ライフサイエンスコーパス: Zea mays

1 sis thaliana) was modified for use in maize (Zea mays).

2 inserts in Nicotiana benthamiana and maize (Zea mays).

3 ranscriptional levels with a focus on maize (Zea mays).

4 nd agronomically important crop plant maize (Zea mays).

5 sis gene transcripts in the C(4) crop maize (Zea mays).

6 neously inducing pathogen defenses in maize (Zea mays).

7 rabidopsis (Arabidopsis thaliana) and maize (Zea mays).

8 eficits occurring during flowering in maize (Zea mays).

9 rus have been shown to induce VIGS in maize (Zea mays).

10 ntogeny of monocot leaf morphology in maize (Zea mays).

11 s directly involved in SC assembly in maize (Zea mays).

12 rabidopsis (Arabidopsis thaliana) and maize (Zea mays).

13 otein against chewing insect pests in maize (Zea mays).

14 ryza sativa) but poorly understood in maize (Zea mays).

15 ased root imaging platform for use in maize (Zea mays).

16 uced mutant alleles of Ca1 and Ca2 in maize (Zea mays).

17 h publicly available information from maize (Zea mays).

18 rabidopsis (Arabidopsis thaliana) and maize (Zea mays).

19 (SMCs) during stomatal development in maize (Zea mays).

20 gain-of-function dominant mutants in maize (Zea mays).

21 (RCA) could improve N acquisition in maize (Zea mays).

22 expanded in a TE-rich genome such as maize (Zea mays).

23 oded by the oil yellow1 (oy1) gene in maize (Zea mays).

24 tein-DNA interaction (PDI) network in maize (Zea mays).

25 attacks many cereal crops, including maize (Zea mays).

26 produced similar gm for Setaria viridis and Zea mays.

27 idopsis thaliana and ZmCKX1 and ZmCKX4a from Zea mays.

28 ccurrences regarded Arabidopsis thaliana and Zea mays.

29 plant Physcomitrella patens and higher plant Zea mays.

30 to an insensitive shuffled variant of maize (Zea mays) 4-hydroxyphenylpyruvate dioxygenase (HPPD), we

31 developmentally regulated splicing in maize (Zea mays), 94 RNA-seq libraries from ear, tassel, and le

32 g) for eye health, while 8 g of cooked mais (Zea mays) a day can provide a high enough level (2 mg) o

33 auxin polar transport, and studies of maize (Zea mays) aberrant phyllotaxy1 (abph1) mutants suggest t

34 l community composition and structure of ten Zea mays accessions along an evolutionary transect (two

35 isorium reilianum causes head smut of maize (Zea mays) after systemic plant colonization.

36 rogen fertilization on GHG fluxes from corn (Zea mays) agro-ecosystems, we conducted a research study

37 find that CENH3 from Lepidium oleraceum and Zea mays, although specifying epigenetically weaker cent

38 We used GRANAR to reanalyze large maize (Zea mays) anatomical datasets from the literature.

39 on of P. nigrum contaminants (Carica papaya, Zea mays and Capsicum annuum) using plant DNA barcodes t

40 resource for constructing the pan-genome of Zea mays and genetic improvement of modern maize varieti

41 alysis of genes in the Arabidopsis thaliana, Zea mays and Oryza sativa anther development pathways sh

42 erved for thousands of Arabidopsis thaliana, Zea mays and Vitis vinifera genes, and have been linked

43 plasmids into rice (Oryza sativa) and maize (Zea mays) and analyzed the results by whole genome seque

44 oop phenotype, whereas sequences from maize (Zea mays) and Arabidopsis (Arabidopsis thaliana) give ph

45 Recombinant maize (Zea mays) and Arabidopsis (Arabidopsis thaliana) NAD(P)H

46 characterization of FNSI enzymes from maize (Zea mays) and Arabidopsis (Arabidopsis thaliana).

47 le-strand breaks in genomes of wheat, maize (Zea mays) and Arabidopsis.

48 mental series performed on soil-grown maize (Zea mays) and barley (Hordeum vulgare) plants.

