ライフサイエンスコーパス: primordia

1 rom the snail (sna) gene, sna-DP (for dorsal primordia).

2 l wall, in guiding organ flattening of organ primordia.

3 plants failed to concurrently initiate leaf primordia.

4 biosynthetic steps induce uninfected nodule primordia.

5 e incorporation of daughter cells into organ primordia.

6 ESR-related (CLE) peptide expressed in organ primordia.

7 S-LIKE (MUL), are overlapped in lateral root primordia.

8 in the shoot apical meristem and young leaf primordia.

9 cruitment for the differentiation of lateral primordia.

10 hoot apical meristem and from incipient leaf primordia.

11 ly in response to zygomorphy of grass floral primordia.

12 ression domain in the ectoderm of the facial primordia.

13 organ boundaries and the emergence of organ primordia.

14 rates of cell division in leaf and vascular primordia.

15 mis, which position incipient leaf or floral primordia.

16 and ECT4 in rapidly dividing cells of organ primordia.

17 loyed to regulate ligule outgrowth from leaf primordia.

18 L1/L2 layers of the shoot meristem and leaf primordia.

19 n in wild-type and liguleless1-R mutant leaf primordia.

20 ssion of infection threads toward the nodule primordia.

21 SoPIN1 functions in the localization of new primordia.

22 red a synthetic morphogen in Drosophila wing primordia.

23 y plan and appropriately positions the organ primordia.

24 precursors and hydathodes in wild-type leaf primordia.

25 ithelial thickness drive elongation of these primordia.

26 caused by abnormal development of the facial primordia.

27 portional subdivision and expansion of these primordia.

28 leaf development program in emerging floral primordia.

29 Loss of GLR3.3 did not affect lateral root primordia.

30 in the subset of cells that give rise to jaw primordia.

31 ction and aberrant placement of lateral root primordia.

32 increased neural crest expands the maxillary primordia.

33 eural crest (CNC) cells into the frontonasal primordia.

34 rt to define the boundary between integument primordia.

35 appear only at the periphery, near the leaf primordia.

36 n auxin distribution and the centers of leaf primordia.

37 ere stunted and aborted most of their flower primordia.

38 erve morphological asymmetries in young leaf primordia.

39 ivity than are developmentally more advanced primordia.

40 le tissues generates reproductive gland-like primordia.

41 apical meristem (SAM) and the flanking leaf primordia.

42 en the shoot apical meristem and leaf/flower primordia.

43 th and the onset of differentiation in organ primordia.

44 cells may be allocated into initiating leaf primordia.

45 ributes to the formation of new lateral root primordia.

46 prevent apoptosis of the extraocular muscle primordia.

47 egenerate after genetic ablation of the wing primordia.

48 s can be caused by signals outside the renal primordia.

49 2a expression is less affected in the facial primordia.

50 evious transplantation of E28 pig pancreatic primordia.

51 ocation of cells within the PZ to form organ primordia.

52 ess diastema mesenchyme of the embryonic jaw primordia.

53 the placement and establishment of new leaf primordia.

54 y arranged primordia and the spacing between primordia.

55 arly stages in the formation of lateral root primordia.

56 nd the subsequent initiation of lateral root primordia.

57 e invagination of mesoderm and posterior gut primordia.

58 fore the divergence of left and right kidney primordia.

59 inconsistent with patterning larger cortical primordia.

60 ve regulator for the outgrowth of young root primordia.

61 ARF3 expression to the medio domain of ovule primordia.

62 ing with the change from flat to dome-shaped primordia.

63 ovule development and is localized in ovule primordia.

64 observed in polyp but not embryonic tentacle primordia.

65 eld for maize foliar (C4) and husk (C3) leaf primordia.

66 hread invasion of the root cortex and nodule primordia.

67 arrest of floral meristems and floral organ primordia.

68 lateral root primordia and all lateral organ primordia.

