ライフサイエンスコーパス: foot-and-mouth disease virus

1 flock house virus, human rhinovirus-14, and foot and mouth disease virus.

2 n, livestock can be made less susceptible to foot and mouth disease virus.

3 2A self-processing peptide derived from the foot-and-mouth disease virus.

4 ere experimentally infected via aerosol with foot-and-mouth disease virus.

5 lved in genome packaging of the picornavirus foot-and-mouth disease virus.

6 xsackievirus, rhinovirus, enterovirus 71 and foot-and-mouth disease virus.

7 ctive peptide (A20FMDV2) derived from VP1 of foot-and-mouth disease virus.

8 polymerases from poliovirus, rhinovirus, and foot-and-mouth disease viruses.

9 sh-ble antibiotic resistance gene, with the foot and mouth disease virus 2A self-cleaving sequence p

10 peptide binding and explains the ability of foot-and-mouth disease virus 3C(pro) to cleave sequences

11 The X-ray crystal structure of the foot-and-mouth disease virus 3C(pro), mutated to replace

12 The foot and mouth disease virus, a picornavirus, encodes tw

13 on mediated a salient genome segmentation of foot-and-mouth disease virus, an important animal pathog

14 agents that produce vesicular lesions, e.g., foot-and-mouth disease virus and others.

15 nked to the gene encoding the 2A protease of foot-and-mouth disease virus and then inserted in frame

16 henotype has been documented for poliovirus, foot-and-mouth disease virus, and coxsackievirus B3 and

17 cally important members, such as poliovirus, foot-and-mouth disease virus, and endomyocarditis virus.

18 icornavirus family, including poliovirus and foot-and-mouth disease virus, are widespread pathogens o

19 AVPNLRGDLQVLAQKVART (A20FMDV2), derived from foot-and-mouth disease virus, as a potent inhibitor of a

20 Foot and mouth disease virus causes a livestock disease

21 The foot-and-mouth disease virus encodes two forms of a cyst

22 uman rhinovirus, coxsackievirus, poliovirus, foot-and-mouth disease virus, enterovirus D-68, and a wi

23 Following infection with foot-and-mouth disease virus, expression of CD62L and CD

24 n from genetic and epidemiological data in a Foot and Mouth Disease Virus (FMDV) veterinary outbreak

25 The viruses in question spanned foot and mouth disease virus (FMDV), African swine fever

26 Foot and mouth disease virus (FMDV), is a highly contagi

27 are effective in reducing the replication of foot and mouth disease virus (FMDV).

28 The foot-and-mouth disease virus (FMDV) "carrier" state was

29 can sterilely protect swine challenged with foot-and-mouth disease virus (FMDV) 1 day later.

30 The ability of foot-and-mouth disease virus (FMDV) 2A to mediate proteo

31 ck in secretion are induced by expression of foot-and-mouth disease virus (FMDV) 3C(pro) and that thi

32 The N-terminal region of the foot-and-mouth disease virus (FMDV) 3D polymerase contai

33 The foot-and-mouth disease virus (FMDV) afflicts livestock i

34 ished data from transmission experiments for foot-and-mouth disease virus (FMDV) and African swine fe

35 s were tested in this study: one recognizing foot-and-mouth disease virus (FMDV) and another recogniz

36 IRESs) of encephalomyocarditis virus (EMCV), foot-and-mouth disease virus (FMDV) and other picornavir

37 e present in highly purified preparations of foot-and-mouth disease virus (FMDV) and poliovirus.

38 the extent to which the genetic diversity of foot-and-mouth disease virus (FMDV) arising over the cou

39 Foot-and-mouth disease virus (FMDV) binds to cell-surfac

40 shown that the leader proteinase (L(pro)) of foot-and-mouth disease virus (FMDV) blocks cap-dependent

41 It has been demonstrated that foot-and-mouth disease virus (FMDV) can utilize at least

42 Foot-and-mouth disease virus (FMDV) causes a fast-spread

43 Foot-and-mouth disease virus (FMDV) causes a highly cont

44 use in stabilizing SAT2 vaccines.IMPORTANCE Foot-and-mouth disease virus (FMDV) causes a highly cont

45 Foot-and-mouth disease virus (FMDV) causes a highly cont

46 Foot-and-mouth disease virus (FMDV) causes a highly cont

47 Foot-and-mouth disease virus (FMDV) causes an acute vesi

48 virus strains; however, the pathogenesis of foot-and-mouth disease virus (FMDV) coinfections is larg

49 The genome of foot-and-mouth disease virus (FMDV) differs from that of

50 Isolates of foot-and-mouth disease virus (FMDV) exist as complex mix

51 for the differential laboratory detection of foot-and-mouth disease virus (FMDV) from viruses that ca

52 Two foot-and-mouth disease virus (FMDV) genome sequences hav

53 hin the RNA genome of all seven serotypes of foot-and-mouth disease virus (FMDV) has been developed.

