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1 l interaction of full-length PsIAA4 in vivo (yeast two-hybrid system).
2  followed by phenotypic screening based on a yeast two-hybrid system.
3 p6, a human cDNA library was screened in the yeast two-hybrid system.
4 gion of AbetaPP have been isolated using the yeast two-hybrid system.
5 e amino-terminal end of P. yoelii MSP-1 in a yeast two-hybrid system.
6 vestigated the interaction directly with the yeast two-hybrid system.
7  proteins that interacted with p35 using the yeast two-hybrid system.
8 ct with each other and self-associate in the yeast two-hybrid system.
9 f the IFT complex was investigated using the yeast two-hybrid system.
10 ns of VacA (termed p-33 and p-55) by using a yeast two-hybrid system.
11 1p as trap were active when tested using the yeast two-hybrid system.
12 apacity to mediate heterodimerization in the yeast two-hybrid system.
13 a cDNA library via a variant of the original yeast two-hybrid system.
14 ize the 4OHT-bound ERalpha conformation in a yeast two-hybrid system.
15 mbrane protein was investigated by using the yeast two-hybrid system.
16 pping of protein-protein interactions is the yeast two-hybrid system.
17 tation, as well as genetic tools such as the yeast two-hybrid system.
18 azE and MazF was also characterized with the yeast two-hybrid system.
19 with actin was originally characterized by a yeast two-hybrid system.
20 s of mouse Rpgr(ORF15) was used as bait in a yeast two-hybrid system.
21  important protein interactions has been the yeast two-hybrid system.
22 nable to interact with wild-type p-55 in the yeast two-hybrid system.
23 ssayed and found to interact strongly in the yeast two-hybrid system.
24  NifL interacted with GlnK and GlnKY51F in a yeast two-hybrid system.
25 terminal regulatory region of p100 using the yeast two-hybrid system.
26 with the Cdh1 substrate-binding protein in a yeast two-hybrid system.
27  sigma(28) was demonstrated by utilizing the yeast two-hybrid system.
28 s factor receptor family, as the bait in the yeast two-hybrid system.
29 protein-protein interaction assays using the yeast two-hybrid system.
30 t with SKR-1, -2, -3, -7, -8, and -10 in the yeast two-hybrid system.
31 lpha-, beta-, gamma-, and delta-zeins in the yeast two-hybrid system.
32  cell complementary DNA library by using the yeast two-hybrid system.
33 n p29 and p67(phox) was demonstrated using a yeast two-hybrid system.
34 16 interacts with AtbZIP68 and AtGBF1 in the yeast two-hybrid system.
35 cDNA expression library was screened using a yeast two-hybrid system.
36 e direct interaction of FleN and FleQ in the yeast two-hybrid system.
37 is interaction was initially found using the yeast two-hybrid system.
38 ed significant dimer formation, by using the yeast two-hybrid system.
39 thermore, LIN-56 and LIN-15A interact in the yeast two-hybrid system.
40   MYOC-MYOC interactions were studied with a yeast two-hybrid system.
41 ibrary for interacting proteins by using the yeast two-hybrid system.
42 necessary for interaction with Src using the yeast two-hybrid system.
43 are confirmed by similar interactions in the yeast two-hybrid system.
44 ts were used to assay for interaction in the yeast two-hybrid system.
45       Munc18-1 was also identified using the yeast two-hybrid system.
46  protein, UBL1, associates with RAD51 in the yeast two-hybrid system.
47  techniques such as mass spectrometry or the yeast two-hybrid system.
48 boxyl terminus (beta(1)AR-CT) as bait in the yeast two-hybrid system.
49 cific binding domains within MUC5B using the yeast two-hybrid system.
50 expression library and screened it using the yeast two-hybrid system.
51  protein, WTAP, which was isolated using the yeast two-hybrid system.
52 of associating with the core protein using a yeast two-hybrid system.
53  it eliminated MucA-MucB interactions in the yeast two-hybrid system.
54 he interaction between these subunits in the yeast two-hybrid system.
55 ntify novel interactors of Smads by use of a yeast two-hybrid system.
56 coding 12-LOX interacting proteins using the yeast two-hybrid system.
57 e proapoptotic BCL-2-related proteins in the yeast two-hybrid system.