69 for rx2 in regulating pax6 within the optic primordia, a function for rx1 in maintaining the pluripo

70 complex expression patterns in floral organ primordia; altering the patterns spatially compromised F

71 by morphogenetic mechanisms that shape organ primordia, although factors that link these processes re

72 reased formation of root hairs, lateral root primordia and adventitious roots.

73 shoot apices, floral meristems, lateral root primordia and all lateral organ primordia.

74 Three of these genes are expressed in vein primordia and all showed transcriptional changes in resp

75 progression of infection threads into nodule primordia and cortical infection thread formation is imp

76 amsh1 mutants that only develop small nodule primordia and display stunted shoot growth, and show tha

77 cinylated succinoglycan still induced nodule primordia and epidermal infections, but further progress

78 Sensory primordia and Frizzled gene expression share domains, wi

79 ll groups of stem cells in the axils of leaf primordia and generate vegetative branches and reproduct

80 t the adaxial-abaxial boundary layer of leaf primordia and governs organization and outgrowth of lami

81 ession of Epr3 in the epidermis and cortical primordia and identified key transcription factors contr

82 signaling responses occur locally in nodule primordia and in developing nodules.

83 primarily in the axillary meristem dome and primordia and in developing stolons.

84 ession in the forming midvein of future leaf primordia and in the vasculature of emerging leaves.

85 in ground meristem cells of developing leaf primordia and in Zmscr1;Zmscr1h mutant leaves, most vein

86 Patterning of the primordia and initial organ differentiation were not aff

87 ndodermal cells overlying early lateral root primordia and is additionally induced by auxin in the ba

88 labeled cells were later found in the ocular primordia and muscle and non-muscle forming tissues of t

89 logy, including NC allocation within the jaw primordia and NC-mediated proliferation, have been impor

90 ulting in altered shapes of the lateral root primordia and of the overlaying cells.

91 iotemporal control of the formation of organ primordia and organ boundaries from the stem cell niche

92 Likewise, tunicate atrial siphon primordia and posterior (otic, lateral line, and epibran

93 broad regions spanning the space between new primordia and previously formed vasculature, suggesting

94 on thread grows toward the developing nodule primordia and rhizobia are taken up into the nodule cell

95 The Fe-stimulated emergence of lateral root primordia and root cell elongation depended on the rootw

96 scribe gene expression changes in early leaf primordia and the meristem using laser microdissection.

97 operiod, whilst its presence in lateral root primordia and the root apical meristem negatively regula

98 is expressed in founder cells, lateral root primordia and the root apical meristem.

99 ells are organized into hexagonally arranged primordia and the spacing between primordia.

100 ression repressed the growth of lateral root primordia and their emergence from the primary root.

101 ow plants control the number of lateral root primordia and their emergence through the main root.

102 to establish the connections between tendon primordia and their respective musculoskeletal counterpa

103 roots and lateral roots, and in lateral root primordia and tips.

104 glandular secretory trichomes (GSTs) of leaf primordia and top expanded leaves.

105 to apical subdomains such as emerging flower primordia, and a large class with high expression in div

106 ected and lobed regions of neighboring petal primordia, and between lower and upper portions of the c

107 nine mFSCs colonize the caudal and anal fin primordia, and daughters of different mFSCs always inter

108 iptomic analysis during Bailinggu's mycelia, primordia, and fruiting body stages to identify genes re

109 X3) homolog expressed at the margins of leaf primordia, and is required for mediolateral outgrowth.

110 und in the inflorescence meristem and floral primordia, and its protein was localized to the nucleoli

111 esoderm upon feeding, migrate into the gonad primordia, and mature into germ cells.

112 ere induced at infection sites and in nodule primordia, and mutation of ARF16a reduced rhizobial infe

113 tumour 1a (wt1a) as a marker to label kidney primordia, and performed quantitative analyses of the mi

114 her, in genetic backgrounds in which the leg primordia are absent, the DP are still partially specifi

115 ertebrate embryonic structures such as organ primordia are composed of confluent cells.

