ライフサイエンスコーパス: tabacum

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

2 ypersensitive response in tobacco (Nicotiana tabacum).

3 thocyanin biosynthesis in tobacco (Nicotiana tabacum).

4 chlorophyll deficiency in tobacco (Nicotiana tabacum).

5 the Solanaceous species, tobacco (Nicotiana tabacum).

6 lants in the higher plant tobacco (Nicotiana tabacum).

7 thyl salicylate (MeSA) in tobacco (Nicotiana tabacum).

8 Arabidopsis thaliana) and tobacco (Nicotiana tabacum).

9 e ((*)NO) production from tobacco (Nicotiana tabacum).

10 ing systemic infection in tobacco (Nicotiana tabacum).

11 (Hordeum vulgare, Vicia faba, and Nicotiana tabacum).

12 naceous species including tobacco (Nicotiana tabacum).

13 oem in systemic leaves of tobacco (Nicotiana tabacum).

14 and onion leaf lectin, in tobacco (Nicotiana tabacum).

15 mary PD at cytokinesis in tobacco (Nicotiana tabacum).

16 a and overexpression in transgenic Nicotiana tabacum.

17 ic stress tolerance in model plant Nicotiana tabacum.

18 nterphase cells in Arabidopsis and Nicotiana tabacum.

19 d into virus particles in infected Nicotiana tabacum.

20 bacco Phylloplanin) and its promoter from N. tabacum.

21 purported purified DAO enzyme from Nicotiana tabacum.

22 relA/spoT genes in the model plant Nicotiana tabacum.

23 the expression of antisense RNA in Nicotiana tabacum.

24 (glyphosate) when compared with wild-type N. tabacum.

25 was significantly reduced in TMV infected N. tabacum.

26 r stable nuclear transformation of Nicotiana tabacum.

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

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

29 nd cocrystallized it with tobacco (Nicotiana tabacum) 14-3-3 proteins to describe the protein complex

30 n systemic leaves of susceptible systems; N. tabacum 9.8% reduction and A. thaliana 12.3% reduction,

31 e effect of downregulating SUT1 in Nicotiana tabacum, a sucrose transporter, and Verbascum phoeniceum

32 arworm (Helicoverpa zea), tobacco (Nicotiana tabacum) after mechanical damage, and tomato (Lycopersic

33 on the production of capsidiol in Nicotiana tabacum, an assumed MVA-derived sesquiterpenoid phytoale

34 When transiently expressed in Nicotiana tabacum, an ECA3-yellow fluorescent protein fusion prote

35 e of the TT in the II interaction between N. tabacum and N. obtusifolia was characterized by evaluati

36 response in nonhost plants such as Nicotiana tabacum and Nicotiana benthamiana.

37 se (HR) in non-host plants such as Nicotiana tabacum and Nicotiana benthamiana.

38 two different species of tobacco, Nicotiana tabacum and Nicotiana sylvestris.

39 ; however, it contributed to HR in Nicotiana tabacum and significantly reduced the progress of diseas

40 NATA1 transient expression in Nicotiana tabacum and the addition of N(delta)-acetylornithine to

41 ys in regulating nicotine accumulation in N. tabacum and the great potential of NtMYC2a overexpressio

42 rase (GalT) activities in tobacco (Nicotiana tabacum) and Arabidopsis (Arabidopsis thaliana) microsom

43 in anthers and pollen of tobacco (Nicotiana tabacum) and Arabidopsis resulted in the abortion of the

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

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

46 Cmpg1 are induced in Cf9 tobacco (Nicotiana tabacum) and Cf9 tomato after Avr9 elicitation.

47 e Clp protease complex of tobacco (Nicotiana tabacum) and identified a set of chloroplast proteins th

48 ion vectors were made for tobacco (Nicotiana tabacum) and lettuce (Lactuca sativa), with endogenous (

49 ene in stably transformed tobacco (Nicotiana tabacum) and maize (Zea mays) plants and in transiently

50 st association in vivo in tobacco (Nicotiana tabacum) and observed weaker tethering to additional unk

51 annin-sensitive manner in tobacco (Nicotiana tabacum) and that it could play an active role in this s

52 d SNAREs SYP121/Syr1 from tobacco (Nicotiana tabacum) and the Arabidopsis thaliana homolog SYP121 ass

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

54 erms rice (Oryza sativa), tobacco (Nicotiana tabacum), and Arabidopsis (Arabidopsis thaliana).

