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Abstract: Fine-scale temporal organization of cortical activity in the gamma range (∼25–80Hz) may play a significant role in information processing, for example by neural grouping ('binding') and phase coding. Recent experimental studies have shown that the precise frequency of gamma oscillations varies with input drive (e.g. visual contrast) and that it can differ among nearby cortical locations. This has challenged theories assuming widespread gamma synchronization at a fixed common frequency. In the present study, we investigated which principles govern gamma synchronization in the presence of input-dependent frequency modulations and whether they are detrimental for meaningful input-dependent gamma-mediated temporal organization. To this aim, we constructed a biophysically realistic excitatory-inhibitory network able to express different oscillation frequencies at nearby spatial locations. Similarly to cortical networks, the model was topographically organized with spatially local connectivity and spatially-varying input drive. We analyzed gamma synchronization with respect to phase-locking, phase-relations and frequency differences, and quantified the stimulus-related information represented by gamma phase and frequency. By stepwise simplification of our models, we found that the gamma-mediated temporal organization could be reduced to basic synchronization principles of weakly coupled oscillators, where input drive determines the intrinsic (natural) frequency of oscillators. The gamma phase-locking, the precise phase relation and the emergent (measurable) frequencies were determined by two principal factors: the detuning (intrinsic frequency difference, i.e. local input difference) and the coupling strength. In addition to frequency coding, gamma phase contained complementary stimulus information. Crucially, the phase code reflected input differences, but not the absolute input level. This property of relative input-to-phase conversion, contrasting with latency codes or slower oscillation phase codes, may resolve conflicting experimental observations on gamma phase coding. Our modeling results offer clear testable experimental predictions. We conclude that input-dependency of gamma frequencies could be essential rather than detrimental for meaningful gamma-mediated temporal organization of cortical activity.
Author Summary: Almost 350 years ago the physicist and polymath Christiaan Huygens first observed the synchronization between two pendulum clocks attached to a common support. Since then synchronization has been recognized as a universal phenomenon from astronomy to biology. The phase-locking (synchrony) and the phase-relation between the two pendulums are determined by two principal forces: the synchronization force exerted over the connection and the tendency to desynchronize due to frequency (speed) differences. We propose that gamma synchronization (25–80Hz) among oscillating cortical neurons in the brain can be understood according to the same principles—like a field of many connected pendula—with the critical addition that input changes the frequency of gamma oscillations, as shown by recent experimental studies. It has been assumed that input-dependent changes in oscillation frequency are detrimental for a meaningful role of gamma synchronization in neural processing. To the contrary, our theoretical analysis demonstrates that because input can change the frequency of the oscillation, phase-locking and phase-relations among neurons relate systematically to input. By analogy, it is because a local push to a pendulum will change its frequency, that resulting changes in phase-locking and phase-relation among the pendula can be used to derive the external force applied.
What happened to the tremendous legacy of juridical knowledge left behind in Italy in the 6th century? Into what labyrinth did it plunge only to re-emerge after the silent age of the early Middle Ages into the light of day, and effectively come to shape the renewal of the jurisprudence at the beginning of the 12th century? One-and-a-half centuries after the fanciful writings of Hermann Fitting, legal historians are still looking for the answers to these questions. Considering the new information we have (especially coming from the paleographical research), this paper re-examines the existence as well as the activities of the school of Rome both during the Justinian Age and in the two centuries thereafter. The aim of this essay is to verify whether Rome, during the very early Middle Ages, continued to represent a centre of juridical culture. According to the hypothesis developed in this contribution, Rome – at that time – not only played a very important role with regard to the material conservation of the Justinian’s libri legales, but also in the initial establishment of the new (i. e., Justinian) imperial law in the West and creation of its image as a significant juridical centre. The absence of such a centre as well as its wide-spread image would truly make the Bolognese renovatio appear "miraculous" and very difficult to explain.
After Justinian, the 7th and 8th centuries can truly be characterised as "silent" in the history of Roman law in the West. However, by studying the medieval manuscript tradition, in particular, that of the Institutiones and the Novellae, we can gather together a series of elements helping us to clarify the situation. Also quite useful is an examination of the manuscript tradition of the Collatio legum Mosaicarum et Romanarum. Through the spread and use of these Late Antique works, we can see how – in conjunction with the actions of the papacy – Rome, toward the end of the 8th century, returned to being a centre of world politics and – given that law follows politics – of the legal culture.
