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Results: 1-25 | 26-28
Results: 1-25/28
From genetics to pathology: tau and alpha-synuclein assemblies in neurodegenerative diseases
Authors: Goedert, M Spillantini, MG Serpell, LC Berriman, J Smith, MJ Jakes, R Crowther, RA
Citation: M. Goedert et al., From genetics to pathology: tau and alpha-synuclein assemblies in neurodegenerative diseases, PHI T ROY B, 356(1406), 2001, pp. 213-227
Pick's disease associated with the novel Tau gene mutation K369I
Authors: Neumann, M Schulz-Schaeffer, W Crowther, RA Smith, MJ Spillantini, MG Goedert, M Kretzschmar, HA
Citation: M. Neumann et al., Pick's disease associated with the novel Tau gene mutation K369I, ANN NEUROL, 50(4), 2001, pp. 503-513
Tau and Parkinson disease
Authors: Spillantini, MG Goedert, M
Citation: Mg. Spillantini et M. Goedert, Tau and Parkinson disease, J AM MED A, 286(18), 2001, pp. 2324-2326
alpha-Synuclein metabolism and aggregation is linked to ubiquitin-independent degradation by the proteasome
Authors: Tofaris, GK Layfield, R Spillantini, MG
Citation: Gk. Tofaris et al., alpha-Synuclein metabolism and aggregation is linked to ubiquitin-independent degradation by the proteasome, FEBS LETTER, 509(1), 2001, pp. 22-26
Familial frontotemporal dementia with ubiquitin-positive inclusions is linked to chromosome 17q2l-22
Authors: Rosso, SM Kamphorst, W de Graaf, B Willemsen, R Ravid, R Niermeijer, MF Spillantini, MG Heutink, P van Swieten, JC
Citation: Sm. Rosso et al., Familial frontotemporal dementia with ubiquitin-positive inclusions is linked to chromosome 17q2l-22, BRAIN, 124, 2001, pp. 1948-1957
Parkinson's disease, dementia with Lewy bodies, and multiple system atrophy as alpha-synucleinopathies
Authors: Goedert, M Jakes, R Crowther, RA Spillantini, MG
Citation: M. Goedert et al., Parkinson's disease, dementia with Lewy bodies, and multiple system atrophy as alpha-synucleinopathies, METH MOL M, 62, 2001, pp. 33-59
Tau mutations in frontotemporal dementia FTDP-17 and their relevance for Alzheimer's disease
Authors: Goedert, M Spillantini, MG
Citation: M. Goedert et Mg. Spillantini, Tau mutations in frontotemporal dementia FTDP-17 and their relevance for Alzheimer's disease, BBA-MOL BAS, 1502(1), 2000, pp. 110-121
A novel tau mutation (N296N) in familial dementia with swollen achromatic neurons and corticobasal inclusion bodies
Authors: Spillantini, MG Yoshida, H Rizzini, C Lantos, PL Khan, N Rossor, MN Goedert, M Brown, J
Citation: Mg. Spillantini et al., A novel tau mutation (N296N) in familial dementia with swollen achromatic neurons and corticobasal inclusion bodies, ANN NEUROL, 48(6), 2000, pp. 939-943
A novel mutation at position+12 in the intron following exon 10 of the taugene in familial frontotemporal dementia (FTD-Kumamoto)
Authors: Yasuda, M Takamatsu, J D'Souza, I Crowther, RA Kawamata, T Hasegawa, M Hasegawa, H Spillantini, MG Tanimukai, S Poorkaj, P Varani, L Varani, G Iwatsubo, T Goedert, M Schellenberg, GD Tanaka, C
Citation: M. Yasuda et al., A novel mutation at position+12 in the intron following exon 10 of the taugene in familial frontotemporal dementia (FTD-Kumamoto), ANN NEUROL, 47(4), 2000, pp. 422-429
A new case of frontotemporal dementia and parkinsonism resulting from an intron 10+3-splice site mutation in the tau gene: clinical and pathological features
Authors: Tolnay, M Spillantini, MG Rizzini, C Eccles, D Lowe, J Ellison, D
Citation: M. Tolnay et al., A new case of frontotemporal dementia and parkinsonism resulting from an intron 10+3-splice site mutation in the tau gene: clinical and pathological features, NEUROP AP N, 26(4), 2000, pp. 368-378
Structural basis for recognition of the RNA major groove in the tau exon 10 splicing regulatory element by aminoglycoside antibiotics
Authors: Varani, L Spillantini, MG Goedert, M Varani, G
Citation: L. Varani et al., Structural basis for recognition of the RNA major groove in the tau exon 10 splicing regulatory element by aminoglycoside antibiotics, NUCL ACID R, 28(3), 2000, pp. 710-719
Tau gene mutation K257T causes a tauopathy similar to Pick's disease
Authors: Rizzini, C Goedert, M Hodges, JR Smith, MJ Jakes, R Hills, R Xuereb, JH Crowther, RