ライフサイエンスコーパス: two-hybrid assay

1 modulate its function, we performed a yeast two-hybrid assay.

2 , and the interaction was confirmed by yeast two-hybrid assay.

3 h FASN and (ii) NS3 interacts with FASN in a two-hybrid assay.

4 e combinations for binary interaction in the two-hybrid assay.

5 that interact with this region using a yeast two-hybrid assay.

6 th V(1) and V(0) subunits were identified by two-hybrid assay.

7 AG1 and other proteins by means of the yeast two-hybrid assay.

8 d is shown to bind Prp43p and Spp382p in the two-hybrid assay.

9 th multiple division proteins in a bacterial two-hybrid assay.

10 o p33 in vitro or in a split-ubiquitin-based two-hybrid assay.

11 lence HMRa and to interact with Orc1BAH in a two-hybrid assay.

12 teracts with both MEI-9 and ERCC1 in a yeast two-hybrid assay.

13 teracting protein(s) in apple, using a yeast two-hybrid assay.

14 d VirB2 and VirB5 were detected in the yeast two-hybrid assay.

15 confirmed that CgtA interacts with SpoT in a two-hybrid assay.

16 of the beta-catenin C terminus in the yeast two-hybrid assay.

17 barley aleurone and physically in the yeast-two-hybrid assay.

18 oprecipitation from HEK293 lysates and yeast two-hybrid assay.

19 lity to interact with Rab4A by using a yeast two-hybrid assay.

20 of yeast vacuolar proteins and in the yeast two-hybrid assay.

21 tigated by coimmunoprecipitation and a yeast two-hybrid assay.

22 teroid receptor coactivator-1 in a mammalian two-hybrid assay.

23 sing pure proteins in solution and the yeast two-hybrid assay.

24 py studies and subsequently confirmed by the two-hybrid assay.

25 subunits including Sgf29 and Spt7 in a yeast two-hybrid assay.

26 racting proteins were screened using a yeast two-hybrid assay.

27 at prevent DEPTOR binding to mTOR in a yeast-two-hybrid assay.

28 ith myocyte enhancer factor 2 in a mammalian two-hybrid assay.

29 sitive interaction with nucleolin in a yeast two-hybrid assay.

30 two polypeptides can be detected in a yeast two-hybrid assay.

31 proteins were identified by a modified yeast two-hybrid assay.

32 cursors was affected, as judged by the yeast two-hybrid assay.

33 ed for interaction with pre-22a in the yeast two-hybrid assay.

34 cally interact with WER and CPC in the yeast two-hybrid assay.

35 high-throughput, array-based, directed yeast two-hybrid assay.

36 ing proteins with GLP-1R by a membrane yeast two-hybrid assay.

37 was further confirmed by Co-IP and mammalian two-hybrid assay.

38 ck proteins, Hsp16.9 and Hsp17.5, in a yeast two-hybrid assay.

39 amK and the two proteins interact in a yeast two-hybrid assay.

40 -interacting proteins using a modified yeast two-hybrid assay.

41 with FeoB or FeoC was detected in the BACTH two-hybrid assay.

42 s DEAD-box helicase/ATPase LOS4 in the yeast two-hybrid assay.

43 e ESCRT-III-related proteins CHMP1A in yeast two hybrid assays.

44 ters, subcellular localization and bacterial two hybrid assays.

45 length protein in vivo, as measured by yeast-two hybrid assays.

46 h other mitochondrial MORF proteins in yeast two hybrid assays.

47 sactivator yeast two-hybrid or reverse yeast two-hybrid assays.

48 s Alix in both immunoprecipitation and yeast-two-hybrid assays.

49 immunoprecipitation, pulldown, and mammalian two-hybrid assays.

50 ) with activity levels measured in bacterial two-hybrid assays.

51 teract with other flavonoid enzymes in yeast two-hybrid assays.

52 with this, AGL61 and AGL80 interact in yeast two-hybrid assays.

53 tween Mst7 and Pmk1 is not observed in yeast two-hybrid assays.

54 inity for LEDGF in either pull-down or yeast two-hybrid assays.

55 pitate from the testis and interact in yeast two-hybrid assays.

56 and Hst 5 were tested by pull-down and yeast two-hybrid assays.

57 ts with Ras1, Ras2, Cdc42, and Mgb1 in yeast two-hybrid assays.

