ライフサイエンスコーパス: maize

1 mycotoxins in whole grain samples (wheat and maize).

2 er-free intra-genomic gene targeting (GT) in maize.

3 resource for functional genetics studies of maize.

4 cinogenic mycotoxins, fumonisins on infested maize.

5 lutionary features with classical mutants in maize.

6 ative, flowering and grain-filling stages of maize.

7 II assembly in mesophyll cells in etiolated maize.

8 the possible basis for inbred instability in maize.

9 ch is consistent with findings in humans and maize.

10 ontributes to the nuclear/cytoplasmic HSR in maize.

11 on has only been developed and exploited for maize.

12 itional KWL paralogs have been identified in maize.

13 lular partitioning of C(4) photosynthesis in maize.

14 expressed higher in tropical than temperate maize.

15 in the modal prices of paddy, groundnut, and maize.

16 gested to be affected by numerous factors in maize.

17 on the occurrence of examined mycotoxins in maize.

18 rnel varieties and high vitamin A content in maize.

19 derstand the genetic architecture of husk in maize.

20 future studies of tritrophic interactions in maize.

21 leiotropic effects on the leaf microbiome in maize.

22 hobo element and the Activator element from maize.

23 68.1% of RS3 from pea and 59.6% from normal maize.

24 Maize, 15% Rice and 6.5% WPC) and F2 (82.4% Maize, 12% Rice and 5.6% WPC) were optimized using a mix

25 We show that a maize 13-lipoxygenase mutant, lox10, colonized by the wi

26 all cakes properties, two formulas F1 (78.5% Maize, 15% Rice and 6.5% WPC) and F2 (82.4% Maize, 12% R

27 ricarp sweetcorn (61.1%) and cherry-aleurone maize (74.6%).

28 p sweetcorn (75.5% of TAC) and blue-aleurone maize (91.6%), while pelargonidin-based glucosides compo

29 Without N fertilizer input, maize (a) benefited less from an increase in atmospheric

30 f 627 RNA-seq analyses are performed for 224 maize accessions which represent a wide genetic diversit

31 ic and morphological analysis of the classic maize adherent1 (ad1) mutant was combined with genome-wi

32 The expanding maize adult leaf displays a dynamic, proximodistal gradi

33 However, a lowland site showed continuous maize agriculture until European conquest but very littl

34 l community response to drought in temperate maize agroecosystems, as well as how these responses to

35 Maize also has two cytosolic isozymes, PGD1 and PGD2, th

36 lic complexes under hydrothermal treatments, maize amylopectin and potato starch were complexed with

37 es were observed for analyzing target AFs in maize and cereal-based chicken feed samples ranged from

38 ptera frugiperda is one of the main pests of maize and cotton in Brazil and has increased its occurre

39 On the other hand, both maize and cowpea anthocyanins were unstable and rapidly

40 bility of sorghum 3-DXA vs anthocyanins from maize and cowpea under microwave-assisted extraction (MA

41 We validate an association between maize and Dyella japonica, a putative producer abundant

42 n a region of chromosome 8 introgressed from maize and encompassing ZCN8, a major flowering time gene

43 matically investigated the MC gene family in maize and identified 11 ZmMCs belonging to two types.

44 Previous studies revealed maize and mixed-food refuse at both sites, but this stud

45 Normal maize and pulse flours formed hard gels after cooking at

46 Maize and rice domestication appears to be associated wi

47 ere used to acquire convergent phenotypes in maize and rice domestication, during which different cen

48 findings of the present study indicated that maize and rice flours, and WPC could be used as a substi

49 The absence of premeiotic 24-nt phasiRNAs in maize and rice suggests a divergence in grass species of

50 ifferences in the domestication processes of maize and rice, two major staple food crops that feed th

51 On average, maize and soybean produced 98% and 77% of SM and SS yiel

52 rip-width for obtaining high grain yields of maize and soybean was 200 cm (medium-strips), which impr

53 ltaneous extraction of multi-mycotoxins from maize and subsequent quantification on LC-MS/MS.

