@misc{ZeiherDuchKrolletal.2019,
  author    = {Zeiher, Johannes and Duch, M. and Kroll, Lars Eric and Mensink, Gerhardus Bernardus Maria and Finger, Jonas David and Keil, Thomas},
  title     = {Domain-specific physical activity patterns and cardiorespiratory fitness among adults in Germany},
  series = {The European Journal of Public Health},
  volume    = {29},
  journal   = {The European Journal of Public Health},
  number    = {Supplement. 4},
  publisher = {Oxford Univ. Press},
  address   = {Oxford},
  issn      = {1101-1262},
  pages     = {1},
  year      = {2019},
  abstract  = {Background Studies show that occupational physical activity (OPA) has less health-enhancing effects than leisure-time physical activity (LTPA). The spare data available suggests that OPA rarely includes aerobic PAs with little or no enhancing effects on cardiorespiratory fitness (CRF) as a possible explanation. This study aims to investigate the associations between patterns of OPA and LTPA and CRF among adults in Germany. Methods 1,204 men and 1,303 women (18-64 years), who participated in the German Health Interview and Examination Survey 2008-2011, completed a standardized sub-maximal cycle ergometer test to estimate maximal oxygen consumption (VO2max). Job positions were coded according to the level of physical effort to construct an occupational PA index and categorized as low vs. high OPA. LTPA was assessed via questionnaires and dichotomized in no vs. any LTPA participation. A combined LTPA/OPA variable was used (high OPA/ LTPA, low OPA/LTPA, high OPA/no LTPA, low OPA/no LTPA). Information on potential confounders was obtained via questionnaires (e.g., smoking and education) or physical measurements (e.g., waist circumference). Multi-variable logistic regression was used to analyze associations between OPA/LTPA patterns and VO2max. Results Preliminary analyses showed that less-active men were more likely to have a low VO2max with odds ratios (ORs) of 0.80 for low OPA/LTPA, 1.84 for high OPA/no LTPA and 3.46 for low OPA/no LTPA compared to high OPA/LTPA. The corresponding ORs for women were 1.11 for low OPA/LTPA, 3.99 for high OPA/no LTPA and 2.44 for low OPA/no LTPA, indicating the highest likelihood of low fitness for women working in physically demanding jobs and not engaging in LTPA. Conclusions Findings confirm a strong association between LTPA and CRF and suggest an interaction between OPA and LTPA patterns on CRF within the workforce in Germany. Women without LTPA are at high risk of having a low CRF, especially if they work in physically demanding jobs. Key messages Women not practicing leisure-time physical activity are at risk of having a low cardiorespiratory fitness, especially if they work in physically demanding jobs. Different impact of domains of physical activity should be considered when planning interventions to enhance fitness among the adult population.},
  language  = {en}
}
@misc{WellenbergWeidesBornhorstetal.2019,
  author    = {Wellenberg, Anna and Weides, L. and Bornhorst, Julia and Crone, Barbara and Karst, U. and Fritz, G. and Honnen, S.},
  title     = {Molecular and electrophysiological analysis of platinum-induced neurotoxicity using the model organism C. elegans},
  series = {Naunyn-Schmiedeberg's archives of pharmacology},
  volume    = {392},
  journal   = {Naunyn-Schmiedeberg's archives of pharmacology},
  publisher = {Springer},
  address   = {New York},
  issn      = {0028-1298},
  doi       = {10.1007/s00210-019-01621-6},
  pages     = {S63 -- S63},
  year      = {2019},
  language  = {en}
}
@misc{UhligGehreKammereretal.2018,
  author    = {Uhlig, Katja and Gehre, Christian P. and Kammerer, Sarah and K{\"u}pper, Jan-Heiner and Coleman, Charles Dominic and P{\"u}schel, Gerhard Paul and Duschl, Claus},
  title     = {Real-time monitoring of oxygen consumption of hepatocytes in a microbioreactor},
  series = {Toxicology letters},
  volume    = {295},
  journal   = {Toxicology letters},
  publisher = {Elsevier},
  address   = {Clare},
  issn      = {0378-4274},
  doi       = {10.1016/j.toxlet.2018.06.652},
  pages     = {S115 -- S115},
  year      = {2018},
  language  = {en}
}
@misc{Steinberg2018,
  author    = {Steinberg, Pablo},
  title     = {Only one Component of a holistic Nutrition Policy},
