ライフサイエンスコーパス: apical meristem

1 esting cell production and an exhausted root apical meristem.

2 postembryonically at the flanks of the shoot apical meristem.

3 e compound leaf as well as a defective shoot apical meristem.

4 r cells, lateral root primordia and the root apical meristem.

5 I4 and ABI5 directly and specifically in the apical meristem.

6 root development by altering the size of the apical meristem.

7 owth from a primordium on flank of the shoot apical meristem.

8 entiation in the stem cell niche in the root apical meristem.

9 nown for their role in maintaining the shoot apical meristem.

10 al to establish a functional embryonic shoot apical meristem.

11 e plant, but are integrated within the shoot apical meristem.

12 ll give rise to the cotyledons and the shoot apical meristem.

13 rol proliferation and cell fate in the shoot apical meristem.

14 ontrols the stem cell population of the root apical meristem.

15 defects characterized by a loss of the shoot apical meristem.

16 nks of the vegetative or inflorescence shoot apical meristem.

17 of a pluripotent structure termed the shoot apical meristem.

18 icle reviews cell proliferation in the shoot apical meristem.

19 e descendents of the stem cells in the shoot apical meristem.

20 ired for the formation of a functional shoot apical meristem.

21 hout the plant but is not found in the shoot apical meristem.

22 le analogous to its requirement in the shoot apical meristem.

23 an abaxial-specific pattern and in the shoot apical meristem.

24 polarity in lateral organs produced from the apical meristem.

25 ype due to reduced cell division in the root apical meristem.

26 to overcome stem cell dormancy at the shoot apical meristem.

27 ely regulates cell proliferation at the root apical meristem.

28 , when the third leaf emerges from the shoot apical meristem.

29 eristem and hypocotyl, cotyledons, and shoot apical meristem.

30 n life as outgrowths from the edges of shoot apical meristems.

31 is the emergence of organ primordia from the apical meristems.

32 umber of cells, compared with wild-type root apical meristems.

33 of the niche/organizing center (OC) of shoot apical meristems.

34 and in the initiation and function of shoot apical meristems.

35 erent root cell types, in embryos, and shoot apical meristems.

36 allus-like floral organs and fasciated shoot apical meristems.

37 atterns are produced by tissues called shoot apical meristems.

38 dine retention experiments in shoot and root apical meristems.

39 duced by pluripotent structures termed shoot apical meristems.

40 uninfected plants only to the shoot and root apical meristems.

41 causing structural abnormalities in the root apical meristems.

42 lls over 3-4 d in Arabidopsis thaliana shoot apical meristems.

43 ablishment and maintenance of shoot and root apical meristems.

44 nate organs derived from indeterminate shoot apical meristems.

45 ell division activity in both shoot and root apical meristems.

46 e the body arises through the activity of an apical meristem (a niche of cells or a single cell).

47 Within the root apical meristem, a group of slowly dividing quiescent ce

48 The shoot apical meristem, a small dome-shaped structure at the sh

49 , hst mutations affect the size of the shoot apical meristem, accelerate vegetative phase change, del

50 e identified three novel regulators of shoot apical meristem activity in Arabidopsis thaliana that en

51 tterning and growth of lateral organs, shoot apical meristem activity, and inflorescence phyllotaxy.

52 isplayed dramatic defects, including reduced apical meristem activity, delayed and abnormal lateral o

53 y a few leaves prior to termination of shoot apical meristem activity.

54 t leaf initiation, leaf expansion, and shoot apical meristem activity.

55 In plants, apical meristems allow continuous growth along the body

56 of globular stage embryos, and in the shoot apical meristem and adaxial domain of cotyledons of hear

57 Leaves arise from the flank of the shoot apical meristem and are asymmetrical along the adaxial/a

58 in the development of the Arabidopsis shoot apical meristem and are part of a complex regulatory net

59 rate of cell elongation is maximal near the apical meristem and decreases steeply toward the middle

60 s of PSD disrupt the initiation of the shoot apical meristem and delay leaf initiation after germinat

61 pecific tissues such as roots, leaves, shoot apical meristem and different stages of panicle and seed

62 rimordia initiate at the flanks of the shoot apical meristem and extend laterally by cell division an

63 the stem cell niche at the tip of the shoot apical meristem and from incipient leaf primordia.