116 y of the nasal capsules and their developing primordia are dependent on Fgf8.

117 However, once arch primordia are established the effects of BMPs become res

118 Organ primordia are formed in the circular peripheral zone (PZ

119 nals from the dorsal forebrain and olfactory primordia are required to specify nasal identity in the

120 ate otic placodes and tunicate atrial siphon primordia are thought to be homologous based on morpholo

121 aves, and the precise arrangement of feather primordia, are lost in the flightless emu and ostrich, t

122 that become incorporated into lateral organ primordia around the meristem periphery.

123 f both STM and LFY/FLO were detected in leaf primordia, associated with regions from which leaflets a

124 are mutated, cells are allocated to lateral primordia at a higher rate, causing a net loss of cells

125 the er erl1 erl2 triple mutant produces leaf primordia at a significantly reduced rate and with alter

126 Rice stems develop adventitious root (AR) primordia at each node that slowly mature but emerge onl

127 The transcripts of LLS1 can be detected in primordia at early stages of leaf initiation and later i

128 , kaempferol accumulated within lateral root primordia at higher levels than wild-type.

129 enish cells that are incorporated into organ primordia at the meristem periphery and leave the merist

130 e coexpressed in incipient and emergent leaf primordia at the shoot apex, but not in the vegetative m

131 l signaling feedback from the incipient leaf primordia back to the meristem that is required to regul

132 signals from differentiating cells in organ primordia back to the stem cell niche and that appears t

133 l stage on, long before the androgenic gland primordia begin to differentiate, and exponentially thro

134 genitally fused, laterally positioned carpel primordia bisected by two medially positioned meristemat

135 in the nuclei of central meristem and organ primordia but at a low level in organ boundary cells to

136 he inability of dgt to initiate lateral root primordia but not the primordia outgrowth.

137 paralogs are co-expressed in lateral floral primordia, but not within the FM.

138 naling axis regulates formation of OFT valve primordia by controlling smooth muscle differentiation o

139 gnaling reporter is blocked in the orofacial primordia by Lrp6 deletion in mice.

140 oliferation and organ growth in flower organ primordia by maintaining the meristematic competence of

141 er, low levels of WUS lead to enlarged organ primordia, by elevating the responsiveness of the PZ cel

142 Rarely, in male genital discs these primordia can develop into sperm-filled testicular sperm

143 port here that the frontonasal and upper jaw primordia cannot be formed after conditional ablation of

144 ce application to epidermal cells above root primordia caused cell death in a dose-dependent manner a

145 ed periclinal divisions in this lateral root primordia cell layer and perturbed the formation of QC p

146 e of MtNSP2 and MtCCS52A in roots and nodule primordia, chromatin immunoprecipitation-quantitative PC

147 r spread of the fusion protein in the mutant primordia compared with the wild type.

148 uction of any PLT clade member in the mutant primordia completely restores layer identities at stage

149 inates from bilateral third pharyngeal pouch primordia containing endodermal progenitors of both thym

150 ts demonstrate that cells from the early leg primordia contribute to both ventral and dorsal appendag

151 h increase in auxin response in lateral root primordia, cotyledon tips, and provascular tissues.

152 ed ectopic stages II, IV, and V lateral root primordia; decreased auxin maxima in indole-3-acetic aci

153 egetative phase change, but ablation of leaf primordia delayed this transition in a miR156-dependent

154 hanges in Shh and Gli1 expression in the vMb primordia delineated their spatial contribution to the e

155 ANT expression in incipient and young floral primordia depends on auxin transport within the inflores

156 rprisingly, however, third-instar wing blade primordia devoid of compartmental dpp expression maintai

157 of photoperiod was studied on inflorescence primordia differentiation and floral pathway related gen

158 fect the developmental delay of marginal ray primordia during their early ontogeny.

159 eristem activity and the formation of needle primordia during this period.

160 emperature affects the development of flower primordia during this preformation period.

