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 llion years ago (MYA), events leading to the Triticum/Aegilops complex occurred at the following inte

4 is one of adaptive radiation of the diploid Triticum/Aegilops species (A, S, D), genome convergence

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

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

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

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

13 Triticum aestivum aluminum-activated malate transporter

14 of the D genome of the allopolyploid species Triticum aestivum and Aegilops cylindrica.

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

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

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

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

19 from those previously seen in winter wheat (Triticum aestivum cv Augusta) and thale cress (Arabidops

20 icity and elasticity were observed in wheat (Triticum aestivum cv Pennmore Winter) coleoptile (type I

21 -, NH4+, NO2-, and urea into roots of wheat (Triticum aestivum cv Yecora Rojo) seedlings from complet

22 4+ transporters in roots of wheat seedlings (Triticum aestivum cv Yercora Rojo) were characterized us

23 tered 327 632 rat ESTs in 47 min and 420 694 Triticum aestivum ESTs in 3 h and 15 min.

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

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

26 Triticum aestivum gliadin derived peptides were employed

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

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

29 Wheat (Triticum aestivum L. cv Bobwhite) was transformed with t

30 Wheat (Triticum aestivum L. cv Fremont) grown in hydroponic cul

31 dly in response to low temperature in wheat (Triticum aestivum L. cv Norstar) and rye (Secale cereale

32 ci in the F7 ITMI population of bread wheat, Triticum aestivum L. emend Thell., where it shortened an

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

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

35 ere is considerable variability among wheat (Triticum aestivum L.) cultivars in their ability to grow

36 r Zn efficiency than comparable bread wheat (Triticum aestivum L.) cultivars.

37 To localize wheat (Triticum aestivum L.) ESTs on chromosomes, 882 homoeolog

38 re believed to play critical roles in wheat (Triticum aestivum L.) grain texture.

39 aphid stylets into the sieve tubes of wheat (Triticum aestivum L.) grains to evaluate the dimensions

40 ed in assimilate flow into developing wheat (Triticum aestivum L.) grains were measured at several po

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

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

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

44 ticeae cDNA libraries, were mapped to wheat (Triticum aestivum L.) homoeologous group 4 chromosomes u

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

46 istance has concentrated on hexaploid wheat (Triticum aestivum L.) lines originating from China.

47 ct cotton (Gossypium hirsutum L.) and wheat (Triticum aestivum L.) plants caused a progressive declin

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

49 mechanisms in the plasma membrane of wheat (Triticum aestivum L.) root cortex cells using the patch-

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

51 d reproductive growth rates of a wheat crop (Triticum aestivum L.) were determined in three separate

52 Wheat plants (Triticum aestivum L.) were grown at the same photosynthe

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

54 ces were produced from Chinese Spring wheat (Triticum aestivum L.), five other hexaploid wheat genoty

55 Wheat (Triticum aestivum L.), rice (Oryza sativa L.), and maize

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

57 of homoeologous group 7 in hexaploid wheat (Triticum aestivum L.), to identify gene distribution in

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

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

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

61 f the hexaploid (2n = 6x = 42) wheat genome (Triticum aestivum L.).

62 gous group 1 chromosomes in hexaploid wheat (Triticum aestivum L.).

63 gous group 3 chromosomes of hexaploid wheat (Triticum aestivum L.).

64 al end of chromosome arm 1DS of bread wheat (Triticum aestivum L.).

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

84 In some species such as wheat (Triticum aestivum) and rice (Oryza sativa), mudrA-simila

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

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

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

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

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

90 Hexaploid wheat (Triticum aestivum) contains triplicated genomes derived

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

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

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

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

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

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

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

98 rop research, we developed a flexible wheat (Triticum aestivum) expression browser (www.wheat-express

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

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

101 nsity physical maps revealed that the wheat (Triticum aestivum) genome is partitioned into gene-rich

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

103 study, Zn-efficient and -inefficient wheat (Triticum aestivum) genotypes were grown for 13 d in chel

104 TRIP inhibited translation in wheat (Triticum aestivum) germ more efficiently than in rabbit

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

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

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

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

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

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

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

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

113 Bread wheat (Triticum aestivum) is an allohexaploid species, consisti

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

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

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

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

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

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

120 3) plants constitutively expressing a wheat (Triticum aestivum) OXO gene.

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

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

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

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

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

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

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

128 identified in the plasma membrane of wheat (Triticum aestivum) root cells.

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

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

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

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

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

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

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

136 rements of CO(2) and O(2) fluxes from wheat (Triticum aestivum) shoots indicated that short-term expo

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 ine zipper transcription factors from wheat (Triticum aestivum) that is specifically bound by PKABA1.

