ライフサイエンスコーパス: Triticum

1 idization has occurred frequently within the Triticum-Aegilops complex which provides a suitable syst

2 The diversity and evolution of wheat (Triticum-Aegilops group) genomes is determined, in part,

3 ument the complete coding sequences from the Triticum/Aegilops taxa, rye and barley including the A,

4 mays), barley (Hordeum vulgare), and wheat (Triticum aesativum), and we verified the inhibitory effe

5 This was demonstrated in Triticum aestivum 'Apogee' (dwarf bread wheat) and resul

6 genome), Triticum turgidum (AB genome), and Triticum aestivum (ABD genome), as well as two Acc-2-rel

7 In Italy, addition of Triticum aestivum (common wheat) during manufacturing is

8 viour on two naturally susceptible varieties Triticum aestivum (L.) variety Solstice and T. monococcu

9 ietary protein sources: Oryza sativa (rice), Triticum aestivum (wheat flour), Lens culinaris (lentils

10 na benthamiana (Nb), Eruca sativa (arugula), Triticum aestivum (wheat) and Gossypium hirsutum (cotton

11 r purifying recombinant hexahistidine-tagged Triticum aestivum (wheat) chlorophyllase from Escherichi

12 The Triticum aestivum (wheat) genome encodes three isoforms

13 te these processes and provide evidence that Triticum aestivum (wheat) plants genetically manipulated

14 za, along with a sesquiterpene synthase from Triticum aestivum (wheat) that is not only closely relat

15 Nicotiana tabacum L. cv Xanthi (tobacco) and Triticum aestivum (wheat) to investigate plant uptake of

16 Triticum aestivum aluminum-activated malate transporter

17 " vary with viability in this species and in Triticum aestivum and Brassica napus seeds.

18 In the polyploid wheats, Triticum aestivum and T. turgidum, the gene is present i

19 large allelic series; for example, in wheat (Triticum aestivum and Triticum turgidum), 17 functional

20 z5A was isolated from an Elymus trachycaulus/Triticum aestivum backcross derivative.

21 recovering fragmentation on the bread wheat, Triticum aestivum cv. Chinese Spring, chromosome 3B; (ii

22 nctional characterization of an orphan gene (Triticum aestivum Fusarium Resistance Orphan Gene [TaFRO

23 ctively consolidating IWGSC CSSv2 and TGACv1 Triticum aestivum genome assemblies and reassembling or

24 Triticum aestivum gliadin derived peptides were employed

25 protective action, mitigating the injury of Triticum aestivum gliadin on cell viability and cytoskel

26 dynamics under grasslands and winter wheat (Triticum aestivum L)-based crop rotations in the inland

27 roscopy to investigate the microstructure of Triticum aestivum L. (wheat) kernels and Arabidopsis lea

28 Given the importance of wheat (Triticum aestivum L.) as a global food crop and the impa

29 Wheat (Triticum aestivum L.) bread doughs were prepared using L

30 nduced phenotypic plasticity in bread wheat (Triticum aestivum L.) by integrating functional mapping

31 e previously reported that transgenic wheat (Triticum aestivum L.) carrying a maize (Zea mays L.) gen

32 acquisition of plant carbon in three wheat (Triticum aestivum L.) cultivars.

33 present a pedigree resource of 2,657 wheat (Triticum aestivum L.) genotypes originating from 38 coun

34 s) in a sand matrix, with and without wheat (Triticum aestivum L.) growth.

35 ly) genes, which together compose the wheat (Triticum aestivum L.) Ha locus that controls grain textu

36 ffects of polyploidy in allohexaploid wheat (Triticum aestivum L.) have primarily been ascribed to in

37 m durum Desf.) in Ethiopia, and bread wheat (Triticum aestivum L.) in India.

38 nding the genomic complexity of bread wheat (Triticum aestivum L.) is a cornerstone in the quest to u

39 fixation in cereals crops like bread wheat (Triticum aestivum L.) is also contributed by ear photosy

40 Winter wheat (Triticum aestivum L.) is essential to maintain food secu

41 ansformed corn (Zea mays L.) with the wheat (Triticum aestivum L.) puroindoline genes (Pina and Pinb)

42 Soil and wheat (Triticum aestivum L.) tissue samples were analyzed to de

43 accumulation of the same nutrients in wheat (Triticum aestivum L.) tissues.

