ライフサイエンスコーパス: mays

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

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

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

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

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

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

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

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

9 blicly available information from maize (Zea mays).

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

11 s) during stomatal development in maize (Zea mays).

12 n-of-function dominant mutants in maize (Zea mays).

13 A) could improve N acquisition in maize (Zea mays).

14 haliana, rice (Oryza sativa), and maize (Zea mays).

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

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

17 r its pathogenic interaction with maize (Zea mays).

18 lturally significant crop species maize (Zea mays).

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

20 ollination in the B73 genotype of maize (Zea mays).

21 e germ lineages and the zygote of maize (Zea mays).

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

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

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

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

26 gronomically important crop plant maize (Zea mays).

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

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

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

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

31 uliarity of cultivation nor inbreeding in Z. mays.

32 duced similar gm for Setaria viridis and Zea mays.

33 sis thaliana and ZmCKX1 and ZmCKX4a from Zea mays.

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

35 n insensitive shuffled variant of maize (Zea mays) 4-hydroxyphenylpyruvate dioxygenase (HPPD), we ach

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

37 or eye health, while 8 g of cooked mais (Zea mays) a day can provide a high enough level (2 mg) of ze

38 Unlike maize (Zea mays), a closely related species also belonging to the g

39 We assessed GS in Zea mays, a species that includes the cultivated crop, maize

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

41 ), and the transposase (TPase) of maize (Zea mays) Activator major transcript X054214.1 on the stable

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

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

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

45 (10-40 degrees C) of C4 gm in S. viridis, Z. mays and Miscanthus x giganteus.

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

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

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

49 genome size of Zea luxurians relative to Zea mays and Zea diploperennis in just the last few million

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

51 actors and histone acetylation in maize (Zea mays) and Arabidopsis (Arabidopsis thaliana) in their pa

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

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

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

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

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

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

58 rolled via annual rotation between corn (Zea mays) and nonhost soybean (Glycine max) in the United St

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

60 hus annuus), Catharanthus roseus, maize (Zea mays) and rice (Oryza sativa), and effectively validated

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

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

63 ion in several nuclear mutants of maize (Zea mays) and that it reveals previously unsuspected defects

64 f Pack-MULEs is observed in rice, maize (Zea mays), and Arabidopsis (Arabidopsis thaliana), suggestin

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

81 ould improve drought tolerance in maize (Zea mays) by reducing the metabolic costs of soil exploratio

82 nts sorghum (Sorghum bicolor) and maize (Zea mays) by the fluorescence recovery after photobleaching

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

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

85 elay signaling in Arabidopsis and maize (Zea mays) cellular assays while retaining its specificity.

86 or indeterminate1 (id1) and the florigen Zea mays CENTRORADIALIS8 (ZCN8), key activators of the flora

87 tabolites) by Cucurbita pepo (zucchini), Zea mays (corn), Solanum lycopersicum (tomato), and Glycine

88 Maize (Zea mays) develops an extensive shoot-borne root system to s

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

90 of these pollen-coat materials in maize (Zea mays) differs completely from that reported in Arabidops

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

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

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

94 esence and economic importance of maize (Zea mays) during the Late Archaic period (3000-1800 B.C.) in

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

96 he imprintome of early developing maize (Zea mays) endosperm, we performed high-throughput transcript

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

98 ample experiment that contains 33 maize (Zea mays 'Fernandez') plants, which were grown for 9 weeks i

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

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

101 one modification distributions in maize (Zea mays), focusing on two maize chromosomes with nearly ful

102 tobacco [Nicotiana tabacum], and maize [Zea mays]) for which controversial findings have been report

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

104 the Arabidopsis thaliana homolog of the Zea mays gene, At3g26430, and studied its biochemical proper

105 llection of mutant alleles for 11 maize (Zea mays) genes predicted to play roles in controlling DNA m

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

107 tructural variations are pervasive in the Z. mays genome and are enriched at loci associated with imp

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

109 eterochromatin in the repeat-rich maize (Zea mays) genome, we performed whole-genome analyses of seve

110 pancy likelihood (NOL) across the maize (Zea mays) genome.

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

112 stimation) can differentiate nine maize (Zea mays) genotypes 8 weeks after planting.

113 The homologs from maize (Zea mays; GRMZM2G161299 and GRMZM2G420119) and Arabidopsis (

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

115 carbon-concentrating mechanism in maize (Zea mays) has two CO2 delivery pathways to the bundle sheath

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

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

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

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

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

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

122 ations affecting paramutations in maize (Zea mays) identify components required for the accumulation

123 xpected involvement of CslD1 from maize (Zea mays) in cell division.

