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1                                              NLV capsid primers demonstrated a greater specificity of
2                                              NLVs also have been found to be a cause of acute gastroe
3                                              NLVs were a major cause of both outbreaks and sporadic d
4                                              NLVs were detected by reverse transcription-polymerase c
5 erologic evidence of infection with > or = 1 NLV was detected in 61 (56%) of 109 patients tested agai
6 ding frame 2 (ORF2) were used to analyze 101 NLV strains, including 2 bovine strains.
7 in 61 (56%) of 109 patients tested against 3 NLV antigens (i.e., Norwalk, Hawaii, and Toronto viruses
8      Unpublished data from laboratories of 4 NLV researchers were also used.
9 elected CMV-specific CD8(+) T cells (HLA-A02/NLV peptide), conferring resistance to glucocorticoids.
10  with genogroup I strains causing 26% of all NLV-positive outbreaks.
11 en (80%) outbreaks met the definition for an NLV outbreak.
12  August 1993 and July 1997, we identified an NLV strain that predominated during the 1995-1996 season
13 g a newly developed and sensitive method, an NLV G2 strain was identified in 2 oyster samples implica
14 he genetic relationship between NLV-BECs and NLV-HuCVs but with the NLV-BECs comprising two clusters
15 sensitive and specific detection of NLV-BEC (NLV-BEC Jena and NA-2) and BEC-NB-like viruses, respecti
16 formation, a functional relationship between NLV p41 and enterovirus 2C is discussed in regard to the
17 ata support the genetic relationship between NLV-BECs and NLV-HuCVs but with the NLV-BECs comprising
18  NLV-BECs, the genetic relationships between NLV from humans and the NLV-BECs commonly circulating in
19 known genotype 2 BoNVs than to genotype 1 Bo/NLV/Jena/80/DE.
20 ene were more closely related to those of Bo/NLV/Jena/80/DE (77 and 87% identities, respectively) tha
21 dentities, respectively) than to those of Bo/NLV/Newbury-2/76/UK (69 and 69% identities, respectively
22 4%, respectively) with the capsid gene of Bo/NLV/Newbury-2/76/UK, whereas the nucleotide and amino ac
23 uses (BoNVs) were more closely related to Bo/NLV/Newbury-2/76/UK (GIII/2) and other known genotype 2
24                    The C7.NLV.HLA-A2 and C25.NLV.HLA-A2 complexes exhibit divergent TCR footprints on
25                                       The C7.NLV.HLA-A2 and C25.NLV.HLA-A2 complexes exhibit divergen
26 n of improved molecular techniques to detect NLVs demonstrates that most outbreaks of nonbacterial ga
27 cent improvements to the method of detecting NLVs in shellfish include enhanced processing of virus a
28  the reverse), giving rise to highly diverse NLV-specific TCR repertoires.
29 ns, suggesting that different mechanisms for NLV attachment likely exist.
30 uct, a regimen similar to current models for NLV vaccination.
31 tool sample from the infant was positive for NLV by RT-PCR, and the sequence of the amplified product
32 taminated shellfish serve as the vehicle for NLV transmission.
33  illness and should encourage monitoring for NLVs in drinking water.
34 , and, of these, 217 (93%) were positive for NLVs.
35 setting, these data support a major role for NLVs as etiologic agents of gastroenteritis in elderly p
36  an assay for the rapid identification of G1 NLVs in fecal specimens.
37 irus (genus Lagovirus), Norwalk virus (genus NLV), and Sapporo virus (genus SLV).
38 veys using electron microscopy often grouped NLVs with other unrelated viruses.
39 transcription-PCR (RT-PCR) primers for human NLV recognize NLV-BECs, the genetic relationships betwee
40 bservation supports the subdivision of human NLVs into two genogroups and provides an assay for the r
41 mer sets designed for the detection of human NLVs or BECs.
42  and from patients involved in a genogroup I NLV outbreak were also tested.
43 ajor capsid protein from another genogroup I NLV strain (NCFL) isolated from a recent outbreak.
44                Ltd., Tokyo, Japan) and IDEIA NLV (DakoCytomation Ltd., Ely, United Kingdom) kits, tha
45 t least 1 year, that specifically identified NLVs.
46 s establishing the diagnosis as genogroup II NLV infection.
47 s specific for the diagnosis of genogroup II NLV infections.
48 gastroenteritis were tested for genogroup II NLV Mexico virus-specific immunoglobulin M (IgM) by use
49 n sera from those infected with genogroup II NLVs in volunteer and outbreak studies, 28 of 47 were rM
50  variable alpha and variable beta regions in NLV-specific T cell repertoires.
51                             This multistrain NLV outbreak investigation illustrates the importance of
52  consisted of fractional anisotropy of NAWM, NLV, and patient age and sex (adjusted R(2) = 0.32, P <
53 ze the immunodominant CMV epitope NLVPMVATV (NLV).
54 ss-reactive HLA-A*02:01 (A2) CMV (NLVPMVATV [NLV])-specific CD8(+) T cells recognizing a specific arr
55  (BECs) have been identified: the norovirus (NLV) Jena and Newbury Agent-2 (NA-2) BECs, which are gen
56  a powerful approach for the design of novel NLV vaccines, either alone or in combination with curren
57                                        NWMV, NLV, and patient sex were the explanatory variables for
58  The final model for NGMV consisted of NWMV, NLV, and patient age and sex (adjusted R(2) = 0.58, P <
59 ific basis for the unified classification of NLV strains detected around the world.
