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2010 Program Meeting Schedule
Vision Sciences Society 10th Annual Meeting, May 7-12, 2010 Naples Grande Resort & Club, Naples, Florida Program Contents Board, Review Committee & Staff . 2 Satellite Events. 22 Keynote Address . 3 Club Vision Dance Party. 22 Meeting Schedule . 4 Open House . 23 Schedule-at-a-Glance . 6 Member-Initiated Symposia . 24 Poster Schedule . 8 Friday Sessions . 29 Talk Schedule . 10 Saturday Sessions . 33 Young Investigator Award . 11 Sunday Sessions . 43 Abstract Numbering System. 11 Monday Sessions . 53 VSS Dinner and Demo Night . 12 Tuesday Sessions . 58 VSS Public Lecture . 15 Wednesday Sessions . 68 VSS at ARVO . 15 Topic Index. 71 Attendee Resources . 16 Author Index . 74 Exhibitors . 19 Hotel Floorplan . 86 Travel Awards . 21 Advertisements. 89 Board, Review Committee & Staff Board of Directors Abstract Review Committee Tony Movshon (2011), President David Alais Laurence Maloney New York University Marty Banks Ennio Mingolla Pascal Mamassian (2012), President Elect Irving Biederman Cathleen Moore CNRS & Université Paris 5 Geoff Boynton Shin’ya Nishida Eli Brenner Tony Norcia Bill Geisler (2010), Past President Angela Brown Aude Oliva University of Texas, Austin David Burr Alice O’Toole Marisa Carrasco (2012), Treasurer Patrick Cavanagh John Reynolds New York University Marvin Chun Anna Roe Barbara Dosher (2013) Jody Culham Brian Rogers University of California, Irvine Greg DeAngelis Jeff Schall James Elder Brian Scholl Karl Gegenfurtner (2013) Steve Engel David Sheinberg Justus-Liebig Universität Giessen, Germany Jim Enns Daniel Simons -
Adrenaline Stimulates Glucagon Secretion by Tpc2-Dependent
1128 Diabetes Volume 67, June 2018 Adrenaline Stimulates Glucagon Secretion by Tpc2- Dependent Ca2+ Mobilization From Acidic Stores in Pancreatic a-Cells Alexander Hamilton,1 Quan Zhang,1 Albert Salehi,2 Mara Willems,1 Jakob G. Knudsen,1 Anna K. Ringgaard,3,4 Caroline E. Chapman,1 Alejandro Gonzalez-Alvarez,1 Nicoletta C. Surdo,5 Manuela Zaccolo,5 Davide Basco,6 Paul R.V. Johnson,1,7 Reshma Ramracheya,1 Guy A. Rutter,8 Antony Galione,9 Patrik Rorsman,1,2,7 and Andrei I. Tarasov1,7 Diabetes 2018;67:1128–1139 | https://doi.org/10.2337/db17-1102 Adrenaline is a powerful stimulus of glucagon secretion. It The ability of the “fight-or-flight” hormone adrenaline to acts by activation of b-adrenergic receptors, but the down- increase plasma glucose levels by stimulating liver gluconeo- stream mechanisms have only been partially elucidated. genesis is in part mediated by glucagon, the body’sprincipal Here, we have examined the effects of adrenaline in mouse hyperglycemic hormone (1). Glucagon is secreted by the and human a-cells by a combination of electrophysiology, a-cells of the pancreas (2). Reduced autonomic stimulation 2+ imaging of Ca and PKA activity, and hormone release of glucagon secretion may result in hypoglycemia, a serious measurements. We found that stimulation of glucagon and potentially fatal complication of diabetes (3). It has been secretion correlated with a PKA- and EPAC2-dependent estimated that up to 10% of insulin-treated patients die of (inhibited by PKI and ESI-05, respectively) elevation of hypoglycemia (4). Understanding the mechanism by which [Ca2+] in a-cells, which occurred without stimulation of i adrenaline stimulates glucagon secretion and how it becomes ISLET STUDIES electrical activity and persisted in the absence of extracel- perturbed in patients with diabetes is therefore essential. -
Back Matter (PDF)
JOBNAME: RNA 12#12 2006 PAGE: 1 OUTPUT: November 10 14:27:49 2006 csh/RNA/125784/reviewers-index RNA: Reviewers for Volume 12, 2006 The editors wish to thank the following individuals whose efforts in reviewing papers for RNA in the past year are greatly appreciated. Juan Alfonzo Donald Burke Fritz Eckstein Carol Greider Frederic Allain John Burke Martin Egli Sam Griffiths-Jones Emily Allen Samuel Butcher Sherif Abou Elela Claudio Gualerzi Sidney Altman Ronald Emeson Alexander Gultyaev Victor Ambros Gail Emilsson Samuel Gunderson Mark Caprara James Anderson Luis Enjuanes Christine Guthrie Paul Anderson Massimo Caputi Anne Ephrussi Raul Andino James Carrington Jay Evans Charles Carter Gordon Hager Mohammed