ライフサイエンスコーパス: tomato

1 n of an important harvesting trait in modern tomato.

2 ting ovule formation in both Arabidopsis and tomato.

3 on has resulted in reduced salt tolerance in tomato.

4 lopment of Anthracnose disease in chilli and tomato.

5 um (SP) is the wild progenitor of cultivated tomato.

6 (+) /K(+) ratio and confer salt tolerance in tomato.

7 causes yield losses to many crops including tomato.

8 sp. lycopersici (Fol), a fungal pathogen of tomato.

9 s are well conserved between Arabidopsis and tomato.

10 ted bipartite begomovirus MYMIV co-infecting tomato.

11 regions with roles in trichome formation in tomato.

12 ruit size in the domestication of cultivated tomatoes.

13 reasing the salinity tolerance of commercial tomatoes.

14 ll.) produces processed foods, such as dried tomatoes.

15 r improving salinity tolerance in commercial tomatoes.

16 N isotope ratios in amino acids derived from tomatoes.

17 fruit locule number and fruit size in modern tomatoes.

18 ple (2.75 +/- 0.23 ng kg(-1)), carbofuran in tomato (11.34 +/- 0.61 ng kg(-1)), and methomyl in water

19 ghts on genes involved in stigma position in tomato, a bulk RNA sequencing (RNA-Seq) approach was ado

20 me-wide association studies (GWAS) using 775 tomato accessions and 2,316,117 SNPs from three GWAS pan

21 Genotyping these SVs in ~600 representative tomato accessions identifies alleles under selection dur

22 was investigated using multiple Pst strains, tomato accessions with available genome sequences, react

23 K(+) ratio in a population consisting of 369 tomato accessions with large natural variations.

24 ssion resistance between cultivated and wild tomato accessions.

25 limonene as potential biomarkers to classify tomatoes according to production systems.

26 stigma is an established phenotype in modern tomatoes, an exserted stigma is still present in several

27 egradation in fruits and vegetables, such as tomatoes, an urgent requirement.

28 hylogenetic comparison of the TPS genes from tomato and Arabidopsis shows expansions in each clade of

29 age but here we show a different pattern in tomato and Arabidopsis.

30 icate that two different mechanisms occur in tomato and Arabidopsis.

31 It is a worldwide pest on tomato and can potently suppress the host's natural resi

32 The ortholog of Ptr1 in tomato and in Solanum pennellii is a pseudogene.

33 ural and recombinant purified allergens from tomato and mustard seeds, we identified 2S albumin and n

34 ecular breeding to improve salt tolerance in tomato and other crops.

35 further studies on epidermal development in tomato and other species of the Solanaceae family.

36 oled leaf samples, collected from individual tomato and pepper fields in Alabama that displayed the c

37 While in tomato and potato samples, the maximum concentrations of

38 ral had a conserved effect on root growth in tomato and rice and generated significantly more compact

39 th half-life of 3.12-3.21 and 1.24-1.35d for tomato and soil, respectively following doses of indoxac

40 the determination of indoxacarb residues in tomato and soil.

41 caused by the fungal pathogen B. cinerea in tomato and tobacco plants, and postharvest products.

42 aCA3 in the high CO(2) -mediated response in tomato and two other Solanaceae crops is distinct from t

43 applicable as specific intake biomarkers for tomatoes and their biological activities as well as meta

44 pene, and rutin were higher in the Tultitlan tomatoes and were associated with the thallium and magne

45 otypical acetylenic lipid present in carrot, tomato, and celery that inhibits growth of fungi and hum

46 RNA-seq transcriptome profiling of tomato, and experiments with jasmonic and salycilic acid

47 Cucumber and tomato are commercially important commodities that are s

48 nvolved in the control of stigma position in tomato are discussed.

49 ess, the majority of divergent FAD2 genes in tomato are upregulated by one or more stresses.

50 Complex dietary foods like soy and tomatoes are composed of active metabolites with anti-in

51 study suggest that the use of indoxacarb in tomato at recommended dose, does not seem to pose any di

52 Tomato Atypical Receptor Kinase 1 (TARK1) is a pseudokin

53 stigated alkaloids were only quantifiable in tomato-based products and the occurrence of N-caprylhist

54 ness, and it offers a potential strategy for tomato breeders to produce firmer fruit.

55 the range of genetic variation available for tomato breeding and research.