  series = {Fleischwirtschaft},
  volume    = {98},
  journal   = {Fleischwirtschaft},
  number    = {11},
  publisher = {Deutscher Fachverlag GmbH},
  address   = {Frankfurt am Main},
  issn      = {0015-363X},
  pages     = {8 -- 9},
  year      = {2018},
  language  = {de}
}
@misc{SchulzeMartinezGonzalezFungetal.2018,
  author    = {Schulze, Matthias Bernd and Martinez-Gonzalez, Miguel A. and Fung, Teresa T. and Lichtenstein, Alice H. and Forouhi, Nita G.},
  title     = {Food based dietary patterns and chronic disease prevention},
  series = {BMJ-British medical journal},
  volume    = {361},
  journal   = {BMJ-British medical journal},
  publisher = {BMJ Publishing Group},
  address   = {London},
  issn      = {1756-1833},
  doi       = {10.1136/bmj.k2396},
  pages     = {6},
  year      = {2018},
  abstract  = {Matthias B Schulze and colleagues discuss current knowledge on the associations between dietary patterns and cancer, coronary heart disease, stroke, and type 2 diabetes, focusing on areas of uncertainty and future research directions.},
  language  = {en}
}
@misc{SchernthanerGroopCooperetal.2016,
  author    = {Schernthaner, G. and Groop, P. and Cooper, M. and Perkovic, V and Hocher, Berthold and Kanasaki, K. and Sharma, K. and Stanton, R. and Toto, R. and Cescutti, Jessica and Gordat, M. and Meinicke, T. and Koitka-Weber, A. and Woerle, H. and Eynatten, M.},
  title     = {EFFECTS OF LINAGLIPTIN ON GLYCAEMIC CONTROL AND ALBUMINURIA IN TYPE 2 DIABETES - THE MARLINA-T2D (TM) TRIAL},
  series = {Nephrology},
  volume    = {21},
  journal   = {Nephrology},
  publisher = {Wiley-Blackwell},
  address   = {Hoboken},
  issn      = {1320-5358},
  doi       = {10.1111/nep.12887},
  pages     = {60 -- 60},
  year      = {2016},
  language  = {en}
}
@misc{RodriguezSillkeSchumannLissneretal.2020,
  author    = {Rodr{\´i}guez Sillke, Yasmina and Schumann, Michael and Lissner, Donata and Branchi, Frederica and Glauben, Rainer and Siegmund, Britta},
  title     = {Small intestinal inflammation but not colitis drives pro-inflammatory nutritional antigen-specific T-cell response},
  series = {Journal of Crohn's and Colitis},
  volume    = {14},
  journal   = {Journal of Crohn's and Colitis},
  publisher = {Oxford Univ. Press},
  address   = {Oxford},
  issn      = {1873-9946},
  doi       = {10.1093/ecco-jcc/jjz203.172},
  pages     = {S154 -- S155},
  year      = {2020},
  abstract  = {Background: Inflammatory bowel disease (IBD) represents a dysregulation of the mucosal immune system. The pathogenesis of Crohn's disease (CD) and ulcerative colitis (UC) is linked to the loss of intestinal tolerance and barrier function. The healthy mucosal immune system has previously been shown to be inert against food antigens. Since the small intestine is the main contact surface for antigens and therefore the immunological response, the present study served to analyse food-antigen-specific T cells in the peripheral blood of IBD patients. Methods: Peripheral blood mononuclear cells of CD, with an affected small intestine, and UC (colitis) patients, either active or in remission, were stimulated with the following food antigens: gluten, soybean, peanut and ovalbumin. Healthy controls and celiac disease patients were included as controls. Antigen-activated CD4+ T cells in the peripheral blood were analysed by a magnetic enrichment of CD154+ effector T cells and a cytometric antigen-reactive T-cell analysis ('ARTE' technology) followed by characterisation of the ef- fector response. Results: The effector T-cell response of antigen-specific T cells were compared between CD with small intestinal inflammation and UC where inflammation was restricted to the colon. Among all tested food antigens, the highest frequency of antigen-specific T cells (CD4+CD154+) was found for gluten. Celiac disease patients were included as control, since gluten has been identified as the disease- causing antigen. The highest frequency of gluten antigen-specific T cells was revealed in active CD when compared with UC, celiac disease on a gluten-free diet (GFD) and healthy controls. Ovalbuminspecific T cells were almost undetectable, whereas the reaction to soybean and peanut was slightly higher. But again, the strong- est reaction was observed in CD with