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1 rotein encoded by Rice stripe virus (RSV), a negative-strand RNA virus.
2 us, Indiana serotype (VSV(IND)), a prototype negative-strand RNA virus.
3 ratory syncytial virus (RSV), a nonsegmented negative-strand RNA virus.
4  loop of the PRNTase domain in non-segmented negative strand RNA viruses.
5 rapy for EVD, as has been proposed for other negative strand RNA viruses.
6 feron induction in cells infected with these negative strand RNA viruses.
7  information is available about SIE of plant negative-strand RNA viruses.
8 As, which are characteristic of nonsegmented negative-strand RNA viruses.
9 has counterparts in a number of nonsegmented negative-strand RNA viruses.
10  previously appreciated for the nonsegmented negative-strand RNA viruses.
11 enters, with an emphasis on the nonsegmented negative-strand RNA viruses.
12 ion of RNA replication in multiple-segmented negative-strand RNA viruses.
13 te efficient RNA synthesis, commonly used by negative-strand RNA viruses.
14 on template preference in multiple-segmented negative-strand RNA viruses.
15 ous recombination, which was not observed in negative-strand RNA viruses.
16  of the RNA polymerase (L) of non-segmented, negative-strand RNA viruses.
17 unique GDNQ motif normally characteristic of negative-strand RNA viruses.
18 ts in the design of new therapeutics against negative-strand RNA viruses.
19 ances led to a resurgence in DIP studies for negative-strand RNA viruses.
20 ire of targets for antiviral therapy against negative-strand RNA viruses.
21  and possibly other families of nonsegmented negative-strand RNA viruses.
22  which are a characteristic hallmark of many negative-strand RNA viruses.
23 autophagy can play an antiviral role against negative-strand RNA viruses.
24 , with implications for many other segmented negative-strand RNA viruses.
25 rget for developing antivirals against other negative-strand RNA viruses.
26                  Arenaviruses are enveloped, negative-strand RNA viruses.
27 let-shaped rhabdovirus and a model system of negative-strand RNA viruses.
28  antiviral therapeutics against nonsegmented negative-strand RNA viruses.
29 virus (VSV), a prototype of the nonsegmented negative-strand RNA viruses.
30              Vesicular stomatitis virus is a negative-stranded RNA virus.
31 habdoviruses that may be applicable to other negative-stranded RNA viruses.
32 hanism of replication of influenza and other negative-stranded RNA viruses.
33  contribute to pathogenicity in a variety of negative-stranded RNA viruses.
34  importance for efficient budding of several negative-stranded RNA viruses.
35 es of a number of L proteins of nonsegmented negative-strand RNA viruses, a cluster of high-homology
36     The large (L) proteins of non-segmented, negative-strand RNA viruses, a group that includes Ebola
37 rate vaccine candidates against nonsegmented negative-strand RNA viruses, a large and expanding group
38 element in control of gene expression of the negative strand RNA viruses and a means by which express
39      J paramyxovirus (JPV) is a nonsegmented negative-strand RNA virus and a member of the proposed g
40 ties in the polymerase proteins of segmented negative-strand RNA viruses and for the search for antiv
41 e viral genome can form during infections of negative-strand RNA viruses and outgrow full-length vira
42 ation strategy should be applicable to other negative-strand RNA viruses and will promote studies int
43                  Replication of genomes from negative strand RNA viruses (and RNA viruses in general)
44 he largest nucleoprotein of the nonsegmented negative-stranded RNA viruses, and like the NPs of other
45      The phosphoproteins (P) of nonsegmented negative strand RNA viruses are viral RNA polymerase sub
46                                          The negative-strand RNA viruses are a broad group of animal
47                                              Negative-stranded RNA viruses are a large group of virus
48  stomatitis virus, a prototypic nonsegmented negative-strand RNA virus, are required for terminal de
49 ratory syncytial virus (RSV), a nonsegmented negative-strand RNA virus, are separated by intergenic r
50            In addition, the use of different negative-strand RNA viruses as vectors to efficiently ex
51 nt RNA polymerase L proteins of nonsegmented negative-strand RNA viruses belonging to the Mononegavir
52 y delineate the evolutionary relationship of negative-strand RNA viruses but also provide insights in
53     Phosphorylation of P proteins in several negative strand RNA viruses by specific cellular kinases
54 tiviral action of IFN against a nonsegmented negative-strand RNA virus by targeting the primary trans
55  that La supports the growth of nonsegmented negative-strand RNA viruses by both IFN suppression and
56  function, against a number of positive- and negative-strand RNA viruses by enhancing type I IFN indu
57                     In addition, recombinant negative-strand RNA viruses can now be designed to have
58 dependent RNA polymerase of the nonsegmented negative-strand RNA viruses carries out two distinct RNA
59      Importance: The paramyxovirus family of negative-strand RNA viruses cause significant disease in
60 ses are a large family of membrane-enveloped negative-stranded RNA viruses causing important diseases
61 irovirus (HAZV) is an enveloped trisegmented negative-strand RNA virus classified within the Nairovir
62                             The nonsegmented negative strand RNA viruses comprise hundreds of human,
63 mal RNA synthesis machinery of non-segmented negative-strand RNA viruses comprises a genomic RNA enca
64                                              Negative-strand RNA viruses condense their genome into h
65 cular stomatitis virus (VSV), a nonsegmented negative-strand RNA virus, directs two discrete RNA synt
66                                     For some negative-strand RNA viruses (e.g., vesicular stomatitis
67 verse members of the Paramyxovirus family of negative-strand RNA viruses effectively suppress host in
68                    Paramyxoviruses and other negative-strand RNA viruses encode matrix proteins that
69                                              Negative-strand RNA viruses encode their own polymerases
70 this control, HDV behaves similarly to other negative-strand RNA viruses, even though there is no gen
71 irus, which represent viruses from different negative-strand RNA virus families.
