508 Publications (Page 15 of 21)
2001
Primary Myopathy and Accumulation of PrPSc-Like Molecules in Peripheral Tissues of Transgenic Mice Expressing a Prion Protein Insertional Mutation
Chiesa, Roberto⋅Chiesa, Roberto⋅Pestronk, Alan⋅Pestronk, Alan⋅Schmidt, Robert E⋅Schmidt, Robert E⋅Tourtellotte, Warren G⋅Tourtellotte, Warren G⋅Ghetti, Bernardino⋅Ghetti, Bernardino⋅Piccardo, Pedro⋅Piccardo, Pedro⋅Harris, David A and Harris, David A
Neurobiology of Disease, vol. 8, (no. 2), pp. 288, April 2001. | Journal Article
 
Prion Proteins with Different Conformations Accumulate in Gerstmann-Sträussler-Scheinker Disease Caused by A117V and F198S Mutations
Piccardo, Pedro⋅Piccardo, Pedro⋅Piccardo, Pedro⋅Piccardo, Pedro⋅Liepnieks, J J⋅Liepnieks, Juris J⋅Liepnieks, Juris J⋅Liepnieks, Juris J⋅William, A⋅William, Albert⋅William, Albert⋅William, Albert⋅Dlouhy, Stephen R⋅Dlouhy, Stephen R⋅Dlouhy, S R⋅Dlouhy, Stephen R⋅Farlow, Martin R⋅Farlow, M R⋅Farlow, Martin R⋅Farlow, Martin R⋅Young, Katherine⋅Young, K⋅Young, Katherine⋅Young, Katherine⋅Nochlin, David⋅Nochlin, David⋅Nochlin, David⋅Nochlin, David⋅Bird, Thomas D⋅Bird, Thomas D⋅Bird, Thomas D⋅Bird, T D⋅Nixon, Randal R⋅Nixon, Randal R⋅Nixon, Randal R⋅Nixon, R R⋅Ball, Melvyn J⋅Ball, M J⋅Ball, Melvyn J⋅Ball, Melvyn J⋅DeCarli, Charles⋅DeCarli, C⋅DeCarli, Charles⋅DeCarli, Charles⋅Bugiani, O⋅Bugiani, Orso⋅Bugiani, Orso⋅Bugiani, Orso⋅Tagliavini, Fabrizio⋅Tagliavini, Fabrizio⋅Tagliavini, F⋅Tagliavini, Fabrizio⋅Benson, Merrill D⋅Benson, Merrill D⋅Benson, Merrill D⋅Benson, M D⋅Ghetti, Bernardino⋅Ghetti, B⋅Ghetti, Bernardino and Ghetti, Bernardino
The American Journal of Pathology, vol. 158, (no. 6), pp. 2207, 2001. | Journal Article
2000
Accumulation of protease-resistant prion protein (PrP) and apoptosis of cerebellar granule cells in transgenic mice expressing a PrP insertional mutation
Chiesa, R.⋅Drisaldi, B.⋅Quaglio, E.⋅Migheli, A.⋅Piccardo, Pedro⋅Ghetti, Bernardino and Harris, David A
Proceedings of the National Academy of Sciences, USA, vol. 97, (no. 10), pp. 5580-5585, 2000. | Journal Article
 
Accumulation of protease-resistant prion protein (PrP) and apoptosis of cerebellar granule cells in transgenic mice expressing a PrP insertional mutation.
Chiesa, R⋅Drisaldi, B⋅Quaglio, E⋅Migheli, A⋅Piccardo, Pedro⋅Ghetti, Bernardino and Harris, David A
Proceedings of the National Academy of Sciences of the United States of America, vol. 97, (no. 10), pp. 5574-9, 2000/May/9. | Journal Article
 
Accumulation of Protease-Resistant Prion Protein (PrP) and Apoptosis of Cerebellar Granule Cells in Transgenic Mice Expressing a PrP Insertional Mutation
Shmuel, A.⋅Chiesa, Roberto⋅Grinvald, Amiram⋅Drisaldi, Bettina⋅Quaglio, Elena⋅Migheli, Antonio⋅Piccardo, Pedro⋅Ghetti, Bernardino and Harris, David
Proceedings of the National Academy of Sciences of the United States of America, vol. 97, (no. 10), pp. 5579, 20000509. | Journal Article
 
