@misc{BehmMuehlbauerKibeleetal.2016,
  author    = {Behm, David George and M{\"u}hlbauer, Thomas and Kibele, Armin and Granacher, Urs},
  title     = {Effects of Strength Training Using Unstable Surfaces on Strength, Power and Balance Performance Across the Lifespan: A Systematic Review and Meta-analysis (vol 45, pg 1645, 2015)},
  series = {Sports medicine},
  volume    = {46},
  journal   = {Sports medicine},
  publisher = {Springer},
  address   = {Northcote},
  issn      = {0112-1642},
  doi       = {10.1007/s40279-016-0497-x},
  pages     = {451 -- 451},
  year      = {2016},
  language  = {en}
}
@misc{AndersonBahnikBarnettCowanetal.2016,
  author    = {Anderson, Christopher J. and Bahnik, Stepan and Barnett-Cowan, Michael and Bosco, Frank A. and Chandler, Jesse and Chartier, Christopher R. and Cheung, Felix and Christopherson, Cody D. and Cordes, Andreas and Cremata, Edward J. and Della Penna, Nicolas and Estel, Vivien and Fedor, Anna and Fitneva, Stanka A. and Frank, Michael C. and Grange, James A. and Hartshorne, Joshua K. and Hasselman, Fred and Henninger, Felix and van der Hulst, Marije and Jonas, Kai J. and Lai, Calvin K. and Levitan, Carmel A. and Miller, Jeremy K. and Moore, Katherine S. and Meixner, Johannes M. and Munafo, Marcus R. and Neijenhuijs, Koen I. and Nilsonne, Gustav and Nosek, Brian A. and Plessow, Franziska and Prenoveau, Jason M. and Ricker, Ashley A. and Schmidt, Kathleen and Spies, Jeffrey R. and Stieger, Stefan and Strohminger, Nina and Sullivan, Gavin B. and van Aert, Robbie C. M. and van Assen, Marcel A. L. M. and Vanpaemel, Wolf and Vianello, Michelangelo and Voracek, Martin and Zuni, Kellylynn},
  title     = {Response to Comment on "Estimating the reproducibility of psychological science"},
  series = {Science},
  volume    = {351},
  journal   = {Science},
  publisher = {American Assoc. for the Advancement of Science},
  address   = {Washington},
  issn      = {0036-8075},
  doi       = {10.1126/science.aad9163},
  pages     = {1162 -- 1165},
  year      = {2016},
  abstract  = {Gilbert et al. conclude that evidence from the Open Science Collaboration's Reproducibility Project: Psychology indicates high reproducibility, given the study methodology. Their very optimistic assessment is limited by statistical misconceptions and by causal inferences from selectively interpreted, correlational data. Using the Reproducibility Project: Psychology data, both optimistic and pessimistic conclusions about reproducibility are possible, and neither are yet warranted.},
  language  = {en}
}
@misc{WippertPuschmannSchiltenwolfetal.2016,
  author    = {Wippert, Pia-Maria and Puschmann, Anne-Katrin and Schiltenwolf, Marcus and Wiebking, Christine and Mayer, Frank},
  title     = {BACK PAIN: THE STUDY OF MECHANISMS AND THE TRANSLATION IN INTERVENTIONS WITHIN THE MISPEX NETWORK},
  series = {Psychosomatic medicine},
  volume    = {78},
  journal   = {Psychosomatic medicine},
  publisher = {Elsevier},
  address   = {Philadelphia},
  issn      = {0033-3174},
  pages     = {A91 -- A91},
  year      = {2016},
  language  = {en}
}
@misc{PuschmannWippert2016,
  author    = {Puschmann, Anne-Katrin and Wippert, Pia-Maria},
  title     = {A LONGITUDINAL INTERDISCIPLINARY APPROACH TO STRESS AND ITS IMPACT ON THE DEVELOPMENT OF CHRONIC PAIN},
  series = {Psychosomatic medicine},
  volume    = {78},
  journal   = {Psychosomatic medicine},
  publisher = {Routledge, Taylor \& Francis Group},
  address   = {Philadelphia},
  issn      = {0033-3174},
  pages     = {A91 -- A91},
  year      = {2016},
  language  = {en}
}
@misc{BattistonFarmerFlacheetal.2016,
  author    = {Battiston, Stefano and Farmer, Doyne and Flache, Andreas and Garlaschelli, Diego and Haldane, Andy and Heesterbeek, Hans and Hommes, Cars and Jaeger, Carlo and May, Robert and Scheffer, Marten},
  title     = {Financial complexity: Accounting for fraud Response},
  series = {Science},
  volume    = {352},
  journal   = {Science},
  publisher = {American Assoc. for the Advancement of Science},
  address   = {Washington},
  issn      = {0036-8075},
  doi       = {10.1126/science.352.6283.302},
  pages     = {302 -- 302},
  year      = {2016},
  language  = {en}
}
@misc{LevermannPetoukhovScheweetal.2016,
  author    = {Levermann, Anders and Petoukhov, Vladimir and Schewe, Jacob and Schellnhuber, Hans Joachim},
  title     = {Abrupt monsoon transitions as seen in paleorecords can be explained by moisture-advection feedback},
  series = {Proceedings of the National Academy of Sciences of the United States of America},
  volume    = {113},
  journal   = {Proceedings of the National Academy of Sciences of the United States of America},
  publisher = {National Acad. of Sciences},
  address   = {Washington},
  issn      = {0027-8424},
  doi       = {10.1073/pnas.1603130113},
  pages     = {E2348 -- E2349},
  year      = {2016},
  language  = {en}
}
@misc{HartmannFischer2016,
  author    = {Hartmann, Matthias and Fischer, Martin H.},
  title     = {Exploring the numerical mind by eye-tracking: a special issue},
  series = {Psychological research : an international journal of perception, attention, memory, and action},
  volume    = {80},
