1,721,659 research outputs found

    Codimension two min-max minimal submanifolds from PDEs

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    A fruitful method to construct min-max minimal hypersurfaces, in an ambient closed Riemannian manifold, is given by the Allen-Cahn functional and its natural rescalings. This approach produces minimal hypersurfaces as limiting interfaces in a phase transition between two different states. A natural attempt to carry out this in codimension two is to use the simplified Ginzburg-Landau functional (with no magnetic potential and no external field) and hope (roughly speaking) to capture a minimal submanifold as a limit of the vortices, as the repulsion parameter tends to infinity. It is known since two decades that one always gets a stationary rectifiable varifold in the limit, but it is an open problem to establish its integrality. After briefly describing the difficulties arising with this functional, we will see how they disappear looking instead at the Yang-Mills-Higgs action (or the full Ginzburg-Landau free energy), with the natural rescalings preserving self-duality, first proposed by Hong-Jost-Struwe in the two-dimensional setting. We will discuss the features of this relaxation of the codimension-two area, which become strikingly similar to those of Allen-Cahn: in particular, integrality of the limit varifold and exponential decay of the energy density (away from vortices) do hold. We also describe how to construct a (codimension two) min-max integer stationary varifold in any ambient closed manifold using this approach. This is joint work with Daniel Stern (Princeton University - University of Toronto)

    Quantization and non-quantization of energy for higher-dimensional Ginzburg-Landau vortices

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    Given a family of critical points uϵ:MnCu_{\epsilon}:M^n\to\mathbb{C} for the complex Ginzburg--Landau energies \begin{align*} &E_\epsilon(u)=\int_{M}\left(\frac{|du|^2}{2}+\frac{(1-|u|^2)^2}{4\epsilon^2}\right), \end{align*} on a manifold MM, with natural energy growth Eϵ(uϵ)=O(logϵ)E_{\epsilon}(u_{\epsilon})=O(|\log\epsilon| ), it is known that the vorticity sets {uϵ12}\{|u_\epsilon|\leq \frac{1}{2}\} converge subsequentially to the support of a stationary, rectifiable (n2)(n-2)-varifold VV in the interior, characterized as the concentrated portion of the limit limϵ0eϵ(uϵ)πlogϵ\lim_{\epsilon\to 0} \frac{e_\epsilon(u_\epsilon)}{\pi|\log\epsilon| } of the normalized energy measures. When n=2n=2 or the solutions uϵu_{\epsilon} are energy-minimizing, it is known moreover that this varifold VV is integral; i.e., the (n2)(n-2)-density Θn2(V,x)\Theta_{n-2}(|V|,x) of V|V| takes values in N\mathbb{N} at V|V|-a.e. xMx\in M. In the present paper, we show that for a general family of critical points with Eϵ(uϵ)=O(logϵ)E_{\epsilon}(u_{\epsilon})=O(|\log\epsilon| ) in dimension n3n\geq 3, this energy quantization phenomenon only holds where the density is less than 22: namely, we prove that the density Θn2(V,x)\Theta_{n-2}(|V|,x) of the limit varifold takes values in {1}[2,)\{1\}\cup [2,\infty) at V|V|-a.e. xMx\in M, and show that this is sharp, in the sense that for any n3n\geq 3 and θ{1}[2,)\theta\in \{1\}\cup [2,\infty), there exists a family of critical points uϵu_{\epsilon} for EϵE_{\epsilon} in the ball B1n(0)B_1^n(0) with concentration varifold VV given by an (n2)(n-2)-plane with density θ\theta.Comment: this is the version published on Ars Inveniendi Analytic