64 eeds the lowest levels, followed by the root apical meristem and hypocotyl, cotyledons, and shoot api

65 OBO1 also is expressed at the root apical meristem and in distinct cell files surrounding t

66 ons to monitor protein movement in the shoot apical meristem and in floral primordia of Arabidopsis,

67 REVOLUTA and is expressed in both the shoot apical meristem and in the cambial zone and secondary va

68 the peripheral zone of the vegetative shoot apical meristem and in the vasculature of immature leave

69 opment correlated with rounding of the shoot apical meristem and induction of TGSQA expression, a tul

70 s expressing OBO1 leads to loss of the shoot apical meristem and lateral organs.

71 specifically at boundaries between the shoot apical meristem and leaf/flower primordia.

72 expressed in specific patterns in the shoot apical meristem and play important roles in plant archit

73 The reduced length of the root apical meristem and primary root of the mutant ashr3-1 i

74 reas SHM2 is mainly transcribed in the shoot apical meristem and roots.

75 a2ox1 mRNAs overlap at the base of the shoot apical meristem and the base of newly initiated leaves,

76 of founder cells at the flanks of the shoot apical meristem and the creation of a functional boundar

77 cally expressed in central zone of the shoot apical meristem and the quiescent center of the root api

78 ws a dynamic expression pattern in the shoot apical meristem and young leaf primordia.

79 FEN1 is abundant in the root and shoot apical meristems and FEN1-GFP shows a nucleolus-localize

80 GFP expression at the boundaries between the apical meristems and lateral organs in Arabidopsis embry

81 parallels the morphogenetic program of shoot apical meristems and may represent a relic of an ancestr

82 Mutant seedlings show disorganized apical meristems and rudimentary true leaves with cluste

83 es of the balance between the determinacy of apical meristems and source-sink cross-talk.

84 ll as in the formation of the root and shoot apical meristems and the cotyledons.

85 e cell division in the seedling, notably the apical meristems and young leaves.

86 at precede formation of plant gametes, their apical-meristem and floral antecedents are continually e

87 a member of the NAC domain [petunia NAM (no apical meristem) and Arabidopsis ATAF1, 2 and CUC2] fami

88 lting in elongated leaves, compromised shoot apical meristem, and delayed bolting.

89 enlarged and deformed plastids in the shoot apical meristem, and develop a mass of callus tissue at

90 dons, abolishes the formation of the primary apical meristem, and in severe cases, eliminates bilater

91 The shoot tip is called the shoot apical meristem, and it acts as a self-renewing source o

92 ABPH1 is expressed in the embryonic shoot apical meristem, and its spatial expression pattern chan

93 notably in root tips, floral buds, stamens, apical meristems, and germinating seeds.

94 D2C were expressed in ovules, embryos, shoot apical meristems, and primary leaves.

95 which resulted from enlarged root and shoot apical meristems, and, additionally, they had a reduced

96 ELEMENT BINDING PROTEIN1 and ORYZA SATIVA No Apical Meristem, Arabidopsis Transcription Activation Fa

97 at the carbon starvation-induced NAC (for NO APICAL MERISTEM/ARABIDOPSIS TRANSCRIPTION ACTIVATION FAC

98 that the transmembrane domain-containing no apical meristem/Arabidopsis transcription activation fac

99 lue light, indicating that regions below the apical meristem are necessary for phototropism.

100 in the shoot apical meristem (SAM) and root apical meristem are necessary for postembryonic developm

101 wering, primordia on the flanks of the shoot apical meristem are specified to form flowers instead of

102 Shoot apical meristems are stem cell niches that balance proli

103 gulation of both ULT genes can lead to shoot apical meristem arrest shortly after germination, reveal

104 gans that arise from the flanks of the shoot apical meristem as polar structures with distinct adaxia

105 cked bidirectionally to sink leaves near the apical meristem as well as to the source leaves at the b

106 lities in cell division patterns at the root apical meristem, as well as reduced growth under ionic,

107 found in leaves and inflorescences, and the apical meristem becomes highly fasciated.

