508 Publications (Page 17 of 21)
1998
Phenotypic variability of Gerstmann-Sträussler-Scheinker disease is associated with prion protein heterogeneity.Piccardo, Pedro⋅Dlouhy, Stephen R⋅Lievens, P M⋅Young, K⋅Bird, Thomas D⋅Nochlin, David⋅Dickson, Dennis W⋅Vinters, Harry V⋅Zimmerman, T R⋅Mackenzie, Ian⋅Kish, S J⋅Ang, L C⋅De Carli, C⋅Pocchiari, M⋅Brown, P⋅Gibbs, C J⋅Gajdusek, D C⋅Bugiani, O⋅Ironside, J. W⋅Tagliavini, F and Ghetti, BernardinoJournal of Neuropathology and Experimental Neurology, vol. 57, (no. 10), pp. 979-88, 1998/Oct.
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1997
A possible role for tyrosine kinases in the regulation of the neuronal dopamine transporter in mouse striatumSimon, Jay R⋅Bare, DJ⋅Ghetti, Bernardino and Richter, Judith ANeuroscience Letters, vol. 224, (no. 3), pp. 201-205, 1997.
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Atrophy and loss of dopaminergic mesencephalic neurons in heterozygous weaver mice.Verina, T⋅Verina, Tatyana⋅Norton, James⋅Norton, J A⋅Sorbel, J J⋅Sorbel, Jeffrey⋅Triarhou, Lazaros⋅Triarhou, L C⋅Laferty, D⋅Laferty, Donald⋅Richter, J A⋅Richter, Judith⋅Simon, Jay⋅Simon, J R⋅Ghetti, B and Ghetti, BernardinoExperimental brain research, vol. 113, (no. 1), pp. 5-12, January 1997.
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Decreased IGF-I gene expression during the apoptosis of Purkinje cells in pcd miceZhang, Wei⋅Ghetti, Bernardino and Lee, Wei-HuaDevelopmental Brain Research, vol. 98, (no. 2), pp. 176, 1997.
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Diverse cell death pathways result from a single missense mutation in weaver mouse.Migheli, A⋅Piva, R⋅Wei, Jian Jun⋅Attanasio, A⋅Casolino, S⋅Hodes, M E⋅Dlouhy, S R⋅Bayer, S A and Ghetti, BThe American journal of pathology, vol. 151, (no. 6), pp. 1629-38, 1997/Dec.
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Familial multiple system tauopathy with presenile dementia: A disease with abundant neuronal and glial tau filamentsSpillantini, Maria G⋅Goedert, M.⋅Crowther, RA⋅Murrell, Jill R⋅Farlow, Martin R and Ghetti, BernardinoProceedings of the National Academy of Sciences, USA, vol. 94, (no. 8), pp. 4113-4118, 1997.
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Familial multiple-system tauopathy with presenile dementia is localized to chromosome 17.Murrell, Jill R⋅Koller, D⋅Foroud, T⋅Goedert, M⋅Spillantini, M G⋅Edenberg, H J⋅Farlow, M R and Ghetti, BAmerican journal of human genetics. , vol. 61, (no. 5), pp. 1131-8, 1997/Nov.
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Gerstmann–Sträussler–Scheinker disease with the PRNP P102L mutation and valine at codon 129Young, Katherine⋅Clark, H.Brent⋅Piccardo, Pedro⋅Dlouhy, Stephen R and Ghetti, BernardinoMolecular Brain Research, vol. 44, (no. 1), pp. 150, 1997.
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In Situ Hybridization Analysis of Girk2 Expression in the Developing Central Nervous System in Normal and Weaver MiceWei, Jianjun⋅Wei, Jian Jun⋅Dlouhy, S R⋅Dlouhy, Stephen⋅Bayer, Shirley⋅Bayer, S⋅Piva, R⋅Piva, Roberto⋅Verina, Tatyana⋅Verina, T⋅Wang, Y⋅Wang, Yi⋅Feng, Y⋅Feng, Yue⋅Dupree, Brenda⋅Dupree, B⋅Hodes, M E⋅Hodes, M⋅Ghetti, Bernardino and Ghetti, BJournal of Neuropathology and Experimental Neurology, vol. 56, (no. 7), pp. 771, 1997-July.
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In vitro evidence that the reduction in mesencepalic dopaminergic neurons in the weaver heterozygote is not due to a failure in target cell interactionWon, Lisa⋅Ghetti, Bernardino⋅Heller, Barbara and Heller, AExperimental Brain Research, vol. 115, (no. 1), pp. 179, 19970600.
