ライフサイエンスコーパス: mays

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

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

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

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

5 gronomically important crop plant maize (Zea mays).

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

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

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

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

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

11 n C and N metabolism in maize (Zea mays ssp. mays).

12 rectly involved in SC assembly in maize (Zea mays).

13 dopsis (Arabidopsis thaliana) and maize (Zea mays).

14 n against chewing insect pests in maize (Zea mays).

15 sativa) but poorly understood in maize (Zea mays).

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

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

18 blicly available information from maize (Zea mays).

19 dopsis (Arabidopsis thaliana) and maize (Zea mays).

20 anded in a TE-rich genome such as maize (Zea mays).

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

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

23 acks many cereal crops, including maize (Zea mays).

24 uliarity of cultivation nor inbreeding in Z. mays.

25 duced similar gm for Setaria viridis and Zea mays.

26 sis thaliana and ZmCKX1 and ZmCKX4a from Zea mays.

27 crop plant and model organism Zea mays ssp. mays.

28 rences regarded Arabidopsis thaliana and Zea mays.

29 er of studies have explored this trait in Z. mays.

30 t Physcomitrella patens and higher plant Zea mays.

31 e characterization of leaf delta(13) C in Z. mays.

32 lopmentally regulated splicing in maize (Zea mays), 94 RNA-seq libraries from ear, tassel, and leaf o

33 n polar transport, and studies of maize (Zea mays) aberrant phyllotaxy1 (abph1) mutants suggest the i

34 mmunity composition and structure of ten Zea mays accessions along an evolutionary transect (two teos

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

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

37 d that CENH3 from Lepidium oleraceum and Zea mays, although specifying epigenetically weaker centrome

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

39 f P. nigrum contaminants (Carica papaya, Zea mays and Capsicum annuum) using plant DNA barcodes trnL

40 ource for constructing the pan-genome of Zea mays and genetic improvement of modern maize varieties.

41 (10-40 degrees C) of C4 gm in S. viridis, Z. mays and Miscanthus x giganteus.

42 is of genes in the Arabidopsis thaliana, Zea mays and Oryza sativa anther development pathways shows

43 Analysis of repeats in Z. mays and other species (Zea diploperennis, Zea luxurians

44 d for thousands of Arabidopsis thaliana, Zea mays and Vitis vinifera genes, and have been linked to d

45 mids into rice (Oryza sativa) and maize (Zea mays) and analyzed the results by whole genome sequencin

46 phenotype, whereas sequences from maize (Zea mays) and Arabidopsis (Arabidopsis thaliana) give phenot

47 Recombinant maize (Zea mays) and Arabidopsis (Arabidopsis thaliana) NAD(P)HX de

48 acterization of FNSI enzymes from maize (Zea mays) and Arabidopsis (Arabidopsis thaliana).

49 trand breaks in genomes of wheat, maize (Zea mays) and Arabidopsis.

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

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

52 ydis infects all aerial organs of maize (Zea mays) and induces tumors in the plant tissues.

53 ion from etiolated coleoptiles of maize (Zea mays) and leaves of Arabidopsis (Arabidopsis thaliana),

54 ation glyphosate-tolerant EPSPS in corn (Zea mays) and now in other crops.

55 tic architecture of senescence in maize (Zea mays) and other cereals.

56 al role in pathogen resistance in maize (Zea mays) and other plants.

57 cumulation have been described in maize (Zea mays) and rice (Oryza sativa) anthers.

58 old-responsive gene expression in maize (Zea mays) and sorghum (Sorghum bicolor) allowed us to identi

59 ionary fates of the subgenomes in maize (Zea mays) and soybean (Glycine max) have followed different

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

61 positive and -negative mutants of maize (Zea mays) and the beneficial fungus Trichoderma virens and i

62 ps rice (Oryza sativa), maize (Zea mays ssp. mays) and wheat (Triticum aestivum) provide half of the

63 abidopsis (Arabidopsis thaliana), maize (Zea mays), and rice (Oryza sativa).

64 abidopsis (Arabidopsis thaliana), maize (Zea mays), and rice (Oryza sativa).

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

66 trong support for a CO2 response of gm in Z. mays, and indicate that gm in maize is probably driven b

67 eviously published data from S. bicolor, Zea mays, and Oryza sativa to identify a small suite of tran

68 heat [Triticum aestivum]) and C4 (maize [Zea mays] and Setaria viridis) monocot species.

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

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

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

72 -indexed insertional libraries in maize (Zea mays) are fundamental resources for functional genetics

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

74 is evolutionary variability using maize (Zea mays) as an experimental system.