44 Natural tolerance in hexaploid bread wheat (Triticum aestivum L.) to synthetic auxin herbicides is p

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

46 Winter wheat (Triticum aestivum L.), a dual-purpose crop, used for bot

47 ple crops, rice (Oryza sativa L.) and wheat (Triticum aestivum L.), and evaluates potential risks ass

48 arrow and thin leaf blades, including wheat (Triticum aestivum L.), maize (Zea may L.), rice (Oryza s

49 s increased branching in the roots of wheat (Triticum aestivum L.), thereby affecting plant biomass.

50 d blight (FHB) is a severe disease of wheat (Triticum aestivum L.).

51 of the Q/q homoeoalleles in hexaploid wheat (Triticum aestivum L.).

52 of glutamine synthetase (GS) genes in wheat (Triticum aestivum L.).

53 for complex polyploid genomes such as wheat (Triticum aestivum L.).

54 regulatory properties of Rca in bread wheat (Triticum aestivum L.).

55 to susceptible common wheat variety Fielder (Triticum aestivum L.).

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

57 The system was created with a Triticum aestivum promoter containing ABA responsive ele

58 ur results do not support this hypothesis as Triticum aestivum spp. vulgare landraces, which were not

59 In this study we identify an E2 enzyme, Triticum aestivum Ubiquitin conjugating enzyme 4 (TaU4)

60 Lys-428 in the CTE of Rca-alpha from wheat (Triticum aestivum) (TaRca2-alpha).

61 tin-binding sites, and interacts with wheat (Triticum aestivum) Actin1 (TaACT1), in planta.

62 iens (Impatiens wallerana) and wheat plants (Triticum aestivum) also elicit directed growth.

63 tic enzymes from maize (Zea mays) and wheat (Triticum aestivum) amyloplasts exist in cell extracts in

64 y to characterize these small RNAs in wheat (Triticum aestivum) and barley (Hordeum vulgare) anthers.

65 The glaucous appearance of wheat (Triticum aestivum) and barley (Hordeum vulgare) plants,

66 systems of intravacuolar membranes in wheat (Triticum aestivum) and barley (Hordeum vulgare) starchy

67 he pooid grasses wheat (Triticum monococcum, Triticum aestivum) and barley (Hordeum vulgare), vernali

68 n, a small temperate grass related to wheat (Triticum aestivum) and barley (Hordeum vulgare).

69 Secale cereale) is closely related to wheat (Triticum aestivum) and barley (Hordeum vulgare).

70 development in the temperate cereals wheat (Triticum aestivum) and barley (Hordeum vulgare).

71 ts distribution in different parts of wheat (Triticum aestivum) and designed an efficient method for

72 ty to drought and heat constraints in wheat (Triticum aestivum) and determined the average sensitivit

73 uctures which grow from the lemmas of wheat (Triticum aestivum) and other grasses that contribute to

74 ols bread-making quality in hexaploid wheat (Triticum aestivum) and represents a recently evolved reg

75 e potential role of ROS in defense of wheat (Triticum aestivum) and rice (Oryza sativa) against Hessi

76 eness of our approach on data sets of wheat (Triticum aestivum) and rice (Oryza sativa) plants as wel

77 As found in wheat (Triticum aestivum) and rice (Oryza sativa), this transge

78 been used to increase grain yields in wheat (Triticum aestivum) and rice (Oryza sativa).

79 of competition for amino acid between roots (Triticum aestivum) and soil microorganisms.

80 ring and inflorescence development of wheat (Triticum aestivum) as daylengths extend naturally in the

81 study, we cloned and characterized a wheat (Triticum aestivum) auxin efflux carrier ABCB1.

82 riant TaAGL22 as the FLC orthologs in wheat (Triticum aestivum) behaving most similar to Brachypodium

83 ith respect to the light gradient for wheat (Triticum aestivum) canopies with the aims of quantifying

84 chitecturally contrasting field-grown wheat (Triticum aestivum) canopies.