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Lack of apolipoprotein E dramatically reduces amyloid β-peptide depositionLittle, Sheila P⋅Piccardo, Pedro⋅Dodel, Richard C⋅Altstiel, Larry⋅Johnstone, Edward M⋅Bales, Kelly R⋅Verina, Tatyana⋅Hyslop, Paul⋅Paul, Steven M⋅Cummins, David J⋅Du, Yansheng⋅Bender, Mark and Ghetti, BernardinoNature Genetics, vol. 17, (no. 3), pp. 264, 199711.
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Neuropsychological function in patients with Gerstmann-Sträussler-Scheinker disease from the Indiana Kindred (F198S)Unverzagt, Frederick W⋅UNVERZAGT, FREDERICK W⋅UNVERZAGT, FREDERICK W⋅Farlow, Martin R⋅Farlow, M R⋅FARLOW, MARTIN R⋅NORTON, JAMES⋅Norton, J⋅NORTON, JAMES⋅DLOUHY, STEPHEN R⋅Dlouhy, S R⋅DLOUHY, STEPHEN R⋅Young, K⋅YOUNG, KATHERINE⋅YOUNG, KATHERINE⋅Ghetti, Bernardino⋅Ghetti, B and GHETTI, BERNARDINOJournal of the International Neuropsychological Society, vol. 3, (no. 2), pp. 178, 19970301.
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Subacute sclerosing panencephalitis manifesting as viral retinitis: clinical and histopathologic findings.Park, D W⋅Boldt, H. C⋅Massicotte, S J⋅Akang, E E⋅Roos, K L⋅Bodnar, A⋅Pless, J⋅Ghetti, B and Pascuzzi, R MAmerican journal of ophthalmology, vol. 123, (no. 4), pp. 533-42, 1997/Apr.
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Subacute sclerosis panencephalitis manifesting as viral retinitis: clinical and histopathologic findingsPark, Donald⋅Roos, Karen⋅Massicotte, Stephen⋅Bodnar, Adriana⋅Pascuzzi, Robert⋅Akang, Effiong⋅Boldt, H.⋅Pless, John⋅Park, Donald⋅Roos, Karen⋅Massicotte, Stephen⋅Bodnar, Adriana⋅Akang, Effiong⋅Boldt, H.⋅Pless, John⋅Ghetti, Bernardino⋅Ghetti, Bernardino and Pascuzzi, RobertAmerican Journal of Ophthalmology, vol. 123, (no. 4), pp. 533, 19970401.
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1996
Cloning a cDNA for Carbonyl Reductase (Cbr) from Mouse Cerebellum: Murine Genes That Express Cbr Map to Chromosomes 16 and 11Wei, Jianjun⋅Wei, Jian Jun⋅Dlouhy, S. R⋅Dlouhy, Stephen R⋅Hara, Akira⋅Hara, A.⋅Ghetti, B.⋅Ghetti, Bernardino⋅Hodes, M.E and Hodes, MEGenomics, vol. 34, (no. 1), pp. 148, 1996-05-15.
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Molecular basis of phenotypic variability in sporadc creudeldt‐jakob diseaseParchi, Piero⋅Parchi, Piero⋅Parchi, P.⋅Parchi, Piero⋅Castellani, R.⋅Castellani, Rudolph⋅Castellani, Rudolph⋅Castellani, Rudolph⋅Capellari, Sabina⋅Capellari, Sabina⋅Capellari, S.⋅Capellari, Sabina⋅Ghetti, B.⋅Ghetti, Bernardino⋅Ghetti, Bernardino⋅Ghetti, Bernardino⋅Young, Katherine⋅Young, Katherine⋅Young, Katherine⋅Young, K.⋅Chen, Shu G⋅Chen, Shu G⋅Chen, S. G.⋅Chen, Shu G.⋅Farlow, M.⋅Farlow, Martin⋅Farlow, Martin⋅Farlow, Martin⋅Dickson, Dennis W⋅Dickson, Dennis W.⋅Dickson, Dennis W⋅Dickson, D. W.⋅Sima, Anders A. F.⋅Sima, A. A.⋅Sima, Anders A. F⋅Sima, Anders A. F⋅Trojanowski, John Q⋅Trojanowski, J. Q.⋅Trojanowski, John Q⋅Trojanowski, John Q.⋅Petersen, Robert B⋅Petersen, R. B.⋅Petersen, Robert B⋅Petersen, Robert B.⋅Gambetti, Pierluigi⋅Gambetti, Pierluigi⋅Gambetti, P. and Gambetti, PierluigiAnnals of Neurology, vol. 39, (no. 6), pp. 778, June 1996.
