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1 opulation originally detached from the shoot apical meristem.
2 ely regulates cell proliferation at the root apical meristem.
3 , when the third leaf emerges from the shoot apical meristem.
4 eristem and hypocotyl, cotyledons, and shoot apical meristem.
5 esting cell production and an exhausted root apical meristem.
6 gulate transition to flowering in leaves and apical meristem.
7 postembryonically at the flanks of the shoot apical meristem.
8 e compound leaf as well as a defective shoot apical meristem.
9 r cells, lateral root primordia and the root apical meristem.
10 I4 and ABI5 directly and specifically in the apical meristem.
11 root development by altering the size of the apical meristem.
12 owth from a primordium on flank of the shoot apical meristem.
13 entiation in the stem cell niche in the root apical meristem.
14 nown for their role in maintaining the shoot apical meristem.
15 al to establish a functional embryonic shoot apical meristem.
16 e plant, but are integrated within the shoot apical meristem.
17 ll give rise to the cotyledons and the shoot apical meristem.
18 rol proliferation and cell fate in the shoot apical meristem.
19 defects characterized by a loss of the shoot apical meristem.
20 nks of the vegetative or inflorescence shoot apical meristem.
21 of a pluripotent structure termed the shoot apical meristem.
22 icle reviews cell proliferation in the shoot apical meristem.
23 for 30-days which was mediated via damaging apical meristem.
24 FT transport through the phloem to the shoot apical meristem.
25 mpacts the mechanics and growth of the shoot apical meristem.
26 ype due to reduced cell division in the root apical meristem.
27 ontrols the stem cell population of the root apical meristem.
28 to overcome stem cell dormancy at the shoot apical meristem.
29 n life as outgrowths from the edges of shoot apical meristems.
30 is the emergence of organ primordia from the apical meristems.
31 umber of cells, compared with wild-type root apical meristems.
32 of the niche/organizing center (OC) of shoot apical meristems.
33 and in the initiation and function of shoot apical meristems.
34 allus-like floral organs and fasciated shoot apical meristems.
35 atterns are produced by tissues called shoot apical meristems.
36 erent root cell types, in embryos, and shoot apical meristems.
37 dine retention experiments in shoot and root apical meristems.
38 causing structural abnormalities in the root apical meristems.
39 lls over 3-4 d in Arabidopsis thaliana shoot apical meristems.
40 ablishment and maintenance of shoot and root apical meristems.
41 nate organs derived from indeterminate shoot apical meristems.
42 ell division activity in both shoot and root apical meristems.
43 e the body arises through the activity of an apical meristem (a niche of cells or a single cell).
46 e identified three novel regulators of shoot apical meristem activity in Arabidopsis thaliana that en
47 tterning and growth of lateral organs, shoot apical meristem activity, and inflorescence phyllotaxy.
48 since dark-grown seedlings have reduced root apical meristem activity, as observed in the clasp-1 nul
49 isplayed dramatic defects, including reduced apical meristem activity, delayed and abnormal lateral o
52 of globular stage embryos, and in the shoot apical meristem and adaxial domain of cotyledons of hear
53 e rate of leaf initiation, an enlarged shoot apical meristem and an increase in the number of juvenil
54 Leaves arise from the flank of the shoot apical meristem and are asymmetrical along the adaxial/a
55 in the development of the Arabidopsis shoot apical meristem and are part of a complex regulatory net
56 these constructs on the lengths of the root apical meristem and cortical cells in the elongation zon
57 rate of cell elongation is maximal near the apical meristem and decreases steeply toward the middle
58 pecific tissues such as roots, leaves, shoot apical meristem and different stages of panicle and seed
59 rimordia initiate at the flanks of the shoot apical meristem and extend laterally by cell division an
61 eeds the lowest levels, followed by the root apical meristem and hypocotyl, cotyledons, and shoot api
63 REVOLUTA and is expressed in both the shoot apical meristem and in the cambial zone and secondary va
64 the peripheral zone of the vegetative shoot apical meristem and in the vasculature of immature leave
65 opment correlated with rounding of the shoot apical meristem and induction of TGSQA expression, a tul
