ライフサイエンスコーパス: Nicotiana benthamiana

1 in the cells of expanded leaves in tobacco (Nicotiana benthamiana).

2 sites on agroinfiltration of tobacco plants (Nicotiana benthamiana).

3 reduces recalcitrance in transgenic tobacco (Nicotiana benthamiana).

4 3IP conferred resistance to RSV infection in Nicotiana benthamiana.

5 onfer methylation of a transgene reporter in Nicotiana benthamiana.

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

7 ed with fluorescent protein and expressed in Nicotiana benthamiana.

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

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

10 era avenae and transiently expressed them in Nicotiana benthamiana.

11 N-glycosylated upon expression in transgenic Nicotiana benthamiana.

12 oactive NLRs when transiently coexpressed in Nicotiana benthamiana.

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

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

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

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

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

18 ke lamellae in both Arabidopsis thaliana and Nicotiana benthamiana.

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

20 g) VLPs and the model antigen GFP in vivo in Nicotiana benthamiana.

21 imeric clone into the laboratory model plant Nicotiana benthamiana.

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

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

24 of inducing cell death when overexpressed in Nicotiana benthamiana.

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

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

27 biosynthesis of MLG by overexpressing it in Nicotiana benthamiana.

28 of RPS5 using transient expression assays in Nicotiana benthamiana.

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

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

31 Agrobacterium tumefaciens infection assay in Nicotiana benthamiana.

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

33 aVCP when transiently expressed in leaves of Nicotiana benthamiana.

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

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

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

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

38 of viral RNA accumulation in agroinfiltrated Nicotiana benthamiana.

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

40 nsensitive DELLA alleles when coexpressed in Nicotiana benthamiana.

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

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

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

44 tive response when co-expressed with Pm1a in Nicotiana benthamiana.

45 gnaling domain when transiently expressed in Nicotiana benthamiana.

46 s effector XopJ4 was identified in the plant Nicotiana benthamiana.

47 ened for activity by transient expression in Nicotiana benthamiana.

48 rabidopsis accessions, and an nrg1 mutant in Nicotiana benthamiana.

49 essful reconstruction of MbA biosynthesis in Nicotiana benthamiana.

50 of specific PTI pathways in both potato and Nicotiana benthamiana.

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

52 ) independent of their enzymatic activity in Nicotiana benthamiana.

53 RX17 was examined by transient expression in Nicotiana benthamiana.

54 uce significant cell death when expressed in Nicotiana benthamiana.

55 were obtained after transient expression in Nicotiana benthamiana.

56 n as demonstrated by transient expression in Nicotiana benthamiana.

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

58 The recent discovery that GLRaV-3 can infect Nicotiana benthamiana, a plant model organism, makes new

59 n virus (CLCuMuV) V2 directly interacts with Nicotiana benthamiana AGO4 (NbAGO4) and that the L76S mu

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

61 Silencing of GCN4 in Nicotiana benthamiana and Arabidopsis thaliana compromis

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

63 y is transferable to the Solanaceous species Nicotiana benthamiana and cannot be substituted by AtEDS

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

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

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

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

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

69 tristeza virus (CTV) triggered ROS burst in Nicotiana benthamiana and in the natural citrus host, th

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

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

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

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

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

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

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

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

78 son with other UGTs in vegetative tissues of Nicotiana benthamiana and peppermint (Mentha x piperita)

79 owever, a functional Ptr1 ortholog exists in Nicotiana benthamiana and potato, and both mediate recog

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

81 small interfering RNA into the model plants Nicotiana benthamiana and tomato (Solanum lycopersicum).

82 of TurboID and miniTurbo in Arabidopsis and Nicotiana benthamiana and versatile vectors enable custo

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

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

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

86 ciates with heterologously expressed NFR5 in Nicotiana benthamiana, and directly binds and phosphoryl

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

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

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

90 encing suppression activity and infection in Nicotiana benthamiana, Arabidopsis and soybean.

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

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

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

94 Transient expression in Nicotiana benthamiana as well as functional complementat

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

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

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

98 Transient expression of both variants in Nicotiana benthamiana by agroinfiltration enhanced P. pa

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

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

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

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

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

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

105 when expressed in Xenopus laevis oocytes and Nicotiana benthamiana cells, Ma1 mediates a malate-depen

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

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

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

109 s interactor FRATAXIN (FH), when silenced in Nicotiana benthamiana, compromised nonhost resistance to

110 Transient expression in Nicotiana benthamiana confirmed involvement in TAG synth

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

112 otinylated proteins expressed transiently in Nicotiana benthamiana coupled to untargeted LC-MS to ide

113 ric IgA1, IgA2m(1), and IgA2m(2) variants in Nicotiana benthamiana DeltaXT/FT plants lacking the enzy

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

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

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

117 Ectopic, transient expression in Nicotiana benthamiana epidermal leaf cells demonstrated

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

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

120 AS) and Flavonoid 3_5 hydroxylase (C75A1) in Nicotiana benthamiana followed by efficacy analysis agai

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

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

123 iltration-based transient gene expression in Nicotiana benthamiana, functionality of the recombinant

124 onses in Marchantia and the model angiosperm Nicotiana benthamiana further reveal a shared set of ort

