ライフサイエンスコーパス: Nicotiana

1 nduces systemic acquired resistance (SAR) in Nicotiana.

2 on-human genome assemblies such as mouse and Nicotiana.

3 on of MYBL1 through stable transformation of Nicotiana.

4 s shaped the evolution of HAE-induced EDS in Nicotiana.

5 The walls of Nicotiana alata pollen tubes contain a linear arabinan c

6 type proteinase inhibitor, named NaStEP (for Nicotiana alata Stigma-Expressed Protein), that is highl

7 Prior studies with Nicotiana and Arabidopsis described failed assembly of t

8 Brassica rapa (extrastaminal nectaries) and Nicotiana attenuata (gynoecial nectaries).

9 Using lines of the wild tobacco Nicotiana attenuata genetically altered in specific well

10 we have planted the annual postfire tobacco Nicotiana attenuata into an experimental field plot in t

11 Nicotiana attenuata plants can distinguish the damage ca

12 We demonstrate that jasmonate-deficient Nicotiana attenuata plants suffer more damage by arthrop

13 ns of IAA accumulation in herbivore-attacked Nicotiana attenuata plants to unravel its role in the re

14 Here, Nicotiana attenuata plants, in which floral volatiles ha

15 p B55, a bacterium naturally associated with Nicotiana attenuata roots, promotes growth and survival

16 Native populations of Nicotiana attenuata, a wild tobacco species, have been s

17 We used Nicotiana attenuata, an ecological model plant with well

18 ore tissue-level metabolic specialization in Nicotiana attenuata, an ecological model with rich secon

19 In Nicotiana attenuata, specific RNA-directed RNA polymeras

20 ed transcriptomic responses in wild tobacco, Nicotiana attenuata, using a phylotranscriptomic approac

21 Here, we used the wild tobacco Nicotiana attenuata, which develops sympetalous flowers

22 ble in native populations of coyote tobacco, Nicotiana attenuata, with some producing no nectar at al

23 ing GLS (SlGLS) and its homolog (NaGLS) from Nicotiana attenuata.

24 n their nicotine-producing native hostplant, Nicotiana attenuata.

25 e 35S promoter in the ecological model plant Nicotiana attenuata.

26 enses against herbivores of the wild tobacco Nicotiana attenuata; whether they also function as gener

27 RBO-sgRNA delivery platform to target GFP in Nicotiana benthamiana (16c) plants, and gene editing was

28 as completely blocked in transgenic lines of Nicotiana benthamiana (ph5.2nb) that are defective in BR

29 andidate genes to combinatorially express in Nicotiana benthamiana (tobacco) and identified six pathw

30 Transient expression in Nicotiana benthamiana (tobacco) and particle bombardment

31 Silencing of GCN4 in Nicotiana benthamiana and Arabidopsis thaliana compromis

32 l-to-cell movement and systemic infection in Nicotiana benthamiana and Arabidopsis thaliana.

33 ratively analyzed by TEM in two susceptible (Nicotiana benthamiana and Chenopodium quinoa) and one no

34 the accumulation of antioxidant flavonols in Nicotiana benthamiana and confers tolerance to abiotic s

35 BAK1 was expressed transiently in Nicotiana benthamiana and immunopurified after treatment

36 persensitive response in transient assays in Nicotiana benthamiana and in wheat demonstrated specific

37 e entire Asp aminotransferase gene family in Nicotiana benthamiana and isolated and cloned the genes

38 heat shock protein70-1 (HSP70-1) inserts in Nicotiana benthamiana and maize (Zea mays).

39 n from P. patens in the heterologous systems Nicotiana benthamiana and Nicotiana tabacum using transi

40 pendent and RPP1/ATR1Delta51-dependent HR in Nicotiana benthamiana and Nicotiana tabacum, respectivel

41 plant morphology by transient expression in Nicotiana benthamiana and overexpression in transgenic N

42 lencing and recombinant expression assays in Nicotiana benthamiana and yeast cells to examine its fun

43 Here we produce moth sex pheromone, using Nicotiana benthamiana as a plant factory, by transient e

44 We sought to develop Nicotiana benthamiana as a system to study NHR against Z

45 Although we use Nicotiana benthamiana as an example, the protocol is ada

46 Transient expression in Nicotiana benthamiana as well as functional complementat

47 e 25 successfully attacked a non-host plant, Nicotiana benthamiana as well as resistant soybean culti