49 re, interactions between the roots of maize (Zea mays) and faba bean (Vicia faba) are characterized.

50 o maydis infects all aerial organs of maize (Zea mays) and induces tumors in the plant tissues.

51 ugation from etiolated coleoptiles of maize (Zea mays) and leaves of Arabidopsis (Arabidopsis thalian

52 eneration glyphosate-tolerant EPSPS in corn (Zea mays) and now in other crops.

53 genetic architecture of senescence in maize (Zea mays) and other cereals.

54 entral role in pathogen resistance in maize (Zea mays) and other plants.

55 f accumulation have been described in maize (Zea mays) and rice (Oryza sativa) anthers.

56 on cold-responsive gene expression in maize (Zea mays) and sorghum (Sorghum bicolor) allowed us to id

57 olutionary fates of the subgenomes in maize (Zea mays) and soybean (Glycine max) have followed differ

58 enic lifestyle during colonization of maize (Zea mays) and soybean (Glycine max), respectively.

59 ISR-positive and -negative mutants of maize (Zea mays) and the beneficial fungus Trichoderma virens a

60 n Arabidopsis (Arabidopsis thaliana), maize (Zea mays), and rice (Oryza sativa).

61 s Arabidopsis (Arabidopsis thaliana), maize (Zea mays), and rice (Oryza sativa).

62 var. italica), carrot (Daucus carota), corn (Zea mays), and tomato (Solanum lycopersicum).

63 the timing of VPC in Populus tremula x alba, Zea mays, and Arabidopsis thaliana to determine its role

64 h previously published data from S. bicolor, Zea mays, and Oryza sativa to identify a small suite of

65 nd wheat [Triticum aestivum]) and C4 (maize [Zea mays] and Setaria viridis) monocot species.

66 C4 plants are major grain (maize [Zea mays] and sorghum [Sorghum bicolor]), sugar (sugarca

67 dful of species (rice [Oryza sativa], maize [Zea mays], and wheat [Triticum aestivum]) providing most

68 ulus, Oryza sativa, Solanum lycopersicum and Zea mays) are analyzed.

69 ence-indexed insertional libraries in maize (Zea mays) are fundamental resources for functional genet

70 Here, using maize (Zea mays) as a model plant system, we determined the tim

71 f this evolutionary variability using maize (Zea mays) as an experimental system.

72 yr BP and maize (Zea mays) at about 6,850 cal.

73 Here, we fully defined the maize (Zea mays) ATG system transcriptionally and characterized

74 tegrated multiomics approach to study maize (Zea mays) autophagy mutants subjected to fixed-carbon st

75 siae) system to functionally annotate maize (Zea mays) auxin signaling components, focusing on genes

76 Osmotic stress was applied to maize (Zea mays) B73 by irrigation with increasing concentratio

77 e of MAKER-P to update and revise the maize (Zea mays) B73 RefGen_v3 annotation build (5b+) in less t

78 roach involving overexpression of the maize (Zea mays) Baby boom (Bbm) and maize Wuschel2 (Wus2) gene

79 of crops such as rice (Oryza sativa), maize (Zea mays), barley (Hordeum vulgare), and wheat (Triticum

80 BE) types by expressing proteins from maize (Zea mays BE2a), potato (Solanum tuberosum BE1), and Esch

81 eld is an essential long-term goal of maize (Zea mays) breeding to meet continual and increasing food

82 stilago maydis causes smut disease in maize (Zea mays) by infecting all plant aerial tissues.

83 N) would improve drought tolerance in maize (Zea mays) by reducing the metabolic costs of soil explor

84 Here, we show that regulation of maize (Zea mays) C(4)-NADP-ME activity is much more elaborate t

85 tion assays of the naturally silenced maize (Zea mays) C2-Idf (inhibitor diffuse) mutant, defective i

86 Stalk lodging in maize (Zea mays) causes significant yield losses due to breakin

87 deliver Cre recombinase protein into maize (Zea mays) cells.

