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1 r fear of spreading the much more contagious foot and mouth disease.
2 l predictions in the event of an outbreak of foot-and-mouth disease.
3 or development as effective vaccines against foot-and-mouth disease.
4 an important animal pathogen responsible for foot-and-mouth disease.
5 study up to now of the epidemiology of hand, foot, and mouth disease.
6 1 continues to cause large outbreaks of hand foot and mouth disease across Asia, associated with neur
7 are emerging pathogens associated with hand, foot, and mouth disease and pediatric respiratory diseas
8 ynamics and immunity patterns of local hand, foot, and mouth disease and to optimise interventions.
9 (EV-A71) is the major cause of severe hand, foot, and mouth disease and viral encephalitis in childr
10 ers a potential route of vaccination against foot-and-mouth disease and may be useful for eliciting p
11 -Mouth disease), two datasets of serotype A (Foot-and-Mouth disease) and two datasets of influenza wh
12 y included 7,200,092 probable cases of hand, foot, and mouth disease (annual incidence, 1.2 per 1000
13 ostly affects children, manifesting as hand, foot, and mouth disease, aseptic meningitis, poliomyelit
14 ue-negative samples) from suspected cases of foot-and-mouth disease collected from 65 countries betwe
18 Here we show that, during the outbreak of foot and mouth disease (FMD) in 2001, there was a signif
20 del uncertainty as management proceeds, with foot-and-mouth disease (FMD) culling and measles vaccina
23 ar ban on fox-hunting during the outbreak of foot-and-mouth disease (FMD) in 2001 to examine this iss
24 ctor expressing IFNs can effectively control foot-and-mouth disease (FMD) in cattle and swine during
25 its potential to control major epidemics of foot-and-mouth disease (FMD) in livestock is contentious
34 ly more stable vaccine candidates.IMPORTANCE Foot-and-mouth disease (FMD) is the most devastating dis
40 f bovine spongiform encephalopathy (BSE) and foot-and-mouth disease (FMD), and the advent of new tech
41 h later with FMDV developed typical signs of foot-and-mouth disease (FMD), including fever, vesicular
42 In the case of notifiable diseases, such as foot-and-mouth disease (FMD), these analyses provide imp
44 6) are the major etiological agents of hand, foot and mouth disease (HFMD) and are often associated w
47 (EV71) is an emerging pathogen causing hand, foot, and mouth disease (HFMD) and fatal neurological di
48 virus A71 (EV-A71) is a major cause of hand, foot, and mouth disease (HFMD) and is particularly preva
49 viridae family and are major causes of hand, foot, and mouth disease (HFMD) and pediatric respiratory
50 f enterovirus 71 (EV71) and associated hand, foot, and mouth disease (HFMD) are recognized as emergin
52 87% (9.8 million/11.3 million) of all hand, foot, and mouth disease (HFMD) cases reported to WHO dur
57 ily Picornaviridae), a common cause of hand, foot, and mouth disease (HFMD), may also cause severe ne
58 picornavirus that causes outbreaks of hand, foot, and mouth disease (HFMD), primarily in the Asia-Pa
59 us 71 (EV71) causes large outbreaks of hand, foot, and mouth disease (HFMD), with severe neurological
61 the primary causes of the epidemics of hand-foot-and-mouth disease (HFMD) that affect more than a mi
62 s recently emerged as a major cause of hand, foot and mouth disease in children worldwide but no vacc
64 , we characterised the epidemiology of hand, foot, and mouth disease in China on the basis of enhance
69 framework is used to analyse an outbreak of foot-and-mouth disease in the UK, enhancing current unde
70 f poliovirus infection and in the control of foot-and-mouth disease infection highlight the problems
71 cellosis) and animal (bovine brucellosis and foot-and-mouth disease) infections clearly differentiati
75 disease virus (FMDV), the causative agent of foot-and-mouth disease, is an Aphthovirus within the Pic
76 disease virus (FMDV), the causative agent of foot-and-mouth disease, is an Apthovirus within the Pico
77 st Nile virus), jump dispersal on a network (foot-and-mouth disease), or a combination of these (Sudd
78 arwick model run for the 2001 United Kingdom foot and mouth disease outbreak and compare the efficacy
80 loped spatio-temporal model of the spread of foot-and-mouth disease, parameterized to match the 2001
82 cal, and laboratory data from cases of hand, foot, and mouth disease reported to the Chinese Center f
84 mine this problem using the specific case of foot-and-mouth disease spreading between farms using the
85 mplifies the severe, atypical cases of hand, foot, and mouth disease that have been reported worldwid
86 terovirus 71 is a picornavirus causing hand, foot, and mouth disease that may progress to fatal encep
88 rediction results on three datasets of SAT2 (Foot-and-Mouth disease), two datasets of serotype A (Foo
90 n from genetic and epidemiological data in a Foot and Mouth Disease Virus (FMDV) veterinary outbreak
91 sh-ble antibiotic resistance gene, with the foot and mouth disease virus 2A self-cleaving sequence p
99 ck in secretion are induced by expression of foot-and-mouth disease virus (FMDV) 3C(pro) and that thi
102 ished data from transmission experiments for foot-and-mouth disease virus (FMDV) and African swine fe
103 s were tested in this study: one recognizing foot-and-mouth disease virus (FMDV) and another recogniz
104 IRESs) of encephalomyocarditis virus (EMCV), foot-and-mouth disease virus (FMDV) and other picornavir
105 e present in highly purified preparations of foot-and-mouth disease virus (FMDV) and poliovirus.
