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1 are specific for spermatogenesis between the two hybrids.
2 haracterized their interactions by bacterial two-hybrid analyses and could show that the permease Bce
3 lize phylogenetic conservation and bacterial two-hybrid analyses to predict residues in Crl important
4                                        Yeast two-hybrid analyses using serial domain deletion constru
5 molecular complementation assays, i.e. yeast two-hybrid analysis and Arabidopsis leaf protoplast spli
6 s actually binds to ankyrin-G, both in yeast two-hybrid analysis and by coimmunoprecipitation in situ
7         We have demonstrated using bacterial two-hybrid analysis and confirmatory coelution experimen
8 nascent PG processing in vivo, and bacterial two-hybrid analysis identified an MltG-PBP1b interaction
9                        Here we use bacterial two-hybrid analysis in vivo and p-benzoyl-phenylalanine
10 oteome, we carried out a comprehensive yeast two-hybrid analysis of all the putative proteins encoded
11                                              Two-hybrid analysis revealed that the dynamins are part
12                                        Yeast two-hybrid analysis reveals that SIX6OS1 interacts with
13                                        Yeast two-hybrid analysis showed no evidence of a direct inter
14                                        Yeast two-hybrid analysis shows that the rod domain of KRT1 in
15                      Here, we used bacterial two-hybrid analysis to identify a surface-exposed alpha-
16     We used yeast (Saccharomyces cerevisiae) two-hybrid analysis to map the binding site of Bud23 on
17                                      A yeast two-hybrid analysis uncovered the actin-depolymerizing f
18 hat disrupted the interaction, as assayed by two-hybrid analysis, did not display a growth defect.
19 vel binding partner of E5, YIPF4 using yeast two-hybrid analysis.
20  loss of interaction that we have defined by two-hybrid analysis.
21 ay crystallography, electron microscopy, and two-hybrid analysis.
22                                        Yeast-two-hybrid and a green-fluorescent protein fragment comp
23  deacetylase subunits were observed in yeast two-hybrid and bimolecular fluorescence assays, consiste
24                                        Yeast two-hybrid and bimolecular fluorescence complementation
25          In yeast (Saccharomyces cerevisiae) two-hybrid and bimolecular fluorescence complementation
26                           Furthermore, yeast two-hybrid and bimolecular fluorescence complementation
27                   Yeast- or protoplast-based two-hybrid and bimolecular fluorescent complementation a
28                      Our complementary yeast two-hybrid and biochemical assays reveal that CHD7 is a
29                                        Yeast two-hybrid and biochemical studies have revealed that th
30                           Results from yeast two-hybrid and co-expression in Escherichia coli confirm
31                                              Two-hybrid and co-immunoprecipitation analysis has been
32                            Here, using yeast two-hybrid and co-immunoprecipitation approaches, we sho
33                                        Yeast two-hybrid and co-immunoprecipitation assays demonstrate
34                                        Yeast two-hybrid and coimmunoprecipitation analyses associated
35                                   Additional two-hybrid and coimmunoprecipitation assays demonstrated
36                        On the basis of yeast two-hybrid and coimmunoprecipitation assays, we demonstr
37                             Using both yeast two-hybrid and copurification approaches, we identified
38 Analysis of interactions using the bacterial two-hybrid and cross-linking assays showed that TraE and
39                                        Yeast two-hybrid and direct pulldown assays revealed that the
40                                    Bacterial two-hybrid and gene-reporter assays demonstrated that Fs
41  (an E3 ubiquitin ligase), as shown by yeast two-hybrid and in vitro pulldown assays.
42                               Combined yeast two-hybrid and protein array experiments demonstrated th
43                           Furthermore, yeast two-hybrid and pull-down experiments indicated that MYC2
44                                              Two-hybrid and pulldown assays demonstrated that UL20, b
45                       Importantly, bacterial two-hybrid and quantitative imaging assays revealed a si
46 therian and avian cDNA libraries using yeast-two-hybrid and split-ubiquitin systems.
47        Transcriptional assays, such as yeast two-hybrid and TANGO, that convert transient protein-pro
48                              Modeling, yeast two-hybrid, and functional data reveal that this PF2-lik
49 our USH proteins using colocalization, yeast two-hybrid, and pull-down assays.
50 coimmunoprecipitation, colocalization, yeast two-hybrid, and small interfering RNA (siRNA) analyses.
