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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 available clinical data presented with hand, foot, and mouth disease.
7 hina and Japan that are known to cause hand, foot, and mouth disease.
8 tle, 16.64% (95% CI: 16.63 to 16.66) against foot and mouth disease, 33.80% (33.43 to 34.38) against
9 rovirus 71 (EV71) is a common cause of hand, foot and mouth disease-a disease endemic especially in t
10 1 continues to cause large outbreaks of hand foot and mouth disease across Asia, associated with neur
11 are emerging pathogens associated with hand, foot, and mouth disease and pediatric respiratory diseas
12 ynamics and immunity patterns of local hand, foot, and mouth disease and to optimise interventions.
13 (EV-A71) is the major cause of severe hand, foot, and mouth disease and viral encephalitis in childr
14 ers a potential route of vaccination against foot-and-mouth disease and may be useful for eliciting p
15 -Mouth disease), two datasets of serotype A (Foot-and-Mouth disease) and two datasets of influenza wh
16 CVA6 was frequently associated with hand, foot and mouth disease, and EV-D68 with respiratory infe
17 al other enteroviruses responsible for hand, foot and mouth disease, and plays a key role in cell ent
18 y included 7,200,092 probable cases of hand, foot, and mouth disease (annual incidence, 1.2 per 1000
19 ostly affects children, manifesting as hand, foot, and mouth disease, aseptic meningitis, poliomyelit
20 eptor for the largest receptor-group of hand-foot-and-mouth disease causing viruses, which includes C
21 ue-negative samples) from suspected cases of foot-and-mouth disease collected from 65 countries betwe
28 Here we show that, during the outbreak of foot and mouth disease (FMD) in 2001, there was a signif
31 del uncertainty as management proceeds, with foot-and-mouth disease (FMD) culling and measles vaccina
33 o estimate the occurrence of transmission of foot-and-mouth disease (FMD) during the incubation phase
36 ar ban on fox-hunting during the outbreak of foot-and-mouth disease (FMD) in 2001 to examine this iss
37 ctor expressing IFNs can effectively control foot-and-mouth disease (FMD) in cattle and swine during
38 its potential to control major epidemics of foot-and-mouth disease (FMD) in livestock is contentious
52 ly more stable vaccine candidates.IMPORTANCE Foot-and-mouth disease (FMD) is the most devastating dis
53 ikelihood of infection with, or exposure to, foot-and-mouth disease (FMD) over the same time period u
59 outh disease virus (FMDV) is responsible for foot-and-mouth disease (FMD), an important disease of fa
60 f bovine spongiform encephalopathy (BSE) and foot-and-mouth disease (FMD), and the advent of new tech
62 h later with FMDV developed typical signs of foot-and-mouth disease (FMD), including fever, vesicular
63 In the case of notifiable diseases, such as foot-and-mouth disease (FMD), these analyses provide imp
64 outh disease virus (FMDV) is the pathogen of foot-and-mouth disease (FMD), which is a highly contagio
67 6) are the major etiological agents of hand, foot and mouth disease (HFMD) and are often associated w
68 the case of a 31-year-old patient with Hand, Foot and Mouth Disease (HFMD) and concurrent acute monoc
71 IOS) framework to simulate and optimize hand foot and mouth disease (HFMD) surveillance in a high-bur
74 (EV71) is an emerging pathogen causing hand, foot, and mouth disease (HFMD) and fatal neurological di
75 virus A71 (EV-A71) is a major cause of hand, foot, and mouth disease (HFMD) and is particularly preva
76 viridae family and are major causes of hand, foot, and mouth disease (HFMD) and pediatric respiratory
77 f enterovirus 71 (EV71) and associated hand, foot, and mouth disease (HFMD) are recognized as emergin
79 87% (9.8 million/11.3 million) of all hand, foot, and mouth disease (HFMD) cases reported to WHO dur
86 ily Picornaviridae), a common cause of hand, foot, and mouth disease (HFMD), may also cause severe ne
87 picornavirus that causes outbreaks of hand, foot, and mouth disease (HFMD), primarily in the Asia-Pa
88 us 71 (EV71) causes large outbreaks of hand, foot, and mouth disease (HFMD), with severe neurological
92 the primary causes of the epidemics of hand-foot-and-mouth disease (HFMD) that affect more than a mi
93 s recently emerged as a major cause of hand, foot and mouth disease in children worldwide but no vacc
95 , we characterised the epidemiology of hand, foot, and mouth disease in China on the basis of enhance
98 nding and quantifying risks for TADs such as Foot-and-Mouth disease in a land-locked country like Uga
