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OPEN FAU

Online publication system of Friedrich-Alexander-Universität Erlangen-Nürnberg

The online publication system OPEN FAU is the central publication platform for Open Access publishing for all members of Friedrich-Alexander-Universität. Qualified works from research and teaching may be published here free of charge, either as a primary or secondary publication. The full texts are permanently available worldwide and are findable and citable via catalogues and search engines.


To search for documents in OPEN FAU, please select "Search" (via the magnifying glass at the top right); this will provide you with various search options. If you want to publish a document, go to "Login" and "My Publications". Then drag you document into the field provided and enter the metadata. In just a few steps, you can submit your document. Please note our guidelines, the publication contract and FAQs.

 

Recent Submissions

Article
Open Access
An Intronic Heterozygous SYNE2 Splice Site Mutation: A Rare Cause for Myalgia and hyperCKemia?
(MDPI, 2024-03-15) Paulus, Theresa; Young, Natalie; Jessop, Emily; Berwanger, Carolin; Clemen, Christoph Stephan; Schröder, Rolf; Ploski, Rafal; Hagel, Christian; Hellenbroich, Yorck; Moser, Andreas; Karakesisoglou, Iakowos; Angelini, Corrado

SYNE2 mutations have been associated with skeletal and cardiac muscle diseases, including Emery-Dreifuss muscular dystrophy (EDMD). Here, we present a 70-year-old male patient with muscle pain and elevated serum creatine kinase levels in whom whole-exome sequencing revealed a novel heterozygous SYNE2 splice site mutation (NM_182914.3:c.15306+2T>G). This mutation is likely to result in the loss of the donor splice site in intron 82. While a diagnostic muscle biopsy showed unspecific myopathological findings, immunofluorescence analyses of skeletal muscle and dermal cells derived from the patient showed nuclear shape alterations when compared to control cells. In addition, a significantly reduced nesprin-2 giant protein localisation to the nuclear envelope was observed in patient-derived dermal fibroblasts. Our findings imply that the novel heterozygous SYNE2 mutation results in a monoallelic splicing defect of nesprin-2, thereby leading to a rare cause of myalgia and hyperCKemia.

Article
Open Access
In Situ Probing the Crystallization Kinetics in Gas‐Quenching‐Assisted Coating of Perovskite Films
(2024-01-07) Qiu, Shudi; Majewski, Martin; Dong, Lirong; Jang, Dongju; Corre, Vincent M. Le; Cerrillo, José Garcia; Ronsin, Olivier J. J.; Yang, Fu; Guo, Fei; Zhang, Kaicheng; Lüer, Larry; Harting, Jens; Du, Tian; Brabec, Christoph J.; Egelhaaf, Hans‐Joachim

The pursuit of commercializing perovskite photovoltaics is driving the development of various scalable perovskite crystallization techniques. Among them, gas quenching is a promising crystallization approach for high‐throughput deposition of perovskite films. However, the perovskite films prepared by gas‐quenching assisted blade coating are susceptible to the formation of pinholes and frequently show inferior crystallinity if the interplay between film coating, film drying, and crystallization kinetics is not fully optimized. That arguably requires a thorough understanding of how single processing steps influence the crystallization kinetics of printed perovskite films. Here, in situ optical spectroscopies are integrated into a doctor‐blading setup that allows to real‐time monitor film formation during the gas‐quenching process. It is found that the essential role of gas quenching treatment is in achieving a smooth and compact perovskite film by controlling the nucleation rate. Moreover, with the assistance of phase‐field simulations, the role of excessive methylammonium iodide is revealed to increase grain size by accelerating the crystal growth rate. These results show a tailored control of crystal growth rate is critical to achieving optimal film quality, leading to fully printed solar cells with a champion power conversion efficiency of 19.50% and mini solar modules with 15.28% efficiency are achieved.

Article
Open Access
Glycerol Trinitrate Acts Downstream of Calcitonin Gene-Related Peptide in Trigeminal Nociception—Evidence from Rodent Experiments with Anti-CGRP Antibody Fremanezumab
(MDPI, 2024-03-25) Benedicter, Nicola; Vogler, Birgit; Kuhn, Annette; Schramm, Jana; Mackenzie, Kimberly D.; Stratton, Jennifer; Dux, Mária; Messlinger, Karl; Dobolyi, Arpad