54 By year 5, maize and wheat availability would decrease by 13% globa

55 extensive data from CIMMYT's (International Maize and Wheat Improvement Center) wheat breeding progr

56 luding tomato, pepper, Brassica, barley, and maize, and concluded an approach for large-scale germina

57 lity of GHG emissions intensities for wheat, maize, and rice in China from 1949 to 2012 using an impr

58 orn, recently developed from purple Peruvian maize, and the effect of kernel maturity on anthocyanin

59 ays of maize embryonic leaves suggested that maize ANT1 (ZmANT1) regulates vascular development.

60 ent cell layers of early developmental stage maize anthers that are important for male sexual reprodu

61 infants, and children in the development of maize as a staple crop.

62 ed role of predicted auxin response genes in maize as well as provide evidence that a synthetic appro

63 The application of the optimal mixture in maize at 0.95 a(w) (0.39 mM NAR, 0.24 mM NEO and 0.40 mM

64 a selected Aspergillus parasiticus strain in maize at 0.95 a(w) were studied by response surface meth

65 maize components, including the ZmAFB2/3 b1 maize AUXIN SIGNALING F-BOX (AFB) receptor, was fully fu

66 All 16 maize auxin/indole-3-acetic acid repressor proteins were

67 Transcriptome analysis of TvWT-treated maize B73 revealed upregulation of 12-OPDA biosynthesis

68 a weaning food (e.g., gruel and/or chicha-a maize beverage), hinting at the significant role of brea

69 multivariate genomic prediction models in a maize breeding program.

70 Since the development of single-hybrid maize breeding programs in the first half of the twentie

71 Especially in maize breeding programs, it emerges as a promising tool

72 nd phenotypic changes associated with modern maize breeding through chronological sampling of 350 eli

73 Our findings suggest that the second wave of maize brought into South America hybridized with long-es

74 Closing the yield gap of maize by increasing N fertilizer use reduced emission in

75 We characterized the deposition of CENH3 in maize by over-expression and mutational analysis.

76 er the past 110 years in symptoms induced in maize by the broad host-range pathogen, maize streak vir

77 da for resistance to single and pyramided Bt maize can result in cross-crop resistance to DAS-444O6-6

78 mmunoprecipitation data demonstrate that the maize CFM1 ortholog is bound to introns whose splicing i

79 The maize chloroplast-localized 6-phosphogluconate dehydroge

80 Maize chlorotic mottle virus (MCMV) combines with a poty

81 Maize chlorotic mottle virus (MCMV) infection is require

82 A maize chromosome variant called abnormal chromosome 10 (

83 The nNILs are a valuable resource for the maize community, providing an extensive collection of in

84 mplete auxin response circuit comprising all maize components, including the ZmAFB2/3 b1 maize AUXIN

85 N balance was associated with fields growing maize continuously and applying higher N inputs without

86 Maize (corn) is the dominant grain grown in the world.

87 The KWL1 protein from maize (corn, Zea mays) specifically inhibits the enzymat

88 a parallel, but earlier, history of reduced maize cultivation and forest regeneration at mid-elevati

89 D 1230 forests had regrown in the valley and maize cultivation was greatly reduced.

90 Forest clearance and maize cultivation were initiated during periods of droug

91 The unaged seeds of two independent maize DEHYDRATION-RESPONSIVE ELEMENT-BINDING2A mutant (z

92 Maize demonstrated root avoidance in maize/maize, with r

93 o, loss-of-function, coding variation, while maize domestication more frequently favored standing, ga

94 volution of the methylation landscape during maize domestication remain largely unknown.

95 open chromatin regions (OCRs) in developing maize ear and tassel primordia using ATAC-seq and charac

96 mental and morphological diversities between maize ear and tassel.

97 is a fungal pathogen that is responsible for maize ear rot and stalk rot diseases worldwide.

98 The husk-the leaf-like outer covering of maize ear-has multiple functions, including protecting t

99 Maize ears and tassels are two separate types of inflore

100 analysis and in situ hybridization assays of maize embryonic leaves suggested that maize ANT1 (ZmANT1

101 Mutation of o2 doubles maize endosperm lysine content, but it causes an inferio

102 Maize exhibits marked growth and yield response to suppl

103 ibuting to the risk assessment of transgenic maize expressing insecticidal dsRNA.

