ライフサイエンスコーパス: cotyledon

1 a, accumulated in whole soybean sprouts and cotyledon.

2 logy and to the identity of the single maize cotyledon.

3 r motion within the glassy matrix of the pea cotyledon.

4 red in the isolated perfused human placental cotyledon.

5 ched at sites of stomatal pore initiation in cotyledons.

6 mobilization from the lipid reserves in the cotyledons.

7 lutathione transferase from soybean seedling cotyledons.

8 lakoid membranes in chloroplasts of seedling cotyledons.

9 5% CHG and 9% CHH contexts was methylated in cotyledons.

10 (C20:1) were preferentially localized to the cotyledons.

11 ent with those previously reported in jojoba cotyledons.

12 First, seedlings detect light and open their cotyledons.

13 yos that could be classified as early curled cotyledons.

14 yos that could be classified as early curled cotyledons.

15 he microsomal membranes of developing peanut cotyledons.

16 determining the boundary region between the cotyledons.

17 t that LAX2 regulates vascular patterning in cotyledons.

18 teral symmetry associated with initiation of cotyledons.

19 he AINTEGUMENTA transcript normally found in cotyledons.

20 tricted auxin distribution pattern in abcb19 cotyledons.

21 s, most strikingly in hypocotyls but also in cotyledons.

22 was expressed in the cytoplasm of developing cotyledons.

23 expansion of cotton (Gossypium hirsutum L.) cotyledons.

24 e family, leading to auxin production in the cotyledons.

25 th, and ectopic root hairs on hypocotyls and cotyledons.

26 e partial-loss-of-function lines have larger cotyledons.

27 d from the kinetics of AA in both leaves and cotyledons.

28 obtained from one day germinated black bean cotyledons.

29 guration in the hypocotyls compared with the cotyledons.

30 e elongation by inducing auxin production in cotyledons.

31 dently of 3-IPA-mediated IAA biosynthesis in cotyledons.

32 is and inducing auxin accumulation in tomato cotyledons.

33 k beans was lower than that observed for raw cotyledons.

34 NA is more highly expressed in roots than in cotyledons.

35 ted flours from roasted and unroasted marama cotyledons.

36 tomatal precursor complexes in mature embryo cotyledons.

37 leaf phloem and to the epidermis of the seed cotyledons.

38 hromatin in a decondensed state in etiolated cotyledons.

39 Furthermore, REF6 targets CUP-SHAPED COTYLEDON 1 (CUC1), which harbors CTCTGYTY motifs, to mo

40 of transcription factors that include LEAFY COTYLEDON 1 (LEC1), LEC1-LIKE (L1L), and B3 domain facto

41 e embryo development master regulators LEAFY COTYLEDON 1 and 2, FUSCA 3, and ABSCICIC ACID INSENSITIV

42 Knockout of GLABRA2 did not affect LEAFY COTYLEDON 1 and PICKLE expression in developing embryo.

43 porter expression and activity of CUP-SHAPED COTYLEDON 2 (CUC2), WUSCHEL (WUS), PIN-FORMED 1 (PIN1),

44 EC1-LIKE (L1L), and B3 domain factors, LEAFY COTYLEDON 2 (LEC2), FUSCA3 (FUS3), and ABSCISIC ACID INS

45 g a lesion in the transcription factor LEAFY COTYLEDON 2 (LEC2; At1g28300).

46 ent mutant using the promoters of CUP-SHAPED COTYLEDON 3 (CUC3) and AINTEGUMENTA (ANT).

47 The npy1 pid double mutants fail to form any cotyledons, a phenotype that is also observed in yuc1 yu

48 Wounding one cotyledon activated the reporter in both aerial and root

49 s revealed a strong expression in the embryo cotyledon and axis throughout the maturation phase.

50 wo 18:3n-3 acyl groups were elevated in both cotyledon and embryonal axis.

51 t apex (meristem and leaf primordia) and the cotyledon and found >5700 differentially expressed genes

52 e flowering time and root growth; control of cotyledon and hypocotyl growth requires simultaneous phy

53 ic metabolic models predicted that the outer cotyledon and hypocotyl/radicle generate the bulk of pla

54 Cotyledon and leaf growth and the accumulation of photos

55 sfc cotyledon and leaf veins are largely fragmented, unlike

56 We show that ADT3 is expressed in the cotyledon and shoot apical meristem, mainly in the cytos

57 ructs enhance luciferase expression in leaf, cotyledon and stem tissues, but to a lesser extent in ro

58 torage metabolism is predicted for the outer cotyledon and the hypocotyl/radicle only.

