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Journal Abstract Search

247 related items for PubMed ID: 33261041

  • 1. Application of Next Generation Sequencing (NGS) in Phage Displayed Peptide Selection to Support the Identification of Arsenic-Binding Motifs.
    Braun R, Schönberger N, Vinke S, Lederer F, Kalinowski J, Pollmann K.
    Viruses; 2020 Nov 27; 12(12):. PubMed ID: 33261041
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  • 2. Phage display biopanning and isolation of target-unrelated peptides: in search of nonspecific binders hidden in a combinatorial library.
    Bakhshinejad B, Zade HM, Shekarabi HS, Neman S.
    Amino Acids; 2016 Dec 27; 48(12):2699-2716. PubMed ID: 27650972
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  • 3. Propagation Capacity of Phage Display Peptide Libraries Is Affected by the Length and Conformation of Displayed Peptide.
    Kamstrup Sell D, Sinkjaer AW, Bakhshinejad B, Kjaer A.
    Molecules; 2023 Jul 10; 28(14):. PubMed ID: 37513190
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  • 4. Depth of Sequencing Plays a Determining Role in the Characterization of Phage Display Peptide Libraries by NGS.
    Sloth AB, Bakhshinejad B, Stavnsbjerg C, Rossing M, Kjaer A.
    Int J Mol Sci; 2023 Mar 11; 24(6):. PubMed ID: 36982469
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  • 5. PHASTpep: Analysis Software for Discovery of Cell-Selective Peptides via Phage Display and Next-Generation Sequencing.
    Brinton LT, Bauknight DK, Dasa SS, Kelly KA.
    PLoS One; 2016 Mar 11; 11(5):e0155244. PubMed ID: 27186887
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  • 7. Screening and Identification of PLK1-Polo Box Binding Peptides by High-Throughput Sequencing of Phage-Selected Libraries.
    Bibi N, Niaz H, Hupp T, Kamal MA, Rashid S.
    Protein Pept Lett; 2019 Mar 11; 26(8):620-633. PubMed ID: 30887917
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  • 9. [Development of a Rapid Identification Method for a Variety of Antibody Candidates Using High-throughput Sequencing].
    Ito Y.
    Yakugaku Zasshi; 2017 Mar 11; 137(7):823-830. PubMed ID: 28674295
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  • 11. Diversity of phage-displayed libraries of peptides during panning and amplification.
    Derda R, Tang SK, Li SC, Ng S, Matochko W, Jafari MR.
    Molecules; 2011 Feb 21; 16(2):1776-803. PubMed ID: 21339712
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  • 12. Comparison of motif-based and whole-unique-sequence-based analyses of phage display library datasets generated by biopanning of anti-Borrelia burgdorferi immune sera.
    Ionov Y, Rogovskyy AS.
    PLoS One; 2020 Feb 21; 15(1):e0226378. PubMed ID: 31940357
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  • 15. Using NGS to Uncover the Corruption of a Peptide Phage Display Selection.
    Sell DK, Bakhshinejad B, Sinkjaer AW, Dawoodi IM, Wiinholt MN, Sloth AB, Stavnsbjerg C, Kjaer A.
    Curr Issues Mol Biol; 2024 Sep 21; 46(9):10590-10605. PubMed ID: 39329979
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  • 19. Prospective identification of parasitic sequences in phage display screens.
    Matochko WL, Cory Li S, Tang SK, Derda R.
    Nucleic Acids Res; 2014 Feb 21; 42(3):1784-98. PubMed ID: 24217917
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  • 20. In vivo phage display: identification of organ-specific peptides using deep sequencing and differential profiling across tissues.
    Pleiko K, Põšnograjeva K, Haugas M, Paiste P, Tobi A, Kurm K, Riekstina U, Teesalu T.
    Nucleic Acids Res; 2021 Apr 19; 49(7):e38. PubMed ID: 33444445
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