56 Fruit firmness is a target trait in tomato breeding because it facilitates transportation an

57 ed as an important germplasm donor in modern tomato breeding.

58 coopted host factors, we have reconstituted Tomato bushy stunt virus (TBSV) replicase using artifici

59 tol 4-phosphate [PI(4)P] phosphatase reduced tomato bushy stunt virus (TBSV) replication in yeast (Sa

60 dissect the roles of various host factors in Tomato bushy stunt virus (TBSV) replication, we have dev

61 rse RNA viruses, including the plant viruses tomato bushy stunt virus, carnation Italian ringspot vir

62 richloro-2-pyridyl phosphorothioate) (CP) in tomato by HPLC-DAD.

63 cipate in the control of ovule initiation in tomato, by promoting an increase on ovule primordia form

64 ection of an important vegetable crop plant, tomato, by two dangerous and peculiarly different viral

65 aluate persistence behaviour of pyridalyl in tomato, cabbage and cultivated field soil over two conse

66 The compound exhibited low persistence in tomato, cabbage and soil.

67 oup reports that bioactive agents in soy and tomatoes can reduce pro-inflammatory cytokines and suppr

68 In the tomato carpoplane, shifts were detected in the families

69 verexpressed under glucose and deproteinized tomato cell wall conditions, respectively.

70 Various cell concentrations (MSK8 tomato cells in Murashige and Skoog media) have been inv

71 as underlying pc10, similar to its effect on tomato chloroplast development.

72 We screened a tomato core collection of 398 accessions from around the

73 d shows the importance of leaf morphology in tomato crop improvement.

74 e have previously reported the phenotypes of tomato cry1a mutants and CRY2 overexpressing plants.

75 causes significant yield loss in commercial tomato cultivation.

76 virulent bacterium Pseudomonas syringae pv. tomato DC3000 and the necrotrophic fungus Botrytis ciner

77 red immunity against Pseudomonas syringae pv tomato DC3000.

78 e virulent pathogen Pseudomonas syringae pv. tomato DC3000.

79 to infection by host pathogen P syringae pv. tomato DC3000.

80 Transcriptomic analysis (RNA-seq) of tomato demonstrated that biochar had a priming effect on

81 Mice with CP fed a soy-tomato diet had a reduction in inflammatory factors (TNF

82 The Galapagos tomatoes displayed greater tolerance to salt stress than

83 To monitor thiocyclam metabolites in tomato, dissipation studies were carried out using a liq

84 ns identifies alleles under selection during tomato domestication, improvement and modern breeding, a

85 ed salinity tolerance of two species of wild tomato endemic to the Galapagos Islands, Solanum cheesma

86 we hypothesize that administration of a soy-tomato enriched diet can reduce inflammation and severit

87 s, mice were administered a control or a soy-tomato enriched diet for 2 weeks.

88 Mice fed a soy-tomato enriched diet had a significantly reduced level o

89 spontaneous activity of mice showed that soy-tomato enriched diet improved total activity and overall

90 ese pre-clinical results indicate that a soy-tomato enriched diet may be a novel treatment approach t

91 ere that analysis of a previously identified tomato ethyl methanesulfonate-induced mutant that exhibi

92 tance to strains of Pseudomonas syringae pv. tomato expressing AvrRpt2 and Ralstonia pseudosolanacear

93 eloped stable transgenic lines of chilli and tomato expressing CgCOM1-RNAi construct employing Agroba

94 13)C data distinguishes two groups of plant (tomato) extracts and highlights biomarkers, in full agre

95 perforans genotypes was obtained in 7 of 10 tomato fields sampled.

96 Tomato flavor has changed over the course of long-term d

97 to constitutively express either Cre-GFP or Tomato for lineage tracing of a mutant and a reference g

98 primary metabolite - remained present in the tomatoes for >60 days.

99 ocess using organic and conventionally grown tomatoes from two Italian regions over two years.

100 demonstrated that biosynthesis of the major tomato fruit carotenoid, lycopene, is sensitive to fruit

101 de and identified putative members affecting tomato fruit development and ripening.

102 The expansion phase of tomato fruit growth was also modelled using a multiphase

103 Ripening of tomato fruit is a complex tightly orchestrated developme

104 a (between-sample) diversity on cucumber and tomato fruit responded to precipitation.