101 framework is used to analyse an outbreak of foot-and-mouth disease in the UK, enhancing current unde
102 ory symptoms (in 1197 [17%] patients), hand, foot, and mouth disease (in 528 [7% patients), and myoca
103 f poliovirus infection and in the control of foot-and-mouth disease infection highlight the problems
104 cellosis) and animal (bovine brucellosis and foot-and-mouth disease) infections clearly differentiati
105 95% CI [1.924, 1.939]; p < 0.001), and hand, foot, and mouth disease (IRR: 2.501, 95% CI [2.491, 2.51
110 disease virus (FMDV), the causative agent of foot-and-mouth disease, is an Aphthovirus within the Pic
111 disease virus (FMDV), the causative agent of foot-and-mouth disease, is an Apthovirus within the Pico
112 st Nile virus), jump dispersal on a network (foot-and-mouth disease), or a combination of these (Sudd
113 arwick model run for the 2001 United Kingdom foot and mouth disease outbreak and compare the efficacy
117 loped spatio-temporal model of the spread of foot-and-mouth disease, parameterized to match the 2001
119 a highly contagious livestock viral disease, foot-and-mouth disease poses a great threat to the beef-
121 cal, and laboratory data from cases of hand, foot, and mouth disease reported to the Chinese Center f
124 mine this problem using the specific case of foot-and-mouth disease spreading between farms using the
125 mplifies the severe, atypical cases of hand, foot, and mouth disease that have been reported worldwid
126 terovirus 71 is a picornavirus causing hand, foot, and mouth disease that may progress to fatal encep
128 rediction results on three datasets of SAT2 (Foot-and-Mouth disease), two datasets of serotype A (Foo
130 n from genetic and epidemiological data in a Foot and Mouth Disease Virus (FMDV) veterinary outbreak
134 liovirus (n=3 each, 18.8%); Brucella spp and foot and mouth disease virus (n=2 each, 12.5%); and vari
135 sh-ble antibiotic resistance gene, with the foot and mouth disease virus 2A self-cleaving sequence p
143 ck in secretion are induced by expression of foot-and-mouth disease virus (FMDV) 3C(pro) and that thi
146 ished data from transmission experiments for foot-and-mouth disease virus (FMDV) and African swine fe
147 s were tested in this study: one recognizing foot-and-mouth disease virus (FMDV) and another recogniz
148 IRESs) of encephalomyocarditis virus (EMCV), foot-and-mouth disease virus (FMDV) and other picornavir
149 e present in highly purified preparations of foot-and-mouth disease virus (FMDV) and poliovirus.
150 the extent to which the genetic diversity of foot-and-mouth disease virus (FMDV) arising over the cou
152 shown that the leader proteinase (L(pro)) of foot-and-mouth disease virus (FMDV) blocks cap-dependent
157 use in stabilizing SAT2 vaccines.IMPORTANCE Foot-and-mouth disease virus (FMDV) causes a highly cont
160 virus strains; however, the pathogenesis of foot-and-mouth disease virus (FMDV) coinfections is larg
163 for the differential laboratory detection of foot-and-mouth disease virus (FMDV) from viruses that ca
165 hin the RNA genome of all seven serotypes of foot-and-mouth disease virus (FMDV) has been developed.
169 ocked the replication of poliovirus (PV) and foot-and-mouth disease virus (FMDV) in a variety of cell
170 ociated with clearance versus persistence of foot-and-mouth disease virus (FMDV) in micro-dissected c
175 ole of T-lymphocyte subsets in recovery from foot-and-mouth disease virus (FMDV) infection in calves
178 ecades of investigation, the manner in which foot-and-mouth disease virus (FMDV) interacts with the i
179 shown that the leader proteinase (L(pro)) of foot-and-mouth disease virus (FMDV) interferes with the
180 Translation initiation dependent on the foot-and-mouth disease virus (FMDV) internal ribosome en
181 iral vectors were constructed containing the foot-and-mouth disease virus (FMDV) internal ribosome en
182 tent infection in African buffalo.IMPORTANCE Foot-and-mouth disease virus (FMDV) is a highly contagio
185 stress response.IMPORTANCE The picornavirus foot-and-mouth disease virus (FMDV) is a notorious anima
189 One of the final steps in the maturation of foot-and-mouth disease virus (FMDV) is cleavage of the V
190 We have previously shown that replication of foot-and-mouth disease virus (FMDV) is highly sensitive
194 n the initiation of immune responses against foot-and-mouth disease virus (FMDV) is poorly understood
199 domestic animals with chemically inactivated foot-and-mouth disease virus (FMDV) is widely practiced
202 dentified an aromatic hydrophobic residue in foot-and-mouth disease virus (FMDV) leader proteinase (L