106 the extent to which the genetic diversity of foot-and-mouth disease virus (FMDV) arising over the cou
108 shown that the leader proteinase (L(pro)) of foot-and-mouth disease virus (FMDV) blocks cap-dependent
113 use in stabilizing SAT2 vaccines.IMPORTANCE Foot-and-mouth disease virus (FMDV) causes a highly cont
118 for the differential laboratory detection of foot-and-mouth disease virus (FMDV) from viruses that ca
120 hin the RNA genome of all seven serotypes of foot-and-mouth disease virus (FMDV) has been developed.
124 ocked the replication of poliovirus (PV) and foot-and-mouth disease virus (FMDV) in a variety of cell
125 ociated with clearance versus persistence of foot-and-mouth disease virus (FMDV) in micro-dissected c
130 ole of T-lymphocyte subsets in recovery from foot-and-mouth disease virus (FMDV) infection in calves
133 ecades of investigation, the manner in which foot-and-mouth disease virus (FMDV) interacts with the i
134 shown that the leader proteinase (L(pro)) of foot-and-mouth disease virus (FMDV) interferes with the
135 Translation initiation dependent on the foot-and-mouth disease virus (FMDV) internal ribosome en
136 iral vectors were constructed containing the foot-and-mouth disease virus (FMDV) internal ribosome en
140 One of the final steps in the maturation of foot-and-mouth disease virus (FMDV) is cleavage of the V
141 We have previously shown that replication of foot-and-mouth disease virus (FMDV) is highly sensitive
144 n the initiation of immune responses against foot-and-mouth disease virus (FMDV) is poorly understood
145 domestic animals with chemically inactivated foot-and-mouth disease virus (FMDV) is widely practiced
149 eta interferon [IFN-alpha/beta]) can inhibit foot-and-mouth disease virus (FMDV) replication in cell
150 and II IFNs have proven effective to inhibit foot-and-mouth disease virus (FMDV) replication in swine
151 g a comparative analysis, of 103 isolates of foot-and-mouth disease virus (FMDV) representing all sev
155 ents from human rhinovirus type 2 (HRV2) and foot-and-mouth disease virus (FMDV) to control the trans
156 previously demonstrated that the ability of foot-and-mouth disease virus (FMDV) to form plaques in c
160 The development of a serological test for foot-and-mouth disease virus (FMDV) which is quick and e
163 the integrin receptors on cultured cells for foot-and-mouth disease virus (FMDV), and high-efficiency
165 ily, and for several diverse species such as foot-and-mouth disease virus (FMDV), hemagglutinin (HA)
170 " We show that the key replication enzyme of foot-and-mouth disease virus (FMDV), the RNA-dependent R
171 s of representatives of several serotypes of foot-and-mouth disease virus (FMDV), we discovered a put
173 mutants were used to map antigenic sites on foot-and-mouth disease virus (FMDV), which resulted in t
183 , we apply the method to two UK epidemics of Foot-and-Mouth Disease Virus (FMDV): the 2007 outbreak,
185 peptide binding and explains the ability of foot-and-mouth disease virus 3C(pro) to cleave sequences
188 nked to the gene encoding the 2A protease of foot-and-mouth disease virus and then inserted in frame
191 n a 4H junction derived from domain 3 of the foot-and-mouth disease virus internal ribosome entry sit
192 (6) and 2 x 10(7) c.f.u./ml, indicating that foot-and-mouth disease virus IRES provides high-titer bi
194 a vector with a multiple cloning site 3' to foot-and-mouth disease virus IRES, was used to construct
195 of the O(1) British field strain serotype of foot-and-mouth disease virus is a high-affinity ligand f
198 ar to those of core catalytic domains of the foot-and-mouth disease virus leader protease and coronav
199 we use these methods to analyze data from a foot-and-mouth disease virus outbreak in the United King
200 Venus and a puromycin-resistant gene via the foot-and-mouth disease virus self-cleaving peptide T2A.
201 odels to predict the antigenic similarity in foot-and-mouth disease virus strains and in influenza st
202 opy of the genome-linked protein, VPg wheras foot-and-mouth disease virus uniquely encodes three copi
203 s in innate responses against infection with foot-and-mouth disease virus was analyzed on consecutive
204 on mediated a salient genome segmentation of foot-and-mouth disease virus, an important animal pathog
205 henotype has been documented for poliovirus, foot-and-mouth disease virus, and coxsackievirus B3 and
206 cally important members, such as poliovirus, foot-and-mouth disease virus, and endomyocarditis virus.
207 icornavirus family, including poliovirus and foot-and-mouth disease virus, are widespread pathogens o
208 AVPNLRGDLQVLAQKVART (A20FMDV2), derived from foot-and-mouth disease virus, as a potent inhibitor of a
210 the prominent G-H loop of the VP1 protein of foot-and-mouth disease virus, raised substantial levels
211 The larger picornavirus IRESs (those of foot-and-mouth disease virus, rhinovirus, encephalomyoca
212 ar viruses, including all seven serotypes of foot-and-mouth disease virus, two serotypes of vesicular
218 imal pathogens: classical swine fever virus; foot-and-mouth disease virus; vesicular stomatitis virus
220 from high affinity ligands of alpha v beta6 (foot-and-mouth-disease virus, latency associated peptide
222 CVA--the predominant pathogens for the hand, foot, and mouth disease--was observed in recent years.
223 TB controls during a nationwide epidemic of foot and mouth disease, which substantially delayed remo
224 for frequent large-scale outbreaks of hand, foot, and mouth disease worldwide and represent a major
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