104 om neighbours in the maize/maize than in the maize/faba bean experiment.

105 reater in the heterogeneous P treatment with maize/faba bean than with maize/maize system.

106 ize (maize/maize) or faba bean (Vicia faba) (maize/faba bean) as a neighbour on one side and with or

107 Thus, EPN from Mexican maize fields can cope with these plant defence metabolit

108 n in magnitude of N balance across irrigated maize fields in the US Corn Belt was explained by persis

109 r cooking at 120 degrees C, and high-amylose maize flour developed the firmest gel after cooking at 1

110 concentrate (WPC) and two flours of rice and maize flours for the production of gluten-free sponge ca

111 However, pulse and high-amylose maize flours required a holding temperature above 95 deg

112 By substituting CA-based maize for rice, similar mean profitability gains were re

113 sively inter-crossing 24 widely used Chinese maize founders.

114 at are closely related to ancient and modern maize from South America.

115 vered dsRNA for the protection of transgenic maize from WCR feeding damage and information contributi

116 To accelerate maize gene discovery and breeding, we present the Comple

117 The maize gene NARROWSHEATH1 (NS1) is a WUSCHEL-related home

118 king proximal promoters, but also 3' ends of maize genes.

119 ntinues to be an invaluable resource for the maize genetics community and has yielded insights into t

120 ilable for free, public distribution via the Maize Genetics Cooperation Stock Center.

121 ical map-based merging pipeline to produce a maize genome (B73-Ab10) composed of 63 contigs and a con

122 is not syntenic with any other region of the maize genome and shows extraordinary sequence divergence

123 feature, present in 25% of cytosines in the maize genome, but variation and evolution of the methyla

124 led view of the distribution of sRNAs in the maize genome, revealing a complex makeup that also shows

125 s, and Sirevirus LTR retrotransposons in the maize genome.

126 Here we report ancient maize genomes (2,300-1,900 cal.

127 We report maize genomic regions associated with indirect defence a

128 As we enter an exciting new stage in maize genomics, this retrospective will summarize the de

129 genome wide association study (GWAS) of 146 maize genotypes comprising of landraces, inbred lines an

130 ned MSV isolates in differentially resistant maize genotypes to phylogenetically infer ancestral symp

131 enotyping-by-sequencing was used to generate maize germplasm SNP data for GWAS.

132 e become some of the most well-characterized maize germplasm, and their de novo assemblies were recen

133 Spanish, and Mexican teosintes as well as in maize germplasm.

134 in 204 maize samples harvested in Serbia in maize growing seasons with extreme drought (2012), extre

135 ic introgression from the high latitude Dent maize grown in Europe.

136 nts, thus improving nutrient acquisition and maize growth.

137 lus thuringiensis (Bt) proteins expressed in maize has been characterized in Brazil, Argentina, Puert

138 -C) is the most commonly used form of CMS in maize hybrid seed production.

139 The elite maize hybrid Zhengdan 958 (ZD958), which has high and st

140 Ten maize hybrids (six newer and four older) were grown in a

141 Breeders have enhanced grain productivity of maize hybrids by pyramiding desirable characteristics fo

142 To this end, we used data from 415 maize hybrids evaluated in 4 years of second season fiel

143 finding provides knowledge basis to enhance maize hybrids grain yield.

144 The orange maize hybrids used for the study were obtained from the

145 Four summer annuals and a collection of maize hybrids were grown in a common garden experiment c

146 roles in gene expression complementation in maize hybrids.

147 conditions and in newer and older generation maize hybrids.

148 tem for the enrichment of the zein gene from maize in eight cereal product samples.

149 an by maintaining the competitive-ability of maize in MSR.

150 s and climatological data were developed for maize in rain-fed conditions.

151 eriment, soybean was relay-intercropped with maize in three different strip-width arrangements (narro

152 ght assemblies for the complex genome of the maize inbred line NC358 using PacBio datasets ranging fr

153 were introgressed into a disease-susceptible maize inbred line.

