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1  the transcription complex in a prototypical dsRNA virus.
2 ruited by the yeast L-A double-stranded RNA (dsRNA) virus.
3  for the packing of dsDNA can be extended to dsRNA viruses.
4 ral entry of other multilayered, nonturreted dsRNA viruses.
5 for virion infectivity in many multi-shelled dsRNA viruses.
6  by growth inhibitors, in contrast to fungal dsRNA viruses.
7 studies and provide much of our knowledge of dsRNA viruses.
8  and similarities and differences with other dsRNA viruses.
9 assembly intermediate of certain prokaryotic dsRNA viruses.
10 for endogenous conservative transcription in dsRNA viruses.
11 ion and diversity of this enormous family of dsRNA viruses.
12 in the RNA-dependent RNA polymerases of some dsRNA viruses.
13 ly efficient endogenous RNA transcription of dsRNA viruses.
14 nces the infectivity of pathogenic dsDNA and dsRNA viruses.
15  (BTV), a member of the Reoviridae family of dsRNA viruses.
16 RNA stages, respectively, between +ssRNA and dsRNA viruses.
17 negative-strand RNA and double-stranded RNA (dsRNA) viruses.
18 olated, however, in recent structures of two dsRNA viruses, a fungal virus from family Partitiviridae
19  the non-A-tailed transcripts of a segmented dsRNA virus and the transcriptome of the infected cell.
20 onservation between RdRps of true ssRNA+ and dsRNA viruses and form a minor, deeply separated cluster
21 that is similar in appearance to the RdRP of dsRNA viruses and multiple accessory appendages that may
22  particle-associated transcription cycles of dsRNA viruses and that small molecules are useful tools
23 s a viral nucleic acid sentinel activated by dsRNA viruses and virus replication intermediates within
24 s, and between a fungal double-stranded RNA (dsRNA) virus and an insect virus, in the yeast host.
25 rise the viral assemblage (ssDNA, dsDNA, and dsRNA viruses) and profile lineage-specific host-virus i
26 nas vaginalis are persistently infected with dsRNA viruses, and growing evidence indicates that at le
27 RNA isolation, detection and inactivation of dsRNA viruses, and prebiotic molecular evolution.
28 e life cycles of double-stranded (ds)DNA and dsRNA viruses are dissimilar.
29                    Most double-stranded RNA (dsRNA) viruses are transcribed and replicated in a speci
30 machine and a detailed comparison with other dsRNA viruses at the secondary-structure level.
31 e 6 of the Cystoviridae family, we show that dsRNA viruses can adopt a dsDNA-like single-spooled geno
32 ber of the Reoviridae, a family of segmented dsRNA viruses characterized by endogenous RNA transcript
33        Upon infection with certain ssRNA and dsRNA viruses, CHO cells fail to generate a significant
34 ide new information on VF trafficking during dsRNA virus coinfection, we rescued two recombinant infe
35        Both repress L-A double-stranded RNA (dsRNA) virus copy number, further suggesting that their
36  infection of segmented double-stranded RNA (dsRNA) virus (CPV; Reoviridae) and highlights the import
37 omparison of PcV and other distantly related dsRNA viruses detected preferential insertion sites at w
38         IMPORTANCE A scenario proposing that dsRNA viruses evolved from +ssRNA viruses is still consi
39                                      The L-A dsRNA virus expression, replication, and RNA packaging a
40 the viral RNA-packaging motif of a segmented dsRNA virus for the first time.
41                      In double-stranded-RNA (dsRNA) viruses found in animals, bacteria and yeast, the
42 e completion of Koch's postulates for a true dsRNA virus from a filamentous fungus and the descriptio
43  orthoreovirus (MRV), a double-stranded RNA (dsRNA) virus from the family Reoviridae.
44 nfected by nonsegmented double-stranded RNA (dsRNA) viruses from the genus Trichomonasvirus, family T
45  core architecture among a broad spectrum of dsRNA viruses, from the mammalian rotaviruses to the Pse
46   The reovirus polymerase and those of other dsRNA viruses function within the confines of a protein
47 um virus 1 (CSpV1) is a double-stranded RNA (dsRNA) virus harbored by Cryptosporidium spp.
48 Analysis of bacterial, protozoal, and fungal dsRNA viruses has improved our understanding of their st
49                                         Most dsRNA viruses have a genome-enclosing capsid that compri
50 NA polymerases from birnaviruses, a group of dsRNA viruses, have their catalytic motifs arranged in a
51 ry and inaugural studies of a novel taxon of dsRNA viruses in five different planarian species.
52  endogenous, persistent double-stranded RNA (dsRNA) virus in each U. maydis subtype.
