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1 infection with a single strain of the agent (bovine spongiform encephalopathy).
2 responsible for diseases such as scrapie and bovine spongiform encephalopathy.
3  transmission to humans of the agent causing bovine spongiform encephalopathy.
4 of maximum global risk for human exposure to bovine spongiform encephalopathy.
5  from eating beef infected with the agent of bovine spongiform encephalopathy.
6 , of variant CJD (vCJD), a disease linked to bovine spongiform encephalopathy.
7 tive prevention of human dietary exposure to bovine spongiform encephalopathy.
8 luding chronic wasting disease, scrapie, and bovine spongiform encephalopathy.
9 n ailments including Alzheimer's disease and bovine spongiform encephalopathy.
10 als, including Creutzfeldt-Jakob disease and bovine spongiform encephalopathy.
11 ived from sheep with scrapie and cattle with bovine spongiform encephalopathy.
12 ditions such as Creutzfeld-Jacob Disease and Bovine Spongiform Encephalopathy.
13 vered from sheep with scrapie or cattle with bovine spongiform encephalopathy.
14 dies reported the emergence of the classical bovine spongiform encephalopathy agent (c-BSE) upon tran
15 features, which results from exposure to the bovine spongiform encephalopathy agent.
16  thought to result from oral exposure to the bovine spongiform encephalopathy agent.
17 thy, chronic wasting disease of cervids, and bovine spongiform encephalopathy) all seem to be lateral
18 for neuroinvasion in many prion diseases, in bovine spongiform encephalopathy and atypical cases of s
19 f natural host systems, including strains of bovine spongiform encephalopathy and chronic wasting dis
20 me synonymous with unusual diseases, such as bovine spongiform encephalopathy and Creutzfeldt-Jakob d
21 nfectious forms of these diseases, including bovine spongiform encephalopathy and Creutzfeldt-Jakob d
22 reutzfeldt-Jakob disease (CJD) in humans and bovine spongiform encephalopathy and scrapie in animals.
23 rol measures have now successfully contained bovine spongiform encephalopathy and the incidence of vC
24 d increased virulence such as in the case of bovine spongiform encephalopathy and variant Creutzfeldt
25 tive diseases that include scrapie in sheep, bovine spongiform encephalopathy, and Creutzfeldt-Jakob
26 monkeys were fed brain of (eleven) cows with bovine spongiform encephalopathy, and some were euthaniz
27 uru; inherited prion disease; sheep scrapie; bovine spongiform encephalopathy; and chronic wasting di
28 "prion") strains, notably those derived from bovine spongiform encephalopathy, are highly resistant t
29 reutzfeldt-Jakob disease (CJD), scrapie, and bovine spongiform encephalopathy because they express hi
30             Since 2005, two cases of natural bovine spongiform encephalopathies (BSE) have been repor
31                      The recent incidents of bovine spongiform encephalopathies (BSE) in humans have
32 en though they were similarly exposed to the bovine spongiform encephalopathy (BSE) agent.
33 son of transmission efficiencies of vCJD and bovine spongiform encephalopathy (BSE) and an assessment
34              However, an association between bovine spongiform encephalopathy (BSE) and bovine PRNP e
35  all of this has to be added the backwash of bovine spongiform encephalopathy (BSE) and foot-and-mout
36                                              Bovine spongiform encephalopathy (BSE) and human Creutzf
37                                              Bovine spongiform encephalopathy (BSE) and its human equ
38 reutzfeldt-Jakob disease (CJD) in humans and bovine spongiform encephalopathy (BSE) and scrapie in an
39 tal neurodegenerative disorders that include bovine spongiform encephalopathy (BSE) and scrapie in an
40 study reports the co-infection of sheep with bovine spongiform encephalopathy (BSE) and scrapie.
41 chemical and neuropathological properties of bovine spongiform encephalopathy (BSE) and variant Creut
42                         Cattle infected with bovine spongiform encephalopathy (BSE) appear to be a re
43  (sCJD), endemic sheep scrapie, and epidemic bovine spongiform encephalopathy (BSE) are caused by a r
44 ssive dementia, whereas scrapie of sheep and bovine spongiform encephalopathy (BSE) are manifest as a
45                               An outbreak of bovine spongiform encephalopathy (BSE) arose in the Unit
46 r the millions of people possibly exposed to bovine spongiform encephalopathy (BSE) by consumption of
47                         An experimental oral bovine spongiform encephalopathy (BSE) challenge study w
48                           However, since the bovine spongiform encephalopathy (BSE) crisis, their use
49 ese proteins is strongly regulated since the bovine spongiform encephalopathy (BSE) crisis.
