ライフサイエンスコーパス: Triticum aestivum

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

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

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

4 (tetraploid Triticum turgidum and hexaploid Triticum aestivum).

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

25 troduced by hybridization into common wheat, Triticum aestivum.

26 rise independently between T. monococcum and Triticum aestivum.

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

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

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

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

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

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

33 Triticum aestivum aluminum-activated malate transporter

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

74 Hexaploid wheat (Triticum aestivum) contains triplicated genomes derived

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

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

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

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

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

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

81 4+ transporters in roots of wheat seedlings (Triticum aestivum cv Yercora Rojo) were characterized us

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

103 Triticum aestivum gliadin derived peptides were employed

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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