ライフサイエンスコーパス: pith

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1 HB15 represses secondary wall development in pith.

2 on of the lignin biosynthetic pathway in the pith.

3 ls) and neurophysiology (he was the first to pith a frog).

4 is accumulated only within the cells of the pith and peridermis layers (peel) of the tuber as it dev

5 e expression occurring in epidermal, cortex, pith and xylem tissue.

6 formed first in the vessels surrounding the pith at stem water potentials of approximately -1.2 mega

7 ympathetically denervated by thoracic spinal pithing, cardiac chronotropic vagal tone was quantified

8 egulated in a thick wall variant with narrow pith cavity, mildly spiral growth, and flat and enlarged

9 plausible mechanism resulting in the narrow pith cavity, weak spiral growth but increased vascular b

10 stp-2d showing secondary wall thickening in pith cells (STP).

11 liana with secondary cell wall thickening in pith cells associated with ectopic deposition of lignin,

12 onsible for the parenchymatous nature of the pith cells in dicotyledonous plants.

13 accumulation of secondary cell walls in the pith cells of the stp-2d mutant.

14 characterize the refilling of xylem fibers, pith cells, and vessels under both excised and in vivo c

15 In contrast, refilling of fibers, pith cells, and vessels was negligible in intact sapling

16 ry forces: fibers refilled more rapidly than pith cells, while vessel refilling was minimal.

17 ry for retaining primary walls in parenchyma pith cells.

18 f caffeoyl coenzyme A O-methyltransferase in pith cells.

19 ural porous materials such as bone, wood and pith evolved to maximize modulus for a given density.

20 n single perfused mesenteric microvessels in pithed frogs (Rana pipiens).

21 measured in single mesenteric capillaries of pithed frogs and anaesthetised rats as perfusion velocit

22 single mesenteric capillaries and venules of pithed frogs to determine whether the rate of increase i

23 n single perfused mesenteric microvessels of pithed frogs, we assessed wall strength from the critica

24 f single perfused mesenteric microvessels in pithed frogs.

25 f single perfused mesenteric microvessels in pithed frogs.

26 nd permeability of mesenteric capillaries in pithed frogs.

27 position were determined in rind (outer) and pith (inner) tissues throughout stem development.

28 kly or unpigmented tissues such as the curd, pith, leaf bases and shoot meristems, and cryptically in

29 llelic elp1 (ectopic deposition of lignin in pith) mutants with altered lignin deposition patterns.

30 osited in patches of parenchyma cells in the pith of both young and mature elp1 stems.

31 The ectopic deposition of lignin in the pith of elp1 stems was accompanied by an increase in the

32 s of cells with incomplete cell walls in the pith of inflorescence stems.

33 asal vascular bundles were identified in the pith of pedicels supporting the fruitlets with the lowes

34 ve regulators of secondary wall formation in pith opens up the possibility of significantly increasin

35 in was ectopically deposited in the walls of pith parenchyma cells in addition to its normal depositi

36 In forsythia and alfalfa, pith parenchyma cells next to the vascular cylinder were

37 bundles and interfascicular cells, and inner pith parenchyma cells with thin primary walls.

38 eaction, including sites around cells of the pith parenchyma, between the vascular elements, and with

39 at the growth displayed a spiral pattern and pith played an important role in promoting the primary t

40 hoxycurcumin are chiefly concentrated in the pith rather than the other parts of the turmeric rhizome

41 ge capacitance was associated with fiber and pith refilling as driven by capillary forces: fibers ref

42 In excised stems that were sealed, fiber and pith refilling was associated with vessel emptying, indi

43 he avb1 stems abnormally penetrated into the pith, which resulted in a disruption in the ring-like ar

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