ライフサイエンスコーパス: aestivum

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

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

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

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

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

6 ortant species, particularly wheat (Triticum aestivum).

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

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

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

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

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

12 ern northern European winter wheat (Triticum aestivum).

13 oid Triticum turgidum and hexaploid Triticum aestivum).

14 Lycopersicum esculentum) and wheat (Triticum aestivum).

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

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

17 the monocotyledonous species wheat (Triticum aestivum).

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

19 cultivated, hexaploid bread wheat (Triticum aestivum).

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

21 y in the hexaploid genome of wheat (Triticum aestivum).

22 erred to as gluten, found in wheat (Triticum aestivum).

23 ting senescence in polyploid wheat (Triticum aestivum).

24 tain grains, including bread wheat (Triticum aestivum).

25 Arabidopsis thaliana) and in wheat (Triticum aestivum).

26 formance and productivity in wheat (Triticum aestivum).

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

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

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

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

31 pendently between T. monococcum and Triticum aestivum.

32 splay nonadditive expression in synthetic T. aestivum.

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

34 homoeologous transcripts in newly formed T. aestivum.

35 by hybridization into common wheat, Triticum aestivum.

36 nlegume cereals Hordeum vulgare and Triticum aestivum.

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

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

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

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

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

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

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

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

45 Triticum aestivum aluminum-activated malate transporter (TaALMT1)

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

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

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

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

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

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

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

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

54 acterize these small RNAs in wheat (Triticum aestivum) and barley (Hordeum vulgare) anthers.

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

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

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

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

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

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

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

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

63 hich grow from the lemmas of wheat (Triticum aestivum) and other grasses that contribute to photosynt

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

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

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

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

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

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

70 ition for amino acid between roots (Triticum aestivum) and soil microorganisms.

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

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

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

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

75 om barley (Hordeum vulgare), wheat (Triticum aestivum), and Medicago truncatula, we demonstrate a rol

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

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

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

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

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

81 This was demonstrated in Triticum aestivum 'Apogee' (dwarf bread wheat) and resulted in an

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

83 inflorescence development of wheat (Triticum aestivum) as daylengths extend naturally in the field, u

84 to hexaploid (AABBDD) common wheat (Triticum aestivum), as well as an 8-kb deletion in MSH4D in hexap

85 e cloned and characterized a wheat (Triticum aestivum) auxin efflux carrier ABCB1.

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

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

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

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

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

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

92 dioxide (CeO(2)) in the tissues of Triticum aestivum, Brassica napus, and Hordeum vulgare, after exp

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

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

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

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

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

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

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

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

101 vailability of the hexaploid wheat (Triticum aestivum) cultivar Chinese Spring reference genome allow

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

103 er ( Helianthus annuus) and wheat ( Triticum aestivum) cultivated on free iron agar medium plates.

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

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

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

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

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

109 g fragmentation on the bread wheat, Triticum aestivum cv. Chinese Spring, chromosome 3B; (ii) by appl

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

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

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

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

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

115 n identified first in common wheat (Triticum aestivum) due to the complex genome.

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

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

118 During this period, bread wheat (Triticum aestivum) emerged as one of the world's most important c

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

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

121 632 rat ESTs in 47 min and 420 694 Triticum aestivum ESTs in 3 h and 15 min.

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

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

124 station in commercial winter wheat (Triticum aestivum) fields in Kansas, USA.

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

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

127 motion in field-grown wheat plants (Triticum aestivum) from time-ordered sequences of red, green, and

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

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

130 Wheat (Triticum aestivum) genetic maps are a key enabling tool for genet

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

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

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

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

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

136 y costs of root growth of 16 wheat (Triticum aestivum) genotypes under three levels of penetration re

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

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

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

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

141 Triticum aestivum gliadin derived peptides were employed as a pos

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

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

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

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

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

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

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

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

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

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

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

153 Wheat (Triticum aestivum) is a major staple food crop worldwide.

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

155 Bread wheat (Triticum aestivum) is an allohexaploid that was formed via two al

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

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

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

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

160 under grasslands and winter wheat (Triticum aestivum L)-based crop rotations in the inland Pacific N

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

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

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

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

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

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

167 7 from hard red winter wheat (HRWW; Triticum aestivum L. cv. Winoka).

