ライフサイエンスコーパス: Oryza sativa

1 eq2 on both mRNA and rRNA structure in rice (Oryza sativa).

2 l-produced LCOs and COs in legumes and rice (Oryza sativa).

3 s japonicus, Arabidopsis thaliana, and rice (Oryza sativa).

4 ved in mechanical stimuli responses in rice (Oryza sativa).

5 it locus for ozone stress tolerance in rice (Oryza sativa).

6 opsis thaliana), maize (Zea mays), and rice (Oryza sativa).

7 for resistance to bacterial blight in rice (Oryza sativa).

8 f calcium-dependent protein kinases in rice (Oryza sativa).

9 liana and more crossovers reported for rice (Oryza sativa).

10 re limited reports on their impacts in rice (Oryza sativa).

11 Arabidopsis (Arabidopsis thaliana) and rice (Oryza sativa).

12 plant genomes and are most abundant in rice (Oryza sativa).

13 to engineer the C(4) pathway into C(3) rice (Oryza sativa).

14 otein expressed in transgenic lines of rice (Oryza sativa).

15 Arabidopsis thaliana) and dwarf (d) of rice (Oryza sativa).

16 (Zea mays) and FRIZZY PANICLE (FZP) in rice (Oryza sativa).

17 ubmergence response of Arabidopsis and rice (Oryza sativa).

18 critical for phosphate homeostasis in rice (Oryza sativa).

19 om both seedling and callus tissues of rice (Oryza sativa).

20 provement of staple food crops such as rice (Oryza sativa).

21 scence caused by prolonged darkness in rice (Oryza sativa).

22 nd UDP-L-arabinofuranose (UDP-Araf) in rice (Oryza sativa).

23 s the most damaging fungal pathogen of rice (Oryza sativa).

24 accuracy (96%), and precision (90%) in rice (Oryza sativa).

25 genomic tools and genetic diversity in rice (Oryza sativa).

26 Arabidopsis (Arabidopsis thaliana) and rice (Oryza sativa).

27 examined the function of OsALMT4 from rice (Oryza sativa).

28 silicon content in nodes and husks of rice (Oryza sativa).

29 thaliana, Brachypodium distachyon and rice (Oryza sativa).

30 e is available for the short-day plant rice (Oryza sativa).

31 during submergence stress tolerance in rice (Oryza sativa).

32 opsis thaliana), maize (Zea mays), and rice (Oryza sativa).

33 lanum lycopersicum, Medicago truncatula, and Oryza sativa.

34 the much more widespread Asian rice species Oryza sativa.

35 thaliana, Vitis vinifera, Musa acuminata and Oryza sativa.

36 /MTP) family of metal cation transporters in Oryza sativa.

37 he biological significance of this method in Oryza sativa.

38 y recent transpositions of a TRIM element in Oryza sativa.

39 transcription factor, SHINE (SHN), in rice (Oryza sativa), a model for the grasses, causes a 34% inc

40 t collections have become available in rice (Oryza sativa), a model organism for monocots.

41 ing survival strategies have been studied in Oryza sativa, a cultivated monocot.

42 fense of wheat (Triticum aestivum) and rice (Oryza sativa) against Hessian fly (Mayetiola destructor)

43 Gene Ontology and rice (Oryza sativa) alignment-based annotation indicated that

44 However, specialized tissues of rice (Oryza sativa) also contain fucogalactoXyG.

45 The pipeline was evaluated using the Oryza sativa and Arabidopsis thaliana genomes.

46 The genus Oryza, which includes rice (Oryza sativa and Oryza glaberrima) and wild relatives, i

47 transposon polymorphisms in the rice species Oryza sativa and Oryza glaberrima, we find that DNA repa

48 A. thaliana could also be applied to predict Oryza sativa and Saccharomyces cerevisiae essential gene

49 tes, both in the compatible interaction with Oryza sativa and the incompatible interaction with the r

50 tolerance to heat stress was investigated in Oryza sativa and two wild rice species, Oryza meridional

51 most devastating disease of cultivated rice (Oryza sativa) and a continuing threat to global food sec

52 rative biochemical characterization of rice (Oryza sativa) and Agave tequilana Rca isoforms demonstra