105 n-sample) diversity measured on cucumber and tomato fruit surfaces, but not tomato leaf surfaces, inc

106 The residues were removed from tomato fruit was in the range of 16.73 to 54.32% using s

107 C and N flows with the purpose of increasing tomato fruit yield.

108 ic network in response to chilling injury in tomato fruit.

109 ic improvement of the nutritional quality of tomato fruit.

110 with accumulation of short-chain FA-VOCs in tomato fruit.

111 traspecific variability of tocochromanols in tomato fruits and genetically engineered their biosynthe

112 tamine-beta-glucoside was isolated from ripe tomato fruits and structurally characterized.

113 As tomato fruits develops, three SlBBXs were found to be up

114 utolanil and etofenprox are usually used for tomato fruits for protecting them against pest infection

115 abundant and important volatile compounds in tomato fruits.

116 , to restrict fungal infection in chilli and tomato fruits.

117 In tomato, GAs act downstream of BRs.

118 We describe a tomato gene cluster on chromosome 7 involved in medium c

119 nd an increase in transcript abundance of 44 tomato genes, with two genes serving as specific reporte

120 Analysis of the updated reference tomato genome found 34 full-length TPS genes and 18 TPS

121 this gap, here BBX protein encoding genes in tomato genome were characterised.

122 shelf life delayed fruit deterioration (dfd) tomato genotype.

123 Transcriptomic analysis of tomato genotypes contrasting for stigma position suggest

124 at these residues are essential for Rep from Tomato golden mosaic virus (TGMV) to interact with the E

125 esmaniae and Solanum galapagense Since these tomatoes grow well despite being constantly splashed wit

126 rafting with vigorous rootstocks could offer tomato growers in Texas sustainable and efficient option

127 nd the bioactive compound content present in tomatoes grown in three regions of Mexico: the state of

128 tic basis underlying the phenotype of purple tomatoes guides an understanding of these varieties whic

129 purified extracts of Cerise and Black Prince tomatoes had the highest ACE (0.50-0.44mg/mL) and AChE (

130 In addition, tomato has seven divergent FAD2 members that lack Delta1

131 fy the plant targets of Me10, we developed a tomato immune induced complementary DNA yeast two-hybrid

132 P maximum residue limit (MRL) for industrial tomato in Brazil, 0.5 mg kg(-1) (1/2 MRL, MRL and 2 MRL)

133 re at unrelated clusters in maize, rice, and tomato indicates that integration of clustered pathway g

134 Tomato is a model for ripening regulation, which require

135 Thus, the FAD2 gene family in tomato is important both to primary fatty acid metabolis

136 bes how drought-induced flower abscission in tomato is regulated similarly, but distinctly via a sing

137 the designed sensor was evaluated in water, tomato juice and hair color.

138 tionally, our team has developed a novel soy-tomato juice currently being studied in healthy individu

139 e determination of TBZ in apple, orange, and tomato juices.

140 f Baumkuchen (Experiment 1) or a spoonful of tomato ketchup (Experiment 2) having different luminance

141 tion of Baumkuchen (a German baked cake) and tomato ketchup on visual perception, flavour expectation

142 In this study, 50 tomato landraces grown in Turkey were investigated in te

143 ality profiles of an important collection of tomato landraces.

144 eaf curl virus (TYLCV), and a betasatellite (Tomato leaf curl betasatellite [ToLCB]).

145 Few taxonomic shifts were detected in the tomato leaf surface (phylloplane).

146 cucumber and tomato fruit surfaces, but not tomato leaf surfaces, increased significantly and remain

147 The method was also applied to Tomato Leaves 1573a SRM to check the accuracy.

148 Here, we examined the global AS changes in tomato leaves infected with Phytophthora infestans, the

149 Local expression of these genes in tomato leaves triggered SAR in distal tissues in the abs

150 istance to fungal and bacterial pathogens in tomato leaves.

151 TfR binds tomato lectin (TL), specific for N-acetyllactosamine (La

152 content in 67 accessions and two commercial tomato lines of Solanum lycopersicum.

153 Resistant tomato lines such as Rio Grande-PtoR (RG-PtoR) recognize

154 encing to capture 238,490 SVs in 100 diverse tomato lines.