58 rotein (GCP)6, as a keratin partner in yeast two-hybrid assays.

59 EBNA2 and EBNA-LP were found with mammalian two-hybrid assays.

60 e pull-down, yeast two-hybrid, and mammalian two-hybrid assays.

61 was shown to ablate the Rad54 interaction in two-hybrid assays.

62 bind the other's cognate effectors in yeast two-hybrid assays.

63 ssary for inter-domain interactions in yeast two-hybrid assays.

64 and Bbp1p and the U2 snRNP protein Prp11p by two-hybrid assays.

65 the Rev nuclear export signal (NES) in yeast two-hybrid assays.

66 olishes this interaction, as determined with two-hybrid assays.

67 sing co-immunoprecipitation and in mammalian two-hybrid assays.

68 ned their impact on pRBR binding using yeast two-hybrid assays.

69 lutathione S-transferase pull-down and yeast two-hybrid assays.

70 cts with MBD2 and MBD3 in vitro and in yeast two-hybrid assays.

71 eciprocal coprecipitation experiments and by two-hybrid assays.

72 ammation by using pyrin as the bait in yeast two-hybrid assays.

73 and the meiotic Rhp51 homolog Dmc1 in yeast two-hybrid assays.

74 acts strongly with mosquito laminin in yeast-two-hybrid assays.

75 an interact with both TTI1 and TTI2 in yeast two-hybrid assays.

76 ptide aptamers for further analysis in yeast two-hybrid assays.

77 with UNC-116 kinesin-1 heavy chain in yeast two-hybrid assays.

78 g relatively little affected by ABA in yeast two-hybrid assays.

79 ies with coimmunoprecipitation and mammalian two-hybrid assays.

80 teracted with both Mst12 and Mata-1 in yeast two-hybrid assays.

81 Using a yeast two-hybrid assay, a protein inhibitor of activated STAT1

82 cted between PMK1 and MST7 or MST11 in yeast two-hybrid assays, a homolog of yeast STE50 in M. grisea

83 that abolished the interaction in the yeast two-hybrid assay also abolished capsid assembly in insec

84 PYL6 and MYC2 interact in yeast two hybrid assays and the interaction is enhanced in the

85 Using the yeast two-hybrid assay and a co-immunoprecipitation assay, we

86 Bacterial two-hybrid assay and accumulation of Gp0.6 only in MreB-

87 Using the yeast two-hybrid assay and affinity chromatography, we demonst

88 high-throughput techniques such as the yeast two-hybrid assay and affinity purification, as well as f

89 Srs2 interacts with Rad51 in the yeast two-hybrid assay and also in vitro.

90 A1 physically interacts with HFR1 in a yeast two-hybrid assay and an in vitro co-immunoprecipitation

91 ts, sigma NS interacts with mu NS in a yeast two-hybrid assay and by coimmunoprecipitation analysis.

92 he globular tail which was verified by yeast two-hybrid assay and by in vivo bimolecular fluorescence

93 Employing yeast two-hybrid assay and coimmunoprecipitation followed by m

94 ally interacts with NLBD using the mammalian two-hybrid assay and coimmunoprecipitation studies in MN

95 anion exchanger 1 (kAE1), detected by yeast two-hybrid assay and confirmed by immunoprecipitation an

96 A mammalian two-hybrid assay and confocal microscopy were used to de

97 By yeast two-hybrid assay and ELISAs using purified proteins, UNC

98 ptic clustering domain, we performed a yeast two-hybrid assay and found that this stargazin domain bi

99 We performed a yeast two-hybrid assay and identified hematopoietically expres

100 GE cytoplasmic domain as "bait" in the yeast two-hybrid assay and identified the formin homology (FH1

101 interact with Hsp90Ecin vivo in a bacterial two-hybrid assay and in vitro in a bio-layer interferome

102 e in ClpB interaction in vivo in a bacterial two-hybrid assay and in vitro in a fluorescence anisotro

103 ns also directly interact in vivo in a yeast two-hybrid assay and in vitro through ammonium sulfate c

104 s transcription factor prey library by yeast two-hybrid assay and isolated six class I members of the

105 Ialpha was therefore used as bait in a yeast two-hybrid assay and microtubule affinity regulating kin

106 Here we show, by using the yeast two-hybrid assay and the glutathione S-transferase pull-

107 Despite the routine use of the two-hybrid assay and the potential of three-hybrid syste

108 Both proteins interacted with DDB1 in yeast two-hybrid assays and associated with DDB1 and CUL4 in v

109 ABD1 directly interacts with ABI5 in yeast two-hybrid assays and associates with ABI5 in vivo by co

110 Erm and TTF-1 were demonstrated by mammalian two-hybrid assays and by co-immunoprecipitation assays.

111 of the p12 subunit were determined by yeast two-hybrid assays and by pulldown assays.

