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Preliminary Program
Europe’s Past, Present, and Future: Utopias and Dystopias University of Iceland | Reykjavik, Iceland June 22-24, 2020 Preliminary Program This preliminary program is subject to change and CES can not be held liable for any reservation/booking made based on the information provided. Updated on February 7, 2020 Chair: Zsuzsanna Fagyal - University of Illinois at MONDAY, JUNE 22 Urbana-Champaign Participants: [1] Austerity, populism and changing policy Are French people white?: Towards an legitimacy: the European welfare states in understanding of whiteness in Republican France comparative perspective Single Paper 6/22/2020 Jean Beaman - University of California, 9:00 AM to 10:45 AM - Room 14 Santa Barbara Paper Panel Colorblindness and Narratives from the ‘Other’ Chair: Maria Petmesidou - Democritus University of (colorful) France Single Paper Thrace Christina Horvath - University of Bath Ana Guillén - University of Oviedo Participants: ‘Migrants’ or ‘Marseillais?’ The Sociolinguistic Construction of French Minority Youth in Nordic welfare states changes especially in the Marseille light of migration and the financial crisis Single Paper Single Paper Cecile Evers - Pomona College, Bent Greve - Roskilde University Department of Anthropology Jon Kvist - Roskilde University Prototypically non-French: the ‘accent of the The post-Brexit liberal welfare state in Europe: suburbs’ as a cultural construct where next for the United Kingdom? Single Paper Single Paper Zsuzsanna Fagyal - University of Illinois Benjamin Leruth - University of at Urbana-Champaign -
3381-001 Donald Sankey Farner Papers Inventory Accession
UNlVERSllY U BRARIJES w UNIVERSITY of WASHI NGTON Spe ial Colle tions 3784 Donald Sankey Farner papers Inventory Accession No: 3381-001 Special Collections Division University of Washington Libraries Box 352900 Seattle, Washington, 98195-2900 USA (206) 543-1929 This document forms part of the Preliminary Guide to the Donald Sankey Farner Papers. To find out more about the history, context, arrangement, availability and restrictions on this collection, click on the following link: http://digital.lib.washington.edu/findingaids/permalink/FarnerDonaldSUA3381/ Special Collections home page: http://www.lib.washington.edu/specialcollections/ Search Collection Guides: http://digital.lib.washington.edu/findingaids/search DONALDS. FARNER Accession No. 3381-88-21 INVENTORY Box Series Folders Dates 1 GENERAL CORRESPONDENCE A 2 1957-60, 1968, 1970-73,1976-87 Abbott, Ian John 1968 Abelson, Philip H. 1980 Abs, Michael 1981 Academic Press Royalty Statement 1977-79 Adam, Hans 1982 Adkisson, C.S. 1979 Ainley, M.G. 1980, 1985 Akesson, Thomas 1979 Akita, Yasukazu n.d. Aldrich, John W. 1946-58, 1961 1968-72 Alexander Von Humboldt-Stiftung 2 1976-85, 1987 Ali, M.A. 1964 Alvarado, Ronald H. 2 1965, n.d. Alvarez, Bonnie 1970-73 Ameel, Donald J. 1961-65 American Elsevier Publishing Co. n.d. American Express 1977, 1984 Amodon, Dean 1947-51, 1961, 1965-66 Amoroso, E.C. 1961-64, 1974-77 Anderson, Berti! G. n.d. Andrewartha, Herbert G. 1959, 1963 Arcese, Peter 1982 Arnold, Arthur P. 1973-74 Aschoff, Jurgen 1965-83 Ashmole, N. Philip 1969-72 Arvey, M. Dale 1949-73 Assenmacher, Ivan 1960-83 American Society of Zoologists 1983 Audubon Conservation Topics West 1980 Austin, O.L. -
Membrane Trafficking in Health and Disease Rebecca Yarwood*, John Hellicar*, Philip G
