508 Publications (Page 18 of 21)
1996
Vascular variant of prion protein cerebral amyloidosis with tau-positive neurofibrillary tangles: the phenotype of the stop codon 145 mutation in PRNP.Ghetti, Bernardino⋅Piccardo, Pedro⋅Spillantini, Maria G⋅Ichimiya, Y⋅Porro, M⋅Perini, F⋅Kitamoto, Tetsuyuki⋅Tateishi, J⋅Seiler, C⋅Frangione, Blas⋅Bugiani, O⋅Giaccone, G⋅Prelli, F⋅Goedert, M⋅Dlouhy, Stephen R and Tagliavini, FProceedings of the National Academy of Sciences of the United States of America, vol. 93, (no. 2), pp. 744-8, 1996/Jan/23.
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Vascular Variant of Prion Protein Cerebral Amyloidosis with τ -Positive Neurofibrillary Tangles: The Phenotype of the Stop Codon 145 Mutation in PRNPGhetti, Bernardino⋅Piccardo, Pedro⋅Spillantini, Maria⋅Ichimiya, Yousuke⋅Porro, Monica⋅Perini, Francesco⋅Kitamoto, Tetsuyuki⋅Tateishi, Jun⋅Seiler, Charles⋅Frangione, Blas⋅Bugiani, Orso⋅Giaccone, Giorgio⋅Prelli, Frances⋅Goedert, Michel⋅Dlouhy, Stephen and Tagliavini, FabrizioProceedings of the National Academy of Sciences of the United States of America, vol. 93, (no. 2), pp. 748, 19960123.
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1995
Altered IGFBP5 gene expression in the cerebellar external germinal layer of weaver mutant miceLee, Wei-Hua⋅Wang, Guo-Ming⋅Lo, Teresa⋅Triarhou, Lazaros C and Ghetti, BernardinoMolecular Brain Research, vol. 30, (no. 2), pp. 268, 1995.
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Detection of apoptosis in weaver cerebellum by electron microscopic in situ end-labeling of fragmented DNAMigheli, Antonio⋅Attanasio, Angelo⋅Lee, Wei-Hua⋅Bayer, Shirley A and Ghetti, BernardinoNeuroscience Letters, vol. 199, (no. 1), pp. 56, 1995.
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Dopaminergic parameters in the striatum and substantia nigra of seven strains of mice: Higher density in striatum of CAST compared to BALB miceRichter, Judith A⋅Brenneman, MG⋅Dlouhy, Stephen R and Ghetti, BernardinoNeurochemical Research, vol. 20, (no. 4), pp. 395-400, 1995.
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Gerstmann-Sträussler-Scheinker disease and the Indiana kindred.Ghetti, Bernardino⋅Dlouhy, Stephen R⋅Giaccone, G⋅Bugiani, O⋅Frangione, Blas⋅Farlow, Martin R and Tagliavini, FBrain Pathology (Zurich, Switzerland), vol. 5, (no. 1), pp. 61-75, 1995/Jan.
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Gerstmann-Sträussler-Scheinker disease (PRNP P102L): amyloid deposits are best recognized by antibodies directed to epitopes in PrP region 90-165.Piccardo, Pedro⋅Ghetti, Bernardino⋅Dickson, Dennis W⋅Vinters, H V⋅Giaccone, G⋅Bugiani, O⋅Tagliavini, F⋅Young, K⋅Dlouhy, S R and Seiler, CJournal of Neuropathology and Experimental Neurology, vol. 54, (no. 6), pp. 790-801, 1995/Nov.
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IMMUNOHISTOCHEMICAL LOCALIZATION OF APOLIPOPROTEIN E AND BETA AMYLOID IN ALZHEIMERʼS DISEASE: 83Basheeruddin, Khaja⋅Ilangovan, Saroja⋅Lee, John⋅Alfieri, Emilio⋅Faraldi, Francesco⋅Vakili, Saeed⋅Ghetti, Bernardino and Reyes, MarcJournal of Neuropathology and Experimental Neurology, vol. 54, (no. 3), pp. 432, 1995-May.
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Neurofibrillary tangles in Niemann-Pick disease type CSuzuki, Kinuko I⋅Suzuki, K⋅Parker, CC⋅Parker, Colette C⋅Pentchev, PG⋅Pentchev, Peter G⋅Katz, D.⋅Katz, David⋅Ghetti, B.⋅Ghetti, Bernardino⋅D'Agostino, AN⋅D'Agostino, Anthony N⋅Carstea, ED and Carstea, Eugene DActa Neuropathologica, vol. 89, (no. 3), pp. 238, 1995-02-01.
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Selective vulnerability of late-generated dopaminergic neurons of the substantia nigra in weaver mutant mice.Bayer, S A⋅Wills, K V⋅Triarhou, L C⋅Verina, T⋅Thomas, J D and Ghetti, BProceedings of the National Academy of Sciences of the United States of America, vol. 92, (no. 20), pp. 9137-9140, September 26, 1995.
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1994
Amyloid fibrils in Gerstmann-Sträussler-Scheinker disease (Indiana and Swedish kindreds) express only PrP peptides encoded by the mutant allele.Tagliavini, F⋅Prelli, F⋅Porro, M⋅Rossi, G⋅Giaccone, G⋅Farlow, Martin R⋅Dlouhy, S R⋅Ghetti, Bernardino⋅Bugiani, O and Frangione, BlasCell, vol. 79, (no. 4), pp. 695-703, 1994/Nov/18.
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Familial Gerstmann-Sträussler-Scheinker disease with neurofibrillary tangles.Ghetti, Bernardino⋅Tagliavini, F⋅Giaccone, G⋅Bugiani, O⋅Frangione, Blas⋅Farlow, M R and Dlouhy, S RMolecular Neurobiology, vol. 8, (no. 1), pp. 41-8, 1994/Feb.