small intestinal involvement compared with UC. Remarkably, in celiac disease on a GFD only antigen-specific cells for gluten were detected. These gluten-specific T cells were characterised by up-regulation of the pro-inflammatory cytokines IFN-γ, IL-17A and TNF-α. IFN-g was exclusively elevated in CD patients with active disease. Gluten-specific T-cells expressing IL-17A were increased in all IBD patients. Furthermore, T cells of CD patients, independent of disease activity, revealed a high expression of the pro-inflammatory cytokine TNF-α. Conclusion: The 'ARTE'-technique allows to analyse and quantify food antigen specific T cells in the peripheral blood of IBD patients indicating a potential therapeutic insight. These data provide evidence that small intestinal inflammation in CD is key for the development of a systemic pro-inflammatory effector T-cell response driven by food antigens.},
  language  = {en}
}
@misc{ReichetzederHocher2017,
  author    = {Reichetzeder, Christoph and Hocher, Berthold},
  title     = {DPP4 inhibition prevents AKI},
  series = {Oncotarget},
  volume    = {8},
  journal   = {Oncotarget},
  publisher = {Impact Journals LLC},
  address   = {Orchard Park},
  issn      = {1949-2553},
  doi       = {10.18632/oncotarget.20212},
  pages     = {64655 -- 64656},
  year      = {2017},
  language  = {en}
}
@misc{PonceSchererBoekstegersetal.2019,
  author    = {Ponce, Carol Barahona and Scherer, Dominique and Boekstegers, Felix and Garate-Calderon, Valentina and Jenab, Mazda and Aleksandrova, Krasimira and Katzke, Verena and Weiderpass, Elisabete and Bonet, Catalina and Moradi, Tahereh and Fischer, Krista and Bossers, Willem and Brenner, Hermann and Sch{\"o}ttker, Ben and Holleczek, Bernd and Hveem, Kristian and Eklund, Niina and Voelker, Uwe and Waldenberger, Melanie and Bermejo, Justo Lorenzo},
  title     = {Arsenic and gallbladder cancer risk},
  series = {International journal of cancer},
  volume    = {146},
  journal   = {International journal of cancer},
  number    = {9},
  publisher = {Wiley},
  address   = {Hoboken},
  issn      = {0020-7136},
  doi       = {10.1002/ijc.32837},
  pages     = {2648 -- 2650},
  year      = {2019},
  language  = {en}
}
@misc{PolzinRassafBoehmetal.2013,
  author    = {Polzin, Amin and Rassaf, Tienush and Boehm, Andreas and Lueth, Anja and Kleuser, Burkhard and Zeus, Tobias and Kelm, Malte and Kroemer, Heyo K. and Schroer, Karsten and Rauch, Bernhard H.},
  title     = {Aspirin inhibits release of platelet-derived sphingosine-1-phosphate in acute myocardial infarction},
  series = {INTERNATIONAL JOURNAL OF CARDIOLOGY},
  volume    = {170},
  journal   = {INTERNATIONAL JOURNAL OF CARDIOLOGY},
  number    = {2},
  publisher = {ELSEVIER IRELAND LTD},
  address   = {CLARE},
  issn      = {0167-5273},
  doi       = {10.1016/j.ijcard.2013.10.050},
  pages     = {E23 -- E24},
  year      = {2013},
  language  = {en}
}
@misc{PlankYeallandMicelietal.2019,
  author    = {Plank, Roswitha and Yealland, Guy and Miceli, Enrico and Cunha, Dulce Lima and Graff, Patrick and Thomforde, Sari and Gruber, Robert and Moosbrugger-Martinz, Verena and Eckl, Katja and Calderon, Marcelo and Hennies, Hans Christian and Hedtrich, Sarah},
  title     = {Transglutaminase 1 Replacement Therapy Successfully Mitigates the Autosomal Recessive Congenital Ichthyosis Phenotype in Full-Thickness Skin Disease Equivalents},
  series = {The journal of investigative dermatology},
  volume    = {139},
  journal   = {The journal of investigative dermatology},
  number    = {5},
  publisher = {Elsevier},
  address   = {New York},
  issn      = {0022-202X},
  doi       = {10.1016/j.jid.2018.11.002},
  pages     = {1191 -- 1195},
  year      = {2019},
  language  = {en}
}
@misc{PischonRadbruchOstrowskietal.2017,
  author    = {Pischon, Hannah and Radbruch, Moritz and Ostrowski, Anja and Schumacher, Fabian and Hoenzke, Stefan and Kleuser, Burkhard and Hedtrich, Sarah and Fluhr, Joachim W. and Gruber, Achim D. and Mundhenk, Lars},
  title     = {How Effective Is Tacrolimus in the Imiquimod},
  series = {The journal of investigative dermatology},
  volume    = {138},
  journal   = {The journal of investigative dermatology},
  number    = {2},
  publisher = {Elsevier},
  address   = {New York},
  issn      = {0022-202X},
