@article{PorschenGartzenGewehretal.1978,
  author    = {Porschen, W. and Gartzen, J. and Gewehr, K. and M{\"u}hlensiepen, H. and Weber, Hans-Joachim and Feinedegen, L E.},
  title     = {In vivo assay of the radiation sensitivity of hypoxic tumour cells : influence of γ-rays, cyclotron neutrons, misonidazole, hyperthermia and mixed modalities},
  series = {The British journal of cancer / Supplement},
  journal   = {The British journal of cancer / Supplement},
  number    = {3},
  publisher = {Lewis},
  address   = {London},
  issn      = {0306-9443},
  pages     = {194 -- 197},
  year      = {1978},
  abstract  = {Tumour cell death can be evaluated in the living mouse by externally measuring the rate of loss of tumour-bound DNA tracer. By sequentially labelling the tumour-bearing animals with ¹²⁵IUdR and ¹³¹IUdR 50 h apart, the average tumour cells at the time of the second injection are labelled by ¹²⁵IUdR and the euoxic tumour cells are specifically labelled with ¹³¹IUdR. Tumour treatment at this stage of labelling permits the observation of the reaction of euoxic cells and average tumour cells and finally yields data on hypoxic cells and thus on the oxygen enhancement ratio. This information adds to results from tumour control and growth delay. With this technique effects were analysed of 60-Co γ-rays, cyclotron neutrons (E = 6 MeV), misonidazole (500 mg/kg body wt) and hyperthermia (42°C water-bath), or combinations of these. Misonidazole (15 min before irradiation) altered the oxygen enhancement ratio by a factor of 1·5 for γ-rays and of 1·1 for neutrons; when evaluated from tumour-growth delay and TCD-50 misonidazole gave a dose modifying factor of 1·47 for γ-rays and of 1·2-1·3 for neutrons. Based on percentage tumour regression 100 days after treatment, the enhancement ratio from hyperthermia (after irradiation) was 2·75 for γ-rays (at 10 Gray) and 2·2 for neutrons (at 3·2 Gray). For neutrons combined with misonidazole and hyperthermia the ratio was 2·4. These results demonstrate that effects of neutron irradiation may be modified by electron-affinic substances and/or hyperthermia.},
  language  = {en}
}
@article{DanhoNaithaniSasakietal.1980,
  author    = {Danho, Waleed and Naithani, Vinod K. and Sasaki, Andr{\´e} N. and F{\"o}hles, Joseph and Berndt, Heinz and B{\"u}llesbach, Erika E. and Zahn, H.},
  title     = {Human proinsulin, VII : synthesis of two protected peptides corresponding to the sequences 1—45 and 46—86 of the prohormone},
  series = {Hoppe-Seyler's Zeitschrift f{\"u}r physiologische Chemie},
  volume    = {361},
  journal   = {Hoppe-Seyler's Zeitschrift f{\"u}r physiologische Chemie},
  number    = {1},
  issn      = {1437-4315},
  doi       = {10.1515/bchm2.1980.361.1.857},
  pages     = {857 -- 863},
  year      = {1980},
  language  = {en}
}
@article{KalbeKuropkaMeyerStorketal.1988,
  author    = {Kalbe, Jochen and Kuropka, Rolf and Meyer-Stork, L. Sebastian and Berndt, Heinz and Sauter, Sybille L. and Loss, Peter and Hendo, Karsten and Riesner, Detlev and H{\"o}cker, Hartwig},
  title     = {Isolation and characterization of high-molecular mass DNA from hair shafts},
  series = {Biological chemistry},
  volume    = {369},
  journal   = {Biological chemistry},
  number    = {1},
  isbn      = {0177-3593},
  doi       = {10.1515/bchm3.1988.369.1.413},
  pages     = {413 -- 416},
  year      = {1988},
  language  = {en}
}
@inproceedings{WeberPorschenDietzel1978,
  author    = {Weber, Hans-Joachim and Porschen, W. and Dietzel, F.},
  title     = {In vivo analysis of the influence of combined hyperthermia and gamma irradiation on euoxic and hypoxic tumor cells},
  series = {Cancer therapy by hyperthermia and radiation : [proceedings of the 2. International Symposium on Cancer Therapy by Hyperthermia and Radiation, Essen, 2.-4.6.1977]},
  booktitle = {Cancer therapy by hyperthermia and radiation : [proceedings of the 2. International Symposium on Cancer Therapy by Hyperthermia and Radiation, Essen, 2.-4.6.1977]},
  editor    = {Streffer, Christian},
  publisher = {Urban and Schwarzenberg},
  address   = {Baltimore ; Munich [u.a.]},
  isbn      = {0-8067-1701-7},
