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In vitro nanobody discovery for integral membrane protein targets
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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Nanobody-based products as research and diagnostic tools
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Molecular evolution by staggered extension process (StEP) in vitro recombination
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Small nanobody drugs win big backing from pharma
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mRNA display for the selection and evolution of enzymes from in vitro-translated protein libraries
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A general protocol for the generation of Nanobodies for structural biology
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Detergent binding explains anomalous SDS-PAGE migration of membrane proteins
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Structures of P-glycoprotein reveal its conformational flexibility and an epitope on the nucleotide-binding domain
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In vitro selection and evolution of functional proteins by using ribosome display
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RNA-peptide fusions for the in vitro selection of peptides and proteins
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Glucose transporter-1 deficiency syndrome: the expanding clinical and genetic spectrum of a treatable disorder
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Nanobodies: Natural Single-Domain Antibodies
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Crystal Structure of a Human Single Domain Antibody Dimer Formed through VH-VH Non-Covalent Interactions
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Advantages of mRNA display selections over other selection techniques for investigation of protein–protein interactions
inferredcites →https://doi.org/10.3389/fimmu.2013.00224openalex-snapshot
Development of Next-Generation Peptide Binders Using In vitro Display Technologies and Their Potential Applications
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Changes in Membrane Protein Structural Biology
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Additional file 1 of Evaluation of the yeast surface display system for screening of functional nanobodies
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Analysis of transcription factor and histone modification dynamics in the nucleus of single living cells using a novel antibody-based imaging approach
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Synthetic single domain antibodies for the conformational trapping of membrane proteins
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