1 Yeast two-hybrid analyses using serial domain deletion c
2 Split-ubiquitin
yeast-two-hybrid analyses revealed that the cell surface
3 Further
yeast two-hybrid analysis also showed that the PHOT2 C-t
4 ent bimolecular complementation assays, i.e.
yeast two-hybrid analysis and Arabidopsis leaf protoplas
5 erminus actually binds to ankyrin-G, both in
yeast two-hybrid analysis and by coimmunoprecipitation i
6 Yeast two-hybrid analysis confirmed RIP1 interaction wit
7 In this investigation,
yeast two-hybrid analysis demonstrated that an E. chaffe
8 Yeast two-hybrid analysis identified whirlin, a PDZ-scaf
9 e MRB1 complex, we performed a comprehensive
yeast two-hybrid analysis of 31 reported MRB1 proteins.
10 ral proteome, we carried out a comprehensive
yeast two-hybrid analysis of all the putative proteins e
11 Yeast two-hybrid analysis reveals that SIX6OS1 interacts
12 Yeast two-hybrid analysis showed no evidence of a direct
13 Yeast two-hybrid analysis shows that Mzt1/Tam4 forms a c
14 Yeast two-hybrid analysis shows that the rod domain of K
15 A
yeast two-hybrid analysis uncovered the actin-depolymeri
16 ing partner for CD16A-CY newly identified by
yeast two-hybrid analysis, inhibits phosphorylation of C
17 Using
yeast two-hybrid analysis, we identified the database-do
18 f a novel binding partner of E5, YIPF4 using
yeast two-hybrid analysis.
19 istone deacetylase subunits were observed in
yeast two-hybrid and bimolecular fluorescence assays, co
20 Yeast two-hybrid and bimolecular fluorescence complement
21 Both
yeast two-hybrid and bimolecular fluorescence complement
22 Furthermore,
yeast two-hybrid and bimolecular fluorescence complement
23 Our complementary
yeast two-hybrid and biochemical assays reveal that CHD7
24 Yeast two-hybrid and biochemical studies have revealed t
25 Results from
yeast two-hybrid and co-expression in Escherichia coli c
26 Here, using
yeast two-hybrid and co-immunoprecipitation approaches,
27 Yeast two-hybrid and co-immunoprecipitation assays demon
28 Yeast two-hybrid and coimmunoprecipitation analyses asso
29 On the basis of
yeast two-hybrid and coimmunoprecipitation assays, we de
30 here that ICP0 interacts with PML.I in both
yeast two-hybrid and coimmunoprecipitation assays.
31 Using both
yeast two-hybrid and copurification approaches, we ident
32 Yeast two-hybrid and direct pulldown assays revealed tha
33 TCP14 and TCP15 interacted with SPY in
yeast two-hybrid and in vitro pull-down assays and were
34 RNF34 (an E3 ubiquitin ligase), as shown by
yeast two-hybrid and in vitro pulldown assays.
35 CagA to the beta1 integrin, as determined by
yeast two-hybrid and in vivo competition assays in H. py
36 Combined
yeast two-hybrid and protein array experiments demonstra
37 In
yeast two-hybrid and pull-down assays, MORF proteins can
38 Yeast two-hybrid and pull-down experiments identify two
39 Furthermore,
yeast two-hybrid and pull-down experiments indicated tha
40 Here, we show by
yeast two-hybrid and pulldown assays that SpoVID also in
41 Split ubiquitin
yeast two-hybrid and split GFP assays indicate that Arab
42 Transcriptional assays, such as
yeast two-hybrid and TANGO, that convert transient prote
43 irm the interaction of OsHOS1 with OsICE1 by
Yeast-Two hybrid and bi-molecular fluorescence complemen
44 Yeast-two-hybrid and a green-fluorescent protein fragmen
45 of eutherian and avian cDNA libraries using
yeast-two-hybrid and split-ubiquitin systems.
46 Modeling,
yeast two-hybrid,
and functional data reveal that this P
47 the four USH proteins using colocalization,
yeast two-hybrid,
and pull-down assays.