85 The availability of the hexaploid wheat (Triticum aestivum) cultivar Chinese Spring reference gen

86 efect that is commonly found in bread wheat (Triticum aestivum) cultivars and can result in commercia

87 h sunflower ( Helianthus annuus) and wheat ( Triticum aestivum) cultivated on free iron agar medium p

88 We identified bacteria in the wheat (Triticum aestivum) cv. Hereward seed environment using e

89 nly 42 have been annotated for common wheat (Triticum aestivum) due to its large genome.

90 s has been identified first in common wheat (Triticum aestivum) due to the complex genome.

91 s on gene co-expression in the mature wheat (Triticum aestivum) embryo.

92 During this period, bread wheat (Triticum aestivum) emerged as one of the world's most im

93 tive analysis of rice nsLtp genes and wheat (Triticum aestivum) EST sequences indexed in the UniGene

94 port on the development of transgenic wheat (Triticum aestivum) events, expressing a maize gene codin

95 f TaALMT1 (formerly named ALMT1) from wheat (Triticum aestivum) expressed in Xenopus laevis oocytes w

96 tor) infestation in commercial winter wheat (Triticum aestivum) fields in Kansas, USA.

97 Z-3-hexenyl acetate (Z-3-HAC) primed wheat (Triticum aestivum) for enhanced defense against subseque

98 We measured the uptake of P by wheat (Triticum aestivum) from radiolabeled nonfiltered (colloi

99 terizing motion in field-grown wheat plants (Triticum aestivum) from time-ordered sequences of red, g

100 Wheat (Triticum aestivum) genetic maps are a key enabling tool

101 owns of field-grown spring and winter wheat (Triticum aestivum) genotypes and their near-isogenic lin

102 the energy costs of root growth of 16 wheat (Triticum aestivum) genotypes under three levels of penet

103 t the function of HSP90 in lysates of wheat (Triticum aestivum) germ.

104 1) mRNA, oat (Avena sativa) globulin, wheat (Triticum aestivum) germin, maize (Zea mays) alcohol dehy

105 anscriptomics analyses revealed three wheat (Triticum aestivum) glycosyltransferase (TaGT) proteins f

106 d alpha-amylase from germinated wheat seeds (Triticum aestivum) has been purified to apparent electro

107 Polyploid wheat (Triticum aestivum) has had a massive increase in genome

108 roposed method is evaluated on winter wheat (Triticum aestivum) images (and demonstrated on Arabidops

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

110 Bread wheat (Triticum aestivum) is a globally important crop, account

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

112 Bread wheat (Triticum aestivum) is an allohexaploid that was formed v

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

114 iron content of staple crops such as wheat (Triticum aestivum) is difficult to change because of gen

115 Wheat (Triticum aestivum) is one of the most important crops in

116 Resistance of wheat (Triticum aestivum) leaves to the necrotrophic fungal pat

117 ur genetically diverse populations of wheat (Triticum aestivum) lines incorporating chromosome segmen

118 on gain (over 1 d) in three different wheat (Triticum aestivum) lines, which are architecturally dive

119 istance to multiple pathogens and the wheat (Triticum aestivum) Lr67 hexose transporter variant (Lr67

120 DEvelopment based on L-systems (ADEL) wheat (Triticum aestivum) model (ADEL-Wheat), which describes t

121 occur in other major cereals such as wheat (Triticum aestivum) or rice (Oryza sativa).

122 athogen, Cochliobolus miyabeanus, the wheat (Triticum aestivum) pathogen, Fusarium graminearum, and t

123 direction, from shoots to roots, the wheat (Triticum aestivum) PC synthase (TaPCS1) gene was express

124 ing growth coordination rules between wheat (Triticum aestivum) plant organs (i.e. between leaves wit

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

126 a novel jacalin-like lectin gene from wheat (Triticum aestivum) plants that responds to infestation b

127 rabidopsis (Arabidopsis thaliana) and wheat (Triticum aestivum) plants to daytime or nighttime elevat

128 tiva), maize (Zea mays ssp. mays) and wheat (Triticum aestivum) provide half of the food eaten by hum

129 (homoeologous) chromosomes, hexaploid wheat (Triticum aestivum) restricts pairing to just true homolo

130 on in the transport properties of the wheat (Triticum aestivum) root malate efflux transporter underl

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

132 e pulse-labelled the soil surrounding wheat (Triticum aestivum) roots with either (1)(5)NH(4)(+) or (

133 ntents of 90 different naturally aged wheat (Triticum aestivum) seed stocks were quantified in an unt

134 Microsomal membranes from etiolated wheat (Triticum aestivum) seedlings cooperatively incorporated

135 y purified XS activity from etiolated wheat (Triticum aestivum) seedlings.

