ライフサイエンスコーパス: Solanum lycopersicum

1 rization of Sl2-MMP and Sl3-MMP from tomato (Solanum lycopersicum).

2 abidopsis (Arabidopsis thaliana) and tomato (Solanum lycopersicum).

3 nthamiana, tobacco (N. tabacum), and tomato (Solanum lycopersicum).

4 ed CO2 -induced stomatal movement in tomato (Solanum lycopersicum).

5 del plants Nicotiana benthamiana and tomato (Solanum lycopersicum).

6 y modulate ripening and softening in tomato (Solanum lycopersicum).

7 s of tobacco (Nicotiana tabacum) and tomato (Solanum lycopersicum).

8 wn to promote arbuscule formation in tomato (Solanum lycopersicum).

9 Daucus carota), corn (Zea mays), and tomato (Solanum lycopersicum).

10 acylsucrose biosynthetic pathway of tomato (Solanum lycopersicum).

11 um species, including the cultivated tomato (Solanum lycopersicum).

12 ototropic seedling1 (Nps1) mutant of tomato (Solanum lycopersicum).

13 ryl diphosphate synthase (NDPS1), in tomato (Solanum lycopersicum).

14 o suppress antiherbivore defenses in tomato (Solanum lycopersicum).

15 unction and host targets of HopQ1 in tomato (Solanum lycopersicum).

16 st important quality traits of fresh tomato (Solanum lycopersicum).

17 overy and repeatability for tomato extracts (Solanum lycopersicum).

18 m transcriptome responses to R:FR in tomato (Solanum lycopersicum).

19 ervation of MIR390-triggered TAS3 in tomato (Solanum lycopersicum).

20 naceous plants, including cultivated tomato (Solanum lycopersicum).

21 castor bean (Ricinus communis), and tomato (Solanum lycopersicum).

22 trophic growth within the host plant tomato (Solanum lycopersicum).

23 e parents and pollen from cultivated tomato (Solanum lycopersicum).

24 ions of lettuce (Lactuca sativa) and tomato (Solanum lycopersicum).

25 anced aphid reproduction on its host tomato (Solanum lycopersicum).

26 , but suppress it in the day-neutral tomato (Solanum lycopersicum).

27 abidopsis (Arabidopsis thaliana) and tomato (Solanum lycopersicum).

28 ulator of carotenoid accumulation in tomato (Solanum lycopersicum).

29 in the background of the cultivated tomato (Solanum lycopersicum).

30 ological function in Arabidopsis and tomato (Solanum lycopersicum).

31 r2 triggers immunity in I-2 carrying tomato (Solanum lycopersicum).

32 of type B Ggamma subunit (SlGGB1) in tomato (Solanum lycopersicum).

33 tible potato (Solanum tuberosum) and tomato (Solanum lycopersicum).

34 belong to the L1L paralogous gene family of Solanum lycopersicum.

35 donor of germplasm for the cultivated tomato Solanum lycopersicum.

36 anum pennellii and its L2 and L3 layers from Solanum lycopersicum.

37 ccessions and two commercial tomato lines of Solanum lycopersicum.

38 homologous genes from the cultivated tomato, Solanum lycopersicum.

39 ucrose biosynthesis in the cultivated tomato Solanum lycopersicum.

40 We investigated the effects of Solanum lycopersicum 1-deoxy-d-xylulose-5-phosphate synt

41 The tomato (Solanum lycopersicum) abscisic acid-induced myb1 (SlAIM1

42 n of an autoinhibited Ca(2+)-ATPase, tomato (Solanum lycopersicum) ACA10, which plays a critical role

43 Folate content was estimated in tomato (Solanum lycopersicum) accessions using microbiological a

44 In tomato (Solanum lycopersicum), acylsugar assembly requires four

45 activation of an immune response in tomato (Solanum lycopersicum) against Pseudomonas syringae relie

46 We describe the different ways in which Solanum lycopersicum and its wild relative S. pennellii

47 metabolic profile of 300 tomato accessions (Solanum lycopersicum and related wild species) by quanti

48 vegetables like Allium cepa, Allium sativum, Solanum lycopersicum and Solanum melongena, irrigated wi

49 o, Homo sapiens, Mus musculus, Oryza sativa, Solanum lycopersicum and Zea mays) are analyzed.