70 a2ox1 mRNAs overlap at the base of the shoot apical meristem and the base of newly initiated leaves,
71 of founder cells at the flanks of the shoot apical meristem and the creation of a functional boundar
74 GFP expression at the boundaries between the apical meristems and lateral organs in Arabidopsis embry
75 parallels the morphogenetic program of shoot apical meristems and may represent a relic of an ancestr
78 a member of the NAC domain [petunia NAM (no apical meristem) and Arabidopsis ATAF1, 2 and CUC2] fami
81 enlarged and deformed plastids in the shoot apical meristem, and develop a mass of callus tissue at
82 istematic activity, for example, of the root apical meristem, and position new sites of outgrowth, su
84 which resulted from enlarged root and shoot apical meristems, and, additionally, they had a reduced
85 ELEMENT BINDING PROTEIN1 and ORYZA SATIVA No Apical Meristem, Arabidopsis Transcription Activation Fa
86 at the carbon starvation-induced NAC (for NO APICAL MERISTEM/ARABIDOPSIS TRANSCRIPTION ACTIVATION FAC
87 that the transmembrane domain-containing no apical meristem/Arabidopsis transcription activation fac
89 in the shoot apical meristem (SAM) and root apical meristem are necessary for postembryonic developm
90 wering, primordia on the flanks of the shoot apical meristem are specified to form flowers instead of
92 gulation of both ULT genes can lead to shoot apical meristem arrest shortly after germination, reveal
93 gans that arise from the flanks of the shoot apical meristem as polar structures with distinct adaxia
94 cked bidirectionally to sink leaves near the apical meristem as well as to the source leaves at the b
95 lities in cell division patterns at the root apical meristem, as well as reduced growth under ionic,
97 ss reminiscent of organogenesis at the shoot apical meristem, but that compound and simple leaves reg
98 s to regulate auxin distribution in the root apical meristem by regulating both the PINs and LAX2.
99 haliana maintain cell proliferation in shoot apical meristems by restricting expression of the transc
101 nd environmental signals acting on the shoot apical meristem cause acquisition of inflorescence meris
102 ;WEE1 is over-expressed in Arabidopsis, root apical meristem cell size increases, and morphogenetic c
103 formation of phyllotactic patterns at plant apical meristems center on either transport of the growt
104 or FLC expression in either leaves or shoot apical meristem, contributing to a threshold expression
106 agenesis of the Arabidopsis vegetative shoot apical meristem demonstrate the broad applicability of t
107 primordia within the periphery of the shoot apical meristem depends on transport of the phytohormone
108 the ptDNA population in a regenerating shoot apical meristem derives from a small number of copies se
112 ild-type plants, SVP expression in the shoot apical meristem falls when plants are exposed to photope
115 and chlorotic, with severe defects in shoot apical meristem formation and cotyledon vein patterning.
116 a novel function of Pgbs in protecting root apical meristems from hypoxia-induced PCD through mechan
117 ost dramatically a progressive loss of shoot apical meristem function that causes premature meristem
120 s able to partially compensate for the shoot apical meristem growth defects in mutants that cannot se
121 hat regulates stem cell numbers of the shoot apical meristem has exclusively been studied in Arabidop
122 rofiles of a meristemoid with shoot and root apical meristems highlighted cytokinin signaling and the
123 a in indole-3-acetic acid (IAA)-treated root apical meristems; hypergravitropic root growth and respo
124 croarray analyses of the rgd2-R mutant shoot apical meristem identified a novel gene, PUNCTATE VASCUL
125 cells in leaves, root vasculature, and shoot apical meristem, implicating it in both local and system
126 eed than in tissues including leaf and shoot apical meristem, implying their function in seed germina
127 t meristems and the reduced size of the root apical meristem in ddl plants suggests a role early in o
128 GFP moves from its site of expression at the apical meristem in embryos and seedlings, yet the extent
129 preferential expression of pBVR in the shoot apical meristem in MERI5::pBVR lines resulted in a phyto
131 proteins are expressed throughout the shoot apical meristem, in leaf primordia, and in the elongatio
132 re expressed coordinately in embryonic shoot apical meristems, in inflorescence and floral meristems,