136 Amino acids in wheat (Triticum aestivum) seeds mainly accumulate in storage pr

137 method to quantify 16 amino acids in wheat (Triticum aestivum) sieve tube (ST) samples as small as 2

138 ase FGL1, is restricted to inoculated wheat (Triticum aestivum) spikelets, whereas the wild-type stra

139 The cell walls of wheat (Triticum aestivum) starchy endosperm are dominated by ar

140 iscovered in lignin preparations from wheat (Triticum aestivum) straw and subsequently in all monocot

141 ining a range of genomic datasets for wheat (Triticum aestivum) that will assist plant breeders and s

142 Fourteen wheat (Triticum aestivum) varieties were grown in soil columns

143 loping starchy endosperm of hexaploid wheat (Triticum aestivum) was determined using RNA-Seq isolated

144 The structure of eIF4E from wheat (Triticum aestivum) was investigated using a combination

145 ug and toxic compound extrusion) from wheat (Triticum aestivum) was isolated and shown to encode a ci

146 lanking sequences from normal fertile wheat (Triticum aestivum) with those of Aegilops kotschyi which

147 ased upon conserved identity with the wheat (Triticum aestivum) xylanase inhibitor TAXI-1, we were ab

148 genes led to impressive increases in wheat (Triticum aestivum) yields during the Green Revolution.

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

150 aize (Zea mays), rice (Oryza sativa), wheat (Triticum aestivum), and barley (Hordeum vulgare) to illu

151 otiana tabacum), Medicago truncatula, wheat (Triticum aestivum), and barley (Hordeum vulgare).

152 t grains of barley (Hordeum vulgare), wheat (Triticum aestivum), and Brachypodium distachyon and that

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

154 utants from barley (Hordeum vulgare), wheat (Triticum aestivum), and Medicago truncatula, we demonstr

155 using muCT scans of maize (Zea mays), wheat (Triticum aestivum), and tomato (Solanum lycopersicum) gr

156 icated into hexaploid (AABBDD) common wheat (Triticum aestivum), as well as an 8-kb deletion in MSH4D

157 ding several important crops, such as wheat (Triticum aestivum), barley (Hordeum vulgare), and oats (

158 domesticated crop species, including wheat (Triticum aestivum), cotton (Gossypium hirsutum), and soy

159 orum as well as three nonpathogens of wheat (Triticum aestivum), including a necrotrophic pathogen of

160 for the three Rca isoforms present in wheat (Triticum aestivum), namely TaRca1-beta, TaRca2-alpha, an

161 conserved in rice (Oryza sativa) and wheat (Triticum aestivum), opening biotechnological perspective

162 staples, including maize (Zea mays), wheat (Triticum aestivum), rice (Oryza sativa), sorghum (Sorghu

163 ncluding barley (Hordeum vulgare) and wheat (Triticum aestivum), suggest that resistance contributed

164 In wheat (Triticum aestivum), the acceleration of flowering under

165 oid (Triticum turgidum) and hexaploid wheat (Triticum aestivum), the spikelet is a short indeterminat

166 plant virus, pea (Pisum sativum) and wheat (Triticum aestivum), was just upstream of a minimal promo

167 BA) and gibberellin (GA) signaling in wheat (Triticum aestivum), we have focused on the transcription

168 ters in responses to Zn deficiency in wheat (Triticum aestivum).

169 es Septoria tritici blotch disease of wheat (Triticum aestivum).

170 grain of barley (Hordeum vulgare) and wheat (Triticum aestivum).

171 ed with other dryland cereals such as wheat (Triticum aestivum).

172 such as barley (Hordeum vulgare) and wheat (Triticum aestivum).

