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1 abdoviridae and Paramyxoviridae in the order Mononegavirales.
2 e negative-stranded-RNA viruses in the order Mononegavirales.
3 hylation domains in different members of the Mononegavirales.
4 g to the Paramyxoviridae family of the order Mononegavirales.
5 virus family, Bornaviridae, within the order Mononegavirales.
6 nome whose organization is characteristic of mononegavirales.
7 nome whose organization is characteristic of Mononegavirales.
8 virus family, Bornaviridae, within the order Mononegavirales.
9 Env and other class 1 fusion proteins of the Mononegavirales.
10 ing to the family Pneumoviridae of the order Mononegavirales.
11 stepwise attenuation of transcription in the Mononegavirales, a group of single-strand negative-sense
12                         Viruses of the order Mononegavirales all encode a large (L) polymerase protei
13 re highly conserved among all members of the Mononegavirales and are believed to constitute the L pro
14 rotein is conserved among all members of the Mononegavirales and has six conserved regions ("domains"
15 e negative-stranded RNA viruses of the order Mononegavirales and have been isolated from vertebrates,
16 able hypotheses regarding the replication of Mononegavirales and suggest that disordered regions with
17 ines and antiviral therapeutics against many Mononegavirales are currently available.
18 nonsegmented negative strand RNA viruses (or Mononegavirales) are believed to be concentrated in the
19                                    The order Mononegavirales (comprised of nonsegmented negative-stra
20 Finally, we discovered that the P of related Mononegavirales contain similarly overlooked motifs in t
21  of the Bornaviridae family within the order Mononegavirales, exhibits high neurotropism and provides
22 diating it are conserved in other members of Mononegavirales Finally, we show that the connector-P in
23 trup virus, a newly discovered member of the Mononegavirales from a leafhopper (Hemiptera), and also
24 spite the highly conserved gene order of the Mononegavirales, gene rearrangement is not lethal or nec
25 ary pressures acting on noncoding regions in Mononegavirales genomes and observed that, despite being
26 ical member of the Paramyxoviridae family of Mononegavirales, has been shown to activate the expressi
27                                              Mononegavirales have a unique machinery to replicate RNA
28 e genome.IMPORTANCEMost viruses of the order Mononegavirales have been demonstrated to naturally gene
29 together with earlier studies, suggests that Mononegavirales have broadly evolved to utilize LLPS as
30                  Viruses within the order of Mononegavirales have phosphoproteins that typically serv
31 NA viruses (nsNSVs), also known as the order Mononegavirales, have a genome consisting of a single st
32 ify a novel RNA virus belonging to the order Mononegavirales in Sf9 cells.
33 segmented negative-strand RNA viruses (order Mononegavirales) include many important human pathogens.
34 ment is conserved among members of the order Mononegavirales, including measles virus and rabies viru
35                                    The order Mononegavirales is composed of viruses that possess sing
36 polymerase of viruses belonging to the order Mononegavirales is part of a large multifunctional L pro
37  emerging pathogen of this order of viruses (Mononegavirales) is one of the main causes of respirator
38 of the Bornaviridae family, within the order Mononegavirales, is highly neurotropic and constitutes a
39 e prototype of a new family within the order Mononegavirales, is unusual in its nuclear localization
40 main cofactor of the viral RNA polymerase of Mononegavirales It is involved in multiple interactions
41                                              Mononegavirales, known as nonsegmented negative-sense (N
42  P protein represents a new understanding of Mononegavirales L protein biology.
43 onal assignment of the connector domain of a Mononegavirales L protein.
44  uniqueness of L and P proteins to the order Mononegavirales, makes disruption of the P-connector sit
45 ns, indicating that the L polymerases of the Mononegavirales may function as multidomain proteins.
46 rvation of the gene order observed among the Mononegavirales may result from immobilization of the an
47                                              Mononegavirales mimic RNA synthesis of their eukaryotic
48 y (cryo-EM) structures of the polymerases of Mononegavirales, namely, VSV, RABV, HRSV, human metapneu
49  Endornaviridae, Fusariviridae, Hypoviridae, Mononegavirales, Narnaviridae, Ophioviridae, Ourmiavirus
50                                          The Mononegavirales, or non-segmented negative-sense RNA vir
51 negative-strand RNA viruses belonging to the Mononegavirales order require their cognate co-factor P
52 studying brain infections by a member of the Mononegavirales order that can cause permanent changes i
53          As all the viruses belonging to the Mononegavirales order, the nonsegmented negative-strand
54 ) RNA virus, prototype of a new taxon in the Mononegavirales order.
55                                              Mononegavirales phosphoproteins lack sequence conservati
56                                 Fragments of Mononegavirales polymerases analyzed to date cannot rest
57                                   Therefore, Mononegavirales polymerases have been extensively invest
58 es We outline the structural analyses of the Mononegavirales polymerases since the first structure of
59 a single polypeptide is not required for the Mononegavirales polymerases to adopt a proper tertiary c
60 ation is anticipated to be applicable to all Mononegavirales polymerases.
61 d cofactor phosphoprotein (P) constitute the Mononegavirales polymerases.
62  of the family Bornaviridae within the order Mononegavirales, provides an important model for the inv
63 nce variation in full-length genomes from 13 Mononegavirales species.
64 egmented negative-strand RNA virus (order of Mononegavirales) that persistently infects specific brai
65 a new family, Bornaviridae, within the order Mononegavirales, that is characterized by nuclear transc
66  RNA viruses, including members of the order Mononegavirales To investigate whether ferrets were susc
67 s virus (MeV), like all viruses of the order Mononegavirales, utilizes a complex consisting of genomi
68 nes and therapeutics against RSV and related Mononegavirales viruses.
69 tis virus (VSV) is an archetypical member of Mononegavirales, viruses with a genome of negative-sense
70 is mechanisms and models of highly conserved Mononegavirales We conclude by the discussion of remaini
71 and the oligomeric multimodular adapter P of Mononegavirales We outline the structural analyses of th
72     As is the case with other members of the Mononegavirales, we detected polar expression of fluores
73 e a similar function in other members of the Mononegavirales, we examined the Sendai virus (SeV) (fam
74             Filoviruses are within the order Mononegavirales, which also includes rabies virus, measl