1 Yeast two-hybrid analyses showed that 4E02 targets A. th
2 Yeast two-hybrid analyses showed that RD21A interacts wi
3 Yeast two-hybrid analyses using serial domain deletion c
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 ral proteome, we carried out a comprehensive
yeast two-hybrid analysis of all the putative proteins e
7 Yeast two-hybrid analysis reveals that SIX6OS1 interacts
8 Yeast two-hybrid analysis showed no evidence of a direct
9 Yeast two-hybrid analysis shows that Mzt1/Tam4 forms a c
10 Yeast two-hybrid analysis shows that the rod domain of K
11 Affinity purification and pairwise
yeast two-hybrid analysis suggest that ZC3H5 forms a com
12 A
yeast two-hybrid analysis uncovered the actin-depolymeri
13 f a novel binding partner of E5, YIPF4 using
yeast two-hybrid analysis.
14 Yeast two-hybrid and bimolecular complementation fluores
15 istone deacetylase subunits were observed in
yeast two-hybrid and bimolecular fluorescence assays, co
16 Yeast two-hybrid and bimolecular fluorescence complement
17 Furthermore,
yeast two-hybrid and bimolecular fluorescence complement
18 Protein-protein interaction studies (
yeast two-hybrid and bimolecular fluorescence complement
19 Yeast two-hybrid and bimolecular fluorescence complement
20 Both
yeast two-hybrid and bimolecular fluorescence complement
21 In this study, using membrane
yeast two-hybrid and bimolecular fluorescence complement
22 otein: protein interaction studies including
yeast two-hybrid and Bimolecular Fluorescence Complement
23 pair (GRMZM2G035341 and GRMZM2G152328) using
yeast two-hybrid and bimolecular fluorescent complementa
24 Our complementary
yeast two-hybrid and biochemical assays reveal that CHD7
25 Yeast two-hybrid and biochemical studies have revealed t
26 Results from
yeast two-hybrid and co-expression in Escherichia coli c
27 Here, using
yeast two-hybrid and co-immunoprecipitation approaches,
28 Yeast two-hybrid and co-immunoprecipitation assays demon
29 Yeast two-hybrid and coimmunoprecipitation analyses asso
30 On the basis of
yeast two-hybrid and coimmunoprecipitation assays, we de
31 ediates cAMP's effects on NCC, and conducted
yeast two-hybrid and coimmunoprecipitation experiments i
32 Using both
yeast two-hybrid and copurification approaches, we ident
33 Yeast two-hybrid and direct pulldown assays revealed tha
34 RNF34 (an E3 ubiquitin ligase), as shown by
yeast two-hybrid and in vitro pulldown assays.
35 Using
yeast two-hybrid and mass-spectrometric analysis, we rep
36 Sequencing" (DoMY-Seq), which leverages both
yeast two-hybrid and next-generation sequencing techniqu
37 Combined
yeast two-hybrid and protein array experiments demonstra
38 Yeast two-hybrid and pull-down experiments identify two
39 Furthermore,
yeast two-hybrid and pull-down experiments indicated tha
40 Split ubiquitin
yeast two-hybrid and split GFP assays indicate that Arab
41 Yeast two-hybrid and subsequent in silico structural pre
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 In the current study, we have used a
yeast two-hybrid approach to identify unknown partners o
52 eraction with DCTN6 were mapped by a reverse
yeast two-hybrid approach using a randomly mutated E2 li
53 In this study, a
yeast two-hybrid approach using the cytoplasmic domain o
54 chanisms and identify putative substrates, a
yeast two-hybrid approach was carried on and a protein w
55 The 3A-DCTN3 interaction identified by the
yeast two-hybrid approach was further confirmed in mamma
56 Here, using a
yeast two-hybrid approach, we have assessed interactions
57 By using the
Yeast Two-Hybrid approach, we identified a disintegrin a
58 Using a
yeast two-hybrid approach, we identified cellular protei
59 Using a
yeast two-hybrid approach, we identified the 5'-3' exonu
60 rate PPI maps at proteome scale, first using
yeast two-hybrid approaches and more recently via affini
61 We used proteomic and
yeast two-hybrid approaches to elucidate host factors in
62 n affinity purification-mass spectrometry or
yeast two-hybrid approaches.