  doi       = {10.1016/j.jid.2017.09.019},
  pages     = {455 -- 458},
  year      = {2017},
  language  = {en}
}
@misc{NojimaKonishiJaptoketal.2016,
  author    = {Nojima, Hiroyuki and Konishi, Takanori and Japtok, Lukasz and Kleuser, Burkhard and Edwards, Michael J. and Gulbins, Erich and Lentsch, Alex B.},
  title     = {Chemokine receptors, CXCR1 and CXCR2, differentially regulate exosome release in hepatocytes},
  series = {Hepatology : official journal of the American Association for the Study of Liver Diseases},
  volume    = {64},
  journal   = {Hepatology : official journal of the American Association for the Study of Liver Diseases},
  publisher = {Wiley-Blackwell},
  address   = {Hoboken},
  issn      = {0270-9139},
  pages     = {165A -- 165A},
  year      = {2016},
  language  = {en}
}
@misc{Mazurek2007,
  author    = {Mazurek, Nicole},
  title     = {Untersuchungen zur Genexpression und Differenzierung muriner embryonaler Stammzellen in vitro zur Pr{\"a}diktion eines embryotoxischen Potentials ausgew{\"a}hlter Chemikalien},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus-68912},
  year      = {2007},
  abstract  = {Der Embryonale Stammzelltest (EST) ist ein validierter In-vitro-Embryotoxizit{\"a}tstest, der zur Untersuchung embryotoxischer Wirkungen von Chemikalien eingesetzt werden kann. W{\"a}hrend des zehnt{\"a}gigen Differenzierungsassays differenzieren sich die pluripotenten murinen embryonalen Stammzellen (ES-Zellen) der Linie D3 in vitro in spontan kontrahierende Herzmuskelzellen. Dabei rekapitulieren sie Prozesse der fr{\"u}hen Embryogenese in vivo. Ein Zytotoxizit{\"a}tsassay mit D3-Zellen und ausdifferenzierten, adulten 3T3-Maus-Fibroblasten dient der Ermittlung allgemeiner zytotoxischer Effekte und unterschiedlicher Sensitivit{\"a}ten beider Zelllinien. Somit basiert der EST auf den beiden wichtigsten Mechanismen pr{\"a}nataler Toxizit{\"a}t, der St{\"o}rung der Differenzierung und der Zytotoxizit{\"a}t. Ziel dieser Arbeit war es, mit Hilfe des EST das embryotoxische Potential der vier Chemikalien Trichostatin A (TSA), Methylazoxymethanolacetat (MAMac), Natriumdodecylsulfat (SDS) und Benzoes{\"a}ure (BA) abzusch{\"a}tzen. Dazu wurde mikroskopisch ermittelt, bei welcher Testsubstanzkonzentration in 50 \% der w{\"a}hrend der In-vitro-Differenzierung gebildeten Embryonalk{\"o}rperchen die Kardiomyozytendifferenzierung inhibiert wird (ID50). Außerdem wurde die halbmaximale Hemmkonzentration des Zellwachstums auf die beiden Zelllinien bestimmt (IC50D3 bzw. IC503T3). Als Erweiterung dieses konventionellen EST wurden mittels quantitativer Real Time-PCR an den Tagen 5, 7 und 10 der Differenzierung zus{\"a}tzlich Genexpressionsanalysen etablierter herzmuskelspezifischer Markergene (Mesoderm Posterior 1, Tag 5; Myosin light chain 1, Tag 7 und 10) durchgef{\"u}hrt. Deren Expression korreliert in den ES-Zellen mit der embryonalen Herzdifferenzierung in vivo und kann zur Ermittlung der von der Pr{\"u}fsubstanz hervorgerufenen halbmaximalen Hemmung der Genexpression in den Kardiomyozyten (IC50 Exp) herangezogen werden. Um letztlich embryotoxische Effekte in vivo auf Grundlage der ermittelten In-vitro-Daten absch{\"a}tzen zu k{\"o}nnen, wurden die ermittelten Parameter mittels eines f{\"u}r den EST empirisch abgeleiteten mathematischen Pr{\"a}diktionsmodells (PM) zur Klassifizierung der Testsubstanzen als nicht, schwach oder stark embryotoxisch herangezogen. F{\"u}r jede der Substanzen waren die ermittelten Halbhemmkonzentrationen in den {\"u}berwiegenden F{\"a}llen vergleichbar und f{\"u}hrten unter Verwendung des PMs im konventionellen und im molekularen EST zu deren identischer Klassifizierung. TSA wurde als „stark embryotoxisch" klassifiziert und beeinflusste insbesondere das Differenzierungspotential der ES-Zellen. Das als „schwach embryotoxisch" klassifizierte SDS wirkte auf die D3-Zellen st{\"a}rker differenzierungsinhibierend als zytotoxisch, hemmte jedoch das Wachstum der 3T3-Zellen bereits in deutlich niedrigeren Konzentrationen. MAMac und BA wurden als „nicht embryotoxisch" klassifiziert. Bei ihnen stand die zytotoxische Wirkung deutlich im Vordergrund. Diese Pr{\"a}diktionen stimmten mit In-vivo-Befunden {\"u}berein, was von der Stabilit{\"a}t und der Brauchbarkeit der im