50 fferent tissue types in domesticated tomato (Solanum lycopersicum) and a wild relative (Solanum penne

51 ion, influence ethylene responses in tomato (Solanum lycopersicum) and Arabidopsis (Arabidopsis thali

52 ally bilaterally symmetric leaves of tomato (Solanum lycopersicum) and Arabidopsis thaliana that are

53 Using tomato (Solanum lycopersicum) and Brassica napus verified the po

54 ar secreting trichomes of cultivated tomato (Solanum lycopersicum) and close relatives produce a vari

55 olatiles is relatively low in tomato fruits (Solanum lycopersicum) and far more abundant in the close

56 olatiles is relatively low in tomato fruits (Solanum lycopersicum) and far more abundant in the close

57 g (VOD) and freeze drying (FD) for tomatoes (Solanum lycopersicum) and ginger (Zingiber officinale) i

58 Glandular trichomes of cultivated tomato (Solanum lycopersicum) and many other species throughout

59 in wild-type Arabidopsis as well as tomato (Solanum lycopersicum) and Nicotiana benthamiana, reveali

60 K alpha ) as a positive regulator in tomato (Solanum lycopersicum) and Nicotiana benthamiana.

61 is thaliana and 93 known pathways in tomato (Solanum lycopersicum) and obtained high-quality cross-va

62 Glandular trichomes from tomato (Solanum lycopersicum) and other species in the Solanacea

63 phorylate AGC kinase substrates from tomato (Solanum lycopersicum) and P. patens at the predicted PDK

64 * Rice, tomato (Solanum lycopersicum) and red clover (Trifolium pratense

65 osynthesis in glandular trichomes of tomato (Solanum lycopersicum) and related wild relatives also oc

66 lates) on six domesticated tomato genotypes (Solanum lycopersicum) and six wild tomato genotypes (Sol

67 ce alters leaf shape in domesticated tomato (Solanum lycopersicum) and wild relatives.

68 s [Arabidopsis thaliana], Helianthus annuus, Solanum lycopersicum, and Beta vulgaris) inoculated with

69 (Arabidopsis thaliana, Medicago truncatula, Solanum lycopersicum, and Oryza sativa) to delineate ope

70 ces of miR482/2118 family members in tomato (Solanum lycopersicum) are functionally significant.

71 but its functions in the model crop tomato (Solanum lycopersicum) are unknown.

72 es are responsible for the key tomato fruit (Solanum lycopersicum) aroma attribute termed "smoky." Re

73 abidopsis (Arabidopsis thaliana) and tomato (Solanum lycopersicum) as models, we show that PDX12 is t

74 egulation of SlARF4, a member of the tomato (Solanum lycopersicum) auxin response factor (ARF) gene f

75 Here we show that the expression of tomato (Solanum lycopersicum) beta-CARBONIC ANHYDRASE 3 (betaCA3

76 process of chlorophyll breakdown in tomato (Solanum lycopersicum), both in leaves and fruits.

77 m), N. benthamiana, N. attenuata and tomato (Solanum lycopersicum) but not to our knowledge in potato

78 onoid and lycopene content from tomato pulp (Solanum lycopersicum) by using response surface methodol

79 Tomato (Solanum lycopersicum) carries three SERK members.

80 hysical map with a cDNA probe of the tomato (Solanum lycopersicum) chromoplast-specific lycopene beta

81 Tomato (Solanum lycopersicum) Cipk6 regulates immune and suscept

82 s microarray hybridization assays in tomato (Solanum lycopersicum; climacteric) and pepper (Capsicum

83 forming pooled CRISPR libraries into tomato (Solanum lycopersicum), collections of mutant lines were

84 and that AtSAUR19 overexpression in tomato (Solanum lycopersicum) confers the same suite of phenotyp

85 sucroses produced by the cultivated tomato (Solanum lycopersicum) contain three or four short chain

86 w here that the genome of cultivated tomato (Solanum lycopersicum) contains 44 terpene synthase (TPS)

87 Tomato (Solanum lycopersicum) contains two close homologs of the

88 In tomato (Solanum lycopersicum), cryptochromes are encoded by a mu

89 esistance as potential resources for tomato (Solanum lycopersicum) cultivar development.

