@misc{Rose2007,
  author    = {Rose, J{\"u}rgen},
  title     = {Wider den „euro-atlantischen Internationalismus" : Berliner Republik und Entgrenzung der Bundeswehr},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus-23212},
  year      = {2007},
  abstract  = {Inhalt: Frieden mit aller Gewalt schaffen? Tatbestand: Staatsterrorismus Das Weißbuch 2006 Bundesverfassungsgericht versus Bundesverwaltungsgericht Weltweites Interventionsrecht Lizenz zum V{\"o}lkerrechtsbruch „Re-Transformation" der Bundeswehr Prinzipien f{\"u}r einen sicherheitspolitischen Grundkonsens Breite {\"o}ffentliche Debatte notwendig},
  language  = {de}
}
@article{SchulmeisterRoseVoigt1996,
  author    = {Schulmeister, Thomas and Rose, J{\"u}rgen and Voigt, Horst},
  title     = {Some extensions of Schmidt's partition method for sequence comparison based on binary character amino acid properties},
  year      = {1996},
  language  = {en}
}
@article{Rose2011,
  author    = {Rose, J{\"u}rgen},
  title     = {R{\"u}ckzug Fehlanzeige},
  series = {WeltTrends-Papiere},
  journal   = {WeltTrends-Papiere},
  number    = {16},
  publisher = {Universit{\"a}tsverlag Potsdam},
  address   = {Potsdam},
  issn      = {1864-0656},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus-63277},
  pages     = {48 -- 57},
  year      = {2011},
  abstract  = {Inhalt: Regime Change und Anti-Terrorkrieg ; „Engagement" der USA ; Deutsche Involvierung ; Ferngesteuerter Krieg ; Abzug nicht in Sicht ; „Sieg" nicht in Sicht ; Reinfall Afghanistan-Strategie ; Menetekel von Saigon},
  language  = {de}
}
@article{SchulmeisterRoseScheller1997,
  author    = {Schulmeister, Thomas and Rose, J{\"u}rgen and Scheller, Frieder W.},
  title     = {Mathematical modelling of exponential amplification in membrane-based enzyme sensors},
  year      = {1997},
  language  = {en}
}
@article{FeoktistovaRoseProkopovicetal.2016,
  author    = {Feoktistova, Natalia and Rose, J{\"u}rgen and Prokopovic, Vladimir Z. and Vikulina, Anna S. and Skirtach, Andre and Volodkin, Dmitry},
  title     = {Controlling the Vaterite CaCO3 Crystal Pores. Design of Tailor-Made Polymer Based Microcapsules by Hard Templating},
  series = {Langmuir},
  volume    = {32},
  journal   = {Langmuir},
  publisher = {American Chemical Society},
  address   = {Washington},
  issn      = {0743-7463},
  doi       = {10.1021/acs.langmuir.6b00717},
  pages     = {4229 -- 4238},
  year      = {2016},
  abstract  = {The spherical vaterite CaCO3 microcrystals are nowadays widely used as sacrificial templates for fabrication of various microcarriers made of biopolymers (e.g., proteins, nucleic acids, enzymes) due to porous structure and mild template elimination conditions. Here, we demonstrated for the first time that polymer microcarriers with tuned internal nanoarchitecture can be designed by employing the CaCO3 crystals of controlled porosity. The layer-by-layer deposition has been utilized to assemble shell-like (hollow) and matrix-like (filled) polymer capsules due to restricted and free polymer diffusion through the crystal pores, respectively. The crystal pore size in the range of few tens of nanometers can be adjusted without any additives by variation of the crystal preparation temperature in the range 745 degrees C. The temperature-mediated growth mechanism is explained by the Ostwald ripening of nanocrystallites forming the crystal secondary structure. Various techniques including SEM, AFM, CLSM, Raman microscopy, nitrogen adsorptiondesorption, and XRD have been employed for crystal and microcapsule analysis. A three-dimensional model is introduced to describe the crystal internal structure and predict the pore cutoff and available surface for the pore diffusing molecules. Inherent biocompatibility of CaCO3 and a possibility to scale the porosity in the size range of typical biomacromolecules make the CaCO3 crystals extremely attractive tools for template assisted designing tailor-made biopolymer-based architectures in 2D to 3D targeted at drug delivery and other bioapplications.},
  language  = {en}
}
@article{UhligMadaboosiSchmidtetal.2012,
  author    = {Uhlig, Katja and Madaboosi, Narayanan and Schmidt, Stephan and J{\"a}ger, Magnus S. and Rose, J{\"u}rgen and Duschl, Claus and Volodkin, Dmitry V.},
  title     = {3d localization and diffusion of proteins in polyelectrolyte multilayers},
  series = {Soft matter},
  volume    = {8},
  journal   = {Soft matter},
  number    = {47},
  publisher = {Royal Society of Chemistry},
  address   = {Cambridge},
  issn      = {1744-683X},
  doi       = {10.1039/c2sm26500a},
  pages     = {11786 -- 11789},
  year      = {2012},
  abstract  = {The interaction of diverse biomaterials with surfaces is more crucial than ever for biomedical applications to ensure efficiency and reproducibility. Very interesting surface materials are micrometer-thick polyelectrolyte multilayers. Not only their surface but also the bulk can be loaded with biomaterials like proteins or DNA for various purposes. Therefore, we established a method to analyze the lateral and vertical distribution of fluorescently labelled proteins of various size and charge in polyelectrolyte films composed of poly(L-lysine) and hyaluronic acid by confocal laser scanning microscopy. This approach enables us to measure the diffusion coefficients of the proteins via fluorescence recovery after photobleaching as a function of their vertical position in the film and facilitates the understanding of molecular interactions in the film with a high resolution in both space and time. As a result, we confirm that protein loading in the film is driven by electrostatic interactions - uncharged dextran molecules of 10 and 500 kDa do not diffuse into the film. Proteins of different sizes (3-11 nm) can diffuse relatively fast (D = 2-4 mm(2) s(-1)) independent of their net charge, indicating complex interpolymer interactions. This approach is a new powerful experimental tool to design the polyelectrolyte multilayers for bio-applications by finding a relationship between intermolecular interactions and mobility and availability of biomolecules to biological samples (e.g. cells) or detection units (e.g. biosensors).},
  language  = {en}
}