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Fatal familial insomnia and familial Creutzfeldt-Jakob disease: Different prion proteins determined by a DNA polymorphismMonari, L.⋅Chen, Shu G⋅Brown, P.⋅Parchi, P.⋅Petersen, Robert B⋅Mikol, J.⋅Gray, F.⋅Cortelli, P.⋅Montagna, P.⋅Ghetti, Bernardino⋅Goldfarb, LG⋅Gajdusek, DC⋅Lugaresi, E.⋅Gambetti, Pierluigi and Autilio-Gambetti, L.Proceedings of the National Academy of Sciences, USA, vol. 91, (no. 7), pp. 2839-2842, 1994.
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Molecular characterization of a novel cDNA from murine cerebellum, developmental expression, and distribution in brain.Kambouris, M⋅Sangameswaran, L⋅Triarhou, L C⋅Kozak, C A⋅Dlouhy, S R⋅Ghetti, B and Hodes, M EBrain research. Molecular brain research, vol. 25, (no. 3-4), pp. 192-199, September 1994.
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Novel cDNA clones obtained by antibody screening of a mouse cerebellar cDNA expression library.Kambouris, M⋅Triarhou, L C⋅Dlouhy, S R⋅Sangameswaran, L⋅Luo, F⋅Ghetti, B and Hodes, M EBrain research. Molecular brain research, vol. 25, (no. 3-4), pp. 183-191, September 1994.
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Studies on the striatal dopamine uptake system of weaver mutant mice and effects of ventral mesencephalic grafts.Triarhou, L C⋅Stotz, E H⋅Low, Walter C⋅Norton, J⋅Ghetti, Bernardino⋅Landwehrmeyer, B⋅Palacios, J M and Simon, Jay RNeurochemical research, vol. 19, (no. 11), pp. 1349-58, 1994/Nov.
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The weaver mutant mouse as a model of nigrostriatal dysfunction.Simon, Jay R and Ghetti, BernardinoMolecular Neurobiology, vol. 9, (no. 1-3), pp. 183-9, 1994 Aug-Dec.
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1993
A68 is a component of paired helical filaments of Gerstmann-Sträussler-Scheinker disease, Indiana kindredTagliavini, Fabrizio⋅Tagliavini, F⋅Giaccone, Giorgio⋅Giaccone, G⋅Prelli, F⋅Prelli, Frances⋅Verga, Laura⋅Verga, L⋅Porro, M⋅Porro, Monica⋅Trojanowski, John Q⋅Trojanowski, John Q⋅Farlow, Martin R⋅Farlow, Martin R⋅Frangione, Blas⋅Frangione, Blas⋅Ghetti, Bernardino⋅Ghetti, B⋅Bugiani, Orso and Bugiani, OBrain Research, vol. 616, (no. 1), pp. 329, 1993.
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Cellular distribution of the RNA transcripts of a newly discovered gene in the brain of normal, weaver, Purkinje cell degeneration and reeler mutant mice as evidenced by in situ hybridization histochemistry.Kambouris, M⋅Sangameswaran, L⋅Dlouhy, S R⋅Hodes, M E⋅Ghetti, B and Triarhou, L CBrain research. Molecular brain research, vol. 18, (no. 4), pp. 321-328, June 1993.
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Corrections: Prion Protein Preamyloid and Amyloid Deposits in Gerstmann- Straussler-Scheinker Disease, Indiana KindredGiaccone, Giorgio⋅Giaccone, Giorgio⋅Verga, Laura⋅Verga, Laura⋅Bugiani, Orso⋅Bugiani, Orso⋅Frangione, Blas⋅Frangione, Blas⋅Serban, Dan⋅Serban, Dan⋅Prusiner, Stanley⋅Prusiner, Stanley⋅Farlow, Martin⋅Farlow, Martin⋅Ghetti, Bernardino⋅Ghetti, Bernardino⋅Tagliavini, Fabrizio and Tagliavini, FabrizioProceedings of the National Academy of Sciences of the United States of America, vol. 90, (no. 1), pp. 362, 19930101.
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Is there a significant somatodendritic uptake of dopamine in the substantia nigra? Evidence from the weaver mutant mouse.Simon, Jay R and Ghetti, BernardinoNeurochemistry International, vol. 22, (no. 5), pp. 471-7, 1993/May.
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Regional Distribution of Amyloid beta -Protein Precursor, Growth-associated Phosphoprotein-43 and Microtubule-associated Protein 2 Messenger RNAs in the Nigrostriatal System of Normal and Weaver Mutant Mice and Effects of Ventral Mesencephalic GraftsSola, C.⋅Mengod, G.⋅Low, Walter C⋅Norton, J.⋅Ghetti, Bernardino⋅Palacios, JM and Triarhou, LCEuropean Journal of Neuroscience, vol. 5, (no. 11), pp. 1442-1452, 1993.
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RFLP analysis for APP 717 mutations associated with Alzheimer's disease.Zeldenrust, Steven R⋅Murrell, Jill R⋅Farlow, Martin R⋅Ghetti, Bernardino⋅Roses, Allen D and Benson, Merrill DJournal of Medical Genetics, vol. 30, (no. 6), pp. 476-478, 1993.
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Synthetic peptides homologous to prion protein residues 106-147 form amyloid-like fibrils in vitro.Tagliavini, F⋅Prelli, F⋅Verga, L⋅Giaccone, G⋅Sarma, R⋅Gorevic, P⋅Ghetti, B⋅Passerini, F⋅Ghibaudi, E and Forloni, GProceedings of the National Academy of Sciences of the United States of America, vol. 90, (no. 20), pp. 9678-9682, October 15, 1993.
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