133 boundary formation in the Arabidopsis shoot apical meristem, including cup-shaped cotyledon, lateral
134 s thaliana) play a role in maintaining shoot apical meristem indeterminacy, and their misexpression i
135 leaves essential KNOX1 function in the shoot apical meristem intact and appears to be a facile way to
138 bidopsis (Arabidopsis thaliana) primary root apical meristem is composed of the quiescent (or organiz
139 ation and differentiation in the plant shoot apical meristem is controlled by regulatory loops involv
141 2 does not recognize CLV3 and that the shoot apical meristem is immune to bacteria independently of C
142 mutation accumulation per unit time in shoot apical meristem is lower than that in root apical tissue
143 naling in the rib meristem (RM) of the shoot apical meristem is necessary and sufficient for stem cel
144 During early seedling development, the shoot apical meristem is protected from damage as the seedling
145 o the shoot apex, where the vegetative shoot apical meristem is restructured into a reproductive meri
146 expression and polarity of PIN1 in the shoot apical meristem is thought to be regulated primarily by
147 eceptor, regulating development of the shoot apical meristem, is involved in autoregulation of nodula
148 used to sequence the transcriptomes of shoot apical meristems isolated from two inbred lines of maize
150 stribution and is enriched in shoot and root apical meristems, lateral root primordia, the vascular s
151 wed that the kinases accumulate in the shoot apical meristem, leaf primordium, and emerging petiole.
152 , and displayed delayed flowering, increased apical meristem life, and altered vascular development r
153 t1 in a gene annotated as encoding a NAM (no apical meristem)-like protein (here designated Medicago
154 late embryo development, and embryonic root apical meristem lines) based on their dominant expressio
156 ADT3 is expressed in the cotyledon and shoot apical meristem, mainly in the cytosol, and that the epi
157 athway genes play an essential role in shoot apical meristem maintenance and floral organ development
158 been proposed to be important regulators of apical meristem maintenance and to be expressed in apica
159 MPY/WOX9 that is required for root and shoot apical meristem maintenance roots and which has previous
160 nd in planta with proteins involved in shoot apical meristem maintenance such as WUSCHEL, KNAT1/BP, K
161 dodermal cell fate; it is also essential for apical meristem maintenance, ground tissue patterning, v
165 ion enriched within a subdomain of the shoot apical meristem, mutant phenotype showing defect in pola
167 aracterized organ boundary gene candidate NO APICAL MERISTEM (NAM) supports the hypothesis that it es
168 er analysis identified potential NAC (for no apical meristem [NAM], Arabidopsis transcription activat
169 sence in lateral root primordia and the root apical meristem negatively regulates root system archite
170 ell division activity in both shoot and root apical meristems observed in fbl17 loss-of-function muta
172 ly dividing fields of cells within the shoot apical meristem of Arabidopsis show dynamic regulation o
179 US) defines the shoot stem cell niche in the apical meristems of many angiosperm species; we show tha
182 ranscriptional profiling in developing shoot apical meristems of vrs3 suggested that VRS3 acts as a t
183 has a documented role, such as in the shoot apical meristem or in the vasculature of Arabidopsis (Ar
185 ts of three major processes: arrest of shoot apical meristem, organ senescence, and permanent suppres
186 meristem maintenance and to be expressed in apical meristem "organizers." Here, we focus on the role
187 showed that the TAS3 ta-siRNA pathway and no apical meristem (ortholog of Arabidopsis cup-shaped coty
188 e meristem e.g. the quiescent centre of root apical meristem (RAM) and the lower half of the central
191 Mutant sav6 plants also show reduced root apical meristem (RAM) size and defective quiescent centr
192 in but also ethylene is able to control root apical meristem (RAM) size through activation of the mul
193 In CLEL peptide-induced long roots, the root apical meristem (RAM) was enlarged and consisted of an i
194 tes, delayed leaf senescence, a smaller root apical meristem (RAM), reduced primary and lateral root
196 onstrate that cells in the Arabidopsis shoot apical meristem respond to local mechanical stresses by
197 d the arrest of mitotic activity in the root apical meristem, resulting in a short-root phenotype.
