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1 years nearly all people have been exposed to metapneumovirus.
2 h acute respiratory tract illness, for human metapneumovirus.
3 za A, respiratory syncytial virus, and human metapneumovirus.
4 al methods, primarily rhinoviruses and human metapneumovirus.
5 tial virus (RSV), human bocavirus, and human metapneumovirus.
9 fluenza virus (PIV), influenza virus (InfV), metapneumovirus, adenovirus (Ad), coronavirus, and enter
10 luenza viruses 1-4, influenza A and B, human metapneumovirus, adenovirus, and human rhinoviruses, cor
11 parainfluenza viruses 1, 2, 3, and 4; human metapneumovirus; adenovirus; enterovirus-rhinovirus; cor
12 -3, influenza viruses AH1, AH3, and B, human metapneumovirus, adenoviruses, and bocavirus) and 3 path
13 s well as respiratory syncytial virus, human metapneumovirus, adenoviruses, picornaviruses, and coron
14 enza, respiratory syncytial virus, and human metapneumovirus among patients with CAP of all ages prob
17 enomic structure and composition of an avian metapneumovirus (aMPV) recently isolated from wild Canad
21 riculturally important viruses such as avian metapneumovirus (aMPV), and Newcastle disease virus (NDV
22 bers, human metapneumovirus (hMPV) and avian metapneumovirus (aMPV), causing respiratory tract infect
25 The first cases of infection caused by avian metapneumoviruses (aMPVs) were described in turkeys with
26 teins from other subtype C viruses and human metapneumovirus and more than 170 aa larger than the G p
27 nome promoters are conserved between the two metapneumoviruses and can be cross-recognized by the pol
28 piratory syncytial viruses A and B and human metapneumovirus, and (iii) parainfluenza virus types 1 t
29 yncytial virus (RSV), influenza, rhinovirus, metapneumovirus, and adenovirus was highly associated wi
31 man rhinoviruses, human coronaviruses, human metapneumovirus, and human bocavirus, as well as the nee
33 viruses, respiratory syncytial virus, human metapneumovirus, and the deadly zoonotic henipaviruses H
35 iruses not covered by DFA and R-mix culture (metapneumovirus, coronaviruses [CoV], parainfluenza viru
37 Paramyxoviridae includes two members, human metapneumovirus (hMPV) and avian metapneumovirus (aMPV),
39 re bronchiolitis and dual infection by human metapneumovirus (hMPV) and human respiratory syncytial v
40 matory chemokine production induced by human metapneumovirus (hMPV) and Nipah virus (NiV), suggesting
41 fections caused by the paramyxoviruses human metapneumovirus (hMPV) and respiratory syncytial virus (
42 eins derived from two human pathogens, human metapneumovirus (hMPV) and respiratory syncytial virus (
44 Respiratory syncytial virus (RSV) and human metapneumovirus (HMPV) are two closely related viruses t
45 Respiratory syncytial virus (RSV) and human metapneumovirus (hMPV) are two important viral pathogens
46 Respiratory syncytial virus (RSV) and human metapneumovirus (hMPV) cause a similar spectrum of respi
50 GFP-expressing AMPV and GFP-expressing human metapneumovirus (HMPV) could be recovered using the supp
57 system resulted from the detection of human metapneumovirus (HMPV) in 9 specimens, human CoV (HCoV)
58 respiratory syncytial virus (RSV) and human metapneumovirus (HMPV) in older adults in comparison wit
60 y MAb-8 was evaluated for detection of human metapneumovirus (HMPV) in shell vial centrifugation cult
61 nocompromised hosts, but the impact of human metapneumovirus (hMPV) in this setting was previously un
63 The inpatient and outpatient burden of human metapneumovirus (HMPV) infection among young children ha
92 rtant clinical implications.IMPORTANCE Human metapneumovirus (HMPV) is a recently discovered pathogen
103 espiratory syncytial virus (hRSV), the human metapneumovirus (hMPV) is one of the leading causes of c
108 challenging B cell-deficient mice with human metapneumovirus (HMPV) several weeks after primary infec
