ライフサイエンスコーパス: mouth disease

1 ions in the event of an outbreak of foot-and-mouth disease.

2 pment as effective vaccines against foot-and-mouth disease.

3 h CNS involvement and 29 with skin, eye, and mouth disease.

4 spreading the much more contagious foot and mouth disease.

5 ant animal pathogen responsible for foot-and-mouth disease.

6 o now of the epidemiology of hand, foot, and mouth disease.

7 ction are usually limited, such as hand-foot-mouth disease.

8 es to cause large outbreaks of hand foot and mouth disease across Asia, associated with neurological

9 DSLINE database was searched using the term "mouth diseases." Additional references were identified f

10 ential route of vaccination against foot-and-mouth disease and may be useful for eliciting protection

11 is a human pathogen that causes hand, foot, mouth disease and neurological complications.

12 ng pathogens associated with hand, foot, and mouth disease and pediatric respiratory disease worldwid

13 d immunity patterns of local hand, foot, and mouth disease and to optimise interventions.

14 is the major cause of severe hand, foot, and mouth disease and viral encephalitis in children across

15 sease), two datasets of serotype A (Foot-and-Mouth disease) and two datasets of influenza when the sc

16 7,200,092 probable cases of hand, foot, and mouth disease (annual incidence, 1.2 per 1000 person-yea

17 cts children, manifesting as hand, foot, and mouth disease, aseptic meningitis, poliomyelitis-like ac

18 ve samples) from suspected cases of foot-and-mouth disease collected from 65 countries between 1965 a

19 present an analysis of the current foot-and-mouth disease epidemic in Great Britain over the first 2

20 of the control policies in the 2001 foot-and-mouth disease epidemic in the UK.

21 Foot-and-mouth disease (FMD) can cause large disruptive epidemics

22 tainty as management proceeds, with foot-and-mouth disease (FMD) culling and measles vaccination as c

23 Candidate foot-and-mouth disease (FMD) DNA vaccines designed to produce vir

24 The foot and mouth disease (FMD) epidemic in British livestock remain

25 ch linked holdings on the size of a Foot-and-Mouth Disease (FMD) epidemic.

26 fox-hunting during the outbreak of foot-and-mouth disease (FMD) in 2001 to examine this issue and fo

27 e show that, during the outbreak of foot and mouth disease (FMD) in 2001, there was a significant red

28 essing IFNs can effectively control foot-and-mouth disease (FMD) in cattle and swine during experimen

29 ntial to control major epidemics of foot-and-mouth disease (FMD) in livestock is contentious.

30 In 1997, a devastating outbreak of foot-and-mouth disease (FMD) in Taiwan was caused by a serotype O

31 Foot-and-mouth disease (FMD) in the UK provides an ideal opportun

32 The recent outbreak of foot-and-mouth disease (FMD) in the United Kingdom is a stark rem

33 Foot-and-mouth disease (FMD) in Turkey is controlled using biannu

34 Foot-and-mouth disease (FMD) is a highly contagious viral disease

35 Foot-and-mouth disease (FMD) is a highly contagious viral disease

36 Foot-and-mouth disease (FMD) is a worldwide problem limiting the

37 Foot-and-mouth disease (FMD) is one of the most feared viral dise

38 table vaccine candidates.IMPORTANCE Foot-and-mouth disease (FMD) is the most devastating disease affe

39 Foot-and-mouth disease (FMD) remains one of the most devastating

40 Production of foot-and-mouth disease (FMD) vaccines requires cytosolic expressi

41 Foot-and-mouth disease (FMD) virus (FMDV) circulates as multiple

42 attle in response to infection with foot-and-mouth disease (FMD) virus.

43 DNA vaccine candidates for foot-and-mouth disease (FMD) were engineered to produce FMD virus

44 spongiform encephalopathy (BSE) and foot-and-mouth disease (FMD), and the advent of new technologies,

45 ith FMDV developed typical signs of foot-and-mouth disease (FMD), including fever, vesicular lesions,

46 ase of notifiable diseases, such as foot-and-mouth disease (FMD), these analyses provide important in

47 ontrol and potential eradication of foot-and-mouth disease (FMD).

