ライフサイエンスコーパス: cambium

1 nd cell-type specification in the procambium/cambium.

2 having wood produced by a bifacial vascular cambium.

3 ing of the vascular tissues derived from the cambium.

4 ore becoming progressively restricted to the cambium.

5 primary meristems are also regulators of the cambium.

6 position of the fasicular and interfasicular cambium.

7 overlapping distribution profiles across the cambium.

8 indeterminacy is maintained in the vascular cambium, a tissue critical to the continuous growth of v

9 Vascular cambium, a wide lateral meristem with an extensive devel

10 a fundamental role in the initiation of the cambium and in regulating the patterning of secondary va

11 nt upon the rate of cell division within the cambium and is controlled by both genetic and environmen

12 pression analysis of PTM5 in staged vascular cambium and other tissues indicated that PTM5 expression

13 In plants, the cambium and procambium are meristems from which vascular

14 divisions in vascular meristems known as the cambium and procambium.

15 nds on the division of cells in the vascular cambium and results in an increase in the diameter of th

16 the skin, the root endodermis, the vascular cambium and the epidermis of the stem.

17 ing between the distribution of auxin in the cambium and the orientation of fusiform initials.

18 e known to be involved in the development of cambium and wood, but how the expression and functional

19 hin a few layers of differentiating vascular cambium and xylem tissues as well as the vascular bundle

20 nt parallel to the flux of auxin through the cambium, and (4) adjacent initials tend to orient parall

21 , in young expanding leaves, in the vascular cambium, and in the phloem, including sieve-element/comp

22 shoot apical meristem (SAM) and the vascular cambium, and is down-regulated in the terminally differe

23 data spanning the secondary phloem, vascular cambium, and wood-forming tissues of Populus tremula The

24 ort the hypothesis that the SAM and vascular cambium are regulated by overlapping genetic programs.

25 ) IAA is transported basipetally through the cambium at a constant speed.

26 dy stem requires the formation of a vascular cambium at an appropriate position and proper patterning

27 pregulated early in the season when the cork cambium becomes active.

28 ction experiments with nine xylem- or phloem-cambium-biased genes.

29 p12 transcripts are present in root and stem cambium, but not in leaves of CB-affected trees, suggest

30 ath is initiated from the infected phloem or cambium cells and spreads to other nearby infected cells

31 r tissues of the leaves and stems, including cambium, differentiating xylem, young xylem fibers and p

32 tem is a primary signal for the induction of cambium differentiation and the plant hormone, auxin, is

33 The stem cells of the vascular cambium divide to produce daughter cells, which in turn

34 ween ARK2 expression level and the timing of cambium formation, the width of the cambial zone and inh

35 An analysis of the members of the phloem-cambium gene set suggested that some genes involved in r

36 ood formation, while transport away from the cambium in the bottom of the stem triggers opposite wood

37 ambium results in auxin transport toward the cambium in the top of the stem, triggering tension wood

38 ization of the xylem, phloem, and procambium/cambium is tightly controlled.

39 ain features of the model are (1) the branch cambium is treated as an approximately cylindrical surfa

40 ide expression profiling of xylem and phloem-cambium isolated from the root-hypocotyl of Arabidopsis

41 content of periosteum 5-fold, with the basal cambium layer exhibiting the greatest enhancement ( appr

42 s most dramatic effect occurred in the basal cambium layer.

43 e in the control tissue sections, nearly all cambium-lining osteoblasts stained intensely positive fo

44 RKNOX1 (ARK1) is a key regulator of vascular cambium maintenance and cell differentiation in Populus.

45 mbination of an entry tunnel through bark, a cambium mother gallery, and up to 11 eggs placed in late

46 phloem-cambium, xylem/nonvascular, or phloem-cambium/nonvascular tissues.

47 ence for topological defects in the vascular cambium of this species.

48 ols the orientation of cells in the vascular cambium of trees, and hence the direction of wood grain,

49 nt of fusiform initial cells in the vascular cambium of trees.

50 air volume sampled by the inner wood layer (cambium) of a tree during a one year growth (sampling) p

51 ially expressed in flowers, roots, xylem and cambium or up-regulated by stress.

52 on significantly biased toward xylem, phloem-cambium, or nonvascular tissue.

53 eporter gene showed activity in the vascular cambium, phloem, and primary xylem in the stem and hypoc

54 ion was preferentially localized in the (pro)cambium region of inflorescence stem and root.

55 ion of PIN3-expressing cells relative to the cambium results in auxin transport toward the cambium in

56 s of IAA synthesis and metabolization in the cambium, so the model is not quantitatively accurate.

57 Members of the WUS clade, except the cambium stem cell regulator WOX4, can substitute for WUS

58 ell proliferation and differentiation of the cambium that acts as vascular stem cells, producing xyle

59 ping vascular tissues including the vascular cambium, the precursor to all woody branches, stems, and

60 and thereafter undergo elimination from the cambium through a process of annihilation.

61 eedlings and mature plants in the fascicular cambium tissue present in roots, stem and leaf petiole.

62 at MADS-box genes were expressed in wood and cambium tissues, which are specific to woody plants.

63 meristematic activities within the vascular cambium (VC) and phloem parenchyma (PP) cells in the reg

64 A cDNA library from CB-affected root cambium was screened with a 60 bp fragment, obtained by

65 genes that promote meristem identity in the cambium were downregulated, while an Altered Phloem Deve

66 gradients were observed in the region of the cambium where cell polarity was changing.

67 on of meristematic cells within the vascular cambium whose daughter cells are recruited to differenti

68 rge multi-instar larval tunnels that consume cambium, wood and bark-is ecologically convergent with E

69 ion significantly biased toward xylem/phloem-cambium, xylem/nonvascular, or phloem-cambium/nonvascula