ライフサイエンスコーパス: ssRNA virus

1 ribed recombination events between ssDNA and ssRNA viruses.

2 ity of viruses other than AaV, including (+) ssRNA viruses.

3 amily Bunyaviridae), a group of enveloped (-)ssRNA viruses.

4 gene transfer between eukaryotic (+) and (-)ssRNA viruses.

5 s into the evolutionary history of dsRNA and ssRNA viruses.

6 order in the packaged genomes of a number of ssRNA viruses.

7 antiviral responses in other positive-sense ssRNA viruses.

8 itro, RBCs bind synthetic ssRNA and RNA from ssRNA viruses.

9 ociated protein 5 (MDA5)-a key receptor for +ssRNA viruses.

10 ffect of Slfn11 on protein synthesis than (-)ssRNA viruses.

11 3 can be harnessed to target a wide range of ssRNA viruses and CARVER's potential broad utility for r

12 troviruses, represent a new linkage between +ssRNA viruses and the intermediate double-stranded RNA (

13 e +ssRNA mycoviruses in the linkage between +ssRNA viruses and the intermediate dsRNA polymycoviruses

14 ic to positive-sense, single-stranded RNA (+ ssRNA) viruses and involves melanoma differentiation-ass

15 respond to unclassified single-stranded RNA (ssRNA) viruses and viruses belonging to the Rhabdovirida

16 termediate between dsRNA and positive-strand ssRNA viruses, as well as between encapsidated and capsi

17 effective antiviral for single-stranded RNA (ssRNA) viruses because it programmably cleaves RNAs comp

18 which resembles that of single-stranded RNA (ssRNA) viruses but differs from the well-established mec

19 ereas negative-sense single-stranded RNA [(-)ssRNA] viruses carry at infection an RNA replicase that

20 co mosaic virus (STMV) is a small, spherical ssRNA virus common in a natural wild plant, Nicotiana gl

21 We used unique characteristics of two ssRNA viruses, dengue virus and influenza virus, to deli

22 atory syncytial virus (RSV), negative strand ssRNA virus, depends upon the ability to recognize speci

23 upport a key role for autophagy in mediating ssRNA virus detection and interferon-alpha secretion by

24 the genome is indeed a primary factor among ssRNA viruses' evolutionary constraints, contributing al

25 enic positive-sense, single-stranded RNA [(+)ssRNA] virus families which carry a macro domain: Corona

26 Single-stranded RNA (ssRNA) viruses form a major class that includes importan

27 ignificantly increased the replication of (+)ssRNA viruses from the Flavivirus genus, including West

28 ound autofluorescence when infected by the + ssRNA virus HcRNAV.

29 ing guide RNA to target and inhibit a human +ssRNA virus, hepatitis C virus, within eukaryotic cells.

30 ay have occurred from a single-stranded RNA (ssRNA) virus (hypovirus) to a dsRNA virus, SsMBV1.

31 nct viruses-a single-stranded (ss) DNA and a ssRNA virus-impacted microbial processing of organic mat

32 ntial to examine the infection dynamics of a ssRNA virus in a host cell at the level of the genomic R

33 s of Slfn11 on the replication of a panel of ssRNA viruses in the human glioblastoma cell line A172,

34 the factors that drive efficient assembly of ssRNA viruses in vivo.

35 like protease domain that commonly exists in ssRNA viruses, including members of the families Potyvir

36 ting different types of single-stranded RNA (ssRNA) viruses independent of whether their structure pr

37 se activity was also substantially higher in ssRNA virus-infected cellular exudates compared to ssDNA

38 i support secondary production and implicate ssRNA virus infection as a source of proteolytic activit

39 In contrast, DOM from ssRNA virus infection did not stimulate growth, but rath

40 o proposing that dsRNA viruses evolved from +ssRNA viruses is still considered controversial due to i

41 s13's potent activity against three distinct ssRNA viruses: lymphocytic choriomeningitis virus (LCMV)

42 DC responses to certain single-stranded RNA (ssRNA) viruses occur only after live viral infection.

43 Rhinovirus (RV), a ssRNA virus of the picornavirus family, is a major cause

44 While most T=3 single-stranded RNA (ssRNA) viruses package in vivo about 3,000 nucleotides (

45 I-IFN upon TLR7 stimulation with agonists or ssRNA viruses-particularly SARS-CoV-2-but not with DNA a

46 ponses triggered by the synthetic analogs of ssRNA viruses (polyuridine) and dsRNA viruses (polyinosi

47 of genome-capsid interactions in a spherical ssRNA virus provides insight into genome delivery via th

48 on of positive-sense single-stranded RNA [(+)ssRNA] viruses requires the immediate translation of the

49 ng signal (PS) with capsid protein(s) (most +ssRNA viruses so far studied); step II, cocondensation o

50 we propose a two-step assembly strategy for +ssRNA viruses: step I, acquisition of packaging specific

51 TLR7 recognizes the genome of ssRNA viruses such as Coxsackievirus B.

52 In simple ssRNA viruses such as the bacteriophage MS2 and small RN

53 nto a preformed capsid, single-stranded RNA (ssRNA) viruses, such as bacteriophage MS2, co-assemble t

54 the prediction was more accurate for the (+) ssRNA virus than the dsDNA virus.

55 circular negative-sense single-stranded RNA (ssRNA) virus that produces three RNAs in infected cells,

56 on the genome packaging of a representative ssRNA virus, the bacteriophage MS2, via a series of biom

57 NA (dsDNA), single-stranded DNA (ssDNA), and ssRNA viruses, the mechanism of genome packaging of dsRN

58 In the class of single-stranded RNA (ssRNA) viruses, the assembly of the capsid takes place i

59 Like ssRNA viruses, there are numerous capsid-genome associat

60 al gene transfer might have occurred from an ssRNA virus to a dsRNA virus, which may provide new insi

61 local assembly rules for the ability of some ssRNA viruses to spontaneously assemble around charged p

62 nificant effect on the replication of the (-)ssRNA viruses vesicular stomatitis virus (VSV) (Rhabdovi

63 HCV is an ssRNA virus, which suggests a role for Toll-like recepto

64 Single-stranded RNA (ssRNA) viruses, which include major human pathogens, pac

65 osterna elaeasa virus (EeV), insect-specific ssRNA+ viruses, which revise a capsid-based classificati

66 1 (HadV1), a capsidless 10- or 11-segmented +ssRNA virus, while proteins encoded by ORFs 4 and 7 show

67 e incoming viral genome, we reasoned that (+)ssRNA viruses will be more sensitive to the effect of Sl

68 suggesting that it should be similar for all ssRNA viruses with a comparable ratio of capsid size/gen