ライフサイエンスコーパス: aestivum

1 orghum (Sorghum bicolor) and wheat (Triticum aestivum).

2 ey, rice (Oryza sativa), and wheat (Triticum aestivum).

3 ern northern European winter wheat (Triticum aestivum).

4 oid Triticum turgidum and hexaploid Triticum aestivum).

5 Lycopersicum esculentum) and wheat (Triticum aestivum).

6 um monococcum) and polyploid wheat (Triticum aestivum).

7 y silence genes in hexaploid wheat (Triticum aestivum).

8 the monocotyledonous species wheat (Triticum aestivum).

9 atula, maize (Zea mays), and wheat (Triticum aestivum).

10 cultivated, hexaploid bread wheat (Triticum aestivum).

11 esponses to Zn deficiency in wheat (Triticum aestivum).

12 ndent selection on its host, wheat (Triticum aestivum).

13 ia tritici blotch disease of wheat (Triticum aestivum).

14 barley (Hordeum vulgare) and wheat (Triticum aestivum).

15 bsent in most tested common wheats (Triticum aestivum).

16 ther dryland cereals such as wheat (Triticum aestivum).

17 barley (Hordeum vulgare) and wheat (Triticum aestivum).

18 role in spike development in wheat (Triticum aestivum).

19 s of rice (Oryza sativa) and wheat (Triticum aestivum).

20 n elongatum) into cultivated wheat (Triticum aestivum).

21 ortant species, particularly wheat (Triticum aestivum).

22 HOX1 (the first homeobox protein in Triticum aestivum).

23 ID331, with those of common wheat (Triticum aestivum).

24 tiller inhibition) mutant of wheat (Triticum aestivum).

25 splay nonadditive expression in synthetic T. aestivum.

26 s loci and nonadditive gene expression in T. aestivum.

27 homoeologous transcripts in newly formed T. aestivum.

28 by hybridization into common wheat, Triticum aestivum.

29 pendently between T. monococcum and Triticum aestivum.

30 nlegume cereals Hordeum vulgare and Triticum aestivum.

31 Triticum aestivum Nor9 haplotypes on two T. aestivum 1A chromosomes in the isogenic background of cv

32 own as the D-genome donor of bread wheat (T. aestivum, 2n = 6x = 42, AABBDD).

33 ies: Triticum turgidum (AABB genomes) and T. aestivum (AABBDD) in the Emmer lineage, and T. timopheev

34 um timopheevii AAGG) and hexaploid (Triticum aestivum, AABBDD) species.

35 Triticum turgidum (AB genome), and Triticum aestivum (ABD genome), as well as two Acc-2-related pseu

36 ypes were found in hexaploid wheat (Triticum aestivum; ABD).

37 ng sites, and interacts with wheat (Triticum aestivum) Actin1 (TaACT1), in planta.

38 atiens wallerana) and wheat plants (Triticum aestivum) also elicit directed growth.

39 Triticum aestivum aluminum-activated malate transporter (TaALMT1)

40 es from maize (Zea mays) and wheat (Triticum aestivum) amyloplasts exist in cell extracts in high mol

41 In wheat (Triticum aestivum), an 18:3 plant, low temperature also influence

42 It is concluded that both T. aestivum and Ae. cylindrica originated recurrently, with

43 genome of the allopolyploid species Triticum aestivum and Aegilops cylindrica.

44 The D genome sequences of T. aestivum and Aegilops tauschii are identical, confirming

45 th viability in this species and in Triticum aestivum and Brassica napus seeds.

46 In the polyploid wheats, Triticum aestivum and T. turgidum, the gene is present in a homoe

47 elic series; for example, in wheat (Triticum aestivum and Triticum turgidum), 17 functional Pm3 allel

48 The glaucous appearance of wheat (Triticum aestivum) and barley (Hordeum vulgare) plants, that is t

49 f intravacuolar membranes in wheat (Triticum aestivum) and barley (Hordeum vulgare) starchy endosperm

50 grasses wheat (Triticum monococcum, Triticum aestivum) and barley (Hordeum vulgare), vernalization re

51 l temperate grass related to wheat (Triticum aestivum) and barley (Hordeum vulgare).

