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1 za A, respiratory syncytial virus, and human metapneumovirus.
2 al methods, primarily rhinoviruses and human metapneumovirus.
3 tial virus (RSV), human bocavirus, and human metapneumovirus.
4 years nearly all people have been exposed to metapneumovirus.
5 h acute respiratory tract illness, for human metapneumovirus.
6 asonal coronavirus, parainfluenza, and human metapneumovirus.
7 re seen among sequences of the related human metapneumovirus.
8 ence except influenza A virus caught up with metapneumovirus.
9 es for parainfluenza virus, and 65 sites for metapneumovirus.
10 ry syncytial virus, parainfluenza virus, and metapneumovirus.
11 ere less frequent overall, followed by human metapneumoviruses.
16 iscordance was common for adenovirus (100%), metapneumovirus (44%), rhinovirus (34%), and parainfluen
18 1, coronavirus NL63, coronavirus OC43, human metapneumovirus A and B, influenza A, influenza A H1, in
21 fluenza virus (PIV), influenza virus (InfV), metapneumovirus, adenovirus (Ad), coronavirus, and enter
22 luenza viruses 1-4, influenza A and B, human metapneumovirus, adenovirus, and human rhinoviruses, cor
23 parainfluenza viruses 1, 2, 3, and 4; human metapneumovirus; adenovirus; enterovirus-rhinovirus; cor
24 -3, influenza viruses AH1, AH3, and B, human metapneumovirus, adenoviruses, and bocavirus) and 3 path
25 s well as respiratory syncytial virus, human metapneumovirus, adenoviruses, picornaviruses, and coron
26 enza, respiratory syncytial virus, and human metapneumovirus among patients with CAP of all ages prob
30 enomic structure and composition of an avian metapneumovirus (aMPV) recently isolated from wild Canad
35 riculturally important viruses such as avian metapneumovirus (aMPV), and Newcastle disease virus (NDV
36 bers, human metapneumovirus (hMPV) and avian metapneumovirus (aMPV), causing respiratory tract infect
39 The first cases of infection caused by avian metapneumoviruses (aMPVs) were described in turkeys with
40 teins from other subtype C viruses and human metapneumovirus and more than 170 aa larger than the G p
41 for two other respiratory pathogens - human metapneumovirus and seasonal coronavirus - from 35 US st
42 nome promoters are conserved between the two metapneumoviruses and can be cross-recognized by the pol
43 piratory syncytial viruses A and B and human metapneumovirus, and (iii) parainfluenza virus types 1 t
44 yncytial virus (RSV), influenza, rhinovirus, metapneumovirus, and adenovirus was highly associated wi
46 man rhinoviruses, human coronaviruses, human metapneumovirus, and human bocavirus, as well as the nee
47 nfluenza, respiratory syncytial virus, human metapneumovirus, and human rhinovirus) in a reconstitute
49 viruses, respiratory syncytial virus, human metapneumovirus, and the deadly zoonotic henipaviruses H
51 s, seasonal coronavirus, picornavirus, human metapneumovirus, and/or SARS-CoV-2 rapid antigen testing
53 RTANCE Respiratory syncytial virus and human metapneumovirus are leading causes of respiratory illnes
54 ry syncytial virus, parainfluenza virus, and metapneumovirus are the most common viruses associated w
55 nued efforts to improve the outcome of human metapneumovirus-associated ALRI among young infants in l
56 , there were an estimated 14.2 million human metapneumovirus-associated ALRI cases (uncertainty range
57 6 100 overall (hospital and community) human metapneumovirus-associated ALRI deaths (5700 to 88 000).
