ライフサイエンスコーパス: pit membrane

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1 ing details of the pores in the margo of the pit membrane.

2 of the pits in the case of margo-torus type pit membrane.

3 unique torus-margo structure of the conifer pit membrane.

4 hrough the pores present in the margo of the pit membrane.

5 e connected to one another via intertracheid pit membranes.

6 y digested regions in the cell wall known as pit membranes.

7 tracheid-bearing plants with more permeable pit membranes.

8 ypical angiosperm conduit with a homogeneous pit membrane and a typical gymnosperm conduit with a tor

9 tional, a result of air entering through the pit membrane and nucleating cavitation in the water colu

10 and central projections of fibers within the pit membrane and the LTTD became visible.

11 electron microscopy in pores of intervessel pit membranes and deposited on vessel wall surfaces.

12 cles may contribute to the disruption of the pit membranes and facilitate systemic virus transport.

13 d pits, suggesting that microchannels in the pit membranes are altered by the swelling and deswelling

14 that electrokinetic effects in the bordered pit membrane (BPM) contribute to this response.

15 For conduits with torus-margo type pits pit membrane deflection was also modeled and pit aspirat

16 ening of the cellulosic mesh of interconduit pit membranes during the water stress and cavitation tre

17 ion and always for conduits with homogeneous pit membranes, embolism growth is more rapid but still m

18 Pit membranes have been well studied in woody plants, bu

19 s pressures (3.8 MPa) compared with bordered pit membranes in vessels located in older annular rings

20 ch revealed a morphological partition of the pit membrane into three well-defined sensory areas with

21 ead and confirm that air seeding through the pit membranes is the principle mechanism of embolism spr

22 pits, particularly through the pores in the pit membrane, is not well understood, but is critical fo

23 ressure required to push gas across bordered pit membranes of current year xylem did not vary with di

24 V in xylem involves chelation of Ca(2+) from pit membranes of infected cells, thereby stabilizing the

25 We found that the bordered pit membranes of vessels located in current year xylem c

26 The pit membrane (PM) is a primary cell wall barrier that se

27 ding enzymes (CWDEs) to break up intervessel pit membranes (PMs) and spread through the vessel system

28 low values when concentrated as they are in pit membrane pores.

29 es on how air-seeding occurs at the level of pit membranes, raising the question of whether capillary

30 We propose that the partial digestion of pit membranes resulting from programmed cell death may p

31 essure required to force air across bordered pit membranes separating individual xylem vessels.

32 are coupled with additional data concerning pit membrane structure and function and are discussed in

33 ypical gymnosperm conduit with a torus-margo pit membrane structure.

34 nd EGFR is incorporated into clathrin-coated pits--membrane structures containing clathrin and other

35 glucans and anti-RYMV antibodies over vessel pit membranes suggests a pathway for virus migration bet

36 and pit aspiration, the displacement of the pit membrane to the low pressure side of the pit chamber

37 In addition, displacement of the Ca2+ from pit membranes to virus particles may contribute to the d

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