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Selective biodegradation of keratin matrix in feather rachis reveals classic bioengineering

https://doi.org/10.1098/rspb.2009.1980
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Outgoing claims: the papers this work cites, builds on, or argues with.

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Keratinization and lipogenesis in epidermal derivatives of the zebrafinch, taeniopygia guttata castanotis (aves, passeriformes, ploecidae) during embryonic development
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New Feather-Degrading Filamentous Fungi
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Dinosaur protofeathers: pushing back the origin of feathers into the Middle Triassic?
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The structure of feather keratin
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Wedge cells during regeneration of juvenile and adult feathers and their role in carving out the branching pattern of barbs
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The self-assembly of keratin intermediate filaments into macrofibrils: Is this process mediated by a mesophase?
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Correlation between concrete-to-concrete bond strength and the roughness of the substrate surface
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Extracellular oxidative systems of the lignin-degrading Basidiomycete Phanerochaete chrysosporium
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Molecular packing in the feather keratin filament
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Young’s modulus varies with differential orientation of keratin in feathers
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The mechanical performance of medullary foam from feathers
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Toughness anisotropy in feather keratin
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Structure of Wool Fibres: Isolation of an α- and β-Protein in Wool
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Molecular Orientation of Some Keratins
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A new Chinese specimen indicates that ‘protofeathers’ in the Early Cretaceous theropod dinosaur Sinosauropteryx are degraded collagen fibres
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Existence of various structural zones in keratinous tissues revealed by X-ray microdiffraction
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Selective Degradation of Wood Components by White‐Rot Fungi
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inferredcites →https://doi.org/10.1242/jeb.198.4.1029openalex-snapshot
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A study of the structure of feathers, with reference to their taxonomic significance

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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The Feather Structure and Bioinspired Rachis Design
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Richard P. Wool's contributions to sustainable polymers from 2000 to 2015
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Peer Review #1 of "Analysis and comparison of protein secondary structures in the rachis of avian flight feathers (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.12919v0.1/reviews/2openalex-snapshot
Peer Review #2 of "Analysis and comparison of protein secondary structures in the rachis of avian flight feathers (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.12919v0.1/reviews/3openalex-snapshot
Peer Review #3 of "Analysis and comparison of protein secondary structures in the rachis of avian flight feathers (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.12919v0.2/reviews/1openalex-snapshot
Peer Review #1 of "Analysis and comparison of protein secondary structures in the rachis of avian flight feathers (v0.2)"
inferred← citeshttps://doi.org/10.7287/peerj.12919v0.2/reviews/2openalex-snapshot
Peer Review #2 of "Analysis and comparison of protein secondary structures in the rachis of avian flight feathers (v0.2)"
inferred← citeshttps://doi.org/10.7287/peerj.3449v0.1/reviews/1openalex-snapshot
Peer Review #1 of "Relating form to function in the hummingbird feeding apparatus (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.3449v0.1/reviews/2openalex-snapshot
Peer Review #2 of "Relating form to function in the hummingbird feeding apparatus (v0.1)"
inferred← citeshttps://doi.org/10.7717/peerj.12919openalex-snapshot
Analysis and comparison of protein secondary structures in the rachis of avian flight feathers
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Relating form to function in the hummingbird feeding apparatus
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