Quantitative assessment of peptide sequence diversity in M13 combinatorial peptide phage display libraries.
about
Cyclosporin A associated helicase-like protein facilitates the association of hepatitis C virus RNA polymerase with its cellular cyclophilin BSelection platforms for directed evolution in synthetic biologyEvolutionary selection of new breast cancer cell-targeting peptides and phages with the cell-targeting peptides fully displayed on the major coat and their effects on actin dynamics during cell internalization.Selective recognition of peptide sequences by glutathione transferases: a possible mechanism for modulation of cellular stress-induced signaling pathways.Phage display of random peptide libraries: applications, limits, and potential.Practical tips for construction of custom Peptide libraries and affinity selection by using commercially available phage display cloning systemsGenome-wide characterisation of the binding repertoire of small molecule drugs.pH-Dependent lytic peptides discovered by phage display.Trinucleotide cassettes increase diversity of T7 phage-displayed peptide library.Immunogenic display of diverse peptides on virus-like particles of RNA phage MS2Developing bifunctional beta-lactamase molecules with built-in target-recognizing module for prodrug therapy: identification of Enterobacter Cloacae P99 cephalosporinase loops suitable for randomization and phage-display selection.Novel beta-lactamase-random peptide fusion libraries for phage display selection of cancer cell-targeting agents suitable for enzyme prodrug therapyPotential of phage-displayed peptide library technology to identify functional targeting peptidesPhage-displayed combinatorial peptide libraries in fusion to beta-lactamase as reporter for an accelerated clone screening: Potential uses of selected enzyme-linked affinity reagents in downstream applications.Cancer cell-specific internalizing ligands from phage displayed beta-lactamase-peptide fusion libraries.Synthetic phage for tissue regenerationSelection dynamic of Escherichia coli host in M13 combinatorial peptide phage display libraries.Identification of target-binding peptide motifs by high-throughput sequencing of phage-selected peptides.Combinatorial library of improved peptide aptamers, CLIPs to inhibit RAGE signal transduction in mammalian cells.Prospective identification of parasitic sequences in phage display screens.Subtractive phage display selection from canine visceral leishmaniasis identifies novel epitopes that mimic Leishmania infantum antigens with potential serodiagnosis applications.Intra-domain phage display (ID-PhD) of peptides and protein mini-domains censored from canonical pIII phage displayBiomathematical description of synthetic peptide libraries.Improved serological detection of rheumatoid arthritis: a highly antigenic mimotope of carbonic anhydrase III selected in a murine model by phage display.Phage display selection of tight specific binding variants from a hyperthermostable Sso7d scaffold protein library.Pulmonary Targeting of Adeno-associated Viral Vectors by Next-generation Sequencing-guided Screening of Random Capsid Displayed Peptide Libraries.Phage display biopanning and isolation of target-unrelated peptides: in search of nonspecific binders hidden in a combinatorial library.Factor Xa active site substrate specificity with substrate phage display and computational molecular modeling.The Use of Phage-Displayed Peptide Libraries to Develop Tumor-Targeting Drugs.Recent developments with B-cell epitope identification for predictive studies.Carbohydrate-mimetic peptides: structural aspects of mimicry and therapeutic implications.Biased selection of propagation-related TUPs from phage display peptide libraries.Biogenic and Synthetic Peptides with Oppositely Charged Amino Acids as Binding Sites for Mineralization.Epitope identification from fixed-complexity random-sequence peptide microarrays.Error analysis of deep sequencing of phage libraries: peptides censored in sequencing.Bypassing bacterial infection in phage display by sequencing DNA released from phage particles.Compositional Bias in Naïve and Chemically-modified Phage-Displayed Libraries uncovered by Paired-end Deep Sequencing.PuLSE: Quality control and quantification of peptide sequences explored by phage display libraries.
P2860
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P2860
Quantitative assessment of peptide sequence diversity in M13 combinatorial peptide phage display libraries.
description
2002 nî lūn-bûn
@nan
2002 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2002 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2002年の論文
@ja
2002年論文
@yue
2002年論文
@zh-hant
2002年論文
@zh-hk
2002年論文
@zh-mo
2002年論文
@zh-tw
2002年论文
@wuu
name
Quantitative assessment of pep ...... ptide phage display libraries.
@ast
Quantitative assessment of pep ...... ptide phage display libraries.
@en
type
label
Quantitative assessment of pep ...... ptide phage display libraries.
@ast
Quantitative assessment of pep ...... ptide phage display libraries.
@en
prefLabel
Quantitative assessment of pep ...... ptide phage display libraries.
@ast
Quantitative assessment of pep ...... ptide phage display libraries.
@en
P2093
P1476
Quantitative assessment of pep ...... ptide phage display libraries.
@en
P2093
Alexei S Soares
Diane J Rodi
Lee Makowski
P304
P356
10.1016/S0022-2836(02)00844-6
P407
P577
2002-10-01T00:00:00Z