88 We named this new virus Zea mays chrysovirus 1.

89 tantly related gene, ZmSUT1 from the monocot Zea mays, did restore phloem loading.

90 Maize (Zea mays) displays an exceptional level of structural ge

91 odel grass Brachypodium distachyon and corn (Zea mays) do not possess orthologs of the currently char

92 ) transcription factors important for maize (Zea mays) endosperm development.

93 The maize (Zea mays) enzyme beta-carotene hydroxylase 2 (ZmBCH2) co

94 n example experiment that contains 33 maize (Zea mays 'Fernandez') plants, which were grown for 9 wee

95 versus left as surplus N in 8 million corn (Zea mays) fields at subfield resolutions of 30 x 30 m (0

96 The activity of the maize (Zea mays) florigen gene ZEA CENTRORADIALIS8 (ZCN8) is as

97 ke product (spaghetti-type), made with corn (Zea mays) flour enriched with 30% broad bean (Vicia faba

98 is], tobacco [Nicotiana tabacum], and maize [Zea mays]) for which controversial findings have been re

99 ombined with Illumina sequencing as a maize (Zea mays) functional genomics tool.

100 A collection of mutant alleles for 11 maize (Zea mays) genes predicted to play roles in controlling D

101 ed mutagenesis, editing of endogenous maize (Zea mays) genes, and site-specific insertion of a trait

102 Using maize (Zea mays) genetic markers and transcript levels from see

103 he non-coding regulatory space in the maize (Zea mays) genome during early reproductive development o

104 ic recombination landscape across the maize (Zea mays) genome will provide insight and tools for furt

105 nd heterochromatin in the repeat-rich maize (Zea mays) genome, we performed whole-genome analyses of

106 rabidopsis (Arabidopsis thaliana) and maize (Zea mays) genomes.

107 al estimation) can differentiate nine maize (Zea mays) genotypes 8 weeks after planting.

108 natomy and architecture of 400 mature maize (Zea mays) genotypes under well-watered and water-stresse

109 Cultivated maize (Zea mays) has retained much of the genetic diversity of

110 hancing fatty acid synthesis (FAS) in maize (Zea mays) has tremendous potential nutritional and econo

111 sis carbon-concentrating mechanism in maize (Zea mays) has two CO2 delivery pathways to the bundle sh

112 Improvements in water-use efficiency in Zea mays have been limited, and warrant a renewed effort

113 Arabidopsis thaliana and maize (Zea mays) have a RidA homolog that is predicted to be pl

114 toplasmic male-sterile (CMS) lines in maize (Zea mays) have been classified by their response to spec

115 The Arabidopsis uORF and its maize (Zea mays) homolog repressed the translation of the main

116 Both ARK1 and a maize (Zea mays) homolog, KNOTTED1, preferentially target evolu

117 A detailed functional analysis of two maize (Zea mays) homologs of At-NPF6.3 (Zm-NPF6.6 and Zm-NPF6.4

118 der varying water availability in six maize (Zea mays) hybrids that differ in yield stability under d

119 orn oil (also named maize oil, obtained from Zea mays, i.e. maize) using Raman spectroscopy and a mat

120 We evaluated evidence in the B73 Zea mays inbred for differences in the activity of the U

121 ot system architectures (RSAs) of two maize (Zea mays) inbred genotypes and their hybrid as they grew

122 used in root and shoot tissues of two maize (Zea mays) inbred lines (B73 and Mo17).

123 n the leaves of several commonly used maize (Zea mays) inbred lines and has been anecdotally linked t

124 the transcriptomic divergence of the maize (Zea mays) inbred lines B73 and Mo17 and their reciprocal

125 Distantly related maize (Zea mays) inbred lines display an exceptional degree of

126 Profiling of DNA methylation in five maize (Zea mays) inbred lines found that while DNA methylation

127 the last 100 years has produced elite maize (Zea mays) inbred lines that combine to produce high-yiel

128 e sequencing of seedling RNA from 503 maize (Zea mays) inbred lines to characterize the maize pan-gen