konventionellen und molekularen EST ermittelten Parameter zeugte. Einzige Ausnahme war das als Entwicklungsneurotoxin in vivo bekannte MAMac. Da der EST auf mesodermaler Differenzierung basiert, k{\"o}nnen spezifische Effekte auf neuronale Entwicklungsprozesse offenbar nicht vollst{\"a}ndig erfasst werden. Substanzkonzentrationen, die sich als differenzierungsinhibierend auf die morphologische Kardiomyozytendifferenzierung erwiesen haben, f{\"u}hrten auch zu einer messbaren Repression der herzmuskelspezifischen Genexpression. Dabei erwies sich die IC50 Exp als ebenso sensitiv wie die konventionellen Parameter und als nutzbringende Erg{\"a}nzung zu diesen, da sie bereits nach 5 bzw. 7 Tagen der In-vitro-Differenzierung eine mit dem mikroskopischen Parameter {\"u}bereinstimmende Einsch{\"a}tzung des embryotoxischen Potentials der Chemikalien in vivo erm{\"o}glichte. Genexpressionsanalysen weiterer differenzierungsspezifischer Gene k{\"o}nnen zus{\"a}tzlich zur Aufkl{\"a}rung zu Grunde liegender Mechanismen der Embryotoxizit{\"a}t von Testsubstanzen dienen. Somit kann der EST durch die Vorteile der Stammzelltechnologie und der Genexpressionsanalyse als neues pr{\"a}diktives Screening-Instrument zur fr{\"u}hzeitigen Detektion embryotoxischer Substanzeffekte in der pharmazeutischen und chemischen Industrie genutzt werden.},
  language  = {de}
}
@misc{Kleuser2018,
  author    = {Kleuser, Burkhard},
  title     = {The enigma of sphingolipids in health and disease},
  series = {International journal of molecular sciences},
  volume    = {19},
  journal   = {International journal of molecular sciences},
  number    = {10},
  publisher = {MDPI},
  address   = {Basel},
  issn      = {1422-0067},
  doi       = {10.3390/ijms19103126},
  pages     = {3},
  year      = {2018},
  language  = {en}
}
@misc{Kleuser2017,
  author    = {Kleuser, Burkhard},
  title     = {Medikamentennebenwirkungen auf Haut und Schleimhaut - allergische oder pharmakologisch erkl{\"a}rbare Reaktionen},
  series = {Allergologie},
  volume    = {40},
  journal   = {Allergologie},
  number    = {10},
  publisher = {Dustri-Verlag},
  address   = {Deisenhofen-M{\"u}nchen},
  issn      = {0344-5062},
  pages     = {420 -- 421},
  year      = {2017},
  language  = {de}
}
@misc{JamnokSanchaisuriyaYamsrietal.2018,
  author    = {Jamnok, Jutatip and Sanchaisuriya, Kanokwan and Yamsri, Supawadee and Fucharoen, Goonnapa and Fucharoen, Supan and Schweigert, Florian J. and Sanchaisuriya, Pattara},
  title     = {Application of a new portable nephelometer for screening thalassemia in countries with limited resources},
  series = {International Journal of Laboratory Hematology},
  volume    = {40},
  journal   = {International Journal of Laboratory Hematology},
  publisher = {Wiley},
  address   = {Hoboken},
  issn      = {1751-5521},
  pages     = {62 -- 62},
  year      = {2018},
  language  = {en}
}
@misc{JamnokSanchaisuriyaYamsrietal.2018,
  author    = {Jamnok, Jutatip and Sanchaisuriya, Kanokwan and Yamsri, Supawadee and Fucharoen, Goonnapa and Fucharoen, Supan and Schweigert, Florian J. and Sanchaisuriya, Pattara},
  title     = {Application of a new portable nephelometer for screening thalassemia in countries with limited resources},
  series = {International journal of laboratory hematology},
  volume    = {40},
  journal   = {International journal of laboratory hematology},
  publisher = {Wiley},
  address   = {Hoboken},
  issn      = {1751-5521},
  pages     = {62 -- 62},
  year      = {2018},
  abstract  = {One-tube osmotic fragility (OF) test is a rapid test used widely for screening thalassemia in countries with limited resources. The test has important limitation in that its accuracy relies on observers' experience. The iCheck Turbidity is a prototype of portable nephelometer developed by BioAnalyt (Bioanalyt GmbH, Germany). In this study, we assessed the applicability of the iCheck Turbidity, for checking turbidity of the OF-test},
  language  = {en}
}
@misc{HonnenWellenbergWeidesetal.2018,
  author    = {Honnen, S. and Wellenberg, Anna and Weides, L. and Bornhorst, Julia and Crone, B. and Karst, U. and Fritz, G.},
  title     = {Identification of potent drug candidates for the prevention of cisplatin-induced neurotoxicity in the model organism C. elegans},
