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1 nfluenza A, respiratory syncytial virus, and human metapneumovirus.
2 ditional methods, primarily rhinoviruses and human metapneumovirus.
3 syncytial virus (RSV), human bocavirus, and human metapneumovirus.
4 ng with acute respiratory tract illness, for human metapneumovirus.
5 man seasonal coronavirus, parainfluenza, and human metapneumovirus.
6 ons were seen among sequences of the related human metapneumovirus.
7 uses were less frequent overall, followed by human metapneumoviruses.
10 us HKU1, coronavirus NL63, coronavirus OC43, human metapneumovirus A and B, influenza A, influenza A
13 arainfluenza viruses 1-4, influenza A and B, human metapneumovirus, adenovirus, and human rhinoviruse
14 ruses; parainfluenza viruses 1, 2, 3, and 4; human metapneumovirus; adenovirus; enterovirus-rhinoviru
15 uses 1-3, influenza viruses AH1, AH3, and B, human metapneumovirus, adenoviruses, and bocavirus) and
16 rus, as well as respiratory syncytial virus, human metapneumovirus, adenoviruses, picornaviruses, and
17 influenza, respiratory syncytial virus, and human metapneumovirus among patients with CAP of all age
18 G proteins from other subtype C viruses and human metapneumovirus and more than 170 aa larger than t
19 l data for two other respiratory pathogens - human metapneumovirus and seasonal coronavirus - from 35
20 irus, parainfluenza virus types 1 and 3, and human metapneumovirus) and identified predictors of supe
21 i) respiratory syncytial viruses A and B and human metapneumovirus, and (iii) parainfluenza virus typ
23 human coronaviruses, parainfluenza viruses, human metapneumovirus, and enteroviruses but not respira
24 of human rhinoviruses, human coronaviruses, human metapneumovirus, and human bocavirus, as well as t
25 ses (influenza, respiratory syncytial virus, human metapneumovirus, and human rhinovirus) in a recons
27 luenza viruses, respiratory syncytial virus, human metapneumovirus, and the deadly zoonotic henipavir
28 including influenza virus, reovirus, HIV-1, human metapneumovirus, and vesicular stomatitis virus.
29 novirus, seasonal coronavirus, picornavirus, human metapneumovirus, and/or SARS-CoV-2 rapid antigen t
31 s.IMPORTANCE Respiratory syncytial virus and human metapneumovirus are leading causes of respiratory
32 continued efforts to improve the outcome of human metapneumovirus-associated ALRI among young infant
33 obally, there were an estimated 14.2 million human metapneumovirus-associated ALRI cases (uncertainty
34 and 16 100 overall (hospital and community) human metapneumovirus-associated ALRI deaths (5700 to 88
35 sociated ALRI in-hospital deaths and overall human metapneumovirus-associated ALRI deaths (both in-ho
38 countries are at greater risk of death from human metapneumovirus-associated ALRI than older childre
39 ed incidence and hospital admission rates of human metapneumovirus-associated ALRI to population esti
40 in-hospital case-fatality ratios (hCFRs) of human metapneumovirus-associated ALRI using a generalise
42 hospital admissions, and deaths by combining human metapneumovirus-associated burden estimates and at
43 [UR] 10.2 million to 20.1 million), 643 000 human metapneumovirus-associated hospital admissions (UR
44 tal admissions (UR 425 000 to 977 000), 7700 human metapneumovirus-associated in-hospital deaths (260
49 ral activity against RSV (EC(50) = 3-46 nM), human metapneumovirus (EC(50) = 210 nM), human rhinoviru
53 family Paramyxoviridae includes two members, human metapneumovirus (hMPV) and avian metapneumovirus (
57 n severe bronchiolitis and dual infection by human metapneumovirus (hMPV) and human respiratory syncy
58 inflammatory chemokine production induced by human metapneumovirus (hMPV) and Nipah virus (NiV), sugg
60 act infections caused by the paramyxoviruses human metapneumovirus (hMPV) and respiratory syncytial v
