ライフサイエンスコーパス: cucumber mosaic virus

1 A viruses, cowpea chlorotic mottle virus and cucumber mosaic virus.

2 Notably, the Cucumber mosaic virus 2b protein, shown previously to fu

3 ypersusceptible to TMV, turnip mosaic virus, cucumber mosaic virus and cauliflower mosaic virus as we

4 ts were infected with two different viruses, cucumber mosaic virus and oilseed rape mosaic virus.

5 s (members of Tobamovirus genus), but not to Cucumber mosaic virus and Potato virus X (members of dif

6 umulation of two other heterologous viruses: cucumber mosaic virus and tobacco mosaic virus.

7 ports describe that the 2b suppressor of the Cucumber mosaic virus binds ARGONAUTE and that the P0 su

8 Finally, the structure of cucumber mosaic virus bound to a loop involved in aphid

9 SDE5 also results in hyper-susceptibility to cucumber mosaic virus but not turnip mosaic virus.

10 RNA (satRNA) with its helper virus, namely, cucumber mosaic virus, causes systemic necrosis in tomat

11 The cucumber mosaic virus (CMV) 2b protein is a potent count

12 The cucumber mosaic virus (CMV) 2b protein suppresses RNA si

13 The cucumber mosaic virus (CMV) 2b protein was among the fir

14 dopsis thaliana targeted during infection by cucumber mosaic virus (CMV) 2b protein, known to suppres

15 ous analysis of replicase recognition of the Cucumber mosaic virus (CMV) and BMV SLCs indicates that

16 A system already under use in field tests is cucumber mosaic virus (CMV) and its satellite RNAs.

17 se gene sequence from RNA-2 of strain Fny of cucumber mosaic virus (CMV) are resistant to systemic CM

18 Cucumber mosaic virus (CMV) comprises numerous isolates

19 onse (systemic necrosis) to seven strains of Cucumber mosaic virus (CMV) from pepper or tomato, but n

20 Cucumber mosaic virus (CMV) has been divided into two su

21 Resistance to Cucumber mosaic virus (CMV) in tobacco lines transformed

22 istance to infection in cowpea by strains of cucumber mosaic virus (CMV) involves a local, hypersensi

23 minent feature on the surfaces of virions of Cucumber mosaic virus (CMV) is a negatively charged loop

24 Cucumber mosaic virus (CMV) is a tripartite RNA virus th

25 Cucumber mosaic virus (CMV) is an RNA plant virus with a

26 Cucumber mosaic virus (CMV) is one of the most successfu

27 The acute plant virus Cucumber mosaic virus (CMV) manipulates its host's volat

28 g of 12 restriction enzyme marker mutants of Cucumber mosaic virus (CMV) onto young leaves of squash

29 ucture and genetic diversity of a California Cucumber mosaic virus (CMV) population was assessed by s

30 inants were observed in the progenies of the Cucumber mosaic virus (CMV) reassortant L(1)L(2)F(3) con

31 D satellite RNA (satRNA) is a strain of cucumber mosaic virus (CMV) satRNA that induces an epide

32 , we demonstrate potent immunosuppression of cucumber mosaic virus (CMV) seed transmission in its nat

33 a and N. clevelandii coexpressing wt BMV and Cucumber mosaic virus (CMV) showed that despite trans-en

34 r maize based on a naturally maize-infecting cucumber mosaic virus (CMV) strain, ZMBJ-CMV.

35 ble for efficient and accurate initiation of cucumber mosaic virus (CMV) subgenomic RNA4.