59 loss of high-complexity vascular networks in cotyledons and a drastic increase in both provascular an

60 g in auxin accumulation in the hypocotyl and cotyledons and a reduction in auxin levels in the root a

61 onfers persistent marginal growth to leaves, cotyledons and floral organs.

62 l and distal cell zones in minimally wounded cotyledons and further enhanced in wounded tissues.

63 highest in rapidly expanding 3- to 4-day-old cotyledons and gradually decreased during the slow-down

64 l seeds grown in Algeria were separated into cotyledons and hulls.

65 apm1 mutants have multiple, fused cotyledons and hypocotyls with enlarged epidermal cells

66 duction into the epidermis of hypocotyls and cotyledons and into the cortex of roots.

67 sive wall ingrowths are ubiquitous in mature cotyledons and juvenile leaves, but dramatically less so

68 Mutations in MtNAM also lead to fused cotyledons and leaflets of the compound leaf as well as

69 omato leafless (lfs) mutants fail to produce cotyledons and leaves and grow a naked pin while maintai

70 lue, and red light) seedlings, as well as in cotyledons and leaves from plants grown in a greenhouse.

71 ermal pavement cells of Arabidopsis thaliana cotyledons and leaves is thought to take place via tip-l

72 At the seedling stage, cotyledons and leaves of nsn1 formed upward curls.

73 In Arabidopsis thaliana, cotyledons and leaves synthesize indole-3-acetic acid (I

74 dically observed in other tissues, including cotyledons and leaves.

75 the developing embryos and the primordia of cotyledons and leaves.

76 topically in the meristem-like outgrowths in cotyledons and leaves.

77 NA level during development were similar for cotyledons and leaves.

78 l, accumulated to over 20% of fatty acids in cotyledons and leaves.

79 In ggt1 plants, the cotyledons and older leaves yellowed early, and GSSG, th

80 Selenium was primarily located in cotyledons and roots of seed embryos.

81 and isoflavones were quantified in sprouts, cotyledons and seed coats of black beans (Phaseolus vulg

82 pif1 seedlings displayed more open cotyledons and slightly reduced hypocotyl length compare

83 ns and flavonoids extracted from seed coats, cotyledons and sprouts.

84 gs responds to an interorgan signal from the cotyledons and that phloem transport of photosynthesis-d

85 occur in a basipetal gradient away from the cotyledons and that this is coincident with a gradient o

86 asts develop in different cell types, namely cotyledons and the dimorphic chloroplasts of the C(4) pl

87 recursors are distributed differently within cotyledons and the hypocotyl/radicle axis in embryos of

88 yogenesis, affecting the shape and number of cotyledons and the hypophysis, and is seedling lethal at

89 distinct regions that will give rise to the cotyledons and the shoot apical meristem.

90 plants, sis3 mutants develop green, expanded cotyledons and true leaves when sown on medium containin

91 re isolated from green cotyledons, etiolated cotyledons and true leaves, and responded to a wide rang

92 fects in rh3-4 were alleviated in 2-week-old cotyledons and true leaves.

93 coat, as shown by the lack of CHS siRNAs in cotyledons and vegetative tissues.

94 cted into the intercellular spaces of cotton cotyledons and, after incubation, the digested substrate

95 n patterns in the major light-sensing organ (cotyledons) and in rapidly elongating hypocotyls of Arab

96 rmal cotyledons (small, cup-shaped, or fused cotyledons), and altered leaf venation.

97 hly reduced venation, initiation of multiple cotyledons, and gradual loss of the SAM accompany these

98 ence red light in the top section (meristem, cotyledons, and hook), and the Trp-independent pathway a

99 ntly to regulate the development of embryos, cotyledons, and leaves.

100 20, 25 or 30 min, then dehulled to separate cotyledons, and pastes were prepared from these.

101 Furthermore, callus formation in roots, cotyledons, and petals is blocked in mutant plants incap

102 d by the root apical meristem and hypocotyl, cotyledons, and shoot apical meristem.

