ライフサイエンスコーパス: Nicotiana benthamiana

1 reduces recalcitrance in transgenic tobacco (Nicotiana benthamiana).

2 nal genome components of FHV in plant cells (Nicotiana benthamiana).

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

4 uce significant cell death when expressed in Nicotiana benthamiana.

5 ke lamellae in both Arabidopsis thaliana and Nicotiana benthamiana.

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

7 imeric clone into the laboratory model plant Nicotiana benthamiana.

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

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

10 of inducing cell death when overexpressed in Nicotiana benthamiana.

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

12 imeric 62-71-3 was successfully expressed in Nicotiana benthamiana.

13 biosynthesis of MLG by overexpressing it in Nicotiana benthamiana.

14 of RPS5 using transient expression assays in Nicotiana benthamiana.

15 were obtained after transient expression in Nicotiana benthamiana.

16 f the Oak1 gene were expressed in transgenic Nicotiana benthamiana.

17 APIP6) are both degraded when coexpressed in Nicotiana benthamiana.

18 Agrobacterium tumefaciens infection assay in Nicotiana benthamiana.

19 encing-based fast-forward genetics screen in Nicotiana benthamiana.

20 aVCP when transiently expressed in leaves of Nicotiana benthamiana.

21 accumulation in yeast and in virus-infected Nicotiana benthamiana.

22 vely regulate Pto-mediated PCD in tomato and Nicotiana benthamiana.

23 irus-induced gene silencing (VIGS) screen in Nicotiana benthamiana.

24 gulator in tomato (Solanum lycopersicum) and Nicotiana benthamiana.

25 ) independent of their enzymatic activity in Nicotiana benthamiana.

26 of viral RNA accumulation in agroinfiltrated Nicotiana benthamiana.

27 P:RFP fusion (chromobody) in the model plant Nicotiana benthamiana.

28 n as demonstrated by transient expression in Nicotiana benthamiana.

29 the translation of virus-encoded proteins in Nicotiana benthamiana.

30 age leaf curl virus (CbLCuV) are enhanced in Nicotiana benthamiana.

31 hytoene desaturase (PDS) gene sequences from Nicotiana benthamiana.

32 m signaling, using transient coexpression in Nicotiana benthamiana.

33 f Solanum demissum, Nicotiana glutinosa, and Nicotiana benthamiana.

34 ha-dependent nuclear import to be assayed in Nicotiana benthamiana.

35 ere selected for further characterization in Nicotiana benthamiana.

36 are greatly reduced in both A. thaliana and Nicotiana benthamiana.

37 roxide-generating paraquat in Arabidopsis or Nicotiana benthamiana.

38 ed vectors can result in RNA1 replication in Nicotiana benthamiana.

39 ircuit in a heterologous Solanaceae species, Nicotiana benthamiana.

40 t hypersensitive response (HR) production in Nicotiana benthamiana.

41 structed by their transient co-expression in Nicotiana benthamiana.

42 ain were required for induction of the HR in Nicotiana benthamiana.

43 s in cassava (Manihot esculenta, Crantz) and Nicotiana benthamiana.

44 nonhost plants such as Nicotiana tabacum and Nicotiana benthamiana.

45 mefaciens to transiently express BMV RNAs in Nicotiana benthamiana.

46 yringae hrp gene cluster and the model plant Nicotiana benthamiana.

47 on-host plants such as Nicotiana tabacum and Nicotiana benthamiana.

48 ells but failed to move from cell to cell in Nicotiana benthamiana.

49 vel specificities by transient expression in Nicotiana benthamiana.

50 onfer methylation of a transgene reporter in Nicotiana benthamiana.

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

52 RX17 was examined by transient expression in Nicotiana benthamiana.

53 ed with fluorescent protein and expressed in Nicotiana benthamiana.

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

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

56 era avenae and transiently expressed them in Nicotiana benthamiana.

57 N-glycosylated upon expression in transgenic Nicotiana benthamiana.

58 oactive NLRs when transiently coexpressed in Nicotiana benthamiana.

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

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

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

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

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

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

65 Nicotiana benthamiana, a plant unable to perceive EF-Tu,

66 d hypersensitive response in both tomato and Nicotiana benthamiana, accompanied by enhanced accumulat

67 Knocking down the NME1 homolog in Nicotiana benthamiana also led to decreased production o

68 Silencing of GCN4 in Nicotiana benthamiana and Arabidopsis thaliana compromis

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

70 ecursors was investigated in leaf tissues of Nicotiana benthamiana and cells of Arabidopsis thaliana.

