TY - CHAP A1 - Lindemann, Markus A1 - Runge, Alexander T1 - Electronic contracting within the reference model for electronic markets T2 - Proceedings of the Sixth European Conference on Information Systems, ECIS 1998, Aix-en-Provence, France, June 4-6, 1998 / Walter Baets (ed.) Y1 - 1998 SN - 849238333X SP - 44 EP - 59 PB - Euro-Arab Management School ER - TY - JOUR A1 - Lindemann, Markus A1 - Runge, Alexander T1 - Permanent IT-support in electronic commerce transactions JF - Electronic markets : the international journal of networked business. Vol. 7 (1997), iss. 1 Y1 - 1997 SN - 1422-8890 SP - 18 EP - 20 ER - TY - GEN A1 - Lindel, Tomasz Dawid A1 - Greiser, Andreas A1 - Waxman, Patrick A1 - Dietterle, Martin A1 - Seifert, Frank A1 - Fontius, Ulrich A1 - Renz, Wolfgang A1 - Dieringer, Matthias A. A1 - Frauenrath, Tobias A1 - Schulz-Menger, Jeanette A1 - Niendorf, Thoralf A1 - Ittermann, Bernd T1 - Cardiac CINE MRI at 7 T using a transmit array T2 - 2012 ISMRM Annual Meeting Proceedings N2 - With its need for high SNR and short acquisition times, Cardiac MRI (CMR) is an intriguing target application for ultrahigh field MRI. Due to the sheer size of the upper torso, however, the known RF issues of 7T MRI are also most prominent in CMR. Recent years brought substantial progress but the full potential of the ultrahigh field for CMR is yet to be exploited. Parallel transmission (pTx) is a promising approach in this context and several groups have already reported B1 shimming for 7T CMR. In such a static pTx application amplitudes and phases of all Tx channels are adjusted individually but otherwise imaging techniques established in current clinical practice 1.5 T and 3 T are applied. More advanced forms of pTx as spatially selective excitation (SSE) using Transmit SENSE promise additional benefits like faster imaging with reduced fields of view or improved SAR control. SSE requires the full dynamic capabilities of pTx, however, and for the majority of today's implemented pTx hardware the internal synchronization of the Tx array does not easily permit external triggering as needed for CMR. Here we report a software solution to this problem and demonstrate the feasibility of CINE CMR at 7 T using a Tx array. Y1 - 2012 SN - 1545-4428 N1 - ISMRM 20th Annual Meeting & Exhibition, 5-11 May 2012, Melbourne, Australia ER - TY - JOUR A1 - Limpert, Nicolas A1 - Wiesen, Patrick A1 - Ferrein, Alexander A1 - Kallweit, Stephan A1 - Schiffer, Stefan T1 - The ROSIN Project and its Outreach to South Africa JF - R&D Journal Y1 - 2019 VL - 35 SP - 1 EP - 6 ER - TY - CHAP A1 - Limpert, Nicolas A1 - Schiffer, Stefan A1 - Ferrein, Alexander T1 - A Local Planner for Ackermann-Driven Vehicles in ROS SBPL T2 - Proceedings of the International Conference on Pattern Recognition Association of South Africa and Robotics and Mechatronics (PRASA-RobMech), 2015 Y1 - 2015 U6 - https://doi.org/10.1109/RoboMech.2015.7359518 SP - 172 EP - 177 ER - TY - JOUR A1 - Li, Anlan A1 - Shi, Young de A1 - Landsmann, B. A1 - Schankowski-Bouvier, P. A1 - Dikta, Gerhard A1 - Bauer, U. A1 - Artmann, Gerhard T1 - Hemorheology and walking distance of Peripheral Arterial Occlusive Disease patients during treatment with Ginkgo-biloba extract JF - Acta Pharmacologica Sinica = ZHONGUO YAOLI XUEBAO. 19 (1998), H. 5 Y1 - 1998 SN - 1745-7254 N1 - ISSN der parallelen Ausgabe 1671-4083; China-Zs.-Code: CN31-1347 abstract frei unter SP - 417 EP - 421 ER - TY - BOOK A1 - Ley, Wilfried A1 - Wittmann, Klaus A1 - Hallmann, Willi T1 - Handbook of space technology Y1 - 2009 SN - 978-0-470-69739-9 PB - Wiley CY - Chichester ER - TY - JOUR A1 - Ley, Wilfried A1 - Plescher, Engelbert A1 - Scholz, Artur A1 - Piepenbrock, Johannes T1 - COMPASS-1 picosatellite project / Ley, Wilfried ; Plescher, Engelbert ; Scholz, Artur ; Piepenbrock, Johannes JF - Small satellites for earth observation : digest of the 6th International symposium of the International Academy of Astronautics, Berlin, April 23 - 26, 2007 / ed. by Rainer Sandau; Hans-Peter Röser; Arnoldo Valenzuela Y1 - 2007 SN - 9783896855718 N1 - Symposium on Small Satellites for Earth Observation ; (6, 2007, Berlin) SP - 147 EP - 150 PB - Wissenschaft und Technik Verl. CY - Berlin ER - TY - JOUR A1 - Levers, A. A1 - Staat, Manfred A1 - Laack, Walter van T1 - Analysis of the long-term effect of the MBST® nuclear magnetic resonance therapy on gonarthrosis JF - Orthopedic Practice Y1 - 2016 VL - 47 IS - 11 SP - 521 EP - 528 ER - TY - JOUR A1 - Leurs, Ulrike A1 - Mezo, Gabor A1 - Öhlschläger, Peter A1 - Orban, Erika A1 - Marquard, Andrea A1 - Manea, Marilena T1 - Design, synthesis, in vitro stability and cytostatic effect of multifunctional anticancer drug-bioconjugates containing GnRH-III as a targeting moiety JF - Peptide Science N2 - Bioconjugates containing the GnRH-III hormone decapeptide as a targeting moiety are able to deliver chemotherapeutic agents specifically to cancer cells expressing GnRH receptors, thereby increasing their local efficacy while limiting the peripheral toxicity. However, the number of GnRH receptors on cancer cells is limited and they desensitize under continuous hormone treatment. A possible approach to increase the receptor mediated tumor targeting and consequently the cytostatic effect of the bioconjugates would be the attachment of more than one chemotherapeutic agent to one GnRH-III molecule. Here we report on the design, synthesis and biochemical characterization of multifunctional bioconjugates containing GnRH-III as a targeting moiety and daunorubicin as a chemotherapeutic agent. Two different drug design approaches were pursued. The first one was based on the bifunctional [4Lys]-GnRH-III (Glp-His-Trp-Lys-His-Asp-Trp-Lys-Pro-Gly-NH2) containing two lysine residues in positions 4 and 8, whose ϵ-amino groups were used for the coupling of daunorubicin. In the second drug design, the native GnRH-III (Glp-His-Trp-Ser-His-Asp-Trp-Lys-Pro-Gly-NH2) was used as a scaffold; an additional lysine residue was coupled to the ϵ-amino group of 8Lys in order to generate two free amino groups available for conjugation of daunorubicin. The in vitro stability/degradation of all synthesized compounds was investigated in human serum, as well as in the presence of rat liver lysosomal homogenate. Their cellular uptake was determined on human breast cancer cells and the cytostatic effect was evaluated on human breast, colon and prostate cancer cell lines. Compared with a monofunctional compound, both drug design approaches resulted in multifunctional bioconjugates with increased cytostatic effect. Y1 - 2012 U6 - https://doi.org/10.1002/bip.21640 SN - 1097-0282 VL - 98 IS - 1 SP - 1 EP - 10 PB - Wiley CY - New York, NY ER -