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

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

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

171 Wheat (Triticum aestivum L.) bread doughs were prepared using LAB strain

172 enotypic plasticity in bread wheat (Triticum aestivum L.) by integrating functional mapping and semia

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

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

175 ion of plant carbon in three wheat (Triticum aestivum L.) cultivars.

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

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

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

179 a pedigree resource of 2,657 wheat (Triticum aestivum L.) genotypes originating from 38 countries, re

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

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

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

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

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

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

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

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

188 esf.) in Ethiopia, and bread wheat (Triticum aestivum L.) in India.

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

190 in cereals crops like bread wheat (Triticum aestivum L.) is also contributed by ear photosynthesis b

191 Winter wheat (Triticum aestivum L.) is essential to maintain food security for

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

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

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

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

196 Soil and wheat (Triticum aestivum L.) tissue samples were analyzed to determine t

197 ion of the same nutrients in wheat (Triticum aestivum L.) tissues.

198 tolerance in hexaploid bread wheat (Triticum aestivum L.) to synthetic auxin herbicides is primarily

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

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

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

202 turgidum L. var. durum) and bread (Triticum aestivum L.) wheat that provides resistance to the wheat

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

204 Winter wheat (Triticum aestivum L.), a dual-purpose crop, used for both forage

205 , rice (Oryza sativa L.) and wheat (Triticum aestivum L.), and evaluates potential risks associated w

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

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

208 thin leaf blades, including wheat (Triticum aestivum L.), maize (Zea may L.), rice (Oryza sativa L.)

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

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

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

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

213 (FHB) is a severe disease of wheat (Triticum aestivum L.).

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

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

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

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

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

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

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

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

222 y properties of Rca in bread wheat (Triticum aestivum L.).

223 tible common wheat variety Fielder (Triticum aestivum L.).

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

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

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

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

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

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

230 o multiple pathogens and the wheat (Triticum aestivum) Lr67 hexose transporter variant (Lr67res) fits

231 nt based on L-systems (ADEL) wheat (Triticum aestivum) model (ADEL-Wheat), which describes the time c

232 hree Rca isoforms present in wheat (Triticum aestivum), namely TaRca1-beta, TaRca2-alpha, and TaRca2-

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

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

235 d in rice (Oryza sativa) and wheat (Triticum aestivum), opening biotechnological perspectives in crop

236 other major cereals such as wheat (Triticum aestivum) or rice (Oryza sativa).

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

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

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

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

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

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

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

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

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

246 ize (Zea mays ssp. mays) and wheat (Triticum aestivum) provide half of the food eaten by humankind.

247 tiva], maize [Zea mays], and wheat [Triticum aestivum]) providing most of the caloric intake of conte

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

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

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

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

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

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

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

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

256 90 different naturally aged wheat (Triticum aestivum) seed stocks were quantified in an untargeted h

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

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

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

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

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

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

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

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

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

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

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

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

269 in the CTE of Rca-alpha from wheat (Triticum aestivum) (TaRca2-alpha).

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

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

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

273 icum turgidum) and hexaploid wheat (Triticum aestivum), the spikelet is a short indeterminate branch

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

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

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

277 onisation increased the attractiveness of T. aestivum var.

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

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

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

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

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

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

284 rus, pea (Pisum sativum) and wheat (Triticum aestivum), was just upstream of a minimal promoter and t

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

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

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

288 miana (Nb), Eruca sativa (arugula), Triticum aestivum (wheat) and Gossypium hirsutum (cotton) leaves

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

290 The Triticum aestivum (wheat) genome encodes three isoforms of Rubisc

291 processes and provide evidence that Triticum aestivum (wheat) plants genetically manipulated to incre

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

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

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

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

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

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

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

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

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