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1 LA orthologue, associated with resilience to African Swine Fever.
2 is no commercially available vaccine against African swine fever.
3 such as Amazonia, coupled with expansion of African swine fever and possibly great economic losses.
4 ave application for preclinical diagnosis of African swine fever and surveillance and/or emergency ma
7 cted from day 10 postimmunization.IMPORTANCE African swine fever (ASF) is endemic in Africa, parts of
11 infection remained free of clinical signs of African swine fever following subsequent challenge with
14 es of the linear DNA genome are found in the African swine fever virus (asfarvirus) and in the Phycod
21 he approximately 165 proteins encoded by the African swine fever virus (ASFV) genome do not have sign
28 ed that the DNA repair system encoded by the African swine fever virus (ASFV) is both extremely error
29 The repair polymerase, Pol X, encoded by the African swine fever virus (ASFV) is one of the most erro
33 ht variable genomic region of the pathogenic African swine fever virus (ASFV) isolate E70 revealed a
42 enic probe hydrolysis (TaqMan) PCR assay for African swine fever virus (ASFV) was developed and evalu
43 Although the Malawi Lil20/1 (MAL) strain of African swine fever virus (ASFV) was isolated from Ornit
45 X), the DNA repair polymerase encoded by the African swine fever virus (ASFV), is extremely error pro
51 es of rat DNA polymerase beta (Pol beta) and African swine fever virus DNA polymerase X (ASFV Pol X)
54 ragment (KF), and a low-fidelity polymerase, African swine fever virus DNA polymerase X (Pol X), and
56 eveal that DNA polymerase X (pol X) from the African swine fever virus incorporates adenine (dATP) op
58 ng to reveal the complex mechanisms by which African swine fever virus interacts with its swine and t
60 tion, we assessed the benefits of adding the African swine fever virus NP868R capping enzyme during r
62 and specificity of interactions between the African swine fever virus polymerase X and gapped DNA su
63 e Xenopus CN (xCN) autoinhibitory domain and African swine fever virus protein A238L] block the Ca(2+
64 netic study of DNA polymerase X (Pol X) from African swine fever virus reported here is the first ana
69 nd is necessary for the proteins produced by African swine fever virus, Canarypox virus, and Herpes s
70 new group or cluster of viruses encompassing African swine fever virus, faustovirus, pacmanvirus, and
71 ts shows that 31 genes are conserved between African swine fever virus, pacmanvirus, faustovirus, and
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