72 ttenuate VSV, and perhaps other nonsegmented negative-strand RNA viruses, for potential application a
73                         The nucleoprotein of negative-strand RNA viruses forms a major component of t
74                                    Rescue of negative-stranded RNA viruses from full-length genomic c
75                          In contrast to most negative-stranded RNA viruses, hantaviruses and other vi
76 etics techniques to manipulate the genome of negative-strand RNA viruses has contributed enormously t
77 w that the mechanism of RNA encapsidation in negative-strand RNA viruses has many common features.
78 ies to genetically manipulate the genomes of negative-strand RNA viruses has provided us with new too
79                          Because monopartite negative strand RNA viruses have not been reported to un
80           Thus, our characterization of this negative-strand RNA virus identified a novel replication
81 encoded by Rice grassy stunt virus (RGSV), a negative-strand RNA virus in the Bunyavirales, causes de
82                         The mumps virus is a negative-strand RNA virus in the family Paramyxoviridae.
83  (VSV) is the prototype virus for 75 or more negative-strand RNA viruses in the rhabdovirus family.
84  the closest relatives of NYNV and MIDWV are negative-stranded-RNA viruses in the order Mononegaviral
85                                              Negative-strand RNA viruses include a diverse set of vir
86  is required for the entry of the prototypic negative-strand RNA virus, including influenza A virus a
87                                 Nonsegmented negative-strand RNA viruses, including measles virus (Me
88                                              Negative-strand RNA viruses, including paramyxoviruses,
89 rnalized viral ribonucleoproteins (vRNPs) of negative-strand RNA viruses induce an early IFN response
90                              Rabies viruses, negative-strand RNA viruses, infect neurons through axon
91 itive-strand RNA virus infections but not in negative-strand RNA virus infections.
92                        The nucleocapsid of a negative-strand RNA virus is assembled with a single nuc
93       Gene expression among the nonsegmented negative-strand RNA viruses is controlled by distance fr
94                   The genome of nonsegmented negative-strand RNA viruses is tightly embedded within a
95   The viral polymerase of influenza virus, a negative-strand RNA virus, is believed to polyadenylate
96  and reveal the structural organization of a negative-strand RNA virus L protein.
97                                          The negative-strand RNA virus measles virus (MeV) uses tissu
98 tinuous RNA-protective path, consistent with negative-strand RNA virus mechanisms.
99 een documented previously for a nonsegmented negative-strand RNA virus (mononegavirus).
100 riation of the adaptability of a debilitated negative-strand RNA virus, namely the generation of defe
101 ding is a departure from other nonsegmented, negative-strand RNA viruses (NNSVs) that have been studi
102        Vesicular stomatitis virus (VSV) is a negative-stranded RNA virus normally sensitive to the an
103 by modeling crystal structures of homologous negative strand RNA virus Ns in NC.
