ライフサイエンスコーパス: Nicotiana tabacum

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

2 nd that of the Solanaceous species, tobacco (Nicotiana tabacum).

3 knockout plants in the higher plant tobacco (Nicotiana tabacum).

4 ied was methyl salicylate (MeSA) in tobacco (Nicotiana tabacum).

5 bidopsis (Arabidopsis thaliana) and tobacco (Nicotiana tabacum).

6 itric oxide ((*)NO) production from tobacco (Nicotiana tabacum).

7 establishing systemic infection in tobacco (Nicotiana tabacum).

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

9 es of Solanaceous species including tobacco (Nicotiana tabacum).

10 it the phloem in systemic leaves of tobacco (Nicotiana tabacum).

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

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

13 ependent hypersensitive response in tobacco (Nicotiana tabacum).

14 egulate anthocyanin biosynthesis in tobacco (Nicotiana tabacum).

15 a strong chlorophyll deficiency in tobacco (Nicotiana tabacum).

16 plasm of interphase cells in Arabidopsis and Nicotiana tabacum.

17 coassembled into virus particles in infected Nicotiana tabacum.

18 oped to a purported purified DAO enzyme from Nicotiana tabacum.

19 bacterial relA/spoT genes in the model plant Nicotiana tabacum.

20 d >90% by the expression of antisense RNA in Nicotiana tabacum.

21 xhibiting greater diffusion of proteins than Nicotiana tabacum.

22 elated CDPK cDNAs (NtCDPK2 and NtCDPK3) from Nicotiana tabacum.

23 lastid genome is reported in a higher plant, Nicotiana tabacum.

24 vectors for stable nuclear transformation of Nicotiana tabacum.

25 benthamiana and overexpression in transgenic Nicotiana tabacum.

26 and abiotic stress tolerance in model plant Nicotiana tabacum.

27 ba], petunia [Petunia hybrida], and tobacco [Nicotiana tabacum]).

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

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

30 ompared the effect of downregulating SUT1 in Nicotiana tabacum, a sucrose transporter, and Verbascum

31 by corn earworm (Helicoverpa zea), tobacco (Nicotiana tabacum) after mechanical damage, and tomato (

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

33 When transiently expressed in Nicotiana tabacum, an ECA3-yellow fluorescent protein fu

34 sensitive response in nonhost plants such as Nicotiana tabacum and Nicotiana benthamiana.

35 ive response (HR) in non-host plants such as Nicotiana tabacum and Nicotiana benthamiana.

36 we grafted two different species of tobacco, Nicotiana tabacum and Nicotiana sylvestris.

37 m other plant species, for example PRB1 from Nicotiana tabacum and PR1 from Brassica napus, at 64% an

38 enthamiana; however, it contributed to HR in Nicotiana tabacum and significantly reduced the progress

39 NATA1 transient expression in Nicotiana tabacum and the addition of N(delta)-acetylorn

40 syltransferase (GalT) activities in tobacco (Nicotiana tabacum) and Arabidopsis (Arabidopsis thaliana

41 ecifically in anthers and pollen of tobacco (Nicotiana tabacum) and Arabidopsis resulted in the abort

42 companion cells of both transgenic tobacco (Nicotiana tabacum) and Arabidopsis.

43 nstitutive expression of CYP76B1 in tobacco (Nicotiana tabacum) and Arabidopsis.

44 opersicum) Cmpg1 are induced in Cf9 tobacco (Nicotiana tabacum) and Cf9 tomato after Avr9 elicitation

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

46 ransformation vectors were made for tobacco (Nicotiana tabacum) and lettuce (Lactuca sativa), with en

47 A fusion gene in stably transformed tobacco (Nicotiana tabacum) and maize (Zea mays) plants and in tr

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

49 in a wortmannin-sensitive manner in tobacco (Nicotiana tabacum) and that it could play an active role

50 identified SNAREs SYP121/Syr1 from tobacco (Nicotiana tabacum) and the Arabidopsis thaliana homolog

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

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

53 d in tomato (Solanum lycopersicum), tobacco (Nicotiana tabacum), and Arabidopsis thaliana.