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 A split-ubiquitin membrane
yeast two-hybrid assay demonstrated specific interaction
67 The
yeast two-hybrid assay identified that proteasome subuni
68 Yeast two-hybrid assay indicated that the PDH45 protein
69 Yeast two-hybrid assay results indicated that MKT1 direc
70 Yeast two-hybrid assay revealed that the N-terminal regi
71 we screened a kidney cDNA library through a
yeast two-hybrid assay using NKCC2 C terminus as bait.
72 teractions with core exocyst subunits in the
yeast two-hybrid assay, cytoplasmic localization, and ge
73 According to a
yeast two-hybrid assay, ORRM1 interacts selectively with
74 We searched for such proteins by
yeast two-hybrid assay, using GARP as a bait to screen a
75 Utilizing a
yeast two-hybrid assay, we discovered several novel inte
76 SAGA subunits including Sgf29 and Spt7 in a
yeast two-hybrid assay.
77 p-interacting proteins were screened using a
yeast two-hybrid assay.
78 cting proteins were identified by a modified
yeast two-hybrid assay.
79 semi-high-throughput, array-based, directed
yeast two-hybrid assay.
80 teracting proteins with GLP-1R by a membrane
yeast two-hybrid assay.
81 at shock proteins, Hsp16.9 and Hsp17.5, in a
yeast two-hybrid assay.
82 e of MamK and the two proteins interact in a
yeast two-hybrid assay.
83 TRPC4-interacting proteins using a modified
yeast two-hybrid assay.
84 GR and modulate its function, we performed a
yeast two-hybrid assay.
85 try or genetic approaches exemplified by the
yeast two-hybrid assay; however, neither assay works wel
86 RISPR-assisted RNA-RNA-binding protein [RBP]
yeast) two-hybrid assay to assess binding of our CEH mut
87 By a combination of
yeast-two hybrid assay, in vitro binding, and coimmunopr
88 nds that prevent DEPTOR binding to mTOR in a
yeast-two-hybrid assay.
89 PYL6 and MYC2 interact in
yeast two hybrid assays and the interaction is enhanced
90 and the ESCRT-III-related proteins CHMP1A in
yeast two hybrid assays.
91 ot with other mitochondrial MORF proteins in
yeast two hybrid assays.
92 ABD1 directly interacts with ABI5 in
yeast two-hybrid assays and associates with ABI5 in vivo
93 15-CD3 and TMC1 or TMC2 was observed in both
yeast two-hybrid assays and coimmunoprecipitation experi
94 Yeast two-hybrid assays and coimmunoprecipitation experi
95 bind to the blue-light photoreceptor FKF1 in
yeast two-hybrid assays and delays flowering in Arabidop
96 ial for the interaction of CRY2 with COP1 in
yeast two-hybrid assays and in planta Mutations in the V
97 quence with beta-catenin was confirmed using
yeast two-hybrid assays and in vitro synthesized protein
98 Yeast two-hybrid assays established a direct interaction
99 Here, using
yeast two-hybrid assays followed by biochemical binding
100 Yeast two-hybrid assays involving seven ABA receptor pro
101 ers for each Chlamydomonas FDX; (b) pairwise
yeast two-hybrid assays measuring FDX interactions with
102 Yeast two-hybrid assays reveal that RgsD can interact wi
103 Furthermore, our
yeast two-hybrid assays show that MoVps17 and MoVps5 can
104 RNA-seq and proteomics data together with
yeast two-hybrid assays suggest that MS23 along with MS3
105 Yeast two-hybrid assays suggested that GID1a has the hig
106 tudy, we used membrane-based split ubiquitin
yeast two-hybrid assays to identify novel GLP1R interact
107 Here, we carry out directional
yeast two-hybrid assays to identify the interactions bet
108 Yeast two-hybrid assays were used to identify ABA signal
109 In
yeast two-hybrid assays ZYX-1 interacts with several kno
110 ombination of pull-downs, mass spectrometry,
yeast two-hybrid assays, and chemical genomics, we demon
111 In
yeast two-hybrid assays, FgMcm1 interacted with Mat1-1-1
112 eracts with P. blakesleeanus Ras homologs in
yeast two-hybrid assays, indicating that MadC is a regul
113 akin family member periplakin, identified in
yeast two-hybrid assays, interacted with a membrane-prox
114 In
yeast two-hybrid assays, MAS2 interacted with splicing a
115 Here we show that in
yeast two-hybrid assays, the non-EAR protein, Related to
116 roism and thermal shift assays, and membrane
yeast two-hybrid assays, to define the mechanism mediati
117 4S]-containing plastidial proteins in binary
yeast two-hybrid assays, we also gained insights into th
118 Using
yeast two-hybrid assays, we determined the interactions
119 fications coupled with mass spectrometry and
yeast two-hybrid assays, we show the Saccharomyces cerev
120 ADP-bound state failed to bind to AvrL567 in
yeast two-hybrid assays, while binding was detected to t
121 the peptide aptamers for further analysis in
yeast two-hybrid assays.
