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1                                              Meristematic activities in root tips initiate changes in
2 pment involved the amplification of existing meristematic activities within the vascular cambium (VC)
3 lar markers of cell division (CYCB1:GUS) and meristematic activity (ANT:GUS).
4 rs root architecture both by inhibiting root meristematic activity and by stimulating lateral root in
5 al repressor of cell proliferation, depletes meristematic activity and causes precocious differentiat
6 s of shby caused poor root growth, decreased meristematic activity and defects in radial patterning t
7 internode of Nicotiana benthamiana to induce meristematic activity and regenerate de novo shoots with
8 o visible metrics of mortality, i.e. lack of meristematic activity and regrowth.
9 velopmental architecture, such as changes in meristematic activity between S. lycopersicum and S. pen
10                    We demonstrate that shoot meristematic activity can occur in the dark through the
11 for survival during starvation and regaining meristematic activity during the recovery from stress.
12 modeling factor PICKLE (PKL) act to restrict meristematic activity in Arabidopsis leaves without repr
13  root growth, root apical meristem size, and meristematic activity in Arabidopsis.
14 termine the capacity for translation to tune meristematic activity in relation to available resources
15          Several intrinsic pathways restrict meristematic activity in the leaf of Arabidopsis; howeve
16 ass III HD-Zip gene activity is required for meristematic activity in the pericycle analogous to its
17 E (MDF) gene lead to a loss of stem cell and meristematic activity in the root and vegetative shoot.
18 do wild-type root tips, suggesting that root meristematic activity is lower in transgenic than in wil
19  indicate that cytokinin signaling specifies meristematic activity through a graded distribution that
20  also inhibited primary root growth, loss of meristematic activity was observed specifically under Pi
21 nhibition of primary root growth and loss of meristematic activity were evident in seedlings grown un
22 onmental Pi status, maintains and fine-tunes meristematic activity, and finally adjusts root system a
23 ellin (GA) growth regulator pathway promotes meristematic activity, both in the natural context of KN
24 ed in organs of the maize plant that possess meristematic activity, but is especially prominent in th
25  meristem growth, as revealed by the ectopic meristematic activity, enhanced branching, and altered f
26     Auxin maxima have been shown to maintain meristematic activity, for example, of the root apical m
27 es, including hormone and calcium signaling, meristematic activity, photosynthesis, flowering time, l
28 otypes in rice were consistent with aberrant meristematic activity, showing reduced formation of till
29 ependent Target of Rapamycin (TOR) kinase in meristematic activity, yet a picture of how these two re
30 the interactions between hormone actions and meristematic activity.
31 nflorescence is specifically associated with meristematic activity.
32 eaf primordia is subject to light control of meristematic activity.
33 chitecture is dictated by precise control of meristematic activity.
34 ort, are crucial for the maintenance of root meristematic activity.
35 rring in more than one leaf, which reflect a meristematic albino cell lineage.
36 differences impact the relative tolerance of meristematic and differentiated tissues.
37  genotype accumulated lower amounts of Al in meristematic and differentiating cells of the root tip a
38  predicted a GA maximum at the border of the meristematic and elongation zones.
39 vealed that they were most abundant in young meristematic and floral tissues, but were expressed cons
40 e and lateral root formation as it represses meristematic and founder cell divisions.
41 is of thyrse architecture development at the meristematic and molecular levels.
42 rts point to the existence of tightly linked meristematic and transgenerational antiviral barriers th
43     This protein appears to also function in meristematic and vegetative plant tissues and under cert
44        We generated multiple markers for the meristematic apical notch region, which have different s
45 llance, this family is activated in specific meristematic areas fundamental for plant shoot developme
46 luding the possibility that ovules represent meristematic axes with their own type of lateral determi
47 ion in surface level relative to the plant's meristematic base and not hindered by prolonged submerge
48 POSITUM 1 (COM1) expressing in inflorescence meristematic boundaries of different grasses.
49 all properties and signaling specifically in meristematic boundaries to establish identity of adjacen
50             During vascular development, the meristematic cambial cells divide down their long axis i
51                     beta-Cyclocitral rescued meristematic cell divisions in ccd1ccd4 biosynthesis mut
52                   It remains unclear how the meristematic cell fate is maintained.
53  (STM) expression in the leaf axil to enable meristematic cell fate maintenance.
54          PRS1 protein accumulates within all meristematic cell layers (L1-L2-L3) when expressed from
55 istems, which are initiated from a leaf axil meristematic cell population originally detached from th
56 g that PFT1/MED25 is an important element of meristematic cell proliferation and cell size control in
57                 The CLAVATA pathway controls meristematic cell proliferation and multiple nonmeristem
58 nges in hormone transport and a reduction in meristematic cell proliferation.
