107 research outputs found

    Gender Mainstreaming in der Forschung zur berufsbegleitenden akademischen Weiterbildung

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    Die Bedeutung von Gender Mainstreaming für den Bereich der berufsbegleitenden akademischen Weiterbildung wurde bislang kaum erörtert. Inwiefern sowohl in der Weiterbildungsforschung als auch in der Konzeption von Weiterbildungsangeboten und in der Weiterbildungspraxis eine gleichstellungsorientierte Perspektive eingenommen wird, kann bislang kaum nachvollzogen werden. Dieser Beitrag möchte verdeutlichen, dass Gender Mainstreaming einerseits als Qualitätskriterium von Weiterbildungen gelten kann und andererseits die Umsetzung von Gender Mainstreaming aufgrund rechtlicher Rahmenbedingungen ein Leitprinzip von öffentlich finanzierten Forschungs- und Entwicklungsprojekten darstellen sollte.

    Flavonoid, Nitrate and Glucosinolate Concentrations in Brassica Species Are Differentially Affected by Photosynthetically Active Radiation, Phosphate and Phosphite

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    We evaluated the effects of phosphate (Pi-deficiency: 0.1 mM; Pi-sufficiency: 0.5 mM), phosphite (low-Phi: 0.1 mM; medium-Phi: 0.5 mM; and high-Phi: 2.5 mM), and two mean daily photosynthetically active radiations (lower PAR: 22.2 mol ⋅ m-2 ⋅ d-1; higher PAR: 29.7 mol ⋅ m-2 ⋅ d-1), as well as their interactions, on flavonoid, nitrate and glucosinolate (GL) concentrations and growth characteristics in hydroponically grown Brassica campestris cv. Mibuna Early and Brassica juncea cv. Red Giant. As expected, higher PAR increased dry matter and contrariwise decreased number of leaves but only in B. campestris. Total flavonoid and individual flavonoid compounds increased with the higher PAR value in B. campestris. Pi-sufficiency resulted in a lower quercetin concentration in both species, the isorhamnetin and total flavonoid concentrations in B. campestris, and the cyanidin concentration in B. juncea, in comparison to Pi-deficiency. Similarly, Pi-sufficient plants exhibited lower GL concentration, especially alkyl-GLs in B. campestris and alkenyl-GLs and an aryl-GL in B. juncea. Pi did not affect the nitrate concentration in either species, and nor did Phi influence the flavonoid concentrations in either species. In B. campestris, medium Phi (0.5 mM) increased the 1-methoxyindol-3-ylmethyl GL concentration by 28.3%, as compared to that observed at low Phi. In B. juncea, high Phi level increased the but-3-enyl-GL concentration by 18.9%, in comparison to values recorded at medium Phi. B. campestris plants exposed to higher PAR increased total flavonoids concentration. In both Brassica species, higher PAR stimulated the alkyl-, alkenyl-, and indole-GLs. The interaction of lower PAR and increasing Phi significantly decreased flavonoid concentration in B. juncea, whereas increasing Phi at higher PAR increased such concentration in this species. The same combination reduced the concentration of 2-phenylethyl- and indol-3-ylmethyl-GL in B. juncea. The highest indol-3-ylmethyl-GL concentration was observed when Pi was deficient combined with medium Phi in B. juncea. Thus, PAR, Pi and Phi may modulate flavonoid, GL and nitrate concentrations in Brassica species, which may be a useful tool to improve the nutraceutical quality of these leafy vegetables if properly managed

    A single, episodic event of unilateral/bilateral scrotal swelling in a group of adult boars at an Austrian boar stud

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    Background Scrotal swelling is a clinical situation which can be caused by different aetiologies. In this case report, we describe a multi-week episode of unilateral and bilateral scrotal swelling in boars at an Austrian boar stud and its diagnostic work-up. Case presentation In the summer of 2020, the herd veterinarian of an Austrian boar stud reported that over a period of six weeks, five out of 70 boars presented with unilateral severe swelling of the left scrotum and three out of 70 boars with bilateral severe swelling of the left and moderate swelling of the right scrotum, respectively. A complete history was obtained and an on-site evaluation of the facility was done. Five boars were necropsied, and a variety of samples harvested for further diagnostic investigations. Infectious differential diagnoses associated with unilateral swelling of the scrotum or the testis were excluded through serological and tissue testing. In three of the five boars, histopathology revealed complete acute haemorrhagic necrosis of the left testis concurrent with strongly congested blood vessels. Review of the collected information with a group of experts in the field of boar stud management resulted with consensus that, most likely, trauma was the etiologic event causing the clinical signs and pathology. Coincident with discussion of implementing video recording cameras in the boar housing area, no further clinical cases followed. As this case occurred during the first lockdown of the COVID-19 pandemic, we propose that the distress and travelling restrictions may have contributed to frustration among boar stud workers, which was consequently expressed as misbehaviour against boars. Conclusions Once all known infectious causes of unilateral swelling of the scrotum were excluded, a critical diagnostic work-up focused on non-infectious causes. Non-infectious causes, such as trauma, need to be carefully evaluated, as it may also include human misbehaviour against boars. Summarizing all findings of this case report, the authors hypothesize that a blunt trauma was the reason for the series of mainly unilateral swelling of the scrota of boars.info:eu-repo/semantics/publishedVersio

