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1 Expression of PttCLE47 peaks in the vascular cambium.
2  and xylem (inside) on opposing sides of the cambium.
3 ) as a YAP-TEAD target gene expressed in the cambium.
4 ly promotes the formation of new phloem, not cambium.
5 ates from cell proliferation of the vascular cambium.
6 overlapping distribution profiles across the cambium.
7 nd cell-type specification in the procambium/cambium.
8  having wood produced by a bifacial vascular cambium.
9 ing of the vascular tissues derived from the cambium.
10 ore becoming progressively restricted to the cambium.
11 tion factors that may intimately control the cambium.
12 primary meristems are also regulators of the cambium.
13 position of the fasicular and interfasicular cambium.
14 um cells and activated later by the vascular cambium(1).
15  produced inside, and phloem outside, of the cambium(1).
16 he classical theory of a uniseriate vascular cambium(3).
17 lem, it arises from one side of the vascular cambium, a bifacial stem cell niche that also produces p
18  In plants, radial growth is mediated by the cambium, a stem cell niche continuously producing wood (
19  indeterminacy is maintained in the vascular cambium, a tissue critical to the continuous growth of v
20                                     Vascular cambium, a wide lateral meristem with an extensive devel
21 a cell-based computational model visualizing cambium activity and integrating the function of central
22 one ethylene has been implicated in vascular cambium activity, but the regulatory network underlying
23 rentiation, including regulation of vascular cambium activity, xylogenesis and its responsiveness tow
24 at ethylene promotes an auxin maximum in the cambium adjacent to the xylem to maintain cambial activi
25  a fundamental role in the initiation of the cambium and in regulating the patterning of secondary va
26 nt upon the rate of cell division within the cambium and is controlled by both genetic and environmen
27 pression analysis of PTM5 in staged vascular cambium and other tissues indicated that PTM5 expression
28 teum is a bilayered tissue composed of inner cambium and outer fibrous layers.
29                               In plants, the cambium and procambium are meristems from which vascular
30 divisions in vascular meristems known as the cambium and procambium.
31 nds on the division of cells in the vascular cambium and results in an increase in the diameter of th
32 le of intercellular communication within the cambium and shows that a limited number of factors are s
33  the skin, the root endodermis, the vascular cambium and the epidermis of the stem.
34 ing between the distribution of auxin in the cambium and the orientation of fusiform initials.
35 ession in the dividing cells of the vascular cambium and the upregulation of MP-like gene expression
36 e known to be involved in the development of cambium and wood, but how the expression and functional
37 hin a few layers of differentiating vascular cambium and xylem tissues as well as the vascular bundle
38 nt parallel to the flux of auxin through the cambium, and (4) adjacent initials tend to orient parall
39 , in young expanding leaves, in the vascular cambium, and in the phloem, including sieve-element/comp
40 shoot apical meristem (SAM) and the vascular cambium, and is down-regulated in the terminally differe
41 tematic tissue called the phellogen, or cork cambium, and its derivatives: the lignosuberized phellem
42 data spanning the secondary phloem, vascular cambium, and wood-forming tissues of Populus tremula The
43 whether the organizer concept applies to the cambium are currently unknown(2).
44 ort the hypothesis that the SAM and vascular cambium are regulated by overlapping genetic programs.
45 ) IAA is transported basipetally through the cambium at a constant speed.
46 dy stem requires the formation of a vascular cambium at an appropriate position and proper patterning
47 em formation during longitudinal growth, the cambium-based formation of secondary phloem depends on t
48                                              Cambium became active when it achieves the desired accum
49 pregulated early in the season when the cork cambium becomes active.
50 ction experiments with nine xylem- or phloem-cambium-biased genes.
51 p12 transcripts are present in root and stem cambium, but not in leaves of CB-affected trees, suggest
52  TDIF-PXY downstream WOX gene that regulates cambium cell proliferation.
53  characterized by a significant reduction in cambium cells and a complete absence of secondary growth
54 ath is initiated from the infected phloem or cambium cells and spreads to other nearby infected cells
55 rier called the periderm, while the vascular cambium contributes with phloem tissues.
56 inst the newly established Arabidopsis early cambium data revealed evolutionary conserved stress-resp
57 t increased the width of the interfascicular cambium-derived (ICD) region.
58 smxl5 double mutants and that the additional cambium-derived cells fail to establish phloem-related f
59 r tissues of the leaves and stems, including cambium, differentiating xylem, young xylem fibers and p
60 tem is a primary signal for the induction of cambium differentiation and the plant hormone, auxin, is
61               The stem cells of the vascular cambium divide to produce daughter cells, which in turn
62 kpoint of cambial activities, explaining how cambium-driven growth is altered in response to environm
63 op is one of the outstanding examples of the cambium-driven growth.
64 about dynamic gene expression changes during cambium-driven root growth and have implications with re
65                                              Cambium drives the lateral growth of stems and roots, co
66 tributes large parts to terrestrial biomass, cambium dynamics eludes direct experimental access due t
67 EM (PXY) receptors promote the expression of CAMBIUM-EXPRESSED AINTEGUMENTA-LIKE (CAIL) transcription
68 ween ARK2 expression level and the timing of cambium formation, the width of the cambial zone and inh
69 f auxin gradients, which is required for the cambium formation.
70     An analysis of the members of the phloem-cambium gene set suggested that some genes involved in r
71                            Although vascular cambium has a unique function among plant meristems, the
72 sterix-expressing cells, which reside in the cambium, impairs periosteal expansion.