A S52R mutation in neuroserpin is associated with myoclonic epilepsy and dementia
Yazaki, Masahide⋅Yazaki, Masahide⋅Benson, Merrill D⋅Benson, Merrill D⋅Liepnieks, Juris J⋅Liepnieks, Juris J⋅Farlow, Martin R⋅Farlow, Martin R⋅Piccardo, Pedro⋅Piccardo, Pedro⋅Takao, Masaki⋅Takao, Masaki⋅Murrell, Jill R⋅Murrell, Jill R⋅Ghetti, Bernardino and Ghetti, Bernardino
Neurobiology of Aging, vol. 21, pp. 66, 2000. | Journal Article
 
A transgenic model of a familial prion disease
Harris, David⋅Harris, David A⋅Chiesa, Roberto⋅Drisaldi, Bettina⋅Quaglio, Elena⋅Migheli, Antonio⋅Piccardo, Pedro and Ghetti, Bernardino
Neurobiology of Aging, vol. 21, pp. 209, 2000. | Journal Article
 
Caspase-3 is activated in Alzheimer disease but not in frontotemporal dementia
Marcon, Gabriella⋅Atzori, Cristiana⋅Srinivasan, Anu N⋅Okazawa, Hitoshi⋅Ghetti, Bernardino and Migheli, Antonio
Neurobiology of Aging, vol. 21, pp. 81, 2000. | Journal Article
 
Caspase-3 mediates apoptosis in Gerstmann-Sträussler-Scheinker (GSS) disease
Migheli, Antonio⋅Atzori, Cristiana⋅Srinivasan, Anu N and Ghetti, Bernardino
Neurobiology of Aging, vol. 21, pp. 266, 2000. | Journal Article
 
Clinical characteristics in a family with early-onset Alzheimer disease caused by a mutation (V717L) in the APP gene
Hake, Ann M⋅Hake, Ann M⋅Hake, Ann M⋅Murrell, Jill R⋅Murrell, Jill R⋅Murrell, Jill R⋅Unverzagt, Frederick W⋅Unverzagt, Frederick W⋅Unverzagt, Frederick W⋅Ghetti, Bernardino⋅Ghetti, Bernardino⋅Ghetti, Bernardino⋅Farlow, Martin R⋅Farlow, Martin R and Farlow, Martin R
Neurobiology of Aging, vol. 21, pp. 59, 2000. | Journal Article
 
Codeposition of cystatin C with amyloid-ß protein in the brain of Alzheimer's disease patients
Pawlik, Monika⋅Sastre, Magdalena⋅Kumar, Asok⋅Gallo, Gloria⋅Ghetti, Bernardino⋅Tagliavini, Fabrizio and Levy, Efrat
Neurobiology of Aging, vol. 21, pp. 194, 2000. | Journal Article
 
Determination of the amino-terminal cleavage site of PRPRES in GSS F198S
Piccardo, Pedro⋅Piccardo, Pedro⋅Liepnieks, Juris J⋅Liepnieks, Juris J⋅William, Albert⋅William, Albert⋅Dlouhy, Stephen R⋅Dlouhy, Stephen R⋅Bugiani, Orso⋅Bugiani, Orso⋅Tagliavini, Fabrizio⋅Tagliavini, Fabrizio⋅Benson, Merrill D⋅Benson, Merrill D⋅Ghetti, Bernardino and Ghetti, Bernardino
Neurobiology of Aging, vol. 21, pp. 268, 2000. | Journal Article
 
Early-onset Alzheimer disease caused by a new mutation (V717L) in the amyloid precursor protein gene.
Murrell, Jill R⋅Murrell, Jill R⋅Hake, Ann M⋅Hake, A M⋅Quaid, Kimberly A⋅Quaid, K A⋅Farlow, M R⋅Farlow, Martin R⋅Ghetti, Bernardino and Ghetti, B
Archives of neurology. , vol. 57, (no. 6), pp. 885-7, 2000/Jun. | Journal Article
 
Evidence of elevated intracellular calcium levels in weaver homozygote mice
Harkins, Amy B⋅Dlouhy, S.⋅Ghetti, B.⋅Cahill, AL⋅Won, L.⋅Heller, B.⋅Heller, A. and Fox, AP
Journal of Physiology (London), vol. 524, (no. 2), pp. 447-455, 2000. | Journal Article
 
Familial presenile dementia with Parkinsonism in a Japanese family
Takao, Masaki⋅Hayakawa, Isao⋅Ikeda, Eiji⋅Murrell, Jill R⋅Piccardo, Pedro⋅Ghetti, Bernardino and Koto, Atsuo
Neurobiology of Aging, vol. 21, pp. 267, 2000. | Journal Article
 