48 using coimmunoprecipitation, colocalization,
yeast two-hybrid,
and small interfering RNA (siRNA) anal
49 Here we use a
yeast two-hybrid approach to demonstrate that Rrp1 and R
50 s of virus replication, we have been using a
yeast two-hybrid approach to identify host proteins that
51 the process of virus replication, we used a
yeast two-hybrid approach to identify host proteins that
52 In this study, a
yeast two-hybrid approach using the cytoplasmic domain o
53 chanisms and identify putative substrates, a
yeast two-hybrid approach was carried on and a protein w
54 The 3A-DCTN3 interaction identified by the
yeast two-hybrid approach was further confirmed in mamma
55 Here, using a
yeast two-hybrid approach, we have assessed interactions
56 By using the
Yeast Two-Hybrid approach, we identified a disintegrin a
57 Using a
yeast two-hybrid approach, we identified cellular protei
58 Using a
yeast two-hybrid approach, we identified the 5'-3' exonu
59 rate PPI maps at proteome scale, first using
yeast two-hybrid approaches and more recently via affini
60 We used proteomic and
yeast two-hybrid approaches to elucidate host factors in
61 n affinity purification-mass spectrometry or
yeast two-hybrid approaches.
62 from high-throughput techniques such as the
yeast two-hybrid assay and affinity purification, as wel
63 We performed a
yeast two-hybrid assay and identified hematopoietically
64 proteins also directly interact in vivo in a
yeast two-hybrid assay and in vitro through ammonium sul
65 idopsis transcription factor prey library by
yeast two-hybrid assay and isolated six class I members
66 The
yeast two-hybrid assay identified that proteasome subuni
67 Yeast two-hybrid assay indicated that the PDH45 protein
68 Yeast two-hybrid assay revealed that the N-terminal regi
69 we screened a kidney cDNA library through a
yeast two-hybrid assay using NKCC2 C terminus as bait.
70 teractions with core exocyst subunits in the
yeast two-hybrid assay, cytoplasmic localization, and ge
71 According to a
yeast two-hybrid assay, ORRM1 interacts selectively with
72 In a
yeast two-hybrid assay, the thioredoxin-like domain of L
73 We searched for such proteins by
yeast two-hybrid assay, using GARP as a bait to screen a
74 teracting proteins with GLP-1R by a membrane
yeast two-hybrid assay.
75 at shock proteins, Hsp16.9 and Hsp17.5, in a
yeast two-hybrid assay.
76 e of MamK and the two proteins interact in a
yeast two-hybrid assay.
77 TRPC4-interacting proteins using a modified
yeast two-hybrid assay.
78 GR and modulate its function, we performed a
yeast two-hybrid assay.
79 idopsis DEAD-box helicase/ATPase LOS4 in the
yeast two-hybrid assay.
80 SAGA subunits including Sgf29 and Spt7 in a
yeast two-hybrid assay.
81 p-interacting proteins were screened using a
yeast two-hybrid assay.
82 cting proteins were identified by a modified
yeast two-hybrid assay.
83 semi-high-throughput, array-based, directed
yeast two-hybrid assay.
84 try or genetic approaches exemplified by the
yeast two-hybrid assay; however, neither assay works wel
85 By a combination of
yeast-two hybrid assay, in vitro binding, and coimmunopr
86 nds that prevent DEPTOR binding to mTOR in a
yeast-two-hybrid assay.
87 PYL6 and MYC2 interact in
yeast two hybrid assays and the interaction is enhanced
88 ot with other mitochondrial MORF proteins in
yeast two hybrid assays.
89 and the ESCRT-III-related proteins CHMP1A in
yeast two hybrid assays.
90 ABD1 directly interacts with ABI5 in
yeast two-hybrid assays and associates with ABI5 in vivo
91 15-CD3 and TMC1 or TMC2 was observed in both
yeast two-hybrid assays and coimmunoprecipitation experi
92 Yeast two-hybrid assays and coimmunoprecipitation experi
93 bind to the blue-light photoreceptor FKF1 in
yeast two-hybrid assays and delays flowering in Arabidop
94 quence with beta-catenin was confirmed using
yeast two-hybrid assays and in vitro synthesized protein
95 Yeast two-hybrid assays detect interactions between the
96 Yeast two-hybrid assays established a direct interaction
97 Here, using
yeast two-hybrid assays followed by biochemical binding
98 Yeast two-hybrid assays identified ETTIN (ETT, or AUXIN
99 ers for each Chlamydomonas FDX; (b) pairwise
yeast two-hybrid assays measuring FDX interactions with
100 Furthermore, our
yeast two-hybrid assays show that MoVps17 and MoVps5 can
101 RNA-seq and proteomics data together with
yeast two-hybrid assays suggest that MS23 along with MS3
102 Yeast two-hybrid assays suggested an interaction of Psb2
103 tudy, we used membrane-based split ubiquitin
yeast two-hybrid assays to identify novel GLP1R interact
104 Here, we carry out directional
yeast two-hybrid assays to identify the interactions bet
105 Furthermore, we used
yeast two-hybrid assays to show that DYT1 forms homodime
106 ein Athb-21 and ESE1 are able to interact in
yeast two-hybrid assays with the ABA responsive element
107 In
yeast two-hybrid assays ZYX-1 interacts with several kno
108 identified as Oas1b interaction partners in
yeast two-hybrid assays, and both in vitro-transcribed/t
109 ombination of pull-downs, mass spectrometry,
yeast two-hybrid assays, and chemical genomics, we demon
110 In
yeast two-hybrid assays, FgMcm1 interacted with Mat1-1-1
111 eracts with P. blakesleeanus Ras homologs in
yeast two-hybrid assays, indicating that MadC is a regul
112 akin family member periplakin, identified in
yeast two-hybrid assays, interacted with a membrane-prox
113 In
yeast two-hybrid assays, MAS2 interacted with splicing a
114 Using
yeast two-hybrid assays, we determined the interactions
115 fications coupled with mass spectrometry and
yeast two-hybrid assays, we show the Saccharomyces cerev
116 ADP-bound state failed to bind to AvrL567 in
yeast two-hybrid assays, while binding was detected to t
117 TEL2 can interact with both TTI1 and TTI2 in
yeast two-hybrid assays.
118 the peptide aptamers for further analysis in
yeast two-hybrid assays.
119 eracts with UNC-116 kinesin-1 heavy chain in
yeast two-hybrid assays.
120 s being relatively little affected by ABA in
yeast two-hybrid assays.
121 Site-directed mutagenesis and
yeast-two hybrid assays identified DnaA and DnaN binding
122 In
yeast-two hybrid assays, ORRM3 interacts with RIP1, ORRM
123 full-length protein in vivo, as measured by
yeast-two hybrid assays.
124 By
yeast-two-hybrid assays and chromatin immunoprecipitatio
125 bimolecular fluorescence complementation and
yeast-two-hybrid assays indicated that the IDR3 domain d
126 tion-mass spectrometry, split-luciferase and
yeast-two-hybrid assays to generate a single reliability
127 Using
yeast two-hybrid,
biochemical, and cellular assays, we d
128 Yeast two-hybrid,
co-immunoprecipitation and pulldown ex
129 , is a binding partner of IL-13Ralpha2 using
yeast two-hybrid,
co-immunoprecipitation, co-localizatio
130 Yeast two-hybrid,
coimmunoprecipitation and bimolecular
131 Yeast two-hybrid,
coimmunoprecipitation, and fluorescenc
132 Furthermore,
yeast two-hybrid data showed that CPTL2 and CPT3 interac
133 Yeast-two-hybrid data and a novel sequence analysis meth
134 ents such as ChIP-Seq, RNA interference, and
yeast two hybrid experiments.
135 Yeast two-hybrid experiments confirmed the direct intera
136 Yeast two-hybrid experiments identified PG core proteins
137 Yeast two-hybrid experiments indicate that the interacti
138 Yeast two-hybrid experiments suggested that the phosphor
139 regulatory subunits of PP2A, Wdb and Wrd, in
yeast two-hybrid experiments.
140 Competitive
yeast-two hybrid experiments indicate that the LIM domai
141 Using a
yeast two-hybrid genome-wide screen, we identified novel
142 Using
yeast two-hybrid,
GST pull-down, co-immunoprecipitation
143 lementary methods-a high-throughput enhanced
yeast two-hybrid (
HT-eY2H) assay and a mammalian-cell-ba
144 mbers of the ABF/AREB clade and the PP2Cs by
yeast two-hybrid,
in vitro phosphatase, and bimolecular
145 CML24 interacts with ATG4b in
yeast two-hybrid,
in vitro pull-down and transient tobac
146 actions between the various MORF proteins by
yeast two-hybrid,
in vitro pulldown, and bimolecular flu
147 ay data, hyphal growth RNA-sequence data and
yeast two hybrid interaction data.
148 ipitations from transfected mammalian cells,
yeast two-hybrid interaction assays, and glutathione S-t
149 and CaM-like (CML) proteins in vitro and in
yeast two-hybrid interaction assays.