Calcitonin gene-related peptide (CGRP) and nitric oxide (NO) have been recognized as important mediators in migraine but their mechanisms of action and interaction have not been fully elucidated. Monoclonal anti-CGRP antibodies like fremanezumab are successful preventives of frequent migraine and can be used to study CGRP actions in preclinical experiments. Fremanezumab (30 mg/kg) or an isotype control monoclonal antibody was subcutaneously injected to Wistar rats of both sexes. One to several days later, glyceroltrinitrate (GTN, 5 mg/kg) mimicking nitric oxide (NO) was intraperitoneally injected, either once or for three consecutive days. The trigeminal ganglia were removed to determine the concentration of CGRP using an enzyme-linked immunosorbent assay (ELISA). In one series of experiments, the animals were trained to reach an attractive sugar solution, the access to which could be limited by mechanical or thermal barriers. Using a semi-automated registration system, the frequency of approaches to the source, the residence time at the source, and the consumed solution were registered. The results were compared with previous data of rats not treated with GTN. The CGRP concentration in the trigeminal ganglia was generally higher in male rats and tended to be increased in animals treated once with GTN, whereas the CGRP concentration decreased after repetitive GTN treatment. No significant difference in CGRP concentration was observed between animals having received fremanezumab or the control antibody. Animals treated with GTN generally spent less time at the source and consumed less sugar solution. Without barriers, there was no significant difference between animals having received fremanezumab or the control antibody. Under mechanical barrier conditions, all behavioral parameters tended to be reduced but animals that had received fremanezumab tended to be more active, partly compensating for the depressive effect of GTN. In conclusion, GTN treatment seems to increase the production of CGRP in the trigeminal ganglion independently of the antibodies applied, but repetitive GTN administration may deplete CGRP stores. GTN treatment generally tends to suppress the animals’ activity and increase facial sensitivity, which is partly compensated by fremanezumab through reduced CGRP signaling. If CGRP and NO signaling share the same pathway in sensitizing trigeminal afferents, GTN and NO may act downstream of CGRP to increase facial sensitivity.

Article
Open Access
The Stokes–Einstein–Sutherland Equation at the Nanoscale Revisited
(2023-10-08) Baer, Andreas; Wawra, Simon E.; Bielmeier, Kristina; Uttinger, Maximilian J.; Smith, David M.; Peukert, Wolfgang; Walter, Johannes; Smith, Ana‐Sunčana

The Stokes–Einstein–Sutherland (SES) equation is at the foundation of statistical physics, relating a particle's diffusion coefficient and size with the fluid viscosity, temperature, and the boundary condition for the particle‐solvent interface. It is assumed that it relies on the separation of scales between the particle and the solvent, hence it is expected to break down for diffusive transport on the molecular scale. This assumption is however challenged by a number of experimental studies showing a remarkably small, if any, violation, while simulations systematically report the opposite. To understand these discrepancies, analytical ultracentrifugation experiments are combined with molecular simulations, both performed at unprecedented accuracies, to study the transport of buckminsterfullerene C60 in toluene at infinite dilution. This system is demonstrated to clearly violate the conditions of slow momentum relaxation. Yet, through a linear response to a constant force, the SES equation can be recovered in the long time limit with no more than 4% uncertainty both in experiments and in simulations. This nonetheless requires partial slip on the particle interface, extracted consistently from all the data. These results, thus, resolve a long‐standing discussion on the validity and limits of the SES equation at the molecular scale.

Article
Open Access
Zum Zusammenhang zwischen Resilienz, Selbstwirksamkeit und Sozialbeziehung in Familie und Schule
(Hogrefe AG, 2024-04-08) Obermeier, Ramona; Lutz, Veronika; Fuchs, Katharina; Nowak, Mareike; Gläser-Zikuda, Michaela

Zusammenfassung: Einigen Schülerinnen und Schülern gelingt es besser als anderen, schulische Herausforderungen zu bewältigen. Dies wird unter anderem auf ihre Resilienz zurückgeführt. Resilienz beschreibt die prozesshafte Fähigkeit, sich an widrige Situationen anpassen zu können, die durch Interaktionen zwischen verschiedenen Systemen angeregt wird. Zentral für diese Anpassungsleistung einzelner Systeme sind individuelle und kontextuelle Faktoren, die sowohl förderlich als auch schützend wirken können und zu denen unter anderem Selbstwirksamkeitserwartungen und Sozialbeziehungen zählen. Die Kontextbedingungen in der Schule zeichnen sich durch eine Mehrebenenstruktur aus, die bei der Analyse der Resilienzentwicklung allerdings bislang nicht berücksichtigt wurde. Die vorliegende Studie zeigt an einer Stichprobe von 655 Schülerinnen und Schülern in 5.–9. Klassen, dass die schulischen Selbstwirksamkeitserwartungen, die Qualität der Beziehung zwischen Lehrkräften und Schülerinnen und Schülern und das Familienklima auf Individualebene sowie die Hilfsbereitschaft der Schülerinnen und Schüler auf Klassenebene einen Zusammenhang mit deren Resilienz aufweisen. Damit liefert die Studie Evidenz für die Bedeutsamkeit individueller und sozialer Ressourcen der Resilienzentwicklung, belegt aber auch einen Zusammenhang von Variablen auf aggregierter Klassenebene. Förderansätze der Resilienzentwicklung müssen demnach sowohl auf Individual- als auch auf Klassenebene ansetzen.