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Results: 1-25 | 26-44
Results: 1-25/44
Primary myopathy and accumulation of PrPSc-like molecules in peripheral tissues of transgenic mice expressing a prion protein insertional mutation
Authors: Chiesa, R Pestronk, A Schmidt, RE Tourtellotte, VG Ghetti, B Piccardo, P Harris, DA
Citation: R. Chiesa et al., Primary myopathy and accumulation of PrPSc-like molecules in peripheral tissues of transgenic mice expressing a prion protein insertional mutation, NEUROBIOL D, 8(2), 2001, pp. 279-288
Evidence that the loss of Purkinje cells and deep cerebellar nuclei neurons in homozygous weaver is not related to neurogenetic patterns
Authors: Marti, J Wills, KV Ghetti, B Bayer, SA
Citation: J. Marti et al., Evidence that the loss of Purkinje cells and deep cerebellar nuclei neurons in homozygous weaver is not related to neurogenetic patterns, INT J DEV N, 19(6), 2001, pp. 599-610
Endocytic disturbances distinguish among subtypes of Alzheimer's disease and related disorders
Authors: Cataldo, A Rebeck, GW Ghetti, B Hulette, C Lippa, C Van Broeckhovan, C van Duijn, C Cras, P Bogdanovic, N Bird, T Peterhoff, C Nixon, R
Citation: A. Cataldo et al., Endocytic disturbances distinguish among subtypes of Alzheimer's disease and related disorders, ANN NEUROL, 50(5), 2001, pp. 661-665
Alzheimer's disease - Molecular consequences of presenilin-1 mutation - Reply
Authors: Russo, C Schettini, G Saido, TC Hulette, C Lippa, C Lannfelt, L Ghetti, B Gambetti, P Tabaton, M Teller, JK
Citation: C. Russo et al., Alzheimer's disease - Molecular consequences of presenilin-1 mutation - Reply, NATURE, 411(6838), 2001, pp. 655-656
Ectopic white matter neurons, a developmental abnormality that may be caused by the PSEN1 S169L mutation in a case of familial AD with myoclonus and seizures
Authors: Takao, M Ghetti, B Murrell, JR Unverzagt, FW Giaccone, G Tagliavini, F Bugiani, O Piccardo, P Hulette, CM Crain, BJ Farlow, MR Heyman, A
Citation: M. Takao et al., Ectopic white matter neurons, a developmental abnormality that may be caused by the PSEN1 S169L mutation in a case of familial AD with myoclonus and seizures, J NE EXP NE, 60(12), 2001, pp. 1137-1152
Activation of the JNK/p38 pathway occurs in diseases characterized by tau protein pathology and is related to tau phosphorylation but not to apoptosis
Authors: Atzori, C Ghetti, B Piva, R Srinivasan, AN Zolo, P Delisle, MB Mirra, SS Migheli, A
Citation: C. Atzori et al., Activation of the JNK/p38 pathway occurs in diseases characterized by tau protein pathology and is related to tau phosphorylation but not to apoptosis, J NE EXP NE, 60(12), 2001, pp. 1190-1197
Codeposition of cystatin C with amyloid-beta protein in the brain of Alzheimer disease patients
Authors: Levy, E Sastre, M Kumar, A Gallo, G Piccardo, P Ghetti, B Tagliavini, F
Citation: E. Levy et al., Codeposition of cystatin C with amyloid-beta protein in the brain of Alzheimer disease patients, J NE EXP NE, 60(1), 2001, pp. 94-104
A 7-kDa prion protein (PrP) fragment, an integral component of the PrP region required for infectivity, is the major amyloid protein in Gerstmann-Straussler-Scheinker disease A117V
Authors: Tagliavini, F Lievens, PMJ Tranchant, C Warter, JM Mohr, M Giaccone, G Perini, F Rossi, G Salmona, M Piccardo, P Ghetti, B Beavis, RC Bugiani, O Frangione, B Prelli, F