103 meristem (ortholog of Arabidopsis cup-shaped cotyledon) antagonistically regulate both leaf margin de

104 phloem transport velocity is correlated with cotyledon area, a pattern that is apparent both during c

105 3 TAG increase occurred predominantly in the cotyledon, as determined with matrix-assisted laser deso

106 tant/ATP via photosynthesis, while the inner cotyledon, being enclosed by the outer cotyledon, is for

107 Post-germination cotyledon blade expansion in abcb19 was 65% slower than

108 oncentrations, NAE 18:3 specifically induced cotyledon bleaching of light-grown seedlings within a re

109 o establish the embryonic SAM and to specify cotyledon boundaries, and STM controls CUC expression po

110 other genes related to the specification of cotyledon boundary and abaxial identity.

111 g the activities of the CUC promoters in the cotyledon boundary during embryogenesis in sensitized ba

112 genes in promoting the establishment of the cotyledon boundary, without affecting the primary shoot

113 ration of carotenoids in fruits, flowers and cotyledons, but not in mature leaves.

114 lls and sub-epidermal cells of the embryonic cotyledons, but rather accumulates with Fe in the cells

115 gely by GNL1 availability at early stages of cotyledon cell expansion but by BFA-sensitive GEFs when

116 plays a major role in driving root hair and cotyledon cell expansion during seedling development.

117 ansion and heterochromatin rearrangements in cotyledon cells are achieved similarly under light and d

118 In lon2 cotyledon cells, matrix proteins were localized to perox

119 sced oil within the void spaces of disrupted cotyledon cells.

120 CHH methylation levels in cotyledons changed greatly from 6% at the early stage to

121 d by the microRNA164A (MIR164A)/ChCUP-SHAPED COTYLEDON (ChCUC) module and ChASYMMETRIC LEAVES1 (ChAS1

122 sable to sustain photosynthesis performed by cotyledons chloroplasts, which is essential for early pl

123 s mapped to Mendel's I locus responsible for cotyledon color (yellow versus green) in peas.

124 yos, visually inspected from torpedo to bent cotyledon, consistent with no reduction in postgerminati

125 the cytosol, and that the epidermis of adt3 cotyledons contains higher levels of ROS Genome-wide pro

126 evelopmental delay only, although leaves and cotyledons continued to show chlorosis and altered chlor

127 actor BZR1 directly represses the cup-shaped cotyledon (CUC) family of organ boundary identity genes.

128 n Arabidopsis thaliana, the three CUP-SHAPED COTYLEDON (CUC) genes are responsible for determining th

129 The CUP-SHAPED COTYLEDON (CUC) genes CUC1, CUC2 and CUC3 act redundantl

130 tion activation factor (ATAF) and cup-shaped cotyledon (CUC) transcription factor 007 in Picea glauca

131 * The CUP-SHAPED COTYLEDON (CUC)/NO APICAL MERISTEM (NAM) family of genes

132 ion activation factor [ATAF], and cup-shaped cotyledon [CUC])-domain transcription factor) and ETHYLE

133 We show that cotyledon-derived auxin is both necessary and sufficient

134 totrophic growth due to severe inhibition of cotyledon development and nutrient mobilization from the

135 eactive oxygen species (ROS) homeostasis and cotyledon development in etiolated Arabidopsis (Arabidop

136 Consistent with a role for auxin in cotyledon development, BOBBER1 mutants fail to express l

137 are involved in embryo apical patterning and cotyledon development.

138 the role of ABCB19 and auxin distribution in cotyledon development.

139 orks for light-regulated meristem, leaf, and cotyledon development.

140 nscript levels during the stages of seedling cotyledon development.

141 the lipid composition of the inner and outer cotyledons differed from each other, a remarkable discov

142 ain and/or to promote the development of the cotyledon domains.

143 re different in embryonic axes compared with cotyledons during germination and seedling growth, with

144 port of auxin through the petioles of abcb19 cotyledons during the period of maximum expansion.

145 scopy showed ABCB19 protein to be present in cotyledons during their main growth phase, but not later

146 GNL1 availability during expansion stages of cotyledon epidermal cells, an exquisite model system for

147 ly, notably so for chloroplast production in cotyledon epidermal cells.

148 In addition, loss of ADT3 disrupts cotyledon epidermal patterning by affecting the number a

149 ABCB19 was present in the plasma membrane of cotyledon epidermal, mesophyll and petiole cells during

150 Petiole cells in the cotyledon epidermis exhibit well-aligned microtubule arr

151 Plants with reduced DEK1 activity produce cotyledon epidermis with protodermal characteristics, de

152 k to understand the cell defects in the adt3 cotyledon epidermis.

153 viable protoplasts were isolated from green cotyledons, etiolated cotyledons and true leaves, and re

154 ulation dominate transcripts specific to the cotyledon, even in etiolated seedlings.