58  Ctr9 as a novel DAT binding partner using a yeast two-hybrid system.
59 efective for multimerization using a reverse yeast two-hybrid system.
60 ins using a highly specific, high-throughput yeast two-hybrid system.
61  binding site, CudA forms a homodimer in the yeast two-hybrid system.
62 eracts directly with the FANCD2 protein in a yeast two-hybrid system.
63 y developed a cost-effective high-throughput yeast two-hybrid system.
64 red for Msi1p to associate with Cac1p in the yeast two-hybrid system.
65 ssessed by using a stringent high-throughput yeast two-hybrid system.
66 d to the Z ring or interact with FtsZ in the yeast two-hybrid system.
67 alpha(2)-Heremans-Schmid glycoprotein in the yeast two-hybrid system.
68  domain in a membrane-bound, split-ubiquitin yeast two-hybrid system.
69  the 22-kDa alpha-zein when expressed in the yeast two-hybrid system.
70 brane anchor in MinD interactions, using the yeast two-hybrid system.
71 ding Drosophila PP1c-binding proteins in the yeast two-hybrid system.
72 E(77-114), in the N terminus of BfpE using a yeast two-hybrid system.
73  PNGase (mPNGase) were detected by using the yeast two-hybrid system.
74  vitro in affinity chromatography and in the yeast two-hybrid system.
75 transcriptional activation and expression in yeast two-hybrid systems.
76                                      Using a yeast two-hybrid system, 38 candidates interacting with
77 in-protein interaction assays done using the yeast two-hybrid system, 56 (approximately 17%) showed p
78                        We report that in the yeast two-hybrid system a domain of U(S)3 essential for
79 he present study we have isolated, using the yeast two-hybrid system, a 182 amino acid residue fragme
80  screen a human liver cDNA library using the yeast two-hybrid system, a cDNA for cytohesin-1, a appro
81                      We use the well studied yeast two-hybrid system adapted for mammalian cells and
82  HPS1 and HPS4 do not interact directly in a yeast two-hybrid system, although HPS4 interacts with it
83                                    Through a yeast two-hybrid system, an in vitro binding assay, and
84 associated polypeptides using the Gal4-based yeast two-hybrid system and a cDNA library derived from
85                                    Using the yeast two-hybrid system and a heterologous cell system,
86                                    Using the yeast two-hybrid system and a protein array membrane, we
87                                    Using the yeast two-hybrid system and affinity immobilization assa
88 een revealed by the RNAi assays, we used the yeast two-hybrid system and an in vitro glutathione-S-tr
89                                    Using the yeast two-hybrid system and bimolecular fluorescence com
90 ms of the importin alpha protein family in a yeast two-hybrid system and by an in planta bimolecular
91 5Delta32, both by genetic criteria using the yeast two-hybrid system and by biochemical criteria usin
92  interaction was confirmed in a conventional yeast two-hybrid system and by direct interaction betwee
93                In a novel application of the yeast two-hybrid system and by immunoprecipitation, we s
94        To explain this process, we show by a yeast two-hybrid system and chemical cross-linking that
95                                  We used the yeast two-hybrid system and co-immunoprecipitation analy
96 nteraction between Rad52 and Rad59 using the yeast two-hybrid system and co-immunoprecipitation from
97                                    Using the yeast two-hybrid system and co-immunoprecipitation metho
98                               Using both the yeast two-hybrid system and coimmunoprecipitation assays
99 teraction was initially demonstrated using a yeast two-hybrid system and corroborated by both in vivo
100                                    Using the yeast two-hybrid system and domain III of perlecan as ba
101 ns on nibrin and Mre11 were mapped using the yeast two-hybrid system and expression of epitope-tagged
102  we screened a prostate cDNA library using a yeast two-hybrid system and found that the cleavage and
103 K1 as a binding partner for UNC5H1 using the yeast two-hybrid system and found that the extreme three
104 etween decorin and EGFR was confirmed in the yeast two-hybrid system and further validated by experim
105                                  We used the yeast two-hybrid system and gel overlays to study intimi
106 X proteins was shown using a split ubiquitin yeast two-hybrid system and gel shift assays.
107  with the cytoplasmic tail of megalin in the yeast two-hybrid system and glutathione-S-transferase pu
108                       We utilized a modified yeast two-hybrid system and identified a new, widely exp
109  to the cytoplasmic domain of ADAM12 using a yeast two-hybrid system and identified a protein called
110  with Nck via the intermediate domain in the yeast two-hybrid system and in a glutathione S-transfera
111 eIF4H interacts physically with eIF4A in the yeast two-hybrid system and in GST pull-down assays and
112 racted with Agrobacterium protein VirE2 in a yeast two-hybrid system and in planta.
