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

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

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

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

7 2A self-processing peptide derived from the 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 Following infection with foot-and-mouth disease virus, expression of CD62L and CD

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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