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2 pment involved the amplification of existing meristematic activities within the vascular cambium (VC)
4 rs root architecture both by inhibiting root meristematic activity and by stimulating lateral root in
5 s of shby caused poor root growth, decreased meristematic activity and defects in radial patterning t
7 velopmental architecture, such as changes in meristematic activity between S. lycopersicum and S. pen
9 modeling factor PICKLE (PKL) act to restrict meristematic activity in Arabidopsis leaves without repr
12 ass III HD-Zip gene activity is required for meristematic activity in the pericycle analogous to its
13 E (MDF) gene lead to a loss of stem cell and meristematic activity in the root and vegetative shoot.
14 do wild-type root tips, suggesting that root meristematic activity is lower in transgenic than in wil
15 indicate that cytokinin signaling specifies meristematic activity through a graded distribution that
16 also inhibited primary root growth, loss of meristematic activity was observed specifically under Pi
17 nhibition of primary root growth and loss of meristematic activity were evident in seedlings grown un
18 onmental Pi status, maintains and fine-tunes meristematic activity, and finally adjusts root system a
19 ellin (GA) growth regulator pathway promotes meristematic activity, both in the natural context of KN
20 ed in organs of the maize plant that possess meristematic activity, but is especially prominent in th
21 otypes in rice were consistent with aberrant meristematic activity, showing reduced formation of till
22 ependent Target of Rapamycin (TOR) kinase in meristematic activity, yet a picture of how these two re
29 genotype accumulated lower amounts of Al in meristematic and differentiating cells of the root tip a
30 vealed that they were most abundant in young meristematic and floral tissues, but were expressed cons
32 This protein appears to also function in meristematic and vegetative plant tissues and under cert
33 luding the possibility that ovules represent meristematic axes with their own type of lateral determi
34 ion in surface level relative to the plant's meristematic base and not hindered by prolonged submerge
37 g that PFT1/MED25 is an important element of meristematic cell proliferation and cell size control in
38 n in the meristem region, differentiation of meristematic cells and altered expression of the meriste
39 s, we attempt to determine whether Al enters meristematic cells and binds to nuclei when roots are ex
40 meristem while limiting overproliferation of meristematic cells and maintaining the meristem structur
41 the SAM suggests distinct wall properties of meristematic cells and specific differences between newl
42 ector and an extra-wounding treatment of the meristematic cells appeared to be most effective in prom
43 s typically associated with active genes) in meristematic cells at the base and expanded cells in the
44 BR) protein regulates the differentiation of meristematic cells at the transition zone by allowing mR
46 Maintenance of mitotic cell clusters such as meristematic cells depends on their capacity to maintain
52 st Oxidase Homologs TUNEL-positive nuclei in meristematic cells indicated the involvement of programm
54 establishment of three major cell types: the meristematic cells of the embryonal mass on one pole and
57 during embryogenesis but originates from the meristematic cells relatively late during development.
58 suppress mutation during mitotic division of meristematic cells that eventually give rise to gametes
59 ortion of the stem of a grass which contains meristematic cells that give rise to new shoots and root
60 K1 in regulating the cytokinin signal in the meristematic cells through modulating activity of CKX pr
62 sis, refuting the unexamined assumption that meristematic cells trigger cell cycle phases upon reachi
63 s that these signals transmit information to meristematic cells where they initiate persistent epigen
64 wth is supported by a dividing population of meristematic cells within the vascular cambium whose dau
66 centromeres through mitosis, in growing root meristematic cells, demonstrated that global centromere
67 ter (QC), stem cells and frequently dividing meristematic cells, in which the timing and the frequenc
68 dization, POTH1 transcripts were detected in meristematic cells, leaf primordia, and the vascular pro
69 or the accumulation of Fe in the apoplast of meristematic cells, triggering the differentiation of me
74 feration and organ growth by maintaining the meristematic competence of cells during organogenesis.
75 in flower organ primordia by maintaining the meristematic competence of cells during organogenesis.