  journal   = {Psychological research : an international journal of perception, attention, memory, and action},
  publisher = {Springer},
  address   = {Heidelberg},
  issn      = {0340-0727},
  doi       = {10.1007/s00426-016-0759-0},
  pages     = {325 -- 333},
  year      = {2016},
  language  = {en}
}
@misc{StroehleRapp2016,
  author    = {Stroehle, Andreas and Rapp, Michael A.},
  title     = {Prevention of Cognitive Decline: A Physical Exercise Perspective on Brain Health in the Long Run},
  series = {Journal of the American Medical Directors Association},
  volume    = {17},
  journal   = {Journal of the American Medical Directors Association},
  publisher = {Elsevier},
  address   = {New York},
  issn      = {1525-8610},
  doi       = {10.1016/j.jamda.2016.02.030},
  pages     = {461 -- 462},
  year      = {2016},
  language  = {en}
}
@misc{MaierHolzloehnerHoenowetal.2016,
  author    = {Maier, Natalia and Holzl{\"o}hner, Pamela and Hoenow, Anja and Scheunemann, Astrid and Weschke, Daniel and Hanack, Katja},
  title     = {Characterization of monoclonal antibodies generated by in vitro immunization},
  series = {The journal of immunology},
  volume    = {196},
  journal   = {The journal of immunology},
  publisher = {American Assoc. of Immunologists},
  address   = {Bethesda},
  issn      = {0022-1767},
  pages     = {2},
  year      = {2016},
  abstract  = {Monoclonal antibodies are highly valuable tools in biomedicine but the generation by hybridoma technology is very time-consuming and elaborate. In order to circumvent the consisting drawbacks an in vitro immunization approach was established by which murine as well as human monoclonal antibodies against a viral coat protein could be developed. The in vitro immunization process was performed by isolation of murine hematopoietic stem cells or human monocytes and an in vitro differentiation into immature dendritic cells. After antigen loading the cells were co-cultivated with naive T and B lymphocytes for three days in order to obtain antigen-specific B lymphocytes in culture, followed by fusion with murine myeloma cells or human/murine heteromyeloma cells. Antigen-specific hybridomas were selected and the generated antibodies were purified and characterized in this study by ELISA, western blot, gene sequencing, affinity measurements. Further the characteristics were compared to a monoclonal antibody against the same target generated by conventional hybridoma technology. Isotype detection revealed a murine IgM and a human IgG4 antibody in comparison to an IgG1 for the conventionally generated antibody. The antibodies derived from in vitro immunization showed indeed a lower affinity for the antigen as compared to the conventionally generated one, which is probably based on the significantly shorter B cell maturation (3 days) during the immunization process. Nevertheless, they were suitable for building up a sandwich based detection system. Therefore, the in vitro immunization approach seems to be a good and particularly fast alternative to conventional hybridoma technology.},
  language  = {en}
}
@misc{HanackSchloerHolzloehneretal.2016,
  author    = {Hanack, Katja and Schloer, Anja and Holzloehner, Pamela and Listek, Martin and Bauer, Cindy and Butze, Monique and Micheel, Burkhard and Hentschel, Christian and Sowa, Mandy and Roggenbuck, Dirk and Schierack, Peter and Fuener, Jonas and Schliebs, Erik and Goihl, Alexander and Reinhold, Dirk},
  title     = {Camelid nanobodies specific to human pancreatic glycoprotein 2},
  series = {The journal of immunology},
  volume    = {196},
  journal   = {The journal of immunology},
  publisher = {American Assoc. of Immunologists},
  address   = {Bethesda},
  issn      = {0022-1767},
  pages     = {313 -- 328},
  year      = {2016},
  abstract  = {Pancreatic secretory zymogen-granule membrane glycoprotein 2 (GP2) has been identified to be a major autoantigenic target in Crohn's disease patients. It was discussed recently that a long and a short isoform of GP2 exists whereas the short isoform is often detected by GP2-specific autoantibodies. In the outcome of inflammatory bowel diseases, these GP2-specific autoantibodies are discussed as new serological markers for diagnosis and therapeutic monitoring. To investigate this further, camelid nanobodies were generated by phage display and selected against the short isoform of GP2 in order to isolate specific tools for the discrimination of both isoforms. Nanobodies are single domain antibodies derived from camelid heavy chain only antibodies and characterized by a high stability and solubility. The selected candidates were expressed, purified and validated regarding their binding properties in different enzyme-linked immunosorbent assays formats, immunofluorescence, immunohistochemistry and surface plasmon resonance spectroscopy. Four different nanobodies could be selected whereof three recognize the short isoform of GP2 very specifically and one nanobody showed a high binding capacity for both isoforms. The KD values measured for all nanobodies were between 1.3 nM and 2.3 pM indicating highly specific binders suitable for the application as diagnostic tool in inflammatory bowel disease.},
  language  = {en}
}