50              A comprehensive analysis of the bovine spongiform encephalopathy (BSE) epidemic in cattl
51                                   The recent bovine spongiform encephalopathy (BSE) epidemic in the U
52 utzfeld-Jakob disease, following on from the bovine spongiform encephalopathy (BSE) epidemic, led to
53 ic prion transmission was reported after the bovine spongiform encephalopathy (BSE) epidemic, when >2
54 hat readily distinguished experimental sheep bovine spongiform encephalopathy (BSE) from classical sc
55 rP-Tg532 mice showed resistance to classical bovine spongiform encephalopathy (BSE) from sheep and so
56                                              Bovine spongiform encephalopathy (BSE) has become a publ
57 ar prion protein PrP(C), such as PrP(BSE) in bovine spongiform encephalopathy (BSE) in cattle and PrP
58 Chronic wasting disease (CWD) in cervids and bovine spongiform encephalopathy (BSE) in cattle are pri
59    It is clear that the prion strain causing bovine spongiform encephalopathy (BSE) in cattle has inf
60 ative diseases and include scrapie in sheep, bovine spongiform encephalopathy (BSE) in cattle, chroni
61 rrence of this disease after the epidemic of bovine spongiform encephalopathy (BSE) in cattle.
62                    Statutory surveillance of bovine spongiform encephalopathy (BSE) indicates that ca
63                                           In bovine spongiform encephalopathy (BSE) infection, the po
64 he region of a 10(-12) dilution of classical bovine spongiform encephalopathy (BSE) inoculum, which i
65                                              Bovine spongiform encephalopathy (BSE) is a transmissibl
66                                              Bovine spongiform encephalopathy (BSE) is a transmissibl
67                                              Bovine spongiform encephalopathy (BSE) is a TSE that occ
68                                              Bovine Spongiform Encephalopathy (BSE) is the only anima
69  concern that bovine prions from cattle with bovine spongiform encephalopathy (BSE) may have been pas
70     More than a million cattle infected with bovine spongiform encephalopathy (BSE) may have entered
71                There is growing concern that bovine spongiform encephalopathy (BSE) may have passed f
72 nt (SR) samples in order to classify them as bovine spongiform encephalopathy (BSE) or non-BSE.
73 n PrP methionine 129, inoculated with either bovine spongiform encephalopathy (BSE) or variant CJD pr
74 Variant Creutzfeldt-Jakob disease (vCJD) and bovine spongiform encephalopathy (BSE) prions are two of
75 n of beef products from cattle infected with bovine spongiform encephalopathy (BSE) prions causes new
76  increasing concern over the extent to which bovine spongiform encephalopathy (BSE) prions have been
77 tion after the extensive dietary exposure to bovine spongiform encephalopathy (BSE) prions in the UK,
78                                              Bovine spongiform encephalopathy (BSE) prions were respo
79 ine prion protein (BoPrP) serially propagate bovine spongiform encephalopathy (BSE) prions without po
80 erstand little about human susceptibility to bovine spongiform encephalopathy (BSE) prions, the causa
81 ototypic mouse line, Tg(CerPrP)1536(+/-), to bovine spongiform encephalopathy (BSE) prions, which hav
82 to be caused by dietary or other exposure to bovine spongiform encephalopathy (BSE) prions.
83  the strain of agent from cattle affected by bovine spongiform encephalopathy (BSE) produces a charac
84   The cause of the original case or cases of bovine spongiform encephalopathy (BSE) remains an enigma
85                    Foodborne transmission of bovine spongiform encephalopathy (BSE) to humans as vari
86                       However, its effect on bovine spongiform encephalopathy (BSE) transmission to g
87  for infection, it remains uncertain whether bovine spongiform encephalopathy (BSE) was transmitted t
88 enerative diseases, including kuru, scrapie, bovine spongiform encephalopathy (BSE), and Creutzfeldt-
89 ldt-Jakob disease (vCJD), experimental ovine bovine spongiform encephalopathy (BSE), and natural shee
90 eutzfeldt-Jakob disease (vCJD) and classical bovine spongiform encephalopathy (BSE), and that with un
91                                              Bovine spongiform encephalopathy (BSE), popularly known
92                                              Bovine spongiform encephalopathy (BSE), scrapie of sheep
93                                              Bovine spongiform encephalopathy (BSE), the prion diseas
94                      After the occurrence of bovine spongiform encephalopathy (BSE), there has been c
95 ritish national sheep flock is infected with bovine spongiform encephalopathy (BSE), we examined the
96                                              Bovine spongiform encephalopathy (BSE)-associated prions
97 sumed that sheep and goats consumed the same bovine spongiform encephalopathy (BSE)-contaminated meat
98 ), almost certainly caused by consumption of bovine spongiform encephalopathy (BSE)-contaminated meat
99 prion disease associated with infection with bovine spongiform encephalopathy (BSE)-like prions.
100 ndistinguishable from the causative agent of bovine spongiform encephalopathy (BSE).
101 train, as is the case for epidemic classical bovine spongiform encephalopathy (BSE).
102  to be a zoonotic form of the cattle disease bovine spongiform encephalopathy (BSE).
103 isease caused by infection with the agent of bovine spongiform encephalopathy (BSE).