154 tion by comparing the microbiomes of diverse maize inbred lines and their F(1) hybrid offspring, whic

155 used transcriptome data of diverse Zea mays (maize) inbreds and hybrids, including 401 samples from f

156 A dominance of larger roots in ruzigrass and maize increased nitrate loss through enhanced solute flo

157 is (bx7, 9) and known resistance genes (e.g. maize insect resistance 1, mir1).

158 Maize is used primarily as an animal feed in the product

159 uencing (WGBS) data on populations of modern maize, landrace, and teosinte (Zea mays ssp. parviglumis

160 le virus (MCMV) combines with a potyvirus in maize lethal necrosis disease (MLND), a serious emerging

161 s of 3' CITEs.IMPORTANCE In the past decade, maize lethal necrosis disease has caused massive crop lo

162 ownstream genes are present in B73, a modern maize line, but absent in teosinte.

163 While some tolerant maize lines have been identified, there are no known res

164 recovered recently from the pollen of select maize lines resulted from the meiotic mobilization of sp

165 We developed aneuploid tetraploid maize lines that contain three copies of chromosome 10 d

166 editing of a waxy allele in 12 elite inbred maize lines, a process that was more than a year faster

167 were identified in 10 independently derived maize lines.

168 unprocessed freshly harvested orange hybrid maize; lutein, zeaxanthin, beta-cryptoxanthin, tannin an

169 ferulate esters were detected in sorghum and maize MAE extracts, indicating cell wall degradation occ

170 (Zea mays) was grown alone (maize), or with maize (maize/maize) or faba bean (Vicia faba) (maize/fab

171 s P treatment with maize/faba bean than with maize/maize system.

172 f, the P patches away from neighbours in the maize/maize than in the maize/faba bean experiment.

173 ays) was grown alone (maize), or with maize (maize/maize) or faba bean (Vicia faba) (maize/faba bean)

174 Maize demonstrated root avoidance in maize/maize, with reduced root growth in 'shared' soil,

175 the functional and nutritional properties of maize meal with SA and has the potential to replace conv

176 ties of infrared heat-moisture treated (HMT) maize meal with stearic acid were studied.

177 -arid Mali and Benin using an ensemble of 25 maize models.

178 yll deficit suppressed tillering in multiple maize mutants, including teosinte branched1, Tillering1,

179 ned with genome-wide binding analysis of the maize MYB transcription factor FUSED LEAVES1 (FDL1), cou

180 n of introgressions from the founders of the maize NAM population in a B73 background combined with d

181 We characterized a panel of 1270 maize NILs derived from crosses between 18 diverse inbre

182 report the functional characterization of a maize NIN-like protein ZmNLP5 as a central hub in a mole

183 This is true for maize (only 41% of N in crops was from current-year N fe

184 Maize (Zea mays) was grown alone (maize), or with maize (maize/maize) or faba bean (Vicia

185 pled the soils annually after harvesting the maize over the following 6 years (from 2005 to 2011).

186 ion affects water relations and growth using maize overexpression (OE; B104 inbred) or knockout (KO;

187 ra; Coleoptera: Chrysomelidae), an important maize pest in America and Europe.

188 s that may be used to control this important maize pest.

189 s, consistent with patterns for nonmicrobial maize phenotypes.

190 ied genomic DNA obtained from a MSV-infected maize plant, a sensitivity 10(5) times higher to that ob

191 Transgenic maize plants expressing dsRNA targeting western corn roo

192 Transgenic maize plants expressing WPGD1 and WPGD2 with an endosper

193 weight (HMW) root exudates of both wheat and maize plants indicate the presence of complex, highly br

194 (0, 25 and 50 uM) was applied to Cd-treated maize plants.

195 iets are high in abrasives, potentially from maize processing.

196 ts into the causes and limitations of global maize production and offer some guidances for water and/

197 Total maize production in 2018 equaled 1.12 billion tons.

198 ystems will be modified if farmers intensify maize production with balanced nutrient management.

199 pathogenic fungi are of constant concern in maize production, as they pose serious risks to human an

200 Maize proliferated more roots, but spent less time to re

201 Conversely, maize proliferated roots in the proximity of neighbourin

202 restored virus replication, respectively, in maize protoplasts and in plants.