36 Cucumber mosaic virus (CMV) systemically infects both to

37 n and deletion mutations of the replicase of Cucumber mosaic virus (CMV) was determined in planta by

38 e plant viruses, Tobacco mosaic virus (TMV), Cucumber mosaic virus (CMV), and Cowpea chlorotic mottle

39 s infected with potato virus Y (PVY) or with cucumber mosaic virus (CMV), but not in plants infected

40 e 3a movement protein (MP) of a plant virus, Cucumber mosaic virus (CMV), forms ribonucleoprotein (RN

41 the effects of a widespread plant pathogen, Cucumber mosaic virus (CMV), on the quality and attracti

42 as detected in another tripartite RNA virus, cucumber mosaic virus (CMV), suggesting that the 1a-1a i

43 Cucumber mosaic virus (CMV), the type member of the genu

44 We previously devised a cucumber mosaic virus (CMV)-based vector system carrying

45 Cucumber mosaic virus (CMV)-encoded 2b protein was among

46 the tripartite positive-strand RNA genome of cucumber mosaic virus (CMV).

47 tatus challenged with a generalist pathogen, Cucumber mosaic virus (CMV).

48 ad significantly reduced symptom severity by Cucumber mosaic virus (CMV).

49 ridae family, alfalfa mosaic virus (AMV) and cucumber mosaic virus (CMV).

50 ns in quantitative resistance to the endemic cucumber mosaic virus (CMV).

51 Here, we describe a mutant of Cucumber mosaic virus (CMV-Delta2b) that is silenced pre

52 The structure of cucumber mosaic virus (CMV; strain Fny) has been determi

53 However, a mixed infection of TYLCV with cucumber mosaic virus compromised the resistance.

54 s study, we used an artificial population of Cucumber mosaic virus consisting of 12 restriction enzym

55 to a virus-like particle (VLP) derived from cucumber mosaic virus containing a tetanus toxoid univer

56 1 and a virus-like particle derived from the cucumber mosaic virus containing the tetanus toxin-deriv

57 c infection with cauliflower mosaic virus or cucumber mosaic virus did not induce the tryptophan path

58 two proteins: a capsid subunit derived from Cucumber mosaic virus engineered with a universal T-cell

59 acco plants infected with the Fny isolate of Cucumber mosaic virus (Fny-CMV) that will direct synthes

60 tobacco, the 3a movement protein (3a MP) of Cucumber mosaic virus fused to green fluorescent protein

61 he tripartite viruses Brome mosaic virus and Cucumber mosaic virus have been shown to induce VIGS in

62 of plant potyviruses and the 2b gene of the cucumber mosaic virus have been shown to interfere with

63 Previous work using Tobacco mosaic virus and Cucumber mosaic virus indicated that evolutionarily rela

64 Symptom enhancement by the satRNA of Cucumber mosaic virus is caused by minus-strand inductio

65 Replication of the satellite RNA (satRNA) of Cucumber Mosaic Virus is dependent on replicase proteins

66 f equine IL-5 (eIL-5) covalently linked to a cucumber mosaic virus-like particle (VLP) containing a u

67 A cucumber mosaic virus-like particle expressing peanut al

68 ic plus-strand initiation was specific since cucumber mosaic virus minus-strand RNA templates were un

69 Here, KN1 and the cucumber mosaic virus movement protein (CMV-MP) were use

70 nts showed enhanced susceptibility to either cucumber mosaic virus or oilseed rape mosaic virus based

71 Tobamovirus, but not Cucumber mosaic virus or Potato virus X, infection of N.

72 One of these proteins, the 2b protein of cucumber mosaic virus, prevents systemic spread of the s

73 in Arabidopsis induced by expression of the Cucumber mosaic virus silencing suppressor protein 2b kn

74 nt of satellite RNA (satRNA) associated with Cucumber mosaic virus strain Q (Q-satRNA) has a propensi

75 ber viroid (PSTVd), a satRNA associated with Cucumber Mosaic Virus strain Q (Q-satRNA) has the propen

76 ript profile for RCY1-mediated resistance to cucumber mosaic virus strain Y (CMV-Y) in Arabidopsis.

77 exhibited enhanced disease susceptibility to cucumber mosaic virus when the virus-encoded function to