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Annals of Neurology|October 17, 2001
Pick's disease associated with the novel Tau gene mutation K369IM Neumann, W Schulz-Schaeffer, R A Crowther, et al.Neurobiology of Aging|May 1, 1995
Molecular dissection of the paired helical filamentM Goedert, M G Spillantini, R Jakes, et al.American Journal of Human Genetics|November 5, 1997
Familial multiple-system tauopathy with presenile dementia is localized to chromosome 17J R Murrell, D Koller, T Foroud, et al.Proceedings of the National Academy of Sciences of the United States of America|July 8, 1999
Structure of tau exon 10 splicing regulatory element RNA and destabilization by mutations of frontotemporal dementia and parkinsonism linked to chromosome 17L Varani, M Hasegawa, M G Spillantini, et al.Pharmacology, Biochemistry, and Behavior|May 1, 1986
Inhibition of penicillin-induced EEG discharges by low doses of morphine or naloxone in the rabbit. Evidence for a possible non-opioid receptor-mediated mechanism at the sensorimotor cortexM G Spillantini, M MassottiCellular and Molecular Life Sciences : CMLS|July 3, 2007
Physiological and pathological properties of alpha-synucleinG K Tofaris, M G SpillantiniJournal of Neuropathology and Experimental Neurology|November 23, 2000
Tau gene mutation K257T causes a tauopathy similar to Pick's diseaseC Rizzini, M Goedert, J R Hodges, et al.Journal of Neuropathology and Experimental Neurology|December 22, 1999
Tau gene mutation G389R causes a tauopathy with abundant pick body-like inclusions and axonal depositsJ R Murrell, M G Spillantini, P Zolo, et al.Brain Pathology (Zurich, Switzerland)|April 18, 1998
Frontotemporal dementia and Parkinsonism linked to chromosome 17: a new group of tauopathiesM G Spillantini, T D Bird, B GhettiFEBS Letters|December 6, 2001
alpha-synuclein metabolism and aggregation is linked to ubiquitin-independent degradation by the proteasomeG K Tofaris, R Layfield, M G SpillantiniPageof 25