ライフサイエンスコーパス: yeast two-hybrid screening

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

2 ify BAFF-R-associated downstream proteins by yeast two-hybrid screening.

3 in called GTRAP3-18 has been identified by a yeast two-hybrid screening.

4 main of EphB1 by using Grb7 as a "bait" in a yeast two-hybrid screening.

5 ed the cytoplasmic region of EGFR as bait in yeast two-hybrid screening.

6 we searched pVHL-interacting proteins using yeast two-hybrid screening.

7 1 (ASK1) as a CDC25A-interacting protein by yeast two-hybrid screening.

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

9 yrosine kinase (RPTK) interacting protein by yeast two-hybrid screening.

10 Rit, we searched for Rit-binding proteins by yeast two-hybrid screening.

11 n (CP) of turnip crinkle virus (TCV) through yeast two-hybrid screening.

12 and-binding domain of PPARgamma as bait in a yeast two-hybrid screening.

13 he Fanconi anemia group C protein (FANCC) by yeast two-hybrid screening.

14 s, we searched for Rap1b-binding proteins by yeast two-hybrid screening.

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

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

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

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

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

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

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

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

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

24 we identified an Akt interaction protein by yeast two-hybrid screening.

25 vation and signal transduction, we performed yeast two-hybrid screening.

26 identified as an IRIP-interacting protein in yeast two-hybrid screening.

27 he second leucine zipper domain of JLP using yeast two-hybrid screening.

28 as an interactive partner of G alpha12 using yeast two-hybrid screening.

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

30 omain of phytochrome A (PhyA) as the bait in yeast two-hybrid screening.

31 of estrogen receptor (ER) alpha was used in yeast two-hybrid screenings.

32 -terminus of ERalpha (E/F domain) as bait in yeast two-hybrid screenings.

33 We have identified through yeast two-hybrid screening a novel protein, periphilin,

34 P/TAK1/JNK1 signaling pathway we isolated by yeast two-hybrid screening a novel X chromosome-linked I

35 Here we use a combination of yeast two-hybrid screening, a high copy suppressor selec

36 By yeast two-hybrid screening, a novel protein termed guany

37 By yeast two-hybrid screening, a specific interaction was i

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

39 We used a yeast two-hybrid screening, an in vitro biochemical meth

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

41 1 (PDZD11) as a new interactor of PLEKHA7 by yeast two-hybrid screening and by mass spectrometry anal

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

43 Through yeast two-hybrid screening and co-immunoprecipitation as

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

45 ify Mcl-1-interacting proteins, we performed yeast two-hybrid screening and found cDNAs encoding tank

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

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

48 (ERalpha) transcriptional activity, we used yeast two-hybrid screening and identified protein argini

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

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

51 he copine target proteins were identified by yeast two-hybrid screening and the interactions were ver

52 We show here, by yeast two-hybrid screenings and biochemical assays, that

53 was identified to interact with LNA through yeast two-hybrid screening, and confirmed by a glutathio

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

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

56 etermine the function(s) of OVCA1, we used a yeast two-hybrid screening approach to identify OVCA1-as

57 and the functions and regulation of HDAC1, a yeast two-hybrid screening approach was chosen to identi

58 Using a yeast two-hybrid screening approach, we cloned a 3-kb cD

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

60 Using in vitro mutagenesis and a yeast two-hybrid screening assay, we have isolated a mut

61 Results obtained from yeast two-hybrid screening, blot overlay binding assays,

62 njugation pathway is regulated, we performed yeast two-hybrid screening by using NEDD8 as a bait and

63 with the Notch4 ligand binding domain, using yeast two-hybrid screening, coimmunoprecipitation, and c

64 Yeast two-hybrid screening combined with bimolecular flu

65 Results obtained from yeast two-hybrid screening, cotransfections, and coimmun

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

67 Yeast two-hybrid screening detected an interaction betwe

68 enerated random TCL1 library combined with a yeast two-hybrid screening detecting loss of interaction

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

70 lated from a mouse embryonic cDNA library in yeast two-hybrid screening experiments by using the liga

