ライフサイエンスコーパス: long-distance movement

1 n productivity, recruitment, and patterns of long-distance movement.

2 al CP functions in host- and strain-specific long-distance movement.

3 eraction in plants, nucleolar targeting, and long-distance movement.

4 ieve elements in particular, to restrict TEV long-distance movement.

5 s TEV replication, cell-to-cell movement, or long-distance movement.

6 cell to cell slowly but were debilitated in long-distance movement.

7 ndirectly with host components to facilitate long-distance movement.

8 ons independently of the complete protein in long-distance movement.

9 systemic infection by vasculature-dependent long-distance movement.

10 short saltatory movements and unidirectional long-distance movements along the microtubule network.

11 This vector is deficient in long-distance movement and is limited to locally inocula

12 mal features, such as the ability to undergo long-distance movement and propensity to accumulate in t

13 cleoprotein (RNP) particles capable of virus long-distance movement and systemic infection.

14 CONCLUSIONS/SIGNIFICANCE: Long-distance movements and disjunct spatial use of adul

15 enome amplification, polyprotein processing, long-distance movement, and suppression of posttranscrip

16 led virus we show that both cell-to-cell and long-distance movement are unusually limited, and the de

17 mosquitoes, likely reflecting their limited long-distance movement compared to avian species.

18 ain had no effect on systemic infection by a long-distance movement-competent chimeric strain, sugges

19 Our work further suggests that barriers to long-distance movement could increase pathogen prevalenc

20 t mutants, several possessed cell-to-cell or long-distance movement defects in tobacco plants.

21 teins that are known to be essential for TEV long-distance movement, failed to infect V20 systemicall

22 In contrast, long-distance movement from leaf to leaf was markedly re

23 protein is multifunctional, with a distinct long-distance movement function in addition to its role

24 possibly altered CP, sat-RNA C reduces virus long-distance movement in a manner that is independent o

25 f RNA silencing-based antiviral defense, and long-distance movement in infected plants.

26 the virus appears to function with only the long-distance movement mechanism, yet is able to survive

27 glycans in the ECM facilitate the remarkable long distance movement of Nodal.

28 To study the role of the coat protein in long-distance movement of AlMV independent of other vita

29 that plant viral MPs cause cell-to-cell and long-distance movement of an animal virus in plants and

30 r results show that rather than enabling the long-distance movement of Fe in the phloem (as is the ca

31 osaic virus (ZYMV) were used to test whether long-distance movement of FLOWERING LOCUS T (FT) mRNA or

32 dence suggesting the existence of short- and long-distance movement of GAs in plants(3-8), the nature

33 try is a decisive step for the initiation of long-distance movement of infectious and endogenous RNAs

34 ve previously been detected in phloem cells, long-distance movement of its mRNA was tested.

35 orticulture and used in science to study the long-distance movement of molecules.

36 mutation in tomato were used to demonstrate long-distance movement of mutant messenger RNA (mRNA) in

37 Long-distance movement of RNA through the phloem is know

38 tionally, we provide direct evidence for the long-distance movement of ShhN across the anteroposterio

39 These results illustrate that efficient long-distance movement of TCV requires both functions af

40 The genetic basis for the restriction of long-distance movement of TEV-GUS in Columbia was invest

41 ion, several strategies for cell-to-cell and long-distance movement of the infectious viral DNA were

42 s have a system to specifically restrict the long-distance movement of tobacco etch potyvirus (TEV) w

43 to exhibit a strain-specific restriction of long-distance movement of tobacco etch potyvirus (TEV).

44 Restriction of long-distance movement of tobacco etch virus (TEV) in Ar

45 e locus RTM1 is necessary for restriction of long-distance movement of tobacco etch virus in Arabidop

46 CPs of other viruses, such as protection and long-distance movement of viral RNA.

47 It is thought that this signal can influence long-distance movement of viruses because protein suppre

48 ovided important details on cell-to-cell and long-distance movement of viruses in plants.

49 Long-distance movements of animals are an important driv

50 We show how the study of individual long-distance movements of insects may contribute to a b

51 igher energetic requirements associated with long-distance movements or consumption of more contamina

52 These data support the hypothesis that long-distance movement requires a set of host functions

53 -to-cell movement between adjacent cells and long-distance movement that allows the virus to rapidly

54 proposed that RTM1 mediates a restriction of long-distance movement through a mechanism that differs

55 sieve elements, suggesting that the block in long-distance movement was associated with entry into, o

56 tantially decreased further, indicating that long-distance movement was reduced in those hosts.

57 me amplification, cell-to-cell movement, and long-distance movement were measured in V20 and a suscep