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Hrudní Endovaskulární Graft Zenith Alpha™ Návod K Použití
MEDICAL EN Zenith Alpha™ Thoracic Endovascular Graft 15 Instructions for Use CS Hrudní endovaskulární graft Zenith Alpha™ 22 Návod k použití DA Zenith Alpha™ torakal endovaskulær protese 29 Brugsanvisning DE Zenith Alpha™ thorakale endovaskuläre Prothese 36 Gebrauchsanweisung EL Θωρακικό ενδαγγειακό μόσχευμα Zenith Alpha™ 44 Οδηγίες χρήσης ES Endoprótesis vascular torácica Zenith Alpha™ 52 Instrucciones de uso FR Endoprothèse vasculaire thoracique Zenith Alpha™ 60 Mode d’emploi HU Zenith Alpha™ mellkasi endovaszkuláris graft 67 Használati utasítás IT Protesi endovascolare toracica Zenith Alpha™ 74 Istruzioni per l’uso NL Zenith Alpha™ thoracale endovasculaire prothese 81 Gebruiksaanwijzing NO Zenith Alpha™ torakalt endovaskulært implantat 88 Bruksanvisning PL Piersiowy stent-graft wewnątrznaczyniowy Zenith Alpha™ 95 Instrukcja użycia PT Prótese endovascular torácica Zenith Alpha™ 103 Instruções de utilização SV Zenith Alpha™ endovaskulärt graft för thorax 110 Bruksanvisning Patient I.D. Card Included I-ALPHA-TAA-1306-436-01 *436-01* ENGLISH ČESKY TABLE OF COntents OBSAH 1 DEVICE DESCRIPTION ....................................................................... 15 1 POPIS ZAŘÍZENÍ ....................................................................................... 22 1.1 Zenith Alpha Thoracic Endovascular Graft .........................................15 1.1 Hrudní endovaskulární graft Zenith Alpha .............................................. 22 1.2 Introduction System ...................................................................................15 -
Customized Book List Life Science
ABCD springer.com Springer Customized Book List Life Science FRANKFURT BOOKFAIR 2007 springer.com/booksellers Life Science 1 M.M. Abdelhaleem, University of Toronto, ON, Canada (Ed.) Transactions on Computational Single Molecules and Systems Biology VIII Nanotechnology Helicases Helicases are enzymes that utilize the energy derived The LNCS journal Transactions on Computation- This book focuses on recent advances in the rapid- from NTP hydrolysis to unwind double standed nu- al Systems Biology is devoted to inter- and multi- ly evolving field of single molecule research. These cleic acids. Significant progress has been achieved in disciplinary research in the fields of computer sci- advances are of importance for the investigation our understanding of the structure and molecular ence and life sciences and supports a paradigmat- of biopolymers and cellular biochemical reactions, mechanisms of helicases. The reader will find proto- ic shift in the techniques from computer and infor- and are essential to the development of quantita- cols utilized by leading experts in the field that span mation science to cope with the new challenges aris- tive biology. Written by leading experts in the field, different species and cover various biological pro- ing from the systems oriented point of view of bio- the articles cover a broad range of topics, including: cesses in which helicases are involved. This volume logical phenomena. The six papers selected quantum photonics of organic dyes and inorgan- will be useful to students and researchers interested for this special issue are:Bio-inspired Network-Cen- ic nanoparticles their use in detecting properties of in this rapidly expanding filed. -
Select Bibliography
Select Bibliography by the late F. Seymour-Smith Reference books and other standard sources of literary information; with a selection of national historical and critical surveys, excluding monographs on individual authors (other than series) and anthologies. Imprint: the place of publication other than London is stated, followed by the date of the last edition traced up to 1984. OUP- Oxford University Press, and includes depart mental Oxford imprints such as Clarendon Press and the London OUP. But Oxford books originating outside Britain, e.g. Australia, New York, are so indicated. CUP - Cambridge University Press. General and European (An enlarged and updated edition of Lexicon tkr WeltliU!-atur im 20 ]ahrhuntkrt. Infra.), rev. 1981. Baker, Ernest A: A Guilk to the B6st Fiction. Ford, Ford Madox: The March of LiU!-ature. Routledge, 1932, rev. 1940. Allen and Unwin, 1939. Beer, Johannes: Dn Romanfohrn. 