Elizabeth M. Gibbs Department of Integrative Biology and Physiology University of California Biography Publications Institution JoVE Articles Elizabeth M. Gibbs has not added a biography. If you are Elizabeth M. Gibbs and would like to personalize this page please email our Author Liaison for assistance. Publications High Levels of Sarcospan Are Well Tolerated and Act As a Sarcolemmal Stabilizer to Address Skeletal Muscle and Pulmonary Dysfunction in DMD Human Molecular Genetics. 12, 2016 | Pubmed ID: 27798107 Differentiation-related Glycan Epitopes Identify Discrete Domains of the Muscle Glycocalyx Glycobiology. Oct, 2016 | Pubmed ID: 27236198 Defective Tubulation Associated with the Myopathy Causing S619L DNM2 Mutation Disease Models & Mechanisms. Oct, 2013 | Pubmed ID: 24135484 Swimming into Prominence: the Zebrafish As a Valuable Tool for Studying Human Myopathies and Muscular Dystrophies The FEBS Journal. Jun, 2013 | Pubmed ID: 23809187 Hemimegalencephaly, a Paradigm for Somatic Postzygotic Neurodevelopmental Disorders Current Opinion in Neurology. Apr, 2013 | Pubmed ID: 23449172 Two Dynamin-2 Genes Are Required for Normal Zebrafish Development PloS One. 2013 | Pubmed ID: 23418470 Neuromuscular Junction Abnormalities in DNM2-related Centronuclear Myopathy Journal of Molecular Medicine (Berlin, Germany). Jun, 2013 | Pubmed ID: 23338057 Congenital Myopathies: an Update Current Neurology and Neuroscience Reports. Apr, 2012 | Pubmed ID: 22392505 Synapses on Demand Require Dendrites at the Ready: How Defining Stages of Dendritic Development in Vitro Could Inform Studies of Behaviorally Driven Information Storage in the Brain Developmental Psychobiology. Jul, 2011 | Pubmed ID: 21678392 The Role of MTMR14 in Autophagy and in Muscle Disease Autophagy. Aug, 2010 | Pubmed ID: 20595810 Loss of Myotubularin Function Results in T-tubule Disorganization in Zebrafish and Human Myotubular Myopathy PLoS Genetics. Feb, 2009 | Pubmed ID: 19197364 Membrane Traffic and Muscle: Lessons from Human Disease Traffic (Copenhagen, Denmark). Jul, 2008 | Pubmed ID: 18266915 ופשוט נמוכים Assay למדידת Ambulation במודלים של העכבר של ניוון Elizabeth M. Gibbs1,2, Rachelle H. Crosbie-Watson1,2,3,4 1Department of Integrative Biology and Physiology, University of California, 2Center for Duchenne Muscular Dystrophy, University of California, 3Department of Neurology, David Geffen School of Medicine, University of California, 4Molecular Biology Institute, University of California JoVE 56772 Behavior ניתוח של עוברי וזחל myofibers שלד דג הזברה מהכנות ניתקו Eric J. Horstick1, Elizabeth M. Gibbs1, Xingli Li1, Ann E. Davidson1, James J. Dowling1 1Departments of Pediatrics and Neurology, University of Michigan JoVE 50259 Biology
ופשוט נמוכים Assay למדידת Ambulation במודלים של העכבר של ניוון Elizabeth M. Gibbs1,2, Rachelle H. Crosbie-Watson1,2,3,4 1Department of Integrative Biology and Physiology, University of California, 2Center for Duchenne Muscular Dystrophy, University of California, 3Department of Neurology, David Geffen School of Medicine, University of California, 4Molecular Biology Institute, University of California JoVE 56772 Behavior
ניתוח של עוברי וזחל myofibers שלד דג הזברה מהכנות ניתקו Eric J. Horstick1, Elizabeth M. Gibbs1, Xingli Li1, Ann E. Davidson1, James J. Dowling1 1Departments of Pediatrics and Neurology, University of Michigan JoVE 50259 Biology