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1 ated pair dolphin morbillivirus and porpoise morbillivirus.
2 ids, consistent with the ultrastructure of a morbillivirus.
3 for the high cell-to-cell fusion activity of morbilliviruses.
4 e, a sequence relatively conserved among the morbilliviruses.
5 active against measles virus (MeV) and other Morbilliviruses.
6 ivergence from characteristics of archetypal morbilliviruses.
7 most closely related to members of the genus Morbillivirus and infect cells through a pH-independent
8 s caused predominantly by viruses, primarily morbillivirus and influenza A.
9                        Rinderpest virus is a morbillivirus and is the causative agent of a widespread
10 protein is a cathepsin, making FeMV a unique morbillivirus and more similar to the closely related zo
11  antibodies against the related pair dolphin morbillivirus and porpoise morbillivirus.
12                        Rinderpest virus is a morbillivirus and the causative agent of an important di
13  it exhibits a broader host range than other morbilliviruses and frequently crosses species barriers.
14 help in the design of new inhibitors against morbilliviruses and provide additional knowledge concern
15 ggest that, in detail, polymerase binding in morbilliviruses and rubulaviruses differs significantly.
16     The trimeric fusion (F) glycoproteins of morbilliviruses are activated by furin cleavage of the p
17                                              Morbilliviruses are among the most contagious viral path
18              Thus, the H proteins of the two morbilliviruses are interchangeable and fully functional
19                                              Morbilliviruses are members of the family Paramyxovirida
20 rtial cross-neutralization of bat-associated morbillivirus by heterologous sera suggested conserved e
21 and data mining, we identified six divergent morbilliviruses by investigating wild bats (38/1,629 RT-
22  this, we investigated the adaptation of the Morbillivirus canine distemper virus to ferrets and comp
23 ycans attached to fusion (F) proteins of the morbilliviruses canine distemper virus and measles virus
24                                              Morbilliviruses cause many diseases of medical and veter
25                          Membrane fusion for morbillivirus cell entry relies on critical interactions
26                                     Cetacean morbillivirus (CeMV) is a global threat to cetaceans.
27                                     Cetacean morbillivirus (CeMV) is considered one of the most impor
28                                         High morbillivirus concentrations of up to 10(9) RNA copies p
29 cies in closely related members of the genus Morbillivirus, currently referred to as Unclassified Mor
30 ry infections as risk factor for exacerbated morbillivirus disease.
31                                      Dolphin morbillivirus (DMV) is a virulent pathogen that causes h
32 mper virus and a wild-type strain of dolphin morbillivirus failed to downregulate CD46.
33               Measles virus, a member of the Morbillivirus family, infects millions of people each ye
34                             The L protein of morbilliviruses (family Paramyxoviridae) was reported to
35 ing of pleomorphic virions, a characteristic morbillivirus feature.
36                                       Feline morbillivirus (FeMV) is a recently discovered pathogen o
37 gglutinin (H) glycoprotein used by all other morbilliviruses for binding and/or fusion activation wit
38                            We report a novel morbillivirus from a Fraser's dolphin (Lagenodelphis hos
39 hest nucleotide identity (77.3%) to porpoise morbillivirus from Northern Ireland and the Netherlands.
40 morbillivirus sequences in bats, full-length morbilliviruses from bats are limited.
41 easles virus (MV) is the type species of the Morbillivirus genus and its RNA-dependent RNA polymerase
42                            H-proteins of the morbillivirus genus consist of a stalk ectodomain suppor
43 g ferrets and dogs, and is the member of the Morbillivirus genus most easily amenable to experimentat
44        Measles virus, a paramyxovirus of the Morbillivirus genus, is responsible for an acute childho
45                       Paramyxoviruses of the morbillivirus genus, such as measles, are highly contagi
46 o-cell fusion activity characteristic of the morbillivirus genus.
47  measles virus (MeV), a paramyxovirus of the morbillivirus genus.