203 Overexpression of ZmDREB2A in maize protoplasts increased the expression of ZmGH3.2, Z

204 omoter was shown to be a target of bZIP60 in maize protoplasts.

205 , we identified proteins that associate with maize psbA mRNA by: (i) formaldehyde cross-linking of le

206 Overexpression of maize PTPN (ZmPTPN) promoted, while knockdown of ZmPTPN

207 nto a genetic mapping population to evaluate maize response to AMF.

208 hromosome structure at unrelated clusters in maize, rice, and tomato indicates that integration of cl

209 the total number of PHAS loci in genomes of maize, rice, barley, and wheat, we identified an expansi

210 ist benzoxazinoids that are sequestered from maize roots by the western corn rootworm (WCR, Diabrotic

211 The foraging strategy of maize roots is an integrated function of heterogeneous d

212 IAA redistribution occurred in maize roots, preceding hydrotropic bending.

213 nd acid phosphatase exudation) compared with maize roots.

214 digestible by amylolytic enzymes than normal maize RS3 because the former possessed double-helical cr

215 Both pea and normal maize RS3 displayed the B-type X-ray diffraction pattern

216 The particles of pea and normal maize RS3 showed a coarse surface and irregular shapes a

217 We propose that maize Rtn1 and Rtn2 act as receptors for autophagy-media

218 Maize Rtn1 and Rtn2 are expressed in the endosperm, loca

219 We have found that maize Rtn1 and Rtn2 control ER homeostasis and autophagi

220 Maize rtn2 mutants display increased autophagy and up-re

221 ervative to improve the shelf-life of stored maize samples against fungal and aflatoxin contamination

222 letely inhibited AFB(1) production in stored maize samples during in situ investigation.

223 Aflatoxin B(1) was detected in 94% and 90% maize samples from 2012 and 2015, respectively.

224 LAMP assay can be used for detecting MSV in maize samples from any region in Africa.

225 stigate the presence of 20 mycotoxins in 204 maize samples harvested in Northern Serbia in the period

226 e of non-regulated fungal metabolites in 204 maize samples harvested in Serbia in maize growing seaso

227 ted ZEA in spiked and naturally contaminated maize samples using liquid chromatography-tandem mass sp

228 and relative standard deviation from spiked maize samples.

229 nce that ZmDREB2A regulates the longevity of maize seed by stimulating the production of raffinose wh

230 plant epiphyte Pseudomonas protegens Pf-5, a maize seed inoculant.

231 ll function and cell-fate acquisition in the maize seedling and provide a valuable scaffold on which

232 phosphate limitation and robustly colonizes maize seedling roots.

233 se in cuticle-dependent leaf permeability in maize seedlings exposed to drought as well as abscisic a

234 Maize shoot biomass and P uptake were greater in the het

235 tion of the transcriptional landscape of the maize shoot stem-cell niche and its differentiating cell

236 ss (Pennisetum purpureum), FeCo supplemented maize silage and FoFeCo a combination of Napier, silage

237 e susceptible, selected for resistance to Bt-maize single (Cry1F) or pyramided (Cry1F/Cry1A.105/Cry2A

238 ntercropping results were compared with sole maize (SM) and sole soybean (SS).

239 re is dominated by a few major annual crops (maize, soybean, wheat) that are mostly grown on fields w

240 Maize/soybean relay intercropping system (MSR) is a popu

241 n encapsulated SNPs prepared from quinoa and maize starch (QR and MR) showed average particle sizes o

242 pared with that generated from native normal maize starch.

243 cles ranged from 20 to -179 g CO(2)e MJ(-1): maize stover >> miscanthus ~ switchgrass ~ native grasse

244 us > poplar > switchgrass > native grasses ~ maize stover (residue) > restored prairie ~ early succes

245 d in maize by the broad host-range pathogen, maize streak virus (MSV).

