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Michael L Hutton

Showing results (21-30 of 41) with videos related to

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Archives of Neurology|January 11, 2007
Progranulin mutations in primary progressive aphasia: the PPA1 and PPA3 familiesMarsel Mesulam, Nancy Johnson, Thomas A Krefft, et al.
The Journal of Biological Chemistry|November 20, 2014
Conformation determines the seeding potencies of native and recombinant Tau aggregatesBenjamin Falcon, Annalisa Cavallini, Rachel Angers, et al.
Archives of Neurology|March 14, 2007
Voxel-based morphometry in frontotemporal lobar degeneration with ubiquitin-positive inclusions with and without progranulin mutationsJennifer L Whitwell, Clifford R Jack, Matthew Baker, et al.
Neuron|December 11, 2012
A plaque-specific antibody clears existing β-amyloid plaques in Alzheimer's disease miceRonald B Demattos, Jirong Lu, Ying Tang, et al.
Acta Neuropathologica|February 18, 2014
A novel in vivo model of tau propagation with rapid and progressive neurofibrillary tangle pathology: the pattern of spread is determined by connectivity, not proximityZeshan Ahmed, Jane Cooper, Tracey K Murray, et al.
Archives of Neurology|April 10, 2002
Association between apolipoprotein E genotype and Alzheimer disease in African American subjectsNeill R Graff-Radford, Robert C Green, Rodney C P Go, et al.
Neurogenetics|October 19, 2013
SLC20A2 and THAP1 deletion in familial basal ganglia calcification with dystoniaMatt Baker, Audrey J Strongosky, Monica Y Sanchez-Contreras, et al.
The American Journal of Pathology|June 5, 2010
Accelerated lipofuscinosis and ubiquitination in granulin knockout mice suggest a role for progranulin in successful agingZeshan Ahmed, Hong Sheng, Ya-Fei Xu, et al.
Parkinsonism & Related Disorders|January 2, 2007
Clinical-pathologic study of biomarkers in FTDP-17 (PPND family with N279K tau mutation)Zoe Arvanitakis, Robert J Witte, Dennis W Dickson, et al.
Journal of Neuropathology and Experimental Neurology|February 7, 2007
Neuropathologic features of frontotemporal lobar degeneration with ubiquitin-positive inclusions with progranulin gene (PGRN) mutationsKeith A Josephs, Zeshan Ahmed, Omi Katsuse, et al.
Pageof 5

Showing results (21-30 of 41) with videos related to

Sort By:
Pageof 5
Archives of Neurology|January 11, 2007
Progranulin mutations in primary progressive aphasia: the PPA1 and PPA3 familiesMarsel Mesulam, Nancy Johnson, Thomas A Krefft, et al.
The Journal of Biological Chemistry|November 20, 2014
Conformation determines the seeding potencies of native and recombinant Tau aggregatesBenjamin Falcon, Annalisa Cavallini, Rachel Angers, et al.
Archives of Neurology|March 14, 2007
Voxel-based morphometry in frontotemporal lobar degeneration with ubiquitin-positive inclusions with and without progranulin mutationsJennifer L Whitwell, Clifford R Jack, Matthew Baker, et al.
Neuron|December 11, 2012
A plaque-specific antibody clears existing β-amyloid plaques in Alzheimer's disease miceRonald B Demattos, Jirong Lu, Ying Tang, et al.
Acta Neuropathologica|February 18, 2014
A novel in vivo model of tau propagation with rapid and progressive neurofibrillary tangle pathology: the pattern of spread is determined by connectivity, not proximityZeshan Ahmed, Jane Cooper, Tracey K Murray, et al.
Archives of Neurology|April 10, 2002
Association between apolipoprotein E genotype and Alzheimer disease in African American subjectsNeill R Graff-Radford, Robert C Green, Rodney C P Go, et al.
Neurogenetics|October 19, 2013
SLC20A2 and THAP1 deletion in familial basal ganglia calcification with dystoniaMatt Baker, Audrey J Strongosky, Monica Y Sanchez-Contreras, et al.
The American Journal of Pathology|June 5, 2010
Accelerated lipofuscinosis and ubiquitination in granulin knockout mice suggest a role for progranulin in successful agingZeshan Ahmed, Hong Sheng, Ya-Fei Xu, et al.
Parkinsonism & Related Disorders|January 2, 2007
Clinical-pathologic study of biomarkers in FTDP-17 (PPND family with N279K tau mutation)Zoe Arvanitakis, Robert J Witte, Dennis W Dickson, et al.
Journal of Neuropathology and Experimental Neurology|February 7, 2007
Neuropathologic features of frontotemporal lobar degeneration with ubiquitin-positive inclusions with progranulin gene (PGRN) mutationsKeith A Josephs, Zeshan Ahmed, Omi Katsuse, et al.
Pageof 5