155 Cotyledons exhibit a net-like array in pavement cells an

156 area, a pattern that is apparent both during cotyledon expansion and after source area manipulation.

157 ion of hypocotyl elongation and promotion of cotyledon expansion and root growth.

158 Taken together, these data indicate that cotyledon expansion during the establishment of photoaut

159 vity to the addition of JA along with ABA in cotyledon expansion experiments.

160 Conversely, primary root growth and cotyledon expansion in blue light were promoted by cytop

161 far-red, and blue light, along with reduced cotyledon expansion in red light.

162 A and developmental defects in root hair and cotyledon expansion that reveal previously unknown roles

163 -mediated end-of-day far-red light response, cotyledon expansion, far-red light block of greening, an

164 dundantly with respect to light promotion of cotyledon expansion, repression of hypocotyl elongation

165 prints revealed that both embryonic axes and cotyledons expressed the allergens.

166 Furthermore, the cotyledons fail to bend over to progress to the bent-cot

167 The results suggest that P. alba cotyledon flour could be a new alternative in the formul

168 According to our results, the P. alba cotyledon flour could be considered as a new alternative

169 nal, phytochemical and functional quality of cotyledon flour from Prosopis alba.

170 anidin synthesis throughout young leaves and cotyledons, followed by death of the plants 1 to 2 weeks

171 nse in leaves; (b) the induction kinetics in cotyledons following MFA treatment differed greatly from

172 g actions of KANADI and HD-ZIPIII factors on cotyledon formation (KANADI represses and HD-ZIPIII prom

173 ion (KANADI represses and HD-ZIPIII promotes cotyledon formation) occur through their opposing action

174 tin remodeling ATPase, that result in strong cotyledon fusion in cuc2-1.

175 atbrm also enhances cotyledon fusion in loss-of-function cuc1 and cuc3 mutan

176 These results show that cotyledon-generated auxin regulates hypocotyl elongation

177 Genetic interactions with the CUP-SHAPED COTYLEDON genes CUC2 and CUC3 revealed a role for LOF1 i

178 ta, AtGRXcp expression was elevated in young cotyledons, green tissues, and vascular bundles.

179 cid-induced blockage of seed germination and cotyledon greening is reduced in CK2 alpha subunit mutan

180 alysis of ABA responses in seed germination, cotyledon greening, and root growth as well as salt and

181 In this mutant, NO supplementation induced cotyledon greening, chloroplast differentiation, and hor

182 m Fusarium oxysporum inhibited both root and cotyledon growth and triggered cell death, thereby gener

183 t inhibition of hypocotyl and stimulation of cotyledon growth as diagnostic criteria for normal deeti

184 more sensitive to inhibition by A2C than is cotyledon growth.

185 Ablation of the root system or cotyledons had no effect on the timing of vegetative pha

186 ation, epicatechin remained in the fermented cotyledon in high concentrations.

187 avoid the medial axis being diverted by the cotyledons in areas where the two come in contact.

188 chain reaction to determine cpDNA levels of cotyledons in dark- and light-grown (low white, high whi

189 on, the saponin concentration in sprouts and cotyledons increased 1.9 and 2.1-fold, respectively.

190 The cpDNA content in cotyledons increased after 3 h of light, decreased with

191 on phenotypic alterations, such as epinastic cotyledons, increased apical dominance, and curled leave

192 ts have altered morphology, including larger cotyledons, increased lateral root density, delayed sepa

193 Cotyledon initiation and development during embryogenesi

194 the level of Asc was elevated just prior to cotyledon initiation.

195 enzyme in the intercellular spaces of cotton cotyledons is very low and could be detected most easily

196 inner cotyledon, being enclosed by the outer cotyledon, is forced to grow essentially heterotrophical

197 shoot apical meristem, including cup-shaped cotyledon, lateral organ boundaries, blade-on-petiole, a

198 tively correlated with slender phenotypes in cotyledon, leaflet, and floral organs, an elongated ovar

199 of multiple ectopic meristems and effects on cotyledons, leaves and flowers.

200 d procambial, cambial, and vascular cells of cotyledons, leaves, roots, hypocotyls, and anthers.

201 rs of seed development and include the LEAFY COTYLEDON (LEC) genes LEC1, LEC1-LIKE, LEC2, and FUS3.

202 ription factor that is a member of the LEAFY COTYLEDON (LEC) group of genes.