129 herbivore-induced volatiles among 26 maize (Zea mays) inbred lines, we conducted a nested associatio

130 ression of ZmMYB167 in the C(4) model system Zea mays increased lignin (~4% to 13%), p-coumaric acid

131 PAA, evidence from mutants in pea and maize (Zea mays) indicate that IAA biosynthetic enzymes are not

132 rabidopsis (Arabidopsis thaliana) and maize (Zea mays) induced aggregation of the target proteins, gi

133 Here, we used the maize (Zea mays) inflorescence to investigate gene networks tha

134 Maize (Zea mays) inflorescences are patterned by a series of br

135 We analyzed a maize (Zea mays) introgression library derived from two elite p

136 we have found a link between them in maize (Zea mays) involving the production of the BASIC LEUCINE

137 Zea mays is an important genetic model for elucidating t

138 Maize (Zea mays) is a globally produced crop with broad genetic

139 To ensure food security, maize (Zea mays) is a model crop for understanding useful trait

140 Maize (Zea mays) is an important C4 plant due to its widespread

141 Hypoxic root growth in maize (Zea mays) is influenced by the expression of phytoglobin

142 eral root branching density (LRBD) in maize (Zea mays) is large (1-41 cm(-1) major axis [i.e. brace,

143 ne editing, that haploid induction in maize (Zea mays) is triggered by a frame-shift mutation in MATR

144 maydis, an edible mushroom growing on maize (Zea mays), is consumed as the food delicacy huitlacoche

145 In maize (Zea mays), it is often attributed to a carbon limitation

146 re as the sole environmental variable during Zea mays kernel-fill, from 12 days after pollination to

147 o were identified in a recent GWAS of maize (Zea mays) kernel carotenoid variation.

148 ok advantage of the large size of the maize (Zea mays) kernel to characterize genome-wide expression

149 and four maternal compartments of the maize (Zea mays) kernel.

150 Grasses, such as Zea mays L. (maize), contain relatively high levels of p

151 inating Ceratopteris spores and (ii) growing Zea mays L. roots.

152 The salt-sensitive crop Zea mays L. shows a rapid leaf growth reduction upon NaC

153 The complex evolutionary history of maize (Zea mays L. ssp. mays) has been clarified with genomic-l

154 riptional enhancers in the crop plant maize (Zea mays L. ssp. mays), we integrated available genome-w

155 and manure amendment experiment in a maize (Zea mays L.) double-cropping system, we quantified chang

156 st suitable for aflatoxin analysis in maize (Zea mays L.) grain based on their relative efficiency an

157 rgifera LeConte) is a serious pest of maize (Zea mays L.) in North America and parts of Europe.

158 enhancers was conducted on no-tillage corn (Zea mays L.) in Tennessee, the USA during 2013-2015.

159 Conte) (WCR) is a major insect pest of corn (Zea mays L.) in the United States (US) and is highly ada

160 omic optimum plant density (AOPD) for maize (Zea mays L.) is a critical management decision, but even

161 Maize (Zea mays L.) is one of the most versatile crops worldwid

162 Increasing grain yield of maize (Zea mays L.) is required to meet the rapidly expanding d

163 Here, we show that in maize (Zea mays L.) mitotic cells, H3T3ph is concentrated at pe

164 The effect of maize (Zea mays L.) plant density on N utilization and N fertil

165 e and water deficit as experienced by maize (Zea mays L.) plants; (2) performing 29 field experiments

166 one functional groups and coated onto maize (Zea mays L.) seeds.

167 ) at a long-term, irrigated continuous corn (Zea mays L.) system in eastern Nebraska, United States.

168 in the above-ground biomass of summer maize (Zea mays L.) under different tillage and residue retenti

169 Maize (Zea mays L.), a model species for genetic studies, is on

170 teomic analyses of expanding leaves of corn (Zea mays L.), we show that this transition in pHapo conv

171 (1MAP), and after harvesting (H) under corn (Zea mays L.)-soybean (Glycine max L.) rotation.

172 nt breeding and selection of high-oil maize (Zea mays L.).