161 hieves distinct Wnt thresholds for the brain primordia earlier compared with diffusion-based transpor

162 n asymmetry in expression in developing leaf primordia early on, while it becomes more symmetric at a

163 In sites of lateral root primordia emergence, both esterified and de-esterified p

164 lantation of wild-type cells into the mutant primordia failed to rescue the krm1(nl10) phenotype, thu

165 s contained large numbers of arrested nodule primordia following B. japonicum inoculation.

166 sna-DP specifically marks the early primordia for both the wing and haltere, collectively re

167 imaginal discs of Drosophila are the larval primordia for the adult cuticular structures of the adul

168 Ovule primordia formation is a complex developmental process w

169 in tomato, by promoting an increase on ovule primordia formation.

170 d PIN7-GFP, normally found below the site of primordia formation.

171 In ern1 mutant roots, nodule primordia formed, but most remained uninfected and bacte

172 lant organogenesis is the emergence of organ primordia from the apical meristems.

173 rol the subsequent separation of these organ primordia from the pharynx are poorly understood.

174 hat is associated with the separation of the primordia from the pharynx is disrupted, resulting in th

175 tional boundary that separates the incipient primordia from the remainder of the meristem.

176 ing face during the crucial period of facial primordia fusion.

177 During the early pupal period (P6-P48) these primordia grow in size and differentiate into the defini

178 Sepal primordia had accelerated cell division, cell enlargemen

179 cluding vertebrates and ascidians, the mouth primordia have been shown to fate to the anterior neural

180 rker for the initiation of adventitious root primordia in Arabidopsis, is enhanced in more axillary g

181 ) signaling in ring muscles defines tentacle primordia in fed polyps.

182 ter revealed that PIN1 expression marks leaf primordia in maize, similarly to Arabidopsis.

183 ssed in the stem tissues that generated root primordia in PtAIL1-overexpressing plants, whereas their

184 ERF12 expression encircles incipient floral primordia in the inflorescence meristem periphery and is

185 nsplanted previously with E28 pig pancreatic primordia in the mesentery, we show normalization of glu

186 prior transplantation of E28 pig pancreatic primordia in the mesentery.

187 The presence of such versatile primordia in the miracrustacean ancestor could account f

188 in subsequently gave rise to the oral siphon primordia in tunicates (with neurosecretory cells being

189 Since both siphon primordia in tunicates give rise to sparse populations o

190 hat Shh null mice have smaller, aparathyroid primordia in which thymus fate specification extends int

191 death correlated with the proximity to root primordia in wild-type and ADVENTITIOUS ROOTLESS1 plants

192 s the formation of more and larger taste bud primordia, including in regions of the tongue normally d

193 The number of lateral root primordia increased in wox7 mutants but decreased in pla

194 ato ontogeny, expression of Tf in young leaf primordia increases, correlating with a rise in leaf dis

195 onic acid also were up-regulated in juvenile primordia; indeed, exogenous application of jasmonic aci

196 It is known that ganglionic primordia initially emerge early and simultaneously duri

197 Dicot leaf primordia initiate at the flanks of the shoot apical mer

198 ty of MSA development had two phases, floret primordia initiated under long and short days, whereas s

199 Emergence of new lateral root primordia, initiated deep inside the root under the infl

200 t AqJAG plays a critical role in controlling primordia initiation and distal growth of floral organs,

201 wing indeterminate inflorescences.(2) Flower primordia initiation and outgrowth depends on the hormon

202 We developed a stochastic model of primordia initiation at the shoot apex, integrating loca

203 ns alter endogenous auxin levels and disrupt primordia initiation in meristems.

204 Primordia initiation is blocked in shr plt1 plt2 mutant.

205 l developmental processes even, as for ovule primordia initiation, if the same set of hormones trigge

206 s (GAs) also play an important role in ovule primordia initiation, inhibiting ovule formation in both

207 Following primordia initiation, the restriction of the broadly act

208 est that LFS transiently acts at the site of primordia initiation, where it provides a specific conte

209 genes and accumulation of auxin at sites of primordia initiation.