48 e major etiological agents of hand, foot and mouth disease (HFMD) and are often associated with neuro

49 an emerging pathogen causing hand, foot, and mouth disease (HFMD) and fatal neurological diseases in

50 (EV-A71) is a major cause of hand, foot, and mouth disease (HFMD) and is particularly prevalent in pa

51 mily and are major causes of hand, foot, and mouth disease (HFMD) and pediatric respiratory disease w

52 rus 71 (EV71) and associated hand, foot, and mouth disease (HFMD) are recognized as emerging public h

53 Epidemiology and etiology of hand, foot, and mouth disease (HFMD) based on large sample size or evalu

54 million/11.3 million) of all hand, foot, and mouth disease (HFMD) cases reported to WHO during 2010-2

55 Hand Foot and Mouth Disease (HFMD) constitutes a considerable burden f

56 Hand, foot, and mouth disease (HFMD) has spread throughout the Asia-Paci

57 To monitor search trends on Hand, Foot and Mouth Disease (HFMD) in Guangdong Province, China, we te

58 nterovirus 71 (EV71) can cause hand-foot-and-mouth disease (HFMD) in young children.

59 Hand, foot, and mouth disease (HFMD) is a common childhood illness cause

60 Hand, foot, and mouth disease (HFMD) is a common childhood illness cause

61 Hand, foot, and mouth disease (HFMD) is a reemerging illness caused by a

62 Hand-foot-mouth disease (HFMD) is an acute, self-limited, highly c

63 ary causes of the epidemics of hand-foot-and-mouth disease (HFMD) that affect more than a million chi

64 aviridae), a common cause of hand, foot, and mouth disease (HFMD), may also cause severe neurological

65 rus that causes outbreaks of hand, foot, and mouth disease (HFMD), primarily in the Asia-Pacific area

66 1) causes large outbreaks of hand, foot, and mouth disease (HFMD), with severe neurological complicat

67 y a major role in the resolution of foot-and-mouth disease in cattle.

68 y emerged as a major cause of hand, foot and mouth disease in children worldwide but no vaccine is av

69 xsackievirus A6 (CVA6) causes hand, foot and mouth disease in children.

70 cterised the epidemiology of hand, foot, and mouth disease in China on the basis of enhanced surveill

71 ccurred during the 2001 epidemic of foot-and-mouth disease in Great Britain.

72 le for seasonal outbreaks of hand, foot, and mouth disease in the Asia-Pacific region.

73 k is used to analyse an outbreak of foot-and-mouth disease in the UK, enhancing current understanding

74 Enterovirus 71 (EV71) causes hand, foot, and mouth disease in young children and infants.

75 rus infection and in the control of foot-and-mouth disease infection highlight the problems caused by

76 and animal (bovine brucellosis and foot-and-mouth disease) infections clearly differentiating infect

77 Hand, foot, and mouth disease is a common childhood illness caused by en

78 Hand-foot-and-mouth disease is a serious public health threat to child

79 Atypical hand, foot, and mouth disease is caused by a new lineage of Coxsackie vi

80 irus (FMDV), the causative agent of foot-and-mouth disease, is an Aphthovirus within the Picornavirid

81 irus (FMDV), the causative agent of foot-and-mouth disease, is an Apthovirus within the Picornavirida

82 irus), jump dispersal on a network (foot-and-mouth disease), or a combination of these (Sudden oak de

83 del run for the 2001 United Kingdom foot and mouth disease outbreak and compare the efficacy of diffe

84 Foot-and-mouth disease outbreaks in non-endemic countries can lea

85 tio-temporal model of the spread of foot-and-mouth disease, parameterized to match the 2001 UK outbre

86 Every year in June, hand, foot, and mouth disease peaked in north China, whereas southern Ch

87 aboratory data from cases of hand, foot, and mouth disease reported to the Chinese Center for Disease