    Development of a rapid detection system for orthopoxviruses

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    Die Famile der Orthopockenviren umschließt neben den zwar ausgerotteten, im Falle einer nicht auszuschließenden bioterroristischen Ausbringung aber hochgefährlichen Variolaviren weitere humanpathogene Viren wie das Affenpocken-, das Kuhpockensowie das Vacciniavirus. Als zoonotische Erreger endemisch in Zentral- und Westafrika, Europa sowie Südamerika, verursachen Sie lokal begrenzt bis systemisch verlaufende pustuläre Erkrankungen, welche in Einzelfällen bis zum Tod führen können. Aufgrund des seltenen Auftretens sind deutschlandweit nur wenige Speziallabore wie das Robert Koch-Institut in der Lage, den Nachweis einer Orthopockenvirusinfektion anhand serologischer, Nukleinsäure- oder Partikel-basierter Nachweisverfahren zu erbringen. Ein im Falle einer bioterroristischen Freisetzung von Variolaviren notwendiges schnelles, sensitives und einfach durchzuführendes Detektionssystem existiert bis heute jedoch nicht. Um diese Lücke zu schließen, war das Ziel dieser Arbeit die Entwicklung eines Antikörper-basierten Schnelldetektionssystems zum Nachweis von Orthopockenviren. Durch Testung Oberflächenprotein-spezifischer polyklonaler Antikörper konnte gezeigt werden, dass das Attachment-Protein A27 am geeignetsten zur Induktion Detektions- optimierter Antikörper ist. In einem mehrstufigen Screeningverfahren wurden daher monoklonale Antikörper gegen A27 generiert, deren Bindungsepitope und Bindungskinetik mittels Peptid-Epitopmapping und Oberflächenplasmonresonanz- Messung bestimmt wurden. Hierbei zeigte sich, dass gute Zugänglichkeit der Bindungsepitope sowie schnelle und multivalente Bindung entscheidend für Detektionsoptimierte Antikörper waren. Die beiden besten Antikörper wurden schließlich auf der Abicap Vor-Ort-Detektionsplattform implementiert und bezüglich Sensitivität und Spezifität beim Orthopockenvirusnachweis charakterisiert. Als Ansatzpunkt für potenzielle Weiterentwicklungen wurden diese zusätzlich in Form rekombinanter single chain fragment variable Antikörper exprimiert und getestet. Das etablierte Detektionssystem war in der Lage, alle getesteten humanpathogenen Orthopockenviren mit hoher Sensitivität von bis zu 1,75×10^2 PFU/ml in 45 Minuten zu detektieren, wobei der Nachweis aus klinischem Material sowie einem verblindetem Probenpanel ohne Kreuzreaktivitäten möglich war. Durch die schnelle und einfache Durchführbarkeit bei gleichzeitig hoher Sensitivität eignet sich das Abicap-System sehr gut für die Vor-Ort-Testung sowohl bioterroristischer als auch klinischer Proben. Darüber hinaus können die in dieser Arbeit gewonnenen Erkenntnisse zur Generierung Detektions-optimierter Antikörper auf anderer Erreger übertragen werden.Besides the eradicated Variola virus, which in the case of an unlikely but non excludable bioterrorist attack nevertheless remains highly dangerous, the Orthopoxvirus family contains further viruses pathogenic for humans like Monkeypox, Cowpox, and Vaccinia virus. As zoonotic agents, they are endemic in Central and Western Africa, Europe, and South America, causing mainly local to systemic pustular diseases which, in rare cases, can lead to death. Due to their rare incidence, only a few specialized laboratories like the Robert Koch-Institute are able to diagnose orthopoxvirus infections via serological, nucleic acid, or virus-particle based detection methods. However, to date there is no fast, sensitive and simple rapid on-site detection system, which in the case of bioterrorist release of Variola virus would be needed. To fill this gap, the aim of this work was to develop an antibody-based rapid detection system for Orthopoxviruses. By testing surface protein-specific polyclonal antibodies, we could show that the attachment protein A27 is most suited for induction of detection-optimized antibodies. Hence, a multi-level screening was used to generate A27-specific monoclonal antibodies whose binding epitopes and kinetics were determined by peptide epitope mapping and surface plason resonance measurement. Hereby, high accessibility of binding epitopes as well as rapid and multivalent binding were hallmarks for detection-optimized antibodies. Finally, two outperforming antibodies were implemented on the Abicap onsite detection platform and characterized regarding their sensitivity and specificity in Orthopoxvirus detection. Additionally, as a starting point for further optimization, both antibodies were expressed as recombinant single-chain variable fragments. The established rapid detection system was able to detect all tested Orthopoxviruses pathogenic to humans with high sensitivity down to 1.75×10^2 PFU/ml within 45 minutes. Detection was possible from clinical samples and a blinded sample panel without cross-reactivity. Due to rapid and simple handling at sustained high sensitivity, the Abicap-platform is highly suited for onsite testing in a bioterrorist as well as a clinical context. Furthermore, findings regarding the generation of detectionoptimized antibodies gained during this work could be transferred to other agents

    Structural and variable-temperature NMR studies of 9-diisopropylphosphanylanthracenes and 9,10-bis(diisopropylphosphanyl)anthracenes and their oxidation products

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    The diisopropylphosphanyl-substituted anthracenes i-Pr(2)P(C(14)H(9)) (1a), i-Pr(2)P(C(14)H(8))Br (2a), and (i-Pr(2)P)(2)(C(14)H(8)) (3a) and some of their oxidation products were prepared from 9-bromoanthracene and 9,10-dibromoanthracene, respectively. Low-temperature (1)H NMR spectra of the 9-monophosphanyl-substituted anthracenes la and 2a are in accordance with a staggered conformer, while above room temperature dynamic processes occur. The low-temperature NMR spectrum of the 9,10-diphosphanylanthracene 3a indicates the presence of two different rotational isomers. The rotational barrier for la was determined from variable-temperature (1)H NMR spectra to be 56 kJ mol(-1) (Delta G(298K)). The crystal structure determinations show the solid-state conformers to be consistent with the prevailing conformer at low temperature

    Etude du suivi régional de la qualité de service par les méthodes d'analyse de données

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    Jambu Michel, Tan Suy Ho, Stern Daniel, Birenbaum Jean. Etude du suivi régional de la qualité de service par les méthodes d'analyse de données. In: NETCOM : Réseaux, communication et territoires / Networks and Communication Studies, vol. 2 n°2, décembre 1988. Le colloque international « Communications et territoires », Issy-les-Moulineaux / Paris-Sorbonne, 21-23 janvier 1988. pp. 144-191

    Going Beyond Counting First Authors in Author Co-citation Analysis

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    The present study examines one of the fundamental aspects of author co-citation analysis (ACA) - the way co-citation counts are defined. Co-citation counting provides the data on which all subsequent statistical analyses and mappings are based, and we compare ACA results based on two different types of co-citation counting - the traditional type that only counts the first one among a cited work's authors on the one hand and a non-traditional type that takes into account the first 5 authors of a cited work on the other hand. Results indicate that the picture produced through this non-traditional author co-citation counting contains more coherent author groups and is therefore considerably clearer. However, this picture represents fewer specialties in the research field being studied than that produced through the traditional first-author co-citation counting when the same number of top-ranked authors is selected and analyzed. Reasons for these effects are discussed
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