210 LLA proteins that will finally promote ovule primordia initiation.

211 to auxin response maxima culminating in leaf primordia initiation.

212 The cellular mechanisms underlying primordia internalization vary greatly among insects and

213 showed progressive outgrowth of lateral root primordia into lateral roots under N-deficient condition

214 ypothesized that transformation of different primordia into plant tumors would require organ-specific

215 Midline convergence of organ primordia is an important mechanism that shapes the vert

216 sts that the process of fusion of the facial primordia is intrinsically buffered against producing ma

217 in maxima and MP direct initiation of flower primordia is poorly understood.

218 The development of leaf primordia is subject to light control of meristematic ac

219 lay in initiation and outgrowth of cotyledon primordia leads to development of an enlarged globular e

220 ession patterns during initiation of lateral primordia (leaves or sporangia).

221 olling the early development of lateral root primordia likely via regulating cell wall synthesis and

222 is enriched in the brain, eyes, pectoral fin primordia, liver and intestinal bulb during embryonic de

223 ts, particularly in zones where lateral root primordia (LRP) initiate and LR differentiate and emerge

224 ateral root formation, when the lateral root primordia (LRP) must traverse three overlying cell layer

225 Lateral root primordia (LRP) originate from pericycle stem cells loca

226 iple mutants, the morphology of lateral root primordia (LRP), the auxin response gradient, and the ex

227 the activation of LR pre-branch sites and LR primordia (LRP).

228 (LRI) and proper development of lateral root primordia (LRP).

229 rmative divisions that generate lateral root primordia (LRP).

230 NRT1.1 represses emergence of lateral root primordia (LRPs) at low concentration or absence of NO3(

231 In Arabidopsis, lateral root primordia (LRPs) originate from pericycle cells located

232 facilitate the emergence of new lateral root primordia (LRPs).

233 pin-like shoots showed reduced expression of primordia markers as well as abnormal auxin distribution

234 eared from boundary subdomains between petal primordia, most likely contributing to formation of cong

235 ansplantation in mesentery of pig pancreatic primordia obtained very early during organogenesis [embr

236 NSN1 gene in the developing embryos and the primordia of cotyledons and leaves.

237 RG-orthologs are expressed in stripes in the primordia of every segment, rather than every other segm

238 e range of transcriptional responses in leaf primordia of G. avellana at different heteroblastic stag

239 e-scale transcriptional analysis of the leaf primordia of G. avellana sheds light on the integration

240 xpressed genes were more highly expressed in primordia of juvenile leaves.

241 caused by reducing EMF1 activity in the leaf primordia of LFYasEMF1 transgenic plants and propose a c

242 expression, relative to amniotes, in the jaw primordia of S. canicula embryos.

243 After initiation, the leaf primordia of species such as Arabidopsis thaliana differ

244 ulature tissue and the outer layer and glume primordia of spikelet pair meristems and floral meristem

245 d DALv2, assemble into structurally distinct primordia of the AOTU, BU, and EB within the late larval

246 the mesenchymal condensations that serve as primordia of the avian limb skeleton.

247 duces regression of the Mullerian ducts, the primordia of the female reproductive tract organs.

248 lefty2 and subsequent reversals in the organ primordia of the heart and gut.

249 By measuring Bmp4 expression in the beak primordia of the species in the genus Geospiza, we provi

250 e of a superoxide-selective probe within the primordia of tt7-2 compared with wild-type, but not in t

251 ased level of kaempferol in the lateral root primordia of tt7-2 reduces superoxide concentration and

252 During flowering, primordia on the flanks of the shoot apical meristem are

253 Subarctic plants develop leaf primordia one or more years prior to flowering (preforma

254 hat de novo QC establishment in lateral root primordia operates via SCR-mediated formative cell divis

255 These differences arise during primordia outgrowth because of more cell divisions in th

256 initiate lateral root primordia but not the primordia outgrowth.