55 o (Solanum lycopersicum), tobacco (Nicotiana tabacum), and Arabidopsis thaliana.

56 ed plastids therefrom) of tobacco (Nicotiana tabacum), and chloroplasts isolated from leaves of trans

57 s (Arabidopsis thaliana), tobacco (Nicotiana tabacum), and cultivated tomato under the control of the

58 or GAMT2 in Arabidopsis, tobacco (Nicotiana tabacum), and petunia (Petunia hybrida) resulted in plan

59 in Arabidopsis thaliana, tobacco (Nicotiana tabacum), and potato (Solanum tuberosum) failed to produ

60 s (Arabidopsis thaliana), tobacco (Nicotiana tabacum), and spinach (Spinacia oleracea) with a resolut

61 us hosts: Nicotiana benthamiana, tobacco (N. tabacum), and tomato (Solanum lycopersicum).

62 ghput Agrobacterium inoculation of Nicotiana tabacum, and a spray-only method (named "agrospray") for

63 in transgenic C3 plants (tobacco [Nicotiana tabacum]) and in in vitro translation extracts.

64 a [Simmondsia chinensis], tobacco [Nicotiana tabacum], and cotton [Gossypium hirsutum]) from warm reg

65 gar beet [Beta vulgaris], tobacco [Nicotiana tabacum], and maize [Zea mays]) for which controversial

66 Plastids in Nicotiana tabacum are normally transmitted to the progeny by the m

67 soybean (Glycine max) and tobacco (Nicotiana tabacum), as monitored by measuring hallmarks of PCD in

68 aliana) Golgi alpha-mannosidase I, Nicotiana tabacum beta1,2-N-acetylglucosaminyltransferase I, Arabi

69 bservations on transgenic tobacco (Nicotiana tabacum) Bright Yellow 2 cells and Arabidopsis (Arabidop

70 n the endosomal system of tobacco (Nicotiana tabacum) Bright Yellow 2 cells and ultimately leads to c

71 Transgenic tobacco (Nicotiana tabacum) Bright Yellow-2 (BY-2) cells stably expressing

72 ortical array assembly in tobacco (Nicotiana tabacum) Bright Yellow-2 cells after cytokinesis and dru

73 ession studies of MAB1 in tobacco (Nicotiana tabacum) Bright Yellow-2 cells revealed a cell cycle-dep

74 drogen peroxide (H2O2) in tobacco (Nicotiana tabacum) Bright Yellow-2 cells, an increase in S-nitrosy

75 n transiently transformed tobacco (Nicotiana tabacum) Bright Yellow-2 cells, showed that the maize an

76 As in Arabidopsis leaf or tobacco (Nicotiana tabacum) Bright Yellow-2 protoplasts identified single c

77 Arabidopsis thaliana) and tobacco (Nicotiana tabacum) Bright Yellow-2 suspension culture cells.

78 ), and expressing them in tobacco (Nicotiana tabacum) Bright-Yellow 2 cells as fusion proteins with g

79 le expression in cultured tobacco (Nicotiana tabacum) Bright-Yellow 2 cells, OsHKT2;1 mediated Na(+)

80 Using tobacco (Nicotiana tabacum) 'Bright Yellow 2' cell suspension and leaves, e

81 g cell plate expansion in tobacco (Nicotiana tabacum) 'Bright Yellow-2' cells: massive delivery of pr

82 nsformation is routine in tobacco (Nicotiana tabacum) but 100-fold less frequent in Arabidopsis (Arab

83 anthocyanin-overproducing tobacco (Nicotiana tabacum), but levels of oligomeric PAs were very low.