90 S1), that is expressed in cultivated tomato (Solanum lycopersicum) cultivar M82 type VI glandular tri

91 (i.e. peach [Prunus persica] and two tomato [Solanum lycopersicum] cultivars, Ailsa Craig and M82) an

92 e used the commercially important crop plant Solanum lycopersicum (cultivated tomato) to investigate

93 se, HT-A and HT-B genes from SI species into Solanum lycopersicum (cultivated tomato).

94 points for two Solanaceous species, tomato (Solanum lycopersicum cv 75 m82D) and Nicotiana benthamia

95 nces, including a pre-release of the tomato (Solanum lycopersicum cv Heinz 1706) reference genome.

96 s in two generations of the well-established Solanum lycopersicum cv M82 x Solanum pennellii ac.

97 trogression lines, but high in the resistant Solanum lycopersicum cv M82, and in C. reflexa itself.

98 soils and in edible parts of two vegetables (Solanum lycopersicum cv. Amal) and (Lactuca sativa L. cv

99 CTOMT1 was cloned from Solanum lycopersicum cv. M82 and expressed in Escherichi

100 rogeny of crosses between cultivated tomato (Solanum lycopersicum cv. M82) and a wild relative (Solan

101 sting the fruit cuticle of wild-type tomato (Solanum lycopersicum cv. M82) with those of cutin-defici

102 Mutations in a tomato (Solanum lycopersicum) cyclophilin A ortholog, DIAGEOTROP

103 Here, we show that the tomato (Solanum lycopersicum) DELLA protein PROCERA (PRO), a neg

104 yanin free (af) mutant of cultivated tomato (Solanum lycopersicum) fail to accumulate both flavonoids

105 ell as pea (Pisum sativum) wilty and tomato (Solanum lycopersicum) flacca ABA-deficient mutants had h

106 ms biology approach was developed in tomato (Solanum lycopersicum) for coordinated induction of biosy

107 Tomato (Solanum lycopersicum) fruit accumulate the red carotenoi

108 observations demonstrate that unripe tomato (Solanum lycopersicum) fruit activate pathogen defense re

109 and embedding the epidermal cells of tomato (Solanum lycopersicum) fruit acts not only as a protectiv

110 alyzed in mitochondria isolated from tomato (Solanum lycopersicum) fruit at two ripening stages.

111 Modulation of the malate content of tomato (Solanum lycopersicum) fruit by altering the expression o

112 emporal distribution of auxin during tomato (Solanum lycopersicum) fruit development and the function

113 -6-P contents of pericarp throughout tomato (Solanum lycopersicum) fruit development.

114 is required for cutin deposition in tomato (Solanum lycopersicum) fruit exocarp.

115 s) make significant contributions to tomato (Solanum lycopersicum) fruit flavor and human preferences

116 The shelf life of tomato (Solanum lycopersicum) fruit is determined by the process

117 rt the fine mapping and cloning of a tomato (Solanum lycopersicum) fruit mass gene encoding the ortho

118 ers such as blossom-end rot (BER) in tomato (Solanum lycopersicum) fruit may be induced by abnormal r

119 eported that cutin polymerization in tomato (Solanum lycopersicum) fruit occurs via transesterificati

120 teins in plastids at three stages of tomato (Solanum lycopersicum) fruit ripening (mature-green, brea

121 R (RIN) is an essential regulator of tomato (Solanum lycopersicum) fruit ripening but the exact mecha

122 Tomato (Solanum lycopersicum) fruit ripening is accompanied by a

123 During tomato (Solanum lycopersicum) fruit ripening, chloroplasts diffe

124 that LeETR4, a critical receptor for tomato (Solanum lycopersicum) fruit ripening, is multiply phosph

125 In tomato (Solanum lycopersicum) fruit, the thick cuticle embedding

126 In tomato (Solanum lycopersicum) fruit, the uniform ripening (u) lo

127 nalysis of the locus surrounding the tomato (Solanum lycopersicum) fruit-shape gene SUN to determine

128 n deposition have been identified in tomato (Solanum lycopersicum) fruit.

129 er at the global scale in developing tomato (Solanum lycopersicum) fruit.

130 with chain lengths beyond C(2)(8) in tomato (Solanum lycopersicum) fruits and C(2)(6) in Arabidopsis

131 Lycopene biosynthesis in tomato (Solanum lycopersicum) fruits has been proposed to procee

132 us on the role of NTRC in developing tomato (Solanum lycopersicum) fruits representing heterotrophic

133 nts of tocochromanol accumulation in tomato (Solanum lycopersicum) fruits.