59 n in the meristem region, differentiation of meristematic cells and altered expression of the meriste
60 psis thaliana) are predominantly confined to meristematic cells and are induced by sucrose and partia
61 s, we attempt to determine whether Al enters meristematic cells and binds to nuclei when roots are ex
62 meristem while limiting overproliferation of meristematic cells and maintaining the meristem structur
63 the SAM suggests distinct wall properties of meristematic cells and specific differences between newl
64 ss the evidence connecting viral invasion of meristematic cells and the ability of plants to recover
65 e either disrupts the supply of glutamate to meristematic cells and/or impairs localized glutamatergi
66 ector and an extra-wounding treatment of the meristematic cells appeared to be most effective in prom
67 s typically associated with active genes) in meristematic cells at the base and expanded cells in the
68 BR) protein regulates the differentiation of meristematic cells at the transition zone by allowing mR
69            Presecretory gland cells resemble meristematic cells because they contain proplastids, sma
70 Maintenance of mitotic cell clusters such as meristematic cells depends on their capacity to maintain
71            Two functionally distinct sets of meristematic cells exist within root tips of pea (Pisum
72                                 We find that meristematic cells express only a core subset of 152 gen
73 moderate high temperature and protected root meristematic cells from heat-induced cell death.
74 nt from seed and bud dormancy, liberation of meristematic cells from the quiescent state, root and sh
75                                Proliferative meristematic cells give rise to differentiating cells, w
76 tributor of membrane for growing vacuoles in meristematic cells has been challenged by a study propos
77             These observations indicate that meristematic cells have discrete but somewhat variable c
78 tic cells, triggering the differentiation of meristematic cells in response to Pi deprivation.
79 re of flowering plants depends on a group of meristematic cells in the shoot apex.
80 st Oxidase Homologs TUNEL-positive nuclei in meristematic cells indicated the involvement of programm
81                        Here, we show that in meristematic cells of the Arabidopsis thaliana root, bio
82 establishment of three major cell types: the meristematic cells of the embryonal mass on one pole and
83             PXY is expressed within dividing meristematic cells of the procambium, whereas CLE41 loca
84 nd plant, growth rate variation patterned by meristematic cells primarily determines shape.
85 during embryogenesis but originates from the meristematic cells relatively late during development.
86 suppress mutation during mitotic division of meristematic cells that eventually give rise to gametes
87 ortion of the stem of a grass which contains meristematic cells that give rise to new shoots and root
88                      However, shoot and root meristematic cells that keep dividing under drought or g
89 K1 in regulating the cytokinin signal in the meristematic cells through modulating activity of CKX pr
90 used to assess the relative contributions of meristematic cells to the developing floral organs.
91 sis, refuting the unexamined assumption that meristematic cells trigger cell cycle phases upon reachi
92 s that these signals transmit information to meristematic cells where they initiate persistent epigen
93 wth is supported by a dividing population of meristematic cells within the vascular cambium whose dau
94           To identify new genes expressed in meristematic cells, a promoter trap insertional mutagene
95  the vasculature, Casparian strips, dividing meristematic cells, and root cap cells, as well as subce
96 centromeres through mitosis, in growing root meristematic cells, demonstrated that global centromere
97 ter (QC), stem cells and frequently dividing meristematic cells, in which the timing and the frequenc
98 dization, POTH1 transcripts were detected in meristematic cells, leaf primordia, and the vascular pro
99  treatment leads to arrest in the S phase of meristematic cells, likely due to the lack of DNA precur
100 or the accumulation of Fe in the apoplast of meristematic cells, triggering the differentiation of me
101 cted RdDM and TGS of a transgene promoter in meristematic cells.
102 aracteristics typical of genes with roles in meristematic cells.
103  abundantly present in the small vacuoles of meristematic cells.
104 chanism that maintains anisotropic growth in meristematic cells.
105 lar and connected vacuolar structures in all meristematic cells.
106 OS staining and TUNEL-positive nuclei in the meristematic cells.
107 feration and organ growth by maintaining the meristematic competence of cells during organogenesis.
108 in flower organ primordia by maintaining the meristematic competence of cells during organogenesis.
109 ture and caused by the decrease in number of meristematic cortical cells due to EPiR.
110 ruitment of leaf founder-cells in a lateral, meristematic domain that contributes to leaf margin deve
111   By this, gene expression differences among meristematic domains giving rise to different tissue and
112  cell population to previously characterized meristematic domains, further supporting the meristemati
113                                  Adaxial and meristematic expression of rld1 is reduced in lbl1 mutan
114 sues, which is essential for maintaining the meristematic fate.