84 n) was integrated into the nuclear DNA of N. tabacum by using Agrobacterium tumefaciens-mediated tran

85 Here, we stably expressed NtPDR1 in N. tabacum BY-2 suspension cells.

86 tation of Cf-9 transgenic tobacco (Nicotiana tabacum) by Avr9 peptide revealed a rapidly upregulated

87 ted to aerial surfaces of tobacco (Nicotiana tabacum) by short procumbent trichomes inhibit spore ger

88 stitutive ectopic expression of NtPDR1 in N. tabacum BY2 cells resulted in increased resistance to se

89 ession by various compounds was tested in N. tabacum BY2 cells.

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

91 ferase (CTOMT1) with homology to a Nicotiana tabacum catechol OMT.

92 The model was further validated using N. tabacum cell extracts or recombinant N. tabacum protein

93 ylable GFP indicator protein expressed in N. tabacum cell lines, which can be chemically complemented

94 ion by the transposable element of Nicotiana tabacum cell type1 (Tnt1) retrotransposon insertion lead

95 M in higher plants using the BY-2 (Nicotiana tabacum) cell line as a model.

96 e transposable element of tobacco (Nicotiana tabacum) cell type 1, is a retrotransposon that replicat

97 e transposable element of tobacco (Nicotiana tabacum) cell type1 (Tnt1), we identified a mutant line

98 n fluorescent protein expressed in Nicotiana tabacum cells produced a fusion glycoprotein with all pr

99 Expression of these P3 analogs in Nicotiana tabacum cells yielded glycoproteins with virtually all P

100 fer from Nicotiana sylvestris into Nicotiana tabacum cells.

101 dly induced when cultured tobacco (Nicotiana tabacum) cells are treated with the mitochondrial electr

102 of HVA22 labels the ER in tobacco (Nicotiana tabacum) cells but its overexpression does not alter ER

103 t production of GhPLA1 in tobacco (Nicotiana tabacum) cells enabled us to purify and analyze a single

104 ved order; however, using tobacco (Nicotiana tabacum) cells expressing either the MBD-DsRed (microtub

105 g assays using transgenic tobacco (Nicotiana tabacum) cells expressing PEPR1 and PEPR2 clearly demons

106 expression in individual tobacco (Nicotiana tabacum) cells from lines transformed by Agrobacterium t

107 ssing human PIPKIalpha in tobacco (Nicotiana tabacum) cells increased plasma membrane PtdIns(4,5)P2 1

108 Tobacco (Nicotiana tabacum) cells that overexpress either Arabidopsis GCR1

109 r transient expression in tobacco (Nicotiana tabacum) cells that were induced to accumulate triacylgl

110 hate (InsP(3)) in plants, tobacco (Nicotiana tabacum) cells were transformed with the human type I in

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

112 he cytoplasm of wild-type tobacco (Nicotiana tabacum) cells.

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

114 ) was integrated into the tobacco (Nicotiana tabacum) chloroplast genome under the control of the lig

115 monstrate intein trans-splicing in Nicotiana tabacum chloroplasts by using the naturally split Ssp Dn

116 is landscape in the ancestral host Nicotiana tabacum Comparing the topographies of the landscape in t

117 ndrial DNA transfer from N. sylvestris to N. tabacum could be recognized by restoration of fertile fl

118 In cultured tobacco (Nicotiana tabacum cv BY-2) cells, addition of boronic acids caused

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

120 tosynthesis in transgenic tobacco (Nicotiana tabacum cv SR1) plants grown under optimal or restricted

121 lkaloid tobacco transgenic plants (Nicotiana tabacum cv. LAMD609).

122 ctase (BVR) in transgenic tobacco (Nicotiana tabacum cv. Maryland Mammoth) resulted in the loss of ph

123 cted and transformed into tobacco (Nicotiana tabacum cv. Xanthi).

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

125 (CMS92) or (ii) normal, with the fertile N. tabacum cytoplasm.

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

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

128 c vacuole exists, in both tobacco (Nicotiana tabacum) epidermal (DeltapH -1.5) and Arabidopsis thalia

129 nd functional analysis of tobacco (Nicotiana tabacum) EXO70 isoforms.

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

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

132 d in and extracted from transformedNicotiana tabacum Gel electrophoresis of leaf extracts revealed a

133 his gene fragment corresponds to a Nicotiana tabacum gene encoding a nicotine uptake permease (NUP1).