88 The Global Foot-and-Mouth Disease Research Alliance (GFRA), an international

89 problem using the specific case of foot-and-mouth disease spreading between farms using the formulat

90 he severe, atypical cases of hand, foot, and mouth disease that have been reported worldwide since 20

91 71 is a picornavirus causing hand, foot, and mouth disease that may progress to fatal encephalitis in

92 e performed experimental studies of foot-and-mouth disease transmission in cattle and estimated this

93 results on three datasets of SAT2 (Foot-and-Mouth disease), two datasets of serotype A (Foot-and-Mou

94 ted at the N-terminal region of the foot-and-mouth disease viral polymerase (3D).

95 The foot-and-mouth disease virus (FMDV) "carrier" state was defined b

96 ilely protect swine challenged with foot-and-mouth disease virus (FMDV) 1 day later.

97 The ability of foot-and-mouth disease virus (FMDV) 2A to mediate proteolytic cle

98 retion are induced by expression of foot-and-mouth disease virus (FMDV) 3C(pro) and that this require

99 The N-terminal region of the foot-and-mouth disease virus (FMDV) 3D polymerase contains the se

100 The foot-and-mouth disease virus (FMDV) afflicts livestock in more th

101 a from transmission experiments for foot-and-mouth disease virus (FMDV) and African swine fever virus

102 sted in this study: one recognizing foot-and-mouth disease virus (FMDV) and another recognizing the 1

103 encephalomyocarditis virus (EMCV), foot-and-mouth disease virus (FMDV) and other picornaviruses comp

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

105 t to which the genetic diversity of foot-and-mouth disease virus (FMDV) arising over the course of in

106 Foot-and-mouth disease virus (FMDV) binds to cell-surface integri

107 t the leader proteinase (L(pro)) of foot-and-mouth disease virus (FMDV) blocks cap-dependent mRNA tra

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

109 Foot-and-mouth disease virus (FMDV) causes a fast-spreading disea

110 tabilizing SAT2 vaccines.IMPORTANCE Foot-and-mouth disease virus (FMDV) causes a highly contagious ac

111 Foot-and-mouth disease virus (FMDV) causes a highly contagious ac

112 Foot-and-mouth disease virus (FMDV) causes a highly contagious in

113 Foot-and-mouth disease virus (FMDV) causes a highly contagious vi

114 Foot-and-mouth disease virus (FMDV) causes an acute vesicular dis

115 The genome of foot-and-mouth disease virus (FMDV) differs from that of other pi

116 Isolates of foot-and-mouth disease virus (FMDV) exist as complex mixtures of

117 ifferential laboratory detection of foot-and-mouth disease virus (FMDV) from viruses that cause clini

118 Two foot-and-mouth disease virus (FMDV) genome sequences have been de

119 NA genome of all seven serotypes of foot-and-mouth disease virus (FMDV) has been developed.

120 Field isolates of foot-and-mouth disease virus (FMDV) have a restricted cell tropis

121 Field isolates of foot-and-mouth disease virus (FMDV) have been shown to use the RG

122 Field isolates of foot-and-mouth disease virus (FMDV) have been shown to use three

123 replication of poliovirus (PV) and foot-and-mouth disease virus (FMDV) in a variety of cells.

124 ith clearance versus persistence of foot-and-mouth disease virus (FMDV) in micro-dissected compartmen

125 ve been identified as receptors for foot-and-mouth disease virus (FMDV) in vitro.

126 ve been identified as receptors for foot-and-mouth disease virus (FMDV) in vitro.

