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The Journal of Biological Chemistry|March 12, 2010
Mutant huntingtin fragments form oligomers in a polyglutamine length-dependent manner in vitro and in vivoJustin Legleiter, Emily Mitchell, Gregor P Lotz, et al.
Frontiers in Synaptic Neuroscience|April 5, 2021
Disposition of Proteins and Lipids in Synaptic Membrane Compartments Is Altered in Q175/Q7 Huntington's Disease Mouse StriatumMaria Iuliano, Connor Seeley, Ellen Sapp, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|April 2, 2010
Aberrant Rab11-dependent trafficking of the neuronal glutamate transporter EAAC1 causes oxidative stress and cell death in Huntington's diseaseXueyi Li, Antonio Valencia, Ellen Sapp, et al.
Journal of Neuroscience Research|July 31, 2009
Mutant huntingtin and glycogen synthase kinase 3-beta accumulate in neuronal lipid rafts of a presymptomatic knock-in mouse model of Huntington's diseaseAntonio Valencia, Patrick B Reeves, Ellen Sapp, et al.
Journal of Neurochemistry|July 2, 2009
Polyglutamine expansion in huntingtin alters its interaction with phospholipidsKimberly B Kegel, Ellen Sapp, Jonathan Alexander, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|January 13, 2004
Huntingtin bodies sequester vesicle-associated proteins by a polyproline-dependent interactionZheng-Hong Qin, Yumei Wang, Ellen Sapp, et al.
The Journal of Biological Chemistry|March 1, 2012
Native mutant huntingtin in human brain: evidence for prevalence of full-length monomerEllen Sapp, Antonio Valencia, Xueyi Li, et al.
Plos One|February 16, 2019
Huntingtin associates with the actin cytoskeleton and α-actinin isoforms to influence stimulus dependent morphology changesAdelaide Tousley, Maria Iuliano, Elizabeth Weisman, et al.
The Journal of Biological Chemistry|June 15, 2014
Preconditioning stimuli induce autophagy via sphingosine kinase 2 in mouse cortical neuronsRui Sheng, Tong-Tong Zhang, Valeria D Felice, et al.
Journal of Huntington'S Disease|October 1, 2016
Cellular Analysis of Silencing the Huntington's Disease Gene Using AAV9 Mediated Delivery of Artificial Micro RNA into the Striatum of Q140/Q140 MiceAllison M Keeler, Ellen Sapp, Kathryn Chase, et al.
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