Cloning of a big tau microtubule-associated protein characteristic of the peripheral nervous system.

Por Goedert, M, Spillantini, M G, Crowther, R A
Publicado em 1992

Different configurational states of beta-amyloid and their distributions relative to plaques and tangles in Alzheimer disease.

Por Spillantini, M G, Goedert, M, Jakes, R, Klug, A
Publicado em 1990

Topographical relationship between beta-amyloid and tau protein epitopes in tangle-bearing cells in Alzheimer disease.

Por Spillantini, M G, Goedert, M, Jakes, R, Klug, A
Publicado em 1990

Influence of Drug-Carrier Polymers on Alpha-Synucleinopathies: A Neglected Aspect in New Therapies Development

Por Tonda-Turo, C., Herva, M., Chiono, V., Ciardelli, G., Spillantini, M. G.
Publicado no Biomed Res Int (2018)

Cloning and sequencing of the cDNA encoding an isoform of microtubule-associated protein tau containing four tandem repeats: differential expression of tau protein mRNAs in human b...

Por Goedert, M, Spillantini, M G, Potier, M C, Ulrich, J, Crowther, R A
Publicado em 1989

Somatodendritic localization and hyperphosphorylation of tau protein in transgenic mice expressing the longest human brain tau isoform.

Por Götz, J, Probst, A, Spillantini, M G, Schäfer, T, Jakes, R, Bürki, K, Goedert, M
Publicado em 1995

Tau Pathology in Two Dutch Families with Mutations in the Microtubule-Binding Region of Tau

Por Spillantini, M.G., Crowther, R.A., Kamphorst, W., Heutink, P., van Swieten, J.C.
Publicado em 1998

Nerve growth factor mRNA and protein increase in hypothalamus in a mouse model of aggression.

Por Spillantini, M G, Aloe, L, Alleva, E, De Simone, R, Goedert, M, Levi-Montalcini, R
Publicado em 1989

From genetics to pathology: tau and alpha-synuclein assemblies in neurodegenerative diseases.

Por Goedert, M, Spillantini, M G, Serpell, L C, Berriman, J, Smith, M J, Jakes, R, Crowther, R A
Publicado em 2001

Familial multiple-system tauopathy with presenile dementia is localized to chromosome 17.

Por Murrell, J R, Koller, D, Foroud, T, Goedert, M, Spillantini, M G, Edenberg, H J, Farlow, M R, Ghetti, B
Publicado em 1997

Atrophy patterns in histologic vs clinical groupings of frontotemporal lobar degeneration

Por Pereira, J M.S., Williams, G B., Acosta-Cabronero, J, Pengas, G, Spillantini, M G., Xuereb, J H., Hodges, J R., Nestor, P J.
Publicado em 2009

Vascular variant of prion protein cerebral amyloidosis with tau-positive neurofibrillary tangles: the phenotype of the stop codon 145 mutation in PRNP.

Por Ghetti, B, Piccardo, P, Spillantini, M G, Ichimiya, Y, Porro, M, Perini, F, Kitamoto, T, Tateishi, J, Seiler, C, Frangione, B, Bugiani, O, Giaccone, G, Prelli, F, Goedert, M, Dlouhy, S R, Tagliavini, F
Publicado em 1996

Worldwide distribution of PSEN1 Met146Leu mutation: A large variability for a founder mutation

Por Bruni, A. C., Bernardi, L., Colao, R., Rubino, E., Smirne, N., Frangipane, F., Terni, B., Curcio, S.A.M., Mirabelli, M., Clodomiro, A., Di Lorenzo, R., Maletta, R., Anfossi, M., Gallo, M., Geracitano, S., Tomaino, C., Muraca, M. G., Leotta, A., Lio, S. G., Pinessi, L., Rainero, I., Sorbi, S., Nee, L., Milan, G., Pappatá, S., Postiglione, A., Abbamondi, N., Forloni, G., St. George Hyslop, P., Rogaeva, E., Bugiani, O., Giaccone, G., Foncin, J. F., Spillantini, M. G., Puccio, G.
Publicado em 2010