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

128 Here, we show that the picornavirus foot-and-mouth disease virus (FMDV) induces the formation of auto

129 lymphocyte subsets in recovery from foot-and-mouth disease virus (FMDV) infection in calves was inves

130 The pathogenesis of persistent foot-and-mouth disease virus (FMDV) infection was investigated in

131 Foot-and-mouth disease virus (FMDV) initiates infection by bindin

132 investigation, the manner in which foot-and-mouth disease virus (FMDV) interacts with the innate and

133 t the leader proteinase (L(pro)) of foot-and-mouth disease virus (FMDV) interferes with the innate im

134 slation initiation dependent on the foot-and-mouth disease virus (FMDV) internal ribosome entry site

135 ors were constructed containing the foot-and-mouth disease virus (FMDV) internal ribosome entry site

136 Foot-and-mouth disease virus (FMDV) is a highly contagious viral

137 Nonstructural protein 3A of foot-and-mouth disease virus (FMDV) is a partially conserved prot

138 Foot-and-mouth disease virus (FMDV) is an important animal pathog

139 he final steps in the maturation of foot-and-mouth disease virus (FMDV) is cleavage of the VP0 protei

140 reviously shown that replication of foot-and-mouth disease virus (FMDV) is highly sensitive to alpha/

141 Infection by field strains of Foot-and-mouth disease virus (FMDV) is initiated by binding to ce

142 The leader proteinase (L(pro)) of foot-and-mouth disease virus (FMDV) is involved in antagonizing t

143 tiation of immune responses against foot-and-mouth disease virus (FMDV) is poorly understood.

144 animals with chemically inactivated foot-and-mouth disease virus (FMDV) is widely practiced to contro

145 Foot-and-mouth disease virus (FMDV) leader proteinase (L(pro)) cl

146 Foot-and-mouth disease virus (FMDV) mediates cell entry by attach

147 Foot-and-mouth disease virus (FMDV) produces one of the most infe

148 feron [IFN-alpha/beta]) can inhibit foot-and-mouth disease virus (FMDV) replication in cell culture,

149 Ns have proven effective to inhibit foot-and-mouth disease virus (FMDV) replication in swine, a simil

150 rative analysis, of 103 isolates of foot-and-mouth disease virus (FMDV) representing all seven seroty

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

152 Foot-and-mouth disease virus (FMDV) RNA-dependent RNA polymerase

153 Adsorption and plaque formation of foot-and-mouth disease virus (FMDV) serotype A12 are inhibited by

154 human rhinovirus type 2 (HRV2) and foot-and-mouth disease virus (FMDV) to control the translation of

155 ly demonstrated that the ability of foot-and-mouth disease virus (FMDV) to form plaques in cell cultu

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

157 Foot-and-mouth disease virus (FMDV) utilizes different cell surfa

158 netic and epidemiological data in a Foot and Mouth Disease Virus (FMDV) veterinary outbreak in Englan

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

160 velopment of a serological test for foot-and-mouth disease virus (FMDV) which is quick and easy to us

161 Foot-and-mouth disease virus (FMDV), a non-enveloped picornavirus

162 However, in foot-and-mouth disease virus (FMDV), a sequence (2A) of just 16-2

163 rin receptors on cultured cells for foot-and-mouth disease virus (FMDV), and high-efficiency utilizat

164 Foot-and-mouth disease virus (FMDV), as with other RNA viruses, r

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

166 Foot-and-mouth disease virus (FMDV), like other RNA viruses, exhi

167 Foot-and-mouth disease virus (FMDV), particularly strains of the

168 Foot-and-mouth disease virus (FMDV), the causative agent of foot-

169 Foot-and-mouth disease virus (FMDV), the causative agent of foot-

170 that the key replication enzyme of foot-and-mouth disease virus (FMDV), the RNA-dependent RNA polyme

171 esentatives of several serotypes of foot-and-mouth disease virus (FMDV), we discovered a putative cre

172 We have previously reported that Foot-and-mouth disease virus (FMDV), which is virulent for cattle

173 were used to map antigenic sites on foot-and-mouth disease virus (FMDV), which resulted in the identi

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

175 ne when challenged 1 day later with foot-and-mouth disease virus (FMDV).

176 ernal ribosome entry site (IRES) of foot-and-mouth disease virus (FMDV).

177 enome packaging in the picornavirus foot-and-mouth disease virus (FMDV).