  pages     = {276 -- 277},
  year      = {1978},
  language  = {en}
}
@incollection{GitterHornhardtKoewiusetal.2003,
  author    = {Gitter, R. and Hornhardt, Ch. and Koewius, A. and Wahle, Michael and Landwein, Th. M. and Linn, W. and Meiners, F. and Wenk, L.},
  title     = {Konstruieren mit Aluminium [Kapitel 4]},
  series = {Aluminium-Taschenbuch / Hrsg.: Aluminium-Zentrale D{\"u}sseldorf. - Bd. 3: Weiterverarbeitung und Anwendung},
  booktitle = {Aluminium-Taschenbuch / Hrsg.: Aluminium-Zentrale D{\"u}sseldorf. - Bd. 3: Weiterverarbeitung und Anwendung},
  edition   = {16. Auflage},
  publisher = {Aluminium-Verlag},
  address   = {D{\"u}sseldorf},
  isbn      = {3-87017-275-4},
  pages     = {355 -- 599},
  year      = {2003},
  language  = {de}
}
@article{KuperjansStarkeEsseretal.2000,
  author    = {Kuperjans, Isabel and Starke, M. and Esser, J. and Meyer, J. and Donner, O.},
  title     = {Analyse und Konzeption von Energieanlagen unter {\"o}kologischen, wirtschaftlichen und technischen Gesichtspunkten},
  series = {WLB : Umwelttechnik f{\"u}r Industrie und Kommune},
  volume    = {44},
  journal   = {WLB : Umwelttechnik f{\"u}r Industrie und Kommune},
  number    = {11/12},
  issn      = {0341-2679},
  pages     = {26 -- 29},
  year      = {2000},
  language  = {de}
}
@incollection{FaboLemke2012,
  author    = {Fabo, Sabine and Lemke, Inga},
  title     = {Gef{\"a}hrliche Liebschaften : Kunst zwischen Wderstand und Umarmung},
  series = {Interventionen : Grenz{\"u}berschreitungen in {\"A}sthetik, Politik und {\"O}konomie},
  booktitle = {Interventionen : Grenz{\"u}berschreitungen in {\"A}sthetik, Politik und {\"O}konomie},
  editor    = {Hartmann, Doreen and Nitsche, Jessica},
  publisher = {Fink},
  address   = {M{\"u}nchen [u.a.]},
  isbn      = {978-3-7705-5283-2},
  pages     = {173 -- 189},
  year      = {2012},
  language  = {de}
}
@article{AlbannaConzenWeissetal.2016,
  author    = {Albanna, Walid and Conzen, Catharina and Weiss, Miriam and Clusmann, Hans and Fuest, Matthias and Mueller, Marguerite and Brockmann, Marc Alexander and Vilser, Walthard and Schmidt-Trucks{\"a}ss, Arno and Hoellig, Anke and Seiz, Marcel and Thom{\´e}, Claudius and Kotliar, Konstantin and Schubert, Gerrit Alexander},
  title     = {Retinal Vessel Analysis (RVA) in the context of subarachnoid hemorrhage: A proof of concept study},
  series = {PLoS ONE},
  volume    = {11},
  journal   = {PLoS ONE},
  number    = {7},
  publisher = {PLOS},
  address   = {San Francisco},
  issn      = {1932-6203},
  doi       = {10.1371/journal.pone.0158781},
  pages     = {13 Seiten},
  year      = {2016},
  abstract  = {Background Timely detection of impending delayed cerebral ischemia after subarachnoid hemorrhage (SAH) is essential to improve outcome, but poses a diagnostic challenge. Retinal vessels as an embryological part of the intracranial vasculature are easily accessible for analysis and may hold the key to a new and non-invasive monitoring technique. This investigation aims to determine the feasibility of standardized retinal vessel analysis (RVA) in the context of SAH. Methods In a prospective pilot study, we performed RVA in six patients awake and cooperative with SAH in the acute phase (day 2-14) and eight patients at the time of follow-up (mean 4.6±1.7months after SAH), and included 33 age-matched healthy controls. Data was acquired using a manoeuvrable Dynamic Vessel Analyzer (Imedos Systems UG, Jena) for examination of retinal vessel dimension and neurovascular coupling. Results Image quality was satisfactory in the majority of cases (93.3\%). In the acute phase after SAH, retinal arteries were significantly dilated when compared to the control group (124.2±4.3MU vs 110.9±11.4MU, p<0.01), a difference that persisted to a lesser extent in the later stage of the disease (122.7±17.2MU, p<0.05). Testing for neurovascular coupling showed a trend towards impaired primary vasodilation and secondary vasoconstriction (p = 0.08, p = 0.09 resp.) initially and partial recovery at the time of follow-up, indicating a relative improvement in a time-dependent fashion. Conclusion RVA is technically feasible in patients with SAH and can detect fluctuations in vessel diameter and autoregulation even in less severely affected patients. Preliminary data suggests potential for RVA as a new and non-invasive tool for advanced SAH monitoring, but clinical relevance and prognostic value will have to be determined in a larger cohort.},