    Parallel sequencing of extrachromosomal circular DNAs and transcriptomes in single cancer cells

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    Extrachromosomal DNAs (ecDNAs) are common in cancer, but many questions about their origin, structural dynamics and impact on intratumor heterogeneity are still unresolved. Here we describe single-cell extrachromosomal circular DNA and transcriptome sequencing (scEC&T-seq), a method for parallel sequencing of circular DNAs and full-length mRNA from single cells. By applying scEC&T-seq to cancer cells, we describe intercellular differences in ecDNA content while investigating their structural heterogeneity and transcriptional impact. Oncogene-containing ecDNAs were clonally present in cancer cells and drove intercellular oncogene expression differences. In contrast, other small circular DNAs were exclusive to individual cells, indicating differences in their selection and propagation. Intercellular differences in ecDNA structure pointed to circular recombination as a mechanism of ecDNA evolution. These results demonstrate scEC&T-seq as an approach to systematically characterize both small and large circular DNA in cancer cells, which will facilitate the analysis of these DNA elements in cancer and beyond

    A non-enzymatic function of 17 beta-hydroxysteroid dehydrogenase type 10 is required for mitochondrial integrity and cell survival

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    Deficiency of the mitochondrial enzyme 2-methyl-3-hydroxybutyryl-CoA dehydrogenase involved in isoleucine metabolism causes an organic aciduria with atypical neurodegenerative course. The disease-causing gene is HSD17B10 and encodes 17beta-hydroxysteroid dehydrogenase type 10 (HSD10), a protein also implicated in the pathogenesis of Alzheimer's disease. Here we show that clinical symptoms in patients are not correlated with residual enzymatic activity of mutated HSD10. Loss-of-function and rescue experiments in Xenopus embryos and cells derived from conditional Hsd17b10(-/-) mice demonstrate that a property of HSD10 independent of its enzymatic activity is essential for structural and functional integrity of mitochondria. Impairment of this function in neural cells causes apoptotic cell death whilst the enzymatic activity of HSD10 is not required for cell survival. This finding indicates that the symptoms in patients with mutations in the HSD17B10 gene are unrelated to accumulation of toxic metabolites in the isoleucine pathway and, rather, related to defects in general mitochondrial function. Therefore alternative therapeutic approaches to an isoleucine-restricted diet are required

    DNA glycosylases: in DNA repair and beyond

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    The base excision repair machinery protects DNA in cells from the damaging effects of oxidation, alkylation, and deamination; it is specialized to fix single-base damage in the form of small chemical modifications. Base modifications can be mutagenic and/or cytotoxic, depending on how they interfere with the template function of the DNA during replication and transcription. DNA glycosylases play a key role in the elimination of such DNA lesions; they recognize and excise damaged bases, thereby initiating a repair process that restores the regular DNA structure with high accuracy. All glycosylases share a common mode of action for damage recognition; they flip bases out of the DNA helix into a selective active site pocket, the architecture of which permits a sensitive detection of even minor base irregularities. Within the past few years, it has become clear that nature has exploited this ability to read the chemical structure of DNA bases for purposes other than canonical DNA repair. DNA glycosylases have been brought into context with molecular processes relating to innate and adaptive immunity as well as to the control of DNA methylation and epigenetic stability. Here, we summarize the key structural and mechanistic features of DNA glycosylases with a special focus on the mammalian enzymes, and then review the evidence for the newly emerging biological functions beyond the protection of genome integrity

    Heterozygous Variants in KMT2E Cause a Spectrum of Neurodevelopmental Disorders and Epilepsy.

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    We delineate a KMT2E-related neurodevelopmental disorder on the basis of 38 individuals in 36 families. This study includes 31 distinct heterozygous variants in KMT2E (28 ascertained from Matchmaker Exchange and three previously reported), and four individuals with chromosome 7q22.2-22.23 microdeletions encompassing KMT2E (one previously reported). Almost all variants occurred de novo, and most were truncating. Most affected individuals with protein-truncating variants presented with mild intellectual disability. One-quarter of individuals met criteria for autism. Additional common features include macrocephaly, hypotonia, functional gastrointestinal abnormalities, and a subtle facial gestalt. Epilepsy was present in about one-fifth of individuals with truncating variants and was responsive to treatment with anti-epileptic medications in almost all. More than 70% of the individuals were male, and expressivity was variable by sex; epilepsy was more common in females and autism more common in males. The four individuals with microdeletions encompassing KMT2E generally presented similarly to those with truncating variants, but the degree of developmental delay was greater. The group of four individuals with missense variants in KMT2E presented with the most severe developmental delays. Epilepsy was present in all individuals with missense variants, often manifesting as treatment-resistant infantile epileptic encephalopathy. Microcephaly was also common in this group. Haploinsufficiency versus gain-of-function or dominant-negative effects specific to these missense variants in KMT2E might explain this divergence in phenotype, but requires independent validation. Disruptive variants in KMT2E are an under-recognized cause of neurodevelopmental abnormalities