54 and isolated plastids therefrom) of tobacco (Nicotiana tabacum), and chloroplasts isolated from leave

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

56 n of GAMT1 or GAMT2 in Arabidopsis, tobacco (Nicotiana tabacum), and petunia (Petunia hybrida) result

57 c promoter-reporter gene fusions in tobacco (Nicotiana tabacum), and phytochrome (phyA, phyB, and hy2

58 these ARFs in Arabidopsis thaliana, tobacco (Nicotiana tabacum), and potato (Solanum tuberosum) faile

59 Arabidopsis (Arabidopsis thaliana), tobacco (Nicotiana tabacum), and spinach (Spinacia oleracea) with

60 high-throughput Agrobacterium inoculation of Nicotiana tabacum, and a spray-only method (named "agros

61 o observed in transgenic C3 plants (tobacco [Nicotiana tabacum]) and in in vitro translation extracts

62 i.e. jojoba [Simmondsia chinensis], tobacco [Nicotiana tabacum], and cotton [Gossypium hirsutum]) fro

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

64 Plastids in Nicotiana tabacum are normally transmitted to the progen

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

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

67 concept observations on transgenic tobacco (Nicotiana tabacum) Bright Yellow 2 cells and Arabidopsis

68 erations in the endosomal system of tobacco (Nicotiana tabacum) Bright Yellow 2 cells and ultimately

69 Transgenic tobacco (Nicotiana tabacum) Bright Yellow-2 (BY-2) cells stably e

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

71 sient expression studies of MAB1 in tobacco (Nicotiana tabacum) Bright Yellow-2 cells revealed a cell

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

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

74 ets of cDNAs in Arabidopsis leaf or tobacco (Nicotiana tabacum) Bright Yellow-2 protoplasts identifie

75 bidopsis (Arabidopsis thaliana) and tobacco (Nicotiana tabacum) Bright Yellow-2 suspension culture ce

76 Val-Pro)(n), and expressing them in tobacco (Nicotiana tabacum) Bright-Yellow 2 cells as fusion prote

77 Upon stable expression in cultured tobacco (Nicotiana tabacum) Bright-Yellow 2 cells, OsHKT2;1 media

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

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

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

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

82 fter elicitation of Cf-9 transgenic tobacco (Nicotiana tabacum) by Avr9 peptide revealed a rapidly up

83 eins secreted to aerial surfaces of tobacco (Nicotiana tabacum) by short procumbent trichomes inhibit

84 Overexpression of GCR1 in tobacco (Nicotiana tabacum) BY-2 cells caused an increase in thym

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

86 xpression of CYP726A1 in transgenic tobacco (Nicotiana tabacum) callus or somatic soybean (Glycine ma

87 ethyltransferase (CTOMT1) with homology to a Nicotiana tabacum catechol OMT.

88 A tobacco (Nicotiana tabacum) cDNA (ASA2) encoding a feedback-insen

89 erevisiae) two-hybrid screen with a tobacco (Nicotiana tabacum) cDNA library, which identified a new

90 inactivation by the transposable element of Nicotiana tabacum cell type1 (Tnt1) retrotransposon inse

91 ion of G2/M in higher plants using the BY-2 (Nicotiana tabacum) cell line as a model.

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

93 ed with the transposable element of tobacco (Nicotiana tabacum) cell type1 (Tnt1), we identified a mu

94 anced green fluorescent protein expressed in Nicotiana tabacum cells produced a fusion glycoprotein w

95 Expression of these P3 analogs in Nicotiana tabacum cells yielded glycoproteins with virtu

96 last transfer from Nicotiana sylvestris into Nicotiana tabacum cells.

97 droxylation and glycosylation in transformed Nicotiana tabacum cells.