© 2020. Published by The Company of Biologists Ltd | Disease Models & Mechanisms (2020) 13, dmm043448. doi:10.1242/dmm.043448 AT A GLANCE Membrane trafficking in health and disease Rebecca Yarwood*, John Hellicar*, Philip G. Woodman‡ and Martin Lowe‡ ABSTRACT KEY WORDS: Disease, Endocytic pathway, Genetic disorder, Membrane traffic, Secretory pathway, Vesicle Membrane trafficking pathways are essential for the viability and growth of cells, and play a major role in the interaction of cells with Introduction their environment. In this At a Glance article and accompanying Membrane trafficking pathways are essential for cells to maintain poster, we outline the major cellular trafficking pathways and discuss critical functions, to grow, and to accommodate to their chemical how defects in the function of the molecular machinery that mediates and physical environment. Membrane flux through these pathways this transport lead to various diseases in humans. We also briefly is high, and in specialised cells in some tissues can be enormous. discuss possible therapeutic approaches that may be used in the For example, pancreatic acinar cells synthesise and secrete amylase, future treatment of trafficking-based disorders. one of the many enzymes they produce, at a rate of approximately 0.5% of cellular protein mass per hour (Allfrey et al., 1953), while in Schwann cells, the rate of membrane protein export must correlate School of Biological Sciences, Faculty of Biology, Medicine and Health, with the several thousand-fold expansion of the cell surface that University of Manchester, Manchester, M13 9PT, UK. occurs during myelination (Pereira et al., 2012). The population of *These authors contributed equally to this work cell surface proteins is constantly monitored and modified via the ‡Authors for correspondence ([email protected]; endocytic pathway. -
Molecular Interactions Between Childhood Acute Lymphoblastic Leukaemia Cells and the Bone Marrow Microenvironment
Molecular Interactions Between Childhood Acute Lymphoblastic Leukaemia Cells And The Bone Marrow Microenvironment Ana Markovic A thesis submitted in fulfilment of the requirements for the degree of Doctor of Philosophy Children’s Cancer Institute Australia for Medical Research School of Women’s and Children’s Health THE UNIVERSITY OF NEW SOUTH WALES 2009 THE UNIVERSITY OF NEW SOUTH WALES Thesis/Dissertation Sheet Surname or Family name: MARKOVIC First name: ANA Other name/s: Abbreviation for degree as given in the University calendar: PhD School: Women’s & Children’s Health Faculty: MEDICINE Title: Molecular Interactions Between Childhood Acute Lymphoblastic Leukaemia Cells And The Bone Marrow Microenvironment. Abstract 350 words maximum Acute lymphoblastic leukaemia (ALL) is the most common cause of death from disease in children. Whilst cure rates over the last 30 years have drastically improved, children that do go on and relapse have a very poor prognosis. Additionally, the ones that do survive can have significant long term side effects from existing treatments. Understanding the molecular mechanisms of the relationship between leukaemia and its microenvironment is essential for the identification of novel targets for treatment and/or the manipulation of existing treatments. Our previous work has established a panel of childhood ALL xenografts from patient biopsies in NOD/SCID mice. Several samples secrete vascular endothelial growth factor (VEGF), an integral component of neovascularisation and normal haematopoiesis, and express FMS-like tyrosine kinase-3 (FLT-3), a receptor tyrosine kinase, which plays an essential role in regulating normal haematopoiesis. This thesis builds on previous work by examining the relationship between VEGF and FLT-3, two widely, yet independently studied molecules in leukaemia, with the aberrant expression of either having adverse outcomes for patients. -
Spinal Muscular Atrophy : Evidence of a Multi-System Disease
