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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.
34 P/TAK1/JNK1 signaling pathway we isolated by yeast two-hybrid screening a novel X chromosome-linked I
38 of the HIV-1 replication cycle, we performed yeast two-hybrid screening against a human cDNA library
41 1 (PDZD11) as a new interactor of PLEKHA7 by yeast two-hybrid screening and by mass spectrometry anal
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
51 he copine target proteins were identified by yeast two-hybrid screening and the interactions were ver
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
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
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
74 HIP1 is a 116-kD protein recently cloned by yeast two-hybrid screening for proteins that interact wi
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
95 ography followed by mass spectrometry and by yeast two-hybrid screening of a bovine retina cDNA libra
101 potential iPLA(2)beta-interacting protein by yeast two-hybrid screening of a cDNA library using iPLA(
105 ling pathways utilized by Tie2, we performed yeast two-hybrid screening of a human endothelial cell c
107 ar proteins interacting with NS5B protein by yeast two-hybrid screening of a human hepatocyte cDNA li
111 se steroidogenic factor 1 (SF1) as bait in a yeast two-hybrid screening of a human mammary gland cDNA
115 l (P1CT), this segment was used as bait in a yeast two-hybrid screening of a kidney epithelial cell l
117 t melanosomal membrane protein, we performed yeast two-hybrid screening of a melanocyte cDNA library.
119 nuclear roles of delta-catenin, we performed yeast two-hybrid screening of a mouse brain cDNA library
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
131 amine the roles of IDRs in CBP, we performed yeast-two-hybrid screenings of placenta and lung cancer
134 ed temporal and spatial expression analysis, yeast two-hybrid screening, promoter activity assays and
142 Pulldown assays of epitope-tagged S100A2 and yeast two-hybrid screening revealed that S100A2 displays
151 it to screen a human liver cDNA library in a yeast two-hybrid screening system, we have isolated seve
158 rugs in prostate cancer cells, we employed a yeast two-hybrid screening to identify cellular proteins
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
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
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
172 ivity at the coactivator level, we performed yeast two-hybrid screening using the NRB domain of the g
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.
187 tagenesis and a double-negative selection in yeast two-hybrid screening, we have identified a dominan
189 containing the two NLS motifs as a bait for yeast two-hybrid screening, we have isolated four clones
195 ing proteins with oncogenic potential by the yeast two-hybrid screening, we identified STAT3 beta as
197 n a search for STAT5-interacting proteins by yeast two-hybrid screening, we identified the nuclear re
203 sing the Fas cytoplasmic domain as bait in a yeast two-hybrid screening, we isolated a mouse cDNA enc
207 Twenty positive clones isolated through yeast two-hybrid screening were deemed potential myocili
209 r understand their functions, we performed a yeast two-hybrid screening with hGab2-(120-587) as bait.
211 ipants in the OSF signaling cascade, we used yeast two-hybrid screening with Saccharomyces cerevisiae
214 ct that binds to c-kinase] was isolated in a yeast two-hybrid screening, with amino acids 1-304 of BR
216 as a Cdc2- or Cdk2-interacting protein by a yeast two-hybrid screening, yet the biological significa
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