257 transiently expressed at incipient and young primordia, overlapping with auxin response maxima.

258 the interplay between cellular mechanics and primordia patterning that results in self-sustained plan

259 hogenetic movements of pronephric glomerular primordia (PGP) occurring during zebrafish embryonic kid

260 main genes, expressed within or around organ primordia, play a key role in the formation, shaping, an

261 he effect of cytokinin on the development of primordia possibly depends on the robustness and stabili

262 tion, we contrasted these profiles to anther primordia prior to fate specification and to msca1 anthe

263 is expressed in cells overlying lateral root primordia, providing auxin signaling that triggers the e

264 h those found in successively initiated leaf primordia, providing evidence against classic hypotheses

265 naling within developing limbs and orofacial primordia regulate proliferation and differentiation of

266 ns pivotal for patterning of early gynoecium primordia remain unknown.

267 3D structures, which also derive from organ primordia, remains unclear.

268 g LR outgrowth are not induced in the mutant primordia, rendering "PLT-null" LRP.

269 repressed by Ubx in the flys haltere and leg primordia, respectively, and led to the differentiation

270 We find that in leaf primordia, shade avoidance is not mediated through canon

271 ll dynamics in chimeric and protein-depleted primordia shows that Cxcl12a-sensing and cadherin-mediat

272 ended GCC-box elements upstream of LFS drove primordia-specific expression in a LFS-dependent but aux

273 tantly reducing apoptosis in nasal cartilage primordia, suggesting that enhanced BMP signaling induce

274 increase in the number of crk5 lateral root primordia, suggests facilitated auxin efflux through the

275 ilar to the endocrine, develop from the same primordia that give rise to the trachea.

276 Here, we compare transcript levels in primordia that will develop into juvenile or adult leave

277 hoot and root apical meristems, lateral root primordia, the vascular system, and the concave side of

278 MtLAX2 is expressed in nodule primordia, the vasculature of developing nodules, and at

279 n, and instead the entire skin gains feather primordia through a later process.

280 ains the passage of the growing lateral root primordia through the overlaying layers, resulting in al

281 ymus hypoplasia and a failure of these organ primordia to completely separate from the pharynx.

282 Signals that provide feedback from organ primordia to control the stem cell niche in plants have

283 es KNOXI gene expression from incipient leaf primordia to initiate leaves and specify leaf adaxial id

284 This pathway impinges upon various organ primordia to instruct their side-specific development.

285 ithin a single tract extend from dome-shaped primordia to thin conical structures with a common axis

286 n the absence of Hox input, prothoracic horn primordia transform to contribute to ectopic wings.

287 In young ear primordia, TU1 proteins are nuclearly localized in speci

288 idermal cells that overlie adventitious root primordia undergo cell death to facilitate root emergenc

289 g the proximal-distal axis of wild-type leaf primordia undergoing ligule initiation and compared tran

290 ns (OCRs) in developing maize ear and tassel primordia using ATAC-seq and characterize combinatorial

291 ssification of gene expression in early leaf primordia, we identified cohorts of genes associated wit

292 ficial horizontal myoseptum and lateral line primordia were not properly formed in the quadruple muta

293 al function, confining VRN2 to meristems and primordia, where it has specific developmental roles, wh

294 is initiated by a signal(s) produced by leaf primordia, which acts by repressing the transcription of

295 enesis is the emergence of the two cotyledon primordia, which marks the transition from radial symmet

296 on and regular, equidistant spacing of ovule primordia, which may serve to minimize competition betwe

297 erived organs that develop from common organ primordia, which undergo a series of morphological event

298 , we compare the development of lateral root primordia with in vitro plant regeneration and discuss p

299 rom the outer layer of stage II lateral root primordia, within which the SCARECROW (SCR) transcriptio

300 ic of birds in general but lays down feather primordia without a wave, akin to the process of hair fo