475 research outputs found

    Fixing education for the AI age: Conrad Wolfram

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    Conrad Wolfram is the CEO and co-founder of Wolfram Research Europe and Strategic Director of Wolfram Research. He is a leading advocate for mathematics education reform and author of “The Math(s) Fix: An Education Blueprint for the AI Age”. He recently gave a public lecture at LSE on this topic. The following is an edited version of an interview by Neil Olver in the Mathematics Department

    Who are the Disciples and Admirers of an Author?

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    Webcast sponsored by the Irving K. Barber Learning Centre and hosted by SLAIS. Recitation (the act of citing a given author or her/his works multiple times) provides an indication of the influence of a cited author. This study investigated patterns of citation and recitation across frequently cited authors' works to better understand how broadly citers have been influenced by cited authors and their publications. Dietmar Wolfram is Interim Dean & Professor School of Information Studies, University of Wisconsin-Milwaukee.Arts, Faculty ofLibrary, Archival and Information Studies (SLAIS), School ofUnreviewedFacult

    Interest rate convexity and the volatility smile

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    When pricing the convexity effect in irregular interest rate derivatives such as, e.g., Libor-in-arrears or CMS, one often ignores the volatility smile, which is quite pronounced in the interest rate options market. This note solves the problem of convexity by replicating the irregular interest flow or option with liquidly traded options with different strikes thereby taking into account the volatility smile. This idea is known among practitioners for pricing CMS caps. We approach the problem on a more general scale and apply the result to various examples. --interest rate options,volatility smile,convexity,,option replication

    Comprehensive overview of disease models for Wolfram syndrome : toward effective treatments

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    Wolfram syndrome (OMIM 222300) is a rare autosomal recessive disease with a devastating array of symptoms, including diabetes mellitus, optic nerve atrophy, diabetes insipidus, hearing loss, and neurological dysfunction. The discovery of the causative gene, WFS1, has propelled research on this disease. However, a comprehensive understanding of the function of WFS1 remains unknown, making the development of effective treatment a pressing challenge. To bridge these knowledge gaps, disease models for Wolfram syndrome are indispensable, and understanding the characteristics of each model is critical. This review will provide a summary of the current knowledge regarding WFS1 function and offer a comprehensive overview of established disease models for Wolfram syndrome, covering animal models such as mice, rats, flies, and zebrafish, along with induced pluripotent stem cell (iPSC)-derived human cellular models. These models replicate key aspects of Wolfram syndrome, contributing to a deeper understanding of its pathogenesis and providing a platform for discovering potential therapeutic approaches

    Algebraic properties and the finite rank problem for Toeplitz operators on the Segal–Bargmann space

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    AbstractWe study three different problems in the area of Toeplitz operators on the Segal–Bargmann space in Cn. Extending results obtained previously by the first author and Y.L. Lee, and by the second author, we first determine the commutant of a given Toeplitz operator with a radial symbol belonging to the class Sym>0(Cn) of symbols having certain growth at infinity. We then provide explicit examples of zero-products of non-trivial Toeplitz operators. These examples show the essential difference between Toeplitz operators on the Segal–Bargmann space and on the Bergman space over the unit ball. Finally, we discuss the “finite rank problem”. We show that there are no non-trivial rank one Toeplitz operators Tf for f∈Sym>0(Cn). In all these problems, the growth at infinity of the symbols plays a crucial role

    A calcium-dependent protease as a potential therapeutic target for Wolfram syndrome

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    Full author list omitted for brevity. For the full list of authors, see article.Wolfram syndrome is a genetic disorder characterized by diabetes and neurodegeneration and considered as an endoplasmic reticulum (ER) disease. Despite the underlying importance of ER dysfunction in Wolfram syndrome and the identification of two causative genes, Wolfram syndrome 1 (WFS1) and Wolfram syndrome 2 (WFS2), a molecular mechanism linking the ER to death of neurons and β cells has not been elucidated. Here we implicate calpain 2 in the mechanism of cell death in Wolfram syndrome. Calpain 2 is negatively regulated by WFS2, and elevated activation of calpain 2 by WFS2-knockdown correlates with cell death. Calpain activation is also induced by high cytosolic calcium mediated by the loss of function of WFS1. Calpain hyperactivation is observed in the WFS1 knockout mouse as well as in neural progenitor cells derived from induced pluripotent stem (iPS) cells of Wolfram syndrome patients. A small-scale small-molecule screen targeting ER calcium homeostasis reveals that dantrolene can prevent cell death in neural progenitor cells derived from Wolfram syndrome iPS cells. Our results demonstrate that calpain and the pathway leading its activation provides potential therapeutic targets for Wolfram syndrome and other ER diseases

    A novel mutation of WFS1 gene in a Japanese man of Wolfram syndrome with positive diabetes-related antibodies

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    Wolfram syndrome is a rare, autosomal recessive disorder characterized by early-onset diabetes mellitus, optic atrophy and neurological and endocrinological abnormalities. A 47-year-old Japanese man with frequent severe hypoglycemic episodes was diagnosed as Wolfram syndrome based on clinical features and laboratory data. He had positive glutamic acid decarboxylase (GAD) and insulinoma-associated antigen-2 (IA-2) antibodies, both uncommon in this syndrome. Genetic analysis revealed that WFS1 gene of the patient has a homozygous 5 base pairs (AAGGC) insertion at position 1279 in exon 8, causing a frameshift at codon 371 leading to premature termination at codon 443

    project-aero/transient-indicators: Files associated with 2020-01-13 manuscript draft. Author correction.

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    The author of the Wolfram Notebook has been corrected to be S. M. O'Regan

    Die geologischen Verhältnisse der Hochfläche von Gräfenhainichen-Bad Schmiedeberg (Dübener Heide)

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    Das Hallesche Jahrbuch ist in Mitteldeutschland das Journal für die Geowissenschaften. Es ist mit einem Band pro Jahr und diversen Beiheften ideal für die Publikation lokaler und überregionaler Beiträge und zugleich ein ideales Medium, um Promotionen und hochqualifizierte Abschlussarbeiten der Öffentlichkeit zugänglich zu machen. So ist das Hallesche Jahrbuch durch sein regelmäßiges Erscheinen und eine zügige Bearbeitung die ideale Plattform für Ihre Publikationen. Solche können in deutscher oder englischer Sprache angenommen werden
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