203 genome scale searches for homologs of LEAFY COTYLEDON-LIKE (L1L; AtNF-YB6), NF-YB transcription fact

204 eld, and that import of amino acids into the cotyledons limits seed protein levels.

205 wn by use of the isolated perfused-placental cotyledon model a decade ago, in vivo confirmation is st

206 n gene expression and the seedling rhythm in cotyledon movement, indicating that the circadian clock

207 easured in isolated perfused human placental cotyledons (n = 5 per experiment) using techniques which

208 a major biosynthetic source of NO in tomato cotyledons, nitrate reductase was shown to be under stri

209 development, several alleles affect seedling cotyledon number.

210 developmental phenotypes, including abnormal cotyledon numbers and higher seed weights.

211 monitor cell cycle progression in leaves and cotyledons of Arabidopsis and/or Nicotiana benthamiana a

212 Cotyledons of cotton cultivar 'Deltapine 5415' bombarded

213 shoot apical meristem and adaxial domain of cotyledons of heart stage embryos.

214 The genes are expressed most strongly in the cotyledons of jojoba seedlings following germination, bu

215 The mineral distribution in the cotyledons of normal and HTC cowpeas were analysed by Pr

216 dly greater in the dark than in the light in cotyledons of the black pine Pinus thunbergii.

217 xisomes (glyoxysomes) mostly confined to the cotyledons of the mature embryos, which resulted in the

218 However, cotyledons of the seedlings from such seeds were abnorma

219 The cotyledons open and expand, the apical hook opens, and t

220 genic processes, including seed germination, cotyledon opening and expansion, chlorophyll accumulatio

221 f1phyB, pif1cry1, and pif1cry2 have enhanced cotyledon opening compared to the single photoreceptor m

222 rated by inhibition of hypocotyl elongation, cotyledon opening, and leaf greening.

223 bition of hypocotyl elongation, induction of cotyledon opening, randomization of gravitropism, and ge

224 However, the hypocotyl and cotyledon-opening phenotypes of shb1 were opposite to th

225 higher concentration of saponins compared to cotyledons or seed coats (p<0.05).

226 the organization of actin filaments in lobed cotyledon pavement cells and the highly elongated single

227 ll catabolism and confer stay-green leaf and cotyledon phenotypes, has been identified in Pisum sativ

228 ased under light conditions, suggesting that cotyledon photomorphogenesis involves a transition from

229 he Aux/IAA protein IAA18 and causes aberrant cotyledon placement in embryos.

230 nstrated cosegregation with the yellow/green cotyledon polymorphism (I/i) first reported by Gregor Me

231 We propose that in cotyledons PPDK may be important in supplying PEP to glu

232 e always observed subjacent to the defective cotyledon primordia cell types in mutant embryos.

233 emporal delay in initiation and outgrowth of cotyledon primordia leads to development of an enlarged

234 to the central domain protodermal cells when cotyledon primordia were first recognizable.

235 nt embryogenesis is the emergence of the two cotyledon primordia, which marks the transition from rad

236 al embryonic domain cell types that generate cotyledon primordia.

237 the embryo including the failure to initiate cotyledon primordia.

238 degradation affects stomatal development in cotyledons, promotes rosette expansion, and modulates gu

239 nating black bean seeds on the production of cotyledon protein hydrolysates (CPH) with antioxidant an

240 PC slides along with antibodies to abundant cotyledon proteins, seed lectin, and Kunitz trypsin inhi

241 tility, reduced hypocotyl length, spoon-like cotyledons, reduced root growth, and ectopic root hairs

242 1 and ara h 3 messenger RNA was detected in cotyledons relative to embryonic axes.

243 de gene expression changes in hypocotyls and cotyledons separately.

244 C1, CUC2 and CUC3 act redundantly to control cotyledon separation in Arabidopsis.

245 ing a general requirement for this ATPase in cotyledon separation.

246 f REF6 causes CUC1 repression and defects in cotyledon separation.

247 ablating or overexpressing PGX3 affects both cotyledon shape and the spacing and pore dimensions of d

248 C and N were measured in different tissues (cotyledons, shells) and extracts (pure theobromine, defa

249 displayed reduced hypocotyl growth, smaller cotyledon size and a reduced number of lateral roots com

250 ayed reduced hypocotyl elongation but normal cotyledon size and only slightly reduced root hair lengt

251 ella cells, root meristem collapse, abnormal cotyledons (small, cup-shaped, or fused cotyledons), and

252 rescent dye traveling in the phloem from the cotyledons (source) to the roots (sink).