48                           The P genes of all morbilliviruses give rise to two proteins in addition to
49                               The individual Morbillivirus glycans have similar functional properties
50 tein, we then predicted the locations of the Morbillivirus glycans: the glycan at position 36 is loca
51                                     However, morbillivirus glycoproteins first assemble intracellular
52 se data and very recently published data for morbillivirus H and henipavirus G proteins, we extend ou
53                                          All morbillivirus H-protein heads appear to be connected to
54 , we devised a strategy based on analysis of morbillivirus H-protein sequences, iterative cycles of m
55                     Our data reveal that the morbillivirus H-stalk domain is composed of four tightly
56  the central region (residues 91-115) of the morbillivirus H-stalk; a sub-domain that also encompasse
57                                              Morbilliviruses have high clinical and veterinary releva
58  available tissues to detect the presence of morbillivirus, herpesvirus, West Nile virus, Toxoplasma
59                  These findings validate the morbillivirus immune amnesia hypothesis, define measles
60  the highest nucleotide identity to porpoise morbillivirus in Northern Ireland and the Netherlands an
61 udies to address the postulated role of this morbillivirus in the development of chronic kidney disea
62 f domestic cats and has been classified as a morbillivirus in the Paramyxovirus family.
63 ated questions and to test interventions for morbilliviruses in a natural host species.IMPORTANCEMorb
64          The immunosuppressive properties of morbilliviruses including measles and canine distemper v
65 t on diabolically elegant mechanisms used by morbilliviruses, including the measles virus, to promote
66 ated CDV strain can be used for experimental morbillivirus infections in ferrets that reflect measles
67 thical and practical constraints, and animal morbillivirus infections in natural host species have be
68 of ferrets is quite similar to that of other Morbillivirus infections, including measles, this model
69                          To understand how a morbillivirus invades the host and causes immunosuppress
70 a new nested-PCR method for the detection of morbillivirus is described here.
71 ing antibodies against a primary vampire bat morbillivirus isolate, suggesting frequent non-fatal inf
72                       Sequence alignments of morbillivirus L polymerases have demonstrated the existe
73 on and demonstrate that FeMV causes an acute morbillivirus-like disease in the cat.
74          Here we characterize the myotis bat morbillivirus (MBaMV) from a bat surveillance programme
75  observed with envelope glycoproteins of the morbilliviruses Measles virus and Canine distemper virus
76                               The prototypic morbillivirus, measles virus (MeV), infects humans and s
77 nidentified mechanism that may contribute to morbillivirus pathogenesis where H-specific IgG antibodi
78 culation with vaccine strains of the related morbillivirus, peste des petits ruminants virus (PPRV).
79 ented here increases the number of confirmed morbillivirus-positive cases within the Canarian archipe
80  2018 that is dissimilar to the beaked whale morbillivirus previously identified from Hawaii and to o
81 tion molecule (SLAM, CD150) is the universal morbillivirus receptor.
82 is research will impact our understanding of morbillivirus-related immunosuppression as well as the a
83 e, currently referred to as the unclassified morbillivirus-related viruses (UMRVs).
84 previous metagenomic surveys have identified morbillivirus sequences in bats, full-length morbillivir
85 ategies to mitigate risks of reservoir-bound morbilliviruses shifting hosts.
86  complete genome sequences of Small ruminant morbillivirus (SRMV) have been reported from different p
87 roteins derived from virulent and attenuated morbillivirus strains and was independent of the nature
88 iruses pertaining to the paramyxoviral genus Morbillivirus, such as measles virus, remains unclear.
89 s caused by PPR virus, a member of the genus Morbillivirus that includes the viruses that cause rinde
90 ne distemper virus (CDV) is an enveloped RNA morbillivirus that triggers respiratory, enteric, and hi
91 espiroviruses (that is, HPIV1 and HPIV3) and morbilliviruses (that is, MeV).
92       NHP-associated, but not bat-associated morbilliviruses, used human CD150 and nectin-4 cellular
93 er, spleen and lymph nodes were positive for morbillivirus using a reverse transcription-polymerase c
94 odel will be useful in testing new candidate Morbillivirus vaccines.
95 mally that SLAM recognition is necessary for morbillivirus virulence.
96    Canine distemper virus (CDV) is an animal morbillivirus with a worldwide circulation that infects
97                       Measles virus (MeV), a morbillivirus within the paramyxovirus family, expresses