173 opulations of rice (Oryza sativa) and wheat (Triticum aestivum).

174 (Agropyron elongatum) into cultivated wheat (Triticum aestivum).

175 rally important species, particularly wheat (Triticum aestivum).

176 d with TaHOX1 (the first homeobox protein in Triticum aestivum).

177 onlis and ID331, with those of common wheat (Triticum aestivum).

178 tin, for tiller inhibition) mutant of wheat (Triticum aestivum).

179 fied in sorghum (Sorghum bicolor) and wheat (Triticum aestivum).

180 lly, barley, rice (Oryza sativa), and wheat (Triticum aestivum).

181 nt in modern northern European winter wheat (Triticum aestivum).

182 (tetraploid Triticum turgidum and hexaploid Triticum aestivum).

183 tomato (Lycopersicum esculentum) and wheat (Triticum aestivum).

184 d (Triticum monococcum) and polyploid wheat (Triticum aestivum).

185 fficiently silence genes in hexaploid wheat (Triticum aestivum).

186 frequency in the hexaploid genome of wheat (Triticum aestivum).

187 ively referred to as gluten, found in wheat (Triticum aestivum).

188 rs regulating senescence in polyploid wheat (Triticum aestivum).

189 , and certain grains, including bread wheat (Triticum aestivum).

190 idopsis (Arabidopsis thaliana) and in wheat (Triticum aestivum).

191 hetic performance and productivity in wheat (Triticum aestivum).

192 ats but absent in most tested common wheats (Triticum aestivum).

193 mportant role in spike development in wheat (Triticum aestivum).

194 repetitive 16 Gbp genome of hexaploid wheat, Triticum aestivum, and assign 7.1 Gb of this assembly to

195 nd cerium dioxide (CeO(2)) in the tissues of Triticum aestivum, Brassica napus, and Hordeum vulgare,

196 f developing caryopses from hexaploid wheat (Triticum aestivum, cv. Hereward) was determined using Af

197 ogenitor of the D genome of hexaploid wheat (Triticum aestivum, genomes AABBDD) and an important gene

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

199 formation, such as the hexaploid bread wheat Triticum aestivum, is accurate annotation of the tags ge

200 rise independently between T. monococcum and Triticum aestivum.

201 s, and nonlegume cereals Hordeum vulgare and Triticum aestivum.

202 on haplotypes were found in hexaploid wheat (Triticum aestivum; ABD).

203 t widely utilized dwarfing alleles in wheat (Triticum aestivum; e.g. Rht-B1b and Rht-D1b) encode GA-r

204 leaves of C3 (rice [Oryza sativa] and wheat [Triticum aestivum]) and C4 (maize [Zea mays] and Setaria

205 [Oryza sativa], maize [Zea mays], and wheat [Triticum aestivum]) providing most of the caloric intake

206 information about Triticeae species (wheat [Triticum aestivum], barley [Hordeum vulgare], rye [Secal

207 t accessions were genotyped, representing 13 Triticum and Aegilops species.

208 n 90 diploid and 300 polyploid accessions of Triticum and Aegilops spp.

209 on haplotypes were detected in all polyploid Triticum and most of the polyploid Aegilops spp.

210 f similar analysis in other genera (Aegilops/Triticum and Oryza), Coffea genomes/subgenomes appeared

211 rghum, Pennisetum, Cynodon, Eragrostis, Zea, Triticum, and Hordeum, 23 (18.5%) seemed to be subject t

212 We examined 10 wild emmer wheat (Triticum dicoccoides Koern.) populations and 10 wild bar

213 he genetic responses of 10 wild emmer wheat (Triticum dicoccoides Koern.; WEW) populations in Israel,

214 accessions of six tetraploid wheat species (Triticum dicoccoides, T. dicoccum, T. turgidum, T. polon

215 tetraploid wheats that include landraces and Triticum dicoccoides.

216 barley, rye, oat, durum wheat, winter wheat, Triticum dicoccum and Triticum monococcum.