104 une deficiency syndrome (AIDS), hepatitis C, bovine spongiform encephalopathy (BSE)/variant Creutzfel
105 ponsible for neurodegenerative diseases like bovine spongiform encephalopathy (BSE; "mad cow" disease
106  sheep are infected with prions from cattle (bovine spongiform encephalopathy [BSE]), both PrP varian
107  of vCJD (sheep experimentally infected with bovine spongiform encephalopathy, BSE) to determine the
108 ion diseases of cattle include the classical bovine spongiform encephalopathy (C-BSE) and the atypica
109                                    Classical bovine spongiform encephalopathy (c-BSE) is the only ani
110  suggest that zoonotic prions from classical bovine spongiform encephalopathy (C-BSE) may copropagate
111          Some animal prion diseases, such as bovine spongiform encephalopathy, can infect humans; how
112 tted to wild-type mice and was also found in bovine spongiform encephalopathy cattle brain, indicatin
113                        Human transmission of bovine spongiform encephalopathy causes the fatal neurod
114  chronic wasting disease (CWD) and classical bovine spongiform encephalopathy (cBSE) prions.
115  13 and 21 overlap with QTLs associated with Bovine spongiform encephalopathy, clinical mastitis or s
116 D", thought to be acquired by consumption of bovine spongiform encephalopathy-contaminated food produ
117                                              Bovine spongiform encephalopathy contamination of the hu
118 ld ensure the safety of processed meats from bovine spongiform encephalopathy contamination, and coul
119 has increased drastically in response to the bovine spongiform encephalopathy epidemic.
120 e-affected sheep and cattle, and cattle with bovine spongiform encephalopathy failed to identify patt
121 health risks posed by prion zoonoses such as bovine spongiform encephalopathy, has focused much atten
122 the human form of a prion disease of cattle, bovine spongiform encephalopathy-have been reported from
123 eldt-Jakob disease in humans and scrapie and bovine spongiform encephalopathy in animals.
124 giform encephalopathy (TSE) diseases such as bovine spongiform encephalopathy in cattle are probably
125 ses--including Creutzfeldt-Jakob disease and bovine spongiform encephalopathy in cattle--is an extend
126 akob disease in humans, scrapie in sheep and bovine spongiform encephalopathy in cattle.
127 e in humans, scrapie in sheep and goats, and bovine spongiform encephalopathy in cattle.
128 ming prime minister; dealing with widespread bovine spongiform encephalopathy in Europe; and respondi
129 f infection proportional to the incidence of bovine spongiform encephalopathy in the United Kingdom a
130 stence of scrapie (in sheep) or unrecognized bovine spongiform encephalopathy (in cattle), the practi
131                        Notably, PrP(Sc) from bovine spongiform encephalopathy-infected brain was susc
132 mals meals in feedstuffs in order to prevent Bovine Spongiform Encephalopathy infection and diffusion
133 o be susceptible to the prion causing L-type bovine spongiform encephalopathy (L-BSE), although RQ171
134 cattle affected by C-BSE and atypical L-type bovine spongiform encephalopathy (L-type BSE or L-BSE) w
135 n of the UK population has been exposed to a bovine spongiform encephalopathy-like prion strain and a
136 rative disorder originating from exposure to bovine-spongiform-encephalopathy-like prions.
137 ted animals (n = 80) and 71% of animals with bovine spongiform encephalopathy (n = 7).
138 , or Ebola virus (n=1, 12.5%) or were due to bovine spongiform encephalopathy (n=1, 12.5%).
139 ort the hypothesis that human infection with bovine spongiform encephalopathy occurred in Saudi Arabi
140                            Just as spread of bovine spongiform encephalopathy prion variant is less i
141                          We demonstrate that bovine spongiform encephalopathy prions maintain their t
142 uman prion strain resulting from exposure to bovine spongiform encephalopathy prions to which the For
143 isk, as in those with primary infection with bovine spongiform encephalopathy prions.
144 e been transmitted from cattle infected with bovine spongiform encephalopathy probably via the food c
145 63K)), chronic waste disease (PrP(CWD)), and bovine spongiform encephalopathy (PrP(BSE)) in lab-scale
146  K-resistant core identical to that found in bovine spongiform encephalopathy-specific scrapie-associ
147 y experimental challenge and the outbreak of bovine spongiform encephalopathy that occurred in the la
148 ansmissible to humans, as has been shown for bovine spongiform encephalopathy (the prion disease of c
149                     Probable transmission of bovine spongiform encephalopathy to humans has focused i
150  as well as the interspecies transmission of bovine spongiform encephalopathy to humans in the form o
151 evastating disease caused by transmission of bovine spongiform encephalopathy to humans.
152 mportance given the apparent transmission of bovine spongiform encephalopathy to humans.
153                 With the potential spread of bovine spongiform encephalopathy to people as a variant
154 vCJD prevalence in the United Kingdom with a bovine spongiform encephalopathy-unexposed population.

 
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