ライフサイエンスコーパス: source-sink

1 ecting a complex interplay between pollution sources, sinks and residence times of different polymers

2 nts, both in relation to picoplankton carbon sources, sinks and transfer to higher trophic levels.

3 time resolution, giving new insight into N2O sources, sinks, and chemistry.

4 nts (POPs) has the potential to characterize sources, sinks, and degradation processes in the environ

5 e observations demonstrate (i) that sediment sources, sinks, and fluxes vary widely over time and spa

6 atmosphere improve our understanding of the sources, sinks, and transport of interplanetary dust thr

7 r injection, P<0.05), which further supports source-sink balance as a critical mediator of Ca(2+)-ind

8 t heart and highlight the critical nature of source-sink balance in initiating focal arrhythmias.

9 Therefore, the source/sink behavior of temperate forest soils likely de

10 nutrient budgets to investigate how the net source/sink behavior of wastewater and irrigated agricul

11 MUA phase-locked to local current source/sink configurations confirmed that alpha rhythms

12 ween the determinacy of apical meristems and source-sink cross-talk.

13 We introduce a source-sink diffusion model for polarization transfer wh

14 Source-sink dynamics and spillover processes may link ad

15 t small intensity of dispersals can generate source-sink dynamics between two patches, while intermed

16 Dispersal, however, induced source-sink dynamics in the presence of specialist preda

17 Understanding source-sink dynamics is important for conservation manag

18 s largely on wintering areas; thus, study of source-sink dynamics of discrete regular wintering units

19 or reproductive seasons differ, the dominant source-sink dynamics of these two congeneric species are

20 When source-sink dynamics were considered, the long-term outc

21 r, currently unoccupied areas, understanding source-sink dynamics, and understanding community dynami

22 ion rates across the region, consistent with source-sink dynamics, whereby more recently colonized sa

23 agmented populations are commonly studied as source-sink dynamics, whereby source populations exhibit

24 tial explanations for these patterns include source-sink dynamics, with asymmetrical gene flow mediat

25 ored the potential impacts of disturbance on source-sink dynamics.

26 virulence in bacterial pathogens subject to source-sink dynamics.

27 on with delta(18)O and delta(15)N, to assess source/sink dynamics of groundwater nitrate beneath allu

28 nuous survival of these organisms in nature, source-sink evolutionary dynamics, or, possibly, a limit

29 eciate is that these effects of dispersal on source-sink extinction arise from the temporal density-d

30 ts to sources is the highest and the risk of source-sink extinction the greatest.

31 l costs to sources is the lowest and risk of source-sink extinction the least.

32 w these subcellular/cellular events overcome source-sink factors in cardiac tissue to generate DADs o

33 mplex I, linking NAD(P)H <--> NAD(P)(+) as a source/sink for electrons.

34 ; these relationships appeared to arise from source-sink imbalances, suggesting potential substrate r

35 n strigolactone production, shoot branching, source-sink interactions and production of arbuscular my

36 of achieving a spatiotemporal resolution of source-sink interactions in crop plant metabolism, a mul

37 cardial Purkinje fibers, which suggests that source-sink interactions may contribute to the greater p

38 s for the regulation of phloem transport and source-sink interactions.

39 ling models and provide support for a graded source-sink mechanism underlying zebrafish dorsal-ventra

40 nism, our analyses support a fourth model, a source-sink mechanism, which relies on a restricted BMP

41 larizations are synchronized to overcome the source-sink mismatch and produce focal arrhythmia in the

42 arose at intermediate pacing rates due to a source-sink mismatch behind the barrier.

43 critically dependent on the presence of the source-sink mismatch imposed by the isthmus.

44 In conclusion, the source-sink mismatch in well-coupled cardiac tissue powe

45 to overcome the robust protective effects of source-sink mismatch.

46 depolarizations (DADs) overcome electrotonic source-sink mismatches in tissue to trigger premature ve

47 Such pattern of dynamics is consistent with source-sink model of virulence evolution.

48 mp2 diffusion and found that it supports the source-sink model, suggesting a new mechanism to shape B

49 ry dynamics is reminiscent of an ecological "source-sink" model of continuous species spread from a s

50 ganic matter, a sink of NO3(-), and variable source/sink of ammonium.

51 hese results suggest that phloem loading and source-sink partitioning of SMM are important for plant

52 edge weighting function so that the shortest source-sink path maximizes exon-level prediction accurac

53 erate a directed acyclic graph in which each source-sink path represents a possible gene structure.

54 abolic and proteomic profiles both along the source-sink pathway and between the STSs of these three

55 imited by the removal of sap, alterations in source-sink patterns, and viral diseases vectored by aph

56 I show that source-sink persistence depends critically on the interp

57 spersal per se does not increase or decrease source-sink persistence relative to density-independent

58 from a four-population n-island model and a source-sink population model.

59 mparison with silique data provides clues to source-sink relations.

60 dian oscillation, CAM-related functions, and source-sink relations.

61 sectors revealed alterations suggestive of a source-sink relationship between the green and white sec

62 e, we investigate the above- and belowground source-sink relationship of the defense compounds glucos

63 fected nonvascular mesophyll tissue when the source-sink relationship of the plant (Solanum sarrachoi

64 e that this behavior reflects alterations in source-sink relationships and paradoxical conduction acr

65 in chlorophyll levels, suggestive of altered source-sink relationships between vegetative shoot and r

66 uable insights into amino acid transport and source-sink relationships during seed development, and r

67 cluding those involved in energy metabolism, source-sink relationships, secondary metabolite producti

68 regulation, suggesting that FT1 might alter source-sink relationships.

69 starch synthesis, and attempts to manipulate source-sink relationships.

70 nt data are essential to correctly ascribing source-sink status and accurately informing development

71 es were used to investigate the influence of source-sink status on protein levels, as well as to anal

72 Source-sink structure was evident via asymmetry in migra

73 roundwater, indicating the complex nature of source-sink terms and the need for care when comparing r

74 I investigate two aspects of source-sink theory that have hitherto received little at

75 s allowed pQBR57 to persist in P. putida via source-sink transfer dynamics.

76 d we analyzed whether SMM phloem loading and source-sink translocation are important for the metaboli

77 AAP2 T-DNA insertion lines showed changes in source-sink translocation of amino acids and a decrease

78 ion can positively affect C assimilation and source-sink transport and benefit sink development and o