73 meristem, root apical meristem, and vascular cambium in plants.
74 ood formation, while transport away from the cambium in the bottom of the stem triggers opposite wood
75 ambium results in auxin transport toward the cambium in the top of the stem, triggering tension wood
76                                 The vascular cambium is the main secondary meristem in plants that pr
77 e many staple crops, the absence of vascular cambium is thought to preclude grafting(2).
78 ization of the xylem, phloem, and procambium/cambium is tightly controlled.
79 ain features of the model are (1) the branch cambium is treated as an approximately cylindrical surfa
80 ide expression profiling of xylem and phloem-cambium isolated from the root-hypocotyl of Arabidopsis
81 content of periosteum 5-fold, with the basal cambium layer exhibiting the greatest enhancement ( appr
82 s most dramatic effect occurred in the basal cambium layer.
83 trate that abnormal activity of the vascular cambium leads to variant secondary growth; however, the
84 e in the control tissue sections, nearly all cambium-lining osteoblasts stained intensely positive fo
85                      XVP is expressed in the cambium, localized on the plasma membrane and forms a co
86 RKNOX1 (ARK1) is a key regulator of vascular cambium maintenance and cell differentiation in Populus.
87                  We conclude that phloem and cambium mortality, and not hydraulic failure, were proba
88 mbination of an entry tunnel through bark, a cambium mother gallery, and up to 11 eggs placed in late
89 ally, all burned saplings showed 100% phloem/cambium necrosis, and roots of burned saplings had reduc
90 phloem-cambium, xylem/nonvascular, or phloem-cambium/nonvascular tissues.
91 ence for topological defects in the vascular cambium of this species.
92 ols the orientation of cells in the vascular cambium of trees, and hence the direction of wood grain,
93 nt of fusiform initial cells in the vascular cambium of trees.
94  air volume sampled by the inner wood layer (cambium) of a tree during a one year growth (sampling) p
95 ially expressed in flowers, roots, xylem and cambium or up-regulated by stress.
96 on significantly biased toward xylem, phloem-cambium, or nonvascular tissue.
97       The origin of periderm production by a cambium (phellogen), an innovation with key roles in pro
98 eporter gene showed activity in the vascular cambium, phloem, and primary xylem in the stem and hypoc
99             Secondary growth from a vascular cambium, present today only in seed plants and isoetalea
100 m two lateral meristems; the phellogen (cork cambium) produces the outermost stem-environment barrier
101       Our results indicate that RBE inhibits cambium proliferation and thereby impacts secondary grow
102 ncreased vascular bundle number and enhanced cambium proliferation in the stem.
103 ytokinin domains are required for phloem and cambium reconstruction.
104 cytokinin differentially regulate phloem and cambium regeneration.
105 ion was preferentially localized in the (pro)cambium region of inflorescence stem and root.
106 expression patterns in the primary xylem and cambium region of Jin668 and TM-1.
107  activity increases tissue production in the cambium region without secondary phloem being formed.
108  RBE gene is expressed in the procambium and cambium regions.
109                   Expression patterns of key cambium regulators and hormone signaling components were
110 k consisting of selected stress-response and cambium regulators indicated ERF-1 as a potential key ch
111 vity and integrating the function of central cambium regulators.
112 e regeneration of phloem prior to continuous cambium restoration, cytokinin only promotes the formati
113 ion of PIN3-expressing cells relative to the cambium results in auxin transport toward the cambium in
114 s of IAA synthesis and metabolization in the cambium, so the model is not quantitatively accurate.
115 -LIKE (CAIL) transcription factors to define cambium stem cell identity in the Arabidopsis root.
116 rently unknown which molecular factors endow cambium stem cell identity.
117         Members of the WUS clade, except the cambium stem cell regulator WOX4, can substitute for WUS
118 nsport through vessel elements, derived from cambium stem cells (CSCs).
119                 The location of the vascular cambium stem cells and whether the organizer concept app
120 ell proliferation and differentiation of the cambium that acts as vascular stem cells, producing xyle
121                                 The vascular cambium, the meristem from which xylem and phloem are de
122 ping vascular tissues including the vascular cambium, the precursor to all woody branches, stems, and
123  and thereafter undergo elimination from the cambium through a process of annihilation.
124 eedlings and mature plants in the fascicular cambium tissue present in roots, stem and leaf petiole.
125 at MADS-box genes were expressed in wood and cambium tissues, which are specific to woody plants.
126 ls suggest that phylloxera exploits vascular cambium to provide meristematic tissue and redirects lea
127 sts in internodes' chlorenchyma, phloem, and cambium underwent significant ultrastructural modificati
128  meristematic activities within the vascular cambium (VC) and phloem parenchyma (PP) cells in the reg
129         A cDNA library from CB-affected root cambium was screened with a 60 bp fragment, obtained by
130  genes that promote meristem identity in the cambium were downregulated, while an Altered Phloem Deve
131 gradients were observed in the region of the cambium where cell polarity was changing.
132 on of meristematic cells within the vascular cambium whose daughter cells are recruited to differenti
133 rge multi-instar larval tunnels that consume cambium, wood and bark-is ecologically convergent with E
134 s 26 clusters representing cell types in the cambium, xylem, phloem, and periderm.
135 ion significantly biased toward xylem/phloem-cambium, xylem/nonvascular, or phloem-cambium/nonvascula

 
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