217 The fermentation of Triticum dicoccum with sourdough enhances the nutritiona

218 mestic cereals, such as Triticum monococcum, Triticum dicoccum, and Hordeum distichon, which were als

219 i.e. Triticum durum, Triticum polonicum and Triticum dicoccum, and to measure the glycemic index (GI

220 olus vulgaris L.) in Nicaragua, durum wheat (Triticum durum Desf.) in Ethiopia, and bread wheat (Trit

221 Durum wheat (Triticum durum Desf.) semolina gluten proteins consist o

222 mitogen-activated protein kinase TdWNK5 [for Triticum durum WITH NO LYSINE (K)5] was able to phosphor

223 In this work, we characterized durum wheat (Triticum durum) RING Finger1 (TdRF1) as a durum wheat nu

224 opulations of rice (Oryza sativa) and wheat (Triticum durum), we developed a method based on Illumina

225 h in pasta made with different cereals, i.e. Triticum durum, Triticum polonicum and Triticum dicoccum

226 Only one Triticum monococcum accession, however, carries both cau

227 loid wheat cultivars in addition to diploids Triticum monococcum and Aegilops tauschii.

228 However, the diploid wheat Triticum monococcum and barley have unusually low Ts/Tv

229 investigate the biological effects of ID331 Triticum monococcum gliadin-derived peptides in human Ca

230 Here, we demonstrate that the Sr35 gene from Triticum monococcum is a coiled-coil, nucleotide-binding

231 he flowering time locus in the diploid wheat Triticum monococcum L. identifying a set of deleted gene

232 r60, a race-specific gene from diploid wheat Triticum monococcum L. that encodes a protein with two p

233 p an early-flowering locus in einkorn wheat (Triticum monococcum L.) that is closely related to the b

234 ties of 2 lines of diploid monococcum wheat (Triticum monococcum ssp. monococcum), Monlis and ID331,

235 ctions from the seeds of 53 accessions among Triticum monococcum subsp. monococcum (T.m.), T. monococ

236 n important role in this process in diploid (Triticum monococcum) and polyploid wheat (Triticum aesti

237 nsible for floral induction in winter wheat (Triticum monococcum) and similar loci in other cereals.

238 this connection, we used two diploid wheat (Triticum monococcum) mutants, maintained vegetative phas

239 Am2) locus on chromosome 5 of diploid wheat (Triticum monococcum) using a cross between frost toleran

240 vernalization requirement in diploid wheat (Triticum monococcum).

241 and S supply for the diploid wheat einkorn (Triticum monococcum).

242 Triticum monococcum, an ancient wheat, is a potential ca

243 In the pooid grasses wheat (Triticum monococcum, Triticum aestivum) and barley (Hord

244 is region consumed domestic cereals, such as Triticum monococcum, Triticum dicoccum, and Hordeum dist

245 m wheat, winter wheat, Triticum dicoccum and Triticum monococcum.

246 r sequences to initiate translation, and the Triticum mosaic virus (TriMV) devotes an astonishing 7%

247 nd that Wheat streak mosaic virus (WSMV) and Triticum mosaic virus (TriMV) encode two independently f

248 d in the 739-nucelotide (nt) sequence of the Triticum mosaic virus (TriMV) leader sequence that disti

249 ong (739-nucleotide [nt]) leader sequence in triticum mosaic virus (TriMV), a recently emerged wheat

250 genus Tritimovirus, family Potyviridae) and Triticum mosaic virus (TriMV; genus Poacevirus, family P

251 Here, we show that the 739-nucleotide-long triticum mosaic virus 5' leader bears a powerful transla

252 d by the fungus Magnaporthe oryzae pathotype Triticum (MoT) is an emerging threat to wheat production

253 with different cereals, i.e. Triticum durum, Triticum polonicum and Triticum dicoccum, and to measure

254 Ag ( Hordeum vulgare) and 94 mg/kg for Ce ( Triticum sativum).

255 f the tribe Triticeae, which includes wheat (Triticum sp. L.) and barley (Hordeum vulgare L.) are cha

256 t species, particularly congeneric ones like Triticum spp, remains a challenging task.

257 Wheat (Triticum spp.

258 chain reaction analysis in 40 accessions of Triticum spp. and Aegilops spp., including diploids, tet

259 ss closely related to cereals such as wheat (Triticum spp.) and barley (Hordeum vulgare L.).