108 fferentiation not only in the root and shoot apical meristems but also in nodule meristems.

109 ss reminiscent of organogenesis at the shoot apical meristem, but that compound and simple leaves reg

110 s to regulate auxin distribution in the root apical meristem by regulating both the PINs and LAX2.

111 haliana maintain cell proliferation in shoot apical meristems by restricting expression of the transc

112 relatively inaccessible region of the shoot apical meristem called the rib zone (RZ).

113 nd environmental signals acting on the shoot apical meristem cause acquisition of inflorescence meris

114 formation of phyllotactic patterns at plant apical meristems center on either transport of the growt

115 or FLC expression in either leaves or shoot apical meristem, contributing to a threshold expression

116 f gibberellin hormones (GAs) in tolerance to apical meristem damage (AMD), we characterized the react

117 Lateral organ distribution at the shoot apical meristem defines specific and robust phyllotaxis

118 agenesis of the Arabidopsis vegetative shoot apical meristem demonstrate the broad applicability of t

119 primordia within the periphery of the shoot apical meristem depends on transport of the phytohormone

120 the ptDNA population in a regenerating shoot apical meristem derives from a small number of copies se

121 al meristem cells partitioned from the shoot apical meristem during reproductive development.

122 ild-type plants, SVP expression in the shoot apical meristem falls when plants are exposed to photope

123 a distinct phase in the derailment of shoot apical meristem fate.

124 g to a threshold expression of SOC1 in shoot apical meristem for floral initiation.

125 and chlorotic, with severe defects in shoot apical meristem formation and cotyledon vein patterning.

126 Cupuliformis mutants are defective in shoot apical meristem formation, but cup plants overcome this

127 a novel function of Pgbs in protecting root apical meristems from hypoxia-induced PCD through mechan

128 ost dramatically a progressive loss of shoot apical meristem function that causes premature meristem

129 s are together required for continuous shoot apical meristem function.

130 oecium (group 2) or systemically through the apical meristem (group 3).

131 s able to partially compensate for the shoot apical meristem growth defects in mutants that cannot se

132 hat regulates stem cell numbers of the shoot apical meristem has exclusively been studied in Arabidop

133 rofiles of a meristemoid with shoot and root apical meristems highlighted cytokinin signaling and the

134 a in indole-3-acetic acid (IAA)-treated root apical meristems; hypergravitropic root growth and respo

135 croarray analyses of the rgd2-R mutant shoot apical meristem identified a novel gene, PUNCTATE VASCUL

136 t meristems and the reduced size of the root apical meristem in ddl plants suggests a role early in o

137 GFP moves from its site of expression at the apical meristem in embryos and seedlings, yet the extent

138 preferential expression of pBVR in the shoot apical meristem in MERI5::pBVR lines resulted in a phyto

139 After germination, cells near the apical meristem in seedlings show a higher size exclusio

140 proteins are expressed throughout the shoot apical meristem, in leaf primordia, and in the elongatio

141 re expressed coordinately in embryonic shoot apical meristems, in inflorescence and floral meristems,

142 boundary formation in the Arabidopsis shoot apical meristem, including cup-shaped cotyledon, lateral

143 s thaliana) play a role in maintaining shoot apical meristem indeterminacy, and their misexpression i

144 out of the epidermal (L1) layer in the shoot apical meristem, indicating that KN1 movement out of the

145 leaves essential KNOX1 function in the shoot apical meristem intact and appears to be a facile way to

146 itiation in the peripheral zone of the shoot apical meristem involves a transition to determinate cel

147 The higher-plant shoot apical meristem is a dynamic structure continuously prod

148 uxin importer LIKE AUX1 and boundary gene NO APICAL MERISTEM is activated.

