1 Yeast three-hybrid analyses demonstrated that the SycN/Y
2 -1 glycoprotein C (gC) mRNA, identified in a
yeast three-hybrid analysis, were screened for binding t
3 Experiments using the
yeast three-hybrid assay also revealed that a 19-aa acid
4 A
yeast three-hybrid assay demonstrates a ternary complex
5 A modified
yeast three-hybrid assay detected Protein 4-RNA interact
6 In contrast, a
yeast three-hybrid assay in which either CK2 alpha and b
7 rated a series of TEP1 deletions and show by
yeast three-hybrid assay that the entire Tetrahymena p80
8 We have used a
yeast three-hybrid assay to demonstrate that [DE]XXXL[LI
9 Using a
yeast three-hybrid assay we demonstrate that several of
10 eral assay for enzyme catalysis based on the
yeast three-hybrid assay, Chemical Complementation, whic
11 lysis, GLD-3 acts upstream of FBF, and, in a
yeast three-hybrid assay, GLD-3 interferes specifically
12 Using the
yeast three-hybrid assay, the glycosynthase activity of
13 yed Tmp-SLF to modulate gene expression in a
yeast three-hybrid assay.
14 ith amino acids 1-871 of TEP1 in an indirect
yeast three-hybrid assay.
15 eporter gene transcription in vivo using the
yeast three-hybrid assay.
16 nd with several of the human vault RNAs in a
yeast three-hybrid assay.
17 Silencing experiments and
yeast three-hybrid assays demonstrated that both ubiquit
18 Gel shift, spectroscopic and
yeast three-hybrid assays show specific interactions bet
19 nteracted by the respective third protein in
yeast three-hybrid assays, pulldown experiments (lumines
20 Combining AlphaFold modeling and
yeast three-hybrid assays, we demonstrate that GID1 bind
21 nd shift assays, fluorescence Job plots, and
yeast three-hybrid assays, we investigate the interactio
22 n and UNC-112, forming a ternary complex, in
yeast three-hybrid assays.
23 agenesis and in vivo random screening in the
yeast three-hybrid binding assay, we have examined the a
24 tion between a reporter gene activation in a
yeast three-hybrid binding system and an in vivo packagi
25 Data from
yeast three-hybrid experiments indicate that a number of
26 Using
yeast three-hybrid experiments, we demonstrate that the
27 e gene encoding Drosophila SLBP (dSLBP) by a
yeast three-hybrid method and have isolated mutations in
28 t' to isolate RNA binding proteins using the
yeast three-hybrid method.
29 Yeast three-hybrid RNA aptamer specificity studies corro
30 We describe in vivo selections from a
yeast three-hybrid RNA library containing sequences pres
31 The
yeast three-hybrid RNA-protein interaction assay indicat
32 Using a
yeast three-hybrid RNA-protein interaction assay, second
33 Using the
yeast three-hybrid screen and RNA gel shift analysis, we
34 The
yeast three-hybrid screen revealed K protein bound to uc
35 t to identify Smad-interacting proteins by a
yeast three-hybrid screen with Smad3 and Smad4 as baits,
36 Using tau exon 10 as a bait in a
yeast three-hybrid screen, we discovered that it interac
37 rs (ITAF) were unaffected by IL-6, we used a
yeast-three-hybrid screen to identify novel ITAFs and id
38 Yeast three-hybrid screening identifies Copb1 as a kor m
39 We carry out
yeast three-hybrid selections with each library against
40 Moreover, in
yeast three-hybrid studies, the Kir2.3 di-isoleucine mot
41 pitously detecting RNA binding by p53 in the
yeast three-hybrid system (Y3H), we are exploring the sp
42 We also used a
yeast three-hybrid system and glutathione S-transferase
43 Several protocols--including the
yeast three-hybrid system and immunoprecipitations that
44 Both in vivo studies using the
yeast three-hybrid system and in vitro binding assays us
45 ine in vivo binding to M. barkeri PylRS in a
yeast three-hybrid system and to measure in vitro tRNA(P
46 The K(D) cutoff of the Mtx
yeast three-hybrid system is found to be ca. 50 nM.
47 In this assay, a small-molecule
yeast three-hybrid system is used to link enzyme catalys
48 We previously showed that the
yeast three-hybrid system provides a genetic assay of bo
49 Therefore, we have developed a new
yeast three-hybrid system that facilitates the rapid scr
50 In this study we used the
yeast three-hybrid system to clone Msy4, which encodes a
51 We also used the
yeast three-hybrid system to study avian retroviral RNA-
52 We have used the
yeast three-hybrid system to study binding of the human
53 The
yeast three-hybrid system was used to demonstrate that e
54 ls of transcription activation in a Mtx-DHFR
yeast three-hybrid system were determined for these vari
55 We report herein a genetic system, named the
yeast three-hybrid system, for detecting ligand-receptor
56 By exploiting the
yeast three-hybrid system, we have found that the histid
57 TPases, we conducted an experiment using the
yeast three-hybrid system.
58 strate an appreciable Gag interaction in the
yeast three-hybrid system.
59 for p85 on IRbeta was also confirmed in the
yeast three-hybrid system.
60 ecognized by its target protein in vivo in a
yeast three-hybrid system.
61 -kappaB (p50(2)) in eukaryotic cells using a
yeast three-hybrid system.
62 zed in vivo using a novel application of the
yeast three-hybrid system.
63 conserved RNA recognition positions using a
yeast three-hybrid system.
64 ive viral protein synthesis, we employed the
yeast three-hybrid system.
65 t with bZIP28 and NF-YA4, respectively, in a
yeast three-hybrid system.
66 ice, and frogs, using the recently developed
yeast three-hybrid system.
67 nary complex analysis, we have developed the
yeast three-hybrid system.
68 Using
yeast three-hybrid technology, we have identified a nove