ライフサイエンスコーパス: Triticum aestivum

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

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

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

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

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

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

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

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

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

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

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

12 (tetraploid Triticum turgidum and hexaploid Triticum aestivum).

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

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

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

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

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

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

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

20 mportant gene pool for breeding bread wheat (Triticum aestivum).

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

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

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

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

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

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

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

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

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

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

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

32 rise independently between T. monococcum and Triticum aestivum.

33 troduced by hybridization into common wheat, Triticum aestivum.

34 Oryza sativa, Zea mays, Sorghum bicolor, and Triticum aestivum.

35 ion crystal structure of chlorophyllase from Triticum aestivum.

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

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

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

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

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

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

42 Triticum aestivum aluminum-activated malate transporter

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

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

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

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

47 LAVATA pathway using genome searches against Triticum aestivum and its wild relatives Triticum turgid

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

87 e (Zea mays), oat (Avena sativa), and wheat (Triticum aestivum); but the dicots pea (Pisum sativum),

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

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

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

93 Hexaploid wheat (Triticum aestivum) contains triplicated genomes derived

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

95 on of Aegilops kotschyi in the background of Triticum aestivum cultivar PBW343.

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

97 e assembly of the South African bread wheat (Triticum aestivum) cultivar Kariega by combining high-fi

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

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

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

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

102 f Al-treated roots of an Al-sensitive wheat (Triticum aestivum cv Victory) cultivar was screened with

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

104 4+ transporters in roots of wheat seedlings (Triticum aestivum cv Yercora Rojo) were characterized us

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

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

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

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

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

110 y-eight (48) grains of free-threshing wheat (Triticum aestivum/durum) represent the largest assemblag

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

126 Bread wheat (Triticum aestivum, genome BBAADD) is a young hexaploid s

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

128 esults of 3 yr of field data using 12 spring Triticum aestivum genotypes which were grown in NW Mexic

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

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

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

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

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

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

135 Triticum aestivum gliadin derived peptides were employed

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

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

138 ibution of genes and recombination in wheat (Triticum aestivum) group 1 chromosomes by comparing high

139 isease-resistance (R) gene cloning in wheat (Triticum aestivum) has been accelerated by the recent su

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

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

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

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

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

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

146 Bread wheat (Triticum aestivum) is a globally dominant crop and major

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

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

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

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

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

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

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

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

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

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

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

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

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

160 ed measurements of root elongation in wheat (Triticum aestivum L. cv Scout 66) seedlings in controlle

161 Growth and photosynthesis of wheat (Triticum aestivum L. cv Super Dwarf) plants grown onboar

162 ated tacr7 from hard red winter wheat (HRWW; Triticum aestivum L. cv. Winoka).

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

164 ation to shoots in seedlings of bread wheat (Triticum aestivum L.) and durum wheat cultivars were stu

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

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

167 Future wheat (Triticum aestivum L.) breeding will heavily rely on diss

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

169 Allopolyploid wheat (Triticum aestivum L.) carries three pairs of homoeologou

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

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

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

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

174 formed on a recombinant population of wheat (Triticum aestivum L.) doubled haploid lines is also prov

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

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

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

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

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

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

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

182 Hexaploid wheat (Triticum aestivum L.) has very low constitutive glutathi

183 d zinc (Zn) biofortification of bread wheat (Triticum aestivum L.) have been hindered by a lack of ge

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

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

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

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

188 Common wheat (Triticum aestivum L.) is a major staple food crop, provi

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

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

191 Winter wheat (Triticum aestivum L.) is the primary host of economic si

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

207 ality, into the Bob White cultivar of wheat (Triticum aestivum L.), in which it is not present in nat

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

209 hich have SafBA, but not in etiolated wheat (Triticum aestivum L.), oat (Avena sativa L.), barley (Ho

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

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

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

213 series of allelic chlorina mutants of wheat (Triticum aestivum L.), which have partial blocks in chlo

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

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

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

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

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

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

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

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

222 hromosomes was developed in hexaploid wheat (Triticum aestivum L.).

223 al crop production globally including wheat (Triticum aestivum L.).

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

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

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

227 n two naturally susceptible wheat varieties, Triticum aestivum (L.) var. Solstice and T. monococcum M

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

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

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

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

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

233 Here, we show the S gene encoding Triticum aestivum m(6)A methyltransferase B (TaMTB) is i

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

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

236 hensive transcriptome analysis of two wheat (Triticum aestivum) near-isogenic lines, the glaucous lin

237 onococcum Nor9 haplotype was substituted for Triticum aestivum Nor9 haplotypes on two T. aestivum 1A

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

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

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

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

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

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

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

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

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

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

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

249 ffecting staple cereal crops of which wheat (Triticum aestivum) plays a critical role in annual agric

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

269 of a natural population of 406 bread wheat (Triticum aestivum ssp.

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

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

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

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

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

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

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

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

278 onse of the glyoxylate cycle in bread wheat (Triticum aestivum) to infection by the obligate biotroph

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

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

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

282 nalysis of 68 pathogen-infected bread wheat (Triticum aestivum) varieties, including three (Oakley, S

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

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

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

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

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

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

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

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

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

292 The Triticum aestivum (wheat) genome encodes three isoforms

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

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

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

296 ntal mapping populations of hexaploid wheat (Triticum aestivum) with a common "Paragon" parent to exp

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

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

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

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