155 The effect of tomato lycopene-rich extract (TLE) addition on shelf-lif

156 The industrial transformation of tomato (Lycopersicon esculentum Mill.) produces processe

157 ties of Pelargonic acid (PA), a component of tomatoes, makes it an attractive candidate as a food add

158 escribe a mosaic analysis system with Cre or Tomato (MASCOT) for tracking mutant cells and demonstrat

159 ance of cv Angela eggplant when grafted onto tomato Maxifort rootstock is attributed to a reduced Na

160 ce was employed to induce protection against tomato mosaic virus (ToMV) infection in tomato plants.

161 flg22 and flgII-28 was greatly reduced in a tomato mutant lacking Fls2 and Fls3, but induction of Fl

162 of prosystemin-mediated responses2 (spr2), a tomato mutant with enhanced aphid resistance and altered

163 We generated two SlWak1 tomato mutants (Deltawak1) using CRISPR/Cas9 gene editin

164 cterized CRISPR/Cas9-generated Fls2 and Fls3 tomato mutants and found that the two receptors contribu

165 s with jasmonic and salycilic acid deficient tomato mutants, were performed to elucidate the in plant

166 In tomato MYMIV was only maintained by TYLCV in the presenc

167 (2) was designed in which 703 g of exogenous tomato oil will be fluxed from the co-solvent tank: the

168 from Maliniak, Cerise, Black Prince and Lima tomatoes on the formation of advanced glycation end prod

169 lfur (S, delta(34)S) was conducted along the tomato passata production process using organic and conv

170 n I in food samples, including chili powder, tomato paste, and ketchup sauce.

171 of acephate, chlorpyrifos, and cyazofamid in tomato peels during pre-harvest intervals using paper sp

172 perimented with five crop species, including tomato, pepper, Brassica, barley, and maize, and conclud

173 address this question by selecting upon the tomato phyllosphere microbiome.

174 rium crown rot and to simultaneously improve tomato plant growth and physiological parameters by up t

175 ld experiments show msh1 grafting effects on tomato plant performance, heritable over five generation

176 of biochar to induce systemic resistance in tomato plants against crown rot caused by a soilborne pa

177 We also performed sequential inoculation of tomato plants by adult psyllids following a 7-day AAP an

178 ised TPTs and cis-prenyltransferases (CPTs), tomato plants can make all cis and trans C(10) , C(15) a

179 lkaline pH; (ii) pole bean, common bean, and tomato plants can uptake mimosine and transport it throu

180 in natural and greenhouse soils, and protect tomato plants from infection.

181 curative effects of EPL were demonstrated on tomato plants inoculated with X. euvesicatoria.

182 R-Cas9 genome editing restructured vine-like tomato plants into compact, early yielding plants suitab

183 mate-tyrosine pathway and VTE, we engineered tomato plants to bypass the pathway at the arogenate bra

184 The growth of tomato plants under contrasting temperature regimes reve

185 ptake in plants, pole bean, common bean, and tomato plants were supplied with mimosine alone and meta

186 oying RNA-seq data previously generated from tomato plants, combined with newly generated data from N

187 boratory bioassays and trials on cabbage and tomato plants, that this can extend the efficacy of the

188 crobial community generated from field-grown tomato plants, we inoculated replicate plants across 5 p

189 parasite infestation compared to non-mutated tomato plants.

190 nus Stenotrophomonas from the rhizosphere of tomato plants.

191 inst tomato mosaic virus (ToMV) infection in tomato plants.

192 pollen development in Solanum lycopersicum (tomato) plants.

193 Like Heterochromatin Protein 1b (SlLHP1b), a tomato Polycomb Repressive Complex 1 (PRC1)-like protein

194 The effect of supercritical fluid extract of tomato pomace (TP) and essential oil of organic peppermi

195 lyc (E:Z) ratio as driving parameters of the tomato pomace (TP) supercritical CO(2) extraction (SFE_C

196 Using Tomato-positive cells as a reference population, we demo

197 Ancient Rcr3 homologs present in tomato, potato, eggplants, pepper, petunia and tobacco c

198 The tomato-potato psyllid (TPP), Bactericera cockerelli, is

199 consumption of peppers, tomatoes, processed tomatoes, potatoes, and tea.

200 Tomato PROCERA/DELLA activity is required to promote flo

201 calculated based on consumption of peppers, tomatoes, processed tomatoes, potatoes, and tea.

202 most promising as starting materials for the tomato processing and breeding industries.

203 We also showed tomato produces endogenous NHP in response to a bacteria

204 or disease control in integrated and organic tomato production systems on disease incidence, yield an

205 antitation of several imidazole alkaloids in tomato products.