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

179 man and animal pathogens, including foot-and-mouth disease virus (FMDV).

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

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

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

183 y the method to two UK epidemics of Foot-and-Mouth Disease Virus (FMDV): the 2007 outbreak, and a sub

184 ng a putative vaccinal peptide from foot-and-mouth disease virus (FMDV15).

185 ntibiotic resistance gene, with the foot and mouth disease virus 2A self-cleaving sequence placed bet

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

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

188 at produce vesicular lesions, e.g., foot-and-mouth disease virus and others.

189 he gene encoding the 2A protease of foot-and-mouth disease virus and then inserted in frame between t

190 Foot and mouth disease virus causes a livestock disease of signif

191 The foot-and-mouth disease virus encodes two forms of a cysteine prot

192 On extensive passage of foot-and-mouth disease virus in baby hamster kidney-21 cells, the

193 nction derived from domain 3 of the foot-and-mouth disease virus internal ribosome entry site (IRES);

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

195 Because foot-and-mouth disease virus IRES structure depends on long-range

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

197 1) British field strain serotype of foot-and-mouth disease virus is a high-affinity ligand for alpha

198 Foot-and-mouth disease virus is a highly contagious pathogen that

199 A genetic variant of foot-and-mouth disease virus lacking the leader proteinase coding

200 se of core catalytic domains of the foot-and-mouth disease virus leader protease and coronavirus PLPs

201 hese methods to analyze data from a foot-and-mouth disease virus outbreak in the United Kingdom in 20

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

203 predict the antigenic similarity in foot-and-mouth disease virus strains and in influenza strains, wh

204 e genome-linked protein, VPg wheras foot-and-mouth disease virus uniquely encodes three copies of VPg

205 te responses against infection with foot-and-mouth disease virus was analyzed on consecutive 5 d foll

206 The foot and mouth disease virus, a picornavirus, encodes two forms o

207 ed a salient genome segmentation of foot-and-mouth disease virus, an important animal pathogen whose

208 has been documented for poliovirus, foot-and-mouth disease virus, and coxsackievirus B3 and can lead

209 ortant members, such as poliovirus, foot-and-mouth disease virus, and endomyocarditis virus.

210 us family, including poliovirus and foot-and-mouth disease virus, are widespread pathogens of humans

211 QVLAQKVART (A20FMDV2), derived from foot-and-mouth disease virus, as a potent inhibitor of alphavbeta

212 Following infection with foot-and-mouth disease virus, expression of CD62L and CD45RO was

213 nent G-H loop of the VP1 protein of foot-and-mouth disease virus, raised substantial levels of antipe

214 larger picornavirus IRESs (those of foot-and-mouth disease virus, rhinovirus, encephalomyocarditis vi

215 s, including all seven serotypes of foot-and-mouth disease virus, two serotypes of vesicular stomatit

216 enome packaging of the picornavirus foot-and-mouth disease virus.

217 tide (A20FMDV2) derived from VP1 of foot-and-mouth disease virus.

218 processing peptide derived from the foot-and-mouth disease virus.

219 use virus, human rhinovirus-14, and foot and mouth disease virus.

220 imentally infected via aerosol with foot-and-mouth disease virus.

221 ock can be made less susceptible to foot and mouth disease virus.

222 rus, rhinovirus, enterovirus 71 and foot-and-mouth disease virus.

223 ogens: classical swine fever virus; foot-and-mouth disease virus; vesicular stomatitis virus, New Jer

224 The foot-and-mouth-disease virus (FMDV) utilizes non-canonical transl

225 affinity ligands of alpha v beta6 (foot-and-mouth-disease virus, latency associated peptide), have a

226 es from poliovirus, rhinovirus, and foot-and-mouth disease viruses.

227 redominant pathogens for the hand, foot, and mouth disease--was observed in recent years.

228 ols during a nationwide epidemic of foot and mouth disease, which substantially delayed removal of TB

229 ent large-scale outbreaks of hand, foot, and mouth disease worldwide and represent a major etiologica