51 irus replication, we have been using a yeast two-hybrid approach to identify host proteins that inter
52                       In this study, a yeast two-hybrid approach using the cytoplasmic domain of TfR2
53 ms and identify putative substrates, a yeast two-hybrid approach was carried on and a protein was ide
54 3A-DCTN3 interaction identified by the yeast two-hybrid approach was further confirmed in mammalian c
55  TolA-pIII complex, we developed a bacterial two-hybrid approach, named Oxi-BTH, suited for studying
56                          Here, using a yeast two-hybrid approach, we have assessed interactions betwe
57                           By using the Yeast Two-Hybrid approach, we identified a disintegrin and met
58                                Using a yeast two-hybrid approach, we identified cellular protein DCTN
59                                Using a yeast two-hybrid approach, we identified the 5'-3' exonuclease
60                            Using a bacterial two-hybrid approach, we show that the three key LTA synt
61 PI maps at proteome scale, first using yeast two-hybrid approaches and more recently via affinity pur
62                  We used proteomic and yeast two-hybrid approaches to elucidate host factors involved
63                              Using bacterial two-hybrid approaches, we showed that the P. aeruginosa
64 nity purification-mass spectrometry or yeast two-hybrid approaches.
65 de, extended-peptide, and protein levels and two "hybrid" approaches (i.e., protein calibrator with S
66                    By a combination of yeast-two hybrid assay, in vitro binding, and coimmunoprecipit
67 s) in human cells, termed mammalian-membrane two-hybrid assay (MaMTH).
68                                    Bacterial two-hybrid assay and accumulation of Gp0.6 only in MreB-
69                         We performed a yeast two-hybrid assay and identified hematopoietically expres
70  interact with Hsp90Ecin vivo in a bacterial two-hybrid assay and in vitro in a bio-layer interferome
71 e in ClpB interaction in vivo in a bacterial two-hybrid assay and in vitro in a fluorescence anisotro
72 ns also directly interact in vivo in a yeast two-hybrid assay and in vitro through ammonium sulfate c
73 s transcription factor prey library by yeast two-hybrid assay and isolated six class I members of the
74 reliminary experiments involving a bacterial two-hybrid assay are presented that corroborate the exis
75                                    The yeast two-hybrid assay identified that proteasome subunit alph
76                                        Yeast two-hybrid assay indicated that the PDH45 protein intera
77                                        Yeast two-hybrid assay revealed that the N-terminal region of
78        Furthermore, results of the mammalian two-hybrid assay showed that cyclin-dependent kinase 3 (
79 reened a kidney cDNA library through a yeast two-hybrid assay using NKCC2 C terminus as bait.
80 h deletion analysis, co-immunoprecipitation, two-hybrid assay, and pulldown assays with expressed pro
81 cessary for the interaction with FeoB in the two-hybrid assay, and when either of these amino acids w
82 ructure was corroborated using the bacterial two-hybrid assay, biochemical characterization of the pu
83 ions with core exocyst subunits in the yeast two-hybrid assay, cytoplasmic localization, and genetic
84                         According to a yeast two-hybrid assay, ORRM1 interacts selectively with penta
85       We searched for such proteins by yeast two-hybrid assay, using GARP as a bait to screen a human
86    Using a modified version of the mammalian two-hybrid assay, we demonstrate that the interaction st
87                    Using the above-mentioned two-hybrid assay, we found that zebrafish Tmc1 and Tmc2a
88 racting proteins were screened using a yeast two-hybrid assay.
89 at prevent DEPTOR binding to mTOR in a yeast-two-hybrid assay.
90 proteins were identified by a modified yeast two-hybrid assay.
91 high-throughput, array-based, directed yeast two-hybrid assay.
92 ing proteins with GLP-1R by a membrane yeast two-hybrid assay.
93 was further confirmed by Co-IP and mammalian two-hybrid assay.
94 ck proteins, Hsp16.9 and Hsp17.5, in a yeast two-hybrid assay.
95 amK and the two proteins interact in a yeast two-hybrid assay.
96 -interacting proteins using a modified yeast two-hybrid assay.
97  modulate its function, we performed a yeast two-hybrid assay.
98 subunits including Sgf29 and Spt7 in a yeast two-hybrid assay.
99              PYL6 and MYC2 interact in yeast two hybrid assays and the interaction is enhanced in the
100          Site-directed mutagenesis and yeast-two hybrid assays identified DnaA and DnaN binding sites
101                                     In yeast-two hybrid assays, ORRM3 interacts with RIP1, ORRM2 and
102 ters, subcellular localization and bacterial two hybrid assays.