206 ingae pv maculicola (Psm) and P. syringae pv tomato (Pst) but not the avirulent strain of Pst that ca

207 yper-susceptible to Pseudomonas syringae pv. tomato (Pst) DC3000, while Arabidopsis lines overexpress

208 gered resistance to Pseudomonas syringae pv. tomato (Pst) DC3000.

209 Pseudomonas syringae pv. tomato (Pst) delivers effector proteins into the plant c

210 bacterial pathogen Pseudomonas syringae pv. tomato (Pst), contains two MAMPs, flg22 and flgII-28, th

211 uding the bacterium Pseudomonas syringae pv. tomato (Pst).

212 ology and investigated the role of SlWak1 in tomato-Pst interactions.

213 mission as well as its relationship with the tomato psyllid at the gut interface.

214 n North America; both are transmitted by the tomato psyllid, Bactericera cockerelli (Sulc), in a circ

215 tion and transmission of LsoA or LsoB by the tomato psyllid.

216 Notably, Pseudomonas syringae pv tomato (Pto) bacterial effectors HrpZ1, HopF3, and AvrPt

217 The replacement of up to 50% tomato pulp by strawberry pulp did not change the acidit

218 The Ptr1 (Pseudomonas tomato race 1) locus in Solanum lycopersicoides confers

219 (rSADS-CoV) as well as a derivative encoding tomato red fluorescent protein (tRFP) in place of ORF3.

220 Heirloom tomatoes retain extensive genetic diversity and a consid

221 ecific CgCOM1 siRNA in transgenic chilli and tomato RNAi lines was confirmed by stem-loop RT-PCR.

222 munities induce specific systemic changes in tomato root exudation.

223 e oxygen species (ROS) signals from attacked tomato roots to the leaves, leading to an increased accu

224 howed the same altered phenotype observed in tomato roots.

225 'Tycoon' (TY) and each grafted on commercial tomato rootstocks 'Estamino' (TAM/ES, TY/ES) and 'Multif

226 The tomato russet mite, Aculops lycopersici, is among the sm

227 has facilitated a deep understanding of the tomato's domestication history.

228 d QuEChERS and SS-LPME method was applied to tomato samples and matrix matching was also used to sign

229 effective routine analysis to monitor CP in tomato samples in processed food industries.

230 ciated bacterial communities of cucumber and tomato samples were profiled by 16 S rRNA gene sequencin

231 cation and control procedures in the organic tomato sector.

232 testing lyc concentrations solubilization in tomato seed oil and E:Z ratios of 75:25, 59:39 and 25:75

233 gnaling network that is implicated in MBI600-tomato seedling interactions was mapped.

234 Therefore, Galapagos tomatoes should be further explored to identify the gene

235 Transgenic tomatoes showed moderate increments in tocopherols (up t

236 and allowed the precise identification of 31 tomato SlBBX proteins.

237 We investigated whether the tomato SlDLK2 is a new regulatory component in the AM sy

238 Knockout mutations in tomato SlHAK20 and the rice homologous genes resulted in

239 Domestication of cultivated tomato (Solanum lycopersicum L.) included the transition

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

241 (FA-VOCs) make significant contributions to tomato (Solanum lycopersicum) fruit flavor and human pre

242 of cutin deposition have been identified in tomato (Solanum lycopersicum) fruit.

243 eterminants of tocochromanol accumulation in tomato (Solanum lycopersicum) fruits.

244 Here, we report that the tomato (Solanum lycopersicum) genome harbors two genes,

245 To gain insight into TARK1's role in tomato (Solanum lycopersicum) immunity, we used a proteo

246 Commercial tomato (Solanum lycopersicum) is one of the most widely

247 umulation of isoprenoid-derived compounds in tomato (Solanum lycopersicum) leaves and fruits.

248 mutants that lack trans- and cis-neoxanthin, tomato (Solanum lycopersicum) neoxanthin-deficient1 (nxd

249 ified by rolling circle amplification from 6 tomato (Solanum lycopersicum) plants with leaf curl symp

250 Tomato (Solanum lycopersicum) provides an excellent syst

251 , flg22 and flgII-28, that are recognized by tomato (Solanum lycopersicum) receptors Flagellin sensin

252 we discovered a biosynthetic gene cluster in tomato (Solanum lycopersicum) required for falcarindiol

253 In tomato (Solanum lycopersicum), cryptochromes are encoded

254 In tomato (Solanum lycopersicum), naturally occurring cis-r

255 In tomato (Solanum lycopersicum), this process is associate

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

257 p in the acylsucrose biosynthetic pathway of tomato (Solanum lycopersicum).