52 reale) is closely related to wheat (Triticum aestivum) and barley (Hordeum vulgare).

53 ent in the temperate cereals wheat (Triticum aestivum) and barley (Hordeum vulgare).

54 bution in different parts of wheat (Triticum aestivum) and designed an efficient method for its isola

55 ught and heat constraints in wheat (Triticum aestivum) and determined the average sensitivities for m

56 -making quality in hexaploid wheat (Triticum aestivum) and represents a recently evolved region uniqu

57 al role of ROS in defense of wheat (Triticum aestivum) and rice (Oryza sativa) against Hessian fly (M

58 our approach on data sets of wheat (Triticum aestivum) and rice (Oryza sativa) plants as well as a un

59 In some species such as wheat (Triticum aestivum) and rice (Oryza sativa), mudrA-similar sequenc

60 As found in wheat (Triticum aestivum) and rice (Oryza sativa), this transgene increa

61 to increase grain yields in wheat (Triticum aestivum) and rice (Oryza sativa).

62 mays), rice (Oryza sativa), wheat (Triticum aestivum), and barley (Hordeum vulgare) to illustrate th

63 bacum), Medicago truncatula, wheat (Triticum aestivum), and barley (Hordeum vulgare).

64 of barley (Hordeum vulgare), wheat (Triticum aestivum), and Brachypodium distachyon and that this eff

65 to barley (Hordeum vulgare), wheat (Triticum aestivum), and maize (Zea mays) ESTs.

66 ), barley (Hordeum vulgare), wheat (Triticum aestivum), and oat (Avena sativa) are anchored by a set

67 (Triticum durum), hexaploid wheat (Triticum aestivum), and tetraploid wild oats (Avena barbata) were

68 T scans of maize (Zea mays), wheat (Triticum aestivum), and tomato (Solanum lycopersicum) grown in a

69 e 16 Gbp genome of hexaploid wheat, Triticum aestivum, and assign 7.1 Gb of this assembly to chromoso

70 C3 (rice [Oryza sativa] and wheat [Triticum aestivum]) and C4 (maize [Zea mays] and Setaria viridis)

71 s tauschii are identical, confirming that T. aestivum arose from hybridization of T. turgidum and Ae.

72 solated from an Elymus trachycaulus/Triticum aestivum backcross derivative.

73 ral important crops, such as wheat (Triticum aestivum), barley (Hordeum vulgare), and oats (Avena sat

74 itance studies in Triticeae (wheat [Triticum aestivum], barley [Hordeum vulgare], and rye [Secale cer

75 ion about Triticeae species (wheat [Triticum aestivum], barley [Hordeum vulgare], rye [Secale cereale

76 sly published method for the detection of T. aestivum, based on the gliadin gene, is inadequate.

77 GL22 as the FLC orthologs in wheat (Triticum aestivum) behaving most similar to Brachypodium ODDSOC2

78 ys), oat (Avena sativa), and wheat (Triticum aestivum); but the dicots pea (Pisum sativum), soybean (

79 ct to the light gradient for wheat (Triticum aestivum) canopies with the aims of quantifying its modu

80 ally contrasting field-grown wheat (Triticum aestivum) canopies.

81 e foliar disease tan spot of wheat (Triticum aestivum), caused by Pyrenophora tritici-repentis, invol

82 Tan spot of wheat (Triticum aestivum), caused by the fungus Pyrenophora tritici-repe

83 icum monococcum is closely homeologous to T. aestivum chromosome 1A but recombines with it little in

84 In Italy, addition of Triticum aestivum (common wheat) during manufacturing is not allo

85 Hexaploid wheat (Triticum aestivum) contains triplicated genomes derived from thre

86 ated crop species, including wheat (Triticum aestivum), cotton (Gossypium hirsutum), and soybean (Gly

87 t is commonly found in bread wheat (Triticum aestivum) cultivars and can result in commercially unacc

88 se previously seen in winter wheat (Triticum aestivum cv Augusta) and thale cress (Arabidopsis thalia

89 elasticity were observed in wheat (Triticum aestivum cv Pennmore Winter) coleoptile (type II) walls,