48 mains are sufficient to induce cell death in Nicotiana benthamiana Autoactive CC domains and full-len

49 vivo in Escherichia coli and subsequently in Nicotiana benthamiana by analyzing carotenoids by HPLC-D

50 titatively analyzed GFP-labeled MT arrays in Nicotiana benthamiana cells transiently expressing GFP-I

51 nucleus and the cytoplasm, but in transgenic Nicotiana benthamiana cells, bimolecular fluorescence co

52 vesiculation were observed in BBSV-infected Nicotiana benthamiana cells.

53 sion of PexRD2 or silencing MAPKKKepsilon in Nicotiana benthamiana enhances susceptibility to P. infe

54 H2O2 sensor, we show that in photosynthetic Nicotiana benthamiana epidermal cells, exposure to high

55 receptor genes in suitable plant cells like Nicotiana benthamiana for testing ligand candidates in r

56 of the RNA Polymerase III in a model species Nicotiana benthamiana had pleiotropic effects, including

57 The plant Nicotiana benthamiana has been shown to be resistant to

58 the class II diTPSs, transient expression in Nicotiana benthamiana identified SdCPS1 as an ent-CPP sy

59 cts with TIFY4B from Arabidopsis, tomato and Nicotiana benthamiana in the nucleus of plant cells.

60 Our data reveal that Nicotiana benthamiana incorporates two different paralog

61 stance to P. syringae Expression of CRK28 in Nicotiana benthamiana induced cell death, which required

62 Here, we show that in leaves of Nicotiana benthamiana infected by potato spindle tuber v

63 r AGO proteins also load vd-sRNAs, leaves of Nicotiana benthamiana infected by potato spindle tuber v

64 cae (green peach aphids) prefer to settle on Nicotiana benthamiana infected with Turnip mosaic virus

65 Heterologous expression of OsSWEET13 in Nicotiana benthamiana leaf cells elevates sucrose concen

66 isoforms were imported into chloroplasts of Nicotiana benthamiana leaf cells, whereas N. munroi CA1a

67 erformed in human embryonic kidney cells and Nicotiana benthamiana leaf cells.

68 reen fluorescent protein fusion construct in Nicotiana benthamiana leaf epidermal and mesophyll cells

69 ization in developing Arabidopsis plants and Nicotiana benthamiana leaf epidermal cells.

70 Using transient expression in Nicotiana benthamiana leaf, we demonstrated that the EXS

71 vage-dependent luciferase gene correction in Nicotiana benthamiana leaves (Johnson et al. in Plant Mo

72 orm homodimers when transiently expressed in Nicotiana benthamiana leaves and heterodimers when coexp

73 luorescence complementation (BiFC) assays in Nicotiana benthamiana leaves and the complex localized i

74 barley (Hordeum vulgare) CSLF6 and CSLH1 in Nicotiana benthamiana leaves and, consistent with our bi

75 uce cell death when transiently expressed in Nicotiana benthamiana leaves but did not affect subcellu

76 Transient overexpression of DXS in Nicotiana benthamiana leaves elevated monoterpene synthe

77 ell death, while transient overexpression in Nicotiana benthamiana leaves induced cell death and tiss

78 riacylglycerol content and FA composition of Nicotiana benthamiana leaves infiltrated with various co

79 of TcADH2 and TcALDH1 together with TcCDS in Nicotiana benthamiana leaves results in the production o

80 Nicotiana benthamiana leaves were exposed to a sucking i

81 This assay consists of co-infiltrating Nicotiana benthamiana leaves with two Agrobacterium tume

82 ucleus of Arabidopsis roots, agroinfiltrated Nicotiana benthamiana leaves, Arabidopsis mesophyll prot

83 sion in Saccharomyces cerevisiae (yeast) and Nicotiana benthamiana leaves.

84 ng Protein 47 (RBP47) upon cotransfection of Nicotiana benthamiana leaves.

85 greater extent than individual expression in Nicotiana benthamiana leaves.

86 ically transactivated the SlTPS5 promoter in Nicotiana benthamiana leaves.

87 hly induced during soybean rust infection in Nicotiana benthamiana leaves.