103 length protein in vivo, as measured by yeast-two hybrid assays.
104 e ESCRT-III-related proteins CHMP1A in yeast two hybrid assays.
105   ABD1 directly interacts with ABI5 in yeast two-hybrid assays and associates with ABI5 in vivo by co
106                                     By yeast-two-hybrid assays and chromatin immunoprecipitation we d
107                                        Yeast two-hybrid assays and coimmunoprecipitation experiments
108  and TMC1 or TMC2 was observed in both yeast two-hybrid assays and coimmunoprecipitation experiments.
109 o the blue-light photoreceptor FKF1 in yeast two-hybrid assays and delays flowering in Arabidopsis wh
110  with beta-catenin was confirmed using yeast two-hybrid assays and in vitro synthesized proteins.
111 fects in vivo, ARC3 interacted with FtsZ2 in two-hybrid assays and inhibited FtsZ2 assembly in a hete
112                                        Yeast two-hybrid assays established a direct interaction of Ce
113 cular fluorescence complementation and yeast-two-hybrid assays indicated that the IDR3 domain does no
114                       Furthermore, our yeast two-hybrid assays show that MoVps17 and MoVps5 can inter
115 -seq and proteomics data together with yeast two-hybrid assays suggest that MS23 along with MS32, bHL
116 ass spectrometry, split-luciferase and yeast-two-hybrid assays to generate a single reliability score
117 we used membrane-based split ubiquitin yeast two-hybrid assays to identify novel GLP1R interactors in
118         Here, we carry out directional yeast two-hybrid assays to identify the interactions between t
119 tion of pull-downs, mass spectrometry, yeast two-hybrid assays, and chemical genomics, we demonstrate
120                           Based on bacterial two-hybrid assays, CelR homodimerizes but does not inter
121                                     In yeast two-hybrid assays, FgMcm1 interacted with Mat1-1-1 and F
122  with P. blakesleeanus Ras homologs in yeast two-hybrid assays, indicating that MadC is a regulator o
123 amily member periplakin, identified in yeast two-hybrid assays, interacted with a membrane-proximal d
124                                     In yeast two-hybrid assays, MAS2 interacted with splicing and rib
125 fatty acid synthase II (FAS-II) in bacterial two-hybrid assays, suggesting essentiality may be linked
126                                  Using yeast two-hybrid assays, we determined the interactions among
127 und state failed to bind to AvrL567 in yeast two-hybrid assays, while binding was detected to the sig
128 an interact with both TTI1 and TTI2 in yeast two-hybrid assays.
129 ptide aptamers for further analysis in yeast two-hybrid assays.
130  with UNC-116 kinesin-1 heavy chain in yeast two-hybrid assays.
131 h the CAR ligand-binding domain in mammalian two-hybrid assays; and 5) disrupts CAR binding to the pr
132                               In this study, two hybrid biochemical routes combining lignin chemical
133                                  Using yeast two-hybrid, biochemical, and cellular assays, we determi
134            Conversely, protein-level and the two hybrid calibrations achieved good quantitative accur
135 offspring phenotypes suggest the presence of two hybrid classes, F1s and var. incana backcrosses, as
136                                        Yeast two-hybrid, co-immunoprecipitation and pulldown experime
137  binding partner of IL-13Ralpha2 using yeast two-hybrid, co-immunoprecipitation, co-localization and
138                                        Yeast two-hybrid, coimmunoprecipitation and bimolecular fluore
139 size exclusion chromatography, and bacterial two-hybrid data revealed that PilM forms dimers mediated
140                           Furthermore, yeast two-hybrid data showed that CPTL2 and CPT3 interact.
141                                    Bacterial two-hybrid data suggested the connectivity of the cytopl
142                            Competitive yeast-two hybrid experiments indicate that the LIM domains and
143 xperiments, chemical crosslinking, bacterial two-hybrid experiments and nuclear magnetic resonance ch
144                                        Yeast two-hybrid experiments confirmed the direct interaction
145                                              Two-hybrid experiments demonstrate self-interaction of t
146                                        Yeast two-hybrid experiments identified PG core proteins ABC1K
147                                        Yeast two-hybrid experiments indicate that the interaction of
148                                        Yeast two-hybrid experiments suggested that the phosphorylatio
149 and IAA7 in yeast (Saccharomyces cerevisiae) two-hybrid experiments, indicating that these proteins w
150 tory subunits of PP2A, Wdb and Wrd, in yeast two-hybrid experiments.