14 vols. Frauwallner, E. and others (eds): Die Welt Stuttgart, Anton Hiersemann, 1950-69. LiU!-alur. 3 vols. Vienna, 1951-4. Supplement Benet, William Rose: The R6athr's Encyc/opludia. (A· F), 1968. Harrap, 1955. Freedman, Ralph: The Lyrical Novel: studies in Bompiani, Valentino: Di.cionario letU!-ario Hnmann Hesse, Andrl Gilk and Virginia Woolf Bompiani dille opn-e 6 tUi personaggi di tutti i Princeton; OUP, 1963. tnnpi 6 di tutu le let16ratur6. 9 vols (including Grigson, Geoffrey (ed.): The Concise Encyclopadia index vol.). Milan, Bompiani, 1947-50. Ap of Motkm World LiU!-ature. Hutchinson, 1970. pendic6. 2 vols. 1964-6. Hargreaves-Mawdsley, W .N .: Everyman's Dic Chambn's Biographical Dictionary. Chambers, tionary of European WriU!-s. -
Adams Adkinson Aeschlimann Aisslinger Akkermann
BUSCAPRONTA www.buscapronta.com ARQUIVO 27 DE PESQUISAS GENEALÓGICAS 189 PÁGINAS – MÉDIA DE 60.800 SOBRENOMES/OCORRÊNCIA Para pesquisar, utilize a ferramenta EDITAR/LOCALIZAR do WORD. A cada vez que você clicar ENTER e aparecer o sobrenome pesquisado GRIFADO (FUNDO PRETO) corresponderá um endereço Internet correspondente que foi pesquisado por nossa equipe. Ao solicitar seus endereços de acesso Internet, informe o SOBRENOME PESQUISADO, o número do ARQUIVO BUSCAPRONTA DIV ou BUSCAPRONTA GEN correspondente e o número de vezes em que encontrou o SOBRENOME PESQUISADO. Número eventualmente existente à direita do sobrenome (e na mesma linha) indica número de pessoas com aquele sobrenome cujas informações genealógicas são apresentadas. O valor de cada endereço Internet solicitado está em nosso site www.buscapronta.com . Para dados especificamente de registros gerais pesquise nos arquivos BUSCAPRONTA DIV. ATENÇÃO: Quando pesquisar em nossos arquivos, ao digitar o sobrenome procurado, faça- o, sempre que julgar necessário, COM E SEM os acentos agudo, grave, circunflexo, crase, til e trema. Sobrenomes com (ç) cedilha, digite também somente com (c) ou com dois esses (ss). Sobrenomes com dois esses (ss), digite com somente um esse (s) e com (ç). (ZZ) digite, também (Z) e vice-versa. (LL) digite, também (L) e vice-versa. Van Wolfgang – pesquise Wolfgang (faça o mesmo com outros complementos: Van der, De la etc) Sobrenomes compostos ( Mendes Caldeira) pesquise separadamente: MENDES e depois CALDEIRA. Tendo dificuldade com caracter Ø HAMMERSHØY – pesquise HAMMERSH HØJBJERG – pesquise JBJERG BUSCAPRONTA não reproduz dados genealógicos das pessoas, sendo necessário acessar os documentos Internet correspondentes para obter tais dados e informações. DESEJAMOS PLENO SUCESSO EM SUA PESQUISA. -
Rūta Stanevičiūtė Nick Zangwill Rima Povilionienė Editors Between Music
Numanities - Arts and Humanities in Progress 7 Rūta Stanevičiūtė Nick Zangwill Rima Povilionienė Editors Of Essence and Context Between Music and Philosophy Numanities - Arts and Humanities in Progress Volume 7 Series Editor Dario Martinelli, Faculty of Creative Industries, Vilnius Gediminas Technical University, Vilnius, Lithuania [email protected] The series originates from the need to create a more proactive platform in the form of monographs and edited volumes in thematic collections, to discuss the current crisis of the humanities and its possible solutions, in a spirit that should be both critical and self-critical. “Numanities” (New Humanities) aim to unify the various approaches and potentials of the humanities in the context, dynamics and problems of current societies, and in the attempt to overcome the crisis. The series is intended to target an academic audience interested in the following areas: – Traditional fields of humanities whose research paths are focused on issues of current concern; – New fields of humanities emerged to meet the demands of societal changes; – Multi/Inter/Cross/Transdisciplinary dialogues between humanities and social and/or natural sciences; – Humanities “in disguise”, that is, those fields (currently belonging to other spheres), that remain rooted in a humanistic vision of the world; – Forms of investigations and reflections, in which the humanities monitor and critically assess their scientific status and social condition; – Forms of research animated by creative and innovative humanities-based -
Shape Dynamics and Lipid Hydrodynamics of Bilayer Membranes: Modeling, Simulation and Experiments