134 re that a closely related tobacco (Nicotiana tabacum) gene previously shown to be induced in leaves a

135 ctifying K(+) channels of tobacco (Nicotiana tabacum) guard cells and show its close parallel with st

136 More recently in our history, Nicotiana tabacum has attracted interest as one of the most econom

137 NtPDR1 from Nicotiana tabacum has been shown to be involved in the constitutiv

138 vation of the plastid PsaI gene in Nicotiana tabacum has no measurable effect on photosynthetic elect

139 , originally developed in tobacco (Nicotiana tabacum), has recently been extended to a number of crop

140 o species Nicotiana sylvestris and Nicotiana tabacum have a recognition mechanism that specifically d

141 d transient expression in tobacco (Nicotiana tabacum) indicate that GTG1 is localized primarily to Go

142 f Petunia hybrida, as well as from Nicotiana tabacum, indicated that migration of organellar DNA into

143 hat receptor targeting in tobacco (Nicotiana tabacum) initially involves a canonical coat protein com

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

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

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

147 We used the model organisms Nicotiana tabacum L. cv Xanthi (tobacco) and Triticum aestivum (wh

148 ly in situ in NN genotype tobacco (Nicotiana tabacum L. cv Xanthi-nc) leaves inoculated with tobacco

149 solubilized proteins from tobacco (Nicotiana tabacum L. cv. Samsun) and Arabidopsis thaliana (cv. Col

150 Nicotiana tabacum L. plants expressing dsRNA homologous to B. taba

151 lated from flower buds of tobacco (Nicotiana tabacum L.) and in vitro culture methods optimised for t

152 all tissues of transgenic tobacco (Nicotiana tabacum L.) examined and there was no indication of its

153 Tobacco (Nicotiana tabacum L.) is a natural allotetraploid derived from the

154 Nicotine biosynthesis in tobacco (Nicotiana tabacum L.) is highly regulated by jasmonic acid (JA).

155 nornicotine conversion in tobacco (Nicotiana tabacum L.) is regulated by an unstable converter locus

156 ine content in cultivated tobacco (Nicotiana tabacum L.) may be of value for industrial purposes, inc

157 loped nfsI transplastomic tobacco (Nicotiana tabacum L.) to reduce pollen-borne transgene flow.

158 e alkaloids in cultivated tobacco (Nicotiana tabacum L.).

159 he NtPMT gene family from tobacco (Nicotiana tabacum L.).

160 ssing cDNA in transformed tobacco (Nicotiana tabacum) leaf cells and by following biosynthesis in the

161 n rapid chlorophyll degradation in Nicotiana tabacum leaves and led to accumulation of pheophorbide (

162 In non-host N. tabacum leaves, the hopPtoN mutant produced more cell de

163 ly expressed in epidermal cells of Nicotiana tabacum leaves.

164 d immunoprecipitated from tobacco (Nicotiana tabacum) leaves after transient expression was active in

165 (TRIP) was isolated from tobacco (Nicotiana tabacum) leaves and purified using ion exchange and gel

166 ncrease 10- to 50-fold in tobacco (Nicotiana tabacum) leaves treated with fungal elicitors.

167 When tobacco (Nicotiana tabacum) leaves were exposed to lethal levels of salt an

168 5e:EGFP fusion protein in tobacco (Nicotiana tabacum) leaves, and immunoblotting using Arabidopsis sh

169 ient expression system of tobacco (Nicotiana tabacum) leaves, we demonstrated that PHO1 and PHO2 are

170 he cytosol in transfected tobacco (Nicotiana tabacum) leaves.

171 escent protein fusions in tobacco (Nicotiana tabacum) leaves.

172 transiently expressed in tobacco (Nicotiana tabacum) leaves.