53  taxon of monosegmented double-stranded RNA (dsRNA) viruses in five planarian species, including the
54 scription characterizes double-stranded RNA (dsRNA) viruses in the Reoviridae, a family that is exemp
55 enveloped, nonsegmented double-stranded RNA (dsRNA) virus infecting Giardia lamblia, the most common
56 aviruses are a group of double-stranded RNA (dsRNA) viruses infecting birds, fish, and insects.
57 idae, a large family of double-stranded RNA (dsRNA) viruses infecting plants, insects, fishes and mam
58 rial genome and the presence or absence of a dsRNA virus influence the phenotype of chromosomal varia
59                        mRNA transcription in dsRNA viruses is a highly regulated process but the mech
60 iruses, the mechanism of genome packaging of dsRNA viruses is poorly understood.
61 ding shells and homologous proteins in other dsRNA viruses: lambda1 in orthoreoviruses and VP3 in orb
62          The endogenous double-stranded RNA (dsRNA) virus Leishmaniavirus (LRV1) has been implicated
63 uence and structure, drive recombination for dsRNA viruses, likely through reinitiation after re-hybr
64 virus (PcV) shows the progenitor fold of the dsRNA virus lineage and suggests a relationship between
65 ated that the hallmark fold preserved in the dsRNA virus lineage shares a long (spinal) alpha-helix t
66 e many examples of inhibitors acting against dsRNA viruses more generally.
67                                 Encapsidated dsRNA viruses, most of which are nonenveloped, infect a
68 (LIV), an unclassified, double-stranded RNA (dsRNA) virus of Agaricus bisporus, were associated with
69 constitutes the viral genome (in the case of dsRNA viruses) or is generated in host cells during vira
70 c analogs of ssRNA viruses (polyuridine) and dsRNA viruses (polyinosinic-polycytidylic acid) were sig
71 mbles the corresponding enzymatic regions of dsRNA virus polymerases and influenza virus polymerase.
72       These observations suggest a model for dsRNA virus recombination in which the polymerase pauses
73 her this arrangement is a general feature of dsRNA viruses remains unknown.
74 antiviral defense modulator are derived from dsRNA viruses (Reoviridae) and dsDNA viruses (Baculoviri
75                           Two strains of the dsRNA virus reovirus differ in the pattern of packaged D
76     We found that for a double-stranded RNA (dsRNA) virus, reovirus, recombination occurs preferentia
77                         The visualization of dsRNA virus replication steps in living cells received m
78 olecular mechanism by which infection with a dsRNA virus results in necroptosis.
79 toplasm triggers host defence mechanisms(9), dsRNA viruses retain their genomes within a core particl
80 lts were obtained with particles of a second dsRNA virus, rhesus rotavirus, from a divergent taxonomi
81          Here, we have characterized a novel dsRNA virus (Sclerotinia sclerotiorum megabirnavirus 1 [
82 -stranded RNA (ssRNA) virus (hypovirus) to a dsRNA virus, SsMBV1.
83    Moreover, GLV is the only known protozoal dsRNA virus that can transmit efficiently by extracellul
84                               Rotavirus is a dsRNA virus that infects epithelial cells that line the
85                           Here, we studied a dsRNA virus that infects the fungus Rosellinia necatrix,
86                    Here, we investigated the dsRNA virus that infects the widespread enteric parasite
87  and follows the architectural principle for dsRNA viruses that a 120-subunit capsid is a conserved a
88 otavirus is a segmented double-stranded RNA (dsRNA) virus that causes severe gastroenteritis in young
89 V) can be infected with double-stranded RNA (dsRNA) viruses that may have important implications for
90 segmented, multipartite double-stranded RNA (dsRNA) viruses that until recently were only known to in
91                                     For most dsRNA viruses, the genome-enclosing capsid comprises 120
92                    We show that unlike other dsRNA viruses, the VP2 attachment trimer has a triskelio
93 tively induces apoptosis in cells containing dsRNA, virus titers were strongly reduced.
94 ment with its unique capacity as a protozoal dsRNA virus to survive and transmit through extracellula
95 ts the first 9-segment, double-stranded RNA (dsRNA) virus to be isolated in nature.
96                               The genomes of dsRNA viruses vary greatly in the degree of segmentation
97 nformation that adds to our understanding of dsRNA virus VF trafficking.
98                                     Overall, dsRNA virus was present in 21 (75%) of 28 TV isolates (9
99 eovirus (reovirus) is a double-stranded RNA (dsRNA) virus which encapsidates its 10 genome segments w
100 might have occurred from an ssRNA virus to a dsRNA virus, which may provide new insights into the evo
101    Bacteriophage 6 is a double-stranded RNA (dsRNA) virus whose genome is packaged sequentially as th
102 read protozoan parasites carry endosymbiotic dsRNA viruses with uncharted implications to the human h
103  BTV is a nonenveloped, double-stranded RNA (dsRNA) virus with two capsids: a well-studied, stable co

 
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