149 bidopsis (Arabidopsis thaliana) primary root apical meristem is composed of the quiescent (or organiz

150 ation and differentiation in the plant shoot apical meristem is controlled by regulatory loops involv

151 During this process, the shoot apical meristem is converted to an inflorescence meriste

152 2 does not recognize CLV3 and that the shoot apical meristem is immune to bacteria independently of C

153 naling in the rib meristem (RM) of the shoot apical meristem is necessary and sufficient for stem cel

154 During early seedling development, the shoot apical meristem is protected from damage as the seedling

155 o the shoot apex, where the vegetative shoot apical meristem is restructured into a reproductive meri

156 expression and polarity of PIN1 in the shoot apical meristem is thought to be regulated primarily by

157 eceptor, regulating development of the shoot apical meristem, is involved in autoregulation of nodula

158 used to sequence the transcriptomes of shoot apical meristems isolated from two inbred lines of maize

159 stribution and is enriched in shoot and root apical meristems, lateral root primordia, the vascular s

160 wed that the kinases accumulate in the shoot apical meristem, leaf primordium, and emerging petiole.

161 This includes the root cap and root apical meristems, leaf primordia, tips of older leaves,

162 , and displayed delayed flowering, increased apical meristem life, and altered vascular development r

163 t1 in a gene annotated as encoding a NAM (no apical meristem)-like protein (here designated Medicago

164 late embryo development, and embryonic root apical meristem lines) based on their dominant expressio

165 , such as leaves, are derived from the shoot apical meristems located at the growing tips.

166 ADT3 is expressed in the cotyledon and shoot apical meristem, mainly in the cytosol, and that the epi

167 been proposed to be important regulators of apical meristem maintenance and to be expressed in apica

168 MPY/WOX9 that is required for root and shoot apical meristem maintenance roots and which has previous

169 nd in planta with proteins involved in shoot apical meristem maintenance such as WUSCHEL, KNAT1/BP, K

170 dodermal cell fate; it is also essential for apical meristem maintenance, ground tissue patterning, v

171 , an essential gene in Arabidopsis, in shoot apical meristem maintenance.

172 al transduction pathway that regulates shoot apical meristem maintenance.

173 ncatula, we isolated a weak allele of the no-apical-meristem mutant mtnam-2.

174 ion enriched within a subdomain of the shoot apical meristem, mutant phenotype showing defect in pola

175 * The CUP-SHAPED COTYLEDON (CUC)/NO APICAL MERISTEM (NAM) family of genes control boundary f

176 We discovered a novel imprinted gene no-apical-meristem (NAM) related protein1 (nrp1) that was e

177 er analysis identified potential NAC (for no apical meristem [NAM], Arabidopsis transcription activat

178 The shoot apical meristem of angiosperm plants generates leaf, ste

179 (KNOTTED1-like homeobox) genes in the shoot apical meristem of Arabidopsis is required for maintenan

180 ly dividing fields of cells within the shoot apical meristem of Arabidopsis show dynamic regulation o

181 SNF2-class ATPase SPLAYED (SYD) in the shoot apical meristem of Arabidopsis.

182 The shoot apical meristem of higher plants is characterized by a c

183 The indeterminate shoot apical meristem of plants is characterized by the expres

184 o formation after germination from the shoot apical meristem of seedlings in culture.

185 The shoot apical meristem of the er erl1 erl2 triple mutant produc

186 in flower tissue, vascular tissue and in the apical meristem of young plants.

187 Shoot apical meristems of higher plants are dome-like structur

188 the expansion of WUS expression in the shoot apical meristems of strong clv1 mutants.

189 ranscriptional profiling in developing shoot apical meristems of vrs3 suggested that VRS3 acts as a t

190 has a documented role, such as in the shoot apical meristem or in the vasculature of Arabidopsis (Ar

191 esophyll, vascular bundles, epidermis, shoot apical meristem, or root.

192 ts of three major processes: arrest of shoot apical meristem, organ senescence, and permanent suppres

193 meristem maintenance and to be expressed in apical meristem "organizers." Here, we focus on the role

194 showed that the TAS3 ta-siRNA pathway and no apical meristem (ortholog of Arabidopsis cup-shaped coty

195 e meristem e.g. the quiescent centre of root apical meristem (RAM) and the lower half of the central

196 ed GR2 is essential for root growth and root apical meristem (RAM) maintenance.