Hereditary lateral sclerosis and Alzheimer disease associated with mutation at codon 261 of the presenilin 1 (PS1) gene
Farlow, Martin R⋅Farlow, Martin R⋅Murrell, Jill R⋅Murrell, Jill R⋅Hulette, Christine M⋅Hulette, Christine M⋅Ghetti, Bernardino and Ghetti, Bernardino
Neurobiology of Aging, vol. 21, pp. 62, 2000. | Journal Article
 
Increased presence of amino-terminally-truncated Aβ-peptides in presenilin 1 early-onset familial Alzheimer disease
Russo, Claudio⋅Saido, Takaomi C⋅Hulette, Christine⋅Price, Kathleen⋅Ghetti, Bernardino⋅Teller, Jan K⋅Tabaton, Massimo⋅Schettini, Gennaro and Gambetti, Pierluigi L
Neurobiology of Aging, vol. 21, pp. 194, 2000. | Journal Article
 
Neuropathology of Gerstmann‐Sträussler‐Scheinker disease
Bugiani, Orso⋅Giaccone, Giorgio⋅Piccardo, Pedro⋅Morbin, Michela⋅Tagliavini, Fabrizio and Ghetti, Bernardino
Microscopy Research and Technique, vol. 50, (no. 1), pp. 15, 1 July 2000. | Journal Article
 
Neuroserpin Mutation S52R Causes Neuroserpin Accumulation in Neurons and Is Associated with Progressive Myoclonus Epilepsy
Takao, M.⋅Benson, Merrill D⋅Murrell, Jill R⋅Yazaki, M.⋅Piccardo, Pedro⋅Unverzagt, Frederick⋅Davis, Robin L⋅Holohan, PD⋅Lawrence, Daniel A⋅Richardson, R.⋅Farlow, Martin R and Ghetti, Bernardino
Journal of Neuropathology & Experimental Neurology, vol. 59, (no. 12), pp. 1070-1086, 2000. | Journal Article
 
Presenilin-1 mutations in Alzheimer's disease
Russo, C.⋅Schettini, G.⋅Saido, TC⋅Hulette, Christine M⋅Lippa, Carol F⋅Lannfelt, L.⋅Ghetti, Bernardino⋅Gambetti, Pierluigi⋅Tabaton, Massimo and Teller, Jan K
Nature, vol. 405, (no. 6786), pp. 531-532, 2000. | Journal Article
 
Presymptomatic Genetic Testing with an APP Mutation in Early-Onset Alzheimer Disease: A Descriptive Study of Sibship Dynamics
Quaid, Kimberly A⋅Murrell, Jill R⋅Hake, Ann M⋅Farlow, Martin R and Ghetti, Bernardino
Journal of Genetic Counseling, vol. 9, (no. 4), pp. 327, Aug 2000. | Journal Article
 
Progress in hereditary tauopathies: a mutation in the Tau gene (G389R) causes a Pick disease-like syndrome.
Ghetti, Bernardino⋅Murrell, J R⋅Zolo, P⋅Spillantini, M G and Goedert, M
Annals of the New York Academy of Sciences. , vol. 920, pp. 52-62, 2000. | Journal Article
 
Tau Gene Mutations in Frontotemporal Dementia and Parkinsonism Linked to Chromosome 17 (FTDP‐17): Their Relevance for Understanding the Neurogenerative Process
GOEDERT, MICHEL⋅Ghetti, Bernardino and SPILLANTINI, MARIA GRAZIA
Annals of the New York Academy of Sciences, vol. 920, (no. 1), pp. 83, December 2000. | Journal Article
 
The weaver gene continues to target late-generated dopaminergic neurons in midbrain areas at P90
Marti, J.⋅Martı́, Joaquı́n⋅Wills, Katherine V⋅Tsiopos, Katherine V⋅Ghetti, B.⋅Ghetti, Bernardino⋅Bayer, SA and Bayer, Shirley A
Developmental Brain Research, vol. 122, (no. 2), pp. 181, 2000. | Journal Article
 
The weaver gene has no effect on the generation patterns of mesencephalic dopaminergic neurons
Martı́, Joaquı́n⋅Marti, J.⋅Wills, Katherine V⋅Tsiopos, Katherine V⋅Ghetti, Bernardino⋅Ghetti, B.⋅Bayer, Shirley A and Bayer, SA
Developmental Brain Research, vol. 122, (no. 2), pp. 172, 2000-08-30. | Journal Article