115 ted in the acquisition and/or maintenance of meristematic fate.
116 his study assessed vegetative propagation of meristematic fragments and the protein content and bioac
117 s review focuses on the expression patterns, meristematic functions and regulation of KNOX genes, and
118 d organ initiation reveal that both of these meristematic functions are progressively compromised in
119  Arabidopsis results in the reprogramming of meristematic gene regulatory networks establishing FM id
120 boundary genes TCP24 and FZP, as well as the meristematic genes AGL6 and ULT1.
121 n lateral organs of eudicots, and repressing meristematic genes in differentiating tissues such as le
122 s expressed in organ primordia interact with meristematic genes to regulate shoot morphogenesis.
123 s, there is also induction of regulatory and meristematic genes, whose predicted activities agree wit
124    Plant body plans arise by the activity of meristematic growing tips during development and radiate
125 s the transition from uniplanar to triplanar meristematic growth in moss.
126 and is, in turn, negatively regulated by the meristematic homeobox gene SHOOT MERISTEMLESS.
127 expression of Knox genes, markers of nonleaf meristematic identity.
128     The margins of the two fused carpels are meristematic in nature and give rise to placentas, ovule
129 s strategically applied in planta to the non-meristematic internode of Nicotiana benthamiana to induc
130                                 Mutations in meristematic layers can propagate into large sectors of
131 different cell layers deriving from distinct meristematic layers.
132 der cells in adult-staged meristems; and (4) meristematic leaf founder cells may be subdivided into s
133 ogenously is limited and usually confined to meristematic-like tissues.
134                                              Meristematic maize tissues had high levels of ZmDHFR-TS
135              However, the characteristics of meristematic mutations remain unclear, limiting our unde
136 meristematic domains, further supporting the meristematic nature of this gynoecial tissue.
137       Shoot development in maize begins when meristematic, non-pigmented cells at leaf base stop divi
138  amount of cenH3 protein at chromocenters of meristematic nuclei, anaphase bridges during mitosis, mi
139 h AIL genes having roles in specification of meristematic or division-competent states.
140 y and distribution of somatic mutations with meristematic origin.
141 his transition from filamentous to triplanar meristematic plant growth are poorly understood.
142  organ initiation and a second that sustains meristematic potential through the maintenance of SHOOTM
143          While CLAVATA ancestrally regulates meristematic proliferation in nonseed plant gametophytes
144 mental and nutritional signals in regulating meristematic proliferation.
145 domains and two medial domains, which retain meristematic properties and later fuse to produce the fe
146 he replum is positioned medially and retains meristematic properties resembling the shoot apical meri
147 e in meristem maintenance and in controlling meristematic properties, such as cell proliferation.
148 iosynthesis within the root occurring in the meristematic region and indicate that the penultimate st
149   The molecular mechanisms that specify this meristematic region and regulate its organogenic potenti
150     Epidermal and proendodermal cells in the meristematic region contained transverse cortical MFs.
151  report the discovery that the dark-arrested meristematic region of Arabidopsis (Arabidopsis thaliana
152 ve genotype and accumulated at nuclei in the meristematic region of the root tip.
153 APETALA3 transcripts are first detected in a meristematic region that will give rise to the petal and
154                      NFL is expressed at the meristematic regions and NFL is localized to the nucleus
155 s less abundant in the vegetative and floral meristematic regions and was present at only a low level
156 rimordia bisected by two medially positioned meristematic regions that give rise to apical and intern
157 and SLK genes support organ development from meristematic regions through two different pathways: one
158 her organs such as the vegetative and floral meristematic regions, fully expanded foliar leaves, the
159 the developing spikelets and three different meristematic regions, which are consistent across spikel
160 2 messages preferentially accumulated in the meristematic regions.
161 athway, coordinating growth between adjacent meristematic regions.
162                                              Meristematic sectors of dual aneuploidy were generated,
163 IRB programs reporter expression in diverse, meristematic somatic cells, paradoxically in those cells
164 te that MADS-domain proteins interact during meristematic stages of flower development.
165  ability of a cell to dedifferentiate into a meristematic state (analogous to stem cells) and develop
166 ed maintenance of cambial-derived cells in a meristematic state was crucial for gall formation; disru
167 uced programmed cell death is limited to the meristematic stem cell niche and its early descendants.
168 nexpectedly, these results also suggest that meristematic stem cells and lateral organ founder cells
169 ly upregulated in the IM compared with a non-meristematic stem tissue.
