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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
7 in 61 (56%) of 109 patients tested against 3 NLV antigens (i.e., Norwalk, Hawaii, and Toronto viruses
9 elected CMV-specific CD8(+) T cells (HLA-A02/NLV peptide), conferring resistance to glucocorticoids.
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
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
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
31 tool sample from the infant was positive for NLV by RT-PCR, and the sequence of the amplified product
35 setting, these data support a major role for NLVs as etiologic agents of gastroenteritis in elderly p
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
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
52 consisted of fractional anisotropy of NAWM, NLV, and patient age and sex (adjusted R(2) = 0.32, P <
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
58 The final model for NGMV consisted of NWMV, NLV, and patient age and sex (adjusted R(2) = 0.58, P <
60 for the sensitive and specific detection of NLV-BEC (NLV-BEC Jena and NA-2) and BEC-NB-like viruses,
63 investigation illustrates the importance of NLV as a cause of waterborne illness and should encourag
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
68 tablish a global network for surveillance of NLV strains that would highlight the importance of NLVs
71 rains that would highlight the importance of NLVs worldwide and allow molecular identification of com
73 a from those infected with genogroup I NV or NLVs in volunteer and outbreak studies, only 3 of 25 wer
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
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.
89 Caliciviruses genetically related to the NLV-BEC Jena and NA-2 strains or to the recently charact
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
96 Extended 3'-terminal genome sequences of two NLV-BECs, designated CV95-OH and CV186-OH, encoding the
99 ide for the diagnosis of Norwalk-like virus (NLV) infection, yet a commonly accepted genetic classifi
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
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
108 HV) is a member of the Norwalk-like viruses (NLVs), one of four genera of the family Caliciviridae.
110 strain of genogroup I Norwalk-like viruses (NLVs), was expressed as virus-like particles using a bac
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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