53 e annual short-day and long-day plants rice (Oryza sativa) and Arabidopsis (Arabidopsis thaliana), wh

54 s identified in genome-wide screens of rice (Oryza sativa) and Arabidopsis thaliana, and at least 10

55 al robustness of human (Homo sapiens), rice (Oryza sativa) and budding yeast (Saccharomyces cerevisia

56 class of SUMO protease gene family in rice (Oryza sativa) and demonstrate a critical role for OsOTS1

57 ond to heat stress as demonstrated for rice (Oryza sativa) and maize (Zea mays), suggesting fundament

58 Rice (Oryza sativa) and other cereals possess stomata that are

59 quence contigs, when compared with the rice (Oryza sativa) and sorghum (Sorghum bicolor) genomes, ret

60 m (Brachypodium distachyon) as well as rice (Oryza sativa) and sorghum (Sorghum bicolor).

61 We have cloned a miR395 gene from rice (Oryza sativa) and studied its function in plant nutritio

62 -sized structural variation (SV) among rice (Oryza sativa) and three of its closest relatives in the

63 l as the antioxidant activity of black rice (Oryza sativa) and to study the stability in relation to

64 ll-characterized mutant populations of rice (Oryza sativa) and wheat (Triticum aestivum).

65 Using mutant populations of rice (Oryza sativa) and wheat (Triticum durum), we developed a

66 piens), fly (Drosophila melanogaster), rice (Oryza sativa), and Arabidopsis (Arabidopsis thaliana) an

67 Comparative genomics of maize, rice (Oryza sativa), and Arabidopsis (Arabidopsis thaliana) se

68 f proteins from Physcomitrella patens, rice (Oryza sativa), and Arabidopsis (Arabidopsis thaliana) wa

69 inearity among the wheat Snn3 regions, rice (Oryza sativa), and Brachypodium distachyon were exploite

70 haranthus roseus, maize (Zea mays) and rice (Oryza sativa), and effectively validated predicted natur

71 en1 mutants from Arabidopsis thaliana, rice (Oryza sativa), and maize (Zea mays), we found 3' truncat

72 ion evolution in Arabidopsis thaliana, rice (Oryza sativa), and maize (Zea mays).

73 ng Arabidopsis (Arabidopsis thaliana), rice (Oryza sativa), and nonvascular plants, while particularl

74 hydrolase, and UAH are also present in rice (Oryza sativa), and orthologous genes occur in all other

75 rachypodium (Brachypodium distachyon), rice (Oryza sativa), and sorghum (Sorghum bicolor), suggesting

76 uences (CDSs) of Arabidopsis thaliana, rice (Oryza sativa), and soybean (Glycine max).

77 P) approach from Arabidopsis thaliana toward Oryza sativa, and demonstrate its applicability in a var

78 nterspecific hybrid between cultivated rice, Oryza sativa, and its wild African relative, Oryza longi

79 stinct species such as Arabidopsis thaliana, Oryza sativa, and Physcomitrella patens to examine the d

80 gous chromosomes of Brachypodium distachyon, Oryza sativa, and Sorghum bicolor, whereas, by applying

81 ty on cell interfaces in leaves of C3 (rice [Oryza sativa] and wheat [Triticum aestivum]) and C4 (mai

82 idopsis thaliana], Brassica napus, and rice [Oryza sativa]), and results are compared with manual ana

83 rass genomes (Brachypodium distachyon, rice [Oryza sativa], and sorghum [Sorghum bicolor]).

84 es in the Arabidopsis thaliana, Zea mays and Oryza sativa anther development pathways shows that anth

85 how virtual transposable elements from rice (Oryza sativa) are assayed for function in transgenic Ara

86 1) in Arabidopsis and DWARF53 (D53) in rice (Oryza sativa) are downstream targets of MAX2.