58 ed ALRI in-hospital deaths and overall human metapneumovirus-associated ALRI deaths (both in-hospital
59 e aimed to estimate the age-stratified human metapneumovirus-associated ALRI global incidence, hospit
61 ries are at greater risk of death from human metapneumovirus-associated ALRI than older children and
62 idence and hospital admission rates of human metapneumovirus-associated ALRI to population estimates
63 spital case-fatality ratios (hCFRs) of human metapneumovirus-associated ALRI using a generalised line
65 al admissions, and deaths by combining human metapneumovirus-associated burden estimates and attribut
66 10.2 million to 20.1 million), 643 000 human metapneumovirus-associated hospital admissions (UR 425 0
67 missions (UR 425 000 to 977 000), 7700 human metapneumovirus-associated in-hospital deaths (2600 to 4
71 iruses not covered by DFA and R-mix culture (metapneumovirus, coronaviruses [CoV], parainfluenza viru
73 tivity against RSV (EC(50) = 3-46 nM), human metapneumovirus (EC(50) = 210 nM), human rhinovirus (EC(
77 The severity of the disease burden of human metapneumovirus (HMPV) among older adults is less well r
78 Paramyxoviridae includes two members, human metapneumovirus (hMPV) and avian metapneumovirus (aMPV),
82 re bronchiolitis and dual infection by human metapneumovirus (hMPV) and human respiratory syncytial v
83 matory chemokine production induced by human metapneumovirus (hMPV) and Nipah virus (NiV), suggesting
85 fections caused by the paramyxoviruses human metapneumovirus (hMPV) and respiratory syncytial virus (
86 eins derived from two human pathogens, human metapneumovirus (hMPV) and respiratory syncytial virus (
88 Respiratory syncytial virus (RSV) and human metapneumovirus (hMPV) are closely related pathogens res
89 iratory syncytial virus (hRSV) and the human metapneumovirus (hMPV) are important human respiratory p
90 (RSV), parainfluenza virus (PIV), and human metapneumovirus (hMPV) are increasingly associated with
91 Respiratory syncytial virus (RSV) and human metapneumovirus (HMPV) are two closely related viruses t
92 Respiratory syncytial virus (RSV) and human metapneumovirus (hMPV) are two important viral pathogens
93 Respiratory syncytial virus (RSV) and human metapneumovirus (HMPV) are two of the leading causes of
96 Respiratory syncytial virus (RSV) and human metapneumovirus (hMPV) cause a similar spectrum of respi
97 Respiratory syncytial virus (RSV) and human metapneumovirus (HMPV) cause acute respiratory infection
98 Respiratory syncytial virus (RSV) and human metapneumovirus (hMPV) cause human respiratory diseases
99 Respiratory syncytial virus (RSV) and human metapneumovirus (HMPV) cause severe respiratory diseases
103 GFP-expressing AMPV and GFP-expressing human metapneumovirus (HMPV) could be recovered using the supp
104 DS-Cav1 vaccination also activated human metapneumovirus (HMPV) cross-reactive B cells capable of
109 respiratory syncytial virus (RSV) and human metapneumovirus (HMPV) from the 52060 respiratory sample
113 d understanding the immune response to human metapneumovirus (hMPV) has lagged behind, although hMPV
115 ent adult with asthma developed severe human metapneumovirus (HMPV) illness complicated by group A St
116 ent adult with asthma developed severe human metapneumovirus (HMPV) illness complicated by group A St
117 respiratory syncytial virus (RSV), or human metapneumovirus (hMPV) illness had pneumococcus detected
118 system resulted from the detection of human metapneumovirus (HMPV) in 9 specimens, human CoV (HCoV)
119 respiratory syncytial virus (RSV) and human metapneumovirus (HMPV) in older adults in comparison wit
121 y MAb-8 was evaluated for detection of human metapneumovirus (HMPV) in shell vial centrifugation cult
122 nocompromised hosts, but the impact of human metapneumovirus (hMPV) in this setting was previously un
124 The inpatient and outpatient burden of human metapneumovirus (HMPV) infection among young children ha
128 e clinical and genomic epidemiology of human metapneumovirus (hMPV) infections in community settings
129 Respiratory syncytial virus (RSV) and human metapneumovirus (hMPV) infections pose a significant hea
173 rtant clinical implications.IMPORTANCE Human metapneumovirus (HMPV) is a recently discovered pathogen
187 espiratory syncytial virus (hRSV), the human metapneumovirus (hMPV) is one of the leading causes of c
189 respiratory syncytial virus (RSV) and human metapneumovirus (hMPV) LRTI in premature children and de
193 m effector proteins and SARS-CoV-2 and human metapneumovirus (HMPV) proteins in yeast to test their e
195 challenging B cell-deficient mice with human metapneumovirus (HMPV) several weeks after primary infec
196 respiratory syncytial virus (hRSV) and human metapneumovirus (hMPV) share virologic and epidemiologic
198 oarray (Virochip) was used to detect a human metapneumovirus (hMPV) strain associated with a critical
199 98-75 (CAN75) and the CAN97-83 (CAN83) human metapneumovirus (HMPV) strains, which represent the two
200 activation of the fusion F protein of human metapneumovirus (HMPV) to replication and pathogenicity
201 roduction by BALB/c mice infected with human metapneumovirus (hMPV) was compared to respiratory syncy
206 capability of MS for the detection of human metapneumovirus (HMPV), a common cause of respiratory tr
212 ry syncytial virus (RSV), enterovirus, human metapneumovirus (hMPV), adenovirus (AdV), and rhinovirus