Universitat Politecnica` de Catalunya Programa de Doctorat en Enginyeria Civil Departament de Matematica` Aplicada III Shape dynamics and lipid hydrodynamics of bilayer membranes: modeling, simulation and experiments by Mohammad Rahimi Doctoral Thesis Advisor: Marino Arroyo Barcelona, December 2012 Abstract Shape dynamics and lipid hydrodynamics of bilayer membranes: modeling, simulation and experiments Mohammad Rahimi Biological membranes are continuously brought out of equilibrium, as they shape organelles, package and transport cargo, or respond to external actions. The dy- namics of lipid membranes are very complex due to the tight interplay between the bilayer architecture, the shape dynamics, the rearrangement of the lipid molecules, and their interactions with adjacent structures. The main goal of the present work is to understand the dynamical shape deformations and reorganizations of lipid bilay- ers, including lipid hydrodynamics, and the mechanical shaping and stabilization of highly curved membrane structures. Towards this goal, we develop theory, simulation methods, and perform experiments. We formulate and numerically implement a continuum model of the shape dynam- ics and lipid hydrodynamics, which describes the bilayer by its mid-surface and by a lipid density field for each monolayer. In this model, the viscoelastic response of bilayers is determined by the stretching and curvature elasticity, and by the inter- monolayer friction and the membrane interfacial shear viscosity. In contrast with previous studies, our numerical approach incorporates the main physics, is fully non- linear, does not assume predefined shapes, and can access a wide range of time and length scales. We apply our model to describe the dynamics of biologically relevant experimental observations, which are insufficiently understood through simpler mod- els introducing geometrical and physical simplifications. -
Influence of Global and Local Membrane
membranes Article Influence of Global and Local Membrane Curvature on Mechanosensitive Ion Channels: A Finite Element Approach Omid Bavi 1,2, Charles D. Cox 2, Manouchehr Vossoughi 1,3, Reza Naghdabadi 1,4, Yousef Jamali 5,6 and Boris Martinac 2,7,* 1 Institute for Nanoscience and Nanotechnology, Sharif University of Technology, 89694-14588 Tehran, Iran; [email protected] (O.B.); [email protected] (M.V.); [email protected] (R.N.) 2 Molecular Cardiology and Biophysics Division/Mechanosensory Biophysics Laboratory, Victor Chang Cardiac Research Institute, Darlinghurst, NSW 2010, Australia; [email protected] (O.B.); [email protected] (C.D.C.) 3 Biochemical & Bioenvironmental Research Center (BBRC), 89694-14588 Tehran, Iran 4 Department of Mechanical Engineering, Sharif University of Technology, 89694-14588 Tehran, Iran 5 Department of Mathematics and Bioscience, Tarbiat Modares University, Jalal Ale Ahmad Highway, 14115-111 Tehran, Iran; [email protected] 6 Computational physical Sciences Research Laboratory, School of Nano-Science, Institute for Research in Fundamental Sciences (IPM), 19395-5531 Tehran, Iran; [email protected] 7 St Vincent’s Clinical School, Faculty of Medicine, University of New South Wales, Darlinghurst, NSW 2010, Australia * Correspondence: [email protected]; Tel.: +61-2-9295-8743; Fax: +61-2-9295-8770 Academic Editor: Serdar Kuyucak Received: 1 January 2016; Accepted: 25 January 2016; Published: 5 February 2016 Abstract: Mechanosensitive (MS) channels are ubiquitous molecular force sensors that respond to a number of different mechanical stimuli including tensile, compressive and shear stress. MS channels are also proposed to be molecular curvature sensors gating in response to bending in their local environment. -
Atomic Force Microscopy Study on the Mechanics of Influenza Viruses and Liposomes