87 Using rice (Oryza sativa) as a model crop species, we performed an i

88 onstrate that OsARID3, a member of the rice (Oryza sativa) AT-rich Interaction Domain (ARID) family,

89 s designed a model to predict methylation in Oryza sativa based on genomic sequence features and gene

90 AL) gene and its potential function in rice (Oryza sativa) based on phylogenetic analyses and transge

91 analysis with the sequenced genomes of rice (Oryza sativa), Brachypodium distachyon, sorghum (Sorghum

92 Arabidopsis (Arabidopsis thaliana) and rice (Oryza sativa) but poorly understood in maize (Zea mays).

93 between abiotic and biotic stresses in rice (Oryza sativa) by performing meta-analyses of microarray

94 A rice (Oryza sativa) calcium-dependent protein kinase (CDPK), C

95 ots as well as a related RDN gene from rice (Oryza sativa) can rescue the phenotype of rdn1-2 when ex

96 Rice (Oryza sativa) can survive flash floods by the emergence

97 Rice (Oryza sativa) carries two such clusters for production o

98 istance to bacterial blight disease of rice (Oryza sativa) caused by Xanthomonas oryzae pv. oryzae (X

99 Loss of DELLA activity in the monocot rice (Oryza sativa) causes complete male sterility, but not in

100 e hyphae (IH) invade successive living rice (Oryza sativa) cells while enclosed in host-derived extra

101 complex and is then translocated into rice (Oryza sativa) cells.

102 The crystallographic structure of a rice (Oryza sativa) cellulose synthase, OsCesA8, plant-conserv

103 tiling array for four fully sequenced rice (Oryza sativa) centromeres and used chromatin immunopreci

104 Recombinant catalytic domains of rice (Oryza sativa) CesA8 cellulose synthase form dimers rever

105 a 'fusion model' for the evolution of rice (Oryza sativa) chromosomes 2 and 3, implying that the gra

106 ize network and a previously described rice (Oryza sativa) coexpression network.

107 lar glucose transporter OsSWEET2b from rice (Oryza sativa), consists of an asymmetrical pair of tripl

108 Rice (Oryza sativa) contains five CYP701A subfamily members in

109 des for over 450 GTs, while the rice genome (Oryza sativa) contains over 600 members.

110 he centromere of chromosome8 (Cen8) of rice (Oryza sativa) contains several transcribed genes.

111 Future rice (Oryza sativa) crops will likely experience a range of gr

112 We confirmed that the rice (Oryza sativa) CslF6 gene mediates the biosynthesis of ML

113 Rice (Oryza sativa) cultivar Azucena--belonging to the Japonic

114 PCS genes-OsPCS1 and OsPCS2 in indica rice (Oryza sativa) cultivar, the OsPCS2 produces an alternati

115 or the response of five tropical Asian rice (Oryza sativa) cultivars to high temperatures, water defi

116 s is essential to breed climate-robust rice (Oryza sativa) cultivars.

117 acterize the biochemical function of a rice (Oryza sativa) cytochrome P450 monooxygenase, CYP76M7, wh

118 We find that the rice (Oryza sativa) d53 mutant, which produces an exaggerated

119 ed transcriptional regulatory networks (i.e. ORYZA SATIVA DEHYDRATION-RESPONSIVE ELEMENT BINDING PROT

120 leotide polymorphism genotyping products for Oryza sativa (domestic rice), we have developed a new ge

121 Higher plants such as Arabidopsis and rice (Oryza sativa) each have a gene family containing this un

122 e regulation of starch biosynthesis in rice (Oryza sativa) endosperm is crucial in tailoring digestib

123 Weedy rice (Oryza sativa f.

124 OsMADS1 controls rice (Oryza sativa) floral fate and organ development.

125 From a library of 400 semi-randomly mutated Oryza sativa FNR, the top hit enabled a 60 % increase in

126 The rice (Oryza sativa) gene xa13 is a recessive resistance allele

127 RS2 were also used to identify several rice (Oryza sativa) genes encoding ARSs, which are likely invo

128 e were able to improve the annotation of the Oryza sativa genome compared to using the standard MAKER

129 tion of genetic variants across the complete Oryza sativa genome, using the 40 million single nucleot

130 he much more GC-rich and heterogeneous rice (Oryza sativa) genome and have often been generalized as

131 ination (GR) and gene densities in the rice (Oryza sativa) genome.