151                                              Two hybrid fluorinated double-chain surfactants with a d
152                                Using a yeast two-hybrid genome-wide screen, we identified novel inter
153 pha-helix(656-666), which are required for a two-hybrid Gln3-Tor1 interaction, also abolished rapamyc
154                                  Using yeast two-hybrid, GST pull-down, co-immunoprecipitation and bi
155 ary methods-a high-throughput enhanced yeast two-hybrid (HT-eY2H) assay and a mammalian-cell-based Ga
156 s between the various MORF proteins by yeast two-hybrid, in vitro pulldown, and bimolecular fluoresce
157                                              Two-hybrid interaction experiments suggest that the inte
158 to its principal endomembrane cargo, a yeast two-hybrid library of Arabidopsis thaliana cDNAs was scr
159     Using a yeast (Saccharomyces cerevisiae) two-hybrid library of S. reilianum-infected maize tissue
160                            Screening a yeast two-hybrid library revealed that UNC-89 interacts with p
161  as a Myb1-binding protein using a bacterial two-hybrid library screening system.
162                              Using bacterial two-hybrid library screening, NR1D1 was identified as a
163                    Here, we screened a yeast two-hybrid library using the Arabidopsis LDAP3 isoform a
164                          We screened a yeast two-hybrid library using the central domain of ubiquilin
165          Therefore, a pancreatic islet yeast two-hybrid library was produced and searched for glucoki
166                   Using an RXR-VDR mammalian two-hybrid (M2H) biologic assay system, we measured vita
167             Recently, we constructed a yeast two-hybrid map around three rice proteins that control t
168 cadherin 23 with expressed exon 68) by yeast two-hybrid mating and co-transformation protocols, pulld
169  we utilized the bacterial adenylate cyclase two-hybrid method and carried out a saturation mutagenes
170 rall prediction accuracy, with the in-silico two-hybrid method contributing most to performance.
171 we used random mutagenesis and the mammalian two-hybrid method MAPPIT (mammalian protein-protein inte
172 re, we present a massively multiplexed yeast two-hybrid method, CrY2H-seq, which uses a Cre recombina
173                Here, we demonstrate by yeast two-hybrid method, immunoprecipitation assays, and surfa
174                                  Using yeast two-hybrid methods, we identified a large set of protein
175 sequence-based prediction methods: in-silico two-hybrid, mirror-tree, gene fusion, phylogenetic profi
176 Sho1p PPIs through the use of membrane yeast two-hybrid (MYTH), an assay specifically suited to ident
177                      The volatile profile of two hybrids of "Radicchio di Chioggia", Corelli and Bott
178 es associated with ontologic cancer sets and two hybrids of separate experimental replicates clustere
179  III where the instability is dependent upon two hybrid-prone sequences.
180                                  Using yeast two-hybrid protein interaction studies, we found that a
181 igh-content imaging and a mammalian membrane two-hybrid protein-protein interaction method, we identi
182 ith our interactions studies including yeast two-hybrid, pull-down, and in planta fluorescence resona
183 ture (SILAC) data with high-throughput yeast two hybrid results, we showed that five of these protein
184 in Containing Protein, HvELMOD_C, in a yeast two hybrid screen for proteins interacting with HvMAGAP1
185                         We performed a yeast two hybrid screen with SR34 as bait and discovered SR45
186 C2.2]) in a yeast (Saccharomyces cerevisiae) two-hybrid screen and have confirmed this interaction th
187 regulation, we performed a large-scale yeast two-hybrid screen and identified CONSTANS-LIKE 3 (COL3)/
188                         We performed a yeast two-hybrid screen and identified the adaptor protein, FH
189 interacting partner of SIS8 based on a yeast two-hybrid screen and in planta bimolecular fluorescence
190  interacting factor for Kbtbd5 using a yeast two-hybrid screen and in vitro binding assays.
191 t with known clock components in a mammalian two-hybrid screen and modulate in vitro cellular rhythms
192                 In this study, using a yeast two-hybrid screen approach, we identified the NF-YB and
193                      On the basis of a yeast two-hybrid screen for the MT1-MMP cytoplasmic tail-bindi
194                                      A yeast two-hybrid screen has identified the adaptor protein X11
195                                      A yeast two-hybrid screen has revealed that the transcriptional
196                                  A bacterial two-hybrid screen identified an interaction between CtsP
197                                Here, a yeast two-hybrid screen revealed that RABV P interacts with th
198                Using a split-ubiquitin yeast two-hybrid screen that covers a test-space of 6.4 x 10(6
199 -terminal subdomain that was used in a yeast two-hybrid screen that identified the proline-rich domai
200     We have previously shown through a yeast two-hybrid screen that it is also a cardiac binding part
201 nding of MTM1 function, we conducted a yeast two-hybrid screen to identify MTM1-interacting proteins.