71 Virus-induced gene silencing of VIP2 in Nicotiana benthamiana and characterization of the Arabid

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

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

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

75 orphyrin chelatase (Chl H) encoding genes in Nicotiana benthamiana and in economically important crop

76 evels were also elevated by leaf ablation in Nicotiana benthamiana and in rejuvenating shoot apices o

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

78 we transiently expressed Arabidopsis RDR6 in Nicotiana benthamiana and investigated the biochemical a

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

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

81 ependent of the FT protein, moves throughout Nicotiana benthamiana and mutant Arabidopsis plants and

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

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

84 One effector, PexRD2, promoted cell death in Nicotiana benthamiana and other solanaceous plants.

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

86 o rattle virus vectors in other species like Nicotiana benthamiana and tomato (Lycopersicon esculentu

87 e assessed the functions of B-class genes in Nicotiana benthamiana and tomato (Solanum lycopersicum)

88 In this study, we utilized Nicotiana benthamiana and virus-induced gene silencing t

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

90 26 nucleotides in two plant hosts, tobacco (Nicotiana benthamiana) and cassava (Manihot esculenta, C

91 train's survival and growth pattern on host (Nicotiana benthamiana) and nonhost (tomato [Solanum lyco

92 es, including tomato (Solanum lycopersicum), Nicotiana benthamiana, and Arabidopsis thaliana.

93 sed a virus-induced gene-silencing screen in Nicotiana benthamiana, and identified the peroxisomal en

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

95 otein bodies when transiently coexpressed in Nicotiana benthamiana, and the analysis of these protein

96 n different silencing pathways and have used Nicotiana benthamiana as a model system.

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

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

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

100 ing Potato spindle tuber viroid infection of Nicotiana benthamiana as the experimental system, we tes

101 Transient expression in Nicotiana benthamiana as well as functional complementat

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

103 leaves and cotyledons of Arabidopsis and/or Nicotiana benthamiana at different stages of development

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

105 initially show a similar infection course in Nicotiana benthamiana, but the absence of an active P19

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

107 cterium-mediated transient transformation of Nicotiana benthamiana by leaf infiltration has been wide

108 nivirus vector was used to silence NbRBR1 in Nicotiana benthamiana by microprojectile bombardment int

109 1-V were produced by transient expression in Nicotiana benthamiana by using a deconstructed tobacco m

110 ikewise, knocking down RanGAP2 expression in Nicotiana benthamiana by virus-induced gene silencing co

111 nduced gene silencing (VIGS) of aconitase in Nicotiana benthamiana caused a 90% reduction in aconitas

112 We show that silencing of SGT1 in Nicotiana benthamiana causes a reduction in steady-state

113 We sequenced six complete Nicotiana benthamiana cDNAs that encode class XI and cla

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

115 HrpP was translocated into Nicotiana benthamiana cells via the DC3000 T3SS when exp

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

117 er, when this same effector is injected into Nicotiana benthamiana cells, it is recognized by the imm

118 protein in yeast, soybean (Glycine max), and Nicotiana benthamiana cells.

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

120 in Chinese hamster ovary and in whole plant (Nicotiana benthamiana) cells.

121 su) were introduced into leaves of wild type Nicotiana benthamiana, circular, yellow spots with an ar

122 Transient expression in Nicotiana benthamiana confirmed involvement in TAG synth

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

124 d VIGS approach to study the function of the Nicotiana benthamiana DEF ortholog (NbDEF).

125 xpression of Pto in the heterologous species Nicotiana benthamiana did not confer resistance to P. sy

126 c circular to total monomeric PSTVd forms in Nicotiana benthamiana Domin plants in which the endogeno

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

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

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

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

131 tein fusion protein transiently expressed in Nicotiana benthamiana, followed by mass spectrometry.