61 coproteins derived from two human pathogens, human metapneumovirus (hMPV) and respiratory syncytial v
65 n respiratory syncytial virus (hRSV) and the human metapneumovirus (hMPV) are important human respira
66 virus (RSV), parainfluenza virus (PIV), and human metapneumovirus (hMPV) are increasingly associated
70 like influenza, information on the burden of human metapneumovirus (HMPV) as a cause of hospitalizati
80 ngly, GFP-expressing AMPV and GFP-expressing human metapneumovirus (HMPV) could be recovered using th
86 HPIV), respiratory syncytial virus (RSV) and human metapneumovirus (HMPV) from the 52060 respiratory
90 toward understanding the immune response to human metapneumovirus (hMPV) has lagged behind, although
92 competent adult with asthma developed severe human metapneumovirus (HMPV) illness complicated by grou
93 competent adult with asthma developed severe human metapneumovirus (HMPV) illness complicated by grou
94 uenza, respiratory syncytial virus (RSV), or human metapneumovirus (hMPV) illness had pneumococcus de
95 imated respiratory syncytial virus (RSV) and human metapneumovirus (hMPV) illness incidences among pr
96 de-PLx system resulted from the detection of human metapneumovirus (HMPV) in 9 specimens, human CoV (
97 den of respiratory syncytial virus (RSV) and human metapneumovirus (HMPV) in older adults in comparis
98 nts (ASRs) (bioMerieux) for the detection of human metapneumovirus (hMPV) in respiratory samples.
99 ntibody MAb-8 was evaluated for detection of human metapneumovirus (HMPV) in shell vial centrifugatio
100 n immunocompromised hosts, but the impact of human metapneumovirus (hMPV) in this setting was previou
105 We aimed to compare the characteristics of human metapneumovirus (hMPV) infection with influenza A
106 derstanding temporal trends of influenza and human metapneumovirus (HMPV) infections among adults and
108 Unlike influenza, information on the risk of human metapneumovirus (HMPV) infections in adults with c
109 The clinical and genomic epidemiology of human metapneumovirus (hMPV) infections in community set
110 sk factors for poor outcomes associated with human metapneumovirus (hMPV) infections in recipients of
155 e important clinical implications.IMPORTANCE Human metapneumovirus (HMPV) is a recently discovered pa
169 uman respiratory syncytial virus (hRSV), the human metapneumovirus (hMPV) is one of the leading cause
171 den of respiratory syncytial virus (RSV) and human metapneumovirus (hMPV) LRTI in premature children
175 cterium effector proteins and SARS-CoV-2 and human metapneumovirus (HMPV) proteins in yeast to test t
177 on by challenging B cell-deficient mice with human metapneumovirus (HMPV) several weeks after primary
178 Human respiratory syncytial virus (hRSV) and human metapneumovirus (hMPV) share virologic and epidemi
180 A microarray (Virochip) was used to detect a human metapneumovirus (hMPV) strain associated with a cr
181 he CAN98-75 (CAN75) and the CAN97-83 (CAN83) human metapneumovirus (HMPV) strains, which represent th
182 eavage activation of the fusion F protein of human metapneumovirus (HMPV) to replication and pathogen
183 kine production by BALB/c mice infected with human metapneumovirus (hMPV) was compared to respiratory
188 ed the capability of MS for the detection of human metapneumovirus (HMPV), a common cause of respirat
194 piratory syncytial virus (RSV), enterovirus, human metapneumovirus (hMPV), adenovirus (AdV), and rhin
195 enza virus (Flu), parainfluenza virus (PIV), human metapneumovirus (HMPV), adenovirus (AdV), rhinovir
198 of Mononegavirales, namely, VSV, RABV, HRSV, human metapneumovirus (HMPV), and human parainfluenza vi
199 es human respiratory syncytial virus (hRSV), human metapneumovirus (hMPV), and human parainfluenza vi
200 ted to influenza B virus, influenza A virus, human metapneumovirus (HMPV), and respiratory syncytial
201 ivatives of the CAN97-83 clinical isolate of human metapneumovirus (HMPV), consensus nucleotide seque