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Phenotypic effects of the weaver gene are evident in the embryonic cerebellum but not in the ventral midbrain.Bayer, S A⋅Wills, K V⋅Wei, Jian Jun⋅Feng, Y⋅Dlouhy, S R⋅Hodes, M E⋅Verina, T and Ghetti, BBrain research. Developmental brain research, vol. 96, (no. 1-2), pp. 130-7, 1996/Oct/23.
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Prion protein amyloidosis.Ghetti, Bernardino⋅Piccardo, P⋅Frangione, B⋅Bugiani, O⋅Giaccone, G⋅Young, K⋅Prelli, F⋅Farlow, M R⋅Dlouhy, S R and Tagliavini, FBrain Pathology (Zurich, Switzerland), vol. 6, (no. 2), pp. 127-45, 1996/Apr.
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Prion Protein AmyloidosisGhetti, Bernardino⋅Piccardo, Pedro⋅Frangione, Bias⋅Bugiani, Orso⋅Giaccone, Giorgio⋅Young, Katherine⋅Prelli, Frances⋅Farlow, Martin R⋅Dlouhy, Stephen R and Tagliavini, FabrizioBrain Pathology, vol. 6, (no. 2), pp. 145, April 1996.
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Prion protein hereditary amyloidosis: Parenchymal and vascularGhetti, Bernardino⋅Piccardo, Pedro⋅Frangione, Blas⋅Bugiani, O.⋅Giaccone, G.⋅Young, K.⋅Prelli, F.⋅Farlow, MR⋅Dlouhy, S. R and Tagliavini, F.Seminars in Virology, vol. 7, (no. 3), pp. 189-200, 1996.
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Proteinase-K-Resistant Prion Protein Isoforms in Gerstmann-Straussler-Scheinker Disease (Indiana Kindred)Piccardo, Pedro⋅Piccardo, Pedro⋅Seiler, Charles⋅Seiler, Charles⋅Dlouhy, Stephen⋅Dlouhy, Stephen⋅Young, Katherine⋅Young, Katherine⋅Farlow, Martin⋅Farlow, Martin⋅Prelli, Frances⋅Prelli, Frances⋅Frangione, Blas⋅Frangione, Blas⋅Bugiani, Orso⋅Bugiani, Orso⋅Tagliavini, Fabrizio⋅Tagliavini, Fabrizio⋅Ghetti, Bernardino and Ghetti, BernardinoJournal of Neuropathology and Experimental Neurology, vol. 55, (no. 11), pp. 1163, 1996-November.
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Proteinase-K-resistant prion protein isoforms in Gerstmann-Sträussler-Scheinker disease (Indiana kindred).Piccardo, Pedro⋅Seiler, C⋅Dlouhy, Stephen R⋅Young, K⋅Farlow, Martin R⋅Prelli, F⋅Frangione, Blas⋅Bugiani, O⋅Tagliavini, F and Ghetti, BernardinoJournal of neuropathology and experimental neurology, vol. 55, (no. 11), pp. 1157-63, 1996/Nov.
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PrP27-30 is a normal soluble prion protein fragment released by human platelets.Perini, F⋅Vidal, Ruben G⋅Ghetti, Bernardino⋅Tagliavini, F⋅Frangione, Blas and Prelli, FBiochemical and biophysical research communications, vol. 223, (no. 3), pp. 572-7, 1996/Jun/25.
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PRP.sub.27-30Is a Normal Soluble Prion Protein Fragment Released by Human PlateletsPerini, Francesco⋅Perini, Francesco⋅Vidal, Ruben⋅Vidal, Ruben⋅Ghetti, Bernardino⋅Ghetti, Bernardino⋅Tagliavini, Fabrizio⋅Tagliavini, Fabrizio⋅Frangione, Blas⋅Frangione, Blas⋅Prelli, Frances and Prelli, FrancesBiochemical and Biophysical Research Communications, vol. 223, (no. 3), pp. 572, 19960625.
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The weaver mutation changes the ion selectivity of the affected inwardly rectifying potassium channel GIRK2Tong, Yanhe⋅Tong, Y⋅Wei, Jianjun⋅Wei, Jian Jun⋅Zhang, Shengwen⋅Zhang, S⋅Strong, Judith A⋅Strong, J A⋅Dlouhy, S R⋅Dlouhy, Stephen R⋅Hodes, M.E⋅Hodes, M E⋅Ghetti, B⋅Ghetti, Bernardino⋅Yu, Lei and Yu, LFEBS Letters, vol. 390, (no. 1), pp. 68, 1996.
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