246 Maize tan1 mutant cells improperly position the preproph

247 Genes linked to phenomic variation in maize using GPWAS shared molecular, population genetic,

248 escribe DNA enrichment of the zein gene from maize using pyrrolidinyl peptide nucleic acid (PNA) immo

249 Biofortified maize varieties form an essential part of a nutritious d

250 Maize was likely used as a weaning food (e.g., gruel and

251 is underlying the dramatic yield increase in maize, we conducted a comprehensive analysis of the geno

252 ed using GPWAS with 260 phenotypic traits in maize were enriched for genes independently linked to ph

253 cal teosintes, the closest wild relatives of maize, were recently reported as new agricultural weeds

254 against a wide range of fungal pathogens of maize, wheat and locusts, without affecting their respec

255 3.95% for the three main staple crops (i.e., maize, wheat, and rice), together accounting for 72% of

256 ies, including important food crops, such as maize, wheat, rice, and potatoes.

257 family that contains important crops such as maize, wheat, rice, and sorghum.

258 els show that global caloric production from maize, wheat, rice, and soybean falls by 13 (+/-1)%, 11

259 rowing season temperature trends for rainfed maize, wheat, rice, and soybean using spatially-explicit

260 Inclusion of mungbean in the rotation (i.e. maize-wheat-mungbean) with CA-based management increased

261 ript-based TE annotation for Arabidopsis and maize, which serves as a blueprint to reduce the bioinfo

262 -Saharan Africa (SSA) currently grow rainfed maize with limited inputs including fertilizer.

263 e detection of FB1 in naturally contaminated maize, with a dynamic range of 0.533-6.81 ng mL-1 and a

264 Here we use satellite remote sensing and maize yield data in the state of Nebraska, USA, combined

265 2) ], temperature and rainfall conditions on maize yield, for different nitrogen (N) inputs (0, 80, 1

266 The input of water increased maize yield, WP, and NUE only when the input was less th

267 d 311 mm, respectively; input of N increased maize yield, WP, and NUE until input was greater than 25

268 the first half of the twentieth century(1), maize yields have increased over sevenfold, and much of

269 induced responses to stemborer egg-laying in maize Zea mays (L.) (Poaceae).

270 t agronomic optimum plant density (AOPD) for maize (Zea mays L.) is a critical management decision, b

271 Maize (Zea mays L.) is one of the most versatile crops w

272 efficient breeding and selection of high-oil maize (Zea mays L.).

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

274 Maize (Zea mays ssp. mays) domestication began in southw

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

276 pathogenic lifestyle during colonization of maize (Zea mays) and soybean (Glycine max), respectively

277 e used ISR-positive and -negative mutants of maize (Zea mays) and the beneficial fungus Trichoderma v

278 Sequence-indexed insertional libraries in maize (Zea mays) are fundamental resources for functiona

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

280 d an integrated multiomics approach to study maize (Zea mays) autophagy mutants subjected to fixed-ca

281 cerevisiae) system to functionally annotate maize (Zea mays) auxin signaling components, focusing on

282 Using maize (Zea mays) genetic markers and transcript levels f

283 igate the non-coding regulatory space in the maize (Zea mays) genome during early reproductive develo

284 root anatomy and architecture of 400 mature maize (Zea mays) genotypes under well-watered and water-

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

286 just over a decade since the release of the maize (Zea mays) Nested Association Mapping (NAM) popula

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

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

289 tate distribution in both N. benthamiana and maize (Zea mays) protoplasts.

290 riation and inheritance among a panel of 108 maize (Zea mays) samples spanning five tissues from eigh

291 e of plant development are controlled by the maize (Zea mays) transcription factor ZmFUSED LEAVES 1 (

292 lyzed a large number of publically available maize (Zea mays) transcriptome data sets including >6000

293 ons in recA, which were fully functional for maize (Zea mays) transformation and confirmed the import

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

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

296 ment is expanded in a TE-rich genome such as maize (Zea mays).

297 is encoded by the oil yellow1 (oy1) gene in maize (Zea mays).

298 the protein-DNA interaction (PDI) network in maize (Zea mays).

299 h a handful of species (rice [Oryza sativa], maize [Zea mays], and wheat [Triticum aestivum]) providi

300 ious work examining Pep-induced responses in maize (Zm) implied specificity of function.