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

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

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

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

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

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

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

131 rofiles of DNA methylation for 20 maize (Zea mays) inbred lines were used to discover differentially

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

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

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

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

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

137 We analyzed a maize (Zea mays) introgression library derived from two elite paren

138 Zea mays is an important genetic model for elucidating trans

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

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

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

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

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

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

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

146 Maize (Zea mays) ISA1 was expressed in Arabidopsis (Arabidopsis tha

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

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

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

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

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

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

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

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

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

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

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

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

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

160 (Vrs4), a barley ortholog of the maize (Zea mays L.) inflorescence architecture gene RAMOSA2 (RA2).

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

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

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

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

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

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

167 egulatory neofunctionalization in maize (Zea mays L.).

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

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

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

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

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

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

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

175 The maize (Zea mays) leaf offers a great tool to study growth processes

176 ale, quantitative analyses of the maize (Zea mays) leaf proteome and phosphoproteome at four developm

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

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

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

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

181 A functions were characterized in maize (Zea mays) leaves to determine whether species-specific disti

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

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

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

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

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

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

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

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

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

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

192 oducts and signals derived from a single Zea mays (maize) lipoxygenase (LOX), ZmLOX10, are critical f

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

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

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

196 ses in Solanum lycopersicum (tomato) and Zea mays (maize), two very important crop plants that are gr

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

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

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

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

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

202 rfamily comes from studies of the maize (Zea mays) Mu elements, whose transposition is mediated by th

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

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

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

206 racterized a seed-specific viable maize (Zea mays) mutant, defective endosperm18 (de18) that is impai

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

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

209 The maize (Zea mays) nucleosome remodeling factor complex component101

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

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

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

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

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

215 -glucan synthase gene GLS1 of the maize (Zea mays) pathogen Colletotrichum graminicola, employing RNA

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

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

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

219 demonstrate that a member of the maize (Zea mays) plant elicitor peptide (Pep) family, ZmPep3, regul

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

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

222 velopmentally distinct tissues in maize (Zea mays) plants of two genetic backgrounds, B73 and Mo17.

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

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

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

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

227 ied from Arabidopsis thaliana and maize (Zea mays) plants.

228 This work focuses on the maize (Zea mays) plasma membrane intrinsic protein (ZmPIP) aquapori

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

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

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

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

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

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

235 th this inference, Arabidopsis or maize (Zea mays) PyrR (At3g47390 or GRMZM2G090068) restored ribofla

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

237 .69 Gb of GBS data were generated on the Zea mays reference inbred B73, utilizing ApeKI for genome re

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

239 The maize (Zea mays) RNA Polymerase IV (Pol IV) largest subunit, RNA Po

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

241 e-3-acetic acid flux near the surface of Zea mays roots.

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

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

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

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

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

247 e leaves to low N was analyzed in maize (Zea mays) seedlings by parallel measurements of transcriptom

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

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

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

251 Using Zea mays somatic embryogenesis as a model system, we report

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

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

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

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

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

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

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

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

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

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

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

263 egion of maize (Zea mays), the Zea teosintes mays ssp. mexicana, luxurians and diploperennis, Tripsac

264 substantially altered the morphology of Zea mays ssp. parviglumis (teosinte) into the currently reco

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

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

267 ripsacum dactyloides, maize and teosinte (Z. mays ssp. parviglumis).

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

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

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

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

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

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

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

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

276 ea (Pisum sativum) homolog of the maize (Zea mays) TEOSINTE BRANCHED1 and the Arabidopsis (Arabidopsi

277 Here, we expressed maize (Zea mays) terpene synthase10 (ZmTPS10), which produces (E)-a

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

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

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

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

282 alyzed the bz gene-rich region of maize (Zea mays), the Zea teosintes mays ssp. mexicana, luxurians a

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

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

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

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

289 cross pre-domestication and domesticated Zea mays varieties, including a representative from the sist

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

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

292 haliana, rice (Oryza sativa), and maize (Zea mays), we found 3' truncation prior to tailing is widesp

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

294 ) and bundle sheath (BS) cells of maize (Zea mays), we isolated large quantities of highly homogeneou

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

296 th mutations in a nuclear gene in maize (Zea mays), white2 (w2), encoding a predicted organellar DNA

297 ly events during the infection of maize (Zea mays) with Colletotrichum graminicola, a model pathosyst

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

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

300 Physcomitrella patens (PpNRH) and maize (Zea mays; ZmNRH), using in vitro and in planta approaches.

301 he function of chloroplast RH3 in maize (Zea mays; ZmRH3) and Arabidopsis (Arabidopsis thaliana; AtRH