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Nature Neuroscience|May 17, 2011
Interferon-γ induces progressive nigrostriatal degeneration and basal ganglia calcificationParamita Chakrabarty, Carolina Ceballos-Diaz, Wen-Lang Lin, et al.Acta Neuropathologica|May 13, 2015
Atypical multiple system atrophy is a new subtype of frontotemporal lobar degeneration: frontotemporal lobar degeneration associated with α-synucleinNaoya Aoki, Philip J Boyer, Cheryl Lund, et al.Journal of Neuropathology and Experimental Neurology|October 2, 2015
A Novel Tau Mutation in Exon 12, p.Q336H, Causes Hereditary Pick DiseasePawel Tacik, Michael DeTure, Kelly M Hinkle, et al.Journal of Neuropathology and Experimental Neurology|May 13, 2006
Atypical progressive supranuclear palsy with corticospinal tract degenerationKeith A Josephs, Omi Katsuse, Dayne A Beccano-Kelly, et al.The American Journal of Pathology|September 1, 2009
Overexpression of wild-type murine tau results in progressive tauopathy and neurodegenerationStephanie J Adams, Richard J P Crook, Michael Deture, et al.Acta Neuropathologica|April 29, 2015
A truncating SOD1 mutation, p.Gly141X, is associated with clinical and pathologic heterogeneity, including frontotemporal lobar degenerationMasataka Nakamura, Kevin F Bieniek, Wen-Lang Lin, et al.Human Molecular Genetics|August 16, 2015
Tau deposition drives neuropathological, inflammatory and behavioral abnormalities independently of neuronal loss in a novel mouse modelCasey Cook, Silvia S Kang, Yari Carlomagno, et al.Neuron|February 19, 2013
Unconventional translation of C9ORF72 GGGGCC expansion generates insoluble polypeptides specific to c9FTD/ALSPeter E A Ash, Kevin F Bieniek, Tania F Gendron, et al.The Journal of Experimental Medicine|February 17, 2019
rAAV-based brain slice culture models of Alzheimer's and Parkinson's disease inclusion pathologiesCara L Croft, Pedro E Cruz, Daniel H Ryu, et al.Human Molecular Genetics|July 2, 2019
Combining P301L and S320F tau variants produces a novel accelerated model of tauopathyEmily J Koller, Elsa Gonzalez De La Cruz, Timothy Machula, et al.Pageof 8