112 By yeast-two-hybrid assays and chromatin immunoprecipitation we d

113 Yeast two-hybrid assays and co-fractionation studies using rec

114 Two-hybrid assays and coimmunoprecipitation analyses dem

115 Yeast two-hybrid assays and coimmunoprecipitation experiments

116 and TMC1 or TMC2 was observed in both yeast two-hybrid assays and coimmunoprecipitation experiments.

117 o the blue-light photoreceptor FKF1 in yeast two-hybrid assays and delays flowering in Arabidopsis wh

118 Yeast two-hybrid assays and fluorescence resonance energy tran

119 Using both in vivo yeast two-hybrid assays and in vitro activity and binding assa

120 with beta-catenin was confirmed using yeast two-hybrid assays and in vitro synthesized proteins.

121 fects in vivo, ARC3 interacted with FtsZ2 in two-hybrid assays and inhibited FtsZ2 assembly in a hete

122 Mammalian two-hybrid assays and pull-down experiments demonstrated

123 Yeast two-hybrid assays and studies in HEK293 cells and primar

124 AcrB, in the absence of both AcrA and TolC, two-hybrid assays and suppressor mutations indicate that

125 reement with these observations, using yeast two-hybrid assays and TAP-tagged protein pull-down analy

126 (I)48 was initially examined using the yeast two-hybrid assay, and a TBP-binding domain was identifie

127 eric interactions were observed in the yeast two-hybrid assay, and Gpr4 was shown to physically inter

128 p, a subunit of mRNA decapping enzyme in the two-hybrid assay, and is enriched in cytoplasmic P bodie

129 h deletion analysis, co-immunoprecipitation, two-hybrid assay, and pulldown assays with expressed pro

130 cessary for the interaction with FeoB in the two-hybrid assay, and when either of these amino acids w

131 Light-scattering studies, yeast two-hybrid assays, and analytical ultracentrifugation me

132 ified as Oas1b interaction partners in yeast two-hybrid assays, and both in vitro-transcribed/transla

133 tion of pull-downs, mass spectrometry, yeast two-hybrid assays, and chemical genomics, we demonstrate

134 le LIM protein) did not interact with WT1 in two-hybrid assays, and WTIP did not interact with an unr

135 based on yeast two-hybrid screens, mammalian two-hybrid assays, and/or coimmunoprecipitation assays.

136 h the CAR ligand-binding domain in mammalian two-hybrid assays; and 5) disrupts CAR binding to the pr

137 reliminary experiments involving a bacterial two-hybrid assay are presented that corroborate the exis

138 ing yeast Smc5/6 complex employing the yeast two-hybrid assay as well as in vitro biochemical approac

139 ted using the GST pull-down assay, the yeast two-hybrid assay, as well as by coimmunoprecipitation.

140 Surprisingly, yeast two-hybrid assays, bimolecular fluorescence complementat

141 ructure was corroborated using the bacterial two-hybrid assay, biochemical characterization of the pu

142 unoprecipitation in vitro and in vivo, yeast two-hybrid assay, bioluminescence resonance energy trans

143 PKC alpha weakly interacted with 4V by yeast two-hybrid assays, but PKC alpha constructs that lack th

144 Based on bacterial two-hybrid assays, CelR homodimerizes but does not inter

145 TIP clone, which interacted with WTIP in the two-hybrid assay, co-localized with WT1 in nuclei, co-pr

146 Furthermore, mammalian two-hybrid assays, coimmunoprecipitation analyses, and b

147 The two-hybrid assay confirmed these findings and revealed t

148 ions with core exocyst subunits in the yeast two-hybrid assay, cytoplasmic localization, and genetic

149 We report two-hybrid assay data that support this model, and resul

150 irect association between Nab2 and Gfd1, and two-hybrid assays delineated Gfd1 binding to the N-termi

151 and both coimmunoprecipitation and mammalian two-hybrid assays demonstrate that TCDD induces interact

152 Finally, a yeast two-hybrid assay demonstrated that SCP-2 directly intera

153 A yeast two-hybrid assay demonstrated that the last 22 amino aci

154 Functional analyses by the yeast two-hybrid assay demonstrated that the p.140 delN mutati

155 Yeast two-hybrid assays detect interactions between the basola

156 In a bacterial two-hybrid assay, DnaK interacts with ClpB and with chim

157 that would occur with the traditional yeast two-hybrid assay due to the transactivating properties o

158 Yeast two-hybrid assays established a direct interaction of Ce

159 Yeast GAL4 two-hybrid assays established that both proteins contain

160 In yeast two-hybrid assays, FgMcm1 interacted with Mat1-1-1 and F

161 Here, using yeast two-hybrid assays followed by biochemical binding experi

162 were screened for function both in the yeast two-hybrid assay for interaction with VP19C and in a gen

163 Results from immunoprecipitation and a two-hybrid assay further indicated that Fliih directly i

164 Mammalian two-hybrid assay further indicates that the amino acids

165 ating enzyme, interacts with NOPO in a yeast two-hybrid assay; furthermore, ben-derived embryos arres

166 In two-hybrid assays, Ggamma13 interacted specifically with

167 esin light chain is demonstrated via a yeast two-hybrid assay, glutathione S-transferase pull down, a

168 nteracts with PIKfyve as determined by yeast two-hybrid assays, glutathione S-transferase (GST) pull-

169 The yeast two-hybrid assay has proven to be a powerful method to d

170 tion of protein-protein interactions through two-hybrid assays has revolutionized our understanding o

171 By using the yeast two-hybrid assay, here we identified HtrA2/Omi, a stress

172 genetic approaches exemplified by the yeast two-hybrid assay; however, neither assay works well for

173 Site-directed mutagenesis and yeast-two hybrid assays identified DnaA and DnaN binding sites

174 A yeast two-hybrid assay identified a novel, WT1-interacting pro

175 The yeast two-hybrid assay identified that proteasome subunit alph

176 pull-down, co-immunoprecipitation, and yeast two-hybrid assays identified a specific interaction betw

177 Yeast two-hybrid assays identified ETTIN (ETT, or AUXIN RESPON

178 Yeast two-hybrid assays identified the S10 region of the K(+)

179 xococcus xanthus was identified from a yeast two-hybrid assay in which MglA was used as bait.

180 By a combination of yeast-two hybrid assay, in vitro binding, and coimmunoprecipit

181 Using a combination of quantitative yeast two-hybrid assays, in planta co-localization studies, fl

182 Two-hybrid assays indicate that Ers1 also directly inter

183 Yeast two-hybrid assays indicate that these newly characterize

184 In vitro pull-down and yeast two-hybrid assays indicate that these splice variants ha

185 Yeast two-hybrid assays indicate weak interactions between MDH

186 Yeast two-hybrid assay indicated that the PDH45 protein intera

187 Bacterial two-hybrid assays indicated strong interactions of M. tu

188 Mammalian two-hybrid assays indicated that Ddx20 can interact with

189 Analysis of mutated proteins in yeast two-hybrid assays indicated that mutations that inactiva

190 Co-immunoprecipitation and two-hybrid assays indicated that RARgamma interacts with

191 cular fluorescence complementation and yeast-two-hybrid assays indicated that the IDR3 domain does no

192 Consistent with these findings, two-hybrid assays indicated that the Sir1 N terminus cou

193 with P. blakesleeanus Ras homologs in yeast two-hybrid assays, indicating that MadC is a regulator o

194 amily member periplakin, identified in yeast two-hybrid assays, interacted with a membrane-proximal d

195 on between Cdc13 and Est1, as monitored by a two-hybrid assay, is dependent on S255 but Tel1-independ

196 s) in human cells, termed mammalian-membrane two-hybrid assay (MaMTH).

197 In yeast two-hybrid assays, MAS2 interacted with splicing and rib

198 r each Chlamydomonas FDX; (b) pairwise yeast two-hybrid assays measuring FDX interactions with protei

199 Here, a yeast two-hybrid assay of LOX-PP-interacting proteins identifi

200 tinal insulin receptor (IRbeta) and used the two-hybrid assay of protein-protein interaction in the y

201 According to a yeast two-hybrid assay, ORRM1 interacts selectively with penta

202 In yeast-two hybrid assays, ORRM3 interacts with RIP1, ORRM2 and

203 The remarkable impact of two-hybrid assay platforms derives from their speed, sim

204 , a cDNA library was screened with the yeast two-hybrid assay, resulting in the identification of hea

205 from reporter transactivation and mammalian two-hybrid assays reveal that DEHP activates CAR2 at low

206 A yeast two-hybrid assay revealed a p204-cytoplasmic Ras protein

207 A yeast two-hybrid assay revealed an interaction between amino a

208 ted from a high-throughput screen of a yeast two-hybrid assay revealed interactions between sigma(54)

209 rminus of the alpha1-subunit using the yeast two-hybrid assay revealed that a distal C-terminal pepti

210 Yeast two-hybrid assay revealed that the N-terminal region of

211 Yeast two-hybrid assays revealed four-and-a-half LIM domain (F

212 Yeast two-hybrid assays revealed that GPC3 interacts with CD81

213 co-immunoprecipitation, pull-down, and yeast two-hybrid assays revealed that mXinalpha directly inter

214 Yeast two-hybrid assays revealed the formation of a ternary co

215 In yeast (Saccharomyces cerevisiae) two-hybrid assays, rice CBLs interact with the kinase pa

216 30 as an ARNT-interacting protein in a yeast two-hybrid assay screen.

217 Yeast two-hybrid assays show that FCL1 interacts with a subset

218 Furthermore, our yeast two-hybrid assays show that MoVps17 and MoVps5 can inter

219 Furthermore, results of the mammalian two-hybrid assay showed that cyclin-dependent kinase 3 (

220 Yeast two-hybrid assays showed that an N-terminal region of GR

221 Co-immunoprecipitation and mammalian two-hybrid assays showed that retinoschisin and the N-te

222 Additional yeast two-hybrid assays showed that the Gbeta(1) subunit also

223 immunoprecipitation, Far-Western assays, and two-hybrid assays showed that TIN2, but not POT1 or PIP1

224 tion between these two proteins in the yeast two-hybrid assay similarly failed to complement the grow

225 In mammalian two hybrid assays, Smad factors recruited the hybrid gen

226 Using a yeast two-hybrid assay, SOS2 interacted with the N terminus of

227 In yeast two-hybrid assays, stronger interactions between DRaf's

228 DLF1 in the yeast (Saccharomyces cerevisiae) two-hybrid assay strongly supports that ZCN8 plays an or

229 -seq and proteomics data together with yeast two-hybrid assays suggest that MS23 along with MS32, bHL

230 n experiments in transfected cells and yeast two-hybrid assays suggest that the C terminus of DFz2 in

231 Yeast two-hybrid assays suggested an interaction of Psb27 with

232 ocardin and SRF as determined by a mammalian two-hybrid assay, suggesting that Ang II-induced increas

233 fatty acid synthase II (FAS-II) in bacterial two-hybrid assays, suggesting essentiality may be linked

234 teracts with the other nucleoporins in yeast two-hybrid assays, suggesting that the proteins affect s

235 using a high-throughput version of the yeast two-hybrid assay that circumvents the difficulties in ex

236 We also show by yeast two-hybrid assay that MEIS proteins can interact with an

237 Bacterial two-hybrid assays that detected interaction between the

238 lyacrylamide gel electrophoresis and a yeast two-hybrid assay, the binding of copper was found to be

239 In a yeast two-hybrid assay, the thioredoxin-like domain of LTO1 in

240 In two-hybrid assays, the interaction of sigma(70) with eit

241 In direct two-hybrid assays, this portion of MAN1 bound to Smad2 a

242 n cross-linking protein filamin in the yeast two-hybrid assay through their highly conserved amino-te

243 otein fragment complement assay, and a yeast two-hybrid assay to analyze the protein-protein interact

244 of NUP98-HOXA9, we used a cytoplasmic yeast two-hybrid assay to avoid the nonspecific trans-activati

245 We used the yeast two-hybrid assay to determine that XPF interacts with th

246 In this study, we used a bacterial two-hybrid assay to identify cellular proteins that inte

247 tions on epithelial cells, we used the yeast two-hybrid assay to identify proteins that interact with

248 In the current studies, we used a yeast two-hybrid assay to identify ten amino acids in Axin tha

249 tially screened for interaction in the yeast two-hybrid assay to identify the domains important for t

