ライフサイエンスコーパス: cotyledon

1 ables are consumed as microgreens (developed cotyledons).

2 epidermal cells of Arabidopsis hypocotyl and cotyledon.

3 a, accumulated in whole soybean sprouts and cotyledon.

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

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

6 red in the isolated perfused human placental cotyledon.

7 is and inducing auxin accumulation in tomato cotyledons.

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

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

10 ted flours from roasted and unroasted marama cotyledons.

11 tomatal precursor complexes in mature embryo cotyledons.

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

13 hromatin in a decondensed state in etiolated cotyledons.

14 mobilization from the lipid reserves in the cotyledons.

15 lutathione transferase from soybean seedling cotyledons.

16 lakoid membranes in chloroplasts of seedling cotyledons.

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

18 ent with those previously reported in jojoba cotyledons.

19 First, seedlings detect light and open their cotyledons.

20 yos that could be classified as early curled cotyledons.

21 yos that could be classified as early curled cotyledons.

22 tene, lutein and neoxanthin in fresh mass of cotyledons.

23 he microsomal membranes of developing peanut cotyledons.

24 determining the boundary region between the cotyledons.

25 t that LAX2 regulates vascular patterning in cotyledons.

26 teral symmetry associated with initiation of cotyledons.

27 he AINTEGUMENTA transcript normally found in cotyledons.

28 tricted auxin distribution pattern in abcb19 cotyledons.

29 cells of Arabidopsis (Arabidopsis thaliana) cotyledons.

30 live-cell imaging experiments using detached cotyledons.

31 ched at sites of stomatal pore initiation in cotyledons.

32 5% CHG and 9% CHH contexts was methylated in cotyledons.

33 cal function(s) of LDs after greening of the cotyledons.

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

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

36 obtained from one day germinated black bean cotyledons.

37 guration in the hypocotyls compared with the cotyledons.

38 e elongation by inducing auxin production in cotyledons.

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

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

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

42 xpression of key seed maturation genes LEAFY COTYLEDON 1/2 (LEC1/2), ABSCISIC ACID INSENSITIVE 3, FUS

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

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

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

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

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

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

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

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

51 Cotyledon and leaf growth and the accumulation of photos

52 We conclude nitrate generally controls cotyledon and leaf size by increasing ploidy levels and

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

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

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

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

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

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

59 pting the model to reflect metabolism in the cotyledons and hypocotyl/root axis (HRA).

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

75 The development of mutant cotyledons and root, and the auxin response of mutant se

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

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

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

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

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

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

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

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

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

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

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

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

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

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

90 displayed delayed chloroplast development in cotyledons and young leaves.

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

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

93 seedlings have reduced root length, smaller cotyledons, and arrested pavement cell expansion.

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

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

96 20, 25 or 30 min, then dehulled to separate cotyledons, and pastes were prepared from these.

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

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

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

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

101 3 TAG increase occurred predominantly in the cotyledon, as determined with matrix-assisted laser deso

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

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

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

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

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

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

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

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

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

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

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

113 Cotyledon cells in kidney beans naturally encapsulate st

114 hat were heated when entrapped within intact cotyledon cells, compared to those thermally treated as

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

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

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

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

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

120 the cocoa testa (cocoa shell) and the cocoa cotyledons (cocoa nibs) of cocoa samples from 15 differe

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

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

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

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

125 While in cotyledons (Cots), formation of an alternative loop, enc

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

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

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

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

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

131 t and transcription factors named CUP SHAPED COTYLEDON (CUCs), which are involved in the establishmen

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

133 cts on phyB's functions in the hypocotyl and cotyledon despite inducing similar photobody dynamics, i

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 nscript levels during the stages of seedling cotyledon development.

138 are involved in embryo apical patterning and cotyledon development.

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

140 orks for light-regulated meristem, leaf, and 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 s SUT1 transporter in the leaf phloem and in cotyledon epidermal cells where import into the embryo o

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

169 n hypocotyls requires temperature sensing in cotyledons, followed by the generation of a mobile auxin

170 eous input of the hormone auxin from the two cotyledons forces the vascular cylinder to develop a dia

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

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

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

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

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

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

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

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

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

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

181 attenuates an NAE-18:3-induced degreening of cotyledons in Arabidopsis (Arabidopsis thaliana) seedlin

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

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

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

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

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

187 Cotyledon initiation and development during embryogenesi

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

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

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

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

192 otstocks or halved cotyledon node and single cotyledon leaf on scions and rootstocks.

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

194 ded that grafting without cotyledon node and cotyledon leaves on rootstocks, and with cotyledon node

195 ions, rootstocks, without cotyledon node and cotyledon leaves on scions and rootstocks or halved coty

196 tstocks, and with cotyledon node but without cotyledon leaves on scions were easy to perform and suit

197 this study focused on the cotyledon node and cotyledon leaves retained on scions, rootstocks, without

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

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

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

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

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

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

204 Cotyledons' mass in the whole plant increased under LED

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 We concluded that grafting without cotyledon node and cotyledon leaves on rootstocks, and w

210 aves retained on scions, rootstocks, without cotyledon node and cotyledon leaves on scions and rootst

211 ting approaches of this study focused on the cotyledon node and cotyledon leaves retained on scions,

212 on leaves on scions and rootstocks or halved cotyledon node and single cotyledon leaf on scions and r

213 and cotyledon leaves on rootstocks, and with cotyledon node but without cotyledon leaves on scions we

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

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

216 Cotyledons of cotton cultivar 'Deltapine 5415' bombarded

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

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

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

220 n, neoxanthin and violaxanthin were found in cotyledons of sprouts growing in RGB LED light.

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

222 Roasted cotyledons of the Chilean hazelnut (Gevuina avellana) ar

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

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

225 investigated separately in the coat and the cotyledons of three chosen varieties (black beans, black

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

227 owering, entrainment of the circadian clock, cotyledon opening and expansion, anthocyanin accumulatio

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

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

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

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

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

233 ere cells are unable to endoreplicate fully, cotyledon organ size is achieved through cell division.

234 ma membrane (PM) during the morphogenesis of cotyledon pavement cells (PC) in Arabidopsis.

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

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

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

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

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

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

241 al embryonic domain cell types that generate cotyledon primordia.

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

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

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

245 1 and ara h 3 messenger RNA was detected in cotyledons relative to embryonic axes.

246 de gene expression changes in hypocotyls and cotyledons separately.

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

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

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

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

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

252 utant plants and increased in LGO-OX plants, cotyledon size remains unchanged relative to wild type a

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

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

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

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

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

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

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

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

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

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

266 distributed via embryonic vasculature toward cotyledon tissues.

267 These had the largest proportion of cotyledons to the mass of plants and the highest content

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

286 mical, and genetic perturbations in seedling cotyledons, we found that augmenting HG modification pro

287 press either EPF1 or Stomagen in Arabidopsis cotyledons, we reveal a range within the epidermis and a

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

289 In particular, from 48 h onward, cotyledons were characterized by the oxidation of fatty

290 Lupin cotyledons were fractionated and bile acid adsorbing act

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

292 lorophyll and carotenoid pigment contents in cotyledons were observed under RGB LED and cold white tr

293 Cotyledons were pale and seedling growth was retarded in

294 ole (i.e. in-shell) beans and shelled seeds (cotyledons) were analysed.

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 on in Arabidopsis resulted in orange-colored cotyledons, which are not observed if PSY or GGPS11 are

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

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