ライフサイエンスコーパス: Oryza

1 genomes that represent the 12 chromosomes of Oryza.

2 mosome variations and evolution in the genus Oryza.

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

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

5 In recent divergence of Oryza, an average of 51.5 de novo genes per million year

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

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

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

9 The rice genus Oryza consists of both recently formed and older allopol

10 opsis LIGHT-DEPENDENT SHORT HYPOCOTYLS 1 and Oryza G1 (ALOG) family protein, named M. polymorpha LATE

11 analysis of their source loci (PHAS) in five Oryza genomes and combined this with analysis of high-th

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

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

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

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

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

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

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

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

23 Oryza meridionalis exhibited intermediate heat tolerance

24 In the recently formed BBCC polyploid, Oryza minuta, genome dominance was not observed and its

25 rain yield QTL in cultivated rice, from four Oryza polyploids of various ages and their likely diploi

26 Strains of the wild rice species Oryza rufipogon also exhibited differential sakuranetin

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

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

29 Oryza sativa (rice) and the wild progenitor Oryza rufipogon.

30 ost serious diseases for the cultivated rice Oryza sativa (O. sativa).

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

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

33 uences from 3,000 accessions of domesticated Oryza sativa (rice) and the wild progenitor Oryza rufipo

34 It uses Oryza sativa (rice) as a reference species for manual cu

35 332 NBS-LRR genes cloned from five resistant Oryza sativa (rice) cultivars for their ability to confe

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

37 A key target for the improvement of Oryza sativa (rice) is the development of heat-tolerant

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

39 As Oryza sativa (rice) seeds represent food for over three

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

41 machine learning models were established in Oryza sativa (rice) that could accurately distinguish be

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

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

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

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

46 From a drought-resistant cultivar of Oryza sativa (rice), we isolated an OsPIP1;3 gene single

47 plast Pi homeostasis is poorly understood in Oryza sativa (rice).

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

49 er (fruit fly), Danio rerio (zebrafish), and Oryza sativa (rice).

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

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

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

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

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

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

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

57 accessions of African cultivated rice, and 7 Oryza sativa cultivars.

58 Mapping the 104 million reads against the Oryza sativa cv.

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

60 Weedy rice (Oryza sativa f.

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

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

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

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

65 Structural and biochemical analysis of Oryza sativa homolog FLO7 reveals identical activity to

66 Here we show that overexpression of Oryza sativa indica AGO17 in rice resulted in robust gro

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

68 and speciation of Cu and As in rice plants ( Oryza sativa japonica 'Koshihikari').

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

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

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

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

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

74 f arsenic, in the rhizosphere of Californian Oryza sativa L. variety M206, grown on Californian paddy

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

76 icum aestivum L.), maize (Zea may L.), rice (Oryza sativa L.) and sorghum (Sorghum bicolor (L.) Moenc

77 and accumulation by two staple crops, rice (Oryza sativa L.) and wheat (Triticum aestivum L.), and e

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

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

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

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

82 39 aromatic indica rice (Oryza sativa L.) cultivars were characterized for Iron,

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

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

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

86 As major food staple, rice (Oryza sativa L.) is cultivated in irrigated fields absor

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

88 The CS8 transgenic rice (Oryza sativa L.) lines expressing an up-regulated glgC g

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

90 This study shows that rice (Oryza sativa L.) roots can acquire aspartate at soil con

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

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

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

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

95 d up genetic improvement in cultivated rice (Oryza sativa L.).

96 ole in modulating phenotypic traits in rice (Oryza sativa L.).

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

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

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

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

101 es in Arabidopsis (Arabidopsis thaliana) and Oryza sativa revealed that several homologs of the candi

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

103 1-methyladenosine (m1A) in a nuclear-encoded Oryza sativa rRNA.

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

105 d young leaf tissues were extracted from the Oryza sativa ssp. indica cv. MR219 and sequenced using I

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

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

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

109 Small ribozymes such as Oryza sativa twister spontaneously cleave their own RNA

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

111 lling tolerance and cell elongation in rice (Oryza sativa) (FSD2, Fe-superoxide dismutase 2).

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

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

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

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

116 d two different circular plasmids into rice (Oryza sativa) and maize (Zea mays) and analyzed the resu

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

118 derstand its role in monocots, such as rice (Oryza sativa) and other cereals of agronomic importance.

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

120 on internode elongation in the monocot rice (Oryza sativa) and petiole elongation in Rumex rosette sp

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

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

123 sacchari, a cyst nematode parasite of rice (Oryza sativa) and sugarcane (Saccharum officinarum).

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

125 e that this phenomenon is conserved in rice (Oryza sativa) and wheat (Triticum aestivum), opening bio

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

127 been described in maize (Zea mays) and rice (Oryza sativa) anthers.