60  for the sensitive and specific detection of NLV-BEC (NLV-BEC Jena and NA-2) and BEC-NB-like viruses,
61                 The small infectious dose of NLV, the large quantity of virus particles in stool, and
62                                Expression of NLV VLPs in mammalian cells offers a powerful approach f
63  investigation illustrates the importance of NLV as a cause of waterborne illness and should encourag
64 otide sequencing, and increased knowledge of NLV genetic diversity.
65 es, reported sporadic cases and outbreaks of NLV-associated gastroenteritis among all age groups.
66 omparison between the consensus sequences of NLV p41 and enterovirus protein 2C revealed regions of h
67             During molecular surveillance of NLV strains from 152 outbreaks of gastroenteritis that o
68 tablish a global network for surveillance of NLV strains that would highlight the importance of NLVs
69 ools, allowing us type-specific detection of NLVs.
70                              Two features of NLVs have hindered the development of simple methods for
71 rains that would highlight the importance of NLVs worldwide and allow molecular identification of com
72 rect electron microscopy for the presence of NLVs.
73 a from those infected with genogroup I NV or NLVs in volunteer and outbreak studies, only 3 of 25 wer
74                          In these outbreaks, NLVs were identified as the probable cause, and crowding
75  of target cells pulsed with the CMV peptide NLV in the presence of dexamethasone (DEX).
76  capsid gene of Norwalk virus, the prototype NLV, has been cloned and expressed in mammalian cells us
77 l infection, the frequency of cross-reactive NLV-specific CD8(+) T cells reduced to previremia levels
78 ed a dynamic expansion of the cross-reactive NLV-specific TCR repertoire before CMV reactivation.
79 ge, of the same A2-restricted cross-reactive NLV-specific TCR-alpha/beta signature (TRAV3TRAJ31_TRBV1
80 PCR (RT-PCR) primers for human NLV recognize NLV-BECs, the genetic relationships between NLV from hum
81  is the first demonstration linking a single NLV strain globally and suggests that the circulation of
82                     These data indicate that NLV infection is a major cause of acute morbidity in mil
83 tine shipboard deployment also suggests that NLVs cause sporadic gastroenteritis.
84                                          The NLV-specific T cell repertoire is characterized by a hig
85 elationships between NLV from humans and the NLV-BECs commonly circulating in cattle is undefined.
86 osely related to the Camberwell virus in the NLV GII/4 genetic cluster was the predominant strain.
87 s more focused on the central portion of the NLV peptide than is C7.
88 stine (duodenum and jejunum), similar to the NLV BEC strains.
89     Caliciviruses genetically related to the NLV-BEC Jena and NA-2 strains or to the recently charact
90 se viruses to be most closely related to the NLV-BEC Jena and NA-2 strains.
91  between NLV-BECs and NLV-HuCVs but with the NLV-BECs comprising two clusters within a third NLV geno
92     Further study of the antigenicity of the NLVs by use of VLPs should allow us to design new detect
93 c clusters within genogroups I and II of the NLVs were detected; a genogroup II (GII) virus closely r
94 -BECs comprising two clusters within a third NLV genogroup.
95 ated gastroenteritis outbreaks attributed to NLV occurred in Louisiana.
96 Extended 3'-terminal genome sequences of two NLV-BECs, designated CV95-OH and CV186-OH, encoding the
97 , and testing identified Norwalk-like virus (NLV) in 8 of 13 stool samples and 1 well.
98            The impact of Norwalk-like virus (NLV) infection on military forces is evaluated in this r
99 ide for the diagnosis of Norwalk-like virus (NLV) infection, yet a commonly accepted genetic classifi
100                        Norwalk-like viruses (NLVs) are a diverse group of single-stranded, nonenvelop
101                        Norwalk-like viruses (NLVs) are the most common cause of acute nonbacterial ga
102 ham showed evidence of Norwalk-like viruses (NLVs) by reverse-transcriptase (RT) polymerase chain rea
103     The three distinct Norwalk-like viruses (NLVs) have various capacities for binding ABH histo-bloo
104          In the 1990s, Norwalk-like viruses (NLVs) were identified in patient specimens as the primar
105 Lagovirus, Vesivirus, "Norwalk-like viruses (NLVs), and "Sapporo-like viruses (SLVs); the latter 2 ge
106 ated with genogroup II Norwalk-like viruses (NLVs), Hawaii virus, and Snow Mountain virus and from pa
107 52%) were positive for Norwalk-like viruses (NLVs), members of the family Caliciviridae.
108 HV) is a member of the Norwalk-like viruses (NLVs), one of four genera of the family Caliciviridae.
109                        Norwalk-like viruses (NLVs), or small round structured viruses, are known to c
110  strain of genogroup I Norwalk-like viruses (NLVs), was expressed as virus-like particles using a bac
111 oup within the genus "Norwalk-like viruses" (NLV) of the family Caliciviridae.
112                      "Norwalk-like viruses" (NLVs) are the most common cause of outbreaks of nonbacte
113  and to characterize "Norwalk-like viruses" (NLVs) in these outbreaks.
114                      "Norwalk-like viruses" (NLVs), members of a newly defined genus of the family Ca
115 tion for testing for "Norwalk-like viruses" (NLVs).
116 not genogroup 2 (G2) "Norwalk-like viruses" (NLVs).
117 cal thickness, and normalized lesion volume (NLV) were quantified.
118 two public TCRs (C7 and C25) in complex with NLV.HLA-A2.
119 re ORF-1 nonstructural-protein sequence with NLV, SLV, vesivirus, and lagovirus strains, while the ov
120 astroenteritis resulting from infection with NLVs, we previously used recombinant-expressed capsid an

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