88 death triggered by overexpression of Fen in Nicotiana benthamiana leaves.

89 for Agrobacterium tumefaciens expression in Nicotiana benthamiana leaves.

90 g cDNAs led to increased oil biosynthesis in Nicotiana benthamiana leaves.

91 e, by virus-induced gene silencing (VIGS) of Nicotiana benthamiana NHEJ genes, and by biochemical ass

92 mefaciens-mediated transient coexpression in Nicotiana benthamiana of an MtVAMP721e-RNAi construct (V

93 were conducted in vegetative or reproductive Nicotiana benthamiana plants (i.e., before or after the

94 is of nuclear and cytoplasmic fractions from Nicotiana benthamiana plants coinfected with Q-satRNA an

95 Transgenic Nicotiana benthamiana plants expressing Rs-cps dsRNA wer

96 attle virus vector to silence these genes in Nicotiana benthamiana plants prior to challenge with TMV

97 w that L2 is unable to suppress silencing in Nicotiana benthamiana plants that have undergone the veg

98 produced these non-enveloped hybrid VLPs in Nicotiana benthamiana plants using a Tobacco mosaic viru

99 nduced by the ToLDeV genotypes in tomato and Nicotiana benthamiana plants were associated with a high

100 Infection of Nicotiana benthamiana plants with such recombinant virus

101 suppressor, caused an efficient infection in Nicotiana benthamiana plants, its viral progeny had very

102 and easily purified in large quantities from Nicotiana benthamiana plants.

103 Transient expression of SGRL in leaves of Nicotiana benthamiana promoted the degradation of chloro

104 robacterium-mediated transient expression in Nicotiana benthamiana provided strong evidence that miR8

105 Overexpression or silencing of IPUT1 in Nicotiana benthamiana resulted in an increase or a decre

106 on, while repression of the NAC1 ortholog in Nicotiana benthamiana resulted in enhanced susceptibilit

107 silencing of two importin-alpha paralogs in Nicotiana benthamiana resulted in significant reduction

108 ts coagroinfiltrated with a reporter gene in Nicotiana benthamiana revealed that P1N-PISPO acts as an

109 ransient expression of WRI1 with OLEOSIN1 in Nicotiana benthamiana stimulates triacylglycerol accumul

110 f a tomato allele of FLS2 does not confer to Nicotiana benthamiana the ability to detect flgII-28, an

111 ficking of P20-defective satBaMV in infected Nicotiana benthamiana The transgene-derived satBaMV, unc

112 accharomyces cerevisiae as well as the plant Nicotiana benthamiana through transgenic expression of R

113 established a transient expression system in Nicotiana benthamiana to study detailed interactions amo

114 iens-mediated transient expression assays in Nicotiana benthamiana to test if NPQ kinetics could be m

115 interact specifically with PRK4 and PRK5 in Nicotiana benthamiana transient expression assays, and a

116 on experiments in these tomato plants and in Nicotiana benthamiana transiently expressing Mi-1.2 and

117 The expression host was Nicotiana benthamiana using a geminiviral vector for tra

118 elf" plant could be transferred to leaves of Nicotiana benthamiana via recombinant expression of PLA2

119 erent fungal species to induce cell death in Nicotiana benthamiana was tested following agroinfiltrat

120 sting of Agrobacterium-infiltrated leaves of Nicotiana benthamiana We observed that one of these pren

121 function by interfamily transfer of ReMAX to Nicotiana benthamiana were successful after using hybrid

122 oteins (CcmK2, CcmM, CcmL, CcmO and CcmN) in Nicotiana benthamiana with fusions that target these pro

123 , Capsella rubella, and Brassica oleracea in Nicotiana benthamiana yielded fungal-type sesterterpenes

124 ransient expression of the entire pathway in Nicotiana benthamiana yields brassinin, demonstrating th

125 uorescence complementation assay in tobacco (Nicotiana benthamiana) epidermal cells.

126 Agroinfiltration of tobacco (Nicotiana benthamiana) epidermal leaf cells with fusions

127 pression of five TX and TN genes in tobacco (Nicotiana benthamiana) induced chlorosis.

128 brane when expressed transiently in tobacco (Nicotiana benthamiana) leaves and Arabidopsis (Arabidops

129 er cell death when overexpressed in tobacco (Nicotiana benthamiana) leaves and does so in a manner th

130 onfirmed by transient expression in tobacco (Nicotiana benthamiana) leaves and grapevine plantlets.