113 ved C-terminal motif in Hook proteins in the yeast two-hybrid system and in tissue culture cells, and
114 ptide also interacts with OASTL based on the yeast two-hybrid system and in vitro binding assays.
115  KorB and IncC interact in vivo by using the yeast two-hybrid system and in vitro by using partially
116  spore coat protein, SafA, in vivo using the yeast two-hybrid system and in vitro.
117 that it directly associates with maspin in a yeast two-hybrid system and in vitro.
118 nitially developed interaction assays (e.g., yeast two-hybrid system and split-ubiquitin assay) usual
119 hways of maspin, we employed a maspin-baited yeast two-hybrid system and subsequently identified Inte
120 d proteins that interacted with INSM1 by the yeast two-hybrid system and the binding of one of them,
121                              We employed the yeast two-hybrid system and used perlecan domain V as ba
122 beta-galactosidase quantitative assay in the yeast two-hybrid system and were confirmed by an in vitr
123                                    Using the yeast-two hybrid system and coprecipitation of recombina
124                       RsbQ bound RsbP in the yeast two-hybrid system, and a large in-frame deletion i
125 ain, Ckigamma2, -gamma3, and -epsilon in the yeast two-hybrid system, and bound Ckidelta and -epsilon
126 , perfluoro-octanoate-PAGE, a membrane-based yeast two-hybrid system, and chemical cross-linking expe
127           3DX bound well to its epitope in a yeast two-hybrid system, and GST-fused 3DX also bound to
128 th the plant SnRK AKIN11 both in vivo in the yeast two-hybrid system, and in vitro in a GST-fusion 'p
129 s with the spliceosome protein U1-70K in the yeast two-hybrid system, and is co-localized with U1-70K
130 y lipoprotein complexes, was identified by a yeast two-hybrid system as a strong and specific binding
131 e 3 (PDCL3, also known as PhLP2A), through a yeast two-hybrid system, as a novel protein involved in
132                                         In a yeast two-hybrid system based on reconstitution of Ras s
133                  Immunoprecipitation and the yeast two-hybrid system both suggest physical interactio
134 etween IDH1 and IDH2 were detected using the yeast two-hybrid system, but interactions between identi
135 ally impaired and unregulated CDPKs with the yeast two-hybrid system can accelerate the discovery of
136                                    Using the yeast two-hybrid system, CCTeta was found to bind to the
137 9 was studied using affinity chromatography, yeast two-hybrid system, coimmunoprecipitation, and gel
138  CDC-42 physically interacts with PAR-6 in a yeast two-hybrid system, consistent with data on the int
139 finity purification-mass spectrometry or the yeast two-hybrid system, contributes a unique and releva
140                                  We used the yeast two-hybrid system coupled with random mutagenesis
141                                          The yeast two-hybrid system data also indicated that CarR is
142 hermore, extensive assays utilizing the Gal4 yeast two-hybrid system demonstrate interactions of syne
143                        Experiments using the yeast two-hybrid system demonstrated a protein-protein i
144                                   Use of the yeast two-hybrid system demonstrated direct interaction
145         In this review we will introduce the yeast two-hybrid system, discuss modifications of the sy
146 nst a library carrying M. xanthus DNA in the yeast two-hybrid system, eight positive, independent clo
147  breast epithelial cell cDNA library using a yeast two-hybrid system for ARHI-interacting proteins.
148 DNA library with a specific antibody and the yeast two-hybrid system for protein interaction using as
149  Since its original description in 1989, the yeast two-hybrid system has been extensively used to ide
150                        In the membrane-based yeast two-hybrid system, homo-oligomeric interactions be
151 ons that occur in E. coli also occurs in the yeast two-hybrid system (i.e., off-DNA).