202 otes genomic stability by performing a yeast two-hybrid screen to identify potential substrates/inter
203                       Using a membrane-based two-hybrid screen to identify proteins that bind to PCDH
204 cular functions of FTO, we performed a yeast two-hybrid screen to identify the protein(s) that could
205  TDP-43 protein interactors found in a yeast two-hybrid screen using an adult human brain cDNA librar
206 teractions, we performed a large-scale yeast two-hybrid screen using both wild-type (WT) and six diff
207                We have now performed a yeast two-hybrid screen using dysbindin as bait against a card
208 hat may remove the CRD, we performed a yeast two-hybrid screen using twitchin kinase as bait.
209 otein interaction partners of NBP35, a yeast-two-hybrid screen was carried out that identified NBP35
210 luence its subcellular localization, a yeast two-hybrid screen was performed.
211                                      A yeast-two-hybrid screen with CPRabA5e as bait revealed 13 inte
212                                Using a yeast two-hybrid screen, we discovered an interaction between
213                                Using a yeast two-hybrid screen, we identified a novel transcription c
214                                Using a yeast two-hybrid screen, we identified cyclin L2 as a DCAF1-in
215                                Using a yeast two-hybrid screen, we identified four cytoskeletal compo
216                                Using a yeast two-hybrid screen, we identified the anti-apoptotic prot
217                                Using a yeast two-hybrid screen, we identified the hematopoietic-restr
218                   Furthermore, using a yeast two-hybrid screen, we identified the motor protein Kif15
219                                Using a yeast two-hybrid screen, we searched for novel AIRE-interactin
220 eneurin-1 ICD interaction partner in a yeast two-hybrid screen.
221 tify Wor1-interacting proteins using a yeast two-hybrid screen.
222  we performed a comprehensive pairwise yeast two-hybrid screen.
223 in was identified by a Split-Ubiquitin Yeast-Two-Hybrid screen.
224 rotein interaction data from a focused yeast two-hybrid screen.
225 genase in a yeast (Saccharomyces cerevisiae) two-hybrid screen; other TX and TN proteins interacted w
226 tein-protein interactions (PPIs) using yeast two-hybrid screening (Y2H).
227 D11) as a new interactor of PLEKHA7 by yeast two-hybrid screening and by mass spectrometry analysis o
228                                  Using yeast two-hybrid screening and co-immunoprecipitation assays,
229 oteins in Vpu function, we carried out yeast two-hybrid screening and identified a previously reporte
230                                        Yeast two-hybrid screening combined with bimolecular fluoresce
231                                  Using yeast two-hybrid screening coupled with a candidate approach,
232             We isolated Myosin Vc in a yeast two-hybrid screening for proteins that interact with Rab
233                                        Yeast two-hybrid screening identified an interaction between N
234          To address this, we performed yeast two-hybrid screening of PRMT7 and identified argininosuc
235                                      A yeast two-hybrid screening revealed a specific interaction wit
236                                        Yeast two-hybrid screening suggests that XB130 interacts with
237 40 was found to be a centrin target by yeast-two-hybrid screening using both Homo sapiens centrin 2 (
238                                         In a two-hybrid screening using the catalytic Sec7 domain as
239  To identify the presumed receptor proteins, two-hybrid screening was performed.
240           SPBB1 was identified through yeast two-hybrid screening with the kinase-dead TbPLK as the b
241  proteins determined using multivector yeast two-hybrid screening, and these PPIs were further suppor
242 By means of yeast (Saccharomyces cerevisiae) two-hybrid screening, we identified basic helix-loop-hel
243                                Through yeast two-hybrid screening, we identified tumor suppressor p27
244                                Through yeast two-hybrid screening, we identify the centrosomal protei
245 ins that can interact with JSRV Env by yeast two-hybrid screening.
246 entified by yeast (Saccharomyces cerevisiae) two-hybrid screening.
247 rotein 1 (SR1IP1) was identified by CytoTrap two-hybrid screening.
248 ified as a Vav3 interacting protein by yeast two-hybrid screening.
249 e interacting partner of NLRC3 through yeast two-hybrid screening.
250 mation efficiency is critical, such as yeast two-hybrid screening.
251 artner of the E2 protein of CSFV using yeast two-hybrid screening.
