ライフサイエンスコーパス: cell-to-cell movement

1 as being necessary and sufficient for SRBP1 cell-to-cell movement.

2 lular mechanisms that take place during CLas cell-to-cell movement.

3 ta size-exclusion limits and promoting virus cell-to-cell movement.

4 y microtubules to promote the range of miRNA cell-to-cell movement.

5 these sites to alter plasmodesmata for virus cell-to-cell movement.

6 odes proteins needed for virion assembly and cell-to-cell movement.

7 a salt bridge, abolished virion assembly and cell-to-cell movement.

8 chanistic link between nuclear transport and cell-to-cell movement.

9 ion spanning these residues was required for cell-to-cell movement.

10 gly suggest that IH co-opt plasmodesmata for cell-to-cell movement.

11 uppression were also non-functional in viral cell-to-cell movement.

12 dependent of silencing but also required for cell-to-cell movement.

13 ship between calreticulin, TMV MP, and viral cell-to-cell movement.

14 ed 3aDeltaC33 MP) resulted in CP-independent cell-to-cell movement.

15 virion tail as a specialized device for BYV cell-to-cell movement.

16 the size of the viral genome at the level of cell-to-cell movement.

17 encoded by RNAbeta but is not essential for cell-to-cell movement.

18 s a tail represents a specialized device for cell-to-cell movement.

19 virus RNA amplification, virus invasion, and cell-to-cell movement.

20 B3), and betad (TGB2), are each required for cell-to-cell movement.

21 nding region resulted in inactivation of TMV cell-to-cell movement.

22 expression, or enhanced virion stability and cell-to-cell movement.

23 leoprotein complexes to facilitate potyvirus cell-to-cell movement.

24 ons that are distinct from those involved in cell-to-cell movement.

25 lones that showed further increased rates of cell-to-cell movement and degrees of systemic invasion i

26 virus (BYV) functions in virion assembly and cell-to-cell movement and is autonomously targeted to pl

27 of MP(TVCV) was necessary for efficient TVCV cell-to-cell movement and systemic infection in Nicotian

28 Cell-to-cell movement and systemic RNA levels were great

29 in a coordinated manner to facilitate virus cell-to-cell movement and that one of these (BR1) is a n

30 omain required for TGB1 self-interaction and cell-to-cell movement and the amino-terminal domain requ

31 a-glucuronidase (GUS), genome amplification, cell-to-cell movement, and long-distance movement were m

32 on of CP-mediated vesicle induction to virus cell-to-cell movement are discussed.

33 viruses is thought to involve two processes: cell-to-cell movement between adjacent cells and long-di

34 f the wild-type TGB3 protein interfered with cell-to-cell movement but movement was not affected by t

35 from TGB2 and TGB3 could function in limited cell-to-cell movement but that the rates of movement dep

36 ficking of the 126-bodies and VRCs and virus cell-to-cell movement, but did not decrease virus accumu

37 ains are capable of genome amplification and cell-to-cell movement, but only TEV-Oxnard is capable of

38 -amino acid peptide was sufficient to impart cell-to-cell movement capacity to GST, a normally cell-a

39 ody and VRC intracellular movement and virus cell-to-cell movement correlates with the disruption of

40 he C terminus of CP functions as a dedicated cell-to-cell movement determinant.

41 component of the viroid infection process is cell-to-cell movement; however, there is virtually no in

42 at while TGB1 self-interaction is needed for cell-to-cell movement, importin-alpha-mediated nucleolar

43 were able to support genome replication and cell-to-cell movement in inoculated leaves.

44 that each of these proteins is required for cell-to-cell movement in monocot and dicot hosts.

45 llular mechanisms of Gram-negative bacterial cell-to-cell movement in plant phloem.

46 Cs, translocation to the rice cytoplasm, and cell-to-cell movement in rice.

47 due to suppression of virus replication and cell-to-cell movement in the inoculated leaves of these

48 single cells, suggesting that essentially no cell-to-cell movement occurred in the latter host.

49 We show that cell-to-cell movement of a KN1 mRNA requires ribosomal R

50 his work, we analyze the virion assembly and cell-to-cell movement of a plant closterovirus and revea

51 The rates of cell-to-cell movement of a reporter-tagged TEV strain (T

52 nses to light cues are processed to regulate cell-to-cell movement of auxin to allow establishment of

53 e inhibitory effect of RFA expression on the cell-to-cell movement of Bean dwarf mosaic virus, a sing

54 Cell-to-cell movement of beet yellows closterovirus requ

55 tion, CMV failed to complement the defective cell-to-cell movement of BMV.