98 t are rapidly induced when cultured tobacco (Nicotiana tabacum) cells are treated with the mitochondr

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

100 Recombinant production of GhPLA1 in tobacco (Nicotiana tabacum) cells enabled us to purify and analyz

101 the observed order; however, using tobacco (Nicotiana tabacum) cells expressing either the MBD-DsRed

102 and binding assays using transgenic tobacco (Nicotiana tabacum) cells expressing PEPR1 and PEPR2 clea

103 tein (GFP) expression in individual tobacco (Nicotiana tabacum) cells from lines transformed by Agrob

104 Expressing human PIPKIalpha in tobacco (Nicotiana tabacum) cells increased plasma membrane PtdIn

105 Tobacco (Nicotiana tabacum) cells that overexpress either Arabido

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

107 -trisphosphate (InsP(3)) in plants, tobacco (Nicotiana tabacum) cells were transformed with the human

108 injection reporter into PTI-induced tobacco (Nicotiana tabacum) cells.

109 s and to the cytoplasm of wild-type tobacco (Nicotiana tabacum) cells.

110 erologous operons expressed via the tobacco (Nicotiana tabacum) chloroplast genome is reported here.

111 lyase (CPL) was integrated into the tobacco (Nicotiana tabacum) chloroplast genome under the control

112 ere, we demonstrate intein trans-splicing in Nicotiana tabacum chloroplasts by using the naturally sp

113 mycin phosphotransferase (NPTII) in tobacco (Nicotiana tabacum) chloroplasts.

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

115 zed to the endoplasmic reticulum of tobacco (Nicotiana tabacum cv Bright-Yellow 2) cells, and reverse

116 In cultured tobacco (Nicotiana tabacum cv BY-2) cells, addition of boronic ac

117 hromes in the qualitative short-day tobacco (Nicotiana tabacum cv Maryland Mammoth) plant.

118 of a bacterial bar gene (b-bar1) in tobacco (Nicotiana tabacum cv Petit Havana) plastids that confers

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

120 cts of photosynthesis in transgenic tobacco (Nicotiana tabacum cv SR1) plants grown under optimal or

121 re of stomata in epidermal peels of tobacco (Nicotiana tabacum cv Xanthi) and Commelina communis at l

122 s of low-alkaloid tobacco transgenic plants (Nicotiana tabacum cv. LAMD609).

123 alpha reductase (BVR) in transgenic tobacco (Nicotiana tabacum cv. Maryland Mammoth) resulted in the

124 re constructed and transformed into tobacco (Nicotiana tabacum cv. Xanthi).

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

126 Overexpressing Pt PAE1 in tobacco (Nicotiana tabacum) decreased the level of acetyl esters

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

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

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

130 C(2)H(4) production in tobacco (Nicotiana tabacum) following inoculation with HR-eliciti

131 truct for plastid transformation of tobacco (Nicotiana tabacum) for the production of the renewable,

132 how that this gene fragment corresponds to a Nicotiana tabacum gene encoding a nicotine uptake permea

133 so show here that a closely related tobacco (Nicotiana tabacum) gene previously shown to be induced i

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

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

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

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

138 sformation, originally developed in tobacco (Nicotiana tabacum), has recently been extended to a numb

139 the tobacco species Nicotiana sylvestris and Nicotiana tabacum have a recognition mechanism that spec

140 tions was studied in cell-engineered cybrids Nicotiana tabacum (+ Hyoscyamus niger) combining the nuc

141 idopsis and transient expression in tobacco (Nicotiana tabacum) indicate that GTG1 is localized prima

142 genitors of Petunia hybrida, as well as from Nicotiana tabacum, indicated that migration of organella

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

144 Nicotine biosynthesis in Nicotiana tabacum is under genetic control by the A and

145 Tobacco (Nicotiana tabacum) is a member of the Solanaceae, one of

146 t nornicotine are two important alkaloids in Nicotiana tabacum L. (tobacco).