250 Here, we have used the yeast two-hybrid assay to isolate molecular partners of harmon

251 In a mammalian two-hybrid assay to measure PR agonist-induced interacti

252 We used a yeast two-hybrid assay to screen for interactors of the golgin

253 on with other proteins, we performed a yeast two-hybrid assay to search for novel interactors of AnxA

254 Initial difficulties in getting the two-hybrid assay to work with full-length Oas1b led to t

255 rt that CEA binds TRAIL-R2 (DR5) directly in two-hybrid assays to decrease anoikis through the extrin

256 ass spectrometry, split-luciferase and yeast-two-hybrid assays to generate a single reliability score

257 we used membrane-based split ubiquitin yeast two-hybrid assays to identify novel GLP1R interactors in

258 Here, we carry out directional yeast two-hybrid assays to identify the interactions between t

259 Furthermore, we used yeast two-hybrid assays to show that DYT1 forms homodimers and

260 Here, we utilized insect two-hybrid assays to show that FTZ-F1 interacts with two

261 th, to interact with sigma(70) region 4 in a two-hybrid assay, to bind to sigma(70) in a native prote

262 d a human prostate cDNA library by the yeast two-hybrid assay using full-length MDM2 protein as the b

263 A yeast two-hybrid assay using IIp45 as bait identified HDAC6 pr

264 reened a kidney cDNA library through a yeast two-hybrid assay using NKCC2 C terminus as bait.

265 n the N-terminus of XPF by the reverse yeast two-hybrid assay using randomly mutagenized XPF.

266 Binary two-hybrid assays using DNA encoding this isoform as bai

267 We searched for such proteins by yeast two-hybrid assay, using GARP as a bait to screen a human

268 Here, a yeast two-hybrid assay was performed to identify FGFR1-binding

269 A yeast two-hybrid assay was used to identify putative OAT3-asso

270 The yeast two-hybrid assay was used to test for interactions betwe

271 interactions with corepressors in mammalian two-hybrid assays was unexpected.

272 By using the yeast two-hybrid assay we found that the ESCP tyrosine-based m

273 eptor-associated factor 2 (TRAF2) in a yeast two-hybrid assay, we demonstrate that Na interacts with

274 Using a modified version of the mammalian two-hybrid assay, we demonstrate that the interaction st

275 Using an E. coli two-hybrid assay, we do not detect an interaction betwee

276 Using the yeast two-hybrid assay, we found an interaction between CaM an

277 Using a yeast two-hybrid assay, we found that Prox1 strongly and speci

278 Using the above-mentioned two-hybrid assay, we found that zebrafish Tmc1 and Tmc2a

279 Using the yeast two-hybrid assay, we have identified ribosomal S6 kinase

280 Using the yeast two-hybrid assay, we have now identified the histone ace

281 Using a two-hybrid assay, we have shown that RocS1 interacts wit

282 Using a two-hybrid assay, we present evidence that FliX regulate

283 Using a yeast two-hybrid assay, we previously identified proliferating

284 Using yeast two-hybrid assays, we determined the interactions among

285 Using yeast two-hybrid assays, we have identified a Rev7-binding sur

286 By yeast two-hybrid assays, we have now demonstrated that Myosin

287 combination of immunoprecipitation and yeast two-hybrid assays, we identified a series of protein-pro

288 Using yeast two-hybrid assays, we identified Spermidine Synthase2 (S

289 By using yeast two-hybrid assays, we identified the carboxyl-terminal r

290 ons coupled with mass spectrometry and yeast two-hybrid assays, we show the Saccharomyces cerevisiae

291 Yeast-two hybrid assays were used to identify two new and inde

292 All interactions identified by yeast two-hybrid assays were confirmed by in vitro binding ass

293 Yeast two-hybrid assays were employed to identify important in

294 Drosophila S2 cell two-hybrid assays were used to describe a novel homotypi

295 Yeast two-hybrid assays were used to identify rice proteins in

296 und state failed to bind to AvrL567 in yeast two-hybrid assays, while binding was detected to the sig

297 moylation sites, and it interacts in a yeast two-hybrid assay with the UBC-9 and GEI-17 components of

298 All four proteins interacted in yeast two-hybrid assays with phragmoplastin, and showed differ

299 hb-21 and ESE1 are able to interact in yeast two-hybrid assays with the ABA responsive element bindin

300 In yeast two-hybrid assays ZYX-1 interacts with several known den