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

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