122 eracts with UNC-116 kinesin-1 heavy chain in
yeast two-hybrid assays.
123 TEL2 can interact with both TTI1 and TTI2 in
yeast two-hybrid assays.
124 Site-directed mutagenesis and
yeast-two hybrid assays identified DnaA and DnaN binding
125 In
yeast-two hybrid assays, ORRM3 interacts with RIP1, ORRM
126 full-length protein in vivo, as measured by
yeast-two hybrid assays.
127 By
yeast-two-hybrid assays and chromatin immunoprecipitatio
128 bimolecular fluorescence complementation and
yeast-two-hybrid assays indicated that the IDR3 domain d
129 tion-mass spectrometry, split-luciferase and
yeast-two-hybrid assays to generate a single reliability
130 dimerization and subcellular localization by
yeast two-hybrid,
bimolecular fluorescence complementati
131 By using
yeast-two-hybrid,
bimolecular fluorescence complementati
132 Using
yeast two-hybrid,
biochemical, and cellular assays, we d
133 Yeast two-hybrid,
co-immunoprecipitation and pulldown ex
134 e genetic approaches, physiological methods,
yeast two-hybrid,
co-immunoprecipitation, and chromatin
135 , is a binding partner of IL-13Ralpha2 using
yeast two-hybrid,
co-immunoprecipitation, co-localizatio
136 Yeast two-hybrid,
coimmunoprecipitation and bimolecular
137 Yeast two-hybrid,
coimmunoprecipitation, and fluorescenc
138 Furthermore,
yeast two-hybrid data showed that CPTL2 and CPT3 interac
139 ents such as ChIP-Seq, RNA interference, and
yeast two hybrid experiments.
140 Yeast two-hybrid experiments confirmed the direct intera
141 Yeast two-hybrid experiments identified PG core proteins
142 Yeast two-hybrid experiments indicate that the interacti
143 Yeast two-hybrid experiments suggested that the phosphor
144 nd Recognition Nexus (MORN) domain; previous
yeast two-hybrid experiments with full-length and MORN-t
145 regulatory subunits of PP2A, Wdb and Wrd, in
yeast two-hybrid experiments.
146 Competitive
yeast-two hybrid experiments indicate that the LIM domai
147 transferase pulldown, coimmunoprecipitation,
yeast two-hybrid,
gel shift, and chromatin immunoprecipi
148 Using a
yeast two-hybrid genome-wide screen, we identified novel
149 Using
yeast two-hybrid,
GST pull-down, co-immunoprecipitation
150 lementary methods-a high-throughput enhanced
yeast two-hybrid (
HT-eY2H) assay and a mammalian-cell-ba
151 CML24 interacts with ATG4b in
yeast two-hybrid,
in vitro pull-down and transient tobac
152 actions between the various MORF proteins by
yeast two-hybrid,
in vitro pulldown, and bimolecular flu
153 and CaM-like (CML) proteins in vitro and in
yeast two-hybrid interaction assays.
