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1 more severe forms of disease associated with human respiratory syncytial virus.
2 l hydrophobic (SH) protein is encoded by the human respiratory syncytial virus.
3 by influenza A virus, influenza B virus, and human respiratory syncytial virus.
5 n conjunction with those being developed for human respiratory syncytial virus and the human parainfl
6 athogens include measles virus, mumps virus, human respiratory syncytial virus, and the zoonotic para
7 tion process has been recently described for human respiratory syncytial virus, another paramyxovirus
8 H protein, 64 amino acids long, found in the human respiratory syncytial virus because of the effect
10 to recover HMPV lacking M2-1 contrasts with human respiratory syncytial virus, for which M2-1 is an
11 ermined the genome sequence of an unpassaged human respiratory syncytial virus from a sample obtained
13 ation and transcription by the pneumoviruses human respiratory syncytial virus (HRSV) and avian pneum
15 otein of aMPV/C were similar to those of the human respiratory syncytial virus (hRSV) attachment G pr
20 imary airway epithelial cells, infected with human respiratory syncytial virus (HRSV) has shown alter
22 t Th2-skewed responses to naturally acquired human respiratory syncytial virus (hRSV) infection obser
37 system was developed to generate infectious human respiratory syncytial virus (HRSV) lacking matrix
38 d (4) that infection of cotton rats with the human respiratory syncytial virus (HRSV) leads to a sign
40 ization and frequency of interactions of the human respiratory syncytial virus (hRSV) nucleocapsid pr
41 nia virus of mice (PVM) is a rodent model of human respiratory syncytial virus (hRSV) pathogenesis.
49 ein cytoplasmic tail (CT) for replication of human respiratory syncytial virus (HRSV) was examined by
50 nfection by human metapneumovirus (hMPV) and human respiratory syncytial virus (hRSV) was investigate
52 changes were compared with those induced by human respiratory syncytial virus (HRSV), a virus with a
53 is a major difference with pre-fusion F from human respiratory syncytial virus (hRSV), and collective
54 mportant human and animal pathogens, such as human respiratory syncytial virus (hRSV), hMPV, bovine R
55 mportant human and animal pathogens, such as human respiratory syncytial virus (hRSV), hMPV, bovine R
65 disease virus (NDV), human pathogens such as human respiratory syncytial virus, human metapneumovirus
66 tein raised in a rabbit neutralized BRSV and human respiratory syncytial virus infectivity when teste
68 The M2-1 protein of the important pathogen human respiratory syncytial virus is a zinc-binding tran
69 n of the open reading frame 2 (ORF-2) of the human respiratory syncytial virus M2 gene initiates at o
70 r than those of other respiratory pathogens: human respiratory syncytial virus, parainfluenza virus 5
71 in mice and provides a convenient model for human respiratory syncytial virus pathogenesis and immun
77 is one of the two nonstructural proteins of human respiratory syncytial virus (RSV) and is encoded b
78 rmini of the genomic and antigenomic RNAs of human respiratory syncytial virus (RSV) are identical at
80 ns required for the packaging and passage of human respiratory syncytial virus (RSV) by reconstructin
92 omising candidate vaccine antigen.IMPORTANCE Human respiratory syncytial virus (RSV) is a global lead
104 tion.IMPORTANCE Despite decades of research, human respiratory syncytial virus (RSV) is still a major
105 An obstacle to developing a vaccine against human respiratory syncytial virus (RSV) is that natural
121 ) and gene end (GE) transcription signals of human respiratory syncytial virus (RSV) strain A2 were a
122 valuated phenotypic reversion of deoptimized human respiratory syncytial virus (RSV) vaccine candidat
123 uences (IGS) between the first nine genes of human respiratory syncytial virus (RSV) vary in length f
125 The characteristic recurrent epidemics of human respiratory syncytial virus (RSV) within communiti
128 Pneumonia virus of mice (PVM), a relative of human respiratory syncytial virus (RSV), causes respirat
132 n previously that the fusion glycoprotein of human respiratory syncytial virus (RSV-F) interacts with
133 tein of an important respiratory pathogen of humans, respiratory syncytial virus (RSV), was mediated
134 In contrast, a highly cytopathic virus, human respiratory syncytial virus that induced NF-kappaB
135 aphic characterization of cell culture-grown human respiratory syncytial virus to determine the archi
136 leads for the research and development of a human respiratory syncytial virus vaccine needed to prot
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