253 ion, -331 to -149, exerts a major control on cotyledon specific expression and the level of expressio

254 It appears that LEC2 is required for cotyledon-specific expression of both SUS genes but it i

255 ontent and a developmental arrest beyond the cotyledon stage, suggesting that PORA is not only transi

256 e a similar lethal phenotype at the seedling cotyledon stage, with disorganized veins, swollen root h

257 os do not develop past late torpedo or early cotyledon stage.

258 ns fail to bend over to progress to the bent-cotyledon stage.

259 os, with seedling development blocked in the cotyledon stage; this developmental block was overcome u

260 mutants arrests between heart and early bent cotyledon stages.

261 arrest immediately upon germination and the cotyledons subsequently bleach.

262 ompared with the area around the tips of the cotyledons, suggesting that the site of silencing signal

263 The soybean cotyledon system, already a model system for defense sig

264 ant displayed shorter root hairs and smaller cotyledons than wild type; these cell expansion defects

265 on of the mature dry seed and opening of the cotyledons, the final stage of seedling establishment.

266 in auxin response in lateral root primordia, cotyledon tips, and provascular tissues.

267 IAA levels are reduced in the cotyledon tissue but not meristems or hypocotyls.

268 distributed via embryonic vasculature toward cotyledon tissues.

269 nhibitors were observed: (a) the response in cotyledons to AA treatment differed greatly in magnitude

270 s included using Jas9-VENUS to determine the cotyledon-to-root JA signal velocities on wounding, reve

271 s transcription activation factor/cup-shaped cotyledon transcription factors (ANAC013, ANAC016, ANAC0

272 S TRANSCRIPTION ACTIVATION FACTOR/CUP-SHAPED COTYLEDON) transcription factor Arabidopsis (Arabidopsis

273 erception of low red to far-red shade by the cotyledons triggers hypocotyl cell elongation and auxin

274 ose-TOR signaling in governing the growth of cotyledons, true leaves, petioles, and primary and secon

275 s has longer hypocotyls and slightly smaller cotyledons under continuous R, FR, and B light compared

276 ings have elongated hypocotyls with enlarged cotyledons under various light conditions.

277 The enhanced responses of gene expression, cotyledon unfolding, hypocotyl growth, and greening obse

278 st lobes formed within the first 24 h of the cotyledons unfurling, during the period of rapid cell ex

279 tion of the brefeldin A (BFA) compartment in cotyledons upon application of BFA, suggesting less effi

280 and OPS are part of a complex that controls cotyledon vascular complexity.

281 etic analyses also revealed interaction with cotyledon vascular pattern2, suggesting that lipid-based

282 COTYLEDON VASCULAR PATTERNING1 (CVP1) encodes C-24 STERO

283 Homozygous vcc mutants displayed cotyledon vein networks of reduced complexity and discon

284 ative to cvp1 mutants, such as discontinuous cotyledon vein pattern, and produce novel phenotypes, in

285 te developmental defects, including aberrant cotyledon vein patterning, serrated floral organs, and r

286 fects in shoot apical meristem formation and cotyledon vein patterning.

287 ips1 mutants are defective in embryogenesis, cotyledon venation patterning, root growth, and root cap

288 and (ii) import of amino acids into the seed cotyledons via epidermal transfer cells.

289 ated that lutein content in whole sprout and cotyledon was closely associated with germination in 'Pu

290 umulation of lutein and beta-carotene in the cotyledons was greater in 'Pungsannamulkong' than in 'Bo

291 Nonetheless, development of abcb19 embryonic cotyledons was very similar to that of wild-type.

292 Here, motional properties within dry pea cotyledons were assessed using dynamic mechanical analys

293 Thiamine levels in the seeds and cotyledons were lower in transketolase-overexpressing li

294 Cotyledons were pale and seedling growth was retarded in

295 ypocotyl apex, with weaker expression in the cotyledons, whereas ANT::P1-GFP was specifically targete

296 crude extracts of all stages of the seedling cotyledons, whereas YABBY seemed to be at the lower limi

297 WAG2) completely abolishes the formation of cotyledons, which phenocopies npy1 pid double mutants an

298 ic and cytosolic proteins were detectable in cotyledons, while in cauline leaves the transcript encod

299 VCC leads to an unusually high proportion of cotyledons with high-complexity vein networks.

300 ng roots and were rapidly transported to the cotyledons with the majority of the accumulation inside