PDF-The cytoskeleton as a soft glassy material (Fredberg & Fabry) Jeffre

The cytoskeleton as a soft glassy material Fredberg Fabry twisting field displacementcell rotation Fig 1a from Fabry Maksym et al 2003 Scanning EM of a bead b. Frank . Candre. Tommy Palm. Vidit. . Talati. Varun. Kumar. Eric Yi. Structure. Microtubules (Tubulin Polymer). Microfilaments (Actin Filaments). Intermediate Filaments. Function. Give mechanical support to the cell and maintain its shape. Network of Protein Filaments. Used in:. Structural Support. Cell Movement. Movement of Vesicles within Cells. Composed of three types of Cytoskeletal fibers. Actin Filaments. Microtubules. Intermediate Filaments. By Kevin Partlow, Neil Perry, and Chris . Paszkiewicz. Cilia and Flagella. Cilia-numerous minute hair like organelles. Flagella-identical to the cilia but there is less of them and they are smaller. Location and Functions. . Spectrographs. Measurements . of the line shift.. a(. sin. a. sin. b. ). g. rating constant. Echelle. spectrometer. The first . standard grating . is optimized for a single lower . order. The . echelle. The cytoskeleton is a network of protein fibers within a cell, that crisscross the cytoplasm of all eukaryotic cells. The cytoskeleton is a very dynamic system that is constantly assembling and . dissembling. . By: Tim Yacoub and Lizette Magdaleno . Cytoskeleton Overview. Cytoskeleton is a “network of fibers that extend[s] throughout the cytoplasm,”(113). . It’s three structures: microtubules, microfilaments, and intermediate filaments. nrtypically have intrinsic coercivity less than 1000 Am-1 They are used primarily to enhance and/or channel the flux produced by an electric current The main parameter often used as a figure of meri Unit 1: Cells and Proteins. Advanced Higher Biology. Miss Aitken. Structure and Function of the Cytoskeleton. The cytoskeleton is a network of fibres made from protein. It extends the whole way through the cytoplasm.. Dr. Michael L. West. Division of Nephrology. Department of Medicine. Dalhousie University. Halifax NS. Canada. mlwest@dal.ca. Fabry Disease. . OMIM #301500. Glycosphingolipid= Gb3. Most specific therapies in Fabry disease increase . IntroductionFabry disease (FD) arises from an X-linked defect in lipid storage, whereby deicient or -galactosidase A (-gal A) activity leads to systemic deposition of glyco-sphingolipids, mainly Page 64 of 69 FMNry diseMse: ProPoPype of IysosomMl SPorMge Gisorder RiPO sysPemic Hrene SMn-Román-MonserrMP*, JuMn-RMmón Gimeno-BlMnes Article InfoArticle Notes Fabry disease is a rare inherited m • What is Fabry Disease?• What Causes Fabry?• How Common is Fabry? Guide to Understanding Fabry Disease mps@mpssociety.or.ukwww.mpssociety.or.uk Dianosis of Fabry DiseaseFabry Dis method. PhD student: . Ameer . Al-. juboory. . Supervisors: . Jem . Rongong. , Charles Lord. sub-structuring. layered damping. This . study involves a composite material comprising stiff platelets distributed within a soft matrix to provide high stiffness and damping simultaneously. Supported by Sanofi Genzyme. Agenda. Pathogenesis of . Fabry. Disease. Evaluation of . Fabry. Disease. Fabry. Disease Management. Learning Objectives. Discuss the pathophysiology of . Fabry. disease and its impact on kidney function to increase awareness.