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

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

77 ated multiomics approach to study maize (Zea mays) autophagy mutants subjected to fixed-carbon starva

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

79 Osmotic stress was applied to maize (Zea mays) B73 by irrigation with increasing concentrations o

80 MAKER-P to update and revise the maize (Zea mays) B73 RefGen_v3 annotation build (5b+) in less than

81 h involving overexpression of the maize (Zea mays) Baby boom (Bbm) and maize Wuschel2 (Wus2) genes, w

82 rops such as rice (Oryza sativa), maize (Zea mays), barley (Hordeum vulgare), and wheat (Triticum aes

83 types by expressing proteins from maize (Zea mays BE2a), potato (Solanum tuberosum BE1), and Escheric

84 Results show that ZmEXPB6 (Z. mays beta-expansin 6) protein is lacking in growth-inhib

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

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

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

88 assays of the naturally silenced maize (Zea mays) C2-Idf (inhibitor diffuse) mutant, defective in th

89 Stalk lodging in maize (Zea mays) causes significant yield losses due to breaking of

90 iver Cre recombinase protein into maize (Zea mays) cells.

91 We named this new virus Zea mays chrysovirus 1.

92 ly related gene, ZmSUT1 from the monocot Zea mays, did restore phloem loading.

93 Maize (Zea mays) displays an exceptional level of structural genomi

94 grass Brachypodium distachyon and corn (Zea mays) do not possess orthologs of the currently characte

95 Maize (Zea mays ssp. mays) domestication began in southwestern Mexico ~9,000

96 irst steps toward maize (Zea mays subspecies mays) domestication occurred in the Balsas region of Mex

97 anscription factors important for maize (Zea mays) endosperm development.

98 The maize (Zea mays) enzyme beta-carotene hydroxylase 2 (ZmBCH2) contro

99 sus left as surplus N in 8 million corn (Zea mays) fields at subfield resolutions of 30 x 30 m (0.09

100 The activity of the maize (Zea mays) florigen gene ZEA CENTRORADIALIS8 (ZCN8) is associ

101 roduct (spaghetti-type), made with corn (Zea mays) flour enriched with 30% broad bean (Vicia faba) fl

102 ned with Illumina sequencing as a maize (Zea mays) functional genomics tool.

103 utagenesis, editing of endogenous maize (Zea mays) genes, and site-specific insertion of a trait gene

104 Using maize (Zea mays) genetic markers and transcript levels from seedlin

105 on-coding regulatory space in the maize (Zea mays) genome during early reproductive development of po

106 ecombination landscape across the maize (Zea mays) genome will provide insight and tools for further

107 dopsis (Arabidopsis thaliana) and maize (Zea mays) genomes.

108 my and architecture of 400 mature maize (Zea mays) genotypes under well-watered and water-stressed co

109 lutionary history of maize (Zea mays L. ssp. mays) has been clarified with genomic-level data from mo

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

111 ing fatty acid synthesis (FAS) in maize (Zea mays) has tremendous potential nutritional and economic

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

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

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

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

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

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

118 lumis, Z. mays mexicana, and particularly Z. mays huehuetenangensis.

119 varying water availability in six maize (Zea mays) hybrids that differ in yield stability under droug

120 oil (also named maize oil, obtained from Zea mays, i.e. maize) using Raman spectroscopy and a mathema

121 We evaluated evidence in the B73 Zea mays inbred for differences in the activity of the UPR b

122 ystem architectures (RSAs) of two maize (Zea mays) inbred genotypes and their hybrid as they grew in

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

124 e leaves of several commonly used maize (Zea mays) inbred lines and has been anecdotally linked to en

125 transcriptomic divergence of the maize (Zea mays) inbred lines B73 and Mo17 and their reciprocal F1

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

127 filing of DNA methylation in five maize (Zea mays) inbred lines found that while DNA methylation leve

128 last 100 years has produced elite maize (Zea mays) inbred lines that combine to produce high-yielding

129 quencing of seedling RNA from 503 maize (Zea mays) inbred lines to characterize the maize pan-genome,

130 bivore-induced volatiles among 26 maize (Zea mays) inbred lines, we conducted a nested association ma

131 ion of ZmMYB167 in the C(4) model system Zea mays increased lignin (~4% to 13%), p-coumaric acid (~8%

132 evidence from mutants in pea and maize (Zea mays) indicate that IAA biosynthetic enzymes are not the

133 dopsis (Arabidopsis thaliana) and maize (Zea mays) induced aggregation of the target proteins, giving

134 Here, we used the maize (Zea mays) inflorescence to investigate gene networks that mo

135 Maize (Zea mays) inflorescences are patterned by a series of branch

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

137 Zea mays is an important genetic model for elucidating trans

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

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

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

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

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

143 diting, that haploid induction in maize (Zea mays) is triggered by a frame-shift mutation in MATRILIN

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

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

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

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

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

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

150 We found that upon U. maydis infection of Z. mays, KWL1-b is expressed at significantly lower levels

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

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

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

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

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

156 uitable for aflatoxin analysis in maize (Zea mays L.) grain based on their relative efficiency and pr

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

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

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

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

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

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

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

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

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

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

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

168 he above-ground biomass of summer maize (Zea mays L.) under different tillage and residue retention t

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

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

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

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

173 reeding and selection of high-oil maize (Zea mays L.).

