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1 species of the genus Orbivirus in the family Reoviridae.
2 t the least similarities to other members of Reoviridae.
3 e-stranded RNA (dsRNA) virus from the family Reoviridae.
4 showed characteristics typical of the family Reoviridae.
5 of a definitive fungal member of the family Reoviridae.
6 nfantile gastroenteritis, is a member of the Reoviridae.
7 rus, which is also a member of the family of Reoviridae.
8 ber of the Orbivirus genus within the family Reoviridae.
9 mber of the Aquareovirus genus of the family Reoviridae, a large family of double-stranded RNA (dsRNA
10 se modulator are derived from dsRNA viruses (Reoviridae) and dsDNA viruses (Baculoviridae), respectiv
11 nted double-stranded RNA (dsRNA) virus (CPV; Reoviridae) and highlights the importance of viral small
12 oviridae, Picornaviridae, Caliciviridae, and Reoviridae) and one DNA virus family (Parvoviridae) were
14 importance to health, members of the family Reoviridae are the basis of most structural and function
15 core has been described in atomic detail for Reoviridae (blue tongue virus and reovirus), the molecul
16 g to identify features common to nonturreted Reoviridae capping enzymes and to predict the domain org
17 -shelled and thus the simplest member of the Reoviridae, cytoplasmic polyhedrosis virus (CPV) provide
18 0) of bluetongue virus (an orbivirus, family Reoviridae) encodes two closely related nonstructural pr
19 is a member of the aquareovirus genus in the Reoviridae family and has a capsid with two shells-a tra
20 olyhedrosis virus (CPV) is unique within the Reoviridae family in having a turreted single-layer caps
21 gates; however, a hallmark of viruses of the Reoviridae family is that they utilize these sites for p
22 wing the lead of previous studies with other Reoviridae family members, most notably orbiviruses and
24 mmalian reoviruses, prototype members of the Reoviridae family of nonenveloped double-stranded RNA vi
25 (ds) RNA genome of viruses belonging to the Reoviridae family requires the RNA-dependent RNA polymer
26 e sickness virus (AHSV), an orbivirus in the Reoviridae family with nine different serotypes, causes
27 , a member of the Orbivirus genus within the Reoviridae family, has a genome of 10 double-stranded RN
28 BTV), a member of the Orbivirus genus in the Reoviridae family, is a double-capsid insect-borne virus
29 otavirus, a double-stranded RNA virus of the Reoviridae family, is the primary etiological agent of s
30 del to study the double-stranded RNA (dsRNA) Reoviridae family, the members of which infect and cause
36 idae, Orthomyxoviridae, Paramyxoviridae, and Reoviridae for RIG-I, MDA5, and interferon promoter-stim
37 ges, like those of eukaryotic viruses of the Reoviridae, function inside the inner capsid shell in bo
38 rate that a large non-enveloped virus of the Reoviridae has specific lipid requirements for membrane
39 ctures of rotavirus and other members of the Reoviridae have been extensively studied, little is know
41 RRSV), in the genus Oryzavirus of the family Reoviridae, is determined to show a core composed of cap
44 e the multiple-shelled organization of other Reoviridae members, cytoplasmic polyhedrosis virus (CPV)
47 nd livestock such as bluetongue virus (BTV) (Reoviridae), Oropouche virus (Bunyaviridae), and likely
48 longing to the picornavirus superfamily, the Reoviridae, Parvoviridae, and Bunyaviridae families, and
49 ridae, Picornaviridae, Picobirnaviridae, and Reoviridae), plants (Alphaflexiviridae, Betaflexiviridae
50 Paramyxoviridae, Picornaviridae, Poxviridae, Reoviridae, Rhabdoviridae and Togaviridae families, with
51 ctural proteins in two members of the family Reoviridae suggests a common mechanism of unwinding vira
52 gue virus (BTV), an archetypal member of the Reoviridae, utilizes the late endosome-specific lipid ly
53 r large complex capsid viruses of the family Reoviridae, which comprises a range of mammalian pathoge
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