ライフサイエンスコーパス: Nicotiana tabacum

1 ependent hypersensitive response in tobacco (Nicotiana tabacum).

2 egulate anthocyanin biosynthesis in tobacco (Nicotiana tabacum).

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

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

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

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

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

8 expression of CsGSTF1 in transgenic tobacco (Nicotiana tabacum).

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

10 establishing systemic infection in tobacco (Nicotiana tabacum).

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

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

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

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

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

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

17 plasm of interphase cells in Arabidopsis and Nicotiana tabacum.

18 ich was confirmed by localization studies in Nicotiana tabacum.

19 coassembled into virus particles in infected Nicotiana tabacum.

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

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

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

23 benthamiana and overexpression in transgenic Nicotiana tabacum.

24 and abiotic stress tolerance in model plant Nicotiana tabacum.

25 lism operating in the glandular trichomes of Nicotiana tabacum.

26 vectors for stable nuclear transformation of 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 mical compounds in cell cultures of tobacco (Nicotiana tabacum); (2) confirmation of the identified h

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

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

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

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

35 of a repeated cybrid between the solanaceae Nicotiana tabacum and Hyoscyamus niger.

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

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

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

39 We found that pollen tubes from Nicotiana tabacum and other plant species with a solid o

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

41 mature Eruca sativa, Nasturtium officinale, Nicotiana tabacum and Spinacia oleracea plants and in is

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

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

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

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

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

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

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

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

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

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

52 e, miR159 function was inhibited in tobacco (Nicotiana tabacum) and rice (Oryza sativa) using miRNA M

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

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

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

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

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

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

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

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

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

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

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

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

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

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

67 mes of N. tabacum The glandular trichomes of Nicotiana tabacum are highly productive in terms of seco

68 Plastids in Nicotiana tabacum are normally transmitted to the progen

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

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

71 utilized the highly synchronizable tobacco (Nicotiana tabacum) Bright yellow 2 (BY2) cell suspension

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

100 last transfer from Nicotiana sylvestris into Nicotiana tabacum cells.

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

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

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

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

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

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

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

108 Tobacco (Nicotiana tabacum) cells that overexpress either Arabido

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

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

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

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

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

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

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

116 xysome linker protein CcmM35 within tobacco (Nicotiana tabacum) chloroplasts.

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

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

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

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

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

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

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

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

125 hosts: Capsicum annuum cv. Marengo (pepper), Nicotiana tabacum cv. Xanthi nc (tobacco), and Cucurbita

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

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

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

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

130 nTag system with the catalytic domain of the Nicotiana tabacum DRM methyltransferase, which efficient

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

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

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

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

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

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

137 MD of Arabidopsis (Arabidopsis thaliana) and Nicotiana tabacum GnTI toward Golgi localization and n-g

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

154 Nicotiana tabacum L. plants expressing dsRNA homologous

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

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

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

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

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

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

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

162 y roles of five BRC gene members in tobacco (Nicotiana tabacum L.) using CRISPR site-directed mutagen

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

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

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

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

167 Using both transient assays in Nicotiana tabacum leaves or Actinidia arguta fruits and

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 Recently, tobacco (Nicotiana tabacum) leaves were engineered to accumulate

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

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

175 When ectopically expressed in tobacco (Nicotiana tabacum) leaves, MtNPD1 colocalized with vacuo

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

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

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

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

180 Transgenic Nicotiana tabacum lines expressing a Juglans regia SDH e

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

182 Here we develop an RNAi-RbcS tobacco (Nicotiana tabacum) master-line, tobRrDeltaS, for produci

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

218 enerated a series of transplastomic tobacco (Nicotiana tabacum) plants to alter tRNA(Glu) expression

219 struct expressing Hvt and lectin in tobacco (Nicotiana tabacum) plants under phloem specific promoter

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

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

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

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

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

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

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

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

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

229 diting site was introduced into the tobacco (Nicotiana tabacum) plastid genome.

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

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

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

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

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

235 gged transmembrane (TM) proteins in tobacco (Nicotiana tabacum) pollen tubes growing normally or trea

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

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

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

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

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

241 ase (nCas9-Target-AID) systems to mutagenize Nicotiana tabacum protoplasts and to regenerate plants h

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

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

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

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

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

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

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

249 51-dependent HR in Nicotiana benthamiana and Nicotiana tabacum, respectively.

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

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

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

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

254 Moreover, plants carrying a tobacco (Nicotiana tabacum) retrotransposon Tnt1 insertion in MtT

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

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

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

258 lation and translation in leaves of tobacco (Nicotiana tabacum) seedlings after transfer from moderat

259 fruits and seeds, and nicotine in tobacco ( Nicotiana tabacum) seedlings.

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

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

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

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

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

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

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

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

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

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

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

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

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

273 m in the dicotyledonous model plant tobacco (Nicotiana tabacum) that allows us to study the leaf deet

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

289 5S promoter in Medicago sativa (alfalfa) and Nicotiana tabacum (tobacco), we show that the 3' UTR pla

290 Tobacco (Nicotiana tabacum) transgenic lines with reduced levels

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

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

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

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

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

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

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

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

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

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