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Journal of Huntington'S Disease|February 27, 2018
Early Neurodegeneration in R6/2 Mice Carrying the Huntington's Disease Mutation with a Super-Expanded CAG Repeat, Despite Normal LifespanCatherine Kielar, A Jennifer MortonPlos One|August 1, 2012
Temporal separation of aggregation and ubiquitination during early inclusion formation in transgenic mice carrying the Huntington's disease mutationBelvin Gong, Catherine Kielar, A Jennifer MortonPlos One|March 7, 2012
Tensor-based morphometry and stereology reveal brain pathology in the complexin1 knockout mouseCatherine Kielar, Stephen J Sawiak, Paloma Navarro Negredo, et al.Experimental Neurology|May 7, 2009
Cerebellar pathology and motor deficits in the palmitoyl protein thioesterase 1-deficient mouseShannon L Macauley, David F Wozniak, Catherine Kielar, et al.Neurobiology of Disease|April 23, 2009
Progressive thalamocortical neuron loss in Cln5 deficient mice: Distinct effects in Finnish variant late infantile NCLCarina von Schantz, Catherine Kielar, Stine N Hansen, et al.Journal of Neuropathology and Experimental Neurology|December 20, 2007
Synaptic changes in the thalamocortical system of cathepsin D-deficient mice: a model of human congenital neuronal ceroid-lipofuscinosisSanna Partanen, Aleksi Haapanen, Catherine Kielar, et al.Neurobiology of Disease|October 19, 2006
Successive neuron loss in the thalamus and cortex in a mouse model of infantile neuronal ceroid lipofuscinosisCatherine Kielar, Lucy Maddox, Ellen Bible, et al.Human Molecular Genetics|July 31, 2009
Molecular correlates of axonal and synaptic pathology in mouse models of Batten diseaseCatherine Kielar, Thomas M Wishart, Alice Palmer, et al.Learning & Memory (Cold Spring Harbor, N.Y.)|May 21, 2011
Insulin receptor substrate 2 is a negative regulator of memory formationElaine E Irvine, Laura Drinkwater, Kasia Radwanska, et al.Pageof 1