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

126 Nicotiana benthamiana has been extensively used as a mod

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

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

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

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

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

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

133 Our data reveal that Nicotiana benthamiana incorporates two different paralog

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

157 expression of the AtCCT1 catalytic domain in Nicotiana benthamiana leaves increased PC content, and S

158 Silencing ISE1 in Nicotiana benthamiana leaves increases the frequency of

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

160 -mediated transient expression of ShMYB78 in Nicotiana benthamiana leaves induced the ectopic deposit

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

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

163 Co-expression of SnRK1alpha with PAL in Nicotiana benthamiana leaves resulted in the severe atte

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

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

166 Here, we used heterologous expression in Nicotiana benthamiana leaves to identify a minimal set o

167 Nicotiana benthamiana leaves were exposed to a sucking i

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

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

170 In Nicotiana benthamiana leaves, SYMRK-yellow fluorescent p

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

172 ile puncta in L. japonicus root hairs and in Nicotiana benthamiana leaves.

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

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

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

176 greater extent than individual expression in Nicotiana benthamiana leaves.

177 ically transactivated the SlTPS5 promoter in Nicotiana benthamiana leaves.

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

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

180 for Agrobacterium tumefaciens expression in Nicotiana benthamiana leaves.

181 nduced by ShMYB78 heterologous expression in Nicotiana benthamiana leaves.

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

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

184 lized in the extracellular space of infected Nicotiana benthamiana leaves.

185 version of a Brassica napus MPK4 (BnMPK4) in Nicotiana benthamiana leaves.

186 nhance crocin accumulation when expressed in Nicotiana benthamiana leaves.plantcell;31/11/2789/FX1F1f

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

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

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

190 its use in transiently transformed tobacco (Nicotiana benthamiana) leaves.

191 encing of the WRKY25/22 orthologous genes in Nicotiana benthamiana led to a delay in programmed cell

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

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

194 Nicotiana benthamiana (Nb) is a natural null mutant carr

195 out transgene integration is accomplished in Nicotiana benthamiana (Nb), Eruca sativa (arugula), Trit

196 DS1 functions in the model Solanaceous plant Nicotiana benthamiana (Nb).

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

198 Silencing of Nicotiana benthamiana NbGPAT6a increased leaf susceptibi

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

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

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

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

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

204 wed the host range of MYMIV not to extend to Nicotiana benthamiana or tomato.

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

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

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

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

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

210 Transgenic Nicotiana benthamiana plants expressing Rs-cps dsRNA wer

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

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

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

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

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

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

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

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

219 Arabidopsis and Nicotiana benthamiana plants with reduced expression of

220 Infection of Nicotiana benthamiana plants with such recombinant virus

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

222 08 and 09) were expressed in glycoengineered Nicotiana benthamiana plants.

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

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

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

226 odify N-glycans upon transient expression in Nicotiana benthamiana plants.

227 display mutual exclusion/cross-protection in Nicotiana benthamiana plants.

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

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

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

231 ant-secreted beta-galactosidase 1 (BGAL1) of Nicotiana benthamiana promotes hydrolytic elicitor relea

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

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

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

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

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

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

238 Moreover, overexpression of PrCYP79D73 in Nicotiana benthamiana resulted in the emission of (E/Z)-

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

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

241 erologous expression in Escherichia coli and Nicotiana benthamiana showed that all five AADC/AAS gene

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

243 Furthermore, silencing of a Nicotiana benthamiana SKP1 ortholog leads to the destabi

244 enzymes in total) to N-formyldemecolcine in Nicotiana benthamiana starting from the amino acids phen

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

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

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

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

249 monas vesicatoria effector protein AvrBsT in Nicotiana benthamiana, suggesting that it may be a broad

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

251 lipid droplets is enhanced in the transient Nicotiana benthamiana system through ectopic production

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

253 y developed a transient expression system in Nicotiana benthamiana that allowed us to demonstrate tha

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

255 Here, we demonstrate in Nicotiana benthamiana that transient expression of the N

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

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

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

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

260 a sgRNA from a single virus-derived mRNA in Nicotiana benthamiana This vector yielded high levels of

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

262 st import assays and transient expression in Nicotiana benthamiana to address this.

263 d a luminescence-based AS reporter system in Nicotiana benthamiana to screen pathogen effectors modul

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

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

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

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

268 e ectopically expressed the OsPIP1;3 gene in Nicotiana benthamiana (tobacco).

269 66 target mimic and three solanaceous hosts: Nicotiana benthamiana, tobacco (N. tabacum), and tomato

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

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

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

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

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

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

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

277 tomato (Solanum lycopersicum cv 75 m82D) and Nicotiana benthamiana Using deep learning, we classified

278 Our goal is to metabolically engineer Nicotiana benthamiana using montbretia genes to achieve

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

280 expression system using agroinfiltration of Nicotiana benthamiana was developed.

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

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

283 osomal protein-encoding gene, RPL10 (QM), in Nicotiana benthamiana We analyzed the expression levels

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

285 ls of Arabidopsis (Arabidopsis thaliana) and Nicotiana benthamiana We present transient expression of

286 ll-free extracts, in yeast, and in the plant Nicotiana benthamiana We propose that there are major di

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

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

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

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

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

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 Q1 (recognition of XopQ 1), an NLR native to Nicotiana benthamiana with a Toll-like interleukin-1 rec

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