134 he and phenylpropanoid metabolism in tomato (Solanum lycopersicum) fruits.

135 dying grapevine (Vitis vinifera) and tomato (Solanum lycopersicum) gene expression atlases and a grap

136 The tomato (Solanum lycopersicum) genome encodes for a single DELLA

137 Here, we report that the tomato (Solanum lycopersicum) genome harbors two genes, SlFAD2-1

138 veral domesticated and wild Solanum species: Solanum lycopersicum (glandular trichome types 1, 6, and

139 ays), wheat (Triticum aestivum), and tomato (Solanum lycopersicum) grown in a range of contrasting so

140 Tomato (Solanum lycopersicum) has a single DELLA gene named PROC

141 at the circadian clock of cultivated tomato (Solanum lycopersicum) has slowed during domestication.

142 Tomato (Solanum lycopersicum) high-pigment mutants with lesions

143 Its tomato (Solanum lycopersicum) homolog is required for host plant

144 s required for protection from HS In tomato (Solanum lycopersicum), HsfA2 acts as coactivator of HsfA

145 abidopsis (Arabidopsis thaliana) and tomato (Solanum lycopersicum) hypocotyls.

146 To gain insight into TARK1's role in tomato (Solanum lycopersicum) immunity, we used a proteomics app

147 round, have been used extensively in tomato (Solanum lycopersicum) improvement.

148 Tomato (Solanum lycopersicum) is a major crop and is highly appr

149 Tomato (Solanum lycopersicum) is a model organism for Solanaceae

150 y metabolites in the human diet, and tomato (Solanum lycopersicum) is a rich source of these health-p

151 Blossom-end rot (BER) in tomato fruit (Solanum lycopersicum) is believed to be a calcium (Ca(2)

152 to Pseudomonas syringae bacteria in tomato (Solanum lycopersicum) is conferred by the Prf recognitio

153 Fruit firmness in tomato (Solanum lycopersicum) is determined by a number of facto

154 Commercial tomato (Solanum lycopersicum) is one of the most widely grown ve

155 Tomato (Solanum lycopersicum) is part of a complex of closely re

156 enotypic diversity within cultivated tomato (Solanum lycopersicum) is particularly evident for fruit

157 rolling the elongated fruit shape of tomato (Solanum lycopersicum) is SUN.

158 Tomato (Solanum lycopersicum) is the primary model for the study

159 The tomato (Solanum lycopersicum) kinase Pto triggers localized prog

160 on and introgression with cultivated tomato, Solanum lycopersicum L.

161 L. (zucchini), Glycine max L. (soybean), and Solanum lycopersicum L. (tomato) was determined.

162 n the leaves of Solanum glaucophyllum Desf., Solanum lycopersicum L. and Capsicum annuum L.

163 o the identification of molecular markers in Solanum lycopersicum L. and Cucurbita pepo L.

164 rt this hypothesis, we show that the tomato (Solanum lycopersicum L.) DNA ligase 1 specifically and e

165 The well-characterized mycorrhizal tomato (Solanum lycopersicum L.) genotype 76R (referred to as MY

166 Tomato (Solanum lycopersicum L.) has been studied extensively du

167 Tomato (Solanum lycopersicum L.) has undergone intensive selecti

168 Domestication of cultivated tomato (Solanum lycopersicum L.) included the transition from al

169 rgeted to the second exon of CCD8 in tomato (Solanum lycopersicum L.) plants.

170 on of 28 genotypes of "long storage" tomato (Solanum lycopersicum L.) was studied for carotenoid and

171 Alternaria solani severely affects tomato (Solanum lycopersicum L.) yield causing early blight (EB)

172 ods to real lipophilic extracts from tomato (Solanum lycopersicum L.), green and red peppers (Capsicu

173 uces fruit quality and shelf-life in tomato (Solanum lycopersicum L.).

174 ular trichomes and leaves from a cultivated (Solanum lycopersicum LA4024) and a wild (Solanum habroch

175 oria (Xcv) that is translocated into tomato (Solanum lycopersicum) leaf cells by the pathogen's type

176 (Nicotiana benthamiana) and nonhost (tomato [Solanum lycopersicum]) leaf surfaces, (2) an assessment

177 n of isoprenoid-derived compounds in tomato (Solanum lycopersicum) leaves and fruits.