152                                      Using a yeast two-hybrid system, immunocolocalization, immunopre
153 lular domains of each immune receptor in the yeast two-hybrid system in a kinase activity-dependent m
154 les of human DNA ligase IV, we have used the yeast two-hybrid system in conjunction with traditional
155                                 By using the yeast two-hybrid system, in vitro coimmunoprecipitation,
156 ts, with the cytoplasmic portion of Ob-Rb in yeast two-hybrid systems, in protein precipitation exper
157            Additional mapping studies in the yeast two-hybrid system indicated that only the N-termin
158                                          The yeast two-hybrid system indicated that regions near the
159                              Analysis in the yeast two-hybrid system indicates that the N-terminal po
160  the HEC proteins can dimerize with SPT in a yeast two-hybrid system, indicating that the HEC genes w
161  gp41 CD failed to interact with PRA1 in the yeast two-hybrid system, its interaction with PRA1 was s
162 ffinity-capture complex purification and the yeast two-hybrid system, may produce inaccurate data set
163                           When tested in the yeast two-hybrid system, mutation of Leu-536 increased t
164 o experiments using either a split ubiquitin yeast two-hybrid system or bimolecular fluorescence comp
165 st, Tie1 did not interact with ABIN-2 in the yeast two-hybrid system or mammalian cells.
166 sduction pathways have successfully used the yeast two-hybrid system or related methods.
167 (1) Using the C-terminus of LPP as bait in a yeast two hybrid system, palladin, an actin-associated p
168                             Using a modified yeast two-hybrid system, PDZ(Omi) mutants were isolated
169                                 By using the yeast two-hybrid system, purified lectin and pilin domai
170                   Here we report that in the yeast two-hybrid system, Rad51D interacts with XRCC2 and
171           Since the first description of the yeast two-hybrid system, related genetic assays for prot
172 it to screen a human heart cDNA library in a yeast two-hybrid system, retrieving two unique clones th
173                  Deletion analysis using the yeast two-hybrid system revealed that the armadillo repe
174                                 Although the yeast two-hybrid system suggested an interaction of six
175                       Third, analysis in the yeast two-hybrid system suggested that all six paralogs
176 ble activation partners for SAF-1, we used a yeast two-hybrid system that detected interaction betwee
177                            Evidence from the yeast two-hybrid system that the D4R and D5R proteins ca
178  However, MA showed binding to TSG101 in the yeast two-hybrid system that was dependent on an intact
179         Utilizing a split-ubiquitin membrane yeast two-hybrid system that was developed to identify i
180 ted in a physical interaction, we employed a yeast-two-hybrid system that revealed a dimerization bet
181                                           In yeast two-hybrid systems, the N-terminus of NIL-16 inter
182 cellular C terminus of the human CaR and the yeast two hybrid system to screen a human kidney cDNA li
183                                  We used the yeast two-hybrid system to analyze the role of Alpharetr
184 romatography, coimmunoprecipitation, and the yeast two-hybrid system to demonstrate that the extracel
185                               We then used a yeast two-hybrid system to detect potential protein-prot
186                                      Using a yeast two-hybrid system to detect protein-protein intera
187                             We have used the yeast two-hybrid system to detect variants of GlnB that
188                   In this study, we used the yeast two-hybrid system to determine the multimerization
189            In the present study, we used the yeast two-hybrid system to determine the site of interac
190                                    Using the yeast two-hybrid system to determine the target host cel
191                         We have modified the yeast two-hybrid system to enable the detection of prote
192  of cellular signaling, we have modified the yeast two-hybrid system to explore the possibility of NO
193 which was used in this report as bait in the yeast two-hybrid system to find other interacting cell t
194                    In this study we used the yeast two-hybrid system to find proteins interacting wit
195                                    We used a yeast two-hybrid system to identify a putative cotton fi
196              In this study, we have used the yeast two-hybrid system to identify an ETS1 interacting
197 m of AR-regulated transcription, we used the yeast two-hybrid system to identify AR-associated protei
198                                  We used the yeast two-hybrid system to identify binding partners of
199 clues about the function of APP, we used the yeast two-hybrid system to identify interaction between
200                                Here we use a yeast two-hybrid system to identify novel TIR1 mutants w
201 regulation of PKCtheta, we have employed the yeast two-hybrid system to identify PKCtheta-interacting
202                                   Use of the yeast two-hybrid system to identify proteins that associ
203 beta PP processing and function, we used the yeast two-hybrid system to identify proteins that intera
204                                  We used the yeast two-hybrid system to identify proteins that intera
205                             We have used the yeast two-hybrid system to identify proteins that intera
206              In this study, we have used the yeast two-hybrid system to identify proteins that intera
207 ignal transduction pathway, we have used the yeast two-hybrid system to identify proteins that physic
208 d random mutagenesis in combination with the yeast two-hybrid system to identify residues in the YopH
209                        Here we have used the yeast two-hybrid system to identify the proteins that in
210                                  We used the yeast two-hybrid system to identify the Prtb (Proline-ri
211  an integrated strategy based on the reverse yeast two-hybrid system to isolate and characterize such
212                             We have used the yeast two-hybrid system to isolate Nova interacting prot
213                Because of the failure of the yeast two-hybrid system to reveal interactions between l
214                           We have employed a yeast two-hybrid system to screen a B lymphoblast-derive
215 ial targets of c-Abl kinase, we utilized the yeast two-hybrid system to screen a murine cDNA library.