Ararzguioui Eduardo Eyras Paul Hagerman Manuel Ares Richard Carthew Jamie Cate Stephen Hajduk Jean Armengaud Dan Fabris Jean Cavarelli Kathleen Hall Brandon Ason Philip Farabaugh Guillaume Chanfreau Michelle Hamm Gil Ast Jean Feagin Tien-Hsien Chang Scott Hammond Pascal Auffinger Martha Fedor Lawrence Chasin Maureen Hanson Johanna Avis Yuriy Fedorov Chang-Zheng Chen Eoghan Harrington Juli Feigon Eric Christian Michael Harris James Fickett Kristian Baker Christine Clayton Roland Hartmann Carol Fierke Alice Barkan Peter Clote Stephen Harvey Susan Baserga Witold Filipowicz Jeffery Coller Michelle Hastings Brenda Bass Andrew Fire Kathleen Collins Christopher Hayes Christoph Flamm David Bartel Richard Collins Christopher Hellen William Folk Robert Batey Elena Conti Matthias Hentze Maurille Fournier Peter Becker Howard Cooke Thomas Herdegen -
Synthesis of the Ca -Mobilizing Messengers NAADP
ARTICLE cro Author’s Choice Synthesis of the Ca2؉-mobilizing messengers NAADP and cADPR by intracellular CD38 enzyme in the mouse heart: Role in -adrenoceptor signaling Received for publication, April 3, 2017, and in revised form, May 13, 2017 Published, Papers in Press, May 24, 2017, DOI 10.1074/jbc.M117.789347 Wee K. Lin‡, Emma L. Bolton‡, Wilian A. Cortopassi§¶, Yanwen Wangʈ, Fiona O’Brien‡, Matylda Maciejewska‡, Matthew P. Jacobson¶, Clive Garnham‡, Margarida Ruas‡, John Parrington‡, Ming Lei‡1, Rebecca Sitsapesan‡2, Antony Galione‡3, and Derek A. Terrar‡4 From the ‡Department of Pharmacology, University of Oxford, Mansfield Road, Oxford OX1 3QT, United Kingdom, the §Department of Chemistry, Chemistry Research Laboratory, University of Oxford, Mansfield Road, Oxford OX1 3TA, United Kingdom, the ¶Department of Pharmaceutical Chemistry, University of California, San Francisco, California 94158, and the ʈFaculty of Biology, Medicine, and Health, University of Manchester, Manchester M13 9NT, United Kingdom Edited by Roger J. Colbran Nicotinic acid adenine dinucleotide phosphate (NAADP) and increase both Ca2؉ transients and the tendency to disturb .cyclic ADP-ribose (cADPR) are Ca2؉-mobilizing messengers heart rhythm important for modulating cardiac excitation–contraction cou- pling and pathophysiology. CD38, which belongs to the ADP- ribosyl cyclase family, catalyzes synthesis of both NAADP and ADP-ribosyl cyclases (ARCs)5 are enzymes capable of con- cADPR in vitro. However, it remains unclear whether this is the verting NAD into cyclic adenosine diphosphate ribose main enzyme for their production under physiological condi- (cADPR). In addition, some of these cyclases (for example, tions. Here we show that membrane fractions from WT but not CD38 and Aplysia cyclase), can (at least under in vitro condi- ؊/؊ CD38 mouse hearts supported NAADP and cADPR synthe- tions) also produce nicotinic acid adenine dinucleotide phos- sis. -
Metabolic Tracing of NAD Precursors Using Strategically Labelled Isotopes of NMN
A thesis submitted in fulfilment of the requirements for the degree of Doctor of Philosophy Metabolic tracing of NAD+ precursors using strategically labelled isotopes of NMN by Lynn-Jee Kim Supervisors Dr. Lindsay E. Wu (Primary) Prof. David A. Sinclair (Joint-Primary) Dr. Lake-Ee Quek (Co-supervisor) School of Medical Sciences Faculty of Medicine Thesis/Dissertation Sheet Surname/Family Name: Kim Given Name/s: Lynn-Jee Abbreviation for degree as give in PhD the University calendar: Faculty: Faculty of Medicine School: School of Medical Sciences + Thesis Title: Metabolic tracing of NAD precursors using strategically labelled isotopes of NMN Abstract 350 words maximum: (PLEASE TYPE) Nicotinamide adenine dinucleotide (NAD+) is an important cofactor and substrate for hundreds of cellular processes involved in redox homeostasis, DNA damage repair and the stress response. NAD+ declines with biological ageing and in age-related diseases such as diabetes and strategies to restore intracellular NAD+ levels are emerging as a promising strategy to protect against metabolic dysfunction, treat age-related conditions and promote healthspan and longevity. One of the most effective ways to increase NAD+ is through pharmacological supplementation with NAD+ precursors such as nicotinamide mononucleotide (NMN) which can be orally delivered. Long term administration of NMN in mice mitigates age-related physiological decline and alleviates the pathophysiologies associated with a high fat diet- and age-induced diabetes. Despite such efforts, there are certain aspects of NMN metabolism that are poorly understood. In this thesis, the mechanisms involved in the utilisation and transport of orally administered NMN were investigated using strategically labelled isotopes of NMN and mass spectrometry. -