173 sting nutritional quality (leaf vs. stalk of Zea mays L.).

174 nd regulatory neofunctionalization in maize (Zea mays L.).

175 G. barbadense L.) and grain yield in maize (Zea mays L.).

176 Smith & Lawrence, is a major pest of maize (Zea mays L.).

177 fera LeConte, is an important pest of maize (Zea mays L.).

178 d responses to stemborer egg-laying in maize Zea mays (L.) (Poaceae).

179 Maize (Zea mays, L.) cultivation has expanded greatly from trop

180 The paralogous maize (Zea mays) LBD (Lateral Organ Boundaries Domain) genes rt

181 In growing maize (Zea mays) leaf blades, a defined developmental gradient

182 ls present in solar radiation inhibit maize (Zea mays) leaf growth without causing any other visible

183 We investigated the consequences of maize (Zea mays) leaf infestation by Spodoptera littoralis cate

184 The maize (Zea mays) leaf is an ideal system to study plant morphog

185 The maize (Zea mays) leaf offers a great tool to study growth proce

186 The maize (Zea mays) leaf provides a robust system to study cellula

187 gh-resolution sampling of the growing maize (Zea mays) leaf with tandem affinity purification followe

188 nd expanded cells in the blade of the maize (Zea mays) leaf.

189 We examined the properties of Zea mays leaves containing Mu and Ds insertions into nuc

190 se required for normal development of maize (Zea mays) leaves, internodes, and inflorescences.

191 work, we provide evidence that three maize (Zea mays) lignin repressors, MYB11, MYB31, and MYB42, pa

192 hromatography-fractionated acetylated maize (Zea mays) lignin revealed that the tricin moieties are f

193 Maize (Zea mays) lines contrasting in root CCS measured as cros

194 eveloped using 19 genetically distant maize (Zea mays) lines from Europe and America.

195 se questions, gm was measured on five maize (Zea mays) lines in response to CO2 , employing three dif

196 maize (Zea mays) PISTILLATA/GLOBOSA ortholog Zea mays mads16 (Zmm16)/sterile tassel silky ear1 (sts1)

197 Pavement cells from the monocot Zea mays (maize) and the eudicot Arabidopsis thaliana (A

198 report that a Mu transposon insertion in the Zea mays (maize) gene encoding a chloroplast dimerizatio

199 e for profiling the rhizosphere chemistry of Zea mays (maize) in agricultural soil, thereby demonstra

200 We used transcriptome data of diverse Zea mays (maize) inbreds and hybrids, including 401 samp

201 is of eight genes in the Bz1-Sh1 interval of Zea mays (maize) indicates significant allele-specific e

202 MALDI-MSI to the asymmetric Kranz anatomy of Zea mays (maize) leaves to study the differential locali

203 iously identified two de novo centromeres on Zea mays (maize) minichromosomes derived from euchromati

204 Here we perform an integrative study of Zea mays (maize) seed development in order to identify k

205 idopsis thaliana, Glycine max (soybean), and Zea mays (maize) to discover new PPIs on a genome-scale.

206 gene expression in the developing leaves of Zea mays (maize), a C(4) plant, and Oryza sativa (rice),

207 In maize (Zea mays), male sterile23 (ms23), necessary for both 24-

208 le parts of three East African staple crops: Zea mays, Manihot esculenta, and Musa acuminata.

209 The origin of maize (Zea mays mays) in the US Southwest remains contentious,

210 Maize (Zea mays mays) is an attractive model for studying centr

211 Maize (Zea mays mays) oil is a rich source of polyunsaturated f

212 The maize (Zea mays) MET1 homolog is enriched in mesophyll chloropl

213 Several GCN studies have been done in maize (Zea mays), mostly using microarray datasets.

214 We discovered a maize (Zea mays) mutant with aberrant leaf architecture, which

215 We isolated a maize (Zea mays) mutant, called rotten ear (rte), that shows di

216 ver a decade since the release of the maize (Zea mays) Nested Association Mapping (NAM) population.