174 g nutritional quality (leaf vs. stalk of Zea mays L.).

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

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

177 sponses to stemborer egg-laying in maize Zea mays (L.) (Poaceae).

178 Maize (Zea mays, L.) cultivation has expanded greatly from tropical

179 The paralogous maize (Zea mays) LBD (Lateral Organ Boundaries Domain) genes rtcs (

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

181 resent in solar radiation inhibit maize (Zea mays) leaf growth without causing any other visible stre

182 investigated the consequences of maize (Zea mays) leaf infestation by Spodoptera littoralis caterpil

183 The maize (Zea mays) leaf is an ideal system to study plant morphogenes

184 The maize (Zea mays) leaf provides a robust system to study cellular di

185 esolution sampling of the growing maize (Zea mays) leaf with tandem affinity purification followed by

186 xpanded cells in the blade of the maize (Zea mays) leaf.

187 We examined the properties of Zea mays leaves containing Mu and Ds insertions into nuclear

188 equired for normal development of maize (Zea mays) leaves, internodes, and inflorescences.

189 k, we provide evidence that three maize (Zea mays) lignin repressors, MYB11, MYB31, and MYB42, partic

190 atography-fractionated acetylated maize (Zea mays) lignin revealed that the tricin moieties are found

191 Maize (Zea mays) lines contrasting in root CCS measured as cross-se

192 oped using 19 genetically distant maize (Zea mays) lines from Europe and America.

193 uestions, gm was measured on five maize (Zea mays) lines in response to CO2 , employing three differe

194 e (Zea mays) PISTILLATA/GLOBOSA ortholog Zea mays mads16 (Zmm16)/sterile tassel silky ear1 (sts1).

195 Pavement cells from the monocot Zea mays (maize) and the eudicot Arabidopsis thaliana (Arabi

196 rt that a Mu transposon insertion in the Zea mays (maize) gene encoding a chloroplast dimerization co

197 r profiling the rhizosphere chemistry of Zea mays (maize) in agricultural soil, thereby demonstrating

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

199 f eight genes in the Bz1-Sh1 interval of Zea mays (maize) indicates significant allele-specific expre

200 I-MSI to the asymmetric Kranz anatomy of Zea mays (maize) leaves to study the differential localizati

201 ly identified two de novo centromeres on Zea mays (maize) minichromosomes derived from euchromatic si

202 Here we perform an integrative study of Zea mays (maize) seed development in order to identify key g

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

204 In maize (Zea mays), male sterile23 (ms23), necessary for both 24-nt p

205 arts of three East African staple crops: Zea mays, Manihot esculenta, and Musa acuminata.

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

207 Maize (Zea mays mays) is an attractive model for studying centromer

208 Maize (Zea mays mays) oil is a rich source of polyunsaturated fatty

209 The maize (Zea mays) MET1 homolog is enriched in mesophyll chloroplasts

210 d its wild relatives Z. mays parviglumis, Z. mays mexicana, and particularly Z. mays huehuetenangensi

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

212 We discovered a maize (Zea mays) mutant with aberrant leaf architecture, which we n

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

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

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

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

217 ed whole-genome duplication in Zea mays ssp. mays occurred after the divergence of Zea and Sorghum.

218 confirmed that At5g32470 and its maize (Zea mays) orthologs GRMZM2G148896 and GRMZM2G078283 are ThMP

219 insertions in genes encoding the maize (Zea mays) orthologs of five such proteins: ZmPTAC2, ZmMurE,

220 occupancy mapping experiments in maize (Zea mays), particular genomic regions are highly susceptible

221 ntromeres in maize and its wild relatives Z. mays parviglumis, Z. mays mexicana, and particularly Z.

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

223 cloning and characterization of a maize (Zea mays) PISTILLATA/GLOBOSA ortholog Zea mays mads16 (Zmm16

224 binant C3 (Arabidopsis thaliana) and C4 (Zea mays) plant enzymes and compared isotope effects using n

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

226 ion and rate of metabolization in mature Zea mays plants grown in hydroponic solution supplemented wi

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

228 moderate transient heat stress on maize (Zea mays) plants at the tetrad stage of pollen development.