90 ted roots of an Al-sensitive wheat (Triticum aestivum cv Victory) cultivar was screened with a degene

91 NO2-, and urea into roots of wheat (Triticum aestivum cv Yecora Rojo) seedlings from complete nutrien

92 orters in roots of wheat seedlings (Triticum aestivum cv Yercora Rojo) were characterized using preci

93 e identified bacteria in the wheat (Triticum aestivum) cv. Hereward seed environment using embryo exc

94 ing caryopses from hexaploid wheat (Triticum aestivum, cv. Hereward) was determined using Affymetrix

95 black truffles Tuber melanosporum and Tuber aestivum), demonstrating the potential and reliability o

96 sistance to the globally important wheat (T. aestivum) disease, Fusarium head blight.

97 ve been annotated for common wheat (Triticum aestivum) due to its large genome.

98 utilized dwarfing alleles in wheat (Triticum aestivum; e.g. Rht-B1b and Rht-D1b) encode GA-resistant

99 co-expression in the mature wheat (Triticum aestivum) embryo.

100 xybenzoic acid, baicalein and kaempferol (T. aestivum), epicatechin and catechin (T. magnatum).

101 ysis of rice nsLtp genes and wheat (Triticum aestivum) EST sequences indexed in the UniGene database.

102 632 rat ESTs in 47 min and 420 694 Triticum aestivum ESTs in 3 h and 15 min.

103 he development of transgenic wheat (Triticum aestivum) events, expressing a maize gene coding for pla

104 (formerly named ALMT1) from wheat (Triticum aestivum) expressed in Xenopus laevis oocytes was conduc

105 rch, we developed a flexible wheat (Triticum aestivum) expression browser (www.wheat-expression.com)

106 nyl acetate (Z-3-HAC) primed wheat (Triticum aestivum) for enhanced defense against subsequent infect

107 measured the uptake of P by wheat (Triticum aestivum) from radiolabeled nonfiltered (colloid-contain

108 characterization of an orphan gene (Triticum aestivum Fusarium Resistance Orphan Gene [TaFROG]) as a

109 y expression experiments, where synthetic T. aestivum gene expression was compared to additive model

110 onsolidating IWGSC CSSv2 and TGACv1 Triticum aestivum genome assemblies and reassembling or mapping o

111 sical maps revealed that the wheat (Triticum aestivum) genome is partitioned into gene-rich and -poor

112 in a total 564 lines of hexaploid wheat (T. aestivum, genome AABBDD) involving all its subspecies an

113 of the D genome of hexaploid wheat (Triticum aestivum, genomes AABBDD) and an important genetic resou

114 ield-grown spring and winter wheat (Triticum aestivum) genotypes and their near-isogenic lines with t

115 n-efficient and -inefficient wheat (Triticum aestivum) genotypes were grown for 13 d in chelate buffe

116 RIP inhibited translation in wheat (Triticum aestivum) germ more efficiently than in rabbit reticuloc

117 ction of HSP90 in lysates of wheat (Triticum aestivum) germ.

118 oat (Avena sativa) globulin, wheat (Triticum aestivum) germin, maize (Zea mays) alcohol dehydrogenase

119 Triticum aestivum gliadin derived peptides were employed as a pos

120 ve action, mitigating the injury of Triticum aestivum gliadin on cell viability and cytoskeleton reor

121 mics analyses revealed three wheat (Triticum aestivum) glycosyltransferase (TaGT) proteins from the G

122 f genes and recombination in wheat (Triticum aestivum) group 1 chromosomes by comparing high-density

123 mylase from germinated wheat seeds (Triticum aestivum) has been purified to apparent electrophoretic

124 Polyploid wheat (Triticum aestivum) has had a massive increase in genome size larg

125 ring between wheat (Triticum turgidum and T. aestivum) homeologous chromosomes is prevented by the ex

126 there are other data sets based on Triticum aestivum, Hordeum vulgare, and Populus subsp.

127 ethod is evaluated on winter wheat (Triticum aestivum) images (and demonstrated on Arabidopsis [Arabi

128 molina and real-time PCR determination of T. aestivum in Triticum spp., was validated.