WE DECOMPOSE INDIVIDUAL INVESTORS’ PORTFOLIO RETURNS INTO PASSIVE BENCHMARK RETURNS, ACTIVE SECURITY SELECTION RETURNS, AND ACTIVE MARKET TIMING RETURNS. FOR THE AVERAGE INVESTOR IN OUR SAMPLE, PASSIVE BENCHMARK RETURNS EXPLAIN SOME 40% OF VARIATION IN LONGITUDINAL PORTFOLIO RETURNS, SECURITY SELECTION EXPLAINS AN ADDITIONAL 50%, AND MARKET TIMING PLAYS ONLY A MINOR ROLE. THIS STANDS IN STARK CONTRAST TO EARLIER RESULTS ON INSTITUTIONAL INVESTORS WHERE PASSIVE BENCHMARK RETURNS (REFLECTING DIFFERENT ASSET ALLOCATION STRATEGIES) EXPLAIN OVER 90%. THE PREDOMINANCE OF SECURITY SELECTION COMES AT A COST FOR INDIVIDUAL INVESTORS: INVESTORS FROM THE HIGHEST QUINTILE IN TERMS OF SECURITY SELECTION ACTIVITY UNDERPERFORM THEIR PEERS FROM THE LOWEST QUINTILE BY MORE THAN 10 PERCENTAGE POINTS PER YEAR. TRANSACTION COSTS EXPLAIN ONLY PART OF THIS UNDERPERFORMANCE. THE LESS INVESTORS DIVERSIFY, THE WORSE THEY DO.
In diesem Jahr hat sich die Paul Ehrlich-Stiftung für zwei Preisträger entschieden, die sich den mit 100.000 Euro dotierten Paul Ehrlich- und Ludwig Darmstaedter-Preis teilen. Am 14.03.2015 überreichte Professor Harald zur Hausen, der Vorsitzende des Stiftungsrates, in der Frankfurter Paulskirche den Preis an Professor James P. Allison vom MD Anderson Cancer Center in Houston (Foto Mitte) und an Professor Carl H. June von der Universität Pennsylvania in Philadelphia (r.). Professor Raja Atreya vom Universitätsklinikum in Erlangen (l.) erhielt den Paul Ehrlich- und Ludwig Darmstaedter-Nachwuchspreis.
Background: The objective measurement of the mechanical component and its role in chronic ankle instability is still a matter of scientific debate. We analyzed known group and diagnostic validity of our ankle arthrometer. Additionally, functional aspects of chronic ankle instability were evaluated in relation to anterior talar drawer.
Methods: By manual stress testing, 41 functionally unstable ankles were divided as mechanically stable (n = 15) or mechanically unstable (n = 26). Ankle laxity was quantified using an ankle arthrometer. Stiffness values from the load displacement curves were calculated between 40 and 60 N. Known group validity and eta2 were established by comparing manual and arthrometer testing results. Diagnostic validity for the ankle arthrometer was determined by a 2 × 2 contingency table. The functional ankle instability severity was quantified by the German version of the Foot and Ankle Ability Measure (FAAM-G). Stiffness (40–60 N) and FAAM-G values were correlated.
Results: Mechanically unstable ankles had lower 40–60 N stiffness values than mechanically stable ankles (p = 0.006 and <0.001). Eta for the relation between manual and arthrometer anterior talar drawer testing was 0.628. With 5.1 N/mm as cut-off value, accuracy, sensitivity, and specificity were 85%, 81%, and 93%, respectively. The correlation between individual 40–60 N arthrometer stiffness values and FAAM-G scores was r = 0.286 and 0.316 (p = 0.07 and 0.04).
Conclusions: In this investigation, the ankle arthrometer demonstrated a high diagnostic validity for the determination of mechanical ankle instability. A clear interaction between mechanical (ankle arthrometer) and functional (FAAM-G) measures could not be demonstrated.
Dies ist der zehnte Artikel unseres Blogfokus „Salafismus in Deutschland“.
