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Molecular Genetics & Genomic Medicine|July 15, 2021
SUMOylated Senataxin functions in genome stability, RNA degradation, and stress granule disassembly, and is linked with inherited ataxia and motor neuron diseaseCraig L Bennett, Albert R La SpadaNeurobiology of Disease|June 1, 2018
TFEB dysregulation as a driver of autophagy dysfunction in neurodegenerative disease: Molecular mechanisms, cellular processes, and emerging therapeutic opportunitiesConstanza J Cortes, Albert R La SpadaAutophagy|April 14, 2009
Development of selective nutrient deprivation as a system to study autophagy induction and regulation in neuronsJessica E Young, Albert R La SpadaNeurology|September 10, 2009
ALS motor phenotype heterogeneity, focality, and spread: deconstructing motor neuron degenerationJohn M Ravits, Albert R La SpadaNeuron|March 13, 2012
Intercellular (mis)communication in neurodegenerative diseaseGwenn A Garden, Albert R La SpadaHandbook of Clinical Neurology|January 13, 2018
The CAG-polyglutamine repeat diseases: a clinical, molecular, genetic, and pathophysiologic nosologyColleen A Stoyas, Albert R La SpadaSTAR Protocols|March 31, 2023
Protocol for mapping double-stranded DNA break sites across the genome with translocation capture sequencingJoe R Delaney, Albert R La SpadaGenome Medicine|September 5, 2012
The expanding world of stem cell modeling of Huntington's disease: creating tools with a promising futureJacqueline M Ward, Albert R La SpadaNature Reviews. Genetics|February 24, 2010
Repeat expansion disease: progress and puzzles in disease pathogenesisAlbert R La Spada, J Paul TaylorAmerican Journal of Medical Genetics. Part A|December 9, 2017
Therapy development in Huntington disease: From current strategies to emerging opportunitiesAudrey S Dickey, Albert R La SpadaPageof 16