170 iana), the carpel margin meristem is a vital meristematic structure that generates ovules from the me
171 tories for individual cells progressing from meristematic through mature stages of root-hair and nonh
172 lloxera exploits vascular cambium to provide meristematic tissue and redirects leaf development towar
173 omerase activity was abundant in cauliflower meristematic tissue and undifferentiated cells from Arab
174                     The periderm comprises a meristematic tissue called the phellogen, or cork cambiu
175 sion pattern, including strong expression in meristematic tissue of an Agave tequilana GlsA/ZRF ortho
176 y network that is responsible for activating meristematic tissue proliferation in Arabidopsis.
177 hybridization using knotted1 as a marker for meristematic tissue show that barren inflorescence2 muta
178 fy the hypocotyl (mesocotyl in grasses) as a meristematic tissue that allows this process.
179  HMGR-FLAG protein were found only in apical meristematic tissue, suggesting post-translational regul
180  vulgare L.) cDNA library prepared from leaf meristematic tissue, was sequenced.
181 from undifferentiated proplastids present in meristematic tissue.
182 pressed constitutively in the root stele and meristematic tissue.
183 ation, followed by cell cycle arrest, in the meristematic tissue.
184 mine the cell biology of CLV1 in Arabidopsis meristematic tissue.
185               This pathogenic fungus infects meristematic tissues and derives nutrients from the plan
186               Altered DKM expression affects meristematic tissues and reproductive organ development,
187 ental regulations, mitotic activities in the meristematic tissues are modulated by nutritional cues,
188                  Telomerase from cauliflower meristematic tissues exhibited relaxed DNA sequence requ
189                                              Meristematic tissues from rye (Secale cereale) and oat (
190 med the occurrence of PCD in S-cells in post-meristematic tissues in the flower stalk as well as in t
191 , we found that WOX13 is expressed mainly in meristematic tissues including the replum.
192 sues, TaABCB1 predominantly expressed in the meristematic tissues likely due to the presence of meris
193 10B to mature leaves was translocated to the meristematic tissues only in line S11.
194    Our results indicate that S-cells in post-meristematic tissues show an extreme degree of metabolic
195  plants, GUS expression is most prominent in meristematic tissues such as root tips, lateral root pri
196 scription factor family, and is expressed in meristematic tissues such as the inflorescence meristem
197 M stages were preferentially enriched in the meristematic tissues that have high proliferation activi
198 ar-applied 10B from the mature leaves to the meristematic tissues verifies that boron is mobile in so
199 n important role in the development of other meristematic tissues, but hormone interaction studies to
200        The KNL2 promoter is mainly active in meristematic tissues, similar to the cenH3 promoter.
201 S fusion gene whose expression is limited to meristematic tissues, the H2A-1 gene is expressed in man
202 box gene STIMPY (STIP or WOX9) expression in meristematic tissues, which is essential for maintaining
203  promoting G2 to M transition in Arabidopsis meristematic tissues.
204 elopment of both vegetative and reproductive meristematic tissues.
205 e PCNA protein was down-regulated throughout meristematic tissues.
206 in plants develop from stem cells located in meristematic tissues.
207  with the entire developmental gradient from meristematic to fully differentiated cells captured.
208  evidence suggests that this transition from meristematic to leaf cell fate requires the down-regulat
209 ionally exhibit hypercolonization around the meristematic zone and a delay of S. indica-induced root-
210 tricate balance between cell division in the meristematic zone and cell elongation in the elongation
211 ems, defining a boundary between the central meristematic zone and the developing organ primordia.
212 osensor, nlsGPS1, and found to be low in the meristematic zone grading to a maximum at the end of the
213  cell structure, and a shorter length of the meristematic zone in root tips.
214 nscripts are expressed preferentially in the meristematic zone of all root types of maize.
215 al cell-type-specific gene expression in the meristematic zone of the Arabidopsis root, while ethylen
216 ys) primary root tissues, the cortex, stele, meristematic zone, and elongation zone, was generated.
217  classes RNA, DNA, and protein peaked in the meristematic zone, cell wall, lipid metabolism, stress,
218  are the two ferritin genes expressed in the meristematic zone, pericycle and endodermis of the Arabi
219 gnaling components in the regulation of root meristematic zone-targeted growth arrest.
220 orescence signals was detected in the apical meristematic zone.
221 ype-specific expression patterns in the root meristematic zone.
222 m de-energized protophloem sieve elements in meristematic zones may be mediated by reversal of SbSUT1
223 altering their concentration gradient in the meristematic zones, and consequently modifying different
224 ed by expansion of cells in rapidly dividing meristematic zones, which are only rarely refreshed by o

 
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