132 the platform's capacity, plants of two rice (Oryza sativa) genotypes, Azucena and IR64, were grown in

133 Cytosolic Oryza sativa glyceraldehyde-3-phosphate dehydrogenase (O

134 * Inorganic arsenic (As(i) ) in rice (Oryza sativa) grains is a possible threat to human healt

135 enome-wide gene expression patterns of rice (Oryza sativa) growing in rainfed and irrigated fields du

136 we report that RNAi-mediated suppression of Oryza sativa GRXS17 (OsGRXS17) improved drought toleranc

137 Rice (Oryza sativa) has been reported to be highly Al tolerant

138 nction of a stress-responsive putative rice (Oryza sativa) histone chaperone of the NAP superfamily:

139 here we analyze two highly homologous rice (Oryza sativa) HKT transporters in plant cells, OsHKT2;1

140 tiple tissues of Arabidopsis thaliana, rice (Oryza sativa), human (Homo sapiens), and mouse (Mus musc

141 We determined the crystal structure of rice (Oryza sativa) importin-alpha1a at 2-A resolution.

142 ance was measured in five cultivars of rice (Oryza sativa) in canopy conditions with PAM fluorescence

143 Arabidopsis (Arabidopsis thaliana) and rice (Oryza sativa) in functional analyses of differentially e

144 mand for premium priced Indian Basmati rice (Oryza sativa) in world commodity market causing fraudule

145 Oryza sativa-infecting isolates showed higher directiona

146 In Asian rice (Oryza sativa), inflorescence (panicle) architecture is c

147 nt-specific HD2 subfamily of HDACs, in rice (Oryza sativa) innate immunity.

148 Asian rice, Oryza sativa is a cultivated, inbreeding species that fe

149 Rice (Oryza sativa) is a semiaquatic plant that is well adapte

150 Rice (Oryza sativa) is a staple crop that supports half the wo

151 that 70% of the overall Pi acquired by rice (Oryza sativa) is delivered via the symbiotic route.

152 Rice (Oryza sativa) is one of the major food crops in world ag

153 Rice (Oryza sativa) is one of the most important cereal grains

154 Rice (Oryza sativa) is one of the world's most important crops

155 is a ubiquitous human carcinogen, and rice (Oryza sativa) is the main contributor to iAs in the diet

156 Rice (Oryza sativa) is the primary food source for more than o

157 ,for resistance to bacterial blight of rice (Oryza sativa), is dependent on the effector genes presen

158 pe complex root systems, like those of rice (Oryza sativa), is fundamental to identifying genes under

159 Asian rice, Oryza sativa, is one of world's oldest and most importan

160 lag leaves of wild-type and transgenic rice (Oryza sativa japonica 'Kitaake') plants expressing ISOPE

161 metabolites in mature seeds of a wide panel Oryza sativa japonica and indica cultivars, revealing co

162 We introduced Xa21 into Oryza sativa L ssp indica (rice 9311), through multi-gen

163 ect on uptake and speciation in rice plants (Oryza sativa L. cv Jiahua).

164 osaic virus-35S promoter in rice transgenic [Oryza sativa L. cv. Pusa Basmati 1 (PB1)] plants confers

165 e canopies of a high-yielding rice cultivar (Oryza sativa L. cv. Takanari) with a common cultivar (cv

166 nate the actions of Cu and Cd in rice roots (Oryza sativa L. cv. TN67).

167 smine (Jasminum nudiflorum), and black rice (Oryza sativa L. indica) by ethanol.

168 termined the crystal structures of DHAR from Oryza sativa L. japonica (OsDHAR) in the native, ascorba

169 Domesticated rice (Oryza sativa L.) accompanied the dawn of Asian civilizat

170 A new resequencing analysis of weedy rice (Oryza sativa L.) biotypes illuminates distinct evolution

171 ice is not of the same origin as Asian rice (Oryza sativa L.) but rather is an entirely different spe

172 crop species closely related to Asian rice (Oryza sativa L.) but was independently domesticated in W

173 Asian cultivated rice (Oryza sativa L.) consists of two main subspecies, indica

174 39 aromatic indica rice (Oryza sativa L.) cultivars were characterized for Iron,

175 For the first time, 91 Indian rice (Oryza sativa L.) cultivars, belonging to non-basmati sce

176 otosynthate allocation to the grain in rice (Oryza sativa L.) has been identified as an effective str