56 ate that p20 is dispensable for assembly and cell-to-cell movement of BYV but is required for the lon

57 propose that the 35S RNA may be involved in cell-to-cell movement of CaMV as an intermediate that is

58 lts imply a role for P6 in intracellular and cell-to-cell movement of CaMV.

59 ification on these residues is essential for cell-to-cell movement of Cm-PP16-1.

60 Cell-to-cell movement of different-sized GFP reporters r

61 Biosynthesis of bioactive BRs relies on the cell-to-cell movement of hormone precursors.

62 utant CP interferes with MP accumulation and cell-to-cell movement of infection.

63 , and MAP kinase signalling is important for cell-to-cell movement of invasive hyphae in M. oryzae.

64 e found that the replication of TuMV and the cell-to-cell movement of its replication vesicles are im

65 s, the TMV-MP was still capable of mediating cell-to-cell movement of itself and the 9.4-kDa F-dextra

66 Cell-to-cell movement of L. monocytogenes is achieved by

67 kinase regulates PWL2 expression during the cell-to-cell movement of M. oryzae at plasmodesmata-cont

68 Demonstrating cell-to-cell movement of mitochondria reconstructs the e

69 We report cell-to-cell movement of mitochondria through a graft ju

70 Plant viral movement proteins mediate the cell-to-cell movement of nucleic acids.

71 Our data show that cell-to-cell movement of plant rhabdoviruses is highly s

72 sor and for the subcellular localization and cell-to-cell movement of plant viral movement protein.

73 The cell-to-cell movement of plant viruses involves transloc

74 vel, PSTVd cDNA also appears able to mediate cell-to-cell movement of plasmid DNA.

75 e are routinely determined by monitoring the cell-to-cell movement of protein tracers of different si

76 We previously proposed that the cell-to-cell movement of RYMV in xylem involves chelatio

77 PDLP5, which functions to restrict the cell-to-cell movement of signals via plasmodesmata, is i

78 The cell-to-cell movement of the Beet yellows virus (BYV) is

79 Here, we present evidence for cell-to-cell movement of the entire 161-kb plastid genom

80 ) along with unlabeled CMV 3a MP resulted in cell-to-cell movement of the F-dextran in control plants

81 Directed cell-to-cell movement of the plant growth hormone auxin

82 Cx43 but not Cx32/Cx26 channels allowed the cell-to-cell movement of the siRNA.

83 t the endoplasmic reticulum as a conduit for cell-to-cell movement of the viral genome.

84 o reach plasmodesmata substantially impaired cell-to-cell movement of the virus.

85 trol stem cell maintenance in plants through cell-to-cell movement of their proteins and mRNAs throug

86 ular proteins known to be involved in local, cell-to-cell movement of tobacco mosaic virus (TMV), is

87 ed by five distinct rhabdoviruses to support cell-to-cell movement of two positive-stranded RNA virus

88 In marked contrast, cell-to-cell movement of two recombinant plant rhabdovir

89 is potentially involved in the regulation of cell-to-cell movement of viral infectious material durin

90 The rates of cell-to-cell movement of virus in inoculated leaves were

91 ts that enhance or suppress TEV replication, cell-to-cell movement, or long-distance movement.

92 ically is not due to defects in replication, cell-to-cell movement, or virion assembly.

93 randed DNA (dsDNA) pararetrovirus capable of cell-to-cell movement presumably through intercellular c

94 This tagged virus was competent in cell-to-cell movement, producing multicellular infection

95 Tomato bushy stunt virus and its cell-to-cell movement protein (MP; P22) provide valuable

96 The structure of p22, the cell-to-cell movement protein from the 30K family widesp

97 , and cooperative interaction with the viral cell-to-cell movement protein MP.

98 e barrier of the plant cell wall by encoding cell-to-cell movement proteins (MPs), which direct newly

99 irus (CaLCuV) and Tobacco mosaic virus (TMV) cell-to-cell movement proteins.

100 Examination of the role of L-Pro in BYV cell-to-cell movement revealed that none of the 20 exami

101 ble for virion assembly but are required for cell-to-cell movement, suggesting that the C terminus of

102 genomes inside cells and spread infection by cell-to-cell movement through cell wall nanochannels cal

103 nucleus for export to the cell periphery and cell-to-cell movement through plasmodesmata.

104 pex symplastically via the phloem and/or via cell-to-cell movement through plasmodesmata.

105 Thus cell-to-cell movement throughout the epithelium of cytos

106 nal cell is requisite for TSWV infection and cell-to-cell movement; thus, this behavior is most likel

107 e required for efficient virion assembly and cell-to-cell movement, while the C-terminal 65 amino aci