260 In winter wheat (Triticum spp.) and barley (Hordeum vulgare) varieties, l

261 N1) is a critical regulatory point in wheat (Triticum spp.) flowering.

262 Hybrid wheat (Triticum spp.) has the potential to boost yields and enh

263 mportant crops but similar efforts in wheat (Triticum spp.) have been more challenging.

264 Wheat (Triticum spp.) is one of the founder crops that likely d

265 Winter wheat (Triticum spp.) varieties require long exposures to low t

266 Arabidopsis (Arabidopsis thaliana) to wheat (Triticum spp.), including many crop and model species.

267 nt parasitic gall midge and a pest of wheat (Triticum spp.), with the aim of identifying genic modifi

268 gene interaction with its host plant, wheat (Triticum spp.).

269 eal-time PCR determination of T. aestivum in Triticum spp., was validated.

270 but maintained in the A genome of tetraploid Triticum timopheevii (AG).

271 Polyploid wheats comprise four species: Triticum turgidum (AABB genomes) and T. aestivum (AABBDD

272 tu (A genome), Aegilops tauschii (D genome), Triticum turgidum (AB genome), and Triticum aestivum (AB

273 leted from the A and B genomes of tetraploid Triticum turgidum (AB).

274 cribed so far in polyploid wheat (tetraploid Triticum turgidum and hexaploid Triticum aestivum).

275 Pairing between wheat (Triticum turgidum and T. aestivum) homeologous chromosom

276 ss is an important agronomic trait of durum (Triticum turgidum L. var. durum) and bread (Triticum aes

277 in wild and domesticated tetraploid wheats, Triticum turgidum ssp. dicoccoides (BBAA) and ssp. durum

278 ll leaf proteome profiles of two wild emmer (Triticum turgidum ssp. dicoccoides TR39477 and TTD22) an

279 Wild emmer (Triticum turgidum ssp. dicoccoides), the tetraploid AB-g

280 Wild emmer wheat (Triticum turgidum ssp. dicoccoides, WEW), the progenitor

281 39477 and TTD22) and one modern durum wheat (Triticum turgidum ssp. durum cv. Kiziltan) genotypes wer

282 rson et Graebener) derived from durum wheat (Triticum turgidum ssp. durum) and the wild barley Hordeu

283 The durum wheat (Triticum turgidum ssp. durum) gene Sr13 confers resistan

284 Durum wheat (Triticum turgidum ssp. durum) is widely grown in the Med

285 show that allotetraploid (AABB) durum wheat (Triticum turgidum ssp. durum) utilizes two pathways of m

286 However, tetraploid wheat (Triticum turgidum ssp., BBAA genome) is an ancestor of m

287 Using durum wheat (Triticum turgidum var durum), this study evaluated the e

288 In tetraploid (Triticum turgidum) and hexaploid wheat (Triticum aestivu

289 as compared in two varieties of durum wheat (Triticum turgidum) L. subsp. durum known to differ in sa

290 for example, in wheat (Triticum aestivum and Triticum turgidum), 17 functional Pm3 alleles confer agr

291 flat block of epoxy-embedded awns of wheat (Triticum turgidum), thin sections of native epidermis ce

292 and the A and B genomes of tetraploid wheat, Triticum turgidum, revealed that, in addition to the con

293 Acc-1 and Acc-2 loci from each of the wheats Triticum urartu (A genome), Aegilops tauschii (D genome)

294 arents, Aegilops longissima (S(l) S(l) ) and Triticum urartu (AA).

295 ), T. monococcum subsp. boeoticum (T.b.) and Triticum urartu (T.u.) were analyzed by immunoblotting a

296 We found that H. vulgare, H. spontaneum, and Triticum urartu DHN3s have a greater number of phosphory

297 ana) disease resistance protein 1 protein in Triticum urartu In this study we determined the molecula

298 endosperm throughout grain-filling stages in Triticum urartu, the A genome donor of common wheat.

299 aea (peanut), Ulex europaeus (gorse, furze), Triticum vulgaris and Concanavalin A (ConA) was used for

300 but retained in the A(m) genome of hexaploid Triticum zhukovskyi (A(m)AG).