177 nd an interesting model monocot plant, rice (Oryza sativa L.) has recently received attention from mo

178 Rice (Oryza sativa L.) is the primary staple food source for m

179 Here, we characterized a rice (Oryza sativa L.) osmogs mutant with shortened roots and

180 d larger bulk particles (BPs) in rice plant (Oryza sativa L.) tissues was evaluated using three ortho

181 Black and red rices (Oryza sativa L.) were analysed for total flavonoids and

182 In rice (Oryza sativa L.), the haplotype at the multigenic SUBMER

183 ore relevant in inbred species such as rice (Oryza sativa L.), which are effectively haploid, allowin

184 fic cell types (INTACT) to the monocot rice (Oryza sativa L.).

185 identification of a specific stage in rice (Oryza sativa) leaf development (P3/P4 transition) when p

186 we have isolated and characterized the rice (Oryza sativa) LESION AND LAMINA BENDING (LLB) gene that

187 hough heat stress reduces seed size in rice (Oryza sativa), little is known about the molecular mecha

188 Overexpression of the rice (Oryza sativa) MADS26 gene in rice has revealed a possibl

189 lysis of AS patterns in B. distachyon, rice (Oryza sativa), maize (Zea mays), sorghum (Sorghum bicolo

190 comparison of the H3K27me3 targets in rice (Oryza sativa), maize, and Arabidopsis thaliana provided

191 To identify previously unknown rice (Oryza sativa) microRNAs (miRNAs) and those regulated by

192 Agrostis stolonifera) overexpressing a rice (Oryza sativa) miR319 gene, Osa-miR319a.

193 ere, a series of expression vectors based on Oryza sativa MIR390 (OsMIR390) precursor was developed f

194 that in rice, transcript level of OsamiR395 (Oryza sativa miR395) increased under sulfate deficiency

195 re, we report that overexpression of a rice (Oryza sativa) miR528 (Osa-miR528) in transgenic creeping

196 ation sequencing, we pyrosequenced two rice (Oryza sativa) mitochondrial genomes that belong to the i

197 y discovered transposable element from rice (Oryza sativa), mPing, and the genes required for its mob

198 In this study, we demonstrated that a rice (Oryza sativa) MULE, Os3378, is capable of excising and r

199 erization of a dominant SL-insensitive rice (Oryza sativa) mutant dwarf 53 (d53) and the cloning of D

200 d loss of responsiveness to AMF in the rice (Oryza sativa) mutant hebiba, reflected by the absence of

201 A rice (Oryza sativa) mutant led to the discovery of a plant-spe

202 udy, we identified and characterized a rice (Oryza sativa) mutant line containing a 750 bp deletion i

203 We identified a male-sterile rice (Oryza sativa) mutant with impaired pollen development an

204 Examination of rice (Oryza sativa) mutants in a grass-expanded and -diverged

205 ass family, as we demonstrate that the rice (Oryza sativa) NECK LEAF1 (NL1) and barley (Hordeum vulga

206 transient growth inhibition response, rice (Oryza sativa 'Nipponbare') seedlings had a slow onset of

207 The rice (Oryza sativa) NLR RGA5 recognizes the Magnaporthe oryzae

208 TION-RESPONSIVE ELEMENT BINDING PROTEIN1 and ORYZA SATIVA No Apical Meristem, Arabidopsis Transcripti

209 erbicide-resistant weeds in crops; (3) rice (Oryza sativa), often infested with feral weedy rice, whi

210 ologs in poplar (Populus trichocarpa), rice (Oryza sativa), or Chlamydomonas reinhardtii.

211 Rice (Oryza sativa) Os9BGlu31 is a glycoside hydrolase family

212 tation of the BT1/BT2 ortholog gene in rice (Oryza sativa) OsBT increased NUE by 20% compared to wild

213 urprisingly, a subfamily 2 member from rice (Oryza sativa), OsHKT2;4, has been proposed to form catio

214 AtSHR), Brachypodium distachyon (BdSHR), and Oryza sativa (OsSHR1 and OsSHR2) function in patterning

215 The rice (Oryza sativa) p-COUMAROYL-Coenzyme A MONOLIGNOL TRANSFER

216 rosophila melanogaste, Arabidopsis thaliana, Oryza sativa, Physcomitrella patens and Chlamydomonas re

217 etermined the substrate specificity of rice (Oryza sativa) phytaspase by using the positional scannin

218 wth media and by altered copper transport in Oryza sativa plants.