198 vels in the hook region (including the shoot apical meristem) reveals genes involved in cell division
200 plays an essential role in regulating shoot apical meristem (SAM) activity and shoot architecture.
203 Expression of proHLP1::GUS in the shoot apical meristem (SAM) after HS coincides with TOR-E2Fa e
204 e CLSM image stacks of the Arabidopsis Shoot Apical Meristem (SAM) and have shown that the AQVT based
206 inct pluripotent cell populations: the shoot apical meristem (SAM) and root meristem (RM), which post
207 the shoot apex, which consists of the shoot apical meristem (SAM) and the flanking leaf primordia.
209 idopsis, the central stem cells of the shoot apical meristem (SAM) are indefinitely maintained, where
212 nnual plants, in perennial plants, the shoot apical meristem (SAM) can undergo seasonal transitions b
217 daries from the stem cell niche in the shoot apical meristem (SAM) determines the patterning and arch
220 leaves, initiate at the flanks of the shoot apical meristem (SAM) following auxin maxima signals; ho
221 ain transcription factor essential for shoot apical meristem (SAM) formation and sustained activity.
222 change that transforms the fate of the shoot apical meristem (SAM) from a leaf-bearing vegetative mer
224 Flowers form on the flanks of the shoot apical meristem (SAM) in response to environmental and e
228 stem cell niche, contained within the shoot apical meristem (SAM) is maintained in Arabidopsis by th
233 re key regulators that function at the shoot apical meristem (SAM) of plants to promote differentiati
235 elf-renewing stem cells located in the shoot apical meristem (SAM) produce leaves from the SAM periph
238 tern of cell shapes in the Arabidopsis shoot apical meristem (SAM) suggests that strict rules govern
239 plants is a small region known as the shoot apical meristem (SAM) that maintains a population of und
240 is a receptor protein expressed in the shoot apical meristem (SAM) that translates perception of a no
241 domain within the Arabidopsis thaliana shoot apical meristem (SAM) to maintain a stem cell niche.
242 s thaliana, multiple genes involved in shoot apical meristem (SAM) transitions have been characterize
245 ing how the distinct cell types of the shoot apical meristem (SAM) withstand ultraviolet radiation (U
248 a stem cell marker in the Arabidopsis shoot apical meristem (SAM), was expressed in expanded regions
249 cell layer structures exists from the shoot apical meristem (SAM), where organ primordia arise, to m
250 ies produce leaves from a conventional shoot apical meristem (SAM), whereas acaulescent species lack
269 light on the transcriptome of columnar shoot apical meristems (SAMs), the molecular mechanisms of col
270 pulations of pluripotent stem cells in shoot apical meristems (SAMs), which continuously produce new
273 ubule-associated protein CLASP sustains root apical meristem size by influencing microtubule organiza
274 ure (RSA), reduces primary root growth, root apical meristem size, and meristematic activity in Arabi
275 erving that shade induces increases in shoot apical meristem size, we then describe gene expression c
276 ry for silencing spread just below the shoot apical meristem that blocks movement upward from the roo
278 rgely unrecognized zone of tissue, below the apical meristem, that is resistant to the silencing sign
279 ore morphological changes occur in the shoot apical meristem, the expression of floral repressors in
282 l contexts, including its role in regulating apical meristems, the patterning of the root, the develo
283 origen, that promotes flowering at the shoot apical meristem; the vernalization process in which expo
286 Growth was modelled as the dynamics of root apical meristems, using Partial Differential Equations.
289 apical hook that protects the fragile shoot apical meristem when it breaks through the soil during g
290 mplex shape and growth patterns in the shoot apical meristem where new organs are initiated shows tha
291 der LDs and is then transported to the shoot apical meristem, where it simultaneously induces the exp
292 s in the presence of an intact primary shoot apical meristem, which at least partially contributes to
294 pluripotent cell population called the shoot apical meristem, which generates the entire above-ground
295 ctures from the peripheral zone of the shoot apical meristem, which requires class I KNOTTED-LIKE HOM