ライフサイエンスコーパス: Zea

1 Zea mays is an important genetic model for elucidating t

2 Zea-NP can be incorporated in yogurt, allowing the dispe

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

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

5 abilities and lacked detectable Zea S(1) and Zea(*+) ESA signals in vivo, which strongly suggests tha

6 al features associated with the Zea S(1) and Zea(*+) excited-state absorption (ESA) signals, respecti

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

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

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

10 ccurrences regarded Arabidopsis thaliana and Zea mays.

11 produced similar gm for Setaria viridis and Zea mays.

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

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

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

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

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

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

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

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

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

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

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

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

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

25 (1MAP), and after harvesting (H) under corn (Zea mays L.)-soybean (Glycine max L.) rotation.

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

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

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

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

30 bited NPQ capabilities and lacked detectable Zea S(1) and Zea(*+) ESA signals in vivo, which strongly

31 . mays and other species (Zea diploperennis, Zea luxurians, and Tripsacum dactyloides) reveals tenfol

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

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

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

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

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

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

38 idopsis thaliana and ZmCKX1 and ZmCKX4a from Zea mays.

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

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

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

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

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

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

45 kely a key mechanism for pollen rejection in Zea and may represent a general mechanism for reproducti

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

171 cluding wheat (Triticum aestivum L.), maize (Zea may L.), rice (Oryza sativa L.) and sorghum (Sorghum

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

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

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

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

176 tructure modification by the roots of maize (Zea maize), palisade grass (Brachiaria brizantha cv. Mar

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

263 ticles (Zea-NP) and zeaxanthin nanoemulsion (Zea-NE) were incorporated in yogurt.

264 Zeaxanthin nanoparticles (Zea-NP) and zeaxanthin nanoemulsion (Zea-NE) were incorp

265 consistent with the transcript abundance of Zea maize Plasma Membrane Intrinsic Protein aquaporins.

266 h strongly suggests that the accumulation of Zea and active LHCX1 is essential for both EET and CT qu

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

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

269 s ssp. mays occurred after the divergence of Zea and Sorghum.

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

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

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

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

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

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

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

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

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

279 ve arrays of CentC may be the norm for other Zea and Tripsacum species, these data also reveal that a

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

281 plant Physcomitrella patens and higher plant Zea mays.

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

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

284 sis of repeats in Z. mays and other species (Zea diploperennis, Zea luxurians, and Tripsacum dactyloi

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

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

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

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

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

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

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

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

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

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

295 erving spectral features associated with the Zea S(1) and Zea(*+) excited-state absorption (ESA) sign

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

297 We named this new virus Zea mays chrysovirus 1.

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

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

300 to investigate chlorophyll (Chl)-zeaxanthin (Zea) excitation energy transfer (EET) and charge transfe