219 mospora indica on interactions between rice (Oryza sativa) plants and its root herbivore rice water w

220 sets of wheat (Triticum aestivum) and rice (Oryza sativa) plants as well as a unique virtual data se

221 5)NH4NO3 The technology was applied to rice (Oryza sativa) plants at different growth stages.

222 Rice (Oryza sativa) presents the lowest content for all AA.

223 representing a developing leaf cell of rice (Oryza sativa) primarily derived from the annotations in

224 Rice (Oryza sativa) produces a variety of labdane-related dite

225 Rice (Oryza sativa) produces momilactone diterpenoids as both

226 e and drought are major constraints to rice (Oryza sativa) production in rain-fed farmlands, both of

227 jor challenges to sustaining irrigated rice (Oryza sativa) production.

228 The rice (Oryza sativa) protein kinase, PHOSPHORUS-STARVATION TOLE

229 ain and a serine/threonine kinase, the rice (Oryza sativa) protein XA21 confers resistance to a broad

230 Rice (Oryza sativa) provides a staple food source for more tha

231 The mechanism is not found in the rice (Oryza sativa) PSY1 5'UTR, consistent with the prevalence

232 Here, we identified a rice (Oryza sativa) remorin gene, OsREM4.1, whose expression i

233 42 and 353 miRNAs from Arabidopsis and rice (Oryza sativa), respectively.

234 m sequence of the KNOX gene Oskn2 from rice (Oryza sativa) resulted in isolation of OsGRF3 and OsGRF1

235 Two NB-LRR protein-coding genes from rice (Oryza sativa), RGA4 and RGA5, were found to be required

236 motif, and promotes vertical shoot growth in Oryza sativa (rice) and Arabidopsis through influencing

237 332 NBS-LRR genes cloned from five resistant Oryza sativa (rice) cultivars for their ability to confe

238 Recent reports in Oryza sativa (rice) identified a role for DEEPER ROOTING

239 ificance of this processing, we isolated two Oryza sativa (rice) mutants (fuct-1 and fuct-2) with los

240 of sequence similarity with LAZY1, a gene in Oryza sativa (rice) shown to participate in the early gr

241 hways in these domains for reference species Oryza sativa (rice) supported by published literature an

242 Here, we use the flowering plant Oryza sativa (rice) to characterize transcriptomes of ti

243 Detailed molecular profiling of Oryza sativa (rice) was carried out to uncover the featu

244 eaves of Zea mays (maize), a C(4) plant, and Oryza sativa (rice), a C(3) plant, using a statistical m

245 sperm cells and pollen vegetative cells from Oryza sativa (rice), and identified transcripts for appr

246 six prioritized key dietary protein sources: Oryza sativa (rice), Triticum aestivum (wheat flour), Le

247 ogen-activated protein kinase (MPK) genes in Oryza sativa (rice).

248 highly expressed in flower and endosperm in Oryza sativa (rice).

249 aracterized the function of class I genes in Oryza sativa root development.

250 1-methyladenosine (m1A) in a nuclear-encoded Oryza sativa rRNA.

251 mensional quantification of changes in rice (Oryza sativa) RSA in response to the physical properties

252 al P content of Pi-deficient wild-type rice (Oryza sativa) seedlings.

253 al endoplasmic reticulum in developing rice (Oryza sativa) seeds.

254 Mutants in five rice (Oryza sativa) SEP genes suggest both redundant and uniqu

255 atlas that includes 40 cell types from rice (Oryza sativa) shoot, root and germinating seed at severa

256 t work on the cultivated microbiome in rice (Oryza sativa) shows that a wide diversity of bacterial s

257 er, Danio rerio, Homo sapiens, Mus musculus, Oryza sativa, Solanum lycopersicum and Zea mays) are ana

258 eny blocks in Brachypodium distachyon, rice (Oryza sativa), sorghum (Sorghum bicolor) and barley (Hor

259 Comparison of rice (Oryza sativa), sorghum (Sorghum bicolor), maize (Zea may

260 n six nontrained eukaryotic organisms (rice [Oryza sativa], soybean [Glycine max], human [Homo sapien

261 mone jasmonic acid (JA) in determining rice (Oryza sativa) spikelet morphogenesis.

