ライフサイエンスコーパス: Oryza

1 ts when comparing Spartina to Sorghum and to Oryza.

2 p and nR of several of specimens of the same Oryza AA genome species provides insight into the evolut

3 In the rice genus (Oryza), about one half of the species are allopolyploids

4 Coix with those of Brachypodium, Setaria and Oryza allows us to infer how the region has evolved by a

5 wo wild rice species, Oryza meridionalis and Oryza australiensis.

6 genomics analyses of 20 O. glaberrima and 94 Oryza barthii accessions support the hypothesis that O.

7 ally is smaller than that of its progenitor, Oryza barthii.

8 ditional Oryza species, Oryza glaberrima and Oryza brachyantha, which diverged from O. sativa 1 and 1

9 lysis in other genera (Aegilops/Triticum and Oryza), Coffea genomes/subgenomes appeared to be dramati

10 8 regions from two additional Oryza species, Oryza glaberrima and Oryza brachyantha, which diverged f

11 African rice (Oryza glaberrima Steud.) is a cereal crop species closel

12 ingly, the grain of African cultivated rice (Oryza glaberrima Steud.) typically is smaller than that

13 ther is an entirely different species (i.e., Oryza glaberrima Steud.).

14 African rice (Oryza glaberrima) and African cultivation practices are

15 Oryza, which includes rice (Oryza sativa and Oryza glaberrima) and wild relatives, is a useful genus

16 The domestication of African rice, Oryza glaberrima, occurred separately from that of the m

17 rphisms in the rice species Oryza sativa and Oryza glaberrima, we find that DNA repair following tran

18 patible interaction with the related species Oryza glaberrima.

19 This suggests that Oryza has a mechanism to maintain the fidelity and funct

20 The genome invasion of Oryza is dated to over 1.8 million years ago (MYA) but p

21 es 100% sequence identity with its allele in Oryza latifolia.

22 Oryza sativa, and its wild African relative, Oryza longistaminata, was analyzed using the new method.

23 d in Oryza sativa and two wild rice species, Oryza meridionalis and Oryza australiensis.

24 Oryza meridionalis exhibited intermediate heat tolerance

25 new executor R gene derived from wild rice (Oryza rufipogon) that confers an extremely broad spectru

26 executor R gene derived from the wild rice (Oryza rufipogon) that confers an extremely broad spectru

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

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

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

30 332 NBS-LRR genes cloned from five resistant Oryza sativa (rice) cultivars for their ability to confe

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

50 Weedy rice (Oryza sativa f.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

71 39 aromatic indica rice (Oryza sativa L.) cultivars were characterized for Iron,

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

87 1-methyladenosine (m1A) in a nuclear-encoded Oryza sativa rRNA.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

284 Oryza sativa-infecting isolates showed higher directiona

285 lanum lycopersicum, Medicago truncatula, and Oryza sativa.

286 the much more widespread Asian rice species Oryza sativa.

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

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

289 he biological significance of this method in Oryza sativa.

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

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

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

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

294 om Mutator-like transposable elements in ten Oryza species and the outgroup Leersia perieri, bridging

295 lineage-specific expansions observed between Oryza species were partly driven by directional selectio

296 d thousands of putative genes in each of the Oryza species, a large proportion of which have evidence

297 orthologous Cen8 regions from two additional Oryza species, Oryza glaberrima and Oryza brachyantha, w

298 ethod to 30 rice specimens belonging to nine Oryza species.

299 ut important issues in the evolution of wild Oryza species.

300 The genus Oryza, which includes rice (Oryza sativa and Oryza glabe