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

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

130 Cereals such as rice (Oryza sativa) are the major dietary source of Mo.

131 Much of humanity relies on rice (Oryza sativa) as a food source, but cultivation is water

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

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

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

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

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

137 lelic variants of wheat and transgenic rice (Oryza sativa) calli demonstrated that XAT catalyzes the

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

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

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

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

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

143 p94b1 Arabidopsis mutant and wild-type rice (Oryza sativa) conferred increased NaCl tolerance to seed

144 rcum-basmati group of cultivated Asian rice (Oryza sativa) contains many iconic varieties and is wide

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

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

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

148 Whereas leaves of rice (Oryza sativa) cultivar Nipponbare predominantly accumula

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

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

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

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

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

154 e distinct chromatin states across the rice (Oryza sativa) genome by integrating multiple chromatin m

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

156 Rice (Oryza sativa) has been recognized as an important cereal

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

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

159 nin histidine kinase (HK) receptors in rice (Oryza sativa) in order to explore the role of cytokinin

160 firmed that people farmed domesticated rice (Oryza sativa) in the interior of Sulawesi Island, Indone

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

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

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

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

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

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

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

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

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

170 The dividing cells also revealed two rice (Oryza sativa) microtubule-associated proteins in the phr

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

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

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

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

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

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

177 A rice (Oryza sativa) mutant with a distinctly prostrate growth

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

179 The rice (Oryza sativa) NLR receptor Piz-t confers broad-spectrum

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

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

182 Rice (Oryza sativa) OsNLA1 has been proposed to play a crucial

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

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

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

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

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

188 Here we show that DGK1 in rice (Oryza sativa) plays important roles in root growth and d

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

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

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

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

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

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

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

196 Transcriptome analysis revealed that a rice (Oryza sativa) receptor-like kinase, WALL-ASSOCIATED KINA

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

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

199 Here, we present evidence that the rice (Oryza sativa) RNA-binding protein, RBP-L, like its inter

200 RO-RICH PROTEIN (RePRP), in regulating rice (Oryza sativa) root growth under water deficit.

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

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

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

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

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

206 We screened rice (Oryza sativa) sRNA expression patterns against Rhizocton

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

208 The indica and japonica rice (Oryza sativa) subspecies differ in nitrate (NO(3)(-)) as

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

210 Here we show in rice (Oryza sativa) that BABY BOOM1 (BBM1), a member of the AP

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

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

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

214 ted in tobacco (Nicotiana tabacum) and rice (Oryza sativa) using miRNA MIM159 technology.

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

216 and 12 loci from weedy and cultivated rice (Oryza sativa) were assembled into the same genetic backg

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

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

219 ortant agronomic traits that determine rice (Oryza sativa) yield.

220 Here we assayed gene expression in rice (Oryza sativa)(3), and used phenotypic selection analysis

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

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

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

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

225 ng Arabidopsis (Arabidopsis thaliana), rice (Oryza sativa), and mouse (Mus musculus).

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

227 Here we identify RAV genes from rice (Oryza sativa), and unravel their regulatory roles in key

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

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

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

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

232 rization of two type I MADS box TFs in rice (Oryza sativa), MADS78 and MADS79 Transcript abundance of

233 The cereal crops rice (Oryza sativa), maize (Zea mays ssp. mays) and wheat (Tri

234 PHO1 uORF in genomes of crops such as rice (Oryza sativa), maize (Zea mays), barley (Hordeum vulgare

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

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

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

238 roducing P. stutzeri JGTA-S1 colonizes rice (Oryza sativa), significantly improving its growth, N con

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

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

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

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

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

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

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

246 a in humans, Arabidopsis thaliana, and rice (Oryza sativa), we present evidence that methylation stat

247 omes (Arabidopsis [Arabidopsis thaliana] and Oryza sativa), we show that LoReAn outperforms popular a

248 of Arabidopsis (Arabidopsis thaliana), rice (Oryza sativa), worm (Caenorhabditis elegans), and human

249 each of the 12 pairs of chromosomes in rice (Oryza sativa).

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

269 to the popcorn-like aroma of fragrant rice (Oryza sativa).

270 s such as wheat (Triticum aestivum) or rice (Oryza sativa).

271 , expressed during seed germination in rice (Oryza sativa).

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

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

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

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

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

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

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

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

280 Oryza sativa-infecting isolates showed higher directiona

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

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

283 lanum lycopersicum, Medicago truncatula, and Oryza sativa.

284 the much more widespread Asian rice species Oryza sativa.

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

286 three datasets from Arabidopsis thaliana and Oryza sativa.

287 he biological significance of this method in Oryza sativa.

288 ulated Arabidopsis 10) and the monocot rice (Oryza sativa; Gibberellic Acid Stimulated Transcript-Rel

289 and function of an OSCA1 homolog from rice (Oryza sativa; OsOSCA1.2), leading to a model of how it c

290 with one of the two Rca isoforms from rice (Oryza sativa; OsRca-beta) and Rca from other species ada

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

292 t on Earth, with a handful of species (rice [Oryza sativa], maize [Zea mays], and wheat [Triticum aes

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

294 High-quality genomes of 13 closely related Oryza species provide unprecedented opportunities to und

295 analyses using these probes in various wild Oryza species revealed that chromosomes from the AA, BB

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

297 ed across 48 accessions representing 11 wild Oryza species, 8 accessions of African cultivated rice,

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

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

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