131 Transgenic tobacco (Nicotiana benthamiana) plants that overexpress three yea

132 ) SEIPIN deletion mutant strain and a plant (Nicotiana benthamiana) transient expression system were

133 es, including Arabidopsis thaliana, tobacco (Nicotiana benthamiana), tomato (Solanum lycopersicum), s

134 reduces recalcitrance in transgenic tobacco (Nicotiana benthamiana).

135 Xa10 induces programmed cell death in rice, Nicotiana benthamiana, and mammalian HeLa cells.

136 me P450 TgCYP76AE2, transiently expressed in Nicotiana benthamiana, converts epikunzeaol into epidihy

137 ce of two homeologs of the AGO1-like gene in Nicotiana benthamiana, NbAGO1-1H and NbAGO1-1L.

138 e characterization of three SACPD genes from Nicotiana benthamiana, NbSACPD-A, -B, and -C.

139 as well as tomato (Solanum lycopersicum) and Nicotiana benthamiana, revealing that the link between P

140 66 target mimic and three solanaceous hosts: Nicotiana benthamiana, tobacco (N. tabacum), and tomato

141 Using heterologous expression in Nicotiana benthamiana, we define multiple sites of N dom

142 Using transient expression assays in Nicotiana benthamiana, we found that Gr(Delta) (SP) UBCE

143 In a virus-induced gene silencing screen in Nicotiana benthamiana, we independently identified two c

144 ing a dual-luciferase based sensor system in Nicotiana benthamiana, we quantitatively assessed the re

145 etic enzymes in Saccharomyces cerevisiae and Nicotiana benthamiana, we reconstitute the complete path

146 nstrated that RBPG1 and PG form a complex in Nicotiana benthamiana, which also involves the Arabidops

147 onance energy transfer studies in transgenic Nicotiana benthamiana, which were used to test the possi

148 efense against Tobacco Mosaic Virus (TMV) in Nicotiana benthamiana.

149 era avenae and transiently expressed them in Nicotiana benthamiana.

150 N-glycosylated upon expression in transgenic Nicotiana benthamiana.

151 oactive NLRs when transiently coexpressed in Nicotiana benthamiana.

152 ized, fucose-free versions of PG9 and RSH in Nicotiana benthamiana.

153 omato, potato, pepper, eggplant, tobacco and Nicotiana benthamiana.

154 uce significant cell death when expressed in Nicotiana benthamiana.

155 to elicit immunity-associated cell death in Nicotiana benthamiana.

156 n and colocalization assays in the CaMV host Nicotiana benthamiana.

157 r gene fusions when coexpressed in citrus or Nicotiana benthamiana.

158 ke lamellae in both Arabidopsis thaliana and Nicotiana benthamiana.

159 tease inhibitor alpha1-antitrypsin (A1AT) in Nicotiana benthamiana.

160 were obtained after transient expression in Nicotiana benthamiana.

161 imeric clone into the laboratory model plant Nicotiana benthamiana.

162 d RNase J, both individually and jointly, in Nicotiana benthamiana.

163 eric KOR1-Fc-GFP fusion protein in leaves of Nicotiana benthamiana.

164 of inducing cell death when overexpressed in Nicotiana benthamiana.

165 ll death and ion leakage in the heterologous Nicotiana benthamiana.

166 siently co-expressed with a GFPP synthase in Nicotiana benthamiana.

167 n as demonstrated by transient expression in Nicotiana benthamiana.

168 ) independent of their enzymatic activity in Nicotiana benthamiana.

169 onfer methylation of a transgene reporter in Nicotiana benthamiana.

170 nity in the non-host solanaceous model plant Nicotiana benthamiana.

171 RX17 was examined by transient expression in Nicotiana benthamiana.

172 ed with fluorescent protein and expressed in Nicotiana benthamiana.

173 tion-dependent cell death in Arabidopsis and Nicotiana benthamiana.

174 ;22,23-dioxide when transiently expressed in Nicotiana bethamiana In contrast, in Lycopodium clavatum

175 1 orthologs appear to be present only in the Nicotiana genus.

176 al, reconstituted, and Nicotiana rustica and Nicotiana glauca tobacco types are also reported.