    Retrospective evaluation of whole exome and genome mutation calls in 746 cancer samples

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    Funder: NCI U24CA211006Abstract: The Cancer Genome Atlas (TCGA) and International Cancer Genome Consortium (ICGC) curated consensus somatic mutation calls using whole exome sequencing (WES) and whole genome sequencing (WGS), respectively. Here, as part of the ICGC/TCGA Pan-Cancer Analysis of Whole Genomes (PCAWG) Consortium, which aggregated whole genome sequencing data from 2,658 cancers across 38 tumour types, we compare WES and WGS side-by-side from 746 TCGA samples, finding that ~80% of mutations overlap in covered exonic regions. We estimate that low variant allele fraction (VAF < 15%) and clonal heterogeneity contribute up to 68% of private WGS mutations and 71% of private WES mutations. We observe that ~30% of private WGS mutations trace to mutations identified by a single variant caller in WES consensus efforts. WGS captures both ~50% more variation in exonic regions and un-observed mutations in loci with variable GC-content. Together, our analysis highlights technological divergences between two reproducible somatic variant detection efforts

    Der gute Ton der Querflöte

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    Die vorliegende Diplomarbeit beschäftigt sich mit der Verknüpfung der Musik mit der Mathematik. Zu Beginn wird kurz die geschichtliche Entwicklung der Querflöte dargestellt. Unter anderem wird die Tonerzeugung bei der Querflöte als physikalischer Prozess mathematisch betrachtet. Abbildungen zeigen Funktionsgraphen musikalischer Schwingungen, welche sich aus mathematischer Sicht aus periodischen Sinus- und Cosinusfunktionen zusammensetzen. Es wird darauf eingegangen, wie die Überlagerung von Wellen in der Physik mit Schwebungen zweier Töne unterschiedlicher Frequenzen zusammenhängt. Im dritten Kapitel geht es um zylindrisch gebohrte Rohre und die darin entstehenden schwingenden Luftsäulen, welche mit Hilfe der Wellengleichung beschrieben werden. Obwohl es sich bei der Querflöte um eine offene Pfeife handelt, werden aus Gründen der Vollständigkeit auch geschlossene Pfeifen betrachtet. In den darauffolgenden Unterkapiteln wird näher auf die sogenannten Partialtöne, die Obertöne, eingegangen und es wird die faszinierende Tatsache, dass gleiche Töne auf verschiedenen Instrumenten eine andere Klangfarbe haben, näher beleuchtet. Um Obertöne und Klangspektren der einzelnen Instrumente sichtbar machen zu können wird die Methode der Fourieranalyse benötigt. Das vierte und umfangreichste Kapitel dieser Arbeit beschäftigt sich mit der Fourier-Theorie, auf welche, vor allem aus mathematischer Sicht, ausführlich eingegangen wird. Zu Beginn wird ein Überblick über das Leben und Schaffen des französischen Mathematikers Jean Baptiste Joseph Fourier gegeben. Er hatte Anfang des 19.Jahrhunderts die großartige Erkenntnis, dass sich alle periodischen Funktionen in Sinus - und Cosinusschwingungen zerlegen lassen. Des Weiteren werden die so wichtigen Fourier Koeffizienten, mit deren Hilfe man die Phase und Amplitude der Schwingung bestimmen kann, berechnet. Das Konvergenzproblem der Fourier - Reihen wird dargestellt und es wird näher auf die Approximation im quadratischen Mittel, gleichmäßige und punktweise Konvergenz eingegangen. Einige Beispiele wie die Sägezahnfunktion, die Rechtecksschwingung, die Zickzack-Welle und die Sprungfunktion werden vorgestellt. Im Anschluss wird das Gibbs-Phänomen untersucht, die komplexe Schreibweise des Fourierpolynoms eingeführt und es werden Fourier-Reihen aus Potenzreihen entwickelt. Der Schluss dieses Kapitels beinhaltet eine kurze Zusammenfassung der wichtigsten Eigenschaften von Fourierpolynomen. Im letzten Kapitel dieser Arbeit wird noch einmal die Verbindung zur Musik verdeutlicht – Obertöne der Querflöte werden mittels ihres Spektrums grafisch dargestellt und die Kunst des Überblasens, die Entstehung der Flageolettöne, wird erklärt
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