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

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

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

232 Here, we compared maize (Zea mays) plants with two, three, and four doses of a 14.6-M

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

234 ted B73 x Mo17 recombinant inbred maize (Zea mays) population using pyrolysis molecular-beam mass spe

235 ant inbred lines of two different maize (Zea mays) populations.

236 ic RNAs in mitochondria and chloroplasts ZEA MAYS: PPR10 is amongst the best studied PPR proteins, wh

237 and phosphoproteome atlas of four maize (Zea mays) primary root tissues, the cortex, stele, meristema

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

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

240 bution in both N. benthamiana and maize (Zea mays) protoplasts.

241 We characterized the maize (Zea mays) RING protein family and identified two novel RING-

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

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

244 ost highly expressed aquaporin in maize (Zea mays) roots.

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

246 inheritance among a panel of 108 maize (Zea mays) samples spanning five tissues from eight inbred pa

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

248 ads, totaling 341 Gb of sequence, from a Zea mays seedling sample.

249 be a refined method optimized for maize (Zea mays) seedling leaves, which not only provides a simple

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

251 (VIGS) in a related crop species, maize (Zea mays), several genes, including a G-BOX BINDING FACTOR 3

252 distachyon, rice (Oryza sativa), maize (Zea mays), sorghum (Sorghum bicolor), Arabidopsis thaliana,

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

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

255 The KWL1 protein from maize (corn, Zea mays) specifically inhibits the enzymatic activity of th

256 expressed and characterized recombinant Zea mays SSIIa and prepared pure ADP-[(13)CU]glucose in a on

257 ize, and four wild teosinte individuals (Zea mays ssp.

258 l-documented whole-genome duplication in Zea mays ssp. mays occurred after the divergence of Zea and

259 cereal crops rice (Oryza sativa), maize (Zea mays ssp. mays) and wheat (Triticum aestivum) provide ha

260 Maize (Zea mays ssp. mays) domestication began in southwestern Mexi

261 Maize (Zea mays ssp. mays) was the primary grain of Native American

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

263 ariation in C and N metabolism in maize (Zea mays ssp. mays).

264 sed on the crop plant and model organism Zea mays ssp. mays.

265 of admixed origin, most likely involving Zea mays ssp. mexicana as one parental taxon, and an unident

266 ect introgression from the wild teosinte Zea mays ssp. mexicana into maize in the highlands of Mexico

267 ish and French teosintes originated from Zea mays ssp. mexicana race "Chalco," a weedy teosinte from

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

269 t the contribution of highland teosinte (Zea mays ssp. mexicana, hereafter mexicana) to modern maize

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

271 terminate1 (id1), and tropical teosinte (Zea mays ssp. parviglumis) under floral inductive and nonind

272 was domesticated from lowland teosinte (Zea mays ssp. parviglumis), but the contribution of highland

273 Here, we microdissected Zea mays stomatal complexes and showed that members of the a

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

275 rated for rice (Oryza sativa) and maize (Zea mays), suggesting fundamental differences in the regulat

276 sults were obtained with the ProRSs from Zea mays, suggesting that the difference in substrate specif

277 A simulation model in maize (Zea mays) suggests that these findings are still compatible

278 The maize (Zea mays) tassel-less1 (tls1) mutant has defects in vegetati

279 ay for use in intact root tips of maize (Zea mays) that includes several different cell lineages and

280 ifera LeConte) is a major pest of maize (Zea mays) that is well adapted to most crop management strat

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

282 In maize (Zea mays), the Sucrose Transporter1 (ZmSut1) gene has been i

283 to predict distal enhancer candidates in Zea mays, thereby providing a basis for a better understandi

284 bing of a closely related model species (Zea mays) to assess correlations in leaf temperature (Tleaf)

285 development are controlled by the maize (Zea mays) transcription factor ZmFUSED LEAVES 1 (FDL1)/MYB94

286 molecular characterization of the maize (Zea mays) transcriptional corepressor RAMOSA1 ENHANCER LOCUS

287 ge number of publically available maize (Zea mays) transcriptome data sets including >6000 RNA sequen

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

289 r the control of the constitutive maize (Zea mays) ubiquitin promoter.

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

291 nal promoter, Ubiquitin-1 (ZMUbi1), from Zea mays was first converted into a synthetic BDP, such that

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

293 Maize (Zea mays ssp. mays) was the primary grain of Native American agricultu

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

295 rs in the crop plant maize (Zea mays L. ssp. mays), we integrated available genome-wide DNA methylati

296 ose accumulation and transport in maize (Zea mays), we isolated carbohydrate partitioning defective33

297 formed with day-neutral maize (Zea mays ssp. mays), where flowering is promoted almost exclusively vi

298 elta(13) C exists across diverse lines of Z. mays, which we show to be heritable across several envir

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

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