150 t technologies and find that high-throughput
yeast two-hybrid is the only available technology for de
151 aches to its principal endomembrane cargo, a
yeast two-hybrid library of Arabidopsis thaliana cDNAs w
152 Screening a
yeast two-hybrid library revealed that UNC-89 interacts
153 Yeast two-hybrid library screening and in vitro protein
154 Here, we screened a
yeast two-hybrid library using the Arabidopsis LDAP3 iso
155 We screened a
yeast two-hybrid library using the central domain of ubi
156 Therefore, a pancreatic islet
yeast two-hybrid library was produced and searched for g
157 the roles of SR45 in splicing, we screened a
yeast two-hybrid library with SR45.
158 Recently, we constructed a
yeast two-hybrid map around three rice proteins that con
159 +68 (cadherin 23 with expressed exon 68) by
yeast two-hybrid mating and co-transformation protocols,
160 Here, we present a massively multiplexed
yeast two-hybrid method, CrY2H-seq, which uses a Cre rec
161 Here, we demonstrate by
yeast two-hybrid method, immunoprecipitation assays, and
162 Using
yeast two-hybrid methods, we identified a large set of p
163 nique Sho1p PPIs through the use of membrane
yeast two-hybrid (
MYTH), an assay specifically suited to
164 Using
yeast two-hybrid protein interaction studies, we found t
165 ther with our interactions studies including
yeast two-hybrid,
pull-down, and in planta fluorescence
166 ll culture (SILAC) data with high-throughput
yeast two hybrid results, we showed that five of these p
167 O Domain Containing Protein, HvELMOD_C, in a
yeast two hybrid screen for proteins interacting with Hv
168 We performed a
yeast two hybrid screen with SR34 as bait and discovered
169 BBX32 regulation, we performed a large-scale
yeast two-hybrid screen and identified CONSTANS-LIKE 3 (
170 We performed a
yeast two-hybrid screen and identified the adaptor prote
171 as an interacting partner of SIS8 based on a
yeast two-hybrid screen and in planta bimolecular fluore
172 direct interacting factor for Kbtbd5 using a
yeast two-hybrid screen and in vitro binding assays.
173 In this study, using a
yeast two-hybrid screen approach, we identified the NF-Y
174 TRN-SR2 was originally identified in a
yeast two-hybrid screen as an interaction partner of HIV
175 Migfilin, originally identified in a
yeast two-hybrid screen for kindlin-2-interacting protei
176 We performed a
yeast two-hybrid screen for novel cofactors, and identif
177 On the basis of a
yeast two-hybrid screen for the MT1-MMP cytoplasmic tail
178 A
yeast two-hybrid screen has identified the adaptor prote
179 A
yeast two-hybrid screen has revealed that the transcript
180 A
yeast two-hybrid screen identified mu2 as a putative int
181 To that end, we report a
yeast two-hybrid screen of all human Rabs for myosin Va-
182 Here, a
yeast two-hybrid screen revealed that RABV P interacts w
183 Using a split-ubiquitin
yeast two-hybrid screen that covers a test-space of 6.4
184 fy key amino acid residues on PXR based on a
yeast two-hybrid screen that examined mutant forms of PX
185 able N-terminal subdomain that was used in a
yeast two-hybrid screen that identified the proline-rich
186 We have previously shown through a
yeast two-hybrid screen that it is also a cardiac bindin
187 n this study, we performed a high throughput
yeast two-hybrid screen to identify additional pathways
188 derstanding of MTM1 function, we conducted a
yeast two-hybrid screen to identify MTM1-interacting pro
189 O promotes genomic stability by performing a
yeast two-hybrid screen to identify potential substrates
190 We used a
yeast two-hybrid screen to identify the plant SnRK1 (for
191 e molecular functions of FTO, we performed a
yeast two-hybrid screen to identify the protein(s) that
192 pecially abundant in retina, was fished with
yeast two-hybrid screen using a constitutively active Ga
193 novel TDP-43 protein interactors found in a
yeast two-hybrid screen using an adult human brain cDNA
194 ein interactions, we performed a large-scale
yeast two-hybrid screen using both wild-type (WT) and si
195 We have now performed a
yeast two-hybrid screen using dysbindin as bait against
196 molecular partners of MIG-10, we conducted a
yeast two-hybrid screen using isoform MIG-10A as bait an
197 ciated protein YejK, which was detected in a
yeast two-hybrid screen using the ParE subunit of topois
198 eins that may remove the CRD, we performed a
yeast two-hybrid screen using twitchin kinase as bait.