205 ts: adenovirus, coronaviruses HKU1 and NL63, human metapneumovirus (hMPV), influenza A virus (to type
206 gnosis of respiratory syncytial virus (RSV), human metapneumovirus (HMPV), parainfluenza virus 1 to 3
208 espiratory syncytial virus (RSV), influenza, human metapneumovirus (HMPV), rhinovirus, and human para
209 u-A, Flu-B, PIV-1, PIV-2, PIV-3, PIV-4, RSV, human metapneumovirus (hMPV), rhinoviruses (RhVs), enter
210 (RSV), Human Parainfluenza Virus (HPIV), and Human Metapneumovirus (hMPV), we adopt a theoretical app
215 man respiratory syncytial viruses (HRSV) and human metapneumoviruses (HMPV) were involved in the etio
218 ciency virus, human parainfluenza virus 1-4, human metapneumovirus, human coronaviruses (229E/OC43/NL
219 s such as human respiratory syncytial virus, human metapneumovirus, human parainfluenza virus type 3,
220 ral infections (respiratory syncytial virus, human metapneumovirus, human rhinovirus, and adenovirus)
223 ates are available for ALRIs associated with human metapneumovirus in children, and no licensed vacci
224 rden estimates and attributable fractions of human metapneumovirus in laboratory-confirmed human meta
226 panzees during the cohort study, we detected human metapneumovirus in two chimpanzees from a February
227 p complex of respiratory syncytial virus and human metapneumovirus incorporate GS-646939 and ATP with
233 compared the gene expression of TCD8 during human metapneumovirus infection to those in acute or chr
234 have disproportionately high risks of severe human metapneumovirus infections across all World Bank i
236 table by both commercial assays (adenovirus, human metapneumovirus, influenza A virus, influenza B vi
237 005 and 2013: adenovirus, human coronavirus, human metapneumovirus, influenza B virus and respiratory
238 he primary analysis tested negative for RSV, human metapneumovirus, influenza, and severe acute respi
242 cture and activities of CR-VI+, a portion of human Metapneumovirus L consisting of CR-VI and the poor
243 ay epithelial cells or mice with recombinant human metapneumovirus lacking SH expression (rhMPV-Delta
246 us types 1, 2, and 3 (PIV1, PIV2, and PIV3), human metapneumovirus (MPV), and adenovirus (AdV) in 1,1
248 workup (respiratory syncytial virus [n = 3], human metapneumovirus [n = 1], and human coronavirus NL6
249 utine clinical testing (influenza A [n = 3], human metapneumovirus [n = 2], and human coronavirus OC4
250 tory syncytial virus, influenza viruses, and human metapneumovirus, often implicated as co-pathogens
251 e found that PD-L1(-/-) mice challenged with human metapneumovirus or influenza showed a similar leve
252 tribute to TCD8 impairment induced by either human metapneumovirus or influenza virus infection.
254 otal of 37 719 incident infections with RSV, human metapneumovirus, or human coronaviruses 229E, NL63
255 er viruses (ie, respiratory syncytial virus, human metapneumovirus, parainfluenza virus, and influenz
256 bacterium effector proteins, SARS-CoV-2 and human metapneumovirus proteins in yeast to test their ef
257 luenza viruses, coronavirus, rhinovirus, and human metapneumovirus, represent a considerable global h
258 missed by the diagnostic panel (rhinovirus, human metapneumovirus, respiratory syncytial virus and p
259 nfluenza virus, coronaviruses, rhinoviruses, human metapneumovirus, respiratory syncytial virus, para
260 of respiratory syncytial virus, adenovirus, human metapneumovirus, rhinovirus, and influenza virus b
262 -negative LRTD events that were negative for human metapneumovirus, SARS-CoV-2, and influenza, and po
263 variation patterns, which were also seen in human metapneumovirus sequences, point to previously def
270 influenza, respiratory syncytial virus, and human metapneumovirus were substantially more common in
271 iratory tract illnesses were attributable to human metapneumovirus, which means that 12 percent of al