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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 putative OGT-interacting proteins through a yeast two-hybrid screen.
6 interaction partner for Ku in a genome-wide yeast two-hybrid screen.
7 inding protein (MTBP) was identified using a yeast two-hybrid screen.
8 DUS2 as a protein interacting with PACT in a yeast two-hybrid screen.
9 to be an hZimp10 interacting protein in the yeast two-hybrid screen.
10 artner of the beta6 cytoplasmic tail using a yeast two-hybrid screen.
11 bait, we isolated clathrin light chain in a yeast two-hybrid screen.
12 e phosphatase named DUSP26 identified from a yeast two-hybrid screen.
13 as a binding partner for Kidins220/ARMS by a yeast two-hybrid screen.
14 t of the AP2 complex and PIPKIgamma661 via a yeast two-hybrid screen.
15 tial interacting proteins were identified by yeast two-hybrid screen.
16 tein-protein interaction data from a focused yeast two-hybrid screen.
17 uman teneurin-1 ICD interaction partner in a yeast two-hybrid screen.
18 o identify Wor1-interacting proteins using a yeast two-hybrid screen.
19 arity, we performed a comprehensive pairwise yeast two-hybrid screen.
20 protein was identified by a Split-Ubiquitin Yeast-Two-Hybrid screen.
21 eracts with three different Cys proteases in yeast two-hybrid screens.
22 nerated through subtractive hybridization or yeast two-hybrid screens.
23 ently available was generated by large-scale yeast two-hybrid screens.
24 e family, as a LOX-interacting partner using yeast two-hybrid screens.
25 l hIP-interacting protein in two independent yeast two-hybrid screens.
26 revious results from electron microscopy and yeast two-hybrid screens.
27 nesulfonate suppressor mutants and performed yeast-two-hybrid screens.
28 P-1L, that was found to bind to Hsf1 through yeast two-hybrid screening.
29 t identified as a binding protein of AKT2 by yeast two-hybrid screening.
30 utative interacting partner of NLRC3 through yeast two-hybrid screening.
31 n family, as a TIMP-1 interacting protein by yeast two-hybrid screening.
32 ansformation efficiency is critical, such as yeast two-hybrid screening.
33 tion, was shown to interact with maspin in a yeast two-hybrid screening.
34 of the human kappa opioid receptor (hKOR) by yeast two-hybrid screening.
35 ding partner of the E2 protein of CSFV using yeast two-hybrid screening.
36 oform of thromboxane A2 receptor (TPbeta) 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 of the HIV-1 replication cycle, we performed yeast two-hybrid screening against a human cDNA library
41 tein targets in the host cells, we performed yeast two-hybrid screens, allowing us to find 48 high-co
43 y SUT-2 interacting proteins, we conducted a yeast two hybrid screen and found SUT-2 binds to ZYG-12,
46 esin-1 light chain KLC-2, as identified in a yeast two-hybrid screen and confirmed by in vitro assays
47 activating transcription factor (ATF) 4 in a yeast two-hybrid screen and confirmed their interaction
49 ed with F(o)F(1) ATP synthase subunit 6 by a yeast two-hybrid screen and had strong antiapoptotic eff
51 f human CD161 (NKR-P1A), we have conducted a yeast two-hybrid screen and identified acid sphingomyeli
52 e the mechanism of action of KAI1, we used a yeast two-hybrid screen and identified an endothelial ce
54 BBX32 regulation, we performed a large-scale yeast two-hybrid screen and identified CONSTANS-LIKE 3 (
56 tify host targets of AvrPtoB, we performed a yeast two-hybrid screen and identified tomato ubiquitin
57 as an interacting partner of SIS8 based on a yeast two-hybrid screen and in planta bimolecular fluore
58 direct interacting factor for Kbtbd5 using a yeast two-hybrid screen and in vitro binding assays.
59 1 (PDZD11) as a new interactor of PLEKHA7 by yeast two-hybrid screening and by mass spectrometry anal
62 ified KDR interactors using a combination of yeast two-hybrid screening and dedicated confirmations w
64 d protein required for ATM activation-1), by yeast two-hybrid screening and found that BAAT1 also bin
65 ell proteins in Vpu function, we carried out yeast two-hybrid screening and identified a previously r
66 teins in Vpu's function, here we carried out yeast two-hybrid screening and identified the V0 subunit
67 th the lambda-isoform 14-3-3 protein both in yeast two-hybrid screening and in an in vitro pull-down
71 G signaling pathway components, we performed yeast two-hybrid screens and identified the muscle-speci
72 ein ensemble in the centrosome, we performed yeast two-hybrid screens and isolated a number of Su48-i
73 identify host targets of AVR1, we performed yeast two-hybrid screens and selected Sec5 as a candidat
74 its mechanism of action, we have employed a yeast-two-hybrid screen and identified serine protease H
75 forming hetero- or homodimers, we conducted yeast-two-hybrid screening and identified an SVP-like MA
76 stone H1.2 as a DME-interacting protein in a yeast two-hybrid screen, and confirmation of their inter
77 entified as a putative cofactor of Jarid2 by yeast two-hybrid screening, and the physical interaction
78 Bam35 proteins determined using multivector yeast two-hybrid screening, and these PPIs were further
79 ify TRPV4-interacting proteins by performing yeast two-hybrid screens, and we isolated with the avian
85 aCC1)) did not disrupt direct interaction in yeast two-hybrid screens but did prevent association by
87 roteins were identified and characterized by yeast two-hybrid screen, co-affinity purification and RN
89 ligase, as an interacting protein of KLF5 by yeast two-hybrid screen, coimmunoprecipitation, and indi
92 lian RSP3 to bind to the MAPK ERK2 through a yeast two-hybrid screen designed to identify interacting
93 accharomyces cerevisiae genome SPA increases yeast two-hybrid screening efficiency by an order of mag
96 O Domain Containing Protein, HvELMOD_C, in a yeast two hybrid screen for proteins interacting with Hv
106 pa can physically interact with ubiquitin by yeast two-hybrid screening, glutathione S-transferase pu
125 ort, we present data from the following: (a) yeast two-hybrid screens, identifying interaction partne
126 t to remedy this situation, a combination of yeast two-hybrid screens, in vitro binding assays and ce
131 eins that interact with KLF5, we performed a yeast two-hybrid screen of a 17-day mouse embryo cDNA li
136 understand the cellular function of ERK8, a yeast two-hybrid screen of a human lung library was perf
138 -residue N-terminal domain, we carried out a yeast two-hybrid screen of a mouse brain cDNA library.
