ライフサイエンスコーパス: Oryza sativa

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

32 lanum lycopersicum, Medicago truncatula, and Oryza sativa.

33 the much more widespread Asian rice species Oryza sativa.

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

35 three datasets from Arabidopsis thaliana and Oryza sativa.

36 he biological significance of this method in Oryza sativa.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

116 Weedy rice (Oryza sativa f.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

134 Oryza sativa-infecting isolates showed higher directiona

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

160 39 aromatic indica rice (Oryza sativa L.) cultivars were characterized for Iron,

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

234 332 NBS-LRR genes cloned from five resistant Oryza sativa (rice) cultivars for their ability to confe

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

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

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

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

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

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

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

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

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

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

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

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

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

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

254 1-methyladenosine (m1A) in a nuclear-encoded Oryza sativa rRNA.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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