Citation: F. Tagliavini et al., A 7-kDa prion protein (PrP) fragment, an integral component of the PrP region required for infectivity, is the major amyloid protein in Gerstmann-Straussler-Scheinker disease A117V, J BIOL CHEM, 276(8), 2001, pp. 6009-6015
A new PRNP mutation (G131V) associated with Gerstmann-Straussler-Scheinkerdisease
Authors: Panegyres, PK Toufexis, K Kakulas, BA Cernevakova, L Brown, P Ghetti, B Piccardo, P Dlouhy, SR
Citation: Pk. Panegyres et al., A new PRNP mutation (G131V) associated with Gerstmann-Straussler-Scheinkerdisease, ARCH NEUROL, 58(11), 2001, pp. 1899-1902
Prion proteins with different conformations accumulate in Geustmann-Straussler-Scheinker disease caused by A117V and F198S mutations
Authors: Piccardo, P Liepnieks, JJ William, A Dlouhy, SR Farlow, MR Young, K Nochlin, D Bird, TD Nixon, RR Ball, MJ DeCarli, C Bugiani, O Tagliavini, F Benson, MD Ghetti, B
Citation: P. Piccardo et al., Prion proteins with different conformations accumulate in Geustmann-Straussler-Scheinker disease caused by A117V and F198S mutations, AM J PATH, 158(6), 2001, pp. 2201-2207
Biochemical characterization of a neuroserpin variant associated with hereditary dementia
Authors: Yazaki, M Liepnieks, JJ Murrell, JR Takao, M Guenther, B Piccardo, P Farlow, MR Ghetti, B Benson, MD
Citation: M. Yazaki et al., Biochemical characterization of a neuroserpin variant associated with hereditary dementia, AM J PATH, 158(1), 2001, pp. 227-233
Familial Alzheimer's disease with spastic paraparesis associated with a mutation at codon 261 of the presenilin 1 gene
Authors: Farlow, MR Murrell, JR Unverzagt, FW Phillips, M Takao, M Hulette, C Ghetti, B
Citation: Mr. Farlow et al., Familial Alzheimer's disease with spastic paraparesis associated with a mutation at codon 261 of the presenilin 1 gene, ALZHEIMER'S DISEASE, 2001, pp. 53-60
Cellular and transgenic models of familial prion diseases
Authors: Harris, DA Chiesa, R Migheli, A Piccardo, P Ghetti, B
Citation: Da. Harris et al., Cellular and transgenic models of familial prion diseases, METH MOL M, 59, 2001, pp. 149-161
Guidelines for the diagnosis of dementia and Alzheimer's disease
Authors: Sorbi, S Alberoni, M Alfieri, P Vesuviana, S Amici, S Antana, D Appollonio, I Avanzi, S Bartoli, A Bergamasco, B Bracco, L Bruni, A Terme, L Bugiani, O Caffarra, P Caltagirone, C Carolei, A Casini, AR Ciannella, L Citterio, A Daniele, A D'Achille, G Del Curatolo, G Dell'Agnello, G Durante, D Farina, E Ferrero, P Forleo, P Gainotti, G Gabriele, P Galante, E Gallai, V Gallassi, R Gasparini, M Ghetti, B Giaccone, G Girotti, F Grimaldi, L Grioli, S Guarnieri, BM Grottoli, S Iemolo, F Latorraca, S Le Pira, F Lenzi, GL Lorusso, S Mariani, C Marcon, G Mascia, V Mearelli, S Morante, M Morbin, M Musicco, M Nardelli, E Nichelli, P Padovani, A Paganini, M Pantieri, R Parisen, P Parnetti, L Passerella, B Pettenati, C Piacentini, S Piccoli, F Piccolini, C Pizzolato, G Provinciali, L Pugliese, N Redi, F Ruggieri, RM Ruggiero, U Saetta, M Schoenuber, R Silveri, MC Sorbi, S Sorrentino, G Sucapane, P Stracciari, A Tabaton, M Tagliavini, F Toso, V Valluzzi, F
Citation: S. Sorbi et al., Guidelines for the diagnosis of dementia and Alzheimer's disease, NEUROL SCI, 21(4), 2000, pp. 187-194
Neuropathology of Gerstmann-Straussler-Scheinker disease
Authors: Bugiani, O Giaccone, G Piccardo, P Morbin, M Tagliavini, F Ghetti, B
Citation: O. Bugiani et al., Neuropathology of Gerstmann-Straussler-Scheinker disease, MICROSC RES, 50(1), 2000, pp. 10-15