Was macht salafistisches Denken in religiöser Hinsicht aus? Was hat Salafismus mit Wahhabismus zu tun? Was hat Dschihadismus mit Salafismus zu tun? Alles Fragen, auf die es keine einfachen Antworten gibt. Trotzdem lohnt der Versuch, eine Antwort zu geben, da die religiösen Vorstellungen zentral für die Identität des Salafismus sind. Es geht hier „nur“ um die religiösen Ideen, die immer wieder in salafistischen Diskussionen auftreten. Freilich ist die innersalafistische Debatte vielgestaltig, so dass sich kein „Katechismus“ aufstellen lässt, der ausweist, woran ein/e SalafistIn glaubt. Deshalb werden im Folgenden entlang einzelner Stränge des salafistischen Diskurses ausgewählte religiöse Ideen beleuchtet....
n the EU there are longstanding and ongoing pressures towards a tax that is levied on the EU level to substitute for national contributions. We discuss conditions under which such a transition can make sense, starting from what we call a "decentralization theorem of taxation" that is analogous to Oates (1972) famous result that in the absence of spill-over effects and economies of scale decentralized public good provision weakly dominates central provision. We then drop assumptions that turn out to be unnecessary for this results. While spill-over effects of taxation may call for central rules for taxation, as long as spill-over effects do not depend on the intra-regional distribution of the tax burden, decentralized taxation plus tax coordination is found superior to a union-wide tax.
Background. Bile leakage testing may help to detect and reduce the incidence of biliary leakage after hepatic resection. This review was performed to investigate the value of the White-test in identifying intraoperative biliary leakage and avoiding postoperative leakage.
Material and methods. A systematic review and meta-analysis was performed. Two researchers performed literature research. Primary outcome measure was the incidence of post-hepatectomy biliary leakage; secondary outcome measure was the ability of detecting intraoperative biliary leakage with the help of the White-test.
Results. A total of 4 publications (including original data from our center) were included in the analysis. Evidence levels of the included studies had medium quality of 2b (individual cohort studies including low quality randomized controlled trials). Use of the White-test led to a significant reduction of post-operative biliary leakage [OR: 0.3 (95% CI: 0.14, 0.63), p = 0.002] and led to a significant higher intraoperative detection of biliary leakages [OR: 0.03 (95%CI: 0.02, 0.07), p < 0.00001].
Conclusion. Existing evidence implicates the use of the White-test after hepatic resection to identify bile leaks intraoperatively and thus reduce incidence of post-operative biliary leakage. Nonetheless, there is a requirement for a high-quality randomized controlled trial with adequately powered sample-size to confirm findings from the above described studies and further increase evidence in this field.
Second mitochondria-derived activator of caspase (Smac) mimetics are considered as promising anticancer therapeutics that are currently under investigation in early clinical trials. They induce apoptosis by antagonizing inhibitor of apoptosis proteins, which are frequently overexpressed in cancer. We previously reported that Smac mimetics, such as BV6, additionally exert non-apoptotic functions in glioblastoma (GBM) cells by stimulating migration and invasion in a nuclear factor kappa B (NF-κB)-dependent manner. Because NF-κB target genes mediating these effects are largely unknown, we performed whole-genome expression analyses. Here, we identify chemokine (C-C motif) ligand 2 (CCL2) as the top-listed NF-κB-regulated gene being upregulated upon BV6 treatment in GBM cells. BV6-induced upregulation and secretion of CCL2 are required for migration and invasion of GBM cells because knockdown of CCL2 in GBM cells abolishes these effects. Co-culture experiments of GBM cells with non-malignant astroglial cells reveal that BV6-stimulated secretion of CCL2 by GBM cells into the supernatant triggers migration of astroglial cells toward GBM cells because CCL2 knockdown in BV6-treated GBM cells impedes BV6-stimulated migration of astroglial cells. In conclusion, we identify CCL2 as a BV6-induced NF-κB target gene that triggers migration and invasion of GBM cells and exerts paracrine effects on the GBM's microenvironment by stimulating migration of astroglial cells. These findings provide novel insights into the biological functions of Smac mimetics with important implications for the development of Smac mimetics as cancer therapeutics.
Wasserbedarfsprognosen sind für Wasserversorger eine wichtige Entscheidungsgrundlage für zukünftige Maßnahmen in der wirtschaftlichen und technischen Betriebsführung sowie beim Ressourcenmanagement. In den letzten zwei Jahrzehnten sanken in Deutschland die spezifischen Wasserbedarfe aufgrund von Technik- und Verhaltensinnovationen. Für Regionen mit Wirtschafts- und Bevölkerungswachstum ist aber das Zusammenspiel dieser für den zukünftigen Bedarf konträren Entwicklungen von besonderem Interesse. Auch die Metropolregion Hamburg ist von diesen Entwicklungen betroffen.