177 virus)), but not in resistant host systems (Nicotiana glutinosa and Chenopodium quinoa with TMV).

178 Species of Nicotiana grow naturally in different parts of the world

179 Nicotiana is an excellent system in which to study allop

180 in Nicotiana suaveolens cineole synthase and Nicotiana langsdorffii terpineol synthase.

181 en fluorescent protein (GFP)-UVR8 fusions in Nicotiana leaves and transgenic Arabidopsis.

182 utein, neoxanthin and violaxanthin levels in Nicotiana leaves were markedly reduced when CsCCD4c is o

183 loss of inhibition of pollen tube growth in Nicotiana obtusifolia (synonym Nicotiana trigonophylla)

184 ifolia (synonym Nicotiana trigonophylla) and Nicotiana repanda.

185 ey, flue-cured, oriental, reconstituted, and Nicotiana rustica and Nicotiana glauca tobacco types are

186 Nicotiana species are frequently investigated for their

187 e platform to a range of wild and cultivated Nicotiana species demonstrated certain evolutionary tren

188 Flowers of Nicotiana species emit a characteristic blend including

189 logy, and medicinal application of different Nicotiana species growing around the globe presented in

190 Nicotiana species of the section Alatae emit a character

191 ced leaf transcriptomes from closely-related Nicotiana species revealed a key gene co-expression netw

192 xpressed in the stigmas of self-incompatible Nicotiana species.

193 igh Top-Band (HT-B), have been identified in Nicotiana species.

194 e protease inhibitors, is essential to SI in Nicotiana spp.

195 RNA interference suppression of NaSIPP in Nicotiana spp. pollen grains disrupts the SI by preventi

196 patible pollen tubes, but its suppression in Nicotiana spp. transgenic plants disrupts S-specific pol

197 often thought of as a smoking drug, tobacco (Nicotiana spp.) is now considered as a plant of choice f

198 egion) of enzyme pairs in leaves of tobacco (Nicotiana spp.), we observed that all tested cis- and me

199 is detected specifically in mature pollen of Nicotiana spp.; however, in self-compatible plants, this

200 ne the different terpineol-cineole ratios in Nicotiana suaveolens cineole synthase and Nicotiana lang

201 t was only shared with the eponymous species Nicotiana suaveolens of the sister section Suaveolentes.

202 XopQ recognition in both the closely-related Nicotiana sylvestris and the distantly-related beet plan

203 STF), and its orthologs in Petunia, pea, and Nicotiana sylvestris are required for leaf blade outgrow

204 Using the classical bladeless lam1 mutant of Nicotiana sylvestris as a genetic tool, we examined the

205 gned to select for chloroplast transfer from Nicotiana sylvestris into Nicotiana tabacum cells.

206 F's ability to complement the lam1 mutant of Nicotiana sylvestris.

207 to compare respiration and photosynthesis of Nicotiana tabacum 'Petit Havana SR1' wild-type plants wi

208 racterization of a Transposable Element from Nicotiana tabacum (Tnt1) insertional mutant line were ca

209 ereas basal subgroup 5 encodes P-proteins in Nicotiana tabacum (tobacco) and Arabidopsis thaliana.

210 idopsis thaliana) Golgi alpha-mannosidase I, Nicotiana tabacum beta1,2-N-acetylglucosaminyltransferas

211 last transfer from Nicotiana sylvestris into Nicotiana tabacum cells.

212 aphy of this landscape in the ancestral host Nicotiana tabacum Comparing the topographies of the land

213 Transgenic tobacco (Nicotiana tabacum cv Samsun) plants containing an INPACT

214 evaluated by gene overexpression in tobacco (Nicotiana tabacum cv. Xanthi).

215 More recently in our history, Nicotiana tabacum has attracted interest as one of the m

216 NtPDR1 from Nicotiana tabacum has been shown to be involved in the c

217 ted inactivation of the plastid PsaI gene in Nicotiana tabacum has no measurable effect on photosynth

218 Nicotiana tabacum L. plants expressing dsRNA homologous

219 Nicotine biosynthesis in tobacco (Nicotiana tabacum L.) is highly regulated by jasmonic ac

220 sing nicotine content in cultivated tobacco (Nicotiana tabacum L.) may be of value for industrial pur

221 have developed nfsI transplastomic tobacco (Nicotiana tabacum L.) to reduce pollen-borne transgene f

222 resulted in rapid chlorophyll degradation in Nicotiana tabacum leaves and led to accumulation of pheo

223 curonidase (uidA) and analyzed in transgenic Nicotiana tabacum plants.