217 sociation study in the 5000-line U.S. maize (Zea mays) nested association mapping panel.

218 The maize (Zea mays) NLR protein Rp1-D21 derives from an intragenic

219 eins confirmed that At5g32470 and its maize (Zea mays) orthologs GRMZM2G148896 and GRMZM2G078283 are

220 oson insertions in genes encoding the maize (Zea mays) orthologs of five such proteins: ZmPTAC2, ZmMu

221 some occupancy mapping experiments in maize (Zea mays), particular genomic regions are highly suscept

222 Further progress in maize (Zea mays) performance under stresses is expected by comb

223 nal cloning and characterization of a maize (Zea mays) PISTILLATA/GLOBOSA ortholog Zea mays mads16 (Z

224 ecombinant C3 (Arabidopsis thaliana) and C4 (Zea mays) plant enzymes and compared isotope effects usi

225 Additionally, as a young, growing maize (Zea mays) plant progressively tapped its soil environmen

226 ulation and rate of metabolization in mature Zea mays plants grown in hydroponic solution supplemente

227 lutions of a soil column experiment in which Zea mays plants were grown for 3 weeks.

228 d a moderate transient heat stress on maize (Zea mays) plants at the tetrad stage of pollen developme

229 As maize (Zea mays) plants undergo vegetative phase change from ju

230 In this study, corn (Zea mays) plants were cultivated to full maturity in soi

231 regulating RIP2 protein accumulation, maize (Zea mays) plants were infested with fall armyworm larvae

232 Here, we compared maize (Zea mays) plants with two, three, and four doses of a 14

233 This work focuses on the maize (Zea mays) plasma membrane intrinsic protein (ZmPIP) aqua

234 from studies of EXPB1 extracted from maize (Zea mays) pollen.

235 ermated B73 x Mo17 recombinant inbred maize (Zea mays) population using pyrolysis molecular-beam mass

236 mbinant inbred lines of two different maize (Zea mays) populations.

237 ecific RNAs in mitochondria and chloroplasts ZEA MAYS: PPR10 is amongst the best studied PPR proteins

238 ome and phosphoproteome atlas of four maize (Zea mays) primary root tissues, the cortex, stele, meris

239 We examined hydrotropism in maize (Zea mays) primary roots.

240 A major challenge in maize (Zea mays) production is to achieve high grain yield (yie

241 stribution in both N. benthamiana and maize (Zea mays) protoplasts.

242 We characterized the maize (Zea mays) RING protein family and identified two novel R

243 We found that the maize (Zea mays) RNA binding motif protein 48 (RBM48) is a U12

244 First, charge mapping at Zea mays root hairs shows that there is a high negative

245 he most highly expressed aquaporin in maize (Zea mays) roots.

246 The century-old maize (Zea mays) salmon silks mutation has been linked to the a

247 and inheritance among a panel of 108 maize (Zea mays) samples spanning five tissues from eight inbre

248 tify genes predominantly expressed in maize (Zea mays) scutellum during maturation.

249 ein in nad5 mature mRNA stability and maize (Zea mays) seed development.

250 q reads, totaling 341 Gb of sequence, from a Zea mays seedling sample.

251 scribe a refined method optimized for maize (Zea mays) seedling leaves, which not only provides a sim

252 g seeds from two different inbreds of maize (Zea mays) seeds, B73 and Mo17.

253 ing (VIGS) in a related crop species, maize (Zea mays), several genes, including a G-BOX BINDING FACT

254 Using Zea mays somatic embryogenesis as a model system, we rep

255 n B. distachyon, rice (Oryza sativa), maize (Zea mays), sorghum (Sorghum bicolor), Arabidopsis thalia

256 Grain Zn and Fe concentration in maize (Zea mays), sorghum (Sorghum bicolor), finger millet (Ele

257 factor binding in leaves of the C(4) grasses Zea mays, Sorghum bicolor, and Setaria italica as well a

258 The KWL1 protein from maize (corn, Zea mays) specifically inhibits the enzymatic activity o

259 We expressed and characterized recombinant Zea mays SSIIa and prepared pure ADP-[(13)CU]glucose in

260 f maize, and four wild teosinte individuals (Zea mays ssp.

