Advances in Bioscience and Biotechnology

Advances in Bioscience and Biotechnology

ISSN Print: 2156-8456
ISSN Online: 2156-8502
www.scirp.org/journal/abb
E-mail: abb@scirp.org
"Strategies to stabilize compact folding and minimize aggregation of antibody-based fragments"
written by Diana Gil, Adam G. Schrum,
published by Advances in Bioscience and Biotechnology, Vol.4 No.4A, 2013
has been cited by the following article(s):
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[15] Production of Plant-Derived Japanese Encephalitis Virus Multi-Epitope Peptide in Nicotiana benthamiana and Immunological Response in Mice
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[17] “Stapling” scFv for multispecific biotherapeutics of superior properties
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[18] Emerging applications of nanobodies in cancer therapy
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[21] Targeting multiple myeloma with nanobody-based heavy chain antibodies, bispecific killer cell engagers, chimeric antigen receptors, and nanobody …
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[22] A 33-residue peptide tag increases solubility and stability of Escherichia coli produced single-chain antibody fragments
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[27] Expression of functional eGFP-fused antigen-binding fragment of ranibizumab in Pichia pastoris
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[28] NMDA-receptor-Fc-fusion constructs neutralize anti-NMDA receptor antibodies
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[30] Development of antibody therapeutic approaches for poultry diseases using avian influenza as a disease model
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[37] Development of BCMA-specific engineered T cells targeting multiple myeloma
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[38] Natural Receptor-and Ligand-Based Chimeric Antigen Receptors: Strategies Using Natural Ligands and Receptors for Targeted Cell Killing
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[39] CAR-NK Cells in the Treatment of Solid Tumors
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[42] Autoinduction as Means for Optimization of the Heterologous Expression of Recombinant Single-Chain Fv (scFv) Antibodies
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[43] Machine Learning Feature Selection for Predicting High Concentration Therapeutic Antibody Aggregation
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[50] CAR-T design: Elements and their synergistic function
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[53] Public and private human T cell clones respond differentially to HCMV antigen when boosted by CD3 co-potentiation
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[54] Driving CARs with alternative navigation tools–the potential of engineered binding scaffolds
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[57] ШАПЕРОННАЯ И ИММУНОГЛОБУЛИНСВЯЗЫВАЮЩАЯ АКТИВНОСТИ Skp ИЗ Yersinia pseudotuberculosis
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[58] Public and private human T-cell clones respond differentially to HCMV antigen when boosted by CD3 copotentiation
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[59] Improved Antitumor Efficacy of Chimeric Antigen Receptor T Cells that Secrete Single-Domain Antibody FragmentsVHH-Secreting CAR T Cells
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[60] Advances in point-of-care testing for cardiovascular diseases
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[61] Development of recombinant antibody fragments for toxin and microbial contaminant detection and investigations of microcystin and azaspiracid toxicity.
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[62] Exploring and exploiting the minor pilins of Type IV pili
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[63] Single-step Protein A and Protein G avidity purification methods to support bispecific antibody discovery and development
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[64] Chaperone and Immunoglobulin-Binding Activities of Skp Protein from Yersinia pseudotuberculosis
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[65] Biochemical and Structural Insights into Carbonic Anhydrase XII/Fab6A10 Complex
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[66] Ice-recrystallization inhibiting polymers protect proteins against freeze-stress and enable glycerol-free cryostorage
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[67] Amino acid induced hyper activation of laccase and its application in dye degradation
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[68] Chimeric Antigen Receptors Incorporating D Domains Targeting CD123 Direct Potent Mono-and Bi-specific Antitumor Activity of T Cells
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[69] Improving developability of an Antigen Binding Fragment by Aspartate Substitutions
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[70] An Antibody Fab Fragment-based Chimeric Antigen Receptor Could Efficiently Eliminate Human Thyroid Cancer Cells
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[71] Design and Production of Bispecific Antibodies
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[72] Developing VHH-based tools to study Ebolavirus infection
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[73] Pre-clinical development of novel ROR1 chimeric antigen receptor T cells and bispecific T cell engagers
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[74] Introduction into Novel Constructs
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[75] Expression of a functional intrabody against hepatitis C virus core protein in Escherichia coli and silkworm pupae
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[76] Strategies to Address Chimeric Antigen Receptor Tonic Signaling
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[77] Expression and neutralization capacity of single domain HIV antibody fragments
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[79] Bacterial communities adapted to higher external resistance can reduce the onset potential of anode in microbial fuel cells
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[80] Optimizing Antibody Expression: the nuts and Bolts
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[83] Antibody Aggregation: Insights from Sequence and Structure
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[85] ECCENTRIC
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