129 grain yield losses of bread wheat (Triticum aestivum) in many parts of the world.

130 ell as three nonpathogens of wheat (Triticum aestivum), including a necrotrophic pathogen of barley,

131 Bread wheat (Triticum aestivum) is a globally important crop, accounting for 2

132 Bread wheat (Triticum aestivum) is an allohexaploid species, consisting of thr

133 Wheat (Triticum aestivum) is an annual crop, cultivated in the winter an

134 tent of staple crops such as wheat (Triticum aestivum) is difficult to change because of genetic comp

135 Wheat (Triticum aestivum) is one of the most important crops in human an

136 , such as the hexaploid bread wheat Triticum aestivum, is accurate annotation of the tags generated.

137 has been identified with chromosome 1D of T. aestivum L.

138 is the same as in the B and D genomes of T. aestivum L.

139 o investigate the microstructure of Triticum aestivum L. (wheat) kernels and Arabidopsis leaves.

140 Wheat (Triticum aestivum L. cv Bobwhite) was transformed with the mtlD g

141 Wheat (Triticum aestivum L. cv Fremont) grown in hydroponic culture unde

142 sponse to low temperature in wheat (Triticum aestivum L. cv Norstar) and rye (Secale cereale L. cv Pu

143 ements of root elongation in wheat (Triticum aestivum L. cv Scout 66) seedlings in controlled medium.

144 Growth and photosynthesis of wheat (Triticum aestivum L. cv Super Dwarf) plants grown onboard the spa

145 7 from hard red winter wheat (HRWW; Triticum aestivum L. cv. Winoka).

146 F7 ITMI population of bread wheat, Triticum aestivum L. emend Thell., where it shortened an existing

147 shoots in seedlings of bread wheat (Triticum aestivum L.) and durum wheat cultivars were studied.

148 Given the importance of wheat (Triticum aestivum L.) as a global food crop and the impact of wat

149 sly reported that transgenic wheat (Triticum aestivum L.) carrying a maize (Zea mays L.) gene (Zmeftu

150 nsiderable variability among wheat (Triticum aestivum L.) cultivars in their ability to grow and yiel

151 ciency than comparable bread wheat (Triticum aestivum L.) cultivars.

152 a recombinant population of wheat (Triticum aestivum L.) doubled haploid lines is also provided.

153 To localize wheat (Triticum aestivum L.) ESTs on chromosomes, 882 homoeologous group

154 ed to play critical roles in wheat (Triticum aestivum L.) grain texture.

155 lets into the sieve tubes of wheat (Triticum aestivum L.) grains to evaluate the dimensions of plasmo

156 imilate flow into developing wheat (Triticum aestivum L.) grains were measured at several points from

157 and matrix, with and without wheat (Triticum aestivum L.) growth.

158 , which together compose the wheat (Triticum aestivum L.) Ha locus that controls grain texture and ma

159 Hexaploid wheat (Triticum aestivum L.) has very low constitutive glutathione S-tra

160 polyploidy in allohexaploid wheat (Triticum aestivum L.) have primarily been ascribed to increases i

161 NA libraries, were mapped to wheat (Triticum aestivum L.) homoeologous group 4 chromosomes using a se

162 genomic complexity of bread wheat (Triticum aestivum L.) is a cornerstone in the quest to unravel th

163 Winter wheat (Triticum aestivum L.) is the primary host of economic significanc

164 as concentrated on hexaploid wheat (Triticum aestivum L.) lines originating from China.

165 (Gossypium hirsutum L.) and wheat (Triticum aestivum L.) plants caused a progressive decline in the

166 corn (Zea mays L.) with the wheat (Triticum aestivum L.) puroindoline genes (Pina and Pinb) to asses

167 ms in the plasma membrane of wheat (Triticum aestivum L.) root cortex cells using the patch-clamp tec

168 GSTs) were cloned from bread wheat (Triticum aestivum L.) treated with the herbicide safener fenchlor

169 ctive growth rates of a wheat crop (Triticum aestivum L.) were determined in three separate studies (

170 Wheat plants (Triticum aestivum L.) were grown at the same photosynthetic photo

171 We transformed wheat (Triticum aestivum L.) with a modified form of the maize (Zea mays

172 produced from Chinese Spring wheat (Triticum aestivum L.), five other hexaploid wheat genotypes (Chey

173 to the Bob White cultivar of wheat (Triticum aestivum L.), in which it is not present in nature, by t

174 SafBA, but not in etiolated wheat (Triticum aestivum L.), oat (Avena sativa L.), barley (Hordeum vul

175 Wheat (Triticum aestivum L.), rice (Oryza sativa L.), and maize (Zea may

176 ed branching in the roots of wheat (Triticum aestivum L.), thereby affecting plant biomass.