104  and replication processes of non-segmented, negative-strand RNA viruses (nsNSVs) are catalyzed by a
105                            The nonsegmented, negative-strand RNA viruses (nsNSVs), also known as the
106                                          The negative-strand RNA viruses (NSRVs) are unique because t
107                               What separates negative-strand RNA viruses (NSVs) from the rest of the
108                                              Negative-strand RNA viruses (NSVs) include some of the m
109 SV genome for viral RNA synthesis.IMPORTANCE Negative-strand RNA viruses (NSVs) include the most path
110                                   Like other negative-strand RNA viruses (NSVs) such as influenza and
111 nfluenza virus type 3 (PIV3), a nonsegmented negative-strand RNA virus of the Paramyxoviridae family
112 nt to be a previously unrecognized enveloped negative-strand RNA virus of the Paramyxoviridae family,
113                            Rhabdoviruses are negative-stranded RNA viruses of the order Mononegaviral
114 nges of the M proteins of other nonsegmented negative-strand RNA viruses on their interactions with m
115 r Mononegavirales (comprised of nonsegmented negative-stranded RNA viruses or NNSVs) contains many im
116 eplication and transcription of nonsegmented negative strand RNA viruses (or Mononegavirales) are bel
117 rus (BDV) is a newly classified nonsegmented negative-strand RNA virus (order of Mononegavirales) tha
118                             The nonsegmented negative-strand RNA viruses (order Mononegavirales) incl
119 that both the N- and C-terminal regions of a negative-strand RNA virus P are involved in binding the
120 itis virus (VSV, a prototype of nonsegmented negative-strand RNA viruses) plays pivotal roles in tran
121 st oligomerisation as a conserved feature of negative strand RNA virus polymerases.
122       The polymerase complex of nonsegmented negative-strand RNA viruses primarily consists of a larg
123                          This suggested that negative-strand RNA viruses produce little, if any, dsRN
124 ing those by ssDNA viruses and positive- and negative-strand RNA viruses, produce dsRNAs detectable b
125 RTANCEMeasles virus (MeV), a non-integrating negative-strand RNA virus, rarely causes subacute sclero
126 of the RNA than the NP protein of some other negative-strand RNA viruses, reflecting the degree of NP
127 polymerase complex.IMPORTANCE Replication of negative-strand RNA viruses relies on two components: a
128 etween arboviruses and ticks, especially for negative-strand RNA viruses, remain largely unexplored.
129             However, the impact of TRIM56 on negative-strand RNA viruses remains unclear.
130 h has served in the past as a model to study negative-strand RNA virus replication.
131                                              Negative-strand RNA viruses represent a significant clas
132                                     MuV is a negative strand RNA virus, similar to rabies virus or Eb
133 bly diverse family of enveloped nonsegmented negative-strand RNA viruses, some of which are the most
134          The nucleoprotein (NP) of segmented negative-strand RNA viruses such as Orthomyxo-, Arena-,
135  Infection of human dendritic cells (DCs) by negative-strand RNA viruses, such as Newcastle disease v
136                           The genomic RNA of negative-strand RNA viruses, such as vesicular stomatiti
137 s instead, suggesting that current segmented negative-strand RNA virus taxonomy may need revision.
138                      Ebola virus (EBOV) is a negative strand RNA virus that causes Ebola virus diseas
139 al virus (RSV) is an enveloped, filamentous, negative-strand RNA virus that causes significant respir
140            Human metapneumovirus (HMPV) is a negative-strand RNA virus that frequently causes respira
141  Borna disease virus (BDV) is a nonsegmented negative-strand RNA virus that replicates and transcribe
142                Paramyxoviruses are enveloped negative-strand RNA viruses that are significant human a
143 Paramyxoviruses are enveloped, nonsegmented, negative-strand RNA viruses that cause a wide spectrum o
144                             Arenaviruses are negative-strand RNA viruses that cause human diseases su
145                   Arenaviruses are enveloped negative-strand RNA viruses that cause significant human
146                           Influenza virus, a negative-stranded RNA virus that causes severe illness i
147                  Arenaviruses are enveloped, negative-stranded RNA viruses that belong to the family
148                        Thus, we examined two negative-stranded RNA viruses that have dsRNA intermedia
149                                         In a negative strand RNA virus, the genomic RNA is sequestere
150                         For the nonsegmented negative-strand RNA viruses, the polymerase is comprised
151 virus (VSV), a prototype of the nonsegmented negative-strand RNA viruses, the two methylase activitie
152     In the replication cycle of nonsegmented negative-strand RNA viruses, the viral RNA-dependent RNA
153                A reverse genetics system for negative-strand RNA viruses was first successfully devel
154 aramyxoviruses, and by analogy for all other negative-strand RNA viruses, we show that directional se
155                  Hantaviruses are enveloped, negative-strand RNA viruses which can be lethal to human
156 d vesicular stomatitis virus, a nonsegmented negative-strand RNA virus, which carries out transcripti
157        Vesicular stomatitis virus (VSV) is a negative-strand RNA virus with a non-segmented genome, c
158        Vesicular stomatitis virus (VSV) is a negative-strand RNA virus with inherent specificity for
159 se virus (BDV) is a neurotropic nonsegmented negative-strand RNA virus with limited homology to rhabd
160           Newcastle disease virus (NDV) is a negative-strand RNA virus with oncolytic activity agains
161                             Lassa virus is a negative-strand RNA virus with only four structural prot
162 es order comprises tick-borne, trisegmented, negative-strand RNA viruses, with several members being

 
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