205 eta interferon [IFN-alpha/beta]) can inhibit foot-and-mouth disease virus (FMDV) replication in cell
206 and II IFNs have proven effective to inhibit foot-and-mouth disease virus (FMDV) replication in swine
207 g a comparative analysis, of 103 isolates of foot-and-mouth disease virus (FMDV) representing all sev
212 ents from human rhinovirus type 2 (HRV2) and foot-and-mouth disease virus (FMDV) to control the trans
213 previously demonstrated that the ability of foot-and-mouth disease virus (FMDV) to form plaques in c
217 The development of a serological test for foot-and-mouth disease virus (FMDV) which is quick and e
220 the integrin receptors on cultured cells for foot-and-mouth disease virus (FMDV), and high-efficiency
222 ily, and for several diverse species such as foot-and-mouth disease virus (FMDV), hemagglutinin (HA)
228 " We show that the key replication enzyme of foot-and-mouth disease virus (FMDV), the RNA-dependent R
229 s of representatives of several serotypes of foot-and-mouth disease virus (FMDV), we discovered a put
231 mutants were used to map antigenic sites on foot-and-mouth disease virus (FMDV), which resulted in t
232 BP1) was documented as an essential ITAF for foot-and-mouth disease virus (FMDV), with no apparent ro
245 , we apply the method to two UK epidemics of Foot-and-Mouth Disease Virus (FMDV): the 2007 outbreak,
248 peptide binding and explains the ability of foot-and-mouth disease virus 3C(pro) to cleave sequences
251 nked to the gene encoding the 2A protease of foot-and-mouth disease virus and then inserted in frame
254 n a 4H junction derived from domain 3 of the foot-and-mouth disease virus internal ribosome entry sit
255 (6) and 2 x 10(7) c.f.u./ml, indicating that foot-and-mouth disease virus IRES provides high-titer bi
257 a vector with a multiple cloning site 3' to foot-and-mouth disease virus IRES, was used to construct
258 of the O(1) British field strain serotype of foot-and-mouth disease virus is a high-affinity ligand f
261 ar to those of core catalytic domains of the foot-and-mouth disease virus leader protease and coronav
262 we use these methods to analyze data from a foot-and-mouth disease virus outbreak in the United King
263 Venus and a puromycin-resistant gene via the foot-and-mouth disease virus self-cleaving peptide T2A.
264 odels to predict the antigenic similarity in foot-and-mouth disease virus strains and in influenza st
265 20FMDV2 is a 20-mer peptide derived from the foot-and-mouth disease virus that exhibits nanomolar and
266 opy of the genome-linked protein, VPg wheras foot-and-mouth disease virus uniquely encodes three copi
267 s in innate responses against infection with foot-and-mouth disease virus was analyzed on consecutive
268 naviruses (e.g., poliovirus, rhinovirus, and foot-and-mouth disease virus), the capsid precursor prot
269 on mediated a salient genome segmentation of foot-and-mouth disease virus, an important animal pathog
270 henotype has been documented for poliovirus, foot-and-mouth disease virus, and coxsackievirus B3 and
271 cally important members, such as poliovirus, foot-and-mouth disease virus, and endomyocarditis virus.
272 icornavirus family, including poliovirus and foot-and-mouth disease virus, are widespread pathogens o
273 AVPNLRGDLQVLAQKVART (A20FMDV2), derived from foot-and-mouth disease virus, as a potent inhibitor of a
274 uman rhinovirus, coxsackievirus, poliovirus, foot-and-mouth disease virus, enterovirus D-68, and a wi
276 the prominent G-H loop of the VP1 protein of foot-and-mouth disease virus, raised substantial levels
277 nal structure of the corresponding domain of foot-and-mouth disease virus, revealing an analogous dom
278 The larger picornavirus IRESs (those of foot-and-mouth disease virus, rhinovirus, encephalomyoca
279 ar viruses, including all seven serotypes of foot-and-mouth disease virus, two serotypes of vesicular
285 imal pathogens: classical swine fever virus; foot-and-mouth disease virus; vesicular stomatitis virus
287 from high affinity ligands of alpha v beta6 (foot-and-mouth-disease virus, latency associated peptide
288 ting cross-neutralization between serotype O foot-and-mouth disease viruses (FMDVs) is critical for g
289 aches, we investigated how highly contagious foot-and-mouth disease viruses persist in the African bu
291 CVA--the predominant pathogens for the hand, foot, and mouth disease--was observed in recent years.
292 TB controls during a nationwide epidemic of foot and mouth disease, which substantially delayed remo
293 for frequent large-scale outbreaks of hand, foot, and mouth disease worldwide and represent a major