@book{Lauth2016,
  author    = {Lauth, Jakob},
  title     = {Physikalische Chemie, 5: Elektrochemie},
  publisher = {Springer},
  address   = {Berlin},
  isbn      = {978-3-662-47559-1},
  pages     = {55 Seiten},
  year      = {2016},
  language  = {de}
}
@book{Lauth2016,
  author    = {Lauth, Jakob},
  title     = {Physikalische Chemie, 4: Reaktionskinetik},
  publisher = {Springer},
  address   = {Berlin},
  isbn      = {978-3-662-47674-1},
  pages     = {52 Seiten},
  year      = {2016},
  language  = {de}
}
@book{Lauth2016,
  author    = {Lauth, Jakob},
  title     = {Physikalische Chemie, 3: Phasengleichgewichte},
  publisher = {Springer},
  address   = {Berlin},
  isbn      = {978-3-662-47571-3},
  pages     = {57 Seiten},
  year      = {2016},
  language  = {de}
}
@book{Lauth2016,
  author    = {Lauth, Jakob},
  title     = {Physikalische Chemie, 2: Chemische Thermodynamik},
  publisher = {Springer},
  address   = {Berlin},
  isbn      = {978-3-662-47621-5},
  pages     = {77 Seiten},
  year      = {2016},
  language  = {de}
}
@book{Lauth2016,
  author    = {Lauth, Jakob},
  title     = {Physikalische Chemie, 1: Grundlagen der Thermodynamik und Verhalten der Gase},
  publisher = {Springer},
  address   = {Berlin},
  isbn      = {978-3-662-47676-5},
  pages     = {57 Seiten},
  year      = {2016},
  language  = {de}
}
@book{LauthKowalczyk2016,
  author    = {Lauth, Jakob and Kowalczyk, J{\"u}rgen},
  title     = {Einf{\"u}hrung in die Physik und Chemie der Grenzfl{\"a}chen und Kolloide},
  publisher = {Springer},
  address   = {Berlin},
  isbn      = {978-3-662-47018-3},
  doi       = {10.1007/978-3-662-47018-3},
  pages     = {Online-Ressource (XIX, 522 S., 341 Abb.)},
  year      = {2016},
  language  = {de}
}
@book{Feuerriegel2016,
  author    = {Feuerriegel, Uwe},
  title     = {Verfahrenstechnik mit EXCEL: Verfahrenstechnische Berechnungen effektiv durchf{\"u}hren und professionell dokumentieren},
  publisher = {Springer Fachmedien},
  address   = {Wiesbaden},
  isbn      = {978-3-658-02902-9},
  doi       = {10.1007/978-3-658-02903-6},
  pages     = {XVII, 381 Seiten},
  year      = {2016},
  language  = {de}
}
@article{ScheerWilson2016,
  author    = {Scheer, Nico and Wilson, Ian D.},
  title     = {A comparison between genetically humanized and chimeric liver humanized mouse models for studies in drug metabolism and toxicity},
  series = {Drug Discovery Today},
  volume    = {21},
  journal   = {Drug Discovery Today},
  number    = {2},
  publisher = {Elsevier},
  address   = {Amsterdam},
  issn      = {1359-6446},
  doi       = {10.1016/j.drudis.2015.09.002},
  pages     = {250 -- 263},
  year      = {2016},
  abstract  = {Mice that have been genetically humanized for proteins involved in drug metabolism and toxicity and mice engrafted with human hepatocytes are emerging and promising in vivo models for an improved prediction of the pharmacokinetic, drug-drug interaction and safety characteristics of compounds in humans. The specific advantages and disadvantages of these models should be carefully considered when using them for studies in drug discovery and development. Here, an overview on the corresponding genetically humanized and chimeric liver humanized mouse models described to date is provided and illustrated with examples of their utility in drug metabolism and toxicity studies. We compare the strength and weaknesses of the two different approaches, give guidance for the selection of the appropriate model for various applications and discuss future trends and perspectives.},
  language  = {en}
}
@incollection{ScheerChuSalphatietal.2016,
  author    = {Scheer, Nico and Chu, Xiaoyan and Salphati, Laurent and Zamek-Gliszczynski, Maciej J.},
  title     = {Knockout and humanized animal models to study membrane transporters in drug development},
  series = {Drug Transporters: Volume 1: Role and Importance in ADME and Drug Development},
  booktitle = {Drug Transporters: Volume 1: Role and Importance in ADME and Drug Development},
  editor    = {Nicholls, Glynis},
  publisher = {Royal Society of Chemistry},
  address   = {Cambridge},
  isbn      = {978-1-78262-379-3},
  doi       = {10.1039/9781782623793-00298},
  pages     = {298 -- 332},
  year      = {2016},
  language  = {en}
}
@article{PaulssenLengkeekLeetal.2016,
  author    = {Paulßen, Elisabeth and Lengkeek, Nigel A. and Le, Van So and Pellegrini, Paul A. and Greguric, Ivan and Weiner, Ron},
  title     = {The role of additives in moderating the influence of Fe(III) and Cu(II) on the radiochemical yield of [⁶⁸Ga(DOTATATE)]},
  series = {Applied Radiation and Isotopes},
  volume    = {107},
  journal   = {Applied Radiation and Isotopes},
  publisher = {Elsevier},
  address   = {Amsterdam},
  issn      = {1872-9800},
  doi       = {10.1016/j.apradiso.2015.09.008},
  pages     = {13 -- 16},
  year      = {2016},
  abstract  = {[⁶⁸Ga(DOTATATE)] has demonstrated its clinical usefulness. Both Fe³⁺ and Cu²⁺, potential contaminants in Gallium-68 generator eluent, substantially reduce the radiochemical (RC) yield of [⁶⁸Ga(DOTATATE)] if the metal/ligand ratio of 1:1 is exceeded. A variety of compounds were examined for their potential ability to reduce this effect. Most had no effect on RC yield. However, addition of phosphate diminished the influence of Fe³⁺ by likely forming an insoluble iron salt. Addition of ascorbic acid reduced Cu²⁺ and Fe³⁺ to Cu⁺ and Fe²⁺ respectively, both of which have limited impact on RC yields. At low ligand amounts (5 nmol DOTATATE), the addition of 30 nmol phosphate (0.19 mM) increased the tolerance of Fe3⁺ from 4 nmol to 10 nmol (0.06 mM), while the addition of ascorbic acid allowed high RC yields (>95\%) in the presence of 40 nmol Fe³⁺ (0.25 mM) and 100 nmol Cu²⁺ (0.63 mM). The effect of ascorbic acid was highly pH-dependant, and gave optimal results at pH 3.},
  language  = {en}
}