Consciousness, Accessibility, and the Mesh Between Psychology and Neuroscience
BEHAVIORAL AND BRAIN SCIENCES (2007) 30, 481–548 Printed in the United States of America doi: 10.1017/S0140525X07002786 Consciousness, accessibility, and the mesh between psychology and neuroscience Ned Block Department of Philosophy, New York University, New York, NY 10003 [email protected] Abstract: How can we disentangle the neural basis of phenomenal consciousness from the neural machinery of the cognitive access that underlies reports of phenomenal consciousness? We see the problem in stark form if we ask how we can tell whether representations inside a Fodorian module are phenomenally conscious. The methodology would seem straightforward: Find the neural natural kinds that are the basis of phenomenal consciousness in clear cases – when subjects are completely confident and we have no reason to doubt their authority – and look to see whether those neural natural kinds exist within Fodorian modules. But a puzzle arises: Do we include the machinery underlying reportability within the neural natural kinds of the clear cases? If the answer is “Yes,” then there can be no phenomenally conscious representations in Fodorian modules. But how can we know if the answer is “Yes”? The suggested methodology requires an answer to the question it was supposed to answer! This target article argues for an abstract solution to the problem and exhibits a source of empirical data that is relevant, data that show that in a certain sense phenomenal consciousness overflows cognitive accessibility. I argue that we can find a neural realizer of this overflow if we assume that the neural basis of phenomenal consciousness does not include the neural basis of cognitive accessibility and that this assumption is justified (other things being equal) by the explanations it allows. -
The International Journal of Developmental Biology
Int. J. Dev. Biol. 53: 725-731 (2009) DEVELOPMENTALTHE INTERNATIONAL JOURNAL OF doi: 10.1387/ijdb.072575mr BIOLOGY www.intjdevbiol.com Molecular tools, classic questions - an interview with Clifford Tabin MICHAEL K. RICHARDSON* Institute of Biology, Leiden University, Leiden, The Netherlands ABSTRACT Clifford J. Tabin has made pioneering contributions to several fields in biology, including retroviruses, oncogenes, developmental biology and evolution. His father, a physicist who worked in the Manhattan project, kindled his interest in science. Cliff later chose to study biology and started his research career when the world of recombinant DNA was opening up. In Robert Weinberg’s lab, he constructed the Moloney leukaemia virus (MLV-tk), the first recombi- nant retrovirus that could be used as a eukaryotic vector. He also discovered the amino acid changes leading to the activation of Ras, the first human oncogene discovered. As an independent researcher, he began in the field of urodele limb regeneration, and described the expression of retinoic acid receptor and Hox genes in the blastema. Moving to the chick model, his was one of the labs that simultaneously cloned the first vertebrate hedgehog cognates and showed that sonic hedgehog functions as a morphogen in certain developmental contexts, in particular as an organizing activity during limb development. Comparative studies by Ann Burke in his lab showed that differences in boundaries of Hox gene expression across vertebrate phylogeny correlated with differences in skeletal morphology. The Tabin lab also discovered a genetic pathway responsible for mediating left-right asymmetry in vertebrates; helped uncover the pathways leading to dorsoventral limb patterning; made contributions to our understanding of skeletal morphogenesis and identified developmental mechanisms that might underpin the diversifica- tion of the beak in Darwin’s finches. -
