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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 from eating beef infected with the agent of bovine spongiform encephalopathy.
5 tive prevention of human dietary exposure to bovine spongiform encephalopathy.
6 luding chronic wasting disease, scrapie, and bovine spongiform encephalopathy.
7 n ailments including Alzheimer's disease and bovine spongiform encephalopathy.
8 als, including Creutzfeldt-Jakob disease and bovine spongiform encephalopathy.
9 ived from sheep with scrapie and cattle with bovine spongiform encephalopathy.
10 of maximum global risk for human exposure to bovine spongiform encephalopathy.
11 ditions such as Creutzfeld-Jacob Disease and Bovine Spongiform Encephalopathy.
12 vered from sheep with scrapie or cattle with bovine spongiform encephalopathy.
15 thy, chronic wasting disease of cervids, and bovine spongiform encephalopathy) all seem to be lateral
16 for neuroinvasion in many prion diseases, in bovine spongiform encephalopathy and atypical cases of s
17 f natural host systems, including strains of bovine spongiform encephalopathy and chronic wasting dis
18 me synonymous with unusual diseases, such as bovine spongiform encephalopathy and Creutzfeldt-Jakob d
19 nfectious forms of these diseases, including bovine spongiform encephalopathy and Creutzfeldt-Jakob d
20 reutzfeldt-Jakob disease (CJD) in humans and bovine spongiform encephalopathy and scrapie in animals.
21 d increased virulence such as in the case of bovine spongiform encephalopathy and variant Creutzfeldt
22 tive diseases that include scrapie in sheep, bovine spongiform encephalopathy, and Creutzfeldt-Jakob
23 monkeys were fed brain of (eleven) cows with bovine spongiform encephalopathy, and some were euthaniz
24 "prion") strains, notably those derived from bovine spongiform encephalopathy, are highly resistant t
25 reutzfeldt-Jakob disease (CJD), scrapie, and bovine spongiform encephalopathy because they express hi
27 son of transmission efficiencies of vCJD and bovine spongiform encephalopathy (BSE) and an assessment
29 all of this has to be added the backwash of bovine spongiform encephalopathy (BSE) and foot-and-mout
32 reutzfeldt-Jakob disease (CJD) in humans and bovine spongiform encephalopathy (BSE) and scrapie in an
33 tal neurodegenerative disorders that include bovine spongiform encephalopathy (BSE) and scrapie in an
34 chemical and neuropathological properties of bovine spongiform encephalopathy (BSE) and variant Creut
36 (sCJD), endemic sheep scrapie, and epidemic bovine spongiform encephalopathy (BSE) are caused by a r
37 ssive dementia, whereas scrapie of sheep and bovine spongiform encephalopathy (BSE) are manifest as a
39 r the millions of people possibly exposed to bovine spongiform encephalopathy (BSE) by consumption of
44 utzfeld-Jakob disease, following on from the bovine spongiform encephalopathy (BSE) epidemic, led to
45 ic prion transmission was reported after the bovine spongiform encephalopathy (BSE) epidemic, when >2
46 hat readily distinguished experimental sheep bovine spongiform encephalopathy (BSE) from classical sc
48 ar prion protein PrP(C), such as PrP(BSE) in bovine spongiform encephalopathy (BSE) in cattle and PrP
49 Chronic wasting disease (CWD) in cervids and bovine spongiform encephalopathy (BSE) in cattle are pri
50 It is clear that the prion strain causing bovine spongiform encephalopathy (BSE) in cattle has inf
51 ative diseases and include scrapie in sheep, bovine spongiform encephalopathy (BSE) in cattle, chroni
57 concern that bovine prions from cattle with bovine spongiform encephalopathy (BSE) may have been pas
61 n PrP methionine 129, inoculated with either bovine spongiform encephalopathy (BSE) or variant CJD pr
62 Variant Creutzfeldt-Jakob disease (vCJD) and bovine spongiform encephalopathy (BSE) prions are two of
63 n of beef products from cattle infected with bovine spongiform encephalopathy (BSE) prions causes new
64 increasing concern over the extent to which bovine spongiform encephalopathy (BSE) prions have been
65 tion after the extensive dietary exposure to bovine spongiform encephalopathy (BSE) prions in the UK,