147 tFUT4, and AtFUT5 were expressed in tobacco (Nicotiana tabacum L. cv BY2) suspension culture cells, a

148 C-40 degrees C) in mature leaves of tobacco (Nicotiana tabacum L. cv W38) was determined using measur

149 We used the model organisms Nicotiana tabacum L. cv Xanthi (tobacco) and Triticum ae

150 antitatively in situ in NN genotype tobacco (Nicotiana tabacum L. cv Xanthi-nc) leaves inoculated wit

151 branes or solubilized proteins from tobacco (Nicotiana tabacum L. cv. Samsun) and Arabidopsis thalian

152 Nicotiana tabacum L. plants expressing dsRNA homologous

153 s were isolated from flower buds of tobacco (Nicotiana tabacum L.) and in vitro culture methods optim

154 leoids in all tissues of transgenic tobacco (Nicotiana tabacum L.) examined and there was no indicati

155 Tobacco (Nicotiana tabacum L.) is a natural allotetraploid derive

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

157 cotine to nornicotine conversion in tobacco (Nicotiana tabacum L.) is regulated by an unstable conver

158 carrot (Daucas carota L.) cells and tobacco (Nicotiana tabacum L.) leaf tissues.

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

160 porter gene and introduced into the tobacco (Nicotiana tabacum L.) plastid genome through homologous

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

162 mbers of the NtPMT gene family from tobacco (Nicotiana tabacum L.).

163 ed pyridine alkaloids in cultivated tobacco (Nicotiana tabacum L.).

164 Here we report that transformation of Nicotiana tabacum leaf explants by an RSF1010-derivative

165 d by expressing cDNA in transformed tobacco (Nicotiana tabacum) leaf cells and by following biosynthe

166 plicate these events in transfected tobacco (Nicotiana tabacum) leaf protoplasts.

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

168 transiently expressed in epidermal cells of Nicotiana tabacum leaves.

169 protein and immunoprecipitated from tobacco (Nicotiana tabacum) leaves after transient expression was

170 obacco RIP (TRIP) was isolated from tobacco (Nicotiana tabacum) leaves and purified using ion exchang

171 r levels increase 10- to 50-fold in tobacco (Nicotiana tabacum) leaves treated with fungal elicitors.

172 When tobacco (Nicotiana tabacum) leaves were exposed to lethal levels

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

174 the transient expression system of tobacco (Nicotiana tabacum) leaves, we demonstrated that PHO1 and

175 lized to the cytosol in transfected tobacco (Nicotiana tabacum) leaves.

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

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

178 Transgenic Nicotiana tabacum lines expressing a Juglans regia SDH e

179 on of PA biosynthesis in T. arvense, whereas Nicotiana tabacum, M. sativa, and T. repens plants const

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

181 ssed in nuclei and distinguished in tobacco (Nicotiana tabacum) mesophyll cells; and (c) shown that i

182 The effect of selective agents on tobacco (Nicotiana tabacum) mesophyll chloroplasts was first exam

183 Efficacy tests in a tobacco (Nicotiana tabacum) model system demonstrated that 14 of

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

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

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

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

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

189 t phosphorylation and glycosylation, on both Nicotiana tabacum NON-CELL-AUTONOMOUS PATHWAY PROTEIN1 (

190 A component in this pathway, Nicotiana tabacum NON-CELL-AUTONOMOUS PATHWAY PROTEIN1 (

191 ation was further analyzed by inoculation of Nicotiana tabacum (NT-1) protoplasts with PVX transcript

192 a benthamiana, Medicago sativa (alfalfa) and Nicotiana tabacum NT1 cells.