  language  = {en}
}
@misc{AlKaidyTippkoetterKaiseretal.2014,
  author    = {Al-Kaidy, Huschyar and Tippk{\"o}tter, Nils and Kaiser, P. and Wollny, S. and Ulber, Roland},
  title     = {Aufreinigung von Cytochrom P450BMP mittels magnetischer Partikel und die enzymatische Synthese von 9, 10-Dihydroxystearins{\"a}ure},
  series = {Chemie Ingenieur Technik},
  volume    = {86},
  journal   = {Chemie Ingenieur Technik},
  number    = {9},
  publisher = {Wiley-VCH},
  address   = {Weinheim},
  issn      = {0009-286X},
  doi       = {10.1002/cite.201450420},
  pages     = {1420},
  year      = {2014},
  abstract  = {Cytochrom P450 sind H{\"a}m-Proteine, die zur Enzymklasse der Oxidoreduktasen (EC 1.14.xy) geh{\"o}ren. Eine wichtige Reaktion ist die Hydroxylierung nichtaktivierter C-H-Bindungen, die in technischen Systemen von großem Interesse ist. Durch die Verwendung von M-IDA-2-Partikeln ist eine direkte Aufreinigung mit gleichzeitiger Immobilisierung und die Applikation der Enzyme aus dem Zelllysat m{\"o}glich. Damit ist das Verfahren mehr als f{\"u}nf Stunden schneller als die konventionelle Chromatographie und mehr als 80 \% der Aufreinigungszeit wird gespart. Mit dem isolierten nativen Enzym konnte die Plattformchemikalie 9,10-Dihydroxystearins{\"a}ure aus {\"O}ls{\"a}ure hergestellt werden. Unter anderem f{\"u}r die Kunststoffindustrie k{\"o}nnen aus diesem Produkt wichtige Monomere wie z. B. Azelains{\"a}ure hergestellt werden. Die Bildung des Produkts erfolgt in einem zweiphasigen Reaktionssystem an der Grenzfl{\"a}che zwischen dem {\"O}l und der w{\"a}ssrigen Phase als Feststoff. Um das immobilisierte Enzym aktiv in die obere Phase zu transportieren, wurde eine neue magnetische Mischvorrichtung entwickelt. Das Reaktionsprodukt wurde mit NMR, GC-MS und HPLC-MS analysiert und mit einem chemisch synthetisierten Standard von 9,10-Dihydroxystearins{\"a}ure verglichen. Derzeit werden Studien des immobilisierten H{\"a}ms des Enzyms durchgef{\"u}hrt.},
  language  = {de}
}
@misc{KuthanAlKaidyTippkoetter2016,
  author    = {Kuthan, K. and Al-Kaidy, Huschyar and Tippk{\"o}tter, Nils},
  title     = {Tropfenbasierte Enzymreaktionen auf Glasoberfl{\"a}chen im μL-Maßstab mit ortsaufgel{\"o}ster pL-Dosierung der Reaktanden},
  series = {Chemie Ingenieur Technik},
  volume    = {88},
  journal   = {Chemie Ingenieur Technik},
  number    = {9},
  publisher = {Wiley-VCH},
  address   = {Weinheim},
  doi       = {10.1002/cite.201650117},
  pages     = {1336 -- 1337},
  year      = {2016},
  abstract  = {Mit der Entwicklung w{\"a}ssriger Tropfen, die mit einer sch{\"u}tzenden H{\"u}lle magnetisierbarer, hydrophober Partikel umgeben sind, ergeben sich neue M{\"o}glichkeiten im Bereich der Mikrofluidik. So k{\"o}nnen die Tropfen als fl{\"u}ssige Mikroreaktoren eingesetzt werden. Der w{\"a}ssrige Kern dieser Mikroreaktoren besteht aus einer Substratl{\"o}sung f{\"u}r enzymatische Umsetzungen. Durch Bewegen der Mikroreaktoren k{\"o}nnen diese {\"u}ber immobilisierten Enzymen positioniert werden, um so einen enzymatischen Umsatz innerhalb der Mikroreaktoren zu realisieren. Hierf{\"u}r wurde eine neue Mikroreaktorplattform-Technologie etabliert. Die Mikroreaktoren k{\"o}nnen aufgrund ihrer magnetisierbaren H{\"u}llenpartikel {\"u}ber elektromagnetische Spulen bewegt werden. Die Bewegung erfolgt dabei mit einer automatisierten Aktuatorplattform, bestehend aus einer 3x3 Doppelspulenmatrix mit Magnetkernen. Als modellhaftes Reaktionssystem wird eine Enzymkaskade eingesetzt, die sich aus einer b-Glucosidase, Glucose-Oxidase und Meerrettichperoxidase zusammensetzt. Prim{\"a}r untersuchte Substrate sind Fluorescein-di-b-D-glucopyranoside, und 1-(3,7-Dihydroxy-10H-phenoxazin-10-yl)-ethanon, bei deren Umsatz fluoreszierende Produkte entstehen.},
  language  = {de}
}