77 ruitment of leaf founder-cells in a lateral, meristematic domain that contributes to leaf margin deve
78 cell population to previously characterized meristematic domains, further supporting the meristemati
82 s review focuses on the expression patterns, meristematic functions and regulation of KNOX genes, and
83 d organ initiation reveal that both of these meristematic functions are progressively compromised in
84 n lateral organs of eudicots, and repressing meristematic genes in differentiating tissues such as le
86 s, there is also induction of regulatory and meristematic genes, whose predicted activities agree wit
87 Plant body plans arise by the activity of meristematic growing tips during development and radiate
91 The margins of the two fused carpels are meristematic in nature and give rise to placentas, ovule
92 der cells in adult-staged meristems; and (4) meristematic leaf founder cells may be subdivided into s
95 amount of cenH3 protein at chromocenters of meristematic nuclei, anaphase bridges during mitosis, mi
98 organ initiation and a second that sustains meristematic potential through the maintenance of SHOOTM
100 domains and two medial domains, which retain meristematic properties and later fuse to produce the fe
101 he replum is positioned medially and retains meristematic properties resembling the shoot apical meri
102 e in meristem maintenance and in controlling meristematic properties, such as cell proliferation.
103 The molecular mechanisms that specify this meristematic region and regulate its organogenic potenti
105 report the discovery that the dark-arrested meristematic region of Arabidopsis (Arabidopsis thaliana
107 APETALA3 transcripts are first detected in a meristematic region that will give rise to the petal and
109 s less abundant in the vegetative and floral meristematic regions and was present at only a low level
110 rimordia bisected by two medially positioned meristematic regions that give rise to apical and intern
111 and SLK genes support organ development from meristematic regions through two different pathways: one
112 her organs such as the vegetative and floral meristematic regions, fully expanded foliar leaves, the
116 IRB programs reporter expression in diverse, meristematic somatic cells, paradoxically in those cells
118 ability of a cell to dedifferentiate into a meristematic state (analogous to stem cells) and develop
119 ed maintenance of cambial-derived cells in a meristematic state was crucial for gall formation; disru
120 uced programmed cell death is limited to the meristematic stem cell niche and its early descendants.
121 nexpectedly, these results also suggest that meristematic stem cells and lateral organ founder cells
122 iana), the carpel margin meristem is a vital meristematic structure that generates ovules from the me
123 omerase activity was abundant in cauliflower meristematic tissue and undifferentiated cells from Arab
124 sion pattern, including strong expression in meristematic tissue of an Agave tequilana GlsA/ZRF ortho
126 hybridization using knotted1 as a marker for meristematic tissue show that barren inflorescence2 muta
127 HMGR-FLAG protein were found only in apical meristematic tissue, suggesting post-translational regul
135 ental regulations, mitotic activities in the meristematic tissues are modulated by nutritional cues,
138 med the occurrence of PCD in S-cells in post-meristematic tissues in the flower stalk as well as in t
141 Our results indicate that S-cells in post-meristematic tissues show an extreme degree of metabolic
142 plants, GUS expression is most prominent in meristematic tissues such as root tips, lateral root pri
143 scription factor family, and is expressed in meristematic tissues such as the inflorescence meristem
144 M stages were preferentially enriched in the meristematic tissues that have high proliferation activi
145 ar-applied 10B from the mature leaves to the meristematic tissues verifies that boron is mobile in so
146 n important role in the development of other meristematic tissues, but hormone interaction studies to
148 S fusion gene whose expression is limited to meristematic tissues, the H2A-1 gene is expressed in man
149 box gene STIMPY (STIP or WOX9) expression in meristematic tissues, which is essential for maintaining
153 evidence suggests that this transition from meristematic to leaf cell fate requires the down-regulat
154 ems, defining a boundary between the central meristematic zone and the developing organ primordia.
156 al cell-type-specific gene expression in the meristematic zone of the Arabidopsis root, while ethylen
157 ys) primary root tissues, the cortex, stele, meristematic zone, and elongation zone, was generated.
158 classes RNA, DNA, and protein peaked in the meristematic zone, cell wall, lipid metabolism, stress,
159 are the two ferritin genes expressed in the meristematic zone, pericycle and endodermis of the Arabi
162 m de-energized protophloem sieve elements in meristematic zones may be mediated by reversal of SbSUT1
163 ed by expansion of cells in rapidly dividing meristematic zones, which are only rarely refreshed by o
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