193 used to produce stably transformed tobacco (Nicotiana tabacum) NT1 cell lines, using Agrobacterium t

194 stores in plant cells, we generated tobacco (Nicotiana tabacum; NT1) suspension cells and Arabidopsis

195 three genes that have orthologs in tobacco (Nicotiana tabacum; NtpreproHypSys), tomato (Solanum lyco

196 ine carboxypeptidase III genes from tobacco (Nicotiana tabacum), NtSCP1 and NtSCP2, belonging to a ph

197 However, expression in tobacco (Nicotiana tabacum) of the major tomato (Lycopersicon esc

198 ed in lily (Lilium longiflorum) and tobacco (Nicotiana tabacum) or for a CaMK similar to those in ani

199 nisms regulating this process, we cloned the Nicotiana tabacum ortholog of PHANTASTICA (NTPHAN) and g

200 Analysis of tobacco (Nicotiana tabacum) Osmotic Stress-Activated Protein Kina

201 f purified protein established that tobacco (Nicotiana tabacum) PAPK is a member of the casein kinase

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

203 ts in Antirrhinum majus, Epilobium hirsutum, Nicotiana tabacum, Petunia hybrida, and the cereal crop

204 und to efficiently ablate pollen in tobacco (Nicotiana tabacum), pine, and Eucalyptus (spp.).

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

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

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

208 We produced transgenic tobacco (Nicotiana tabacum) plants carrying an I-SceI endonucleas

209 Transplastomic tobacco (Nicotiana tabacum) plants expressing beta-glucosidase (B

210 Transgenic tobacco (Nicotiana tabacum) plants expressing green fluorescent p

211 h content from genetically modified tobacco (Nicotiana tabacum) plants in which the activity of the C

212 gon (Antirrhinum majus) GPPS.SSU in tobacco (Nicotiana tabacum) plants increased the total GPPS activ

213 channeling, we generated transgenic tobacco (Nicotiana tabacum) plants independently expressing epito

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

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

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

217 bosomes in the leaves of transgenic tobacco (Nicotiana tabacum) plants transferred to the dark for 2

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

219 We transformed tobacco (Nicotiana tabacum) plants with the cholesterol oxidase c

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

221 n salicylate hydroxylase-expressing tobacco (Nicotiana tabacum) plants, where SA levels were reduced,

222 asite dodder (Cuscuta pentagona) on tobacco (Nicotiana tabacum) plants.

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

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

225 ion experiments were performed on a tobacco (Nicotiana tabacum) plasmodesmal-enriched cell wall prote

226 obifida fusca and inserted into the tobacco (Nicotiana tabacum) plastid genome.

227 rbcL-accD intergenic region of the tobacco (Nicotiana tabacum) plastid genome.

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

229 In transformed tobacco (Nicotiana tabacum) plastids, we flank the marker genes w

230 e from Schizosaccharomyces pombe in tobacco (Nicotiana tabacum) plastids.

231 Screening a Nicotiana tabacum pollen cDNA library yielded a pollen-s

232 show that a green fluorescent protein-tagged Nicotiana tabacum pollen-expressed Rab11b is localized p

233 mosanum and Lilium longiflorum) and tobacco (Nicotiana tabacum) pollen tubes using three markers: (1)

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

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

236 Overexpression of AtCCX3 in tobacco (Nicotiana tabacum) produced lesions in the leaves, stunt

237 ecently, it has been shown that the tobacco (Nicotiana tabacum) protein SABP2 (salicylic acid binding

238 lucuronidase marker, translation in tobacco (Nicotiana tabacum) protoplasts was repressed by those co

239 ously shown that, when expressed in tobacco (Nicotiana tabacum) protoplasts, the A chain of the heter

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

241 -stranded forms of a gusA gene into tobacco (Nicotiana tabacum) protoplasts.

242 Mi-1 homologs for degradation with tobacco (Nicotiana tabacum) rattle virus (TRV)-based virus-induce

243 avioural assays showing that tobacco plants (Nicotiana tabacum) release herbivore-induced volatiles d

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

245 the salicylic acid (SA)-inducible RdRP from Nicotiana tabacum required for defense against viruses.

246 51-dependent HR in Nicotiana benthamiana and Nicotiana tabacum, respectively.

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

248 rexpression of MtDFR1 in transgenic tobacco (Nicotiana tabacum) resulted in visible increases in anth

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

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

251 ltrastructure of columella cells in tobacco (Nicotiana tabacum) root tips preserved by high-pressure

252 monoclonal antibody complex from transgenic Nicotiana tabacum roots has been demonstrated.