197 Mutant sav6 plants also show reduced root apical meristem (RAM) size and defective quiescent centr

198 In CLEL peptide-induced long roots, the root apical meristem (RAM) was enlarged and consisted of an i

199 tes, delayed leaf senescence, a smaller root apical meristem (RAM), reduced primary and lateral root

200 y a significant role, including cells in the apical meristem region and in young leaves that would be

201 velop embryo-like proliferations in root and apical meristem regions.

202 onstrate that cells in the Arabidopsis shoot apical meristem respond to local mechanical stresses by

203 d the arrest of mitotic activity in the root apical meristem, resulting in a short-root phenotype.

204 vels in the hook region (including the shoot apical meristem) reveals genes involved in cell division

205 in rapidly growing tissues such as the shoot apical meristem, roots and seeds.

206 plays an essential role in regulating shoot apical meristem (SAM) activity and shoot architecture.

207 An analysis of several shoot apical meristem (SAM) activity-related gene expression p

208 The shoot apical meristem (SAM) acts as a reservoir for stem cells

209 e CLSM image stacks of the Arabidopsis Shoot Apical Meristem (SAM) and have shown that the AQVT based

210 Plant stem cells in the shoot apical meristem (SAM) and root apical meristem are neces

211 inct pluripotent cell populations: the shoot apical meristem (SAM) and root meristem (RM), which post

212 the shoot apex, which consists of the shoot apical meristem (SAM) and the flanking leaf primordia.

213 ARK1 is expressed in the shoot apical meristem (SAM) and the vascular cambium, and is d

214 idopsis, the central stem cells of the shoot apical meristem (SAM) are indefinitely maintained, where

215 The maize (Zea mays) shoot apical meristem (SAM) arises early in embryogenesis and

216 ase); the upper blade emerges from the shoot apical meristem (SAM) before the expansion of the lower

217 nnual plants, in perennial plants, the shoot apical meristem (SAM) can undergo seasonal transitions b

218 The shoot apical meristem (SAM) comprises a group of undifferentia

219 The maize shoot apical meristem (SAM) comprises a small pool of stem cel

220 daries from the stem cell niche in the shoot apical meristem (SAM) determines the patterning and arch

221 The shoot apical meristem (SAM) determines these patterns, which v

222 u (han), which affects both flower and shoot apical meristem (SAM) development in Arabidopsis thalian

223 leaves, initiate at the flanks of the shoot apical meristem (SAM) following auxin maxima signals; ho

224 ain transcription factor essential for shoot apical meristem (SAM) formation and sustained activity.

225 change that transforms the fate of the shoot apical meristem (SAM) from a leaf-bearing vegetative mer

226 Flowers form on the flanks of the shoot apical meristem (SAM) in response to environmental and e

227 The shoot apical meristem (SAM) is a collection of stem cells that

228 Enlargement and doming of the shoot apical meristem (SAM) is a hallmark of the transition fr

229 The shoot apical meristem (SAM) is a small population of stem cell

230 stem cell niche, contained within the shoot apical meristem (SAM) is maintained in Arabidopsis by th

231 The shoot apical meristem (SAM) is specified by two complementary

232 CM) from the developmentally important shoot apical meristem (SAM) of maize (Zea mays L.).

233 Different with model plants, the shoot apical meristem (SAM) of Moso is composed of six layers

234 Stem cells in the shoot apical meristem (SAM) of plants are the self-renewable r

235 re key regulators that function at the shoot apical meristem (SAM) of plants to promote differentiati

236 The shoot apical meristem (SAM) produces all of the plant's aerial

237 Shoot apical meristem (SAM) structure varies markedly within t

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

243 Leaves develop from the shoot apical meristem (SAM) via recruitment of leaf founder ce

244 We address this question for the shoot apical meristem (SAM) which harbors pluripotent stem cel

245 The shoot apical meristem (SAM), a specialized tissue producing pl

246 The cell walls of the shoot apical meristem (SAM), containing the stem cell niche th

247 a stem cell marker in the Arabidopsis shoot apical meristem (SAM), was expressed in expanded regions

248 growth depends on the activity of the shoot apical meristem (SAM), where organ primordia are initiat

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

251 ically through the phloem to reach the shoot apical meristem (SAM).