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

143 Resistance in wheat (Triticum aestivum) to the Hessian fly (Mayetiola destruc

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

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

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

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

148 A carboxylase (ACCase; EC 6.4.1.2) of wheat (Triticum aestivum) were cloned and sequenced.

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

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

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

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

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

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

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

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

157 m bicolor), barley (Hordeum vulgare), wheat (Triticum aestivum), and oat (Avena sativa) are anchored

158 oid wheat (Triticum durum), hexaploid wheat (Triticum aestivum), and tetraploid wild oats (Avena barb

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

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

161 The foliar disease tan spot of wheat (Triticum aestivum), caused by Pyrenophora tritici-repent

162 Tan spot of wheat (Triticum aestivum), caused by the fungus Pyrenophora tri

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

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

165 d sequences expressed in seedlings of wheat (Triticum aestivum), oat (Avena strigosa), rice (Oryza sa

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

167 ositions of corresponding loci on the wheat (Triticum aestivum), rice, maize, sugarcane, and Arabidop

168 responsible for toxic Na(+) influx in wheat (Triticum aestivum), root plasma membrane preparations we

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

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

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

172 icularly barley (Hordeum vulgare) and wheat (Triticum aestivum), with reference to methods of gene is

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

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

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

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

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

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

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

180 (tetraploid Triticum turgidum and hexaploid Triticum aestivum).

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

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

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

184 olved in the monocotyledonous species wheat (Triticum aestivum).

185 ago truncatula, maize (Zea mays), and wheat (Triticum aestivum).

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

187 ession in cultivated, hexaploid bread wheat (Triticum aestivum).

188 ency-dependent selection on its host, wheat (Triticum aestivum).

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

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

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

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

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

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

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

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

197 nd Triticum timopheevii AAGG) and hexaploid (Triticum aestivum, AABBDD) species.

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

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

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

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

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

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

204 troduced by hybridization into common wheat, Triticum aestivum.

205 rise independently between T. monococcum and Triticum aestivum.

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

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

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

209 es, inheritance studies in Triticeae (wheat [Triticum aestivum], barley [Hordeum vulgare], and rye [S

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

211 The diploid Triticum and Aegilops progenitors of the A, B, D, G, and

212 o determine phylogenetic relationships among Triticum and Aegilops species of the wheat lineage and t

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

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

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

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

217 persicon, Medicago, Oryza, Solanum, Sorghum, Triticum and Zea (www.tigr.org/tdb/e2k1/plant.repeats/in

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

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

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

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

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

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

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

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

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

227 barley (Hordeum vulgare), tetraploid wheat (Triticum durum), hexaploid wheat (Triticum aestivum), an

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

229 e major storage proteins of wheat endosperm (Triticum durum, Desf. cv Monroe), were reduced in vitro

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

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

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

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

234 physical contig spanning the Q locus using a Triticum monococcum BAC library.

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

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

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

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

239 und between the last two genes in the 324-kb Triticum monococcum sequence or in the colinear regions

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

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

242 ombination of chromosomes 3A(m) and 5A(m) of Triticum monococcum with closely homeologous chromosomes

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

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

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

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

247 vernalization requirement in diploid wheat (Triticum monococcum).

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

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

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

251 osely related homoeologous chromosome 1Am of Triticum monococcum.

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

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

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

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

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

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

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

259 GST) gene expression was examined in several Triticum species, differing in genome constitution and p

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

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

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

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

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

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

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

269 l. (2n = 2x = 14, DD) (syn. A. squarrosa L.; Triticum tauschii) is well known as the D-genome donor o

270 and D genome progenitor to cultivated wheat, Triticum tauschii.

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

272 the tetraploid (Triticum turgidum AABB, and Triticum timopheevii AAGG) and hexaploid (Triticum aesti

273 species cytoplasm-specific gene derived from Triticum timopheevii) and Vi (vitality) genes can be obs

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

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

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

277 onvergence and divergence of the tetraploid (Triticum turgidum AABB, and Triticum timopheevii AAGG) a

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

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

280 Durum wheat (Triticum turgidum L. var durum) cultivars exhibit lower

281 In durum wheat (Triticum turgidum L., AABB), an alloplasmic durum line [

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

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

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

285 39477 and TTD22) and one modern durum wheat (Triticum turgidum ssp. durum cv. Kiziltan) genotypes wer

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

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

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

289 es from the B genome of the tetraploid wheat Triticum turgidum were identified, each of which contain

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

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

292 enin locus from the A genome of durum wheat (Triticum turgidum, AABB) with the orthologous regions fr

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

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

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

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

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

298 Triticum urartu was confirmed as the A genome donor of t

299 from T. gondii antigen labeled with succinyl Triticum vulgare lectin (S-WGA) and represents the major

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

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