199 ht influence its subcellular localization, a
yeast two-hybrid screen was performed.
200 stone H1.2 as a DME-interacting protein in a
yeast two-hybrid screen, and confirmation of their inter
201 Using a
yeast two-hybrid screen, we discovered an interaction be
202 Using a
yeast two-hybrid screen, we found that splice cassette I
203 Employing C2GnT1 CT as the bait to perform a
yeast two-hybrid screen, we have identified Golgi phosph
204 Through a
yeast two-hybrid screen, we have identified XPLN (exchan
205 Using a
yeast two-hybrid screen, we identified a novel transcrip
206 Using a
yeast two-hybrid screen, we identified a RING domain ubi
207 Using a
yeast two-hybrid screen, we identified cyclin L2 as a DC
208 Using a
yeast two-hybrid screen, we identified espin, an actin-b
209 Using a
yeast two-hybrid screen, we identified four cytoskeletal
210 Using a
yeast two-hybrid screen, we identified the anti-apoptoti
211 Using a
yeast two-hybrid screen, we identified the hematopoietic
212 Using a
yeast two-hybrid screen, we identified the human homolog
213 Furthermore, using a
yeast two-hybrid screen, we identified the motor protein
214 Using a
yeast two-hybrid screen, we searched for novel AIRE-inte
215 Using a
yeast two-hybrid screen, we show that RBBP6 interacts wi
216 o identify Wor1-interacting proteins using a
yeast two-hybrid screen.
217 arity, we performed a comprehensive pairwise
yeast two-hybrid screen.
218 tein-protein interaction data from a focused
yeast two-hybrid screen.
219 uman teneurin-1 ICD interaction partner in a
yeast two-hybrid screen.
220 ind protein interaction partners of NBP35, a
yeast-two-hybrid screen was carried out that identified
221 A
yeast-two-hybrid screen with CPRabA5e as bait revealed 1
222 protein was identified by a Split-Ubiquitin
Yeast-Two-Hybrid screen.
223 st protein-protein interactions (PPIs) using
yeast two-hybrid screening (Y2H).
224 1 (PDZD11) as a new interactor of PLEKHA7 by
yeast two-hybrid screening and by mass spectrometry anal
225 Using
yeast two-hybrid screening and co-immunoprecipitation as
226 ell proteins in Vpu function, we carried out
yeast two-hybrid screening and identified a previously r
227 Yeast two-hybrid screening combined with bimolecular flu
228 Using
yeast two-hybrid screening coupled with a candidate appr
229 We isolated Myosin Vc in a
yeast two-hybrid screening for proteins that interact wi
230 Yeast two-hybrid screening identified an interaction bet
231 Yeast two-hybrid screening identified Isl1, a LIM/homeod
232 To address this, we performed
yeast two-hybrid screening of PRMT7 and identified argin
233 A
yeast two-hybrid screening revealed a specific interacti
234 Yeast two-hybrid screening suggests that XB130 interacts
235 We first discovered by
yeast two-hybrid screening that the C termini of ENaC al
236 uences differentiation of neurons, we used a
yeast two-hybrid screening to search for new binding par
237 SPBB1 was identified through
yeast two-hybrid screening with the kinase-dead TbPLK as
238 entified as a putative cofactor of Jarid2 by
yeast two-hybrid screening, and the physical interaction
239 Bam35 proteins determined using multivector
yeast two-hybrid screening, and these PPIs were further
240 Using a
yeast two-hybrid screening, we found that the Pkd2L1 N t
241 By
yeast two-hybrid screening, we identified the Polycomb-l
242 Through
yeast two-hybrid screening, we identified tumor suppress
243 Through
yeast two-hybrid screening, we identify the centrosomal
244 proteins that can interact with JSRV Env by
yeast two-hybrid screening.
245 identified as a Vav3 interacting protein by
yeast two-hybrid screening.
246 Aedes CYC as a MET-interacting protein using
yeast two-hybrid screening.
247 utative interacting partner of NLRC3 through
yeast two-hybrid screening.
248 ansformation efficiency is critical, such as
yeast two-hybrid screening.
249 ding partner of the E2 protein of CSFV using
yeast two-hybrid screening.
250 oform of thromboxane A2 receptor (TPbeta) by
yeast two-hybrid screening.