71 Using a yeast two-hybrid screening followed by mammalian cell an

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

73 Yeast two-hybrid screening for CIB1-interacting partners

74 HIP1 is a 116-kD protein recently cloned by yeast two-hybrid screening for proteins that interact wi

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

76 Through a yeast two-hybrid screening for the effectors of Etk, a n

77 d as a GF14(lambda)-interacting protein in a yeast two-hybrid screening (GF14(lambda) is a 14-3-3 pro

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

79 Yeast two-hybrid screening has led to the identification

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

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

82 Yeast two-hybrid screening identified a number of secret

83 Yeast two-hybrid screening identified an interaction bet

84 Using the GATA-3-Nf as a bait, our yeast two-hybrid screening identified friend of GATA (FO

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

86 A yeast two-hybrid screening identified Mint-3 as the EWV-

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

88 Yeast two-hybrid screening identified Rieske FeS protein

89 Yeast two-hybrid screening indicated that XERICO interac

90 P50, identified by yeast two-hybrid screening, interacts physically with th

91 The yeast two-hybrid screening method was used to identify n

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

93 Bioinformatics and yeast two-hybrid screening methods were therefore used t

94 By yeast two-hybrid screening of a B cell library with TACI

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

96 Yeast two-hybrid screening of a bovine retinal cDNA libr

97 Yeast two-hybrid screening of a bovine retinal cDNA libr

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

99 By yeast two-hybrid screening of a cDNA library prepared fr

100 DRBP76 was also cloned by the yeast two-hybrid screening of a cDNA library using a mut

101 potential iPLA(2)beta-interacting protein by yeast two-hybrid screening of a cDNA library using iPLA(

102 A yeast two-hybrid screening of a human aorta cDNA library

103 Yeast two-hybrid screening of a human brain cDNA library

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

105 ling pathways utilized by Tie2, we performed yeast two-hybrid screening of a human endothelial cell c

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

107 ar proteins interacting with NS5B protein by yeast two-hybrid screening of a human hepatocyte cDNA li

108 Yeast two-hybrid screening of a human kidney cDNA librar

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

110 Yeast two-hybrid screening of a human lymphocyte library

111 se steroidogenic factor 1 (SF1) as bait in a yeast two-hybrid screening of a human mammary gland cDNA

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

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

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

115 l (P1CT), this segment was used as bait in a yeast two-hybrid screening of a kidney epithelial cell l

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

117 t melanosomal membrane protein, we performed yeast two-hybrid screening of a melanocyte cDNA library.

118 Yeast two-hybrid screening of a mouse brain cDNA library

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

120 Employing yeast two-hybrid screening of a mouse kidney cDNA librar

121 Yeast two-hybrid screening of a neuroblastoma cDNA libra

122 Yeast two-hybrid screening of a porcine coronary artery

123 Yeast two-hybrid screening of a rabbit parietal cell cDN

124 The yeast two-hybrid screening of a retinal cDNA library, us

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

126 t kinase II (CaMKII) interacting proteins by yeast two-hybrid screening of an adult head cDNA library

127 ons underlying these functions, we performed yeast two-hybrid screening of an embryonic rat lens libr

128 Employing yeast two-hybrid screening of an HL60 cDNA library using

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

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

131 amine the roles of IDRs in CBP, we performed yeast-two-hybrid screenings of placenta and lung cancer

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

133 This protein was identified by the yeast two-hybrid screening procedure via its interaction

134 ed temporal and spatial expression analysis, yeast two-hybrid screening, promoter activity assays and

135 ssion and/or function of MDM2, we utilized a yeast two-hybrid screening protocol.

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

137 Yeast two-hybrid screening revealed a direct interaction

138 A yeast two-hybrid screening revealed a specific interacti

139 The yeast two-hybrid screening revealed interaction of the S

140 Yeast two-hybrid screening revealed that GRASP interacte

141 Yeast two-hybrid screening revealed that POG interacted

142 Pulldown assays of epitope-tagged S100A2 and yeast two-hybrid screening revealed that S100A2 displays

143 Yeast two-hybrid screening revealed that the phosphatidy

144 Yeast two-hybrid screening showed that this new GABA(B)R

145 Using yeast two-hybrid screening, small ubiquitin-like modifie

146 We used a yeast two-hybrid screening strategy and identified eukar

147 a human aorta cDNA library was screened by a yeast two-hybrid screening strategy.