Atomic force microscopy study on the mechanics of influenza viruses and liposomes Dissertation for the award of the degree “Doctor rerum naturalium” In the program of Physics of Biological and Complex Systems Göttingen Graduate School for Neurosciences, Biophysics, and Molecular Biosciences of the Georg-August-Universität Göttingen submitted by Sai Li from Hubei, China Göttingen, 2012 Members of the Thesis Committee Dr. Iwan A.T. Schaap (Reviewer, Examination board) Atomic Force Microscopy group at the III. Physikalisches Institut Faculty of Physics Prof. Dr. Andreas Janshoff (Reviewer, Examination board) Institute for Physical Chemistry Faculty of Chemistry Prof. Dr. Christoph F. Schmidt (Examination board) III. Physikalisches Institut Faculty of Physics Prof. Dr. Jörg Enderlein (Examination board) III. Physikalisches Institut Faculty of Physics Prof. Dr. Sarah Köster (Examination board) Institute for X-Ray Physics Faculty of Physics Prof. Dr. Bert de Groot (Examination board) Computational Biomolecular Dynamics Group Max Planck Institute for Biophysical Chemistry Date of oral examination: November, 2012 II I, Sai Li, hereby certify that my doctoral thesis entitled “Atomic force microscopy study on the mechanics of influenza viruses and liposomes” has been written independently and with no other sources and aids than quoted. Signature: III IV Table of contents Abbreviations ........................................................................................................ 1 Abstract ................................................................................................................ -
Biophysical Implications of Lipid Bilayer Rheometry for Mechanosensitive Channels
Biophysical implications of lipid bilayer rheometry for mechanosensitive channels Navid Bavia,b, Yoshitaka Nakayamab, Omid Bavic, Charles D. Coxb, Qing-Hua Qind, and Boris Martinaca,b,1 aSt. Vincent’s Clinical School, Faculty of Medicine, University of New South Wales, Darlinghurst, NSW 2010, Australia; bMolecular Cardiology and Biophysics Division, Victor Chang Cardiac Research Institute, Darlinghurst, NSW 2010, Australia; cInstitute for Nanoscience and Nanotechnology, Sharif University of Technology, 8969414588 Tehran, Iran; and dResearch School of Engineering, Australian National University, Canberra, ACT 0200, Australia Edited by Ching Kung, University of Wisconsin–Madison, Madison, WI, and approved August 14, 2014 (received for review May 15, 2014) The lipid bilayer plays a crucial role in gating of mechanosensitive model, of including in the calculations the boundary conditions (MS) channels. Hence it is imperative to elucidate the rheological caused by a rigid cylindrical pipette and no assumption for volume properties of lipid membranes. Herein we introduce a framework conservation during MA. The material properties resulting from to characterize the mechanical properties of lipid bilayers by these models were imported separately into a continuum FE model combining micropipette aspiration (MA) with theoretical model- (Fig. S1 A–C). This permitted comparisons between the FE model ing. Our results reveal that excised liposome patch fluorometry is parameters and experimentally derived results to define the best superior to traditional cell-attached MA for measuring the intrinsic description of the continuum behavior of azolectin bilayers. Using our alternative models, we compare the membrane tension in an mechanical properties of lipid bilayers. The computational results ’ also indicate that unlike the uniform bilayer tension estimated by azolectin liposome patch estimated using Laplace slawwiththe ’ membrane tension obtained from our computations. -
Analysis of MESSENGER High-Resolution Images of Mercury's
PUBLICATIONS Journal of Geophysical Research: Planets RESEARCH ARTICLE Analysis of MESSENGER high-resolution images 10.1002/2016JE005070 of Mercury's hollows and implications Key Points: for hollow formation • Average depth of 2518 hollows in 552 high-resolution images of Mercury is David T. Blewett1, Amanda C. Stadermann2, Hannah C. Susorney3, Carolyn M. Ernst1, Zhiyong Xiao4,5, 24 ± 16 m 1 1 1 6 1 • Hollows enlarge by scarp retreat and Nancy L. Chabot , Brett W. Denevi , Scott L. Murchie , Francis M. McCubbin , Mallory J. Kinczyk , 7 8,9 cease to deepen when a devolatilized Jeffrey J. Gillis-Davis , and Sean C. Solomon lag becomes thick enough to prevent further volatile loss 1Planetary Exploration Group, The Johns Hopkins University Applied Physics Laboratory, Laurel, Maryland, USA, • Carbon could be lost from Mercury's 2Department of Earth and Planetary Sciences, Washington University, St. Louis, Missouri, USA, 3Department of Earth and surface via ion sputtering or Planetary Sciences, The Johns Hopkins University, Baltimore, Maryland, USA, 4China University of Geosciences, Wuhan, conversion of graphite to methane by 5 6 proton bombardment