258 lf-compatible potato (Solanum tuberosum) and tomato (Solanum lycopersicum).

259 both Arabidopsis (Arabidopsis thaliana) and tomato (Solanum lycopersicum).

260 o the model plants Nicotiana benthamiana and tomato (Solanum lycopersicum).

261 f cryogenically milled cutins extracted from tomatoes (Solanum lycopersicum 'Micro-Tom'; the wild typ

262 naceae, including 15 accessions of five wild tomato species.

263 Tomato spotted wilt tospovirus (TSWV), one of the most i

264 Thrips tabaci, which transmits Tomato spotted wilt virus (TSWV) in a persistent and pro

265 Tomato spotted wilt virus (TSWV) is a devastating diseas

266 Tomato spotted wilt virus (TSWV) is a generalist pathoge

267 structure of glycoprotein N (G(N)) from the tomato spotted wilt virus (TSWV), a representative membe

268 Using the model plant bunyavirus tomato spotted wilt virus (TSWV), and the most efficient

269 yellow leaf curl Sardinia virus (TYLCSV) and Tomato spotted wilt virus (TSWV).

270 We identified a regulator of tomato stem length (SlER) and devised a trait-stacking s

271 This cluster co-localizes with a tomato steroidal alkaloid gene cluster and is syntenic t

272 e resistant to Pseudomonas syringae pathovar tomato strain DC3000-induced stomatal reopening, and TAR

273 ants were insensitive to P syringae pathovar tomato strain DC3118 (coronatine deficit)-induced stomat

274 Sauces were made using different tomato/strawberry pulp ratios (100:0; 75:25; 50:50; 25:7

275 nhost resistance to Pseudomonas syringae pv. tomato T1.

276 y "knocking-in" a fluorochrome, tandem-dimer Tomato (tdTom), into exon 1alpha of the p16 (INK4a) locu

277 Rcr3 is a secreted protease of tomato that is targeted by fungal effector Avr2, a secre

278 e models for close relatives of domesticated tomatoes that can serve as a useful resource for breedin

279 activate a membrane-bound immune receptor of tomato, the Cuscuta Receptor 1 (CuRe1), leading to defen

280 For goosegrass detection in tomato, the F-score was 0.56 and 0.65 for the EP and LB

281 In tomatoes, the exCNLs display exceptional modes of evolut

282 e exploit the MSH1 system in Arabidopsis and tomato to introduce rootstock epigenetic variation to gr

283 crop plant Solanum lycopersicum (cultivated tomato) to investigate the interaction between simulated

284 ed to backcross selected introgressions into tomato, to recover a uniform genetic background, to isol

285 e deficiency in salt tolerance in cultivated tomato varieties.

286 ts of citrus greening, potato zebra chip and tomato vein greening diseases.

287 ntrol citrus greening, potato zebra chip and tomato vein greening diseases.

288 of economically important diseases including tomato vein-greening and potato zebra chip.

289 The reduced ET production by RIN-deficient tomatoes was due to an inability to induce autocatalytic

290 and generating transgenic pathway mutants in tomato, we demonstrate a direct role of the cluster in f

291 Genotypes (G) of grafted and non-grafted tomato were grown in different environments (E) in the 2

292 The purified extracts of Black Prince tomatoes were the most potent inhibitors of AGEs in BSA-

293 importance of leaf shape to fruit quality in tomato, with rounder leaves having significantly improve

294 onsible for heavy yield losses in chilli and tomato worldwide.

295 Expression of both tomato WRKY genes is also induced upon treatment with fl

296 Using RNA-seq, we identified two tomato WRKY transcription factor genes, SlWRKY22 and SlW

297 us and peculiarly different viral pathogens, Tomato yellow leaf curl Sardinia virus (TYLCSV) and Toma

298 mber of monopartite begomoviruses, including Tomato yellow leaf curl virus (TYLCV), and a betasatelli

299 effects of production system and grafting on tomato yield traits, (ii) determine the size of genotypi

300 These results suggest that high tomato yields could be consistently achieved with grafte