178 of the diversity of leaf shape, and tomato (Solanum lycopersicum) leaves are compound due to prolong

179 Importantly, tomato (Solanum lycopersicum) leaves treated with AA exhibited r

180 rol and Cladosporium fulvum-infected tomato (Solanum lycopersicum) leaves were subjected to the same

181 mmed cell death (PCD) in susceptible tomato (Solanum lycopersicum) leaves.

182 Tomato (Solanum lycopersicum), like most plants, contains two GL

183 Tomato (Solanum lycopersicum), like other Solanaceous species, a

184 nravel the transcriptional regulation of the Solanum lycopersicum linalool synthase (SlMTS1, recently

185 ipt levels are higher in leaves of a tomato (Solanum lycopersicum) line resistant to Tomato yellow le

186 pathway genes were overexpressed in tomato (Solanum lycopersicum) lines and the effects on carotenoi

187 Transgenic tomato (Solanum lycopersicum) lines overexpressing yeast spermid

188 Tomato (Solanum lycopersicum) local varieties are having an incr

189 icated tomato species, Solanum pennellii and Solanum lycopersicum 'M82.' We found extensive differenc

190 the cold/freezing-sensitive species tomato (Solanum lycopersicum [M82 cv]).

191 The RLPs Cf-4 and Ve1 of tomato (Solanum lycopersicum) mediate resistance to the fungal p

192 rrhization in three different plant species: Solanum lycopersicum, Medicago truncatula, and Oryza sat

193 cally milled cutins extracted from tomatoes (Solanum lycopersicum 'Micro-Tom'; the wild type and the

194 f fruit surface, we investigated the tomato (Solanum lycopersicum) MIXTA-like gene.

195 In tomato (Solanum lycopersicum), molecular cloning has revealed th

196 the environment on fruit metabolism, tomato (Solanum lycopersicum 'Moneymaker') plants were grown und

197 procera (pro) is a tall tomato (Solanum lycopersicum) mutant carrying a point mutation i

198 with that of simple leaves, and the tomato (Solanum lycopersicum) mutant clausa (clau) exposes a pot

199 sterile, whereas the JA-insensitive tomato (Solanum lycopersicum) mutant jai1 is female sterile.

200 ular identification of the classical tomato (Solanum lycopersicum) mutant lyrate, which is impaired i

201 The late termination (ltm) tomato (Solanum lycopersicum) mutant shows severely delayed flow

202 fication and characterization of new tomato (Solanum lycopersicum) mutants affected in fruit pigmenta

203 This study utilized tomato (Solanum lycopersicum) mutants with altered flavonoid bio

204 ecently identified a defense-related tomato (Solanum lycopersicum) NAC (NAM, ATAF1,2, CUC2) transcrip

205 d the regulation of a stress-related tomato (Solanum lycopersicum) NAC1 (SlNAC1) transcription factor

206 In tomato (Solanum lycopersicum), naturally occurring cis-regulator

207 that lack trans- and cis-neoxanthin, tomato (Solanum lycopersicum) neoxanthin-deficient1 (nxd1) and A

208 y documenting dynamic changes in the tomato (Solanum lycopersicum) nuclear proteome during infection

209 Furthermore, delivery of GroEL into tomato (Solanum lycopersicum) or Arabidopsis through Pseudomonas

210 at Tomato AGAMOUS-LIKE1 (TAGL1), the tomato (Solanum lycopersicum) ortholog of the duplicated SHATTER

211 the proteins extracted from dewaxed tomato (Solanum lycopersicum) peels, we identified GDSL1, a memb

212 in their capacity to invade and kill tomato (Solanum lycopersicum) plants and immunodepressed mice.

