ライフサイエンスコーパス: Solanum

1 ilarity to known sesquiterpenes in the genus Solanum.

2 is the first genome wide comparison between Solanum A and B genomes and establishes a foundation for

3 sting possible chromosome divergence between Solanum A and B genomes.

4 ort that the wild, diploid non-tuber-bearing Solanum americanum harbors multiple Rpi genes.

5 n cereal (wheat, rye, barley and Triticale), Solanum and amaranthus seeds.

6 ssess genetic variation within tuber-bearing Solanum and the impact of domestication on genome divers

7 Solanum habrochaites LA0407, and SC Solanum arcanum LA2157, which lack functional S-RNase ex

8 Wild relative, Solanum arcanum Peralta could be a potential source of E

9 At least 20 tuber-bearing, wild species of Solanum are known from North and Central America, yet th

10 le fruits, seeds, pulp and skin from chilto (Solanum betaceum Cav) cultivated in the ecoregion of Yun

11 Tamarillo (Solanum betaceum Cav.) is an underutilised fruit in Mala

12 e and the pulp fractions from red tamarillo (Solanum betaceum Cav.) mesocarp, and characterisation of

13 We evaluated 23 tree tomato (Solanum betaceum) accessions from five cultivar groups a

14 tomatoes (Solanum lycopersicum), tamarillos (Solanum betaceum) and goldenberries (Physalis peruviana)

15 Tamarillo (Solanum betaceum) is a tropical exotic fruit whose polys

16 Wild potato Solanum bulbocastanum is a rich source of genetic resist

17 five cultivar groups and one wild relative (Solanum cajanumense) for 26 composition traits.

18 perimentally inbred and outcrossed plants of Solanum carolinense (horsenettle) for three years.

19 resistance and growth (tolerance) traits in Solanum carolinense (Solanaceae).

20 e, 523-3, of the diploid wild potato species Solanum chacoense.

21 One species, Solanum chmielewskii, was found to have many accessions

22 The TPS genes in the Solanum cluster encoding cis-prenyl diphosphate-utilizin

23 Here, we report the draft genome sequence of Solanum commersonii, which consists of approximately 830

24 esis in the fruit fly Bactrocera cacuminata (Solanum fly) have been investigated using a series of de

25 Thus, the Solanum functional gene cluster evolved by duplication a

26 copene beta-cyclase (beta-Cyc) allele from a Solanum galapagense background.

27 The Solanum gene cluster also contains an ortholog of Nt-CPS

28 In the tomato clade of the Solanum genus, acylsugars consist of aliphatic acids of

29 ing UVB- and heat-treatment in the leaves of Solanum glaucophyllum Desf., Solanum lycopersicum L. and

30 Solanum habrochaites LA0407 and in SC S. arcanum LA2157

31 Solanum habrochaites LA0407, and SC Solanum arcanum LA21

32 re identified in extracts of the wild tomato Solanum habrochaites LA1777 trichomes.

33 ed (Solanum lycopersicum LA4024) and a wild (Solanum habrochaites LA1777) tomato accession.

34 Two enzymes, Solanum habrochaites methylketone synthase1 (ShMKS1) and

35 reference genome revealed a close homolog of Solanum habrochaites MOMT1 3'/5' myricetin O-methyltrans

36 Wild tomato (Solanum habrochaites), a relative of the cultivated toma

37 In the orthologous cluster in Solanum habrochaites, a new sesquiterpene synthase gene

38 by the orthologous CPT1 locus in tomato and Solanum habrochaites, respectively.

39 chains on acylsucroses was most striking in Solanum habrochaites.

40 in 19 populations of the wild tomato species Solanum habrochaites.

41 tic bacteria decreased plant defenses in all Solanum hosts and there were different gut bacterial com

42 se granules have been identified as those of Solanum jamesii Torr.

43 astidic FRK, we generated transgenic tomato (Solanum lycopersicon) plants with RNAi suppression of Sl

44 expressed in the tangerine mutant of tomato (Solanum lycopersicon) which accumulates cis-carotene iso

45 mine B-class GATAs from Arabidopsis, tomato (Solanum lycopersicon), Brachypodium (Brachypodium distac

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

76 8-1/8-1-1) that causes the cultivated tomato Solanum lycopersicum to shift from producing acylsucrose

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

98 Tomato (Solanum lycopersicum) carries three SERK members.

99 Tomato (Solanum lycopersicum) Cipk6 regulates immune and suscept

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

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

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

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

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

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

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

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

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

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

110 -6-P contents of pericarp throughout tomato (Solanum lycopersicum) fruit development.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

210 donor of germplasm for the cultivated tomato Solanum lycopersicum.

