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

3 te the mechanistic actions of BPA, BPAF, and Zea on estrogen receptor (ER) alpha and ERbeta.

4 APK pathway were activated by BPA, BPAF, and Zea.

5 dividual contributions of PSII complexes and Zea to chlorophyll (Chl) fluorescence quenching in a mem

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

7 ze of Zea luxurians relative to Zea mays and Zea diploperennis in just the last few million years.

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

9 -II was observed in the presence of PsbS and Zea, although neither Zea nor PsbS alone was sufficient

10 ts on liposomes containing LHC-II, PsbS, and Zea showed an increase of electronic interactions betwee

11 nt in the Pennisetum, Saccharum, Sorghum and Zea lineages.

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

13 produced similar gm for Setaria viridis and Zea mays.

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

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

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

17 AF was via the AF-2 function of ERalpha, but Zea activated via both the AF-1 and AF-2 functions.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

36 ed for indeterminate1 (id1) and the florigen Zea mays CENTRORADIALIS8 (ZCN8), key activators of the 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 inating Ceratopteris spores and (ii) growing Zea mays L. roots.

41 As in Zea, different patterns of interspersion between genes a

42 LTR retrotransposon amplification bursts in Zea may have been initiated by polyploidy, but the great

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

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

45 t recent activity of Ji and Opie elements in Zea and of Leviathan elements in Sorghum and Saccharum s

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

47 nde family of retrotransposons is present in Zea species and is characterized by an unusually long in

48 , and both repeats have become widespread in Zea species.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

208 riculturally significant crop species maize (Zea mays).

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

234 -1,3-glucan synthase gene GLS1 of the maize (Zea mays) pathogen Colletotrichum graminicola, employing

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

260 e presence of PsbS and Zea, although neither Zea nor PsbS alone was sufficient to induce the same que

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

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

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

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

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

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

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

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

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

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

271 ave approximately doubled the genome size of Zea luxurians relative to Zea mays and Zea diploperennis

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

290 further document the size flexibility of the Zea genome, but also point to a drastic shift in pattern

291 In a detailed analysis of the Zea lineage, the combined action of several families of

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

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

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

295 ted several micro-rearrangements relative to Zea, including addition, truncation and deletion of gene

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

297 antagonist for ERbeta in HeLa cells, whereas Zea was only a partial antagonist for ERalpha.

298 (BPA), bisphenol AF (BPAF), and zearalenone (Zea), but mechanisms of action and diversity of effects

299 SII (LHC-II) and the xanthophyll zeaxanthin (Zea) into proteoliposomes, we have tested the individual

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