213 Transgenic tomato (Solanum lycopersicum) plants expressing a fragment of th

214 ating fruit, we generated transgenic tomato (Solanum lycopersicum) plants expressing an OXDC (FvOXDC)

215 arthropod herbivores and disease in tomato (Solanum lycopersicum) plants grown from seed treated wit

216 ddition, the firmness of fruits from tomato (Solanum lycopersicum) plants overexpressing VvABF2 was s

217 Here, we show that tomato (Solanum lycopersicum) plants with impaired SiR expressio

218 rolling circle amplification from 6 tomato (Solanum lycopersicum) plants with leaf curl symptoms ide

219 ion of an entire bacterial operon in tomato (Solanum lycopersicum) plants without the need for plasti

220 nvestigated S-RNase-independent rejection of Solanum lycopersicum pollen by SC Solanum pennellii LA07

221 he lutescent1 (l1) and l2 mutants of tomato (Solanum lycopersicum) possess a range of chlorophyll-def

222 ar secreting trichomes of cultivated tomato (Solanum lycopersicum) produce a wide array of volatile a

223 copene metabolites are found in both tomato (Solanum lycopersicum) products and in their consumers, m

224 Tomato (Solanum lycopersicum) provides an excellent system in wh

225 ible part of different vegetables (tomatoes (Solanum lycopersicum "Raf") peppers (Capsicum annuum), c

226 A pollen-specific tomato (Solanum lycopersicum) RALF (SlPRALF) has been identified

227 rison of At-FLS2 and the orthologous tomato (Solanum lycopersicum) receptor Sl-FLS2.

228 and flgII-28, that are recognized by tomato (Solanum lycopersicum) receptors Flagellin sensing2 (Fls2

229 ) was reported as a key regulator of tomato (Solanum lycopersicum) reproductive development, mainly i

230 vered a biosynthetic gene cluster in tomato (Solanum lycopersicum) required for falcarindiol producti

231 with cell death induction during the tomato (Solanum lycopersicum) resistance response to its pathoge

232 In tomato (Solanum lycopersicum), resistance to Pseudomonas syringa

233 abidopsis (Arabidopsis thaliana) and tomato (Solanum lycopersicum), respectively.

234 on of the sticky peel (pe) mutant of tomato (Solanum lycopersicum) revealed several phenotypes indica

235 Comparison of SiR expression in tomato (Solanum lycopersicum 'Rheinlands Ruhm') and Arabidopsis

236 MADS1 and MaMADS2, homologous to the tomato (Solanum lycopersicum) RIN-MADS ripening gene.

237 NADP-dependent malic enzyme (ME) on tomato (Solanum lycopersicum) ripening.

238 LP with structural similarity to the tomato (Solanum lycopersicum) RLP Eix2, which detects fungal xyl

239 to study global mRNA translation in tomato (Solanum lycopersicum) roots.

240 g and chloroplast differentiation in tomato (Solanum lycopersicum) seedlings are mediated by an intri

241 Metabolite profiling of tomato (Solanum lycopersicum) shoots and roots from plants expos

242 Here, two isoenzymes from tomato (Solanum lycopersicum), SlAMADHs, and three AMADHs from m

243 In tomato (Solanum lycopersicum), SlPIF1a and SlPIF3 regulate fruit

244 Analysis of tomato (Solanum lycopersicum) small RNA data sets revealed the p

245 , we show that a cluster of genes in tomato (Solanum lycopersicum; Solanaceae) contains genes for ter

246 IGG marker files for three sets of genomes, Solanum lycopersicum/Solanum pennellii, Arabidopsis (Ara

247 na, tobacco (Nicotiana benthamiana), tomato (Solanum lycopersicum), sunflower (Helianthus annuus), Ca

248 aites), a relative of the cultivated tomato (Solanum lycopersicum), synthesizes large amounts of 2-me

249 Characterization of a new tomato (Solanum lycopersicum) T-DNA mutant allowed for the isola

250 nalysis of regulated pesticides in tomatoes (Solanum lycopersicum), tamarillos (Solanum betaceum) and

251 del species Arabidopsis thaliana and tomato (Solanum lycopersicum) that auxin is depleted from leaf a

252 using genetically modified lines of tomato (Solanum lycopersicum) that vary incrementally in the exp

253 In tomato (Solanum lycopersicum), this process is associated with e

254 8-1/8-1-1) that causes the cultivated tomato Solanum lycopersicum to shift from producing acylsucrose

255 d Solanum pennellii and domesticated tomato (Solanum lycopersicum) to identify the genetic basis of t

256 Resistance in tomato (Solanum lycopersicum) to infection by Pseudomonas syring

257 ns (RLPs) that mediate resistance of tomato (Solanum lycopersicum) to the foliar pathogen Cladosporiu

258 have been successfully validated in tomato (Solanum lycopersicum), tobacco (Nicotiana tabacum), Medi