213 irus (Flu), parainfluenza virus (PIV), human metapneumovirus (HMPV), adenovirus (AdV), rhinovirus (RV
215 onegavirales, namely, VSV, RABV, HRSV, human metapneumovirus (HMPV), and human parainfluenza virus (H
216 Respiratory syncytial virus (RSV), human metapneumovirus (HMPV), and human parainfluenza virus ty
217 an respiratory syncytial virus (hRSV), human metapneumovirus (hMPV), and human parainfluenza virus ty
218 influenza B virus, influenza A virus, human metapneumovirus (HMPV), and respiratory syncytial virus
219 es of the CAN97-83 clinical isolate of human metapneumovirus (HMPV), consensus nucleotide sequencing
221 A recently discovered paramyxovirus, human metapneumovirus (hMPV), has been studied by our group in
223 enovirus, coronaviruses HKU1 and NL63, human metapneumovirus (hMPV), influenza A virus (to type level
224 of respiratory syncytial virus (RSV), human metapneumovirus (HMPV), parainfluenza virus 1 to 3 (PIV1
226 tory syncytial virus (RSV), influenza, human metapneumovirus (HMPV), rhinovirus, and human parainflue
227 lu-B, PIV-1, PIV-2, PIV-3, PIV-4, RSV, human metapneumovirus (hMPV), rhinoviruses (RhVs), enterovirus
228 Human Parainfluenza Virus (HPIV), and Human Metapneumovirus (hMPV), we adopt a theoretical approach
233 spiratory syncytial viruses (HRSV) and human metapneumoviruses (HMPV) were involved in the etiology o
236 virus, human parainfluenza virus 1-4, human metapneumovirus, human coronaviruses (229E/OC43/NL63/HKU
237 as human respiratory syncytial virus, human metapneumovirus, human parainfluenza virus type 3, and m
238 fections (respiratory syncytial virus, human metapneumovirus, human rhinovirus, and adenovirus) were
241 re available for ALRIs associated with human metapneumovirus in children, and no licensed vaccines or
242 stimates and attributable fractions of human metapneumovirus in laboratory-confirmed human metapneumo
243 We sought to determine the role of human metapneumovirus in lower respiratory tract illness in pr
244 s during the cohort study, we detected human metapneumovirus in two chimpanzees from a February 2023
245 lex of respiratory syncytial virus and human metapneumovirus incorporate GS-646939 and ATP with simil
251 red the gene expression of TCD8 during human metapneumovirus infection to those in acute or chronic l
252 isproportionately high risks of severe human metapneumovirus infections across all World Bank income
254 by both commercial assays (adenovirus, human metapneumovirus, influenza A virus, influenza B virus, p
255 d 2013: adenovirus, human coronavirus, human metapneumovirus, influenza B virus and respiratory syncy
256 mary analysis tested negative for RSV, human metapneumovirus, influenza, and severe acute respiratory
260 and activities of CR-VI+, a portion of human Metapneumovirus L consisting of CR-VI and the poorly con
261 thelial cells or mice with recombinant human metapneumovirus lacking SH expression (rhMPV-DeltaSH) en
262 SARS-CoV-2 nucleocapsid protein and human metapneumovirus M2-1 protein are shown to enhance TBSV R
264 istence of two distinct sublineages of avian metapneumovirus (MPV) subtype C, a virus which has cause
265 es 1, 2, and 3 (PIV1, PIV2, and PIV3), human metapneumovirus (MPV), and adenovirus (AdV) in 1,138 spe
266 (RSV), parainfluenza virus, influenza virus, metapneumovirus (MPV), and coronavirus (CoV) detected in
269 (respiratory syncytial virus [n = 3], human metapneumovirus [n = 1], and human coronavirus NL63 [n =
270 clinical testing (influenza A [n = 3], human metapneumovirus [n = 2], and human coronavirus OC43 [n =
271 yncytial virus, influenza viruses, and human metapneumovirus, often implicated as co-pathogens with p
274 ory syncytial virus, parainfluenza virus, or metapneumovirus, or a combination of these, for at least
275 f 37 719 incident infections with RSV, human metapneumovirus, or human coronaviruses 229E, NL63, OC43
276 uses (ie, respiratory syncytial virus, human metapneumovirus, parainfluenza virus, and influenza viru
277 coronavirus, enteroviruses, influenza virus, metapneumovirus, parainfluenza virus, rhinovirus, and re
278 ytic choriomeningitis virus, measles, mumps, metapneumovirus, parainfluenza, rotavirus, respiratory s
279 rium effector proteins, SARS-CoV-2 and human metapneumovirus proteins in yeast to test their effects
280 viruses, coronavirus, rhinovirus, and human metapneumovirus, represent a considerable global health
281 d by the diagnostic panel (rhinovirus, human metapneumovirus, respiratory syncytial virus and parainf
282 za virus, coronaviruses, rhinoviruses, human metapneumovirus, respiratory syncytial virus, parainflue
283 spiratory syncytial virus, adenovirus, human metapneumovirus, rhinovirus, and influenza virus but not
285 tion patterns, which were also seen in human metapneumovirus sequences, point to previously defined i
287 were multibasic sequences derived from avian metapneumovirus type A (R-R-R-R) or type C (R-K-A-R), wi
296 enza, respiratory syncytial virus, and human metapneumovirus were substantially more common in patien
297 y tract illnesses were attributable to human metapneumovirus, which means that 12 percent of all lowe
298 st attachment (G) gene of any pneumovirus or metapneumovirus, with the predicted G protein of 585 ami
300 zuelan equine encephalitis virus, norovirus, metapneumovirus, yellow fever virus, Japanese encephalit