252 of thromboxane A2 receptor (TPbeta) by yeast two-hybrid screening.
253 the roles of IDRs in CBP, we performed yeast-two-hybrid screenings of placenta and lung cancer cDNA l
254              Employing pooled RNAi and yeast two-hybrid screenings, we report that the mitochondrial
255 aling pathway components, we performed yeast two-hybrid screens and identified the muscle-specific pr
256 ify host targets of AVR1, we performed yeast two-hybrid screens and selected Sec5 as a candidate.
257                                        Yeast-two-hybrid screens identify RhoC as a Fam65b binding par
258                      Here we performed yeast two-hybrid screens of 3,305 baits against 3,606 preys (
259                                        Yeast two-hybrid screens revealed that CEFIP interacts with th
260 olycystic kidney disease, we performed yeast two-hybrid screens using the C-terminus of polycystin-1
261 tor-protein interactions, we conducted yeast two-hybrid screens using the cytosolic domains of ETR1 a
262                     In addition, using yeast two-hybrid screens we identified several candidates of N
263 argets in the host cells, we performed yeast two-hybrid screens, allowing us to find 48 high-confiden
264                 Using STK38 as bait in yeast-two-hybrid screens, we discovered STK38 as a novel bindi
265 s results from electron microscopy and yeast two-hybrid screens.
266 er NCX1 was found to interact with Ano6 in a two-hybrid split-ubiquitin screen.
267                                        Yeast two-hybrid studies revealed that meiosis-expressed gene
268 n interaction which we confirmed using yeast two-hybrid studies.Taken together, we find evidence for
269                                   In a yeast two-hybrid study, we identified a novel interaction betw
270  TaFROG-interacting protein based on a yeast two-hybrid study.
271                                  A Bacterial Two Hybrid system indicates that DauA and the sensor com
272                     By employing a bacterial two hybrid system, pull down assays and surface plasmon
273 is sensitivity issue, we introduced in vitro two-hybrid system (IVT2H) into microfluidic drops and de
274 r-binding protein PspF to create an in vitro two-hybrid system (IVT2H), capable of carrying out gene
275                              Using the yeast two-hybrid system and bimolecular fluorescence complemen
276 were systematically mapped using a mammalian two-hybrid system and confirmed using a co-immunoprecipi
277 ly developed interaction assays (e.g., yeast two-hybrid system and split-ubiquitin assay) usually are
278 brane-based yeast (Saccharomyces cerevisiae) two-hybrid system established that tetraspanins can phys
279  its original description in 1989, the yeast two-hybrid system has been extensively used to identify
280 domains of each immune receptor in the yeast two-hybrid system in a kinase activity-dependent manner.
281 criptional effectors (LITEs), an optogenetic two-hybrid system integrating the customizable TALE DNA-
282 d the Sos recruitment system, an alternative two-hybrid system method to detect protein-protein inter
283                                  A bacterial two-hybrid system screen identified bacterioferritins an
284                          Here we use a yeast two-hybrid system to identify novel TIR1 mutants with al
285 we used the yeast (Saccharomyces cerevisiae) two-hybrid system to screen for NF-YC1-interacting prote
286                          Here, using a yeast two-hybrid system to search for AtRALF1-interacting prot
287 raction of full-length PsIAA4 in vivo (yeast two-hybrid system).
288                            Using a bacterial two-hybrid system, it could be shown that the N-terminus
289 y-capture complex purification and the yeast two-hybrid system, may produce inaccurate data sets owin
290    Using a modified yeast substrate trapping two-hybrid system, we identified a cytosolic adaptor pro
291 as a novel DAT binding partner using a yeast two-hybrid system.
292 aptured proteins was verified in a bacterial two-hybrid system.
293 also detected with the yeast split-ubiquitin two-hybrid system.
294 -immunoprecipitation assay and the mammalian two-hybrid system.
295         PIP5K6 interacted with MPK6 in yeast two-hybrid tests, immuno-pull-down assays, and by bimole
296 f the NS4A TM domain in a well-characterized two-hybrid TM protein interaction system.
297 teractions (PPIs) of HEV by systematic Yeast two-hybrid (Y2H) and LuMPIS screens, providing a basis f
298 ystems, such as affinity purification, yeast two-hybrid (Y2H) and protein-fragment complementation as
299                         We performed a yeast two-hybrid (Y2H) screen and uncovered TNKS as a putative
300                       We recently used yeast two-hybrid (Y2H) screening to identify a small set of no

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