140 e N-terminal domain of TGMV AL1 as bait in a yeast two-hybrid screen of a random peptide aptamer libr
142 CDH23-interacting proteins, a membrane-based yeast two-hybrid screen of an outer hair cell (OHC) cDNA
143 ntified as an Mst1-interacting protein, in a yeast two-hybrid screen of human adult prostate cDNA lib
146 ography followed by mass spectrometry and by yeast two-hybrid screening of a bovine retina cDNA libra
153 nuclear roles of delta-catenin, we performed yeast two-hybrid screening of a mouse brain cDNA library
158 IC-directed assembly of TFIIIB, we conducted yeast two-hybrid screens of Brf1 peptide libraries again
159 otein-protein interactions using a stringent yeast two-hybrid screen; of 75 pairs tested, 83% of the
160 surface plasmon resonance spectroscopy, NMR, yeast two-hybrid screens, peptide tagging combined with
173 cting proteins, we used a recently developed yeast two-hybrid screen (split ubiquitin method) to dete
177 fy key amino acid residues on PXR based on a yeast two-hybrid screen that examined mutant forms of PX
178 ursor, proRTD1a, into a bait construct for a yeast two-hybrid screen that identified rhesus macaque s
179 of SATB1 in cellular events, we performed a yeast two-hybrid screen that identified SUMO-1, Ubc9, an
180 able N-terminal subdomain that was used in a yeast two-hybrid screen that identified the proline-rich
185 I5-interacting proteins were identified by a yeast two-hybrid screen; the most prevalent interactors
186 transcription factor that was isolated in a yeast two-hybrid screen through its binding property to
189 interacting proteins were identified using a yeast two-hybrid screen to functionally characterize the
190 n this study, we performed a high throughput yeast two-hybrid screen to identify additional pathways
192 derstanding of MTM1 function, we conducted a yeast two-hybrid screen to identify MTM1-interacting pro
195 O promotes genomic stability by performing a yeast two-hybrid screen to identify potential substrates
199 e molecular functions of FTO, we performed a yeast two-hybrid screen to identify the protein(s) that
201 rugs in prostate cancer cells, we employed a yeast two-hybrid screening to identify cellular proteins
203 uences differentiation of neurons, we used a yeast two-hybrid screening to search for new binding par
207 pecially abundant in retina, was fished with yeast two-hybrid screen using a constitutively active Ga
209 novel TDP-43 protein interactors found in a yeast two-hybrid screen using an adult human brain cDNA
212 ein interactions, we performed a large-scale yeast two-hybrid screen using both wild-type (WT) and si
214 molecular partners of MIG-10, we conducted a yeast two-hybrid screen using isoform MIG-10A as bait an
215 s of the alpha1D-adrenergic receptor (AR), a yeast two-hybrid screen using the alpha1D-AR C terminus
216 protein that interacts with C kinase) from a yeast two-hybrid screen using the amino terminus of PKCb
217 ciated protein YejK, which was detected in a yeast two-hybrid screen using the ParE subunit of topois
218 eins that may remove the CRD, we performed a yeast two-hybrid screen using twitchin kinase as bait.
221 tify PIF1-interacting proteins, we performed yeast two-hybrid screening using PIF1 as a bait and iden
222 nant polycystic kidney disease, we performed yeast two-hybrid screens using the C-terminus of polycys
223 receptor-protein interactions, we conducted yeast two-hybrid screens using the cytosolic domains of
224 Prp40 was found to be a centrin target by yeast-two-hybrid screening using both Homo sapiens centr
228 address the function of DJ-1 in prostate, a yeast two-hybrid screen was done to identify novel DJ-1
229 n EF-1alpha and other cellular components, a yeast two-hybrid screen was performed for the archaeon M
230 1/2/4-mediated transcriptional repression, a yeast two-hybrid screen was performed that identified p6
231 n regulation of the RPW8 protein function, a yeast two-hybrid screen was performed using RPW8.2 as ba
232 es toward disease lesions, a Sos-recruitment yeast two-hybrid screen was performed with human Ckidelt
234 signaling events underlying this process, a yeast-two hybrid screen was performed on the C terminus
235 ind protein interaction partners of NBP35, a yeast-two-hybrid screen was carried out that identified
246 Employing C2GnT1 CT as the bait to perform a yeast two-hybrid screen, we have identified Golgi phosph
256 for potential regulators of Smad3 through a yeast two-hybrid screen, we identified casein kinase 1 g
283 Using a plant Rho GTPase (ROP1) as bait in yeast two-hybrid screens, we identified a family of Rho
285 he competency of Gal4-based baits prior to a yeast two-hybrid screen, which allows determination of w
287 used the WFS1-C-terminal domain as bait in a yeast two-hybrid screen with a human brain cDNA library.
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
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