Familial Alzheimer's disease: Site of mutation influences clinical phenotype
Authors: Lippa, CF Swearer, JM Kane, KJ Nochlin, D Bird, TD Ghetti, B Nee, LE St George-Hyslop, P Pollen, DA Drachman, DA
Citation: Cf. Lippa et al., Familial Alzheimer's disease: Site of mutation influences clinical phenotype, ANN NEUROL, 48(3), 2000, pp. 376-379
A transgenic model of a familial prion disease
Authors: Harris, DA Chiesa, R Drisaldi, B Quaglio, E Migheli, A Piccardo, P Ghetti, B
Citation: Da. Harris et al., A transgenic model of a familial prion disease, ARCH VIROL, 2000, pp. 103-112
The weaver gene has no effect on the generation patterns of mesencephalic dopaminergic neurons
Authors: Marti, J Wills, KV Ghetti, B Bayer, SA
Citation: J. Marti et al., The weaver gene has no effect on the generation patterns of mesencephalic dopaminergic neurons, DEV BRAIN R, 122(2), 2000, pp. 165-172
The weaver gene continues to target late-generated dopaminergic neurons inmidbrain areas at P90
Authors: Marti, J Wills, KV Ghetti, B Bayer, SA
Citation: J. Marti et al., The weaver gene continues to target late-generated dopaminergic neurons inmidbrain areas at P90, DEV BRAIN R, 122(2), 2000, pp. 173-181
Neurobiology - Presenilin-1 mutations in Alzheimer's disease
Authors: Russo, C Schettini, G Saido, TC Hulette, C Lippall, C Lannfelt, L Ghetti, B Gambetti, P Tabaton, M Teller, JK
Citation: C. Russo et al., Neurobiology - Presenilin-1 mutations in Alzheimer's disease, NATURE, 405(6786), 2000, pp. 531-532
Genetic influence on the structural variations of the abnormal prion protein
Authors: Parchi, P Zou, WQ Wang, W Brown, P Capellari, S Ghetti, B Kopp, N Schulz-Schaeffer, WJ Kretzschmar, HA Head, MW Ironside, JW Gambetti, P Chen, SG
Citation: P. Parchi et al., Genetic influence on the structural variations of the abnormal prion protein, P NAS US, 97(18), 2000, pp. 10168-10172
Accumulation of protease-resistant prion protein (PrP) and apoptosis of cerebellar granule cells in transgenic mice expressing a PrP insertional mutation
Authors: Chiesa, R Drisaldi, B Quaglio, E Migheli, A Piccardo, P Ghetti, B Harris, DA
Citation: R. Chiesa et al., Accumulation of protease-resistant prion protein (PrP) and apoptosis of cerebellar granule cells in transgenic mice expressing a PrP insertional mutation, P NAS US, 97(10), 2000, pp. 5574-5579
Evidence of elevated intracellular calcium levels in weaver homozygote mice
Authors: Harkins, AB Dlouhy, S Ghetti, B Cahill, AL Won, L Heller, B Heller, A Fox, AP
Citation: Ab. Harkins et al., Evidence of elevated intracellular calcium levels in weaver homozygote mice, J PHYSL LON, 524(2), 2000, pp. 447-455
Neuroserpin mutation S52R causes neuroserpin accumulation in neurons and is associated with progressive myoclonus epilepsy
Authors: Takao, M Benson, MD Murrell, JR Yazaki, M Piccardo, P Unverzagt, FW Davis, RL Holohan, PD Lawrence, DA Richardson, R Farlow, MR Ghetti, B
Citation: M. Takao et al., Neuroserpin mutation S52R causes neuroserpin accumulation in neurons and is associated with progressive myoclonus epilepsy, J NE EXP NE, 59(12), 2000, pp. 1070-1086
Early-onset Alzheimer disease caused by a new mutation (V717L) in the amyloid precursor protein gene
Authors: Murrell, JR Hake, AM Quaid, KA Farlow, MR Ghetti, B
Citation: Jr. Murrell et al., Early-onset Alzheimer disease caused by a new mutation (V717L) in the amyloid precursor protein gene, ARCH NEUROL, 57(6), 2000, pp. 885-887
Risultati: 1-25 | 26-44