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1 on pathogens including Ureaplasma parvum and Bocavirus.
2 SV, rhinovirus, enterovirus, adenovirus, and bocavirus.
3 , and human rhinoviruses, coronaviruses, and bocavirus.
4 oronaviruses NL63, HKU1, 229E, and OC43; and bocavirus.
5 nes for these viruses or the related enteric bocaviruses.
10 rAAV2) genome is pseudopackaged by the human bocavirus 1 (HBoV1) capsid, has been shown to be highly
14 arvovirus replication was modeled with human bocavirus 1 (HBoV1) duplex genomes whose 5' hairpin stru
21 g and viral DNA replication.IMPORTANCE Human bocavirus 1 (HBoV1) is one of the significant pathogens
22 of recombinant HBoV vectors.IMPORTANCE Human bocavirus 1 (HBoV1) is pathogenic to humans, causing acu
23 the hairpin-deleted duplex genomes of human bocavirus 1 (HBoV1) replicate in human embryonic kidney
33 ed three new nonstructural proteins of human bocavirus 1 that are expressed during infection of polar
34 ve been discovered in human-derived samples: bocaviruses 1-4, parvovirus 4, bufavirus, tusavirus, and
38 us (PuBoV) in a tiger and serval cat, canine bocavirus 2 (CBoV-2) in raccoon dogs, and feline bocavir
40 says (rhinovirus [RV]/enterovirus [EV], 118; bocavirus, 8; coronavirus, 7; parainfluenza virus 4, 4;
41 en may have recently evolved from an enteric bocavirus after acquiring an expanded tropism favoring t
45 uenza A detections were usually symptomatic; bocavirus and rhinovirus detections were often asymptoma
48 B, human metapneumovirus, adenoviruses, and bocavirus) and 3 pathogenic airway bacteria (Streptococc
49 tions caused by respiratory syncytial virus, bocavirus, and adenovirus in addition to acute otitis me
50 ovirus, astrovirus, sapovirus, parechovirus, bocavirus, and aichivirus were detected in the stool spe
55 ainfluenza virus 4 (aOR 9.3, P = .12), human bocavirus (aOR 9.1, P < .01), Coxsackieviruses (aOR 5.1,
56 human bocavirus infections.IMPORTANCE Human bocaviruses are one of only a few members of the Parvovi
57 onaviruses, human metapneumovirus, and human bocavirus, as well as the need for new treatment and pre
58 ted data exist regarding the impact of human bocavirus (BoV) in hematopoietic cell transplant (HCT) r
62 ific and conserved antigenic epitopes of the bocaviruses can be instrumental in characterization of t
63 stem-cell recipients, including adenovirus, bocavirus, coronavirus, human herpesvirus-6, lymphocytic
64 ll noncoding RNA of 140 nucleotides known as bocavirus-encoded small RNA (BocaSR), in addition to vir
65 virus, Aichi virus, Anellovirus, Astrovirus, Bocavirus, Enterovirus, Parechovirus, Picobirnavirus, an
66 as observed for adenoviruses, anelloviruses, bocaviruses, enteroviruses, parechoviruses, and picobirn
68 ee of genetic diversity seen among the human bocaviruses found in feces specimens, relative to the hi
70 as recently discovered and classified in the Bocavirus genus (family Parvoviridae, subfamily Parvovir
86 itive regions of the capsid.IMPORTANCE Human bocaviruses (HBoVs) are associated with disease in human
87 rvoviruses B19 and recently discovered human bocaviruses (HBoVs) are widespread, while PARV4 infectio
91 ossible role of the newly identified enteric bocaviruses in human diseases, including acute flaccid p
94 ent of antiviral strategies to control human bocavirus infections.IMPORTANCE Human bocaviruses are on
97 ll leukemia virus type 1; hepatitis E virus; bocavirus; KI and WU polyomaviruses; coronaviruses HKU1
98 erization of a single-cycle infection of the bocavirus minute virus of canines (MVC) in canine WRD ce
100 dependoviruses, sapoviruses, enteroviruses, bocaviruses, noroviruses, adenoviruses, parechoviruses,
101 Here, we report the structure of the human bocavirus NS1 N-terminal domain, the first for any auton
102 ic-residue-rich subdomain that is present in bocavirus NS1 proteins but not in the NS1 orthologs in e
103 irus of canines (MVC), a member of the genus Bocavirus of the Parvoviridae family; however, the mecha
105 amino acid residues of NS1s from four human bocavirus species onto the structure shows a scattered p
107 ldren and adults, the most commonly detected bocavirus species were, in descending order, HBoV2, HBoV
108 throvirus or dependovirus, which may mediate bocavirus-specific interaction with DNA or potential hos
109 lyses of data from 194 children, adenovirus, bocavirus, Streptococcus pneumoniae, Haemophilus influen
110 vealed important information about the genus Bocavirus that may eventually help us to clone the human
111 rst member of the family Parvoviridae, genus Bocavirus, to be potentially associated with human disea
112 udy, we identified an additional HBoV1 gene, bocavirus-transcribed small noncoding RNA (BocaSR), with
114 I), parechovirus (types 1, 3, 4, and 5), and bocavirus (types 1, 2, and 3) were found cocirculating.
118 dae family and of DNA circoviruses and human bocaviruses were detected, expanding the known genetic d
119 le novel species of porcine astroviruses and bocaviruses were generated and phylogenetically analyzed