173 The alloplasmic N. tabacum line we used carries Nicotiana undulata cytoplas

174 Transgenic Nicotiana tabacum lines expressing a Juglans regia SDH exhibited a

175 bidopsis thaliana, Nicotiana benthamiana, N. tabacum, Lycopersicon esculentum and others could be use

176 iosynthesis in T. arvense, whereas Nicotiana tabacum, M. sativa, and T. repens plants constitutively

177 of FT induced flowering in the short-day N. tabacum Maryland Mammoth tobacco under long-day conditio

178 o (Solanum lycopersicum), tobacco (Nicotiana tabacum), Medicago truncatula, wheat (Triticum aestivum)

179 clei and distinguished in tobacco (Nicotiana tabacum) mesophyll cells; and (c) shown that interaction

180 ct of selective agents on tobacco (Nicotiana tabacum) mesophyll chloroplasts was first examined by tr

181 Efficacy tests in a tobacco (Nicotiana tabacum) model system demonstrated that 14 of these elem

182 nstrate that manipulating tobacco (Nicotiana tabacum) MTHFR gene (NtMTHFR1) expression dramatically a

183 Both homoplastomic tobacco (Nicotiana tabacum) mutants psbN-F and psbN-R show essentially the

184 generating transplastomic tobacco (Nicotiana tabacum) mutants with point mutations in the aSD coupled

185 es including A. thaliana, tobacco (Nicotiana tabacum), N. benthamiana, N. attenuata and tomato (Solan

186 ional characterization of tobacco (Nicotiana tabacum) Nin88, a presumed fully active cwINV playing a

187 ylation and glycosylation, on both Nicotiana tabacum NON-CELL-AUTONOMOUS PATHWAY PROTEIN1 (Nt-NCAPP1)

188 A component in this pathway, Nicotiana tabacum NON-CELL-AUTONOMOUS PATHWAY PROTEIN1 (NtNCAPP1),

189 further analyzed by inoculation of Nicotiana tabacum (NT-1) protoplasts with PVX transcripts containi

190 ana, Medicago sativa (alfalfa) and Nicotiana tabacum NT1 cells.

191 roduce stably transformed tobacco (Nicotiana tabacum) NT1 cell lines, using Agrobacterium tumefaciens

192 es that have orthologs in tobacco (Nicotiana tabacum; NtpreproHypSys), tomato (Solanum lycopersicum;

193 ypeptidase III genes from tobacco (Nicotiana tabacum), NtSCP1 and NtSCP2, belonging to a phylogenetic

194 hich gentamycin resistance encoded in the N. tabacum nucleus was combined with spectinomycin resistan

195 However, expression in tobacco (Nicotiana tabacum) of the major tomato (Lycopersicon esculentum) A

196 infected A. thaliana by 19.6% but not in N. tabacum or the resistant systems.

197 (Lilium longiflorum) and tobacco (Nicotiana tabacum) or for a CaMK similar to those in animals or ye

198 lating this process, we cloned the Nicotiana tabacum ortholog of PHANTASTICA (NTPHAN) and generated a

199 Analysis of tobacco (Nicotiana tabacum) Osmotic Stress-Activated Protein Kinase activit

200 protein established that tobacco (Nicotiana tabacum) PAPK is a member of the casein kinase I family.

201 respiration and photosynthesis of Nicotiana tabacum 'Petit Havana SR1' wild-type plants with that of

202 rrhinum majus, Epilobium hirsutum, Nicotiana tabacum, Petunia hybrida, and the cereal crop Setaria it

203 iciently ablate pollen in tobacco (Nicotiana tabacum), pine, and Eucalyptus (spp.).

204 aic virus or Potato virus X, infection of N. tabacum plants resulted in 50% reductions in Rca and Atp

205 whiteflies exposed to dsRNA by feeding on N. tabacum plants, compared to non-dsRNA expressing plants,

206 (uidA) and analyzed in transgenic Nicotiana tabacum plants.

207 riched fractions from TMV-infected Nicotiana tabacum plants.