  series = {Naunyn-Schmiedeberg's archives of pharmacology},
  volume    = {391},
  journal   = {Naunyn-Schmiedeberg's archives of pharmacology},
  publisher = {Springer},
  address   = {New York},
  issn      = {0028-1298},
  doi       = {10.1007/s00210-018-1477-5},
  pages     = {S4 -- S4},
  year      = {2018},
  language  = {en}
}
@misc{HollmannReuterWerneretal.2016,
  author    = {Hollmann, C. and Reuter, D. and Werner, S. and Avota, Elita and Mueller, N. and Japtok, Lukasz and Kleuser, Burkhard and Becker, Katrin Anne and Gulbins, Erich and Schneider-Schaulies, J{\"u}rgen and Beyersdorf, Niklas},
  title     = {Pharmacological inhibition of acid sphingomyelinase or genetic ablation enhances CD4(+) Foxp3(+) regulatory T cell activity},
  series = {European journal of immunology},
  volume    = {46},
  journal   = {European journal of immunology},
  publisher = {Wiley-Blackwell},
  address   = {Hoboken},
  issn      = {0014-2980},
  pages     = {14 -- 14},
  year      = {2016},
  language  = {en}
}
@misc{HocherZeng2018,
  author    = {Hocher, Berthold and Zeng, Shufei},
  title     = {Clear the fog around parathyroid hormone assays},
  series = {Clinical journal of the American Society of Nephrology},
  volume    = {13},
  journal   = {Clinical journal of the American Society of Nephrology},
  number    = {4},
  publisher = {American Society of Nephrology},
  address   = {Washington},
  issn      = {1555-9041},
  doi       = {10.2215/CJN.01730218},
  pages     = {524 -- 526},
  year      = {2018},
  language  = {en}
}
@misc{HocherZeng2018,
  author    = {Hocher, Berthold and Zeng, Shufei},
  title     = {Need for better PTH assays for clinical research and patient treatment},
  series = {Clinical chemistry and laboratory medicine : journal of the Forum of the European Societies of Clinical Chemistry - the European Branch of the International Federation of Clinical Chemistry and Laboratory Medicine},
  volume    = {56},
  journal   = {Clinical chemistry and laboratory medicine : journal of the Forum of the European Societies of Clinical Chemistry - the European Branch of the International Federation of Clinical Chemistry and Laboratory Medicine},
  number    = {2},
  publisher = {De Gruyter},
  address   = {Berlin},
  issn      = {1434-6621},
  doi       = {10.1515/cclm-2017-0617},
  pages     = {183 -- 185},
  year      = {2018},
  language  = {en}
}
@misc{HocherTsuprykov2017,
  author    = {Hocher, Berthold and Tsuprykov, Oleg},
  title     = {Renoprotective effects of GLP1R agonists and SGLT2 inhibitors},
  series = {Nature reviews nephroloy},
  volume    = {13},
  journal   = {Nature reviews nephroloy},
  publisher = {Nature Publ. Group},
  address   = {New York},
  issn      = {1759-5061},
  doi       = {10.1038/nrneph.2017.140},
  pages     = {728 -- 729},
  year      = {2017},
  abstract  = {New data from the LEADER trial show that the glucagon-like peptide 1 receptor agonist liraglutide protects against diabetic nephropathy in patients with type 2 diabetes mellitus. The renoprotective efficacy of liraglutide is not, however, as great as that reported for the sodium-glucose cotransporter 2 inhibitor emplagiflozin in the EMPA-REG OUTCOME trial.},
  language  = {en}
}
@misc{Henze2018,
  author    = {Henze, Andrea},
  title     = {Proteinoxidation als Indikator des Alterungsph{\"a}notyps und Target einer individualisierten Ern{\"a}hrungsintervention (ProAID)},
  series = {Ern{\"a}hrungs-Umschau : Forschung \& Praxis},
  volume    = {65},
  journal   = {Ern{\"a}hrungs-Umschau : Forschung \& Praxis},
  number    = {10},
  publisher = {Umschau-Zeitschriftenverl.},
  address   = {Frankfurt, Main},
  issn      = {0174-0008},
  pages     = {M566 -- M567},
  year      = {2018},
  abstract  = {Oxidative posttranslationale Modifikationen endogener Proteine werden v. a. durch reaktive Sauerstoff- und Stickstoffspezies (engl:. Reactive Oxygen Species, ROS, reactive nitrogen species, RNS) hervorgerufen und k{\"o}nnen sowohl reversibel (z. B. Disulfidbindungen) als auch irreversibel (z. B. Proteincarbonyle) erfolgen [1-3]. Lange wurde angenommen, dass oxidative posttranslationale Proteinmodifikationen (oxPTPM) nur von untergeordneter Bedeutung f{\"u}r den Metabolismus sind. Tats{\"a}chlich handelt es sich jedoch um einen physiologischen Prozess, der {\"u}ber die Modulation der Proteinstruktur auch die Proteinfunktion (z. B. Enzymaktivit{\"a}t, Stabilit{\"a}t) und somit zahlreiche Stoffwechselwege wie den Energiestoffwechsel, die Immunfunktion, die vaskul{\"a}re Funktion sowie Apoptose und Genexpression beeinflussen kann. Die Bildung von oxPTPM ist dabei hochreguliert und h{\"a}ngt u. a. von der Proteinstruktur, der Verf{\"u}gbarkeit von ROS und RNS sowie dem lokalen Mikromilieu der Zelle ab [2, 4].},