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

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

134 Nicotiana benthamiana has been employed as a heterologou

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

136 ts role, we down-regulated expression of the Nicotiana benthamiana homolog, NbRDR6, and examined the

137 nsitivity response (HR) when inoculated into Nicotiana benthamiana; however, it contributed to HR in

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

139 er, it promotes chlorosis in the model plant Nicotiana benthamiana in a manner independent of type II

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

141 erial growth when delivered by Pta 6606 into Nicotiana benthamiana in which AvrRPS4 is not recognized

142 Our data reveal that Nicotiana benthamiana incorporates two different paralog

143 Downregulation of XRCC4 in Arabidopsis and Nicotiana benthamiana increased stable transformation du

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

145 ent expression of truncated RPS4 proteins in Nicotiana benthamiana induced hypersensitive response-li

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

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

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

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

150 Silencing of RPN9 in Nicotiana benthamiana inhibits systemic spread of two ta

151 rates that basal resistance in the leaves of Nicotiana benthamiana is accompanied by reduced vascular

152 plast phosphoglycerate kinase (chl-PGK) from Nicotiana benthamiana is one of the viral RNA binding pr

153 Nicotiana benthamiana leaf areas expressing basal resist

154 m tumefaciens-mediated protein expression in Nicotiana benthamiana leaf cells and site-specific mutag

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

156 a sub-pool of SRFR1 transiently expressed in Nicotiana benthamiana leaf cells localizes to the nucleu

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

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

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

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

161 aggregates when overexpressed transiently in Nicotiana benthamiana leaf epidermis cells.

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

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

164 Silencing of ISE1 in mature Nicotiana benthamiana leaves also leads to increased PD

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

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

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

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

169 Nicotiana benthamiana leaves display a visible plant cel

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

171 of immunofluorescence confocal microscopy to Nicotiana benthamiana leaves expressing replication-deri

172 Silencing ISE1 in Nicotiana benthamiana leaves increases the frequency of

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

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

175 Finally, silencing of DSE1 in Nicotiana benthamiana leaves leads to reduced movement o

176 constructs of B1 or B2 or B3 and CP mRNAs in Nicotiana benthamiana leaves resulted in packaging of TL

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

178 icroscopy analysis after agroinfiltration of Nicotiana benthamiana leaves showed that SN1-green fluor

179 nt protein-fused TGBp3 in epidermal cells of Nicotiana benthamiana leaves to study the TGBp3 intracel

180 ur pair-wise combinations and infiltrated to Nicotiana benthamiana leaves to systematically evaluate

181 Nicotiana benthamiana leaves were exposed to a sucking i

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

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

184 When transiently expressed in Nicotiana benthamiana leaves, full-length RPS5 protein t

185 ar import of a plant transcription factor in Nicotiana benthamiana leaves, indicating that excess AtN

186 In Nicotiana benthamiana leaves, SYMRK-yellow fluorescent p

187 Here, by agroinfiltrating Nicotiana benthamiana leaves, we show that brome mosaic

188 ically transactivated the SlTPS5 promoter in Nicotiana benthamiana leaves.

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

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

191 for Agrobacterium tumefaciens expression in Nicotiana benthamiana leaves.

192 om palisade mesophyll to spongy mesophyll in Nicotiana benthamiana leaves.

193 RNA accumulation in plant protoplasts and in Nicotiana benthamiana leaves.

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

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

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

197 greater extent than individual expression in Nicotiana benthamiana leaves.

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

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

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

201 Additionally, we have generated transgenic Nicotiana benthamiana lines that express fluorescent pro

202 Virus-induced gene silencing of the Nicotiana benthamiana myosin XI-2 gene, but not three ot

203 from model plants like Arabidopsis thaliana, Nicotiana benthamiana, N. tabacum, Lycopersicon esculent

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

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

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

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

208 Nicotiana benthamiana often displays more intense sympto

209 xtracted from purified membrane fractions of Nicotiana benthamiana or Arabidopsis thaliana.

210 sease Susceptibility 1 after coexpression in Nicotiana benthamiana or in yeast cells.

211 We show here that the solanaceous species Nicotiana benthamiana perceives the flagellin proteins o

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

213 n of anti-SEB antibodies was explored in the Nicotiana benthamiana plant expression system.