54 Field isolates of foot-and-mouth disease virus (FMDV) have a restricted ce

55 Field isolates of foot-and-mouth disease virus (FMDV) have been shown to u

56 Field isolates of foot-and-mouth disease virus (FMDV) have been shown to u

57 ocked the replication of poliovirus (PV) and foot-and-mouth disease virus (FMDV) in a variety of cell

58 ociated with clearance versus persistence of foot-and-mouth disease virus (FMDV) in micro-dissected c

59 beta8, have been identified as receptors for foot-and-mouth disease virus (FMDV) in vitro.

60 ta(6), have been identified as receptors for foot-and-mouth disease virus (FMDV) in vitro.

61 Foot-and-mouth disease virus (FMDV) induces a very rapid

62 Here, we show that the picornavirus foot-and-mouth disease virus (FMDV) induces the formatio

63 ole of T-lymphocyte subsets in recovery from foot-and-mouth disease virus (FMDV) infection in calves

64 The pathogenesis of persistent foot-and-mouth disease virus (FMDV) infection was invest

65 Foot-and-mouth disease virus (FMDV) initiates infection

66 ecades of investigation, the manner in which foot-and-mouth disease virus (FMDV) interacts with the i

67 shown that the leader proteinase (L(pro)) of foot-and-mouth disease virus (FMDV) interferes with the

68 iral vectors were constructed containing the foot-and-mouth disease virus (FMDV) internal ribosome en

69 Translation initiation dependent on the foot-and-mouth disease virus (FMDV) internal ribosome en

70 tent infection in African buffalo.IMPORTANCE Foot-and-mouth disease virus (FMDV) is a highly contagio

71 Foot-and-mouth disease virus (FMDV) is a highly contagio

72 Foot-and-mouth disease virus (FMDV) is a highly contagio

73 stress response.IMPORTANCE The picornavirus foot-and-mouth disease virus (FMDV) is a notorious anima

74 Nonstructural protein 3A of foot-and-mouth disease virus (FMDV) is a partially conse

75 Foot-and-mouth disease virus (FMDV) is a picornavirus, w

76 Foot-and-mouth disease virus (FMDV) is an important anim

77 One of the final steps in the maturation of foot-and-mouth disease virus (FMDV) is cleavage of the V

78 We have previously shown that replication of foot-and-mouth disease virus (FMDV) is highly sensitive

79 Infection by field strains of Foot-and-mouth disease virus (FMDV) is initiated by bind

80 The leader proteinase (L(pro)) of foot-and-mouth disease virus (FMDV) is involved in antag

81 Foot-and-mouth disease virus (FMDV) is one of the most d

82 n the initiation of immune responses against foot-and-mouth disease virus (FMDV) is poorly understood

83 The 5' UTR of foot-and-mouth disease virus (FMDV) is predicted to incl

84 IMPORTANCE Foot-and-mouth disease virus (FMDV) is responsible for f

85 Foot-and-mouth disease virus (FMDV) is the first animal

86 Foot-and-mouth disease virus (FMDV) is the pathogen of f

87 domestic animals with chemically inactivated foot-and-mouth disease virus (FMDV) is widely practiced

88 Foot-and-mouth disease virus (FMDV) leader proteinase (L

89 dentified an aromatic hydrophobic residue in foot-and-mouth disease virus (FMDV) leader proteinase (L

90 Foot-and-mouth disease virus (FMDV) leader proteinase (L

91 Foot-and-mouth disease virus (FMDV) mediates cell entry

92 Foot-and-mouth disease virus (FMDV) produces one of the

93 eta interferon [IFN-alpha/beta]) can inhibit foot-and-mouth disease virus (FMDV) replication in cell

94 and II IFNs have proven effective to inhibit foot-and-mouth disease virus (FMDV) replication in swine

95 g a comparative analysis, of 103 isolates of foot-and-mouth disease virus (FMDV) representing all sev

96 Infection of cells by foot-and-mouth disease virus (FMDV) results in the rapid

97 Foot-and-mouth disease virus (FMDV) RNA-dependent RNA po

98 The low fidelity of foot-and-mouth disease virus (FMDV) RNA-dependent RNA po

99 Adsorption and plaque formation of foot-and-mouth disease virus (FMDV) serotype A12 are inh

100 ents from human rhinovirus type 2 (HRV2) and foot-and-mouth disease virus (FMDV) to control the trans

101 previously demonstrated that the ability of foot-and-mouth disease virus (FMDV) to form plaques in c

102 Adaptation of field isolates of foot-and-mouth disease virus (FMDV) to grow in cells in

103 Foot-and-mouth disease virus (FMDV) utilizes different c

104 VHH proteins recognizing foot-and-mouth disease virus (FMDV) were used for making

105 The development of a serological test for foot-and-mouth disease virus (FMDV) which is quick and e

106 Foot-and-mouth disease virus (FMDV), a non-enveloped pic

107 However, in foot-and-mouth disease virus (FMDV), a sequence (2A) of

108 the integrin receptors on cultured cells for foot-and-mouth disease virus (FMDV), and high-efficiency

