ライフサイエンスコーパス: Zea mays

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

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

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

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

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

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

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

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

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

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

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

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

13 is thaliana, rice (Oryza sativa), and maize (Zea mays).

14 ate carboxylase (C4-Pepc) promoter in maize (Zea mays).

15 on canopy energy and water fluxes of maize (Zea mays).

16 l for its pathogenic interaction with maize (Zea mays).

17 riculturally significant crop species maize (Zea mays).

18 ycle of the Suc transporter SUT1 from maize (Zea mays).

19 ng pollination in the B73 genotype of maize (Zea mays).

20 n the germ lineages and the zygote of maize (Zea mays).

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

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

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

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

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

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

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

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

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

30 produced similar gm for Setaria viridis and Zea mays.

31 ucture exhibits remarkable plasticity within Zea mays.

32 idopsis thaliana and ZmCKX1 and ZmCKX4a from Zea mays.

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

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

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

36 Unlike maize (Zea mays), a closely related species also belonging to t

37 We assessed GS in Zea mays, a species that includes the cultivated crop, m

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

39 (GFP), and the transposase (TPase) of maize (Zea mays) Activator major transcript X054214.1 on the st

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

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

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

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

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

45 the genome size of Zea luxurians relative to Zea mays and Zea diploperennis in just the last few mill

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

47 ng factors and histone acetylation in maize (Zea mays) and Arabidopsis (Arabidopsis thaliana) in thei

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

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

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

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

52 ity genes branched silkless1 (bd1) in maize (Zea mays) and FRIZZY PANICLE (FZP) in rice (Oryza sativa

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

54 controlled via annual rotation between corn (Zea mays) and nonhost soybean (Glycine max) in the Unite

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

56 ianthus annuus), Catharanthus roseus, maize (Zea mays) and rice (Oryza sativa), and effectively valid

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

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

59 ression in several nuclear mutants of maize (Zea mays) and that it reveals previously unsuspected def

60 es of Pack-MULEs is observed in rice, maize (Zea mays), and Arabidopsis (Arabidopsis thaliana), sugge

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

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

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

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

68 le functions of jasmonic acid (JA) in maize (Zea mays) are revealed by comprehensive analyses of JA-d

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

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

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

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

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

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

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

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

77 plants sorghum (Sorghum bicolor) and maize (Zea mays) by the fluorescence recovery after photobleach

78 lines allow the effects of individual maize (Zea mays; C(4)) chromosomes to be investigated in an oat

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

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

81 phorelay signaling in Arabidopsis and maize (Zea mays) cellular assays while retaining its specificit

82 ed for indeterminate1 (id1) and the florigen Zea mays CENTRORADIALIS8 (ZCN8), key activators of the f

83 Maize (Zea mays) contains three chloroplast FNR proteins with t

84 + metabolites) by Cucurbita pepo (zucchini), Zea mays (corn), Solanum lycopersicum (tomato), and Glyc

85 Maize (Zea mays) develops an extensive shoot-borne root system

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

87 fer of these pollen-coat materials in maize (Zea mays) differs completely from that reported in Arabi

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

89 The tie-dyed2 (tdy2) mutant of maize (Zea mays) displays variegated green and yellow leaves.

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

91 The maize (Zea mays) drought transcriptome was studied using RNA-Se

92 e presence and economic importance of maize (Zea mays) during the Late Archaic period (3000-1800 B.C.

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

94 fy the imprintome of early developing maize (Zea mays) endosperm, we performed high-throughput transc

95 duced mesotrione metabolism in MCR and corn (Zea mays) excised leaves but not in ACR.

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

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

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

99 histone modification distributions in maize (Zea mays), focusing on two maize chromosomes with nearly

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

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

102 oned the Arabidopsis thaliana homolog of the Zea mays gene, At3g26430, and studied its biochemical pr

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

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

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

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

107 occupancy likelihood (NOL) across the maize (Zea mays) genome.

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

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

110 The homologs from maize (Zea mays; GRMZM2G161299 and GRMZM2G420119) and Arabidops

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

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

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

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

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

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

117 In maize (Zea mays), however, selection for a strong central stalk

118 Mutations affecting paramutations in maize (Zea mays) identify components required for the accumulat

119 unexpected involvement of CslD1 from maize (Zea mays) in cell division.

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

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

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

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

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

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

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

127 de profiles of DNA methylation for 20 maize (Zea mays) inbred lines were used to discover differentia

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

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

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

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

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

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

134 Zea mays is an important genetic model for elucidating t

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

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

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

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

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

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

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

142 Maize (Zea mays) ISA1 was expressed in Arabidopsis (Arabidopsis

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

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

145 The maize (Zea mays) kernel plays a critical role in feeding humans

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

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

148 Cu, Mn, and Zn distributions around roots of Zea mays L. demonstrate the new opportunities offered by

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

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

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

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

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

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

155 is the most destructive insect pest of corn (Zea mays L.) in the United States.

156 ike4 (Vrs4), a barley ortholog of the maize (Zea mays L.) inflorescence architecture gene RAMOSA2 (RA

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

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

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

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

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

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

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

164 alk strength is an important trait in maize (Zea mays L.).

