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1 identified using a filamentous bacteriophage random peptide library.
2 icroglobulin in the presence or absence of a random peptide library.
3 talytic site of DMPK using a phage-displayed random peptide library.
4 rosine kinase (PTK) by screening a secondary random peptide library.
5 ecipients, using recombinant phages encoding random peptide libraries.
6 nd is more efficient in epitope mapping than random peptide libraries.
7 gh-throughput screening of a phage-displayed random peptide library and classified the cell lines acc
8 sing a genetic selection, we have screened a random peptide library and identified a group of C-termi
11 ons relations, we designed a phage-displayed random peptide library based on previous knowledge of st
12 We have displayed a 12-amino-acid (12-mer) random peptide library between the H and I sheets of the
13 of synthetic peptides as well as a screen of random peptide libraries by the yeast two-hybrid system.
14 odon sequence was previously isolated from a random peptide library by binding to growth hormone bind
15 stigate protein interactions of FXI, a large random peptide library consisting of 10(6) to 10(7) pept
16 es in SK, we used unconstrained 15 and 6-mer random peptide libraries displayed on phage (theoretical
18 elective enrichment from two phage-displayed random peptide libraries enabled us to isolate and ident
22 ces, but will also allow the construction of random peptide libraries from which specific binding act
23 esides natural peptide ligands, screening of random peptide libraries has yielded novel bioactive pep
24 uccess reemphasizes the utility of searching random peptide libraries in protein design projects, and
27 a motif was established by the panning of a random peptide library in which peptide sequences are di
32 Qa-1 that had been folded in the presence of random peptide libraries or pools of Qdm derivatives ran
34 tion, epitope mapping with a phage-displayed random peptide library revealed that one of these mAbs (
36 recognized by LIM domains, we have utilized random peptide library selection, the yeast two-hybrid s
37 itochondria, and that an internalizing-phage random peptide library selects for peptide motifs that l
38 istance were selected from in vivo expressed random peptide libraries to study structural features im
40 rget-assisted iterative screening applied to random peptide libraries unveiled a novel and atypical r
41 tein-DNA interactions can be identified from random peptide libraries using phage display techniques.
42 To overcome these obstacles, we screened random peptide libraries using sera from HIV-infected su
43 and (000-1) substrates, were selected from a random peptide library using the phage display technique
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