Function Follows Form: How Connectivity Patterns Govern Neural Responses by David Eugene Osher B.Sc
Function Follows Form: How Connectivity Patterns Govern Neural Responses by David Eugene Osher B.Sc. Psychology The Ohio State University 2006 SUBMITTED TO THE DEPARTMENT OF BRAIN AND COGNITIVE SCIENCES IN PARTIAL FULFILLMENT OF THE REQUIREMENTS FOR THE DEGREE OF DOCTOR OF PHILOSOPHY IN NEUROSCIENCE AT THE MASSACHUSETTS INSTITUTE OF TECHNOLOGY June 2013 © David E. Osher, MMXIII. All rights reserved The author hereby grants to MIT permission to reproduce and distribute publicly paper and electronic copies of this thesis document in whole or in part in any medium now known or hereafter created. Author.......................................................................................................................... David E. Osher Department of Brain and Cognitive Sciences May 3, 2013 Certified by.................................................................................................................. John D. E. Gabrieli Grover Hermann Professor in Health Sciences, Technology and Cognitive Neuroscience Thesis Supervisor Accepted by................................................................................................................. Matthew A. Wilson Sherman Fairchild Professor of Neuroscience Director of Graduate Education for Brain and Cognitive Sciences Page 1 of 129 Function Follows Form: How Connectivity Patterns Govern Neural Responses by David Eugene Osher Submitted to the Department of Brain and Cognitive Sciences on May 3 2013, in partial fulfillment of the requirements for the degree of Doctor of Philosophy -
Human Brain Mapping Foundational Issues in Human Brain Mapping
edited by Stephen José Hanson and Martin Bunzl FOUNDATIONAL ISSUES IN Human Brain Mapping Foundational Issues in Human Brain Mapping Foundational Issues in Human Brain Mapping edited by Stephen Jose´ Hanson and Martin Bunzl A Bradford Book The MIT Press Cambridge, Massachusetts London, England ( 2010 Massachusetts Institute of Technology All rights reserved. No part of this book may be reproduced in any form by any electronic or mechanical means (including photocopying, recording, or information storage and retrieval) without permission in writing from the publisher. MIT Press books may be purchased at special quantity discounts for business or sales promotional use. For information, please email [email protected] or write to Special Sales Depart- ment, The MIT Press, 55 Hayward Street, Cambridge, MA 02142. This book was set in Stone Serif and Stone Sans on 3B2 by Asco Typesetters, Hong Kong. Printed and bound in the United States of America. Library of Congress Cataloging-in-Publication Data Foundational issues in human brain mapping / edited by Stephen Jose´ Hanson and Martin Bunzl. p. ; cm. ‘‘A Bradford Book.’’ Includes bibliographical references and index. ISBN 978-0-262-01402-1 (hardcover : alk. paper)—ISBN 978-0-262-51394-4 (pbk. : alk. paper) 1. Brain mapping. 2. Brain—Magnetic resonance imaging. I. Hanson, Stephen Jose´. II. Bunzl, Martin. [DNLM: 1. Brain Mapping. 2. Brain—physiology. 3. Data Interpretation, Statistical. 4. Magnetic Resonance Imaging. 5. Research Design. WL 335 F771 2010] QP385.F68 2010 612.8'2—dc22 2009036078 10 9 8 7 6 5 4 3 2 1 Contents Acknowledgments vii Introduction ix I Location and Representation 1 1 A Critique of Functional Localizers 3 Karl J. -
Biologie Moléculaire De LA CELLULE Biologie Moléculaire De Sixième Édition
Sixième édition BRUCE ALEXANDER JULIAN DAVID MARTIN KEITH PETER ALBERTS JOHNSON LEWIS MORGAN RAFF ROBERTS WALTER Biologie moléculaire de LA CELLULE Biologie moléculaire de Sixième édition LA CELLULESixième édition Biologie moléculaire de moléculaire Biologie LA CELLULE LA BRUCE ALBERTS BRUCE ALBERTS ALEXANDER JOHNSON ALEXANDER JOHNSON JULIAN LEWIS JULIAN LEWIS DAVID MORGAN DAVID MORGAN MARTIN RAFF MARTIN RAFF KEITH ROBERTS KEITH ROBERTS PETER WALTER PETER WALTER -:HSMCPH=WU[\]\: editions.lavoisier.fr 978-2-257-20678-7 20678-Albers2017.indd 1-3 08/09/2017 11:09 Chez le même éditeur Culture de cellules animales, 3e édition, par G. Barlovatz-Meimon et X. Ronot Biochimie, 7e édition, par J. M. Berg, J. L. Tymoczko, L. Stryer L’essentiel de la biologie cellulaire, 3e édition, par B. Alberts, D. Bray, K. Hopkin, A. Johnson, A. J. Lewis, M. Ra", K. Roberts et P. Walter Immunologie, par L. Chatenoud et J.