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

212 ucrose biosynthesis in the cultivated tomato Solanum lycopersicum.

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

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

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

216 yclic triterpene, from the hexane extract of Solanum melongena L.

217 The common or brinjal eggplant (Solanum melongena L.) belongs to the Leptostemonum Clade

218 pa, Allium sativum, Solanum lycopersicum and Solanum melongena, irrigated with wastewater in Mardan a

219 ELR (elicitin response) from the wild potato Solanum microdontum mediates extracellular recognition o

220 receptor-like protein, from the wild potato Solanum microdontum, which mediates response to a broad

221 Pepino (Solanum muricatum) fruits from 15 accessions of cultivat

222 es as part of a larger revision of the spiny solanums of Africa.

223 ongs to the Leptostemonum Clade (the "spiny" solanums) of the species-rich genus Solanum (Solanaceae)

224 Solanum paniculatum L. (Solanaceae) is a plant species w

225 ation developed from the wild desert-adapted Solanum pennellii and domesticated tomato (Solanum lycop

226 n lines (ILs) derived from the desert tomato Solanum pennellii and identified quantitative trait loci

227 ericlinal chimera that has its L1 layer from Solanum pennellii and its L2 and L3 layers from Solanum

228 of a wild and a domesticated tomato species, Solanum pennellii and Solanum lycopersicum 'M82.' We fou

229 pulation derived from the wild desert tomato Solanum pennellii at ultrahigh density, providing the ex

230 titions the whole genome of the wild species Solanum pennellii in the background of the cultivated to

231 ously reported overlapping S. lycopersicum x Solanum pennellii introgression lines (ILs) that fail to

232 iling of acylsugars in the S. lycopersicum x Solanum pennellii introgression lines identified a chrom

233 ysis was performed on the well-characterized Solanum pennellii introgression lines to investigate the

234 A tomato Solanum pennellii introgression population was assessed

235 Solanum pennellii is a wild tomato species endemic to An

236 y identified a region of chromosome 8 in the Solanum pennellii LA0716 genome (IL8-1/8-1-1) that cause

237 pic screen of a set of S. lycopersicum M82 x Solanum pennellii LA0716 introgression lines identified

238 jection of Solanum lycopersicum pollen by SC Solanum pennellii LA0716, SC.

239 patible accession of the wild tomato species Solanum pennellii We describe the assembly of its genome

240 trometry and HPLC, of introgression lines of Solanum pennellii with a domesticated line in order to a

241 (Solanum lycopersicum) and a wild relative (Solanum pennellii).

242 three sets of genomes, Solanum lycopersicum/Solanum pennellii, Arabidopsis (Arabidopsis thaliana) Co

243 more abundant in the closely related species Solanum pennellii.

244 In the wild tomato, Solanum peruvianum, herbivory limits pollinator visits,

245 ere evaluated by qRT-PCR during infection in Solanum phureja.

246 The Pto protein kinase from Solanum pimpinellifolium interacts with Pseudomonas syri

247 recognition of AvrPtoB and it differed from Solanum pimpinellifolium Pto by only 14 amino acids, inc

248 rsicum, S. lycopersicum var cerasiforme, and Solanum pimpinellifolium to map loci controlling variati

249 and fruit tissues of the wild tomato species Solanum pimpinellifolium.

250 (CPB; Leptinotarsa decemlineata) use several Solanum plants as hosts in their natural environment.

251 n of induced defenses in wild and cultivated Solanum plants of CPB.

252 ted species in the tomato clade of the genus Solanum provide a model to better understand these barri

253 our-active volatile compounds of lulo fruit (Solanum quitoense Lam.) were isolated by solvent extract

254 nd reproductively diverse wild tomato clade (Solanum sect.

255 nting more than 100 tuber-bearing relatives (Solanum section Petota).

256 "spiny" solanums) of the species-rich genus Solanum (Solanaceae).