224 and VRC-enriched fractions from TMV-infected Nicotiana tabacum plants.

225 ion of the mature transmitting tract (TT) in Nicotiana tabacum resulted in the loss of inhibition of

226 NtPDR1 was originally identified in Nicotiana tabacum suspension cells (BY2), in which its e

227 terologous systems Nicotiana benthamiana and Nicotiana tabacum using transient and stable nuclear tra

228 ore the RNA content of TAC preparations from Nicotiana tabacum was determined using whole genome tili

229 orter gene and two varieties of A. annua and Nicotiana tabacum were transformed.

230 development in two susceptible host systems (Nicotiana tabacum with TMV (Tobacco mosaic virus), and A

231 Using tobacco (Nicotiana tabacum) 'Bright Yellow 2' cell suspension and

232 ases during cell plate expansion in tobacco (Nicotiana tabacum) 'Bright Yellow-2' cells: massive deli

233 of KAT1 and cocrystallized it with tobacco (Nicotiana tabacum) 14-3-3 proteins to describe the prote

234 tegy to the Clp protease complex of tobacco (Nicotiana tabacum) and identified a set of chloroplast p

235 chloroplast association in vivo in tobacco (Nicotiana tabacum) and observed weaker tethering to addi

236 responses in specific cultivars of tobacco (Nicotiana tabacum) and tomato (Solanum lycopersicum).

237 udies of cortical array assembly in tobacco (Nicotiana tabacum) Bright Yellow-2 cells after cytokines

238 (HS) or hydrogen peroxide (H2O2) in tobacco (Nicotiana tabacum) Bright Yellow-2 cells, an increase in

239 fusions in transiently transformed tobacco (Nicotiana tabacum) Bright Yellow-2 cells, showed that th

240 lastid transformation is routine in tobacco (Nicotiana tabacum) but 100-fold less frequent in Arabido

241 patens for transient expression and tobacco (Nicotiana tabacum) BY2 cells for stable transformation.

242 Tnt1, the transposable element of tobacco (Nicotiana tabacum) cell type 1, is a retrotransposon tha

243 c isoform of HVA22 labels the ER in tobacco (Nicotiana tabacum) cells but its overexpression does not

244 plets after transient expression in tobacco (Nicotiana tabacum) cells that were induced to accumulate

245 gated the expression of matK across tobacco (Nicotiana tabacum) development at the transcriptional, p

246 o the lytic vacuole exists, in both tobacco (Nicotiana tabacum) epidermal (DeltapH -1.5) and Arabidop

247 ization, and functional analysis of tobacco (Nicotiana tabacum) EXO70 isoforms.

248 inward-rectifying K(+) channels of tobacco (Nicotiana tabacum) guard cells and show its close parall

249 we show that receptor targeting in tobacco (Nicotiana tabacum) initially involves a canonical coat p

250 of CPRabA5e:EGFP fusion protein in tobacco (Nicotiana tabacum) leaves, and immunoblotting using Arab

251 reen fluorescent protein fusions in tobacco (Nicotiana tabacum) leaves.

252 drial when transiently expressed in tobacco (Nicotiana tabacum) leaves.

253 e, we demonstrate that manipulating tobacco (Nicotiana tabacum) MTHFR gene (NtMTHFR1) expression dram

254 Both homoplastomic tobacco (Nicotiana tabacum) mutants psbN-F and psbN-R show essent

255 Here, by generating transplastomic tobacco (Nicotiana tabacum) mutants with point mutations in the a

256 the functional characterization of tobacco (Nicotiana tabacum) Nin88, a presumed fully active cwINV

257 ing high levels of botryococcene in tobacco (Nicotiana tabacum) plants by diverting carbon flux from

258 used on the transport in transgenic tobacco (Nicotiana tabacum) plants of a human alpha-mannosidase,

259 This result was confirmed in tobacco (Nicotiana tabacum) plants overexpressing the TRXm4 ortho

260 ation was explored using transgenic tobacco (Nicotiana tabacum) plants that have either high (PAO) or

261 photosynthetic capacity and growth, tobacco (Nicotiana tabacum) plants with increased levels of trans

262 isoprene-emitting and non-emitting tobacco (Nicotiana tabacum) plants, to examine: the response of i

263 nt monoclonal antibody expressed in tobacco (Nicotiana tabacum) plants.