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

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

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

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

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

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

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

172 e-scale, quantitative analyses of the maize (Zea mays) leaf proteome and phosphoproteome at four deve

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

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

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

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

177 ISA functions were characterized in maize (Zea mays) leaves to determine whether species-specific d

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

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

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

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

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

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

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

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

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

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

188 t products and signals derived from a single Zea mays (maize) lipoxygenase (LOX), ZmLOX10, are critic

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

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

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

192 efenses in Solanum lycopersicum (tomato) and Zea mays (maize), two very important crop plants that ar

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

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

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

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

197 superfamily comes from studies of the maize (Zea mays) Mu elements, whose transposition is mediated b

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

199 rsion of the high-lysine opaque2 (o2) maize (Zea mays) mutant, but the genes involved in modification

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

201 characterized a seed-specific viable maize (Zea mays) mutant, defective endosperm18 (de18) that is i

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

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

204 Here, we present evidence that the maize (Zea mays) nuclear gene Pentatricopeptide repeat 2263 (PP

205 The maize (Zea mays) nucleosome remodeling factor complex component

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

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

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

209 -1,3-glucan synthase gene GLS1 of the maize (Zea mays) pathogen Colletotrichum graminicola, employing

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

211 iously showed that the traffic of the maize (Zea mays) PIP2;5 to the plasma membrane is dependent on

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

213 , we demonstrate that a member of the maize (Zea mays) plant elicitor peptide (Pep) family, ZmPep3, r

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

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

216 e developmentally distinct tissues in maize (Zea mays) plants of two genetic backgrounds, B73 and Mo1

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

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

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

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

221 urified from Arabidopsis thaliana and maize (Zea mays) plants.

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

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

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

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

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

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

228 Zeins, the maize (Zea mays) prolamin storage proteins, accumulate at very

229 t with this inference, Arabidopsis or maize (Zea mays) PyrR (At3g47390 or GRMZM2G090068) restored rib

230 We used maize (Zea mays) recombinant inbred lines to map a quantitative

231 ly 8.69 Gb of GBS data were generated on the Zea mays reference inbred B73, utilizing ApeKI for genom

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

233 The maize (Zea mays) RNA Polymerase IV (Pol IV) largest subunit, RN

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

235 ndole-3-acetic acid flux near the surface of Zea mays roots.

236 In maize (Zea mays), Rubisco accumulates in bundle sheath but not

237 required for Rubisco accumulation in maize (Zea mays), RUBISCO ACCUMULATION FACTOR1 (RAF1), which la

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

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

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

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

242 ource leaves to low N was analyzed in maize (Zea mays) seedlings by parallel measurements of transcri

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

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

245 umulation of insecticidal flavones in maize (Zea mays) silks and red phlobaphene pigments in pericarp

246 ydis is a biotrophic pathogen causing maize (Zea mays) smut disease.

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

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

249 sess diversity of AM fungi colonizing maize (Zea mays), soybean (Glycene max) and field violet (Viola

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

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

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

253 ve demonstrated that mutations in the maize (Zea mays ssp. mays) gene teosinte glume architecture (tg

254 Maize (Zea mays ssp. mays) is among the world's most important

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

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

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

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

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

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

261 have substantially altered the morphology of Zea mays ssp. parviglumis (teosinte) into the currently

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

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

264 b1) gene in natural populations of teosinte (Zea mays ssp. parviglumis, Z. mays ssp. mexicana, and Z.

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

266 In addition, corn ( Zea mays ) stover, corn grains, and soil were collected

267 sites occur among haplotypes from different Zea mays sub-species, but not outside the species.

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

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

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

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

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

273 he pea (Pisum sativum) homolog of the maize (Zea mays) TEOSINTE BRANCHED1 and the Arabidopsis (Arabid

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

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

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

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

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

279 In maize (Zea mays), the three isozymes were transiently expressed

280 e analyzed the bz gene-rich region of maize (Zea mays), the Zea teosintes mays ssp. mexicana, luxuria

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

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

283 s, as well as for RNA-Seq reads of the corn (Zea mays) transcriptome.

284 Maize (Zea mays) transformation routinely produces stable trans

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

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

287 Pod corn (Zea mays var tunicata) was once regarded as ancestral to

288 es across pre-domestication and domesticated Zea mays varieties, including a representative from the

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

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

291 is thaliana, rice (Oryza sativa), and maize (Zea mays), we found 3' truncation prior to tailing is wi

292 l (M) and bundle sheath (BS) cells of maize (Zea mays), we isolated large quantities of highly homoge

293 ism (SNP) genotyping across a large panel of Zea mays, we have identified an approximately 50-Mb regi

294 tility of RooTrak using muCT scans of maize (Zea mays), wheat (Triticum aestivum), and tomato (Solanu

295 d with mutations in a nuclear gene in maize (Zea mays), white2 (w2), encoding a predicted organellar

296 early events during the infection of maize (Zea mays) with Colletotrichum graminicola, a model patho

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

298 cum), SlAMADHs, and three AMADHs from maize (Zea mays), ZmAMADHs, were kinetically investigated to ob

299 ts, Physcomitrella patens (PpNRH) and maize (Zea mays; ZmNRH), using in vitro and in planta approache

300 The function of chloroplast RH3 in maize (Zea mays; ZmRH3) and Arabidopsis (Arabidopsis thaliana;