216            Using the era gene as bait in the yeast two-hybrid system to screen E. coli genomic librar
217                     We developed a sensitive yeast two-hybrid system to screen for hERalpha variants
218  phosphorylation, we modified the Gal4-based yeast two-hybrid system to screen for phosphorylation-de
219 s of BCSG1 in breast cancer cells, we used a yeast two-hybrid system to screen for proteins that coul
220 or cell invasion and metastasis, we used the yeast two-hybrid system to screen for proteins that inte
221                         We used an optimized yeast two-hybrid system to screen mouse pregnancy-associ
222                                Here, using a yeast two-hybrid system to search for AtRALF1-interactin
223     Thus, we screened a cDNA library using a yeast two-hybrid system to search for interacting protei
224  results also demonstrate the utility of the yeast two-hybrid system to study protein-protein interac
225                        Here we have used the yeast two-hybrid system to test for direct interaction b
226 FBP-5, we screened a human cDNA library by a yeast two-hybrid system using IGFBP-5 as bait and identi
227            In the present study, we employed yeast two-hybrid system using the N-terminal domain of A
228 brain microvascular endothelial cells by the yeast two-hybrid system using the N-terminal domain of C
229 ing with Rb in muscle cells, we utilized the yeast two-hybrid system, using the A-B and C pockets of
230 interaction was identified by screening of a yeast two-hybrid system vascular endothelial cell librar
231                                          The yeast two hybrid system was used to confirm these intera
232 ential nucleator of enamel crystallites, the yeast two-hybrid system was applied to a mouse tooth exp
233 the role of RGSZ1 in cellular signaling, the yeast two-hybrid system was employed to identify potenti