-F. Bach Génétique moléculaire humaine, 4e édition, par T. Strachan et A. Read Manuel de poche de biologie cellulaire, par H. Plattner et J. Hentschel Manuel de poche de microbiologie médicale, par F. H. Kayser, E. C. Böttger, P. Deplazes, O. Haller, A. Roers Atlas de poche de génétique, par E. Passarge Atlas de poche de biotechnologie et de génie génétique, par R.D. Schmid Les biosimilaires, par J.-L. Prugnaud et J.-H. Trouvin Bio-informatique moléculaire : une approche algorithmique (Coll. IRIS), par P. A. Pevzner et N. Puech Cycle cellulaire et cytométrie en "ux, par D. Grunwald, J.-F. Mayol et X. Ronot La cytométrie en "ux, par X. Ronot, D. -
Physiology News
PN Issue 91 / Summer 2013 Physiology News Language, culture and international relations Reports from national and international associations The female faces of physiology International special issue Annual General Meeting 2013 The Annual General Meeting (AGM) of The Physiological Society will be held on 24 July 2013, commencing at 1.00pm at the Symphony Ballroom, Hyatt Regency, 2 Bridge Street, Birmingham B1 2JZ. Ordinary and Honorary Members have the right to attend and vote at the AGM. Affiliates have the right to attend, but may not vote. Please note that you do not have to register for IUPS 2013 to attend the AGM. Questions can be submitted in advance online. The Annual Review, Annual Report and Accounts, and agenda for the 2013 AGM, as well as minutes of last year’s meeting, can be downloaded via the link below. The Annual Report and Accounts, which received an unqualified audit opinion, should be consulted for a complete understanding of the financial affairs of The Society. www.physoc.org/agm2013 Physiology News / Summer 2013 / Issue 91 Contents Annual General Meeting 2013 Welcome to the Summer 2013 edition of Physiology News Introduction Features The Annual General Meeting (AGM) of 05 Editorial 18 The international dimensions of the physiological sciences The Physiological Society will be held on 22 Physiology in Africa 24 July 2013, commencing at 1.00pm at 25 Physiology in Australia News in brief 28 Physiology in Brazil: the Symphony Ballroom, Hyatt Regency, The Rhythms of Life: IUPS 2017 in Rio de Janeiro Vote now: 2013 Council elections 2 Bridge Street, Birmingham B1 2JZ. -
Genetic Basis of Metabolic Evolution in the Cave Fish Astyanax Mexicanus
Genetic Basis of Metabolic Evolution in the Cave Fish Astyanax Mexicanus The Harvard community has made this article openly available. Please share how this access benefits you. Your story matters Citable link http://nrs.harvard.edu/urn-3:HUL.InstRepos:40050145 Terms of Use This article was downloaded from Harvard University’s DASH repository, and is made available under the terms and conditions applicable to Other Posted Material, as set forth at http:// nrs.harvard.edu/urn-3:HUL.InstRepos:dash.current.terms-of- use#LAA Gene�c Basis of Metabolic Evolu�on in the Cave fish Astyanax mexicanus A disserta�on presented by Ariel Cacayuran Aspiras to The Division of Medical Sciences in par�al fulfillment of the requirements for the degree of Doctor of Philosophy in the subject of Biological and Biomedical Sciences Harvard University Cambridge, Massachuse�s May 2018 ©2018 by Ariel Cacayuran Aspiras All rights reserved. iii Dissertation Advisor: Dr. Clifford Tabin Ariel Cacayuran Aspiras Genetic Basis of Metabolic Evolution in the Cave fish Astyanax mexicanus Abstract Organisms evolve to thrive in new environments. In spite of the role metabolism plays in adaptation, the genetic basis for metabolic variation remains poorly understood. Here we use independently derived populations of Astyanax mexicanus, a Mexican tetra, to interrogate the genetic basis of extreme metabolic variation between surface and cave adapted populations. In the cave environment, food is much more scarce than in nutrient-rich rivers. Cave populations of Astyanax mexicanus rely on sporadic input of food from outside the cave. As a result, cave fish populations have evolved a suite of metabolic traits such as: starvation resistance, hyperphagia, hyperglycemia, and insulin resistance.