidemiological parameters included human pegivirus load, patient age and sex, HIV load, CD4+ T-ce
44 ic bloodborne viruses like anelloviruses and pegiviruses might be at greater risk of acquiring a bloo
46 ditis: Epstein Barr virus (n=11, 41%), human pegivirus (n=1, 4%), human endogenous retrovirus K (n=27
47 dy provides the first cell culture model for pegivirus, opening new possibilities for studies of pegi
48 SIV-infected African monkeys coinfected with pegiviruses, possibly because SIV causes little to no di
50 (SIVagm; in 42% of animals), a novel simian pegivirus (SPgVagm; in 7% of animals), and numerous nove
51 se embryo fibroblasts, and is thus the first pegivirus that can be efficiently cultured in vitro Expe
53 ntified pathogenicity of previously reported pegiviruses, which sheds lights on the pathobiology of p