177 ologous group 7 in hexaploid wheat (Triticum aestivum L.), to identify gene distribution in these chr

178 allelic chlorina mutants of wheat (Triticum aestivum L.), which have partial blocks in chlorophyll (

179 q homoeoalleles in hexaploid wheat (Triticum aestivum L.).

180 ine synthetase (GS) genes in wheat (Triticum aestivum L.).

181 ex polyploid genomes such as wheat (Triticum aestivum L.).

182 aploid (2n = 6x = 42) wheat genome (Triticum aestivum L.).

183 p 1 chromosomes in hexaploid wheat (Triticum aestivum L.).

184 p 3 chromosomes of hexaploid wheat (Triticum aestivum L.).

185 chromosome arm 1DS of bread wheat (Triticum aestivum L.).

186 s was developed in hexaploid wheat (Triticum aestivum L.).

187 the huge size of the common wheat (Triticum aestivum L., 2n = 6x = 42, AABBDD) genome of 17,300 Mb,

188 two naturally susceptible varieties Triticum aestivum (L.) variety Solstice and T. monococcum MDR037,

189 Resistance of wheat (Triticum aestivum) leaves to the necrotrophic fungal pathogen Myc

190 pression was characterized in a synthetic T. aestivum line and the T. turgidum and Aegilops tauschii

191 cally diverse populations of wheat (Triticum aestivum) lines incorporating chromosome segments from T

192 over 1 d) in three different wheat (Triticum aestivum) lines, which are architecturally diverse.

193 Nor9 haplotype was substituted for Triticum aestivum Nor9 haplotypes on two T. aestivum 1A chromosom

194 es expressed in seedlings of wheat (Triticum aestivum), oat (Avena strigosa), rice (Oryza sativa), so

195 constitutively expressing a wheat (Triticum aestivum) OXO gene.

196 Cochliobolus miyabeanus, the wheat (Triticum aestivum) pathogen, Fusarium graminearum, and the Arabid

197 with the activation of the defense Triticum aestivum Pathogenesis-Related-1 (TaPR1) gene.

198 n, from shoots to roots, the wheat (Triticum aestivum) PC synthase (TaPCS1) gene was expressed under

199 h coordination rules between wheat (Triticum aestivum) plant organs (i.e. between leaves within a ste

200 We generated transgenic wheat (Triticum aestivum) plants expressing AtEFR driven by the constitu

201 acalin-like lectin gene from wheat (Triticum aestivum) plants that responds to infestation by Hessian

202 s (Arabidopsis thaliana) and wheat (Triticum aestivum) plants to daytime or nighttime elevated CO2 an

203 The system was created with a Triticum aestivum promoter containing ABA responsive elements (AB

204 gous) chromosomes, hexaploid wheat (Triticum aestivum) restricts pairing to just true homologs at mei

205 including maize (Zea mays), wheat (Triticum aestivum), rice (Oryza sativa), sorghum (Sorghum bicolor

206 of corresponding loci on the wheat (Triticum aestivum), rice, maize, sugarcane, and Arabidopsis genom

207 ed in the plasma membrane of wheat (Triticum aestivum) root cells.

208 transport properties of the wheat (Triticum aestivum) root malate efflux transporter underlying Al r

209 le for toxic Na(+) influx in wheat (Triticum aestivum), root plasma membrane preparations were screen

210 Uptake of soil microbes by wheat (Triticum aestivum) roots appears to take place in soil.

211 abelled the soil surrounding wheat (Triticum aestivum) roots with either (1)(5)NH(4)(+) or (1)(5)N-gl

212 90 different naturally aged wheat (Triticum aestivum) seed stocks were quantified in an untargeted h

213 mal membranes from etiolated wheat (Triticum aestivum) seedlings cooperatively incorporated xylose (X

214 d XS activity from etiolated wheat (Triticum aestivum) seedlings.