264 isum sativum) Fd isoform (PsFd1) in tobacco (Nicotiana tabacum) plants.

265 ins by stable transformation of the tobacco (Nicotiana tabacum) plastid genome.

266 In steady-state growing tobacco (Nicotiana tabacum) pollen tubes, SEC3a displayed amino-t

267 In transient expression assays in tobacco (Nicotiana tabacum) protoplasts, TSAR1 and TSAR2 exhibit

268 A tobacco (Nicotiana tabacum) retrotransposon (Tnt1) insertion rsd

269 Here, we show that the tobacco (Nicotiana tabacum) retrotransposon Tnt1 efficiently tran

270 is of the cytochrome b6f complex in tobacco (Nicotiana tabacum) seems to be restricted to young leave

271 membrane surface of Bright Yellow 2 tobacco (Nicotiana tabacum) suspension cells labeled with an envi

272 ization of GFP fusion constructs in tobacco (Nicotiana tabacum) suspension cells, indicated mitochond

273 bcellular localization studies with tobacco (Nicotiana tabacum) suspension-cultured cells indicate th

274 ted them by metabolite profiling of tobacco (Nicotiana tabacum) tissues.

275 e, we report the application of the tobacco (Nicotiana tabacum) Tnt1 retrotransposon as an insertiona

276 Tobacco (Nicotiana tabacum) transgenic lines with reduced levels

277 Here, we show that tobacco (Nicotiana tabacum) trichomes contain a specific Rubisco

278 he angiosperms rice (Oryza sativa), tobacco (Nicotiana tabacum), and Arabidopsis (Arabidopsis thalian

279 Arabidopsis (Arabidopsis thaliana), tobacco (Nicotiana tabacum), and cultivated tomato under the cont

280 tomato in soybean (Glycine max) and tobacco (Nicotiana tabacum), as monitored by measuring hallmarks

281 roots and anthocyanin-overproducing tobacco (Nicotiana tabacum), but levels of oligomeric PAs were ve

282 d in tomato (Solanum lycopersicum), tobacco (Nicotiana tabacum), Medicago truncatula, wheat (Triticum

283 eral species including A. thaliana, tobacco (Nicotiana tabacum), N. benthamiana, N. attenuata and tom

284 In tobacco (Nicotiana tabacum), pollen tube tip growth is controlled

285 In tobacco (Nicotiana tabacum), replicons based on the bean yellow d

286 ighlighted, with a special focus on tobacco (Nicotiana tabacum).

287 xin (Hvt) and onion leaf lectin, in tobacco (Nicotiana tabacum).

288 ted in primary PD at cytokinesis in tobacco (Nicotiana tabacum).

289 nt species (Hordeum vulgare, Vicia faba, and Nicotiana tabacum).

290 onoterpene on the production of capsidiol in Nicotiana tabacum, an assumed MVA-derived sesquiterpenoi

291 51-dependent HR in Nicotiana benthamiana and Nicotiana tabacum, respectively.

292 vectors for stable nuclear transformation of Nicotiana tabacum.

293 benthamiana and overexpression in transgenic Nicotiana tabacum.

294 and abiotic stress tolerance in model plant Nicotiana tabacum.

295 lina sativa]) or just the beta-Rca (tobacco [Nicotiana tabacum]).

296 aliana, sugar beet [Beta vulgaris], tobacco [Nicotiana tabacum], and maize [Zea mays]) for which cont

297 erated response to natural shading events in Nicotiana (tobacco), resulting in increased leaf carbon

298 was identified to be the target of miR395 in Nicotiana tobacum, which belongs to low affinity sulfate

299 ube growth in Nicotiana obtusifolia (synonym Nicotiana trigonophylla) and Nicotiana repanda.

300 alloplasmic N. tabacum line we used carries Nicotiana undulata cytoplasmic genomes, and its flowers

301 ts of allopolyploidy on floral morphology in Nicotiana, using corolla tube measurements and geometric