257 This study uncovers a historic role of wild Solanum species in the diversification of long-day-adapt

258 olanum tuberosum L.), domesticated from wild Solanum species native to the Andes of southern Peru, po

259 t segregating populations involving the wild Solanum species S. berthaultii (Rpi-ber2) and S. ruiz-ce

260 tudy, 75 Andean native potato samples from 7 Solanum species with different colors were characterized

261 in secreting glandular trichomes of various Solanum species, including the cultivated tomato (Solanu

262 In tomato and related Solanum species, two genes, ui1.1 and ui6.1, are require

263 e biosynthesis in the glandular trichomes of Solanum species.

264 se, a key protein expressed in pistils of SI Solanum species.

265 on of >33,000 leaflets from a set of tomato (Solanum spp) introgression lines grown under controlled

266 ia were isolated from dormant potato tubers (Solanum tuberosum 'Folva') and their proteome investigat

267 endodermis, bark, specialized organs (e.g., Solanum tuberosum (potato) tubers), and seed coats.

268 accessions, and S. lycopersicum/S. pennellii/Solanum tuberosum (three-way polymorphic) are included.

269 Andean potatoes (Solanum tuberosum andigenum) are a staple food for Andea

270 proteins from maize (Zea mays BE2a), potato (Solanum tuberosum BE1), and Escherichia coli (glycogen B

271 fully applied RenSeq to the sequenced potato Solanum tuberosum clone DM, and increased the number of

272 Transgenic potato (Solanum tuberosum cv. Jowon) constitutively overexpressi

273 for the high throughput field phenotyping of Solanum tuberosum for differences in stomatal behaviour.

274 or unintended composition changes in potato (Solanum tuberosum L. cv. Desiree) tubers, which have bee

275 ght on the composition of transgenic potato (Solanum tuberosum L. cv. Desiree) with reduced glycoalka

276 omes of six accessions of cultivated potato (Solanum tuberosum L.), a vegetatively propagated autotet

277 Cultivated potatoes (Solanum tuberosum L.), domesticated from wild Solanum sp

278 temperature on the RS contents of potatoes (Solanum tuberosum L.).

279 (Momordica charantia Descourt.), and potato (Solanum tuberosum L.).

280 ly cultivar amongst those tested with a pure Solanum tuberosum origin and A cooking type.

281 We identified eight putative StYUC (Solanum tuberosum YUCCA) genes whose deduced amino acid

282 ual reproduction in the crop species potato (Solanum tuberosum) and strawberry (Fragaria spp), where

283 StBEL5 of potato (Solanum tuberosum) functions as a mobile RNA signal that

284 nchored to 12 chromosomes, using the potato (Solanum tuberosum) genome sequence as a reference.

285 Potato (Solanum tuberosum) multicystatin (PMC) is a unique cysta

286 nalyses, we previously identified in potato (Solanum tuberosum) StRGGA, coding for an Arginine Glycin

287 CLAVATA2-like receptor (StCLV2) from potato (Solanum tuberosum) than its nonglycosylated forms.

288 ymbiont infection by exposing potato plants (Solanum tuberosum) to psyllids infected with "Candidatus

289 and Rx1, which confer resistance in potato (Solanum tuberosum) to the cyst nematode Globodera pallid

290 Potato (Solanum tuberosum) tuber, a swollen underground stem, is

291 evidence concerning the early use of potato (Solanum tuberosum) within its botanical locus of origin

292 Arabidopsis (Arabidopsis thaliana), potato (Solanum tuberosum), and white lupin, making them ideal c

293 usal agent of late blight disease of potato (Solanum tuberosum), depends on multilayered defense resp

294 ghum bicolor), Arabidopsis thaliana, potato (Solanum tuberosum), Medicago truncatula, and poplar (Pop

295 In cultivated potato (Solanum tuberosum), six PP2A catalytic subunits (StPP2Ac

296 In potato (Solanum tuberosum), StBEL5 and its Knox protein partner

297 In potato (Solanum tuberosum), tuber integrity is dependent on sube

298 In potato (Solanum tuberosum), tubers develop from underground stol

299 ant architecture and tuberization in potato (Solanum tuberosum).

300 ral crops, has not been developed in potato (Solanum tuberosum).