252 dependent upon the maintenance of the shoot apical meristem (SAM).

253 s in all lateral organs as well as the shoot apical meristem (SAM).

254 the adoption of floral identity by the shoot apical meristem (SAM).

255 , ADF9, is moderately expressed in the shoot apical meristem (SAM).

256 expressed in floral meristems and the shoot apical meristem (SAM).

257 differentially regulated in the maize shoot apical meristem (SAM).

258 lure of bps1 mutants to maintain their shoot apical meristem (SAM).

259 lower half of the central zone of the shoot apical meristem (SAM).

260 n of a population of stem cells in the shoot apical meristem (SAM).

261 a from a specialized tissue called the shoot apical meristem (SAM).

262 evelopmental cues that converge at the shoot apical meristem (SAM).

263 that is transported from leaves to the shoot apical meristem (SAM).

264 meristematic properties resembling the shoot apical meristem (SAM).

265 Shoot apical meristems (SAMs) harbor a small set of stem cells

266 oring individual cell divisions in the shoot apical meristems (SAMs) of Arabidopsis thaliana.

267 Shoot apical meristems (SAMs) of higher plants harbor a set of

268 Shoot apical meristems (SAMs) of higher plants harbor stem-cel

269 light on the transcriptome of columnar shoot apical meristems (SAMs), the molecular mechanisms of col

270 perpetuation of stem cell pools called shoot apical meristems (SAMs).

271 e-ground plant organs are derived from shoot apical meristems (SAMs).

272 ure (RSA), reduces primary root growth, root apical meristem size, and meristematic activity in Arabi

273 erving that shade induces increases in shoot apical meristem size, we then describe gene expression c

274 eristem and the quiescent center of the root apical meristem, suggesting that they may somehow functi

275 ry for silencing spread just below the shoot apical meristem that blocks movement upward from the roo

276 rgely unrecognized zone of tissue, below the apical meristem, that is resistant to the silencing sign

277 ore morphological changes occur in the shoot apical meristem, the expression of floral repressors in

278 In the shoot apical meristem, the PIN-FORMED1 (PIN1) efflux carrier c

279 The targets of CLV1/CLV2 in the shoot apical meristem, the WUSCHEL (WUS)-RELATED HOMEOBOX (WOX

280 l contexts, including its role in regulating apical meristems, the patterning of the root, the develo

281 origen, that promotes flowering at the shoot apical meristem; the vernalization process in which expo

282 ation between different regions of the shoot apical meristem to coordinate loss of stem cells from th

283 in that travels from the leaves to the shoot apical meristem to promote flowering.

284 e-responsive element binding protein, and no apical meristem transcription factors.

285 as sufficient to accelerate flowering at the apical meristem under noninductive (short-day) condition

286 Growth was modelled as the dynamics of root apical meristems, using Partial Differential Equations.

287 Differentiation of new apical meristems was forced by decapitating the plants a

288 Trajectories of root apical meristems were used to deform root domains, the b

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

293 In the root apical meristem, which contains the stem cells that feed

294 pluripotent cell population called the shoot apical meristem, which generates the entire above-ground

295 cture results from the activity of the shoot apical meristem, which initiates leaves, internodes, and

296 ctures from the peripheral zone of the shoot apical meristem, which requires class I KNOTTED-LIKE HOM

297 species display a delayed maturation only in apical meristems, which leads to modest branching.

298 Leaf primordia initiate from the shoot apical meristem with inherent polarity; the adaxial side

299 In Arabidopsis shoot apical meristems, WUSCHEL (WUS), a stem cell-promoting t

300 essed BR genes prevailed in the stele of the apical meristem zone.