253 rabidopsis thaliana (Columbia-0 ecotype) and Nicotiana tabacum ('Samsun') under the control of a comp

254 hat the endosperm cell walls of the tobacco (Nicotiana tabacum) seed are rich in a galactomannan with

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

256 mprehensive characterization of two tobacco (Nicotiana tabacum) SEO genes (NtSEO).

257 ways of the apoplasmic loader Vicia faba and Nicotiana tabacum showed, to our knowledge for the first

258 sis thaliana) AtMPK6 and AtMPK3 (or tobacco [Nicotiana tabacum] SIPK and WIPK), respectively.

259 omain of Hevea brasiliensis HMGR (tHMGR) and Nicotiana tabacum SMT1 in tobacco, under control of both

260 A tobacco cDNA (NtSLT1, for Nicotiana tabacum sodium- and lithium-tolerant) was isol

261 ng enzymes are closely related to a tobacco (Nicotiana tabacum; Solanaceae) diterpene synthase encodi

262 ated that the activation of SIPK, a tobacco (Nicotiana tabacum) stress-responsive MAPK, induces the b

263 The vector carrying a fragment from the Nicotiana tabacum sulfur gene (su), encoding one unit of

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

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

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

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

268 To fill this void, we have analysed tobacco (Nicotiana tabacum) TFs using a dataset of 1,159,022 gene

269 psis thaliana) was overexpressed in tobacco (Nicotiana tabacum) that grows well at light intensities

270 We show that in tobacco (Nicotiana tabacum) the presence of leaves is essential f

271 bidopsis (Arabidopsis thaliana) and tobacco (Nicotiana tabacum), the maize proteins contain a carboxy

272 In transgenic tobacco (Nicotiana tabacum), the pea (Pisum sativum) Ferredoxin 1

273 rances of floral buds in thin-layer tobacco (Nicotiana tabacum) tissue culture was studied by followi

274 ed with Ros1, we show that infected tobacco (Nicotiana tabacum) tissues turn bright red, demonstratin

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

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

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

278 by studying the responses of tobacco plants (Nicotiana tabacum) to systemin.

279 water washes (LWW) of the experimental plant Nicotiana tabacum tobacco introduction (TI) 1068 contain

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

281 toxoid genes were then transformed into the Nicotiana tabacum (tobacco) cell line NT-1 by Agrobacter

282 Identification of a genetically stable Nicotiana tabacum (tobacco) plant with a uniform populat

283 We follow GRD evolution in Nicotiana tabacum (tobacco), an allotetraploid, and its

284 We isolated four novel FT-like genes from Nicotiana tabacum (tobacco), and determined their expres

285 5S promoter in Medicago sativa (alfalfa) and Nicotiana tabacum (tobacco), we show that the 3' UTR pla

286 Tobacco (Nicotiana tabacum) transgenic lines with reduced levels

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

288 subunit ribosomal protein L3 (RPL3) genes in Nicotiana tabacum using post-transcriptional gene silenc

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

290 levels of expression in transgenic tobacco (Nicotiana tabacum var. Petit Havana) plants.

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

292 Here, Nicotiana tabacum was transformed with a gene encoding C

293 e, antisense suppression of CP12 in tobacco (Nicotiana tabacum) was observed to impact on NAD-induced

294 toxic nicotine released by the tobacco plant Nicotiana tabacum, we investigate here whether specific

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

296 Regenerating protoplasts from tobacco (Nicotiana tabacum) were used to determine whether cells

297 nsient protein expression system in tobacco (Nicotiana tabacum), which allowed us to perform coimmuno

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

299 own-regulation was also observed in tobacco (Nicotiana tabacum) with similar temporal and fluence-res

300 the levels of 16:0 was observed in tobacco (Nicotiana tabacum, WT-SR) leaves overexpressing So KAS I