208 evels of botryococcene in tobacco (Nicotiana tabacum) plants by diverting carbon flux from the cytoso

209 We produced transgenic tobacco (Nicotiana tabacum) plants carrying an I-SceI endonuclease recognit

210 Transplastomic tobacco (Nicotiana tabacum) plants expressing beta-glucosidase (Bgl-1) show

211 Transgenic tobacco (Nicotiana tabacum) plants expressing green fluorescent protein (GF

212 rhinum majus) GPPS.SSU in tobacco (Nicotiana tabacum) plants increased the total GPPS activity and mo

213 , we generated transgenic tobacco (Nicotiana tabacum) plants independently expressing epitope-tagged

214 e transport in transgenic tobacco (Nicotiana tabacum) plants of a human alpha-mannosidase, MAN2B1, wh

215 s result was confirmed in tobacco (Nicotiana tabacum) plants overexpressing the TRXm4 orthologous gen

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

217 etic capacity and growth, tobacco (Nicotiana tabacum) plants with increased levels of transketolase p

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

219 te hydroxylase-expressing tobacco (Nicotiana tabacum) plants, where SA levels were reduced, JA levels

220 um) Fd isoform (PsFd1) in tobacco (Nicotiana tabacum) plants.

221 er (Cuscuta pentagona) on tobacco (Nicotiana tabacum) plants.

222 nal antibody expressed in tobacco (Nicotiana tabacum) plants.

223 ments were performed on a tobacco (Nicotiana tabacum) plasmodesmal-enriched cell wall protein prepara

224 sca and inserted into the tobacco (Nicotiana tabacum) plastid genome.

225 intergenic region of the tobacco (Nicotiana tabacum) plastid genome.

226 ble transformation of the tobacco (Nicotiana tabacum) plastid genome.

227 ed green fluorescent protein (smGFP) into N. tabacum plastids.

228 In transformed tobacco (Nicotiana tabacum) plastids, we flank the marker genes with recomb

229 izosaccharomyces pombe in tobacco (Nicotiana tabacum) plastids.

230 Screening a Nicotiana tabacum pollen cDNA library yielded a pollen-specific PM

231 a green fluorescent protein-tagged Nicotiana tabacum pollen-expressed Rab11b is localized predominant

232 d Lilium longiflorum) and tobacco (Nicotiana tabacum) pollen tubes using three markers: (1) changes i

233 In steady-state growing tobacco (Nicotiana tabacum) pollen tubes, SEC3a displayed amino-terminal Pl

234 In tobacco (Nicotiana tabacum), pollen tube tip growth is controlled by the RA

235 erexpression of AtCCX3 in tobacco (Nicotiana tabacum) produced lesions in the leaves, stunted growth,

236 g N. tabacum cell extracts or recombinant N. tabacum protein prenyltransferases expressed in Escheric

237 t has been shown that the tobacco (Nicotiana tabacum) protein SABP2 (salicylic acid binding protein 2

238 se marker, translation in tobacco (Nicotiana tabacum) protoplasts was repressed by those constructs c

239 n that, when expressed in tobacco (Nicotiana tabacum) protoplasts, the A chain of the heterodimeric t

240 ient expression assays in tobacco (Nicotiana tabacum) protoplasts, TSAR1 and TSAR2 exhibit different

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

242 logs for degradation with tobacco (Nicotiana tabacum) rattle virus (TRV)-based virus-induced gene sil

243 In tobacco (Nicotiana tabacum), replicons based on the bean yellow dwarf virus

244 ylic acid (SA)-inducible RdRP from Nicotiana tabacum required for defense against viruses.

245 nt HR in Nicotiana benthamiana and Nicotiana tabacum, respectively.

246 mature transmitting tract (TT) in Nicotiana tabacum resulted in the loss of inhibition of pollen tub

247 Mild NtSUT1 downregulation in N. tabacum resulted in the pronounced phenotype associated

248 n of MtDFR1 in transgenic tobacco (Nicotiana tabacum) resulted in visible increases in anthocyanin ac

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

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

251 l antibody complex from transgenic Nicotiana tabacum roots has been demonstrated.

252 thaliana (Columbia-0 ecotype) and Nicotiana tabacum ('Samsun') under the control of a companion cell

253 dosperm cell walls of the tobacco (Nicotiana tabacum) seed are rich in a galactomannan with a very lo

254 cytochrome b6f complex in tobacco (Nicotiana tabacum) seems to be restricted to young leaves, suggest

255 e characterization of two tobacco (Nicotiana tabacum) SEO genes (NtSEO).

256 e apoplasmic loader Vicia faba and Nicotiana tabacum showed, to our knowledge for the first time in v

257 na) AtMPK6 and AtMPK3 (or tobacco [Nicotiana tabacum] SIPK and WIPK), respectively.