109 respiratory syncytial virus (hRSV) and human metapneumovirus (hMPV) share virologic and epidemiologic
110 oarray (Virochip) was used to detect a human metapneumovirus (hMPV) strain associated with a critical
111 98-75 (CAN75) and the CAN97-83 (CAN83) human metapneumovirus (HMPV) strains, which represent the two
112 activation of the fusion F protein of human metapneumovirus (HMPV) to replication and pathogenicity
113 roduction by BALB/c mice infected with human metapneumovirus (hMPV) was compared to respiratory syncy
117 capability of MS for the detection of human metapneumovirus (HMPV), a common cause of respiratory tr
123 ry syncytial virus (RSV), enterovirus, human metapneumovirus (hMPV), adenovirus (AdV), and rhinovirus
125 an respiratory syncytial virus (hRSV), human metapneumovirus (hMPV), and human parainfluenza virus ty
126 es of the CAN97-83 clinical isolate of human metapneumovirus (HMPV), consensus nucleotide sequencing
128 A recently discovered paramyxovirus, human metapneumovirus (hMPV), has been studied by our group in
130 enovirus, coronaviruses HKU1 and NL63, human metapneumovirus (hMPV), influenza A virus (to type level
131 of respiratory syncytial virus (RSV), human metapneumovirus (HMPV), parainfluenza virus 1 to 3 (PIV1
133 lu-B, PIV-1, PIV-2, PIV-3, PIV-4, RSV, human metapneumovirus (hMPV), rhinoviruses (RhVs), enterovirus
134 Human Parainfluenza Virus (HPIV), and Human Metapneumovirus (hMPV), we adopt a theoretical approach
137 spiratory syncytial viruses (HRSV) and human metapneumoviruses (HMPV) were involved in the etiology o
139 as human respiratory syncytial virus, human metapneumovirus, human parainfluenza virus type 3, and m
140 fections (respiratory syncytial virus, human metapneumovirus, human rhinovirus, and adenovirus) were
142 We sought to determine the role of human metapneumovirus in lower respiratory tract illness in pr
148 red the gene expression of TCD8 during human metapneumovirus infection to those in acute or chronic l
149 by both commercial assays (adenovirus, human metapneumovirus, influenza A virus, influenza B virus, p
152 and activities of CR-VI+, a portion of human Metapneumovirus L consisting of CR-VI and the poorly con
153 thelial cells or mice with recombinant human metapneumovirus lacking SH expression (rhMPV-DeltaSH) en
155 istence of two distinct sublineages of avian metapneumovirus (MPV) subtype C, a virus which has cause
156 es 1, 2, and 3 (PIV1, PIV2, and PIV3), human metapneumovirus (MPV), and adenovirus (AdV) in 1,138 spe
157 (RSV), parainfluenza virus, influenza virus, metapneumovirus (MPV), and coronavirus (CoV) detected in
161 uses (ie, respiratory syncytial virus, human metapneumovirus, parainfluenza virus, and influenza viru
162 coronavirus, enteroviruses, influenza virus, metapneumovirus, parainfluenza virus, rhinovirus, and re
163 ytic choriomeningitis virus, measles, mumps, metapneumovirus, parainfluenza, rotavirus, respiratory s
164 viruses, coronavirus, rhinovirus, and human metapneumovirus, represent a considerable global health
165 za virus, coronaviruses, rhinoviruses, human metapneumovirus, respiratory syncytial virus, parainflue
166 spiratory syncytial virus, adenovirus, human metapneumovirus, rhinovirus, and influenza virus but not
169 were multibasic sequences derived from avian metapneumovirus type A (R-R-R-R) or type C (R-K-A-R), wi
176 enza, respiratory syncytial virus, and human metapneumovirus were substantially more common in patien
177 y tract illnesses were attributable to human metapneumovirus, which means that 12 percent of all lowe
178 st attachment (G) gene of any pneumovirus or metapneumovirus, with the predicted G protein of 585 ami
180 zuelan equine encephalitis virus, norovirus, metapneumovirus, yellow fever virus, Japanese encephalit
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