  language  = {de}
}
@misc{HalibasicFuerstHeidenetal.2017,
  author    = {Halibasic, Emina and Fuerst, Elisabeth and Heiden, Denis and Japtok, Lukasz and Diesner, Susanne C. and Hillebrand, P. and Trauner, Michael and Kleuser, Burkhard and Kazemi-Shirazi, Lili and Untersmayr, Eva},
  title     = {Significantly reduced plasma levels of the bioactive sphingolipid S1P in lung transplanted cystic fibrosis patients are associated with gastrointestinal symptoms},
  series = {Allergy},
  volume    = {72},
  journal   = {Allergy},
  number    = {S103},
  publisher = {Wiley},
  address   = {Hoboken},
  issn      = {0105-4538},
  pages     = {195 -- 195},
  year      = {2017},
  language  = {en}
}
@misc{FernandoDrescherDeubeletal.2018,
  author    = {Fernando, Raquel and Drescher, Cathleen and Deubel, Stefanie and Grune, Tilman and Castro, Jose Pedro},
  title     = {Distinct proteasomal activity for fast and slow twitch skeletal muscle during aging},
  series = {Free radical biology and medicine : the official journal of the Oxygen Society, a constituent member of the International Society for Free Radical Research},
  volume    = {120},
  journal   = {Free radical biology and medicine : the official journal of the Oxygen Society, a constituent member of the International Society for Free Radical Research},
  publisher = {Elsevier},
  address   = {New York},
  issn      = {0891-5849},
  doi       = {10.1016/j.freeradbiomed.2018.04.393},
  pages     = {S119 -- S119},
  year      = {2018},
  abstract  = {Skeletal muscle alterations during aging lead to dysfunctional metabolism, correlating with frailty and early mortality. The loss of proteostasis is a hallmark of aging. Whether proteostasis loss plays a role in muscle aging remains elusive. To address this question we collected muscles, Soleus (SOL, type I) and Extensor digitorum longus (EDL, type II), from young (4 months) and old (25 months) C57BL/6 mice and evaluated the proteasomal system. Initial work showed decreased 26 S activity in old SOL. EDL displayed lower proteasomal activity in both ages compared to any of the SOL ages. Moreover, in order to understand if during aging there is the so-called "fiber switch from fast-to-slow", we performed western blots against sMHC and fMHC (slow and fast myosin heavy chain, respectively). Preliminary results suggest that young SOL is composed by slow twitch fibers but also contains fast twitch fibers, while young EDL seems to be mostly composed by fast twitch fibers that level down during aging, suggesting the switch. As a conclusion, EDL seems to have less proteasomal activity, however, if this is a contributor or a consequence to the muscle fiber switch during aging still needs further investigation.},
  language  = {en}
}
@misc{DoegeSchumacherBalzusetal.2017,
  author    = {D{\"o}ge, Nadine and Schumacher, Fabian and Balzus, Benjamin and Colombo, Miriam and Hadam, Sabrina and Rancan, Fiorenza and Blume-Peytavi, Ulrike and Kleuser, Burkhard and Bodmeier, Roland and Vogt, Annika},
  title     = {Particle- based formulations and controlled skin barrier disruption have a signifi cant impact on the delivery and penetration kinetics of dexamethasone as assessed in an ex vivo microdialysis},
  series = {Journal der Deutschen Dermatologischen Gesellschaft},
  volume    = {15},
  journal   = {Journal der Deutschen Dermatologischen Gesellschaft},
  publisher = {Wiley},
  address   = {Berlin},
  issn      = {1610-0379},
  pages     = {182 -- 182},
  year      = {2017},