China, Centre for Earth Evolution and Dynamics, University of Oslo, Oslo, Norway, NASA Johnson Space Center, Houston, Texas, USA, 7Hawaii Institute of Geophysics and Planetology, University of Hawaii, Honolulu, Hawaii, USA, 8Lamont-Doherty Earth Observatory, Columbia University, Palisades, New York, USA, 9Department of Terrestrial Magnetism, Carnegie Supporting Information: Institution of Washington, Washington, District of Columbia, USA • Supporting Information S1 • Data Set S1 • Data Set S2 Abstract High-resolution images from MESSENGER provide morphological information on the nature and Correspondence to: origin of Mercury's hollows, small depressions that likely formed when a volatile constituent was lost from the D. -
Lipid Bilayer Composition Modulates the Unfolding Free Energy of a Knotted Α-Helical Membrane Protein
Lipid bilayer composition modulates the unfolding free PNAS PLUS energy of a knotted α-helical membrane protein M. R. Sandersa, H. E. Findlaya, and P. J. Bootha,1 aDepartment of Chemistry, King’s College London, SE1 1DB London, United Kingdom Edited by David Baker, University of Washington, Seattle, WA, and approved January 12, 2018 (received for review August 18, 2017) α-Helical membrane proteins have eluded investigation of their gregation, most helical proteins are thought to insert directly into thermodynamic stability in lipid bilayers. Reversible denaturation the membrane cotranslationally with the assistance of the curves have enabled some headway in determining unfolding free translocon apparatus. Although the exact mechanism of mem- energies. However, these parameters have been limited to deter- brane protein insertion is unclear, the final stages of protein gent micelles or lipid bicelles, which do not possess the same me- folding are most likely to occur in the lipid bilayer (4, 5). Equally, chanical properties as lipid bilayers that comprise the basis of lipids can induce posttranslational repositioning of helices and natural membranes. We establish reversible unfolding of the protein orientation within the membrane (6, 7). If the unique membrane transporter LeuT in lipid bilayers, enabling the compar- folded state is an equilibrium structure, then it should be possible ison of apparent unfolding free energies in different lipid composi- to achieve the folded structure via other pathways, as has been demonstrated for example from coexpression (8), from reas- tions. LeuT is a bacterial ortholog of neurotransmitter transporters sembly of protein fragments (9), or from cell-free synthesis (10). -
Lipid Bilayer Composition Modulates the Unfolding Free Energy of A
Lipid bilayer composition modulates the unfolding free PNAS PLUS energy of a knotted α-helical membrane protein M. R. Sandersa, H. E. Findlaya, and P. J. Bootha,1 aDepartment of Chemistry, King’s College London, SE1 1DB London, United Kingdom Edited by David Baker, University of Washington, Seattle, WA, and approved January 12, 2018 (received for review August 18, 2017) α-Helical membrane proteins have eluded investigation of their gregation, most helical proteins are thought to insert directly into thermodynamic stability in lipid bilayers. Reversible denaturation the membrane cotranslationally with the assistance of the curves have enabled some headway in determining unfolding free translocon apparatus. Although the exact mechanism of mem- energies. However, these parameters have been limited to deter- brane protein insertion is unclear, the final stages of protein gent micelles or lipid bicelles, which do not possess the same me- folding are most likely to occur in the lipid bilayer (4, 5). Equally, chanical properties as lipid bilayers that comprise the basis of lipids can induce posttranslational repositioning of helices and natural membranes. We establish reversible unfolding of the protein orientation within the membrane (6, 7). If the unique membrane transporter LeuT in lipid bilayers, enabling the compar- folded state is an equilibrium structure, then it should be possible ison of apparent unfolding free energies in different lipid composi- to achieve the folded structure via other pathways, as has been demonstrated for example from coexpression (8), from reas- tions. LeuT is a bacterial ortholog of neurotransmitter transporters sembly of protein fragments (9), or from cell-free synthesis (10).