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1 ntification in domestic dogs of a nonprimate hepacivirus.
2 longing to the family flaviviridae and genus hepacivirus.
3 ce of ancient recombination with these other hepaciviruses.
4 t on the genetic diversity and host range of hepaciviruses.
5 es has resulted in escape from antagonism by hepaciviruses.
6 s) of the RNA genomes of Flaviviridae of the Hepacivirus and Pestivirus genera contain internal ribos
7 four cysteine residues, conserved among the Hepacivirus and Pestivirus genera, fitting the formula o
8 data highlight the similarities between the Hepacivirus and Pestivirus NS5A proteins and suggest tha
9 on the natural history and evolution of the hepaciviruses and on the extent of structural variation
10 major and ancient natural reservoir for both hepaciviruses and pegiviruses and provide insights into
12 erse group of bat-derived viruses related to hepaciviruses and pegiviruses within the family Flavirid
13 volutionary analyses revealed that all known hepaciviruses and pegiviruses, including those previousl
14 about the origin and evolution of the animal hepaciviruses as well as their potential usage as surrog
15 tics, the IRES of hepatitis C virus (HCV), a Hepacivirus belonging to Flaviviridae, cannot as yet be
16 of HCV include a recently discovered canine hepacivirus (CHV) and GB virus B (GBV-B), both viruses w
17 parative phylogenetic analysis of the canine hepacivirus (CHV) confirmed it to be the most geneticall
20 gy caused by another, more rapidly resolving hepacivirus, GB virus B (GBV-B), in infections of common
23 of hepatitis C virus (HCV), a member of the Hepacivirus genus of the family Flaviviridae, has been d
25 xpanded the previously mammal-only pegivirus-hepacivirus group to include a virus from the graceful c
26 B virus B (GBV-B; family Flaviviridae, genus Hepacivirus) has been studied in New World primates as a
29 ow that NS3 proteases from all other primate hepaciviruses, including the highly divergent GBV-A and
30 enetically with GBV-B and recently described hepaciviruses infecting African bats and North American
31 netic and biological characterization of new hepaciviruses infecting animals contributes to our under
32 st that NK cell and DC mobilization in acute hepacivirus infection can dampen virus replication but a
35 ile GB virus B (GBV-B), another hepatotropic hepacivirus, infects small New World primates (tamarins
41 he natural host of the only known nonprimate hepacivirus (NPHV), CHV, which is also the closest phylo
42 sest homolog of HCV is the equine nonprimate hepacivirus (NPHV), which shares similar features with H
43 Among these novel viruses, the nonprimate hepaciviruses (NPHV) that infect horses are the closest
45 The mechanism of translation initiation on hepacivirus/pestivirus (HP) IRESs, which involves factor
46 n the closest genetic relatives of the human hepaciviruses, providing an intriguing clue to the zoono
47 animal and primate hepaciviruses, the equine hepaciviruses remain the closest genetic relatives of th
49 inants between HCV and GB virus B (GBV-B), a hepacivirus that infects small New World primates (tamar
50 ntification of these many animal and primate hepaciviruses, the equine hepaciviruses remain the close
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