  abstract  = {Preclinical assessment of penetration not only in intact, but also in barrier-disrupted skin is important to explore the surplus value of novel drug delivery systems, which can be specifically designed for diseased skin. Here, we characterized physical and chemical barrier disruption protocols for short-term ex vivo skin cultures with regard to structural integrity, physiological and biological parameters. Further, we compared the penetration of dexamethasone (Dex) in different nanoparticle-based formulations in stratum corneum, epidermis and dermis extracts of intact vs. barrier-disrupted skin as well as by dermal microdialysis at 6, 12 and 24 hours after topical application. Dex was quantified by liquid-chromatography - tandem-mass spectrometry (LC-MS/MS). Simultaneously, we investigated the Dex efficacy by interleukin (IL) analysis. Tape-stripping (TS) and 4 hours sodium lauryl sulfate 5 \% (SLS) exposure were identified as highly effective barrier disruption methods assessed by reproducible transepidermal water loss (TEWL) changes and IL-6/8 increase which was more pronounced in SLS-treated skin. The barrier state has also a significant impact on the Dex penetration kinetics: for all formulations, TS highly increased dermal Dex concentration despite the fact that nanocrystals quickly and effectively penetrated both, intact and barrier-disrupted skin reaching significantly higher dermal Dex concentration after 6 hours compared to Dex cream. The surplus value of encapsulation in ethyl cellulose nanocarriers could mostly be observed when applied on intact skin, in general showing a delayed Dex penetration. Estimation of cytokines was limited due to the trauma caused by probe insertion. In summary, ex vivo human skin is a highly interesting short-term preclinical model for the analysis of penetration and efficacy of novel drug delivery systems.},
  language  = {en}
}
@misc{DoegeHoenzkeSchumacheretal.2016,
  author    = {Doege, N. and Hoenzke, S. and Schumacher, Fabian and Balzus, Benjamin and Colombo, Miriam and Hadam, S. and Rancan, F. and Blume-Peytavi, Ulrike and Schindler, A. and Ruehl, E. and Skov, P. and Church, Martin K. and Hedtrich, Sarah and Kleuser, Burkhard and Bodmeier, Roland and Vogt, A.},
  title     = {Ex vivo microdialysis used for the preclinical assessment of anti-inflammatory therapy},
  series = {Experimental dermatology : the official journal of the European Immunodermatology Society},
  volume    = {25},
  journal   = {Experimental dermatology : the official journal of the European Immunodermatology Society},
  publisher = {Wiley-Blackwell},
  address   = {Hoboken},
  issn      = {0906-6705},
  pages     = {E32 -- E32},
  year      = {2016},
  language  = {en}
}
@misc{ChenBornhorstNeelyetal.2018,
  author    = {Chen, Pan and Bornhorst, Julia and Neely, M. Diana and Avila, Daiana Silva},
  title     = {Mechanisms and Disease Pathogenesis Underlying Metal-Induced Oxidative Stress},
  series = {Oxidative Medicine and Cellular Longevity},
  journal   = {Oxidative Medicine and Cellular Longevity},
  publisher = {Hindawi},
  address   = {London},
  issn      = {1942-0900},
  doi       = {10.1155/2018/7612172},
  pages     = {3},
  year      = {2018},
  language  = {en}
}
@misc{BaeumerRossbachMischkeetal.2011,
  author    = {B{\"a}umer, Wolfgang and Rossbach, Kristine and Mischke, Reinhard and Reines, Ilka and Langbein-Detsch, Ines and L{\"u}th, Anja and Kleuser, Burkhard},
  title     = {Decreased concentration and enhanced metabolism of sphingosine-1-Phosphate in lesional skin of dogs with atopic dermatitis disturbed Sphingosine-1-Phosphate homeostasis in atopic Dermatitis},
  series = {The journal of investigative dermatology},
  volume    = {131},
  journal   = {The journal of investigative dermatology},
  number    = {1},
  publisher = {Nature Publ. Group},
  address   = {New York},
  issn      = {0022-202X},
  doi       = {10.1038/jid.2010.252},
  pages     = {266 -- 268},
  year      = {2011},
  language  = {en}
}
@misc{BijleveldZoutewelleTerovanHuscheketal.2016,
  author    = {Bijleveld, Catrien and Zoutewelle-Terovan, Mioara and Huschek, Doreen and Liefbroer, Aart C.},
  title     = {Criminal careers and demographic outcomes: An introduction to the special issue},
  series = {Advances in life course research},
  volume    = {28},
  journal   = {Advances in life course research},
  publisher = {Elsevier},
  address   = {Oxford},
  issn      = {1569-4909},
  doi       = {10.1016/j.alcr.2016.05.001},
  pages     = {1 -- 5},
  year      = {2016},
  language  = {en}
}