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  • 1
    In: Journal of Sleep Research, Wiley, Vol. 30, No. 5 ( 2021-10)
    Abstract: Narcolepsy type 1 (NT1) is a disorder with well‐established markers and a suspected autoimmune aetiology. Conversely, the narcoleptic borderland (NBL) disorders, including narcolepsy type 2, idiopathic hypersomnia, insufficient sleep syndrome and hypersomnia associated with a psychiatric disorder, lack well‐defined markers and remain controversial in terms of aetiology, diagnosis and management. The Swiss Primary Hypersomnolence and Narcolepsy Cohort Study (SPHYNCS) is a comprehensive multicentre cohort study, which will investigate the clinical picture, pathophysiology and long‐term course of NT1 and the NBL. The primary aim is to validate new and reappraise well‐known markers for the characterization of the NBL, facilitating the diagnostic process. Seven Swiss sleep centres, belonging to the Swiss Narcolepsy Network (SNaNe), joined the study and will prospectively enrol over 500 patients with recent onset of excessive daytime sleepiness (EDS), hypersomnia or a suspected central disorder of hypersomnolence (CDH) during a 3‐year recruitment phase. Healthy controls and patients with EDS due to severe sleep‐disordered breathing, improving after therapy, will represent two control groups of over 50 patients each. Clinical and electrophysiological (polysomnography, multiple sleep latency test, maintenance of wakefulness test) information, and information on psychomotor vigilance and a sustained attention to response task, actigraphy and wearable devices (long‐term monitoring), and responses to questionnaires will be collected at baseline and after 6, 12, 24 and 36 months. Potential disease markers will be searched for in blood, cerebrospinal fluid and stool. Analyses will include quantitative hypocretin measurements, proteomics/peptidomics, and immunological, genetic and microbiota studies. SPHYNCS will increase our understanding of CDH and the relationship between NT1 and the NBL. The identification of new disease markers is expected to lead to better and earlier diagnosis, better prognosis and personalized management of CDH.
    Type of Medium: Online Resource
    ISSN: 0962-1105 , 1365-2869
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2021
    detail.hit.zdb_id: 2007459-1
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  • 2
    In: Contributions to Plasma Physics, Wiley, Vol. 60, No. 5-6 ( 2020-06)
    Abstract: Applying gyrokinetic simulations in theoretical turbulence and transport studies for the plasma edge and scrape‐off layer (SOL) presents significant challenges. To particularly account for steep density and temperature gradients in the SOL, the “full‐f” code PICLS was developed. PICLS is a gyrokinetic particle‐in‐cell (PIC) code, is based on an electrostatic model with a linearized field equation, and uses kinetic electrons. In previously published results, we applied PICLS to the well‐studied 1D parallel transport problem during an edge‐localized mode (ELM) in the SOL without collisions. As an extension to this collision‐less case and in preparation for 3D simulations, in this work, a collisional model will be introduced. The implemented Lenard–Bernstein collision operator and its Langevin discretization will be shown. Conservation properties of the collision operator, as well as a comparison of the collisional and non‐collisional case, will be discussed.
    Type of Medium: Online Resource
    ISSN: 0863-1042 , 1521-3986
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2020
    detail.hit.zdb_id: 2018082-2
    SSG: 12
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  • 3
    Online Resource
    Online Resource
    Wiley ; 2021
    In:  Magnetic Resonance in Medicine Vol. 85, No. 5 ( 2021-05), p. 2882-2891
    In: Magnetic Resonance in Medicine, Wiley, Vol. 85, No. 5 ( 2021-05), p. 2882-2891
    Abstract: Click here for author‐reader discussions
    Type of Medium: Online Resource
    ISSN: 0740-3194 , 1522-2594
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2021
    detail.hit.zdb_id: 1493786-4
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  • 4
    In: Experimental Dermatology, Wiley, Vol. 21, No. 10 ( 2012-10), p. 765-770
    Abstract: Mechanical forces are highly variable ranging from the ubiquitous gravity force to compression, fluid shear, torsion, tension and other forms. Mechanical forces act on cells and modulate their biological responses by regulating gene transcription, enzyme and growth factor activity. In soft connective tissues, formation of myofibroblasts strictly requires a mechanically loaded environment in addition to local transforming growth factor ( TGF )‐β activity, which itself can be modulated by the mechanical status of the environment. The aim of this study was to monitor the adaptive responses of primary dermal fibroblasts towards cyclic mechanical stress under conditions of high force to better understand the regulation of gene expression in normal skin and mechanisms of gene regulation in mechanically altered fibrotic skin. Primary murine dermal fibroblasts were exposed to equi‐biaxial tensile strain. Cyclic mechanical tension was applied at a frequency of 0.1  H z (6× /min) for 24 h with a maximal increase in surface area of 15%. This treatment resulted in downregulation of alpha smooth muscle actin (α SMA ) and connective tissue growth factor ( CTGF ) but not of TGF β1 expression. Cyclic strain also strongly reduced endothelin‐1 ( ET ‐1) expression and supplementing strained cultures with exogenous ET ‐1 rescued α SMA and CTGF levels. Of note, no biologically significant levels of TGF β1 activity were detected in strained cultures. We provide evidence for a novel, TGF β1‐independent mechanism regulating ET ‐1 expression in dermal fibroblasts by biomechanical forces. Modulation of ET ‐1‐dependent activities regulates downstream fibrotic marker genes; this pathway might therefore provide an approach to attenuate myofibroblast differentiation.
    Type of Medium: Online Resource
    ISSN: 0906-6705 , 1600-0625
    URL: Issue
    RVK:
    Language: English
    Publisher: Wiley
    Publication Date: 2012
    detail.hit.zdb_id: 2026228-0
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