234 MP, a functional genetic screen based on the yeast two-hybrid system was performed.
235                                            A yeast two-hybrid system was used to analyze interactions
236                                              Yeast two-hybrid system was used to demonstrate that a h
237                               In addition, a yeast two-hybrid system was used to detect the interacti
238                                          The yeast two-hybrid system was used to identify a groucho h
239                                          The yeast two-hybrid system was used to isolate the ATP bind
240                                          The yeast two-hybrid system was used to search for proteins
241 biguous interaction, first observed with the yeast two-hybrid system, was corroborated by co-immunopr
242                                    Using the yeast two-hybrid system we have identified an RNA-bindin
243               Using that domain as bait in a yeast two-hybrid system we now report the identification
244                                    Using the yeast-two hybrid system we isolated a novel Numb interac
245                                    Using the yeast two hybrid system, we show that the iaa17/axr3-1 m
246                                    Using the yeast two-hybrid system, we cloned an apolipoprotein (ap
247 entifying Jak2-interacting proteins with the yeast two-hybrid system, we cloned the human homologue o
248 ys, radioligand binding experiments, and the yeast two-hybrid system, we demonstrate that FGF7 binds
249                                      Using a yeast two-hybrid system, we found that both SPECs intera
250                                    Using the yeast two-hybrid system, we found that HAP1 also interac
251                                    Using the yeast two-hybrid system, we found that these mutations d
252                                    Using the yeast two-hybrid system, we found that TRIM32 binds and
253                                    Using the yeast two-hybrid system, we found that VZV IE63 interact
254             In the present study employing a yeast two-hybrid system, we found that zyxin, a molecule
255                                    Using the yeast two-hybrid system, we have identified a human cell
256                    In this report, using the yeast two-hybrid system, we have identified a novel inte
257                                    Using the yeast two-hybrid system, we have identified a novel inte
258                                 By using the yeast two-hybrid system, we have identified a novel memb
259 kinase 1 (Plk1)-interacting proteins using a yeast two-hybrid system, we have identified histone acet
260                                    Using the yeast two-hybrid system, we have now identified two sper
261                                    Using the yeast two-hybrid system, we have observed a strong inter
262                                        Using yeast two-hybrid system, we have previously identified C
263                                    Using the yeast two-hybrid system, we here report an interaction b
264                                      Using a yeast two-hybrid system, we identified a calmodulin-rela
265                                   By using a yeast two-hybrid system, we identified a gene, invasion
266                                    Using the yeast two-hybrid system, we identified a novel calcineur
267                                    Using the yeast two-hybrid system, we identified a number of prote
268                                    Using the yeast two-hybrid system, we identified a transcriptional
269                                    Using the yeast two-hybrid system, we identified an interaction be
270                                      Using a yeast two-hybrid system, we identified Arabidopsis thali
271 may underlie the disease phenotype.Using the yeast two-hybrid system, we identified ETO/MTG8, a compo
272                          With the use of the yeast two-hybrid system, we identified filamin-A (an act
273                                    Using the yeast two-hybrid system, we identified Hsp90, a chaperon
274                                    Using the yeast two-hybrid system, we identified importin alpha1 (
275                                Utilizing the yeast two-hybrid system, we identified protein phosphata
276                                    Using the yeast two-hybrid system, we identified several second-si
277                                    Using the yeast two-hybrid system, we identified Sprouty2 as an in
278                                    Using the yeast two-hybrid system, we identified uridine kinase li
279                                    Using the yeast two-hybrid system, we isolated a membrane-associat
280                       Using DAZ as bait in a yeast two-hybrid system, we isolated two DAZAP (DAZ-asso
281                                    Using the yeast two-hybrid system, we previously isolated a novel
282                                      Using a yeast two-hybrid system, we screened for galectin-3-inte
283         Using chemical cross-linking and the yeast two-hybrid system, we show that sortilin interacts
284                                    Using the yeast two-hybrid system, we show that the Mod(mdg4) prot
285                                      Using a yeast two-hybrid system, we show that these SOS2-like ki
286                          With the use of the yeast two-hybrid system, we show that this Dnm1p oligome
287           Using a stringent, high-throughput yeast two-hybrid system, we tested pairwise interactions
288 ne was changed to alanine could activate the yeast two-hybrid system when paired with RsbW, whereas m
289 s with the Aspergillus NUDE coiled-coil in a yeast two-hybrid system, while human LIS1 interacts with
290 cer-associated C terminus (BRCT) domain in a yeast two-hybrid system, while increased sensitivity of
291           Here we report the cloning, by the yeast two hybrid system with dominant negative caspase-2
292 enesis, Pipkz1, was shown to interact in the yeast two-hybrid system with a putative bZIP transcripti
293  factor, interleukin-1, and ROS, we used the yeast two-hybrid system with ASK1 as bait to identify AS
294 on factor-1gamma (EF1gamma) interacts in the yeast two-hybrid system with DOA, the LAMMER protein kin
295 d caveolin-1 was determined by the Pro-Quest yeast two-hybrid system with full-length NSP4 and seven
296                                Combining the yeast two-hybrid system with genetic analysis, we show h
297                                          The yeast two-hybrid system with myocilin as the bait and a
298                                    Using the yeast two-hybrid system with syntaxin-1A as bait, we iso
299  co-regulatory proteins in RKO cells using a yeast two-hybrid system with the intact TRbeta1 as bait.
300 g sites for VHb on the cytochrome, using the yeast two-hybrid system with VHb as the bait and testing

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