S
Stephan Söder
Researcher at University of Erlangen-Nuremberg
Publications - 38
Citations - 1322
Stephan Söder is an academic researcher from University of Erlangen-Nuremberg. The author has contributed to research in topics: Cartilage & Regulation of gene expression. The author has an hindex of 19, co-authored 38 publications receiving 1170 citations.
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Journal ArticleDOI
Comparison of the chondrosarcoma cell line SW1353 with primary human adult articular chondrocytes with regard to their gene expression profile and reactivity to IL-1β
Mathias Gebauer,Joachim Saas,Florian Sohler,Jochen Haag,Stephan Söder,M. Pieper,Eckart Bartnik,J. Beninga,Ralf Zimmer,Thomas Aigner +9 more
TL;DR: The data characterize SW1353 cells as a cell line with only a very limited potential to mimic PHCs, though SW13 53 cells can be of value to study the induction of protease expression within cells, a phenomenon also seen in chondrocytes.
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Osteophyte development--molecular characterization of differentiation stages.
TL;DR: Tissue architecture and matrix composition in mature osteophytes suggests that metaplastic neo-cartilagenous tissue might be one potential source of cartilage repair tissue in the adult joint.
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Human lymphoid organ dendritic cell identity is predominantly dictated by ontogeny, not tissue microenvironment
Gordon F. Heidkamp,Jil Sander,Christian H. K. Lehmann,Lukas Heger,Nathalie Eissing,Anna Baranska,Jennifer J. Lühr,Alana Hoffmann,Katharina C. Reimer,Anja Lux,Stephan Söder,Arndt Hartmann,Johannes Zenk,Thomas Ulas,Naomi McGovern,Christoph Alexiou,Bernd M. Spriewald,Andreas Mackensen,Gerold Schuler,Burkhard Schauf,Anja Forster,Roland Repp,Peter A. Fasching,Ariawan Purbojo,Robert Cesnjevar,Evelyn Ullrich,Evelyn Ullrich,Florent Ginhoux,Andreas Schlitzer,Andreas Schlitzer,Andreas Schlitzer,Falk Nimmerjahn,Joachim L. Schultze,Joachim L. Schultze,Diana Dudziak +34 more
TL;DR: It is demonstrated that DC subpopulations in organs of the lymphohematopoietic system (spleen, thymus, and blood) are strongly defined by ontogeny rather than by signals from the microenvironment, strongly arguing that DCs react toward modulatory signals from tissue microenvironments.
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Ultrastructural localization of type VI collagen in normal adult and osteoarthritic human articular cartilage
TL;DR: The authors' immunohistochemical and ultrastructural data are compatible with two ways of degradation of type VI collagen in osteoarthritic cartilage: the pathologically increased physiological molecular degradation leading to the complete loss oftype VI collagen filaments from the pericellular chondrocyte matrix and the transformation of the fine filaments to the band-like form of type VII collagen.
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The C5 domain of Col6A3 is cleaved off from the Col6 fibrils immediately after secretion.
TL;DR: The results suggest that at least in human adult articular cartilage the C5 domain of alpha3(VI) collagen is synthesized and initially incorporated into the newly formed type VI collagen fibrils, but immediately after secretion is cut off and is not present in the mature pericellular type VI matrix of articular Cartilage.