67 ine prion protein (BoPrP) serially propagate bovine spongiform encephalopathy (BSE) prions without po
68 erstand little about human susceptibility to bovine spongiform encephalopathy (BSE) prions, the causa
69 ototypic mouse line, Tg(CerPrP)1536(+/-), to bovine spongiform encephalopathy (BSE) prions, which hav
71 the strain of agent from cattle affected by bovine spongiform encephalopathy (BSE) produces a charac
72 The cause of the original case or cases of bovine spongiform encephalopathy (BSE) remains an enigma
75 for infection, it remains uncertain whether bovine spongiform encephalopathy (BSE) was transmitted t
76 enerative diseases, including kuru, scrapie, bovine spongiform encephalopathy (BSE), and Creutzfeldt-
77 ldt-Jakob disease (vCJD), experimental ovine bovine spongiform encephalopathy (BSE), and natural shee
82 ritish national sheep flock is infected with bovine spongiform encephalopathy (BSE), we examined the
84 sumed that sheep and goats consumed the same bovine spongiform encephalopathy (BSE)-contaminated meat
85 ), almost certainly caused by consumption of bovine spongiform encephalopathy (BSE)-contaminated meat
90 une deficiency syndrome (AIDS), hepatitis C, bovine spongiform encephalopathy (BSE)/variant Creutzfel
91 ponsible for neurodegenerative diseases like bovine spongiform encephalopathy (BSE; "mad cow" disease
92 sheep are infected with prions from cattle (bovine spongiform encephalopathy [BSE]), both PrP varian
93 ion diseases of cattle include the classical bovine spongiform encephalopathy (C-BSE) and the atypica
96 tted to wild-type mice and was also found in bovine spongiform encephalopathy cattle brain, indicatin
99 13 and 21 overlap with QTLs associated with Bovine spongiform encephalopathy, clinical mastitis or s
100 D", thought to be acquired by consumption of bovine spongiform encephalopathy-contaminated food produ
102 ld ensure the safety of processed meats from bovine spongiform encephalopathy contamination, and coul
104 e-affected sheep and cattle, and cattle with bovine spongiform encephalopathy failed to identify patt
105 health risks posed by prion zoonoses such as bovine spongiform encephalopathy, has focused much atten
106 the human form of a prion disease of cattle, bovine spongiform encephalopathy-have been reported from
108 giform encephalopathy (TSE) diseases such as bovine spongiform encephalopathy in cattle are probably
109 ses--including Creutzfeldt-Jakob disease and bovine spongiform encephalopathy in cattle--is an extend
112 f infection proportional to the incidence of bovine spongiform encephalopathy in the United Kingdom a
113 stence of scrapie (in sheep) or unrecognized bovine spongiform encephalopathy (in cattle), the practi
115 mals meals in feedstuffs in order to prevent Bovine Spongiform Encephalopathy infection and diffusion
116 o be susceptible to the prion causing L-type bovine spongiform encephalopathy (L-BSE), although RQ171
117 cattle affected by C-BSE and atypical L-type bovine spongiform encephalopathy (L-type BSE or L-BSE) w
118 n of the UK population has been exposed to a bovine spongiform encephalopathy-like prion strain and a
121 ort the hypothesis that human infection with bovine spongiform encephalopathy occurred in Saudi Arabi
124 uman prion strain resulting from exposure to bovine spongiform encephalopathy prions to which the For
126 e been transmitted from cattle infected with bovine spongiform encephalopathy probably via the food c
127 63K)), chronic waste disease (PrP(CWD)), and bovine spongiform encephalopathy (PrP(BSE)) in lab-scale
128 K-resistant core identical to that found in bovine spongiform encephalopathy-specific scrapie-associ
129 y experimental challenge and the outbreak of bovine spongiform encephalopathy that occurred in the la
130 ansmissible to humans, as has been shown for bovine spongiform encephalopathy (the prion disease of c
132 as well as the interspecies transmission of bovine spongiform encephalopathy to humans in the form o
135 vCJD prevalence in the United Kingdom with a bovine spongiform encephalopathy-unexposed population.
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