258 evea brasiliensis HMGR (tHMGR) and Nicotiana tabacum SMT1 in tobacco, under control of both constitut

259 are closely related to a tobacco (Nicotiana tabacum; Solanaceae) diterpene synthase encoding Z-abien

260 the activation of SIPK, a tobacco (Nicotiana tabacum) stress-responsive MAPK, induces the biosynthesi

261 llen tube growth in normal and TT-ablated N. tabacum styles at various post-pollination times and dev

262 ector carrying a fragment from the Nicotiana tabacum sulfur gene (su), encoding one unit of the chlor

263 ired accumulation of PELPIII in the TT of N. tabacum, supporting PELPIII function in pre-zygotic II.

264 tPDR1 was originally identified in Nicotiana tabacum suspension cells (BY2), in which its expression

265 urface of Bright Yellow 2 tobacco (Nicotiana tabacum) suspension cells labeled with an environment se

266 GFP fusion constructs in tobacco (Nicotiana tabacum) suspension cells, indicated mitochondrial, plas

267 localization studies with tobacco (Nicotiana tabacum) suspension-cultured cells indicate that interac

268 is void, we have analysed tobacco (Nicotiana tabacum) TFs using a dataset of 1,159,022 gene-space seq

269 ana) was overexpressed in tobacco (Nicotiana tabacum) that grows well at light intensities much highe

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

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

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

273 s1, we show that infected tobacco (Nicotiana tabacum) tissues turn bright red, demonstrating that in

274 y metabolite profiling of tobacco (Nicotiana tabacum) tissues.

275 ion of a Transposable Element from Nicotiana tabacum (Tnt1) insertional mutant line were carried out

276 rt the application of the tobacco (Nicotiana tabacum) Tnt1 retrotransposon as an insertional mutagen

277 g the responses of tobacco plants (Nicotiana tabacum) to systemin.

278 es (LWW) of the experimental plant Nicotiana tabacum tobacco introduction (TI) 1068 contained highly

279 l subgroup 5 encodes P-proteins in Nicotiana tabacum (tobacco) and Arabidopsis thaliana.

280 In dicotyledonous plants, such as Nicotinana tabacum (tobacco) and Solanum lycopersicum (tomato), gre

281 nes were then transformed into the Nicotiana tabacum (tobacco) cell line NT-1 by Agrobacterium tumefa

282 tification of a genetically stable Nicotiana tabacum (tobacco) plant with a uniform population of tra

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

284 ated four novel FT-like genes from Nicotiana tabacum (tobacco), and determined their expression profi

285 r in Medicago sativa (alfalfa) and Nicotiana tabacum (tobacco), we show that the 3' UTR plays a major

286 Tobacco (Nicotiana tabacum) transgenic lines with reduced levels of ASR pro

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

288 by capsidiol, a sesquiterpene produced by N. tabacum upon pathogen attack.

289 bosomal protein L3 (RPL3) genes in Nicotiana tabacum using post-transcriptional gene silencing (PTGS)

290 systems Nicotiana benthamiana and Nicotiana tabacum using transient and stable nuclear transformatio

291 A content of TAC preparations from Nicotiana tabacum was determined using whole genome tiling arrays.

292 GUS expression in transgenic N. tabacum was localized to glandular heads.

293 Here, Nicotiana tabacum was transformed with a gene encoding CV-N to exp

294 se suppression of CP12 in tobacco (Nicotiana tabacum) was observed to impact on NAD-induced PRK and G

295 ural products already exists, mostly from N. tabacum, we focus our attention on the ecological roles

296 When extracts from the mature TT of N. tabacum were injected into the TT-ablated style prior to

297 and two varieties of A. annua and Nicotiana tabacum were transformed.

298 tein expression system in tobacco (Nicotiana tabacum), which allowed us to perform coimmunoprecipitat

299 t in two susceptible host systems (Nicotiana tabacum with TMV (Tobacco mosaic virus), and Arabidopsis

300 tion was also observed in tobacco (Nicotiana tabacum) with similar temporal and fluence-response kine