262 expanded the expression domain of the rice (Oryza sativa ssp japonica) OsSHR2 gene, which we show is

263 genic methylation patterns to those of rice (Oryza sativa ssp. japonica).

264 ueprint of the genetic architecture of rice (Oryza sativa) stem nonstructural carbohydrates (NSC) at

265 We previously characterized the rice (Oryza sativa) Submergence1 (Sub1) locus encoding three e

266 e now available for Arabidopsis thaliana and Oryza sativa, such profiles remain static and do not pro

267 Rice (Oryza sativa) takes up arsenite mainly through the silic

268 ubisco with higher thermal sensitivity (e.g. Oryza sativa) than others (e.g. Lactuca sativa), intersp

269 e of five calmodulins known to be present in Oryza sativa that relays the increase of cytosolic [Ca(2

270 CM) and limit yield of cereals such as rice (Oryza sativa) that feeds half the world.

271 ergrass) is a major weed of California rice (Oryza sativa) that has evolved cytochrome P450-mediated

272 In rice (Oryza sativa), the chitin elicitor binding protein (CEBi

273 In rice (Oryza sativa), the CYTOKININ-RESPONSIVE GATA TRANSCRIPTI

274 In rice (Oryza sativa), the GF14e gene, which encodes a 14-3-3 pr

275 ial for chitin recognition, whereas in rice (Oryza sativa), the LysM-containing protein, CEBiP (for c

276 Rice (Oryza sativa), the most important food crop, is salt sen

277 In rice (Oryza sativa), the plastid-localized protein DWARF27 (Os

278 In rice (Oryza sativa), the reproductive phase is initiated by ex

279 Rice (Oryza sativa), the staple crop for the largest number of

280 For Oryza sativa, the technique has been initiated in callus

281 found in wheat (Triticum aestivum) and rice (Oryza sativa), this transgene increases maize yield by i

282 ublished data from S. bicolor, Zea mays, and Oryza sativa to identify a small suite of transcription

283 of herbicide-resistant (HR) Clearfield rice (Oryza sativa) to control weedy rice has increased in the

284 dicago truncatula, Solanum lycopersicum, and Oryza sativa) to delineate open chromatin regions and tr

285 ruce (Picea abies) and the angiosperms rice (Oryza sativa), tobacco (Nicotiana tabacum), and Arabidop

286 tified salt-responsive ERF1 (SERF1), a rice (Oryza sativa) transcription factor (TF) gene that shows

287 onal gene clusters were discovered for rice (Oryza sativa) using a global, knowledge-independent para

288 wo-component elements from the monocot rice (Oryza sativa) using several complementary approaches.

289 the node, internode and leaf sheath of rice (Oryza sativa) using synchrotron X-ray fluorescence (S-XR

290 charum officinarum) callus, and indica rice (Oryza sativa var. indica) callus.

291 that confers submergence tolerance in rice (Oryza sativa) via limiting shoot elongation during the i

292 In rice (Oryza sativa), we computed a body methylation level (pro

293 ut of the three homologs identified in rice (Oryza sativa), we have functionally characterized OsbZIP

294 psis (Arabidopsis thaliana) to a crop, rice (Oryza sativa), we identified evolutionarily conserved N-

295 Sperm cells of rice (Oryza sativa) were isolated from field-grown, disease-fr

296 the positions of cenH3 nucleosomes in rice (Oryza sativa), which has centromeres composed of both th

297 LLA during infection of the model crop rice (Oryza sativa) with four different pathogens exhibiting d

298 and impact of BRs during infection of rice (Oryza sativa) with the root oomycete Pythium graminicola

299 similar in domain architecture to the rice (Oryza sativa) XA21 Binding Protein3, a defense protein.

300 Genomes of the rice (Oryza sativa) xylem and mesophyll pathogens Xanthomonas