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

215 of epitope-tagged Bs2-expressing transgenic Nicotiana benthamiana plants and engineered strains of P

216 high levels within 8 days of infiltration in Nicotiana benthamiana plants and retained high-affinity

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

218 Transgenic Nicotiana benthamiana plants expressing Rs-cps dsRNA wer

219 patite) of extracts from healthy or infected Nicotiana benthamiana plants in combination with in vitr

220 Infection with Potato virus X (PVX) in Nicotiana benthamiana plants leads to increased transcri

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

222 criptome sequencing of Verticillium-infected Nicotiana benthamiana plants revealed only a single high

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

224 tive CaMV35S promoter for over-expression in Nicotiana benthamiana plants to study its effect on lepi

225 n multigram quantities after extraction from Nicotiana benthamiana plants transduced with a tobacco m

226 Nicotiana benthamiana plants treated with SA showed decr

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

228 BMV) were transiently expressed in leaves of Nicotiana benthamiana plants using engineered Agrobacter

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

230 Infection of Nicotiana benthamiana plants with such recombinant virus

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

232 o mutants were generated and inoculated onto Nicotiana benthamiana plants, to reveal that (i) they we

233 fragment (EPO-Fc) by transient expression in Nicotiana benthamiana plants.

234 e p1-5b CPm mutant genotype (agro-pR6-5b) in Nicotiana benthamiana plants.

235 ation (RdDM) in wild-type and RDR6-deficient Nicotiana benthamiana plants.

236 -R(ER) produced from plant-optimized cDNA in Nicotiana benthamiana plants.

237 ion in tobacco cells and during infection of Nicotiana benthamiana plants.

238 o Potato virus X for transient expression in Nicotiana benthamiana plants.

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

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

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

242 channel blocker impeded TBSV replication in Nicotiana benthamiana protoplasts or in whole plants.

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

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

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

246 polypeptide GalNAc-transferase in leaves of Nicotiana benthamiana resulted in GalNAc O-glycosylation

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

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

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

250 A Nicotiana benthamiana Sgt1 VIGS construct silencing both

251 hypersensitive cell death was suppressed in Nicotiana benthamiana silenced for expression of CRT1 ho

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

253 cco mosaic virus or potato X virus infecting Nicotiana benthamiana, stressing the general applicabili

254 all trigger a similar cell death response in Nicotiana benthamiana, suggesting an evolutionarily cons

255 PCD when transiently expressed in leaves of Nicotiana benthamiana, suggesting D1416 plays an importa

256 the coexpression of SPRYSEC-19 in leaves of Nicotiana benthamiana suppresses programmed cell death m

257 between replicase protein and CP using a FHV-Nicotiana benthamiana system.

258 ty in both tomato (Solanum lycopersicum) and Nicotiana benthamiana that degrades RIN4 and requires th

259 We confirm, using transient expression in Nicotiana benthamiana, that miR482 targets mRNAs for NBS

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

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

262 Upon transient expression in Nicotiana benthamiana, the TPS enzymes colocalize in ves

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

264 silencing (VIGS) has been used routinely in Nicotiana benthamiana to assess functions of candidate g

265 n RNA silencing system in the protoplasts of Nicotiana benthamiana to investigate the functions of vi

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

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

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

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

270 s also pathogenic on the model plant species Nicotiana benthamiana (tobacco).

271 66 target mimic and three solanaceous hosts: Nicotiana benthamiana, tobacco (N. tabacum), and tomato

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

273 In the plant virus model host Nicotiana benthamiana, Tomato bushy stunt virus (TBSV) P

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

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

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

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

278 form complexes with RPS2 in Arabidopsis and Nicotiana benthamiana using a pulldown assay and fluores

279 mutant plant, which contrasts to reports in Nicotiana benthamiana using virus-induced gene silencing

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

281 expression system using agroinfiltration of Nicotiana benthamiana was developed.

282 Growth of DC3000D28E in Nicotiana benthamiana was symptomless and 4 logs lower t

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

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

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

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

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

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

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

290 for functional analysis in which transgenic Nicotiana benthamiana were generated and screened for re

291 -length myosin cDNAs from the BYV host plant Nicotiana benthamiana were sequenced and shown to encode

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

293 green fluorescent protein (GFP) transgene in Nicotiana benthamiana when overexpressed from a Potato v

294 HaRxL96 suppresses immunity in Nicotiana benthamiana, whereas PsAvh163 induces an HR-li

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

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

297 i-mediated viral RNA degradation in infected Nicotiana benthamiana, while P19/75-78 is unable to prev

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

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

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