109 Foot-and-mouth disease virus (FMDV), as with other RNA v

110 ily, and for several diverse species such as foot-and-mouth disease virus (FMDV), hemagglutinin (HA)

111 3D(pol), the RdRp of the foot-and-mouth disease virus (FMDV), is responsible for

112 Foot-and-mouth disease virus (FMDV), like other RNA viru

113 Foot-and-mouth disease virus (FMDV), particularly strain

114 Foot-and-mouth disease virus (FMDV), the causative agent

115 Foot-and-mouth disease virus (FMDV), the causative agent

116 " We show that the key replication enzyme of foot-and-mouth disease virus (FMDV), the RNA-dependent R

117 s of representatives of several serotypes of foot-and-mouth disease virus (FMDV), we discovered a put

118 We have previously reported that Foot-and-mouth disease virus (FMDV), which is virulent f

119 mutants were used to map antigenic sites on foot-and-mouth disease virus (FMDV), which resulted in t

120 BP1) was documented as an essential ITAF for foot-and-mouth disease virus (FMDV), with no apparent ro

121 lfate has an important role in cell entry by foot-and-mouth disease virus (FMDV).

122 tion is a common feature in the evolution of foot-and-mouth disease virus (FMDV).

123 lved in genome packaging in the picornavirus foot-and-mouth disease virus (FMDV).

124 merous human and animal pathogens, including foot-and-mouth disease virus (FMDV).

125 deoptimize the capsid-coding region (P1) of foot-and-mouth disease virus (FMDV).

126 which acts as a primer in the replication of foot-and-mouth disease virus (FMDV).

127 tionally been used to map antigenic sites on foot-and-mouth disease virus (FMDV).

128 proof of principle concept to the capsid of foot-and-mouth disease virus (FMDV).

129 caffer) are the principal "carrier" hosts of foot-and-mouth disease virus (FMDV).

130 subsequent evolution of RNA viruses such as foot-and-mouth disease virus (FMDV).

131 ected swine when challenged 1 day later with foot-and-mouth disease virus (FMDV).

132 f the internal ribosome entry site (IRES) of foot-and-mouth disease virus (FMDV).

133 , we apply the method to two UK epidemics of Foot-and-Mouth Disease Virus (FMDV): the 2007 outbreak,

134 Like other viruses, the picornavirus foot-and-mouth disease virus (FMDV; genus Aphthovirus),

135 The foot-and-mouth-disease virus (FMDV) utilizes non-canonic

136 recognizing a putative vaccinal peptide from foot-and-mouth disease virus (FMDV15).

137 ting cross-neutralization between serotype O foot-and-mouth disease viruses (FMDVs) is critical for g

138 On extensive passage of foot-and-mouth disease virus in baby hamster kidney-21 c

139 n a 4H junction derived from domain 3 of the foot-and-mouth disease virus internal ribosome entry sit

140 (6) and 2 x 10(7) c.f.u./ml, indicating that foot-and-mouth disease virus IRES provides high-titer bi

141 Because foot-and-mouth disease virus IRES structure depends on l

142 a vector with a multiple cloning site 3' to foot-and-mouth disease virus IRES, was used to construct

143 of the O(1) British field strain serotype of foot-and-mouth disease virus is a high-affinity ligand f

144 Foot-and-mouth disease virus is a highly contagious path

145 A genetic variant of foot-and-mouth disease virus lacking the leader proteina

146 from high affinity ligands of alpha v beta6 (foot-and-mouth-disease virus, latency associated peptide

147 ar to those of core catalytic domains of the foot-and-mouth disease virus leader protease and coronav

148 liovirus (n=3 each, 18.8%); Brucella spp and foot and mouth disease virus (n=2 each, 12.5%); and vari

149 we use these methods to analyze data from a foot-and-mouth disease virus outbreak in the United King

150 aches, we investigated how highly contagious foot-and-mouth disease viruses persist in the African bu

151 the prominent G-H loop of the VP1 protein of foot-and-mouth disease virus, raised substantial levels

152 nal structure of the corresponding domain of foot-and-mouth disease virus, revealing an analogous dom

153 The larger picornavirus IRESs (those of foot-and-mouth disease virus, rhinovirus, encephalomyoca

154 Venus and a puromycin-resistant gene via the foot-and-mouth disease virus self-cleaving peptide T2A.

155 odels to predict the antigenic similarity in foot-and-mouth disease virus strains and in influenza st

156 20FMDV2 is a 20-mer peptide derived from the foot-and-mouth disease virus that exhibits nanomolar and

157 naviruses (e.g., poliovirus, rhinovirus, and foot-and-mouth disease virus), the capsid precursor prot

158 ar viruses, including all seven serotypes of foot-and-mouth disease virus, two serotypes of vesicular

159 opy of the genome-linked protein, VPg wheras foot-and-mouth disease virus uniquely encodes three copi

160 imal pathogens: classical swine fever virus; foot-and-mouth disease virus; vesicular stomatitis virus

161 s in innate responses against infection with foot-and-mouth disease virus was analyzed on consecutive