261 well-documented whole-genome duplication in Zea mays ssp. mays occurred after the divergence of Zea

262 The cereal crops rice (Oryza sativa), maize (Zea mays ssp. mays) and wheat (Triticum aestivum) provid

263 Maize (Zea mays ssp. mays) domestication began in southwestern

264 Maize (Zea mays ssp. mays) was the primary grain of Native Amer

265 alysis was performed with day-neutral maize (Zea mays ssp. mays), where flowering is promoted almost

266 ic variation in C and N metabolism in maize (Zea mays ssp. mays).

267 focused on the crop plant and model organism Zea mays ssp. mays.

268 is of admixed origin, most likely involving Zea mays ssp. mexicana as one parental taxon, and an uni

269 detect introgression from the wild teosinte Zea mays ssp. mexicana into maize in the highlands of Me

270 Spanish and French teosintes originated from Zea mays ssp. mexicana race "Chalco," a weedy teosinte f

271 from sympatric MVs into LRs and into the WR Zea mays ssp. mexicana sampled after the year 2000.

272 , but the contribution of highland teosinte (Zea mays ssp. mexicana, hereafter mexicana) to modern ma

273 ons of modern maize, landrace, and teosinte (Zea mays ssp. parviglumis) to estimate epimutation rates

274 indeterminate1 (id1), and tropical teosinte (Zea mays ssp. parviglumis) under floral inductive and no

275 aize was domesticated from lowland teosinte (Zea mays ssp. parviglumis), but the contribution of high

276 Here, we microdissected Zea mays stomatal complexes and showed that members of t

277 The first steps toward maize (Zea mays subspecies mays) domestication occurred in the

278 onstrated for rice (Oryza sativa) and maize (Zea mays), suggesting fundamental differences in the reg

279 c results were obtained with the ProRSs from Zea mays, suggesting that the difference in substrate sp

280 A simulation model in maize (Zea mays) suggests that these findings are still compati

281 The maize (Zea mays) tassel-less1 (tls1) mutant has defects in vege

282 Here, we expressed maize (Zea mays) terpene synthase10 (ZmTPS10), which produces (

283 assay for use in intact root tips of maize (Zea mays) that includes several different cell lineages

284 virgifera LeConte) is a major pest of maize (Zea mays) that is well adapted to most crop management s

285 s of paramutation are well studied in maize (Zea mays), the responsible mechanisms remain unclear.

286 In maize (Zea mays), the Sucrose Transporter1 (ZmSut1) gene has be

287 ied to predict distal enhancer candidates in Zea mays, thereby providing a basis for a better underst

288 probing of a closely related model species (Zea mays) to assess correlations in leaf temperature (Tl

289 ant development are controlled by the maize (Zea mays) transcription factor ZmFUSED LEAVES 1 (FDL1)/M

290 and molecular characterization of the maize (Zea mays) transcriptional corepressor RAMOSA1 ENHANCER L

291 large number of publically available maize (Zea mays) transcriptome data sets including >6000 RNA se

292 recA, which were fully functional for maize (Zea mays) transformation and confirmed the importance of

293 under the control of the constitutive maize (Zea mays) ubiquitin promoter.

294 This method was evaluated in maize (Zea mays) using the well-characterized kernel row number

295 ctional promoter, Ubiquitin-1 (ZMUbi1), from Zea mays was first converted into a synthetic BDP, such

296 Maize (Zea mays) was grown alone (maize), or with maize (maize/

297 the mechanisms governing seed size in maize (Zea mays), we examined transcriptional and developmental

298 sucrose accumulation and transport in maize (Zea mays), we isolated carbohydrate partitioning defecti

299 Whereas normal maize (Zea mays [Zm]) has a single aleurone layer, naked endosp

300 The maintenance DNA methyltransferase from Zea mays, ZMET2, recognizes dimethylation of H3K9 via a