ライフサイエンスコーパス: Solanum

1 ilarity to known sesquiterpenes in the genus Solanum.

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

3 Extracts of Solanum aculeastrum root bark and Sesamum calycinum subs

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 Wild potato Solanum bulbocastanum is a rich source of genetic resist

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

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

18 ild tomato endemic to the Galapagos Islands, Solanum cheesmaniae and Solanum galapagense Since these

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

20 amily of giant LTR retrotransposons from the Solanum clade, named MESSI, with transcriptional compete

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

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

23 e Galapagos Islands, Solanum cheesmaniae and Solanum galapagense Since these tomatoes grow well despi

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

25 ya by co-opting the pre-existing Rcr3 in the Solanum genus.

26 Solanum habrochaites LA0407 and in SC S. arcanum LA2157

27 Solanum habrochaites LA0407, and SC Solanum arcanum LA21

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

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

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

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

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

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

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

35 chains on acylsucroses was most striking in Solanum habrochaites.

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

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

38 he Ptr1 (Pseudomonas tomato race 1) locus in Solanum lycopersicoides confers resistance to strains of

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

77 8-1/8-1-1) that causes the cultivated tomato Solanum lycopersicum to shift from producing acylsucrose

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

194 acylsucrose biosynthetic pathway of tomato (Solanum lycopersicum).

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

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

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

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

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

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

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

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

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

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

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

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

207 ucrose biosynthesis in the cultivated tomato Solanum lycopersicum.

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

209 donor of germplasm for the cultivated tomato Solanum lycopersicum.

210 ccessions and two commercial tomato lines of Solanum lycopersicum.

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

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

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

214 mosome-anchored genome assembly of eggplant (Solanum melongena), containing 34,916 genes, confirming

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

216 ophthora infestans as a model, we identified Solanum microdontum plants that recognize the apoplastic

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

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

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

220 ll-established Solanum lycopersicum cv M82 x Solanum pennellii ac.

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

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

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

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

225 specialized metabolites in the seeds of the Solanum pennellii introgression lines identifying 338 pu

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

227 A tomato Solanum pennellii introgression population was assessed

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

229 Solanum pennellii is a wild tomato species endemic to An

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

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

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

233 - and high-acylsugar-producing accessions of Solanum pennellii revealed that expression levels of kno

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

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

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

237 more abundant in the closely related species Solanum pennellii.

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

239 Solanum pimpinellifolium (SP) is the wild progenitor of

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

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

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

243 lycopersicum) and six wild tomato genotypes (Solanum pimpinellifolium).

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

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

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

247 RLP/KSeq in a segregating Solanum population confirmed the localization of the INF

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

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

250 South American fruit crop naranjilla (lulo; Solanum quitoense) produces acylsugars containing a myoi

251 Buffalobur (Solanum rostratum Dunal), which belongs to the Solanacea

252 shade leaves, comprising two African species Solanum scabrum and S. nigrum, and from two distinct cul

253 nd reproductively diverse wild tomato clade (Solanum sect.

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

255 of 202 wild and cultivated diploid potatoes, Solanum section Petota, to explore its phylogenetic util

256 The wild tomato relative Solanum sitiens is a xerophyte endemic to the Atacama De

257 With approximately 450 species, spiny Solanum species constitute the largest monophyletic grou

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

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

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

266 s study identified three BiP homologs in the Solanum tuberosum (potato) genome using phylogenetic, am

267 As a proof-of-concept, we generated Solanum tuberosum (potato) macro-chloroplast lines overe

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

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

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

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

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

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

274 tuberization in the major crop plant potato (Solanum tuberosum L.) is of importance to secure yield e

275 Potato (Solanum tuberosum L.) is the most important tuber crop w

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

280 eld, but stimulates aerial tubers in potato (Solanum tuberosum ssp andigena) under short-day (SD) pho

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

282 S-locus remnants of self-compatible potato (Solanum tuberosum) and tomato (Solanum lycopersicum).

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 produced here incorporated differing potato (Solanum tuberosum) rbcL-rbcS operons that either encoded

286 ty to this phenomenon, we analyzed potatoes (Solanum tuberosum) regenerated from either protoplasts o

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

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

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

290 effect of reduced N availability on potato (Solanum tuberosum) tuber yield and quality traits using

291 develop high-resolution DHS maps in potato (Solanum tuberosum) using chromatin isolated from tubers

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

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 spp.), cassava (Manihot esculenta), potato (Solanum tuberosum), sweet potato (Ipomoea batatas), and

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

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

299 ted from a segregating population of potato (Solanum tuberosum).

300 d species, such as the autotetraploid potato Solanum tuberosum, face a variety of challenges during m