251 Using
yeast-two hybrid screening followed by co-immunoprecipit
252 Prp40 was found to be a centrin target by
yeast-two-hybrid screening using both Homo sapiens centr
253 By
yeast two-hybrid screenings, we found a specific interac
254 Employing pooled RNAi and
yeast two-hybrid screenings, we report that the mitochon
255 amine the roles of IDRs in CBP, we performed
yeast-two-hybrid screenings of placenta and lung cancer
256 G signaling pathway components, we performed
yeast two-hybrid screens and identified the muscle-speci
257 identify host targets of AVR1, we performed
yeast two-hybrid screens and selected Sec5 as a candidat
258 Here we performed
yeast two-hybrid screens of 3,305 baits against 3,606 pr
259 Here, large-scale
yeast two-hybrid screens repeatedly identified a surpris
260 Yeast two-hybrid screens revealed that CEFIP interacts w
261 nant polycystic kidney disease, we performed
yeast two-hybrid screens using the C-terminus of polycys
262 receptor-protein interactions, we conducted
yeast two-hybrid screens using the cytosolic domains of
263 In addition, using
yeast two-hybrid screens we identified several candidate
264 tein targets in the host cells, we performed
yeast two-hybrid screens, allowing us to find 48 high-co
265 ort, we present data from the following: (a)
yeast two-hybrid screens, identifying interaction partne
266 revious results from electron microscopy and
yeast two-hybrid screens.
267 Yeast-two-hybrid screens identify RhoC as a Fam65b bindi
268 Using STK38 as bait in
yeast-two-hybrid screens, we discovered STK38 as a novel
269 nesulfonate suppressor mutants and performed
yeast-two-hybrid screens.
270 Yeast two-hybrid studies revealed that meiosis-expressed
271 protein interaction which we confirmed using
yeast two-hybrid studies.Taken together, we find evidenc
272 In a
yeast two-hybrid study, we identified a novel interactio
273 d as a TaFROG-interacting protein based on a
yeast two-hybrid study.
274 In vitro study with
yeast two-hybrid suggests that most alpha-helices of R16
275 Using the
yeast two-hybrid system and bimolecular fluorescence com
276 ms of the importin alpha protein family in a
yeast two-hybrid system and by an in planta bimolecular
277 racted with Agrobacterium protein VirE2 in a
yeast two-hybrid system and in planta.
278 nitially developed interaction assays (e.g.,
yeast two-hybrid system and split-ubiquitin assay) usual
279 Since its original description in 1989, the
yeast two-hybrid system has been extensively used to ide
280 lular domains of each immune receptor in the
yeast two-hybrid system in a kinase activity-dependent m
281 sduction pathways have successfully used the
yeast two-hybrid system or related methods.
282 Here we use a
yeast two-hybrid system to identify novel TIR1 mutants w
283 Here, using a
yeast two-hybrid system to search for AtRALF1-interactin
284 Combining the
yeast two-hybrid system with genetic analysis, we show h
285 l interaction of full-length PsIAA4 in vivo (
yeast two-hybrid system).
286 e 3 (PDCL3, also known as PhLP2A), through a
yeast two-hybrid system, as a novel protein involved in
287 ffinity-capture complex purification and the
yeast two-hybrid system, may produce inaccurate data set
288 Using the
yeast two-hybrid system, we identified Sprouty2 as an in
289 cer-associated C terminus (BRCT) domain in a
yeast two-hybrid system, while increased sensitivity of
290 Ctr9 as a novel DAT binding partner using a
yeast two-hybrid system.
291 s of mouse Rpgr(ORF15) was used as bait in a
yeast two-hybrid system.
292 with the Cdh1 substrate-binding protein in a
yeast two-hybrid system.
293 protein-protein interaction assays using the
yeast two-hybrid system.
294 16 interacts with AtbZIP68 and AtGBF1 in the
yeast two-hybrid system.
295 Using the
yeast-two hybrid system we isolated a novel Numb interac
296 PIP5K6 interacted with MPK6 in
yeast two-hybrid tests, immuno-pull-down assays, and by
297 ein interactions (PPIs) of HEV by systematic
Yeast two-hybrid (
Y2H) and LuMPIS screens, providing a b
298 ntal systems, such as affinity purification,
yeast two-hybrid (
Y2H) and protein-fragment complementat
299 We performed a
yeast two-hybrid (
Y2H) screen and uncovered TNKS as a pu
300 We recently used
yeast two-hybrid (
Y2H) screening to identify a small set