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1 ity of viruses other than AaV, including (+) ssRNA viruses.
2 amily Bunyaviridae), a group of enveloped (-)ssRNA viruses.
3  gene transfer between eukaryotic (+) and (-)ssRNA viruses.
4 s into the evolutionary history of dsRNA and ssRNA viruses.
5 order in the packaged genomes of a number of ssRNA viruses.
6 termediate between dsRNA and positive-strand ssRNA viruses, as well as between encapsidated and capsi
7 which resembles that of single-stranded RNA (ssRNA) viruses but differs from the well-established mec
8 co mosaic virus (STMV) is a small, spherical ssRNA virus common in a natural wild plant, Nicotiana gl
9        We used unique characteristics of two ssRNA viruses, dengue virus and influenza virus, to deli
10 atory syncytial virus (RSV), negative strand ssRNA virus, depends upon the ability to recognize speci
11 upport a key role for autophagy in mediating ssRNA virus detection and interferon-alpha secretion by
12  the genome is indeed a primary factor among ssRNA viruses' evolutionary constraints, contributing al
13 enic positive-sense, single-stranded RNA [(+)ssRNA] virus families which carry a macro domain: Corona
14                         Single-stranded RNA (ssRNA) viruses form a major class that includes importan
15 ing guide RNA to target and inhibit a human +ssRNA virus, hepatitis C virus, within eukaryotic cells.
16 ay have occurred from a single-stranded RNA (ssRNA) virus (hypovirus) to a dsRNA virus, SsMBV1.
17 the factors that drive efficient assembly of ssRNA viruses in vivo.
18 like protease domain that commonly exists in ssRNA viruses, including members of the families Potyvir
19 DC responses to certain single-stranded RNA (ssRNA) viruses occur only after live viral infection.
20                           Rhinovirus (RV), a ssRNA virus of the picornavirus family, is a major cause
21          While most T=3 single-stranded RNA (ssRNA) viruses package in vivo about 3,000 nucleotides (
22 ponses triggered by the synthetic analogs of ssRNA viruses (polyuridine) and dsRNA viruses (polyinosi
23 of genome-capsid interactions in a spherical ssRNA virus provides insight into genome delivery via th
24 ng signal (PS) with capsid protein(s) (most +ssRNA viruses so far studied); step II, cocondensation o
25 we propose a two-step assembly strategy for +ssRNA viruses: step I, acquisition of packaging specific
26                TLR7 recognizes the genome of ssRNA viruses such as Coxsackievirus B.
27 nto a preformed capsid, single-stranded RNA (ssRNA) viruses, such as bacteriophage MS2, co-assemble t
28  on the genome packaging of a representative ssRNA virus, the bacteriophage MS2, via a series of biom
29 al gene transfer might have occurred from an ssRNA virus to a dsRNA virus, which may provide new insi
30                                    HCV is an ssRNA virus, which suggests a role for Toll-like recepto
31                         Single-stranded RNA (ssRNA) viruses, which include major human pathogens, pac
32 osterna elaeasa virus (EeV), insect-specific ssRNA+ viruses, which revise a capsid-based classificati
33 suggesting that it should be similar for all ssRNA viruses with a comparable ratio of capsid size/gen

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