154 Yeast-two-hybrid interaction and complementation assays
155 ed a tomato immune induced complementary DNA
yeast two-hybrid library and screened it with Me10 as ba
156 and PKG's mechanism of action, we screened a
yeast two-hybrid library for P. falciparum proteins that
157 aches to its principal endomembrane cargo, a
yeast two-hybrid library of Arabidopsis thaliana cDNAs w
158 Screening a
yeast two-hybrid library revealed that UNC-89 interacts
159 Here, we screened a
yeast two-hybrid library using the Arabidopsis LDAP3 iso
160 We screened a
yeast two-hybrid library using the central domain of ubi
161 Therefore, a pancreatic islet
yeast two-hybrid library was produced and searched for g
162 Recently, we constructed a
yeast two-hybrid map around three rice proteins that con
163 +68 (cadherin 23 with expressed exon 68) by
yeast two-hybrid mating and co-transformation protocols,
164 Here, we present a massively multiplexed
yeast two-hybrid method, CrY2H-seq, which uses a Cre rec
165 Here, we demonstrate by
yeast two-hybrid method, immunoprecipitation assays, and
166 Using
yeast two-hybrid methods, we identified a large set of p
167 nique Sho1p PPIs through the use of membrane
yeast two-hybrid (
MYTH), an assay specifically suited to
168 Using
yeast two-hybrid protein interaction studies, we found t
169 ther with our interactions studies including
yeast two-hybrid,
pull-down, and in planta fluorescence
170 iching for the interacting fragments using a
yeast two-hybrid reporter system.
171 ll culture (SILAC) data with high-throughput
yeast two hybrid results, we showed that five of these p
172 O Domain Containing Protein, HvELMOD_C, in a
yeast two hybrid screen for proteins interacting with Hv
173 We performed a
yeast two hybrid screen with SR34 as bait and discovered
174 The interaction was found in a
yeast two-hybrid screen (human leukocyte and mononuclear
175 Both a
yeast two-hybrid screen and a pull-down assay identified
176 Using a
yeast two-hybrid screen and coimmunoprecipitation assays
177 BBX32 regulation, we performed a large-scale
yeast two-hybrid screen and identified CONSTANS-LIKE 3 (
178 We performed a
yeast two-hybrid screen and identified the adaptor prote
179 as an interacting partner of SIS8 based on a
yeast two-hybrid screen and in planta bimolecular fluore
180 direct interacting factor for Kbtbd5 using a
yeast two-hybrid screen and in vitro binding assays.
181 In this study, using a
yeast two-hybrid screen approach, we identified the NF-Y
182 Here, we conducted
yeast two-hybrid screen assay and identified an E3 ligas
183 Using an unbiased
yeast two-hybrid screen for interactions between murine
184 Migfilin, originally identified in a
yeast two-hybrid screen for kindlin-2-interacting protei
185 Here, using a
yeast two-hybrid screen for proteins interacting with it
186 On the basis of a
yeast two-hybrid screen for the MT1-MMP cytoplasmic tail
187 A
yeast two-hybrid screen has identified the adaptor prote
188 A
yeast two-hybrid screen has revealed that the transcript
189 To that end, we report a
yeast two-hybrid screen of all human Rabs for myosin Va-
190 Here, a
yeast two-hybrid screen revealed that RABV P interacts w
191 Using a split-ubiquitin
yeast two-hybrid screen that covers a test-space of 6.4
192 able N-terminal subdomain that was used in a
yeast two-hybrid screen that identified the proline-rich
193 We have previously shown through a
yeast two-hybrid screen that it is also a cardiac bindin
194 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
196 e molecular functions of FTO, we performed a
yeast two-hybrid screen to identify the protein(s) that
197 pecially abundant in retina, was fished with
yeast two-hybrid screen using a constitutively active Ga
198 novel TDP-43 protein interactors found in a
yeast two-hybrid screen using an adult human brain cDNA
199 ein interactions, we performed a large-scale
yeast two-hybrid screen using both wild-type (WT) and si
200 We have now performed a
yeast two-hybrid screen using dysbindin as bait against
201 ciated protein YejK, which was detected in a
yeast two-hybrid screen using the ParE subunit of topois
202 eins that may remove the CRD, we performed a
yeast two-hybrid screen using twitchin kinase as bait.
203 ht influence its subcellular localization, a
yeast two-hybrid screen was performed.
204 Using a
yeast two-hybrid screen, we discovered an interaction be
205 Using a
yeast two-hybrid screen, we found that splice cassette I
206 Through a
yeast two-hybrid screen, we have identified XPLN (exchan
207 Using a
yeast two-hybrid screen, we identified a novel transcrip
208 Using a
yeast two-hybrid screen, we identified cyclin L2 as a DC
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 Furthermore, using a
yeast two-hybrid screen, we identified the motor protein
213 Using a
yeast two-hybrid screen, we searched for novel AIRE-inte
214 tein-protein interaction data from a focused
yeast two-hybrid screen.
215 uman teneurin-1 ICD interaction partner in a
yeast two-hybrid screen.
216 o identify Wor1-interacting proteins using a
yeast two-hybrid screen.
217 arity, we performed a comprehensive pairwise
yeast two-hybrid screen.
218 ind protein interaction partners of NBP35, a
yeast-two-hybrid screen was carried out that identified
219 A
yeast-two-hybrid screen with CPRabA5e as bait revealed 1
220 protein was identified by a Split-Ubiquitin
Yeast-Two-Hybrid screen.
221 st protein-protein interactions (PPIs) using
yeast two-hybrid screening (Y2H).
222 1 (PDZD11) as a new interactor of PLEKHA7 by
yeast two-hybrid screening and by mass spectrometry anal
223 Using
yeast two-hybrid screening and co-immunoprecipitation as
224 Using an unbiased
yeast two-hybrid screening and complementary approaches,
225 ified KDR interactors using a combination of
yeast two-hybrid screening and dedicated confirmations w
226 ell proteins in Vpu function, we carried out
yeast two-hybrid screening and identified a previously r
227 teins in Vpu's function, here we carried out
yeast two-hybrid screening and identified the V0 subunit
228 Using
yeast two-hybrid screening and pull-down assays, MDT-28/
229 Yeast two-hybrid screening combined with bimolecular flu
230 Using
yeast two-hybrid screening coupled with a candidate appr
231 We isolated Myosin Vc in a
yeast two-hybrid screening for proteins that interact wi
232 Yeast two-hybrid screening identified an interaction bet
233 To address this, we performed
yeast two-hybrid screening of PRMT7 and identified argin
234 A
yeast two-hybrid screening revealed a specific interacti
235 Yeast two-hybrid screening revealed several interactive
236 Yeast two-hybrid screening suggests that XB130 interacts
237 uences differentiation of neurons, we used a
yeast two-hybrid screening to search for new binding par
238 SPBB1 was identified through
yeast two-hybrid screening with the kinase-dead TbPLK as
239 Bam35 proteins determined using multivector
yeast two-hybrid screening, and these PPIs were further
240 Here, using
yeast two-hybrid screening, co-immunoprecipitation, and
241 Through
yeast two-hybrid screening, we identified tumor suppress
242 Through
yeast two-hybrid screening, we identify the centrosomal
243 ansformation efficiency is critical, such as
yeast two-hybrid screening.
244 ding partner of the E2 protein of CSFV using
yeast two-hybrid screening.
245 oform of thromboxane A2 receptor (TPbeta) by
yeast two-hybrid screening.
246 proteins that can interact with JSRV Env by
yeast two-hybrid screening.
247 identified as a Vav3 interacting protein by
yeast two-hybrid screening.
248 utative interacting partner of NLRC3 through
yeast two-hybrid screening.
249 forming hetero- or homodimers, we conducted
yeast-two-hybrid screening and identified an SVP-like MA
250 Here, we have used
yeast-two-hybrid screening to identify OsPIP5K1, a membe
251 Prp40 was found to be a centrin target by
yeast-two-hybrid screening using both Homo sapiens centr
252 Employing pooled RNAi and
yeast two-hybrid screenings, we report that the mitochon
253 amine the roles of IDRs in CBP, we performed
yeast-two-hybrid screenings of placenta and lung cancer
254 G signaling pathway components, we performed
yeast two-hybrid screens and identified the muscle-speci
255 identify host targets of AVR1, we performed
yeast two-hybrid screens and selected Sec5 as a candidat
256 Yeast two-hybrid screens indicated that GhDsPTP3a intera
257 Here we performed
yeast two-hybrid screens of 3,305 baits against 3,606 pr
258 Here, large-scale
yeast two-hybrid screens repeatedly identified a surpris
259 Yeast two-hybrid screens revealed that CEFIP interacts w
260 nant polycystic kidney disease, we performed
yeast two-hybrid screens using the C-terminus of polycys
261 receptor-protein interactions, we conducted
yeast two-hybrid screens using the cytosolic domains of
262 In addition, using
yeast two-hybrid screens we identified several candidate
263 tein targets in the host cells, we performed
yeast two-hybrid screens, allowing us to find 48 high-co
264 ort, we present data from the following: (a)
yeast two-hybrid screens, identifying interaction partne
265 revious results from electron microscopy and
yeast two-hybrid screens.
266 Yeast-two-hybrid screens identify RhoC as a Fam65b bindi
267 Using STK38 as bait in
yeast-two-hybrid screens, we discovered STK38 as a novel
268 Yeast two-hybrid studies revealed that meiosis-expressed
269 with contradicting bacterial two-hybrid and
yeast two-hybrid studies suggesting that either the form
270 protein interaction which we confirmed using
yeast two-hybrid studies.Taken together, we find evidenc
271 In a
yeast two-hybrid study, we identified a novel interactio
272 d as a TaFROG-interacting protein based on a
yeast two-hybrid study.
273 In vitro study with
yeast two-hybrid suggests that most alpha-helices of R16
274 lished interactions naively tested using the
yeast two-hybrid system and 2.7 times better than for ra
275 Using the
yeast two-hybrid system and bimolecular fluorescence com
276 nitially developed interaction assays (e.g.,
yeast two-hybrid system and split-ubiquitin assay) usual
277 Since its original description in 1989, the
yeast two-hybrid system has been extensively used to ide
278 lular domains of each immune receptor in the
yeast two-hybrid system in a kinase activity-dependent m
279 sduction pathways have successfully used the
yeast two-hybrid system or related methods.
280 Here we use a
yeast two-hybrid system to identify novel TIR1 mutants w
281 Here, using a
yeast two-hybrid system to search for AtRALF1-interactin
282 ce the temporal control of NCKX4 activity, a
yeast two-hybrid system was used to search for protein i
283 Combining the
yeast two-hybrid system with genetic analysis, we show h
284 l interaction of full-length PsIAA4 in vivo (
yeast two-hybrid system).
285 the decapping complex VARICOSE (VCS) in the
yeast two-hybrid system, and co-localizes with component
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 previously identified a swin
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 -transcription factor interactions using the
yeast two-hybrid system.
292 ins involved in PPIs by advancing the use of
yeast two-hybrid technology.
293 PIP5K6 interacted with MPK6 in
yeast two-hybrid tests, immuno-pull-down assays, and by
294 own by cosubcellular enrichment analysis and
yeast two-hybrid validation.
295 ein interactions (PPIs) of HEV by systematic
Yeast two-hybrid (
Y2H) and LuMPIS screens, providing a b
296 ntal systems, such as affinity purification,
yeast two-hybrid (
Y2H) and protein-fragment complementat
297 We performed a
yeast two-hybrid (
Y2H) screen and uncovered TNKS as a pu
298 We recently used
yeast two-hybrid (
Y2H) screening to identify a small set
299 We applied a
yeast-two-hybrid (
Y2H) analysis to screen for ubiquitin
300 We employed
yeast-two-hybrid (
Y2H) assays, co-immunoprecipitation, t