Missense and splice site mutations in tau associated with FTDP-17: Multiple pathogenic mechanismsHUTTON, Michael.Neurology. 2001, Vol 56, Num 11, pp S21-S25, issn 0028-3878, SUP4Article

A novel calcium-binding protein is associated with tau proteins in tauopathyVEGA, Irving E; TRAVERSE, Edwin E; FERRER-ACOSTA, Yancy et al.Journal of neurochemistry. 2008, Vol 106, Num 1, pp 96-106, issn 0022-3042, 11 p.Article

MAX II : A low-cost, high-performance LUT-based CPLDLEVENTIS, Paul; VEST, Brad; HUTTON, Michael et al.Custom integrated circuits conference. 2004, pp 443-446, isbn 0-7803-8495-4, 1Vol, 4 p.Conference Paper

Filamentous Tau in oligodendrocytes and astrocytes of transgenic mice expressing the human tau isoform with the P301L mutationLIN, Wen-Lang; LEWIS, Jada; YEN, Shu-Hui et al.The American journal of pathology. 2003, Vol 162, Num 1, pp 213-218, issn 0002-9440, 6 p.Article

Frontotemporal dementia and parkinsonism associated with the IVSI+IG→A mutation in progranulin : a clinicopathologic studyGOEDERT, Michel; GRAZIA SPILLANTINI, Maria; RADEMAKERS, Rosa et al.Brain. 2006, Vol 129, issn 0006-8950, 2808-2810,3103-3114 [15 p.], 11Article

Heritability of plasma amyloid β in typical late-onset Alzheimer's disease pedigreesERTEKIN-TANER, Nilufer; GRAFF-RADFORD, Neill; YOUNKIN, Linda H et al.Genetic epidemiology. 2001, Vol 21, Num 1, pp 19-30, issn 0741-0395Article

Elevated amyloid β protein (Aβ42) and late onset Alzheimer's disease are associated with single nucleotide polymorphisms in the urokinase-type plasminogen activator geneERTEKIN-TANER, Nilüfer; RONALD, James; KELLY, Jason et al.Human molecular genetics (Print). 2005, Vol 14, Num 3, pp 447-460, issn 0964-6906, 14 p.Article

Rapid neurofibrillary tangle formation after localized gene transfer of mutated tauKLEIN, Ronald L; LIN, Wen-Lang; DICKSON, Dennis W et al.The American journal of pathology. 2004, Vol 164, Num 1, pp 347-353, issn 0002-9440, 7 p.Article

A novel tau mutation in exon 9 (1260V) causes a four-repeat tauopathyGROVER, Andrew; ENGLAND, Elisabet; HUTTON, Michael et al.Experimental neurology (Print). 2003, Vol 184, Num 1, pp 131-140, issn 0014-4886, 10 p.Article

Clinical features and disease haplotypes of individuals with the N279K tau gene mutation: A comparison of the pallidopontonigral degeneration kindred and a French familyTSUBOI, Yoshio; UITTI, Ryan J; WSZOLEK, Zbigniew K et al.Archives of neurology (Chicago). 2002, Vol 59, Num 6, pp 943-950, issn 0003-9942Article

A decade of modeling Alzheimer's disease in transgenic miceMCGOWAN, Eileen; ERIKSEN, Jason; HUTTON, Michael et al.Trends in genetics (Regular ed.). 2006, Vol 22, Num 5, pp 281-289, issn 0168-9525, 9 p.Article

Adaptive delay estimation for partitioning-driven PLD placement : System-level interconnect prediction (SLIP)HUTTON, Michael; ADIBSAMII, Khosrow; LEAVER, Andrew et al.IEEE transactions on very large scale integration (VLSI) systems. 2003, Vol 11, Num 1, pp 60-63, issn 1063-8210, 4 p.Article

Tau genotype: No effect on onset, symptom severity, or survival in progressive supranuclear palsyLITVAN, Irene; BAKER, Matt; HUTTON, Michael et al.Neurology. 2001, Vol 57, Num 1, pp 138-140, issn 0028-3878Article

H1/H1 Genotype Influences Symptom Severity in Corticobasal SyndromeLITVAN, Irene; CHISM, Amanda; LITVAN, Juan et al.Movement disorders. 2010, Vol 25, Num 6, pp 760-763, issn 0885-3185, 4 p.Article

Whole-genome analysis of sporadic amyotrophic lateral sclerosisDUNCKLEY, Travis; HUENTELMAN, Matthew J; HESTERLEE, Sharon E et al.The New England journal of medicine. 2007, Vol 357, Num 8, pp 775-788, issn 0028-4793, 14 p.Article

A family with tau-negative frontotemporal dementia and neuronal intranuclear inclusions linked to chromosome 17MACKENZIE, Ian R; BAKER, Matthew; MELQUIST, Stacey et al.Brain. 2006, Vol 129, pp 853-867, issn 0006-8950, 15 p., 4Article

Fine mapping of the α-T catenin gene to a quantitative trait locus on chromosome 10 in late-onset Alzheimer's disease pedigreesERTEKIN-TANER, Nilüfer; RONALD, James; SINGLETON, Adam et al.Human molecular genetics (Print). 2003, Vol 12, Num 23, pp 3133-3143, issn 0964-6906, 11 p.Article

The L266V tau mutation is associated with frontotemporal dementia and Pick-like 3R and 4R tauopathyHOGG, Marion; GRUJIC, Zoran M; GAMBLIN, T. C et al.Acta neuropathologica. 2003, Vol 106, Num 4, pp 323-336, issn 0001-6322, 14 p.Article

The genetic and pathological classification of familial frontotemporal dementiaMORRIS, Huw R; KHAN, M. Nadeem; LEES, Andrew J et al.Archives of neurology (Chicago). 2001, Vol 58, Num 11, pp 1813-1816, issn 0003-9942Article

Progranulin Is a Chemoattractant for Microglia and Stimulates Their Endocytic ActivityPICKFORD, Fiona; MARCUS, Jacob; HUTTON, Michael et al.The American journal of pathology. 2011, Vol 178, Num 1, pp 284-295, issn 0002-9440, 12 p.Article

Progranulin expression correlates with dense-core amyloid plaque burden in Alzheimer disease mouse modelsPERESON, Sandra; WILS, Hans; VAN BROECKHOVEN, Christine et al.Journal of pathology (Print). 2009, Vol 219, Num 2, pp 173-181, issn 0022-3417, 9 p.Article

Risk-reducing effect of education in Alzheimer's diseaseSANDO, Sigrid Botne; MELQUIST, Stacey; CANNON, Ashley et al.International journal of geriatric psychiatry. 2008, Vol 23, Num 11, pp 1156-1162, issn 0885-6230, 7 p.Article

Clinical features of pathologic subtypes of behavioral-variant frontotemporal dementiaHU, William T; MANDREKAR, Jayawant N; PARISI, Joseph E et al.Archives of neurology (Chicago). 2007, Vol 64, Num 11, pp 1611-1616, issn 0003-9942, 6 p.Article

Presenilin 1 mutation in an African American family presenting with atypical Alzheimer dementiaRIPPON, Gregory A; CROOK, Richard; BAKER, Matthew et al.Archives of neurology (Chicago). 2003, Vol 60, Num 6, pp 884-888, issn 0003-9942, 5 p.Article

Epidemiology and genetics of frontotemporal dementia/Pick's diseaseBIRD, Thomas; KNOPMAN, David; VANSWIETEN, John et al.Annals of neurology. 2003, Vol 54, pp S29-S31, issn 0364-5134, SUP5Conference Paper