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1 c similarity to bovine parvovirus and canine minute virus.
9 se (DDR) is essential for DNA replication of minute virus of canines (MVC), a member of the genus Boc
10 was constructed, based on a chimera between minute virus of mice (MVM) and LuIII, which expresses Bo
11 ng DNA replication, the hairpin telomeres of Minute Virus of Mice (MVM) are extended and copied to cr
12 e of the simplest virus particles known, the minute virus of mice (MVM) capsid, and experimentally an
14 o initiate DNA synthesis, the NS1 protein of minute virus of mice (MVM) first binds to a simple cogna
15 igin of DNA replication at the 3' end of the minute virus of mice (MVM) genome and functions as an es
17 ns surrounding the fivefold-symmetry axes in minute virus of mice (MVM) harbor central pores that pen
18 ion.IMPORTANCE Replication of the parvovirus minute virus of mice (MVM) induces a sustained cellular
20 The small nonstructural protein NS2 of the minute virus of mice (MVM) is required for efficient vir
21 The DNA damage response to infection with minute virus of mice (MVM) leads to activated p53; howev
27 d vectors based on the autonomous parvovirus minute virus of mice (MVM) that were designed to introdu
28 he Fab molecules inhibits the binding of the minute virus of mice (MVM) to permissive cells but can a
29 ral protein NS1 of the autonomous parvovirus minute virus of mice (MVM), a protein essential for vira
30 eningitis virus, an ambisense RNA virus, and minute virus of mice (MVM), a single-stranded DNA (ssDNA
33 cleotide NS2-specific exon of the parvovirus minute virus of mice (MVM), which is flanked by a large
40 rine fibroblasts, the lymphotropic strain of minute virus of mice (MVMi) does not efficiently produce
41 he lymphotropic, immunosuppressive strain of minute virus of mice (MVMi) in complex with the neutrali
42 l rearrangement that can occur in parvovirus minute virus of mice (MVMp) virions following prolonged
43 ing a truncated version of NS1, as seen with minute virus of mice and adeno-associated virus 2, was a
45 9 promoter was detected; however, similar to minute virus of mice and other members of the Parvovirus
46 s the interaction between the NS2 protein of minute virus of mice and the nuclear export factor Crm1
48 The linear single-stranded DNA genome of minute virus of mice can be ejected, in a 3'-to-5' direc
49 spectrometry to analyze the dynamics of the minute virus of mice capsid at increasing temperatures.
51 rated pre-mRNAs of the autonomous parvovirus minute virus of mice caused a decrease in the accumulate
52 rus (PRV), adeno-associated virus (AAV), and minute virus of mice i-strain (MVMi) and MVMp all infect
54 he P38 promoter of the autonomous parvovirus minute virus of mice is strongly transactivated by the n
55 nity for CRM1 that is 100-fold less than the minute virus of mice NS2 protein, a high affinity cargo
56 ing enhancer within the NS2-specific exon of minute virus of mice P4 promoter-generated pre-mRNA caus
58 ependovirus (AAV) and autonomous parvovirus (minute virus of mice) replication centers can colocalize
59 e parvovirus (ADV), canine parvovirus (CPV), minute virus of mice, and bovine parvovirus, also bind s
61 parvovirus capsids, along with those of the minute virus of mice, have also advanced our understandi
62 rvovirus) and prototypic parvovirus species (minute virus of mice, Kilham's rat virus, and H-1) than
63 s to those observed in canine parvovirus and minute virus of mice, two members of the genus Parvoviru
64 ranscriptional attenuation of the parvovirus minute virus of mice, which is mediated by a stem-loop s
67 revealed that induced disassembly of single minute-virus-of-mice particles is frequently initiated b
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