Spinal muscular atrophy : Evidence of a multi-system disease Marc-Olivier Deguise This thesis is submitted as a partial fulfillment of the Ph.D. program in Cellular and Molecular Medicine of the University of Ottawa September 6th 2019 Department of Cellular and Molecular Medicine Faculty of Medicine University of Ottawa © Marc-Olivier Deguise, Ottawa, Canada, 2020 Authorization The content of this document consists of Marc-Olivier Deguise’s original work. All previously published work as produced by Marc-Olivier Deguise & al. obtained permissions from the publishers for publication within this document, whether unaltered or modified. Licenses are provided below. 1. Deguise M.O. & al. (20XX) Myopathic phenotype precedes neuronal phenotype in a new mild mouse model of spinal muscular atrophy (Not yet submitted) 2. Deguise M.O. & al. (20XX). Spinal muscular atrophy: providing a novel framework to elucidate NAFLD molecular pathogenesis (Not yet submitted). 3. Marc-Olivier Deguise & al. (2019) Low fat diets increase survival of a mouse model of spinal muscular atrophy. Ann Clin Transl Neurol (IF: 4.656). DOI : 10.1002/acn3.50920 This is an open access article under the terms of the Creative Commons Attribution- NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/), which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made. If you remix, transform or build upon the material, you may not distribute the modified material. This work has been altered as part of the thesis. II 4. Deguise M.O. & al. -
Uncovering the Variability, Regulatory Roles and Mutation Rates of Short Tandem Repeats by Thomas F
Uncovering the variability, regulatory roles and mutation rates of short tandem repeats by Thomas F. Willems B.S. in Chemical Engineering, University of California, Berkeley (2011) Submitted to the Computational and Systems Biology Program in partial fulfillment of the requirements for the degree of Doctor of Philosophy at the MASSACHUSETTS INSTITUTE OF TECHNOLOGY June 2016 ○c Massachusetts Institute of Technology 2016. All rights reserved. Author............................................................................ Computational and Systems Biology Program April 26, 2016 Certified by . Yaniv Erlich, PhD Assistant Professor of Computer Science, Columbia University Thesis Supervisor Certified by . Manolis Kellis, PhD Associate Professor of Computer Science, MIT Thesis Supervisor Accepted by....................................................................... Christopher B. Burge, PhD Professor of Biology and Biological Engineering Director, Computational and Systems Biology Graduate Program 2 Uncovering the variability, regulatory roles and mutation rates of short tandem repeats by Thomas F. Willems Submitted to the Computational and Systems Biology Program on April 26, 2016, in partial fulfillment of the requirements for the degree of Doctor of Philosophy Abstract Over the past decade, the advent of next-generation DNA sequencing technologies has ushered in an exciting era of biological research. Through large-scale sequencing projects, scientists have begun to unveil the variability and function of millions of DNA mutations called single nucleotide polymorphisms. Despite this rapid growth in understanding, short tandem repeats (STRs), ge- nomic elements consisting of a repeating pattern of 2-6 bases, have remained poorly understood. Mutating orders of magnitude more rapidly than most of the human genome, STRs have been identified as the causal variants in diseases such as Fragile X syndrome and Huntington’s disease. -
Ravi Arvind Palat
Department of Sociology Phone (607) 777-4756 Binghamton University Fax (607) 777-4197 Binghamton, NY 13902 E-mail [email protected] Ravi Arvind Palat Education 1981 - 1988 State University of New York Binghamton, NY Ph. D (Sociology) • Awarded with Distinction. 1978 - 1981 Jawaharlal Nehru University New Delhi M. Phil History 1976 - 1978 Jawaharlal Nehru University New Delhi M. A. History 1973- 1976 University of Madras Madras B. A. Economics Citizenship Indian Permanent residency in New Zealand and the United States Academic Posts 2009- 2011 State University of New York Binghamton, NY Chair, Department of Sociology 2008 - present Professor of Sociology • Courses taught include World-systems Studies; Contemporary Capitalism; Asia in World-Historical Perspective; Comparative Hegemonies; Political Economy of Asia; Consuming Interests: Sociology of Food; Empire, Hegemony, and Terror; Sociology of Colonialism; Sociology of Contemporary Asia; Advanced Seminar on India and China; Social Change: Introduction to Sociology; Binghamton and the World-Economy 2006 - 2008 Associate Chair and Director of Graduate Studies in Sociology 2000 - 2008 Associate Professor of Sociology 2000 Johns Hopkins University Baltimore, MD Visiting Associate Professor of Sociology • Fall Semester 1998 - 2000 University of Auckland New Zealand Senior Lecturer in Sociology • Courses taught include Sociology: Issues and Themes, Social Change and Modernization, Sociology of Colonialism, Social Theory: Change and Conflict, Sociology of Contemporary Asia, Asia and the Modern -
C-Met: a Potential Therapeutic Target for Hepatocellular Carcinoma
ISSN 1881-7831 Online ISSN 1881-784X DD&T Drug Discoveries & Therapeutics Volume 5 ● Number 1 ● 2011 www.ddtjournal.com ISSN: 1881-7831 Online ISSN: 1881-784X CODEN: DDTRBX Issues/Year: 6 Language: English Publisher: IACMHR Co., Ltd. Drug Discoveries & Therapeutics is one of a series of peer-reviewed journals of the International Research and Cooperation Association for Bio & Socio-Sciences Advancement (IRCA-BSSA) Group and is published bimonthly by the International Advancement Center for Medicine & Health Research Co., Ltd. (IACMHR Co., Ltd.) and supported by the IRCA-BSSA and Shandong University China-Japan Cooperation Center for Drug Discovery & Screening (SDU-DDSC). Drug Discoveries & Therapeutics publishes contributions in all fields of pharmaceutical and therapeutic research such as medicinal chemistry, pharmacology, pharmaceutical analysis, pharmaceutics, pharmaceutical administration, and experimental and clinical studies of effects, mechanisms, or uses of various treatments. Studies in drug-related fields such as biology, biochemistry, physiology, microbiology, and immunology are also within the scope of this journal. Drug Discoveries & Therapeutics publishes Original Articles, Brief Reports, Reviews, Policy Forum articles, Case Reports, News, and Letters on all aspects of the field of pharmaceutical research. All contributions should seek to promote international collaboration in pharmaceutical science. Editorial Board Editor-in-Chief: Masahiro MURAKAMI Osaka Ohtani University, Osaka, Japan Kazuhisa SEKIMIZU Yutaka ORIHARA -
19 by UCL Press University College London Gower Street London WC1E 6BT
Re-Mapping Centre and Periphery Re-Mapping Centre and Periphery Asymmetrical Encounters in European and Global Contexts Edited by Tessa Hauswedell, Axel Körner and Ulrich Tiedau First published in 2019 by UCL Press University College London Gower Street London WC1E 6BT Available to download free: www.ucl.ac.uk/ucl-press Text © Authors, 2019 Images © Authors and copyright holders named in captions, 2019 The authors have asserted their rights under the Copyright, Designs and Patents Act 1988 to be identified as authors of this work. A CIP catalogue record for this book is available from The British Library. This book is published under a Creative Commons 4.0 International licensee (CC BY 4.0). This license allows you to share, copy, distribute and transmit the work; to adapt the work and to make commercial use of the work providing attribution is made to the authors (but not in any way that suggests that they endorse you or your use of the work). Attribution should include the following information: Hauswedell, T., Körner, A., Tiedau, U. Re-Mapping Centre and Periphery: Asymmetri- cal Encounters in European and Global Contexts. London: UCL Press. https://doi.org/ 10.14324/111.9781787350991 Further details about Creative Commons licenses are available at http://creativecom- mons.org/licenses/ ISBN: 978–1-78735–101-1 (Hbk.) ISBN: 978–1-78735–100-4 (Pbk.) ISBN: 978–1-78735–099-1 (PDF) ISBN: 978–1-78735–102-8 (epub) ISBN: 978–1-78735–103-5 (mobi) ISBN: 978–1-78735–104-2 (html) DOI: https://doi.org/10.14324/111.9781787350991 Contents 1. -
Matrix Type Transdermal Therapeutic Systems of Glibenclamide: Formulation, Ex Vivo and in Vivo Characterization
Drug Discoveries & Therapeutics. 2011; 5(1):53-59. 53 Original Article DOI: 10.5582/ddt.v5.1.53 Matrix type transdermal therapeutic systems of glibenclamide: Formulation, ex vivo and in vivo characterization Asgar Ali1, Anupam Trehan1, Zabih Ullah2, Mohammed Aqil1,*, Yasmin Sultana1 1 Department of Pharmaceutics, Faculty of Pharmacy, Hamdard University, New Delhi, India; 2 Department of Pharmaceutical Medicine, Faculty of Pharmacy, Hamdard University, New Delhi, India. ABSTRACT: Matrix type transdermal therapeutic 1. Introduction systems (TTS) of glibenclamide were formulated using polymers Eudragit RL 100, ethyl cellulose, Diabetes mellitus is a metabolic disorder characterized PVP K-30, and polyvinyl acetate, and citral was by high blood glucose level (fasting plasma glucose > used as the penetration enhancer. The polymer fi lms 7.0 mM, or plasma glucose > 11.1 mM 2 h after meal) were formulated with Eudragit RL 100 and PVP (1). In total diabetic patients more than 90% suffer K-30 in different ratios and subsequently subjected from type 2 diabetes (2). Globally, the burden of type 2 to ex vivo studies (drug permeation through rat diabetes is rising fast. The global prevalence of diabetes skin) followed by interaction studies, skin irritation among adults was estimated at 150 million in 1995, studies, accelerated stability analysis, and in vivo and this is projected to rise up to 300 million by 2025 studies (determination of blood glucose level in (3). Developing countries may experience the largest rabbits). The drug content of the formulations was proportional increase in diabetes (4). Type 2 diabetes is found to be 99.1-99.2%. The cumulative percentages caused by insulin defi ciency in the body due to partial of drug permeated through rat skin from the three or incomplete inactivation/destruction of β cells of selected formulations in 48 h were 95.3%, 98.8%, pancreas and often associated with insulin resistance and 99%, respectively. -
La Sclérose Latérale Amyotrophique Chez Les Souris Sod1g86r Thibaut Burg
Détermination du rôle des neurones corticospinaux dans le déclenchement et la progression de la sclérose latérale amyotrophique chez les souris Sod1G86R Thibaut Burg To cite this version: Thibaut Burg. Détermination du rôle des neurones corticospinaux dans le déclenchement et la pro- gression de la sclérose latérale amyotrophique chez les souris Sod1G86R. Neurosciences [q-bio.NC]. Université de Strasbourg, 2019. Français. NNT : 2019STRAJ046. tel-02539135 HAL Id: tel-02539135 https://tel.archives-ouvertes.fr/tel-02539135 Submitted on 9 Apr 2020 HAL is a multi-disciplinary open access L’archive ouverte pluridisciplinaire HAL, est archive for the deposit and dissemination of sci- destinée au dépôt et à la diffusion de documents entific research documents, whether they are pub- scientifiques de niveau recherche, publiés ou non, lished or not. The documents may come from émanant des établissements d’enseignement et de teaching and research institutions in France or recherche français ou étrangers, des laboratoires abroad, or from public or private research centers. publics ou privés. UNIVERSITÉ DE STRASBOURG ÉCOLE DOCTORALE DES SCIENCES DE LA VIE ET DE LA SANTÉ UMR-S INSERM 1118 THÈSE présentée par : Thibaut BURG soutenue le : 06 septembre 2019 pour obtenir le grade de : Docteur de l’université de Strasbourg Discipline/ Spécialité : Neurosciences Détermination du rôle des neurones corticospinaux dans le déclenchement et la progression de la sclérose latérale amyotrophique chez les souris Sod1G86R THÈSE dirigée par : Mme ROUAUX Caroline CR,