148 Yeast two-hybrid screening suggests that XB130 interacts

149 Using a yeast two-hybrid screening system, we have identified Ra

150 Using the yeast two-hybrid screening system, we have isolated and

151 it to screen a human liver cDNA library in a yeast two-hybrid screening system, we have isolated seve

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

153 Using yeast two-hybrid screening, the N terminus of Grb10 was

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

155 Using a yeast two-hybrid screening to clone MTA1-interacting pro

156 Using a yeast two-hybrid screening to clone MTA1s-interacting pr

157 We have used yeast two-hybrid screening to identify a 116-kDa human p

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

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

160 volved in PTTG biological functions, we used yeast two-hybrid screening to identify proteins that int

161 responsible for this coupling, we performed yeast two-hybrid screening to identify proteins that int

162 In this report, we used the yeast two-hybrid screening to isolate MEK interacting pr

163 mediated transcriptional regulation, we used yeast two-hybrid screening to isolate NRL-interacting pr

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

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

166 Yeast two-hybrid screening using an AtBT1 fragment as ba

167 1C-binding segments of Nek2 were isolated by yeast two-hybrid screening using Inh2 bait.

168 Yeast two-hybrid screening using libraries prepared from

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

170 nation of comparative sequence alignment and yeast two-hybrid screening using short conserved peptide

171 In a yeast two-hybrid screening using the C-terminal domain o

172 ivity at the coactivator level, we performed yeast two-hybrid screening using the NRB domain of the g

173 Through the yeast two-hybrid screening using the tail domain of myos

174 Sy (XPIASy), a member of the PIAS family, by yeast two-hybrid screening using Xenopus Smad2 (XSmad2)

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

176 -related protein 3 (ERR3), was identified by yeast two-hybrid screening, using the transcriptional co

177 ed from a rat neonatal heart cDNA library by yeast two-hybrid screening, using YB-1 as the bait.

178 Yeast two-hybrid screening was performed to identify pro

179 Yeast two-hybrid screening was used to explore novel pro

180 Through yeast two-hybrid screening we have cloned and characteri

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

182 In yeast two-hybrid screening, we found that TCL1 interacts

183 Using yeast two-hybrid screening, we found that the alpha subu

184 Using yeast two-hybrid screening, we found that the alpha4-sub

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

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

187 tagenesis and a double-negative selection in yeast two-hybrid screening, we have identified a dominan

188 Using cytohesin 2 as bait in yeast two-hybrid screening, we have isolated a cDNA enco

189 containing the two NLS motifs as a bait for yeast two-hybrid screening, we have isolated four clones

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

191 Through yeast two-hybrid screening, we identified an apparent in

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

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

194 Using yeast two-hybrid screening, we identified SHARP, one of

195 ing proteins with oncogenic potential by the yeast two-hybrid screening, we identified STAT3 beta as

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

197 n a search for STAT5-interacting proteins by yeast two-hybrid screening, we identified the nuclear re

198 Using yeast two-hybrid screening, we identified the polyamine

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

200 By yeast two-hybrid screening, we identified the regulatory

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

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

203 sing the Fas cytoplasmic domain as bait in a yeast two-hybrid screening, we isolated a mouse cDNA enc

204 By yeast two-hybrid screenings, we found a specific interac

205 Employing pooled RNAi and yeast two-hybrid screenings, we report that the mitochon

206 Results from yeast two-hybrid screening were confirmed by direct prot

207 Twenty positive clones isolated through yeast two-hybrid screening were deemed potential myocili

208 We find by yeast two-hybrid screening with a PDEdelta bait that it

209 r understand their functions, we performed a yeast two-hybrid screening with hGab2-(120-587) as bait.

210 Recently, we performed yeast two-hybrid screening with NUB1 as bait and isolate

211 ipants in the OSF signaling cascade, we used yeast two-hybrid screening with Saccharomyces cerevisiae

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

213 Specifically, yeast two-hybrid screening with the rel homology domain

214 ct that binds to c-kinase] was isolated in a yeast two-hybrid screening, with amino acids 1-304 of BR

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

216 as a Cdc2- or Cdk2-interacting protein by a yeast two-hybrid screening, yet the biological significa

217 Yeast two-hybrid screening yielded a CLP-interacting clo