215 Amino acids in wheat (Triticum aestivum) seeds mainly accumulate in storage proteins ca

216 sed the total GST activity extracted from T. aestivum shoots 9-fold when assayed with dimethenamid as

217 f CO(2) and O(2) fluxes from wheat (Triticum aestivum) shoots indicated that short-term exposures to

218 o quantify 16 amino acids in wheat (Triticum aestivum) sieve tube (ST) samples as small as 2 nL colle

219 is restricted to inoculated wheat (Triticum aestivum) spikelets, whereas the wild-type strain coloni

220 s do not support this hypothesis as Triticum aestivum spp. vulgare landraces, which were not subjecte

221 The cell walls of wheat (Triticum aestivum) starchy endosperm are dominated by arabinoxyla

222 in lignin preparations from wheat (Triticum aestivum) straw and subsequently in all monocot samples

223 barley (Hordeum vulgare) and wheat (Triticum aestivum), suggest that resistance contributed by the ch

224 ccessions of six hexaploid wheat species (T. aestivum, T. compactum, T. sphaerococcum, T. spelta, T.

225 r transcription factors from wheat (Triticum aestivum) that is specifically bound by PKABA1.

226 ange of genomic datasets for wheat (Triticum aestivum) that will assist plant breeders and scientists

227 In wheat (Triticum aestivum), the acceleration of flowering under long days

228 Resistance in wheat (Triticum aestivum) to the Hessian fly (Mayetiola destructor), a m

229 T activity in crude protein extracts from T. aestivum, Triticum durum, and Triticum tauschii was sepa

230 his study we identify an E2 enzyme, Triticum aestivum Ubiquitin conjugating enzyme 4 (TaU4) that func

231 onisation increased the attractiveness of T. aestivum var.

232 Fourteen wheat (Triticum aestivum) varieties were grown in soil columns packed to

233 iently explored black summer truffles (Tuber aestivum Vittad.) and white (Tuber magnatum Pico) truffl

234 sely homeologous chromosomes 3A and 5A of T. aestivum was compared with recombination across correspo

235 archy endosperm of hexaploid wheat (Triticum aestivum) was determined using RNA-Seq isolated at five

236 The structure of eIF4E from wheat (Triticum aestivum) was investigated using a combination of x-ray

237 xic compound extrusion) from wheat (Triticum aestivum) was isolated and shown to encode a citrate tra

238 ibberellin (GA) signaling in wheat (Triticum aestivum), we have focused on the transcription factor T

239 lase (ACCase; EC 6.4.1.2) of wheat (Triticum aestivum) were cloned and sequenced.

240 otein sources: Oryza sativa (rice), Triticum aestivum (wheat flour), Lens culinaris (lentils), Pangus

241 ng recombinant hexahistidine-tagged Triticum aestivum (wheat) chlorophyllase from Escherichia coli.

242 with a sesquiterpene synthase from Triticum aestivum (wheat) that is not only closely related to dit

243 tabacum L. cv Xanthi (tobacco) and Triticum aestivum (wheat) to investigate plant uptake of 10-, 30-

244 equences from normal fertile wheat (Triticum aestivum) with those of Aegilops kotschyi which is the s

245 barley (Hordeum vulgare) and wheat (Triticum aestivum), with reference to methods of gene isolation.

246 romosome pairing by 1.6 chiasmata/cell in T. aestivum x Ae. speltoides hybrids and was additive to th

247 creased homeologous chromosome pairing in T. aestivum x Ae. speltoides hybrids by 8.4 and 5.8 chiasma

248 creased homeologous chromosome pairing in T. aestivum x Ae. speltoides hybrids to the same level as S

249 conserved identity with the wheat (Triticum aestivum) xylanase inhibitor TAXI-1, we were able to dev

250 d to impressive increases in wheat (Triticum aestivum) yields during the Green Revolution.