259 Fruits of Solanum lycopersicum (tomato) accumulate high levels of

260 Solanum lycopersicum (tomato) and its wild relatives har

261 composition and transcriptomes of suberized Solanum lycopersicum (tomato) and russet apple (Malus x

262 res) that either induce/suppress defenses in Solanum lycopersicum (tomato) and Zea mays (maize), two

263 Here we identified and characterized the Solanum lycopersicum (tomato) ARF10 homolog (SlARF10), d

264 There is extensive natural variation in Solanum lycopersicum (tomato) but it has not been fully

265 Studies with Solanum lycopersicum (tomato) fruit have shown that poll

266 onin content of Capsicum annuum (pepper) and Solanum lycopersicum (tomato) fruits.

267 cell degeneration and pollen development in Solanum lycopersicum (tomato) plants.

268 e role of SERK1 in Mi-1-mediated resistance, Solanum lycopersicum (tomato) SlSERK genes were cloned.

269 nd fruit-ripening specific (E8) promoters in Solanum lycopersicum (tomato), and determined alteration

270 Cucurbita pepo (zucchini), Zea mays (corn), Solanum lycopersicum (tomato), and Glycine max (soybean)

271 ts, such as Nicotinana tabacum (tobacco) and Solanum lycopersicum (tomato), greater than 10-fold enha

272 tor of the late branch of wound signaling in Solanum lycopersicum (tomato).

273 associated bacteria in mediating defenses in Solanum lycopersicum (tomato).

274 We characterized a tomato (Solanum lycopersicum) TPS-e/f gene, TPS46, encoding GLS

275 pecialized (secondary) metabolism in tomato (Solanum lycopersicum) trichomes, 454 sequencing of cDNA

276 eae and Rhizophagus intraradices) on tomato (Solanum lycopersicum) under the WS condition was studied

277 etabolites in glandular trichomes of tomato (Solanum lycopersicum) using (13)CO2 and analyzing (13)C

278 s genes in Nicotiana benthamiana and tomato (Solanum lycopersicum) using virus-induced gene silencing

279 gnificant reduction of root-galls on tomato (Solanum lycopersicum var. Rutgers).

280 Modern tomato (Solanum lycopersicum) varieties are bred for uniform rip

281 This gene was termed Solanum lycopersicum virus resistant/susceptible lipocal

282 In tomato (Solanum lycopersicum), wall-associated kinase 1 (SlWak1)

283 he vacuolar amino acid transporter CAT2 from Solanum lycopersicum was investigated in this work.

284 ression of the Arabidopsis etr1-1 in tomato (Solanum lycopersicum) was achieved using an inducible pr

285 In tomato (Solanum lycopersicum), we find that ABA-increased ROS is

286 Ile and OPDA to insect resistance in tomato (Solanum lycopersicum), we silenced the expression of OPD

287 ing the mechanism of BR signaling in tomato (Solanum lycopersicum), we used liquid chromatography-tan

288 tome and metabolome reprogramming in tomato (Solanum lycopersicum), we used plants that express both

289 , six BCAT genes from the cultivated tomato (Solanum lycopersicum) were identified and characterized.

290 hree senescence-related NAC TFs from tomato (Solanum lycopersicum) were identified, namely SlORE1S02,

291 With 47 homologues in tomato (Solanum lycopersicum) were reported, but the individual

292 echanism of ethylene biosynthesis of tomato (Solanum lycopersicum) when fruit have reached their maxi

293 diated responses2 (spr2) mutation in tomato (Solanum lycopersicum), which eliminates the function of

294 ng extended dark, SO was enhanced in tomato (Solanum lycopersicum) wild-type leaves, while the other

295 Tomato (Solanum lycopersicum) wiry mutants represent a class of

296 abidopsis (Arabidopsis thaliana) and tomato (Solanum lycopersicum) with caterpillar herbivory, applic

297 ssing of prosystemin, a precursor of tomato (Solanum lycopersicum) wound hormone systemin, is perform

298 galactosyl and fucosyl substituents, tomato (Solanum lycopersicum) XyG contains arabinofuranosyl resi

299 pv. tomato (Pto) T1 is pathogenic in tomato (Solanum lycopersicum) yet nonpathogenic in Arabidopsis.

300 Cultivated tomato (Solanum lycopersicum Zinc Finger2 [SIZF2]) is a cysteine