Im Auftrag des Wasserversorgers HAMBURG WASSER aktualisierte das ISOE (Forschungsschwerpunkt Wasserressourcen und Landnutzung) in Kooperation mit dem ifo Institut München seine mittel- und langfristige Wasserbedarfsprognose aus dem Jahr 2007 für das Versorgungsgebiet des Auftraggebers. In einem innovativen Konzept wurden dafür Forschungsmethoden aus Natur-, Wirtschafts-, Planungs- und Sozialwissenschaften kombiniert. Mit dem gewählten transdisziplinären Forschungsmodus war das Projekt darauf angelegt, im laufenden Forschungsprozess gemeinsam mit den wissenschaftlichen und außerwissenschaftlichen Projektpartnern das Prognosekonzept weiterzuentwickeln. Der vorliegende Studientext basiert auf dem Projektbericht an HAMBURG WASSER und fasst Prognosekonzept, Modellentwicklung, Prognoseergebnissen und Schlussfolgerungen zusammen.
Rain- and floodwater harvesting (RFWH) technologies and water reuse are ideal and generalpurpose technologies to improve water security and to contribute to climate adaptation – in particular for semi-arid regions. These technologies are part of a multi-resources mix within an integrated water resources management (IWRM). They create capacities to buffer water fluctuations and alleviate water scarcity. In this way, they reduce the pressure on existing resources, and can stimulate local economies. However, in order to be sustainable, these technologies need to be adapted to the local context – through suitable design, adapted operation requirements, and a back-up by training users and operators accordingly.
Background: The introduction of modern troponin assays has facilitated diagnosis of acute myocardial infarction due to improved sensitivity with corresponding loss of specificity. Atrial fibrillation (AF) is associated with elevated levels of troponin. The aim of the present study was to evaluate the diagnostic performance of troponin I in patients with suspected acute coronary syndrome and chronic AF.
Methods: Contemporary sensitive troponin I was assayed in a derivation cohort of 90 patients with suspected acute coronary syndrome and chronic AF to establish diagnostic cut-offs. These thresholds were validated in an independent cohort of 314 patients with suspected myocardial infarction and AF upon presentation. Additionally, changes in troponin I concentration within 3 hours were used.
Results: In the derivation cohort, optimized thresholds with respect to a rule-out strategy with high sensitivity and a rule-in strategy with high specificity were established. In the validation cohort, application of the rule-out cut-off led to a negative predictive value of 97 %. The rule-in cut-off was associated with a positive predictive value of 88 % compared with 71 % if using the 99th percentile cut-off. In patients with troponin I levels above the specificity-optimized threshold, additional use of the 3-hour change in absolute/relative concentration resulted in a further improved positive predictive value of 96 %/100 %.
Conclusions: Troponin I concentration and the 3-hour change in its concentration provide valid diagnostic information in patients with suspected myocardial infarction and chronic AF. With regard to AF-associated elevation of troponin levels, application of diagnostic cut-offs other than the 99th percentile might be beneficial.
Patienten mit einer BCR/ABL positiven (Ph+) akuten lymphatischen Leukämie (ALL) bilden die größte genetisch definierte Untergruppe der ALL und gelten wegen ihrer schlechten Prognose als Höchstrisiko ALL. Die bisherigen Therapieergebnisse werden durch die Kombination von Tyrosin-Kinase-Inhibitoren (TKI) wie Imatinib und Chemotherapeutika verbessert, sind aber durch das Auftreten von Resistenzen gegen TKI in ihrer langfristigen Wirkung limitiert. Die derzeitige Forschung fokussiert sich weitestgehend auf konstitutive aktive Kinasen, die für die leukämische Transformation verantwortlich sind. Allerdings kann die Deregulation von Phosphatasen, die als Gegenspieler von Kinasen fungieren, durch eine verminderte Inaktivierung dieser Kinasen, ebenso zur Leukämogenese beitragen, indem ihre physiologische Funktion vermindert wird. Im Vorfeld konnte bereits gezeigt werden, dass die deregulierte Protein Tyrosin Phosphatase 1B (PTP1B) bei Ph+ Leukämien eine partielle Resistenz gegenüber TKI vermitteln kann.1 Darüber hinaus zeigen von Juric et al. (2007)2 publizierte Microarrays von 54 Ph+ ALL Patienten eine transkriptionelle Hochregulierung der Phosphatase „Supressor of T-Cell receptor Signalling 1“ (STS-1).2 STS-1 (TULA-2) gehört zusammen mit STS-2 (TULA-1) zur Familie der STS/TULA Proteine, von denen keine weiteren Mitglieder bekannt sind. STS-1 dephosphoryliert diverse Rezeptor-Tyrosin-Kinasen wie z.B. den T-Cell Receptor (TCR) und den Epidermal-Growth-Factor Receptor (EGFR) und verhindert somit deren Internalisierung und proteosomalen Abbau.3 Weitere durch STS-1 dephosphorylierte Substrate sind die Proteintyrosinkinase Syk, die eine wichtige Rolle bei der Signalweiterleitung des B-Cell-Receptors (BCR) spielt sowie andere SRC-Kinasen (z.B. FYN).4 Aufgrund der oben beschriebenen Zusammenhänge zwischen STS-1 und der Ph+ ALL ist die Untersuchung einer möglichen funktionellen Bedeutung von STS-1 bei der Entwicklung einer mutationsunabhängigen Resistenz von Ph+ ALL Inhalt dieser Arbeit. Als Modellsystem dienen in der hier vorliegenden Arbeit aus der BCR/ABL Zelllinie Sup B15 abgeleitete TKI resistente Zellen (Sup B15 RT). Imatinib ist in diesen immer noch in der Lage BCR/ABL zu binden und führt zu einer Verschiebung der Dosiswirkungskurve ohne Apoptose zu induzieren. Mutationen in der Tyrosinkinase Domäne von BCR/ABL konnten als zugrunde liegender Resistenzmechanismus durch Sequenzanalysen ausgeschlossen werden, ebenso wie zusätzliche Translokationen oder genomischen Amplifikationen von BCR/ABL. Eine Analyse der STS-1 Expression zeigte sowohl transkriptionell als auch auf Proteinebene eine deutliche Herunterregulierung von STS-1 in Sup B15 RT Zellen. Die Interaktion zwischen STS-1 und BCR/ABL wurde in verschiedenen Zellmodellen gezeigt. Dabei konnten bezüglich der Interaktion keine Unterschiede zwischen dem p210BCR/ABL und p185BCR/ABL Fusionsprotein festgestellt werden. Auch die „Gatekeeper“ Mutation T315I hatte keinen Einfluss auf die Interaktion. Die Unabhängigkeit der Bindung von STS-1 und BCR/ABL von einer aktiven BCR/ABL Kinase wurde durch die Zugabe von Imatinib gezeigt. Lediglich auf endogenem Level konnte eine Imatinib vermittelte Reduktion der Interaktion nachgewiesen werden. Durch die Verwendung unterschiedlich trunkierter BCR/ABL Proteine wurde gezeigt, dass STS-1 sowohl mit c-ABL als auch mit dem ABL-Anteil von BCR/ABL interagiert und dass eine Oligomerisierung für diese Interaktion nicht notwendig ist. Als Folge der Interaktion kommt es zu einer Dephosphorylierung von BCR/ABL durch STS-1, wobei vor allem die im ABL Anteil lokalisierten und für die Autophosphorylierung wichtigen Tyrosine 245 und 412 dephosphoryliert werden. Mittels eines Proliferations-Kompetitions-Assay konnte gezeigt werden, dass STS-1 sowohl die Proliferationsrate reduziert als auch erheblich die Sensitivität von SupB15 RT Zellen gegenüber Imatinib steigert. Dieser Befund steht im Einklang mit der Annahme, dass diese Sensitivitätssteigerung durch eine gegenüber den sensitiven Sup B15 WT deutlich verminderte STS-1 Expression bedingt ist. Dexamethason in klinisch relevanten Konzentrationen (10-6 M - 10-9 M) konnte sowohl in SupB15 WT als auch in SupB15 RT Zellen die STS-1 Expression um ein Vielfaches steigern und führte in Kombination mit 1 μM Imatinib sogar in den resistenten Zellen zu einer hoch signifikanten Inhibition der Proliferation sowie einer gesteigerten Apoptose. Die Resultate dieser Arbeit rücken Phosphatasen und im speziellen STS-1 in einen stärkeren Fokus, wenn es um die Bildung von Resistenzen geht. Dadurch können sich eine Vielzahl neuer Behandlungsstrategien sowie neue Ansätze für die klinische Wirkstoffforschung ergeben.