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Methods in Molecular Biology (Clifton, N.J.)|January 9, 2010
Protein aggregate characterization in models of neurodegenerative diseaseAndrew T N Tebbenkamp, David R Borchelt
Human Molecular Genetics|February 11, 2011
Premature death and neurologic abnormalities in transgenic mice expressing a mutant huntingtin exon-2 fragmentAndrew T N Tebbenkamp, Debbie Swing, Lino Tessarollo, et al.
Current Opinion in Neurology|February 26, 2014
The developmental transcriptome of the human brain: implications for neurodevelopmental disordersAndrew T N Tebbenkamp, A Jeremy Willsey, Matthew W State, et al.
Journal of Neuropathology and Experimental Neurology|May 8, 2010
Partial depletion of CREB-binding protein reduces life expectancy in a mouse model of Huntington diseaseAlexandra M Klevytska, Andrew T N Tebbenkamp, Alena V Savonenko, et al.
Journal of Neuropathology and Experimental Neurology|April 7, 2007
Characterization of huntingtin pathologic fragments in human Huntington disease, transgenic mice, and cell modelsGabriele Schilling, Alexandra Klevytska, Andrew T N Tebbenkamp, et al.
Journal of Huntington'S Disease|July 27, 2014
Experimental mutagenesis of huntingtin to map cleavage sites: different outcomes in cell and mouse modelsAndrew T N Tebbenkamp, Guilian Xu, Zoe B Siemienski, et al.
Biorxiv : the Preprint Server for Biology|June 25, 2024
Early Developmental Origins of Cortical Disorders Modeled in Human Neural Stem CellsXoel Mato-Blanco, Suel-Kee Kim, Alexandre Jourdon, et al.
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