ライフサイエンスコーパス: yeast two-hybrid screen

1 ntified as a Bicoid-interacting protein in a yeast two-hybrid screen.

2 n interacting protein of LYRIC/AEG through a yeast two-hybrid screen.

3 IA gamma) as a Runx2-interacting factor in a yeast two-hybrid screen.

4 inin-2 was found to associate with eNOS in a yeast two-hybrid screen.

5 tein-protein interaction data from a focused yeast two-hybrid screen.

6 putative OGT-interacting proteins through a yeast two-hybrid screen.

7 interaction partner for Ku in a genome-wide yeast two-hybrid screen.

8 inding protein (MTBP) was identified using a yeast two-hybrid screen.

9 DUS2 as a protein interacting with PACT in a yeast two-hybrid screen.

10 to be an hZimp10 interacting protein in the yeast two-hybrid screen.

11 artner of the beta6 cytoplasmic tail using a yeast two-hybrid screen.

12 bait, we isolated clathrin light chain in a yeast two-hybrid screen.

13 e phosphatase named DUSP26 identified from a yeast two-hybrid screen.

14 as a binding partner for Kidins220/ARMS by a yeast two-hybrid screen.

15 t of the AP2 complex and PIPKIgamma661 via a yeast two-hybrid screen.

16 tial interacting proteins were identified by yeast two-hybrid screen.

17 ct interaction with NudE, as determined by a yeast two-hybrid screen.

18 uman teneurin-1 ICD interaction partner in a yeast two-hybrid screen.

19 o identify Wor1-interacting proteins using a yeast two-hybrid screen.

20 arity, we performed a comprehensive pairwise yeast two-hybrid screen.

21 protein was identified by a Split-Ubiquitin Yeast-Two-Hybrid screen.

22 eracts with three different Cys proteases in yeast two-hybrid screens.

23 nerated through subtractive hybridization or yeast two-hybrid screens.

24 ently available was generated by large-scale yeast two-hybrid screens.

25 e family, as a LOX-interacting partner using yeast two-hybrid screens.

26 l hIP-interacting protein in two independent yeast two-hybrid screens.

27 revious results from electron microscopy and yeast two-hybrid screens.

28 nesulfonate suppressor mutants and performed yeast-two-hybrid screens.

29 P-1L, that was found to bind to Hsf1 through yeast two-hybrid screening.

30 ansformation efficiency is critical, such as yeast two-hybrid screening.

31 t identified as a binding protein of AKT2 by yeast two-hybrid screening.

32 ding partner of the E2 protein of CSFV using yeast two-hybrid screening.

33 oform of thromboxane A2 receptor (TPbeta) by yeast two-hybrid screening.

34 n family, as a TIMP-1 interacting protein by yeast two-hybrid screening.

35 tion, was shown to interact with maspin in a yeast two-hybrid screening.

36 of the human kappa opioid receptor (hKOR) by yeast two-hybrid screening.

37 proteins that can interact with JSRV Env by yeast two-hybrid screening.

38 identified as a Vav3 interacting protein by yeast two-hybrid screening.

39 Aedes CYC as a MET-interacting protein using yeast two-hybrid screening.

40 utative interacting partner of NLRC3 through yeast two-hybrid screening.

41 of the HIV-1 replication cycle, we performed yeast two-hybrid screening against a human cDNA library

42 tein targets in the host cells, we performed yeast two-hybrid screens, allowing us to find 48 high-co

43 Inhibitor of Apoptosis Protein (XIAP), using yeast two-hybrid screening analyses.

44 y SUT-2 interacting proteins, we conducted a yeast two hybrid screen and found SUT-2 binds to ZYG-12,

45 esin-1 light chain KLC-2, as identified in a yeast two-hybrid screen and confirmed by in vitro assays

46 activating transcription factor (ATF) 4 in a yeast two-hybrid screen and confirmed their interaction

47 ha-interacting protein in this study using a yeast two-hybrid screen and GST pull-down assays.

48 ed with F(o)F(1) ATP synthase subunit 6 by a yeast two-hybrid screen and had strong antiapoptotic eff

49 In the present study, we used a yeast two-hybrid screen and identified a novel interacti

50 f human CD161 (NKR-P1A), we have conducted a yeast two-hybrid screen and identified acid sphingomyeli

51 e the mechanism of action of KAI1, we used a yeast two-hybrid screen and identified an endothelial ce

52 Furthermore, we performed a yeast two-hybrid screen and identified carboxypeptidase

53 BBX32 regulation, we performed a large-scale yeast two-hybrid screen and identified CONSTANS-LIKE 3 (

54 We performed a yeast two-hybrid screen and identified the adaptor prote

55 tify host targets of AvrPtoB, we performed a yeast two-hybrid screen and identified tomato ubiquitin

56 as an interacting partner of SIS8 based on a yeast two-hybrid screen and in planta bimolecular fluore

57 direct interacting factor for Kbtbd5 using a yeast two-hybrid screen and in vitro binding assays.

58 1 (PDZD11) as a new interactor of PLEKHA7 by yeast two-hybrid screening and by mass spectrometry anal

59 Using yeast two-hybrid screening and co-immunoprecipitation as

60 In this report, we performed a yeast two-hybrid screening and discovered that Nod1 inte

61 d protein required for ATM activation-1), by yeast two-hybrid screening and found that BAAT1 also bin

62 ell proteins in Vpu function, we carried out yeast two-hybrid screening and identified a previously r

63 th the lambda-isoform 14-3-3 protein both in yeast two-hybrid screening and in an in vitro pull-down

64 Yeast two-hybrid screening and in vitro and in vivo anal

65 Using a combination of yeast two-hybrid screens and biochemical analyses, we re

66 G signaling pathway components, we performed yeast two-hybrid screens and identified the muscle-speci

67 ein ensemble in the centrosome, we performed yeast two-hybrid screens and isolated a number of Su48-i

68 identify host targets of AVR1, we performed yeast two-hybrid screens and selected Sec5 as a candidat

69 its mechanism of action, we have employed a yeast-two-hybrid screen and identified serine protease H

70 stone H1.2 as a DME-interacting protein in a yeast two-hybrid screen, and confirmation of their inter

71 entified as a putative cofactor of Jarid2 by yeast two-hybrid screening, and the physical interaction

72 Bam35 proteins determined using multivector yeast two-hybrid screening, and these PPIs were further

73 ify TRPV4-interacting proteins by performing yeast two-hybrid screens, and we isolated with the avian

74 In this study, using a yeast two-hybrid screen approach, we identified the NF-Y

75 Using a yeast two-hybrid screening approach, we identified 14-3-

76 Yeast two-hybrid screens are an important method to map

77 TRN-SR2 was originally identified in a yeast two-hybrid screen as an interaction partner of HIV

78 aCC1)) did not disrupt direct interaction in yeast two-hybrid screens but did prevent association by

79 We performed a yeast two-hybrid screen by using the NH(2) terminus of P

80 roteins were identified and characterized by yeast two-hybrid screen, co-affinity purification and RN

81 ligase, as an interacting protein of KLF5 by yeast two-hybrid screen, coimmunoprecipitation, and indi

82 Yeast two-hybrid screening combined with bimolecular flu

83 Using yeast two-hybrid screening coupled with a candidate appr

84 lian RSP3 to bind to the MAPK ERK2 through a yeast two-hybrid screen designed to identify interacting

85 accharomyces cerevisiae genome SPA increases yeast two-hybrid screening efficiency by an order of mag

86 A yeast two-hybrid screen first suggested a direct interac

87 Using yeast-two hybrid screening followed by co-immunoprecipit

88 Using a yeast two-hybrid screen, followed by a series of coimmun

89 O Domain Containing Protein, HvELMOD_C, in a yeast two hybrid screen for proteins interacting with Hv

90 In a yeast two-hybrid screen for binding partners of RAB-10 w

91 We performed a yeast two-hybrid screen for HMGA1-interacting proteins a

92 Migfilin, originally identified in a yeast two-hybrid screen for kindlin-2-interacting protei

93 We performed a yeast two-hybrid screen for novel cofactors, and identif

94 In a yeast two-hybrid screen for TAN1-interacting proteins, a

95 On the basis of a yeast two-hybrid screen for the MT1-MMP cytoplasmic tail

96 Yeast two-hybrid screening for CIB1-interacting partners

97 We isolated Myosin Vc in a yeast two-hybrid screening for proteins that interact wi

98 pa can physically interact with ubiquitin by yeast two-hybrid screening, glutathione S-transferase pu

99 A yeast two-hybrid screen has identified the adaptor prote

100 A yeast two-hybrid screen has revealed that the transcript

101 Major advances in large-scale yeast two-hybrid screening have provided a global view o

102 A yeast two-hybrid screen identified a novel UBX-containin

103 A yeast two-hybrid screen identified an interaction of the

104 A yeast two-hybrid screen identified Arabidopsis pectin me

105 The yeast two-hybrid screen identified MOG1 as a new protein

106 A yeast two-hybrid screen identified mu2 as a putative int

107 In this study, a yeast two-hybrid screen identified PC2, a component of t

108 After a yeast two-hybrid screen identified prosaposin as a poten

109 A yeast two-hybrid screen identified SEM-5 as able to inte

110 Yeast two-hybrid screening identified a number of DNA bi

111 Yeast two-hybrid screening identified a number of secret

112 Yeast two-hybrid screening identified an interaction bet

113 Yeast two-hybrid screening identified Isl1, a LIM/homeod

114 Subsequent yeast two-hybrid screening identified PIAS3 (protein inh

115 Yeast-two-hybrid screens identify RhoC as a Fam65b bindi

116 ort, we present data from the following: (a) yeast two-hybrid screens, identifying interaction partne

117 t to remedy this situation, a combination of yeast two-hybrid screens, in vitro binding assays and ce

118 Yeast two-hybrid screening indicated that XERICO interac

119 A yeast two-hybrid screen led to the identification of the

120 Using a yeast two-hybrid screen, mass spectrometry, coimmunoprec

121 o identify Nde1-interacting molecules by the yeast two-hybrid screening method.

122 eins that interact with KLF5, we performed a yeast two-hybrid screen of a 17-day mouse embryo cDNA li

123 Through a yeast two-hybrid screen of a cDNA library made from tiss

124 To explore this possibility, we used a yeast two-hybrid screen of a human cDNA library with p35

125 A yeast two-hybrid screen of a human cDNA library yielded

126 ve used the N terminus of AC8 as a bait in a yeast two-hybrid screen of a human embryonic kidney (HEK

127 Using a yeast two-hybrid screen of a human kidney cDNA library w

128 understand the cellular function of ERK8, a yeast two-hybrid screen of a human lung library was perf

129 A yeast two-hybrid screen of a human placenta cDNA library

130 -residue N-terminal domain, we carried out a yeast two-hybrid screen of a mouse brain cDNA library.

131 Filamin A was identified in a yeast two-hybrid screen of a neuronal transcriptome usin

132 e N-terminal domain of TGMV AL1 as bait in a yeast two-hybrid screen of a random peptide aptamer libr

133 issect the STARS/SRF pathway, we performed a yeast two-hybrid screen of a skeletal muscle cDNA librar

134 To that end, we report a yeast two-hybrid screen of all human Rabs for myosin Va-

135 CDH23-interacting proteins, a membrane-based yeast two-hybrid screen of an outer hair cell (OHC) cDNA

136 ntified as an Mst1-interacting protein, in a yeast two-hybrid screen of human adult prostate cDNA lib

137 In a yeast two-hybrid screen of mouse brain cDNA library, usi

138 We performed a yeast two-hybrid screen of pollen cDNAs using sequences

139 ography followed by mass spectrometry and by yeast two-hybrid screening of a bovine retina cDNA libra

140 A yeast two-hybrid screening of a cDNA library made from t

141 From yeast two-hybrid screening of a human embryonic stem cel

142 Here we report that yeast two-hybrid screening of a human fetal brain cDNA l

143 Using yeast two-hybrid screening of a human kidney cDNA librar

144 Yeast two-hybrid screening of a human testis cDNA librar

145 Using yeast two-hybrid screening of a human thymus cDNA librar

146 Yeast two-hybrid screening of a mammary gland cDNA libra

147 nuclear roles of delta-catenin, we performed yeast two-hybrid screening of a mouse brain cDNA library

148 Through a yeast two-hybrid screening of adult human heart cDNA lib

149 To address this, we performed yeast two-hybrid screening of PRMT7 and identified argin

150 Furthermore, yeast two-hybrid screening of the accessory Sec system r

151 Here we performed yeast two-hybrid screens of 3,305 baits against 3,606 pr

152 IC-directed assembly of TFIIIB, we conducted yeast two-hybrid screens of Brf1 peptide libraries again

153 otein-protein interactions using a stringent yeast two-hybrid screen; of 75 pairs tested, 83% of the

154 surface plasmon resonance spectroscopy, NMR, yeast two-hybrid screens, peptide tagging combined with

155 A yeast two-hybrid screen performed with the C-terminal 17

156 During our yeast two-hybrid screening, PP2calpha was pulled out by

157 Here, large-scale yeast two-hybrid screens repeatedly identified a surpris

158 Proteomics analysis and yeast two-hybrid screening reveal that Miz1 is a JNK-ass

159 Our yeast two-hybrid screen revealed CARP-1 binding with the

160 A yeast two-hybrid screen revealed that HP1 interacts with

161 Here, a yeast two-hybrid screen revealed that RABV P interacts w

162 A yeast two-hybrid screening revealed a specific interacti

163 Yeast two-hybrid screens revealed several RNA-binding pr

164 Yeast two-hybrid screens revealed that CEFIP interacts w

165 Yeast two-hybrid screens revealed that the cytoplasmic p

166 A yeast-two-hybrid screen revealed that the mutant protein

167 In a yeast two-hybrid screen, SCNM1 interacted with LUC7L2, a

168 cting proteins, we used a recently developed yeast two-hybrid screen (split ubiquitin method) to dete

169 Yeast two-hybrid screens suggested that lysyl-tRNA synth

170 Yeast two-hybrid screening suggests that XB130 interacts

171 Using a split-ubiquitin yeast two-hybrid screen that covers a test-space of 6.4

172 fy key amino acid residues on PXR based on a yeast two-hybrid screen that examined mutant forms of PX

173 ursor, proRTD1a, into a bait construct for a yeast two-hybrid screen that identified rhesus macaque s

174 of SATB1 in cellular events, we performed a yeast two-hybrid screen that identified SUMO-1, Ubc9, an

175 able N-terminal subdomain that was used in a yeast two-hybrid screen that identified the proline-rich

176 We have previously shown through a yeast two-hybrid screen that it is also a cardiac bindin

177 In a yeast two-hybrid screen that used the C-terminal cytopla

178 We first discovered by yeast two-hybrid screening that the C termini of ENaC al

179 minal head domain of golgin-160 as bait in a yeast two-hybrid screen, the postsynaptic density-95/Dis

180 Through a yeast two-hybrid screen, the Src homology 3 domains of t

181 I5-interacting proteins were identified by a yeast two-hybrid screen; the most prevalent interactors

182 transcription factor that was isolated in a yeast two-hybrid screen through its binding property to

183 In the current study, by using yeast two-hybrid screening, Tip60 was identified as a KL

184 We conducted a yeast two hybrid screen to identify SUT-1 binding partne

185 interacting proteins were identified using a yeast two-hybrid screen to functionally characterize the

186 n this study, we performed a high throughput yeast two-hybrid screen to identify additional pathways

187 In this study, we conducted a yeast two-hybrid screen to identify molecules that physi

188 derstanding of MTM1 function, we conducted a yeast two-hybrid screen to identify MTM1-interacting pro

189 In this study, we have used a yeast two-hybrid screen to identify novel binding partne

190 Here we use a yeast two-hybrid screen to identify potential binding pa

191 O promotes genomic stability by performing a yeast two-hybrid screen to identify potential substrates

192 We have now used a yeast two-hybrid screen to identify proteins that bind t

193 We used a yeast two-hybrid screen to identify putative interacting

194 We used a yeast two-hybrid screen to identify the plant SnRK1 (for

195 e molecular functions of FTO, we performed a yeast two-hybrid screen to identify the protein(s) that

196 We initially used a yeast two-hybrid screen to look for an interaction betwe

197 rugs in prostate cancer cells, we employed a yeast two-hybrid screening to identify cellular proteins

198 We used yeast two-hybrid screening to identify MAGI-2 (membrane

199 uences differentiation of neurons, we used a yeast two-hybrid screening to search for new binding par

200 We conducted a series of yeast two-hybrid screens to identify proteins interactin

201 We carried out a yeast two-hybrid screen using a BRCA1 bait composed of a

202 pecially abundant in retina, was fished with yeast two-hybrid screen using a constitutively active Ga

203 A yeast two-hybrid screen using a library from human mamma

204 novel TDP-43 protein interactors found in a yeast two-hybrid screen using an adult human brain cDNA

205 In a yeast two-hybrid screen using Arabidopsis SKD1 as bait,

206 A yeast two-hybrid screen using ATBS1 as bait discovered f

207 ein interactions, we performed a large-scale yeast two-hybrid screen using both wild-type (WT) and si

208 We have now performed a yeast two-hybrid screen using dysbindin as bait against

209 molecular partners of MIG-10, we conducted a yeast two-hybrid screen using isoform MIG-10A as bait an

210 s of the alpha1D-adrenergic receptor (AR), a yeast two-hybrid screen using the alpha1D-AR C terminus

211 protein that interacts with C kinase) from a yeast two-hybrid screen using the amino terminus of PKCb

212 ciated protein YejK, which was detected in a yeast two-hybrid screen using the ParE subunit of topois

213 eins that may remove the CRD, we performed a yeast two-hybrid screen using twitchin kinase as bait.

214 Yeast two-hybrid screening using a portion of UNC-89 inc

215 Yeast two-hybrid screening using libraries prepared from

216 tify PIF1-interacting proteins, we performed yeast two-hybrid screening using PIF1 as a bait and iden

217 nant polycystic kidney disease, we performed yeast two-hybrid screens using the C-terminus of polycys

218 receptor-protein interactions, we conducted yeast two-hybrid screens using the cytosolic domains of

219 Prp40 was found to be a centrin target by yeast-two-hybrid screening using both Homo sapiens centr

220 egulators during development, we performed a yeast two-hybrid screen, using Ap2delta's TAD.

221 A yeast two-hybrid screen, using the carboxyl tail of the

222 A yeast two-hybrid screen was carried out using yjbH as ba

223 address the function of DJ-1 in prostate, a yeast two-hybrid screen was done to identify novel DJ-1

224 n EF-1alpha and other cellular components, a yeast two-hybrid screen was performed for the archaeon M

225 1/2/4-mediated transcriptional repression, a yeast two-hybrid screen was performed that identified p6

226 n regulation of the RPW8 protein function, a yeast two-hybrid screen was performed using RPW8.2 as ba

227 stand the biological function of ADAMTS-1, a yeast two-hybrid screen was performed using the carboxyl

228 es toward disease lesions, a Sos-recruitment yeast two-hybrid screen was performed with human Ckidelt

229 ht influence its subcellular localization, a yeast two-hybrid screen was performed.

230 signaling events underlying this process, a yeast-two hybrid screen was performed on the C terminus

231 ind protein interaction partners of NBP35, a yeast-two-hybrid screen was carried out that identified

232 Through the yeast two-hybrid screen we have identified dynamin-2 as

233 In addition, using yeast two-hybrid screens we identified several candidate

234 Using an MCF-7 cell cDNA library in a yeast two-hybrid screen, we cloned a factor that mediate

235 Using a yeast two-hybrid screen, we discovered an interaction be

236 Using a directed yeast two-hybrid screen, we found several novel and prev

237 Using a yeast two-hybrid screen, we found that SNIP1 (Smad nucle

238 Using a yeast two-hybrid screen, we found that splice cassette I

239 Here, using the yeast two-hybrid screen, we have discovered a novel SSTK

240 Using a yeast two-hybrid screen, we have found that Def-6, a gua

241 Using ERalpha as bait in a yeast two-hybrid screen, we have identified a novel ERal

242 Employing C2GnT1 CT as the bait to perform a yeast two-hybrid screen, we have identified Golgi phosph

243 In a yeast two-hybrid screen, we have identified TSG101 as a

244 Through a yeast two-hybrid screen, we have identified XPLN (exchan

245 Using a yeast two-hybrid screen, we identified a novel protein,

246 Using a yeast two-hybrid screen, we identified a novel transcrip

247 Using a yeast two-hybrid screen, we identified a RING domain ubi

248 Using a yeast two-hybrid screen, we identified an interaction be

249 Using a yeast two-hybrid screen, we identified an interaction be

250 Using a yeast two-hybrid screen, we identified Bicaudal D1 (BicD

251 Using a yeast two-hybrid screen, we identified cAMP-dependent pr

252 for potential regulators of Smad3 through a yeast two-hybrid screen, we identified casein kinase 1 g

253 Using a yeast two-hybrid screen, we identified cyclin L2 as a DC

254 Using a yeast two-hybrid screen, we identified dynein light chai

255 Using a yeast two-hybrid screen, we identified espin, an actin-b

256 Using a yeast two-hybrid screen, we identified four cytoskeletal

257 By using a yeast two-hybrid screen, we identified HRS as a novel PE

258 Using a yeast two-hybrid screen, we identified integrin-linked k

259 By using a yeast two-hybrid screen, we identified MEA and a related

260 Using a yeast two-hybrid screen, we identified PELP1 as a novel

261 Using a yeast two-hybrid screen, we identified the anti-apoptoti

262 From a yeast two-hybrid screen, we identified the cellular prot

263 Using a yeast two-hybrid screen, we identified the hematopoietic

264 Using a yeast two-hybrid screen, we identified the human homolog

265 Furthermore, using a yeast two-hybrid screen, we identified the motor protein

266 Using a yeast two-hybrid screen, we identify a novel interaction

267 Using a yeast two-hybrid screen, we identify Hook2, a linker pro

268 Using a yeast two-hybrid screen, we searched for novel AIRE-inte

269 Using a yeast two-hybrid screen, we show that RBBP6 interacts wi

270 Using a yeast two-hybrid screening, we found an interaction of t

271 Using a yeast two-hybrid screening, we found that the Pkd2L1 N t

272 By yeast two-hybrid screening, we found three novel interac

273 Using a yeast two-hybrid screening, we identified a novel gene f

274 By yeast two-hybrid screening, we identified as a galectin-

275 Through a yeast two-hybrid screening, we identified Notch3 as a ca

276 By yeast two-hybrid screening, we identified the E3 ubiquit

277 By yeast two-hybrid screening, we identified the Polycomb-l

278 Through yeast two-hybrid screening, we identified tumor suppress

279 Through yeast two-hybrid screening, we identify the centrosomal

280 Using unbiased yeast two-hybrid screens, we here identify a direct inte

281 Using a plant Rho GTPase (ROP1) as bait in yeast two-hybrid screens, we identified a family of Rho

282 Using STK38 as bait in yeast-two-hybrid screens, we discovered STK38 as a novel

283 he competency of Gal4-based baits prior to a yeast two-hybrid screen, which allows determination of w

284 We performed a yeast two hybrid screen with SR34 as bait and discovered

285 used the WFS1-C-terminal domain as bait in a yeast two-hybrid screen with a human brain cDNA library.

286 Here, we performed a yeast two-hybrid screen with calcineurin B as bait, whic

287 te genes causing neutropenia, we performed a yeast two-hybrid screen with Gfi1.

288 A yeast two-hybrid screen with HeLa cell lysates revealed

289 We used a yeast two-hybrid screen with myocardin as bait to search

290 In a yeast two-hybrid screen with pericentrin we identified c

291 Using a yeast two-hybrid screen with POSH (plenty of SH3 domains

292 cal roles of these enzymes, we carried out a yeast two-hybrid screen with the class III E2, UbcM2.

293 WD-repeat protein SWAN-1 was identified in a yeast two-hybrid screen with the LIM domains of the Rac

294 SPBB1 was identified through yeast two-hybrid screening with the kinase-dead TbPLK as

295 gulating neutrophil production, we conducted yeast two-hybrid screens with Gfi1 and neutrophil elasta

296 (JNK-interacting leucine zipper protein) in yeast-two hybrid screens with the phosphoinositide kinas

297 A yeast-two-hybrid screen with CPRabA5e as bait revealed 1

298 We used a yeast two-hybrid screen, with myocardin as bait in a sea

299 We performed a yeast two-hybrid screen (Y2H) to search for proteins tha

300 st protein-protein interactions (PPIs) using yeast two-hybrid screening (Y2H).