Caren Linnemann
University of Tübingen
17 Papers
43 Citations
Caren Linnemann is an academic researcher from University of Tübingen. The author has contributed to research in topics: Mesenchymal stem cell & Neutrophil extracellular traps. The author has an hindex of 6, co-authored 12 publications.
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Papers
Donor Site Location Is Critical for Proliferation, Stem Cell Capacity, and Osteogenic Differentiation of Adipose Mesenchymal Stem/Stromal Cells: Implications for Bone Tissue Engineering.
Marie K. Reumann,Caren Linnemann,Romina H. Aspera-Werz,Sigrid Arnold,Manuel Held,Claudine Seeliger,Andreas K. Nussler,Sabrina Ehnert +7 more
TL;DR: The data clearly show that the donor tissue site affects the proliferation and osteogenic differentiation of Ad-MSCs significantly, and for bone tissue engineering, the donor site of the adipose tissue from which the Ad- MSCs are derived should be adapted depending on the requirements.
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One-Step ARMS-PCR for the Detection of SNPs-Using the Example of the PADI4 Gene.
Sabrina Ehnert,Caren Linnemann,Bianca Braun,Josephine Botsch,Karolin Leibiger,Philipp Hemmann,And Andreas K Nussler +6 more
- 25 Jul 2019
TL;DR: ARMS-PCR proved to be the most suitable method regarding handling, duration, and cost of experiments and using the method with SYBR-green based real-time PCR reagents further diminished handling steps and thus potential sources of error.
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Modulation of Macrophage Activity by Pulsed Electromagnetic Fields in the Context of Fracture Healing
Yangmengfan Chen,Maximilian M. Menger,Benedikt J. Braun,Sara Schweizer,Caren Linnemann,Karsten Falldorf,Michael Ronniger,Hongbo Wang,Tina Histing,Andreas K. Nussler,Sabrina Ehnert +10 more
TL;DR: In this paper, the authors identify the specific ELF-PEMFs able to modulate macrophage activity to indirectly promote mesenchymal stem/stromal cell (SCP-1 cells) function.
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Cell-Type-Specific Quantification of a Scaffold-Based 3D Liver Co-Culture
Marc Ruoß,Vanessa Kieber,Silas Rebholz,Caren Linnemann,Helen Rinderknecht,Victor Häussling,Marina Häcker,Leon Olde Damink,Sabrina Ehnert,Andreas K. Nussler +9 more
- 23 Dec 2019
TL;DR: A PCR-based method is developed that allows the quantification of HepG2 cells and 3T3-J2 cells separately in a 3D scaffold culture and shows that this method allows better comparability between 2D and 3D cultures in comparison to the often-used approaches based on metabolic activity measurements.
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