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Georg N. Duda

Researcher at Charité

Publications -  613
Citations -  31004

Georg N. Duda is an academic researcher from Charité. The author has contributed to research in topics: Bone healing & Bone regeneration. The author has an hindex of 81, co-authored 563 publications receiving 25802 citations. Previous affiliations of Georg N. Duda include Humboldt University of Berlin & University of Ulm.

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A method to determine the 3-D stiffness of fracture fixation devices and its application to predict inter-fragmentary movement

TL;DR: A 6 x 6 stiffness matrix is introduced which completely describes the linear relationship between the 6 inter-fragmentary movements and the resulting bony loading (3 forces and 3 moments) and the authors conclude that a single value is not sufficient to describe the mechanical relationship.
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Composite transcriptome assembly of RNA-seq data in a sheep model for delayed bone healing

TL;DR: A first atlas of gene expression profiles and differentially expressed genes in standard and delayed bone healing in a large-animal model is provided and a number of clues as to the shifts in gene expression that underlie delayedBone healing are provided.
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Geometry-driven cell organization determines tissue growths in scaffold pores: consequences for fibronectin organization

TL;DR: Scaffold pore size directed the time required for pore closure and furthermore impacted the organization of the fibronectin matrix, indicating a reorganization of the cell/ECM network.
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Mechanical induction of critically delayed bone healing in sheep: Radiological and biomechanical results

TL;DR: The presented ovine model provides the basis for a comparative evaluation of mechanisms controlling delayed and standard bone healing and led to the development of a hypertrophic non-union in sheep.
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The multifaceted roles of macrophages in bone regeneration: A story of polarization, activation and time

TL;DR: In this paper, the authors discuss the high degree of plasticity of macrophages and the relevant contribution of the different and more specific M2 subtypes (M2a-M2f) during bone regeneration.