ライフサイエンスコーパス: Solanum lycopersicum

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

18 pA) is a late wound-response gene of tomato (Solanum lycopersicum).

19 ed into a heterospecific genetic background (Solanum lycopersicum).

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

21 ere explored using the GGH system of tomato (Solanum lycopersicum).

22 including that conditioned by Mi in tomato (Solanum lycopersicum).

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

24 gena), pepper (Capsicum annuum), and tomato (Solanum lycopersicum).

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

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

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

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

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

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

31 donor of germplasm for the cultivated tomato Solanum lycopersicum.

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

33 homologous genes from the cultivated tomato, Solanum lycopersicum.

34 ucrose biosynthesis in the cultivated tomato Solanum lycopersicum.

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

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

37 In tomato (Solanum lycopersicum), a plant with dissected leaves, KN

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

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

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

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

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

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

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

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

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

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

48 Pst DC3000), which causes disease in tomato (Solanum lycopersicum) and Arabidopsis (Arabidopsis thali

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

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

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

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

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

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

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

56 ogenous proteolytic activity in both tomato (Solanum lycopersicum) and Nicotiana benthamiana that deg

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

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

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

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

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

62 In many fruits, including tomato (Solanum lycopersicum) and pepper (Capsicum annuum), ther

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

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

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

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

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

68 Other plants including tomato, Solanum lycopersicum, are chilling sensitive and incur i

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

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

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

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

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

74 ode (Meloidogyne spp.) yield loss in tomato (Solanum lycopersicum), but the resistance is ineffective

75 Tomato (Solanum lycopersicum) carries three SERK members.

76 chemical characterization of a tomato EGase, Solanum lycopersicum Cel8 (SlCel9C1), with a distinct C-

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

78 Tomato (Solanum lycopersicum) Cipk6 regulates immune and suscept

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

80 evels of Nt CMPG1 and the homologous tomato (Solanum lycopersicum) Cmpg1 are induced in Cf9 tobacco (

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

82 The Pto gene of tomato (Solanum lycopersicum) confers specific recognition of th

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

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

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

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

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

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

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

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

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

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

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

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

95 ope labeling in planta) using tomato plants (Solanum lycopersicum cv. Rutgers) as a method that allow

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

97 tic plant Cuscuta pentagona impacted tomato (Solanum lycopersicum) defenses against the chewing insec

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

99 softening of fleshy fruits, such as tomato (Solanum lycopersicum), during ripening is generally repo

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

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

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

103 Tomato (Solanum lycopersicum) fruit accumulate the red carotenoi

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

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

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

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

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

109 -6-P contents of pericarp throughout tomato (Solanum lycopersicum) fruit development.

110 ite profiling analyses of transgenic tomato (Solanum lycopersicum) fruit engineered to accumulate the

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

126 Tomato (Solanum lycopersicum) fruits provide an attractive exper

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

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

129 DEA1 is a circadian-regulated tomato (Solanum lycopersicum) gene with sequence similarity to E

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

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

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

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

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

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

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

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

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

139 taining the G107R amino acid substitution in Solanum lycopersicum indicated that this polymorphism al

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

160 c variation has been observed within tomato (Solanum lycopersicum L.), although no studies have exten

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

162 s of light-induced ripening of tomato fruit (Solanum lycopersicum L.).

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

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

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

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

167 olated from arachidonic acid-treated tomato (Solanum lycopersicum) leaves by differential display PCR

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

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

170 e stages of infection in susceptible tomato (Solanum lycopersicum) leaves.

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

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

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

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

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

176 Here, we characterize two tomato (Solanum lycopersicum) lines (sp12 and sp5) that overexpr

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

178 Transgenic tomato (Solanum lycopersicum) lines overexpressing yeast spermid

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

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

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

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

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

184 The tomato (Solanum lycopersicum) Mi-1 gene encodes a protein with p

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

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

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

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

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

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

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

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

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

194 Analysis of tomato (Solanum lycopersicum) mutants and inhibitor studies indi

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

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

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

198 in several plant species, including tomato (Solanum lycopersicum), Nicotiana benthamiana, and Arabid

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

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

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

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

203 quenced plant genomes but present in tomato (Solanum lycopersicum), pepper (Capsicum annuum), and pot

204 fferentially expressed in developing tomato (Solanum lycopersicum) pericarp.

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

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

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

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

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

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

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

212 ut of Manduca sexta larvae reared on tomato (Solanum lycopersicum) plants.

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

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

215 omato MADS box gene 6 (TM6) lineage, tomato (Solanum lycopersicum) possesses both euAP3 and TM6 genes

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

231 onine (Thr) deaminase (TD), which in tomato (Solanum lycopersicum) serves a dual role in isoleucine (

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

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

234 (Nicotiana tabacum; NtpreproHypSys), tomato (Solanum lycopersicum; SlpreproHypSys), petunia (Petunia

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

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

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

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

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

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

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

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

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

244 e species within this clade, such as tomato (Solanum lycopersicum), the anther cone is held together

245 8-1/8-1-1) that causes the cultivated tomato Solanum lycopersicum to shift from producing acylsucrose

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

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

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

249 kinase activity that is conserved in tomato (Solanum lycopersicum), tobacco (Nicotiana tabacum), and

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

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

252 Solanum lycopersicum (tomato) and its wild relatives har

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

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

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

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

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

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

259 stribution of recombination nodules (RNs) on Solanum lycopersicum (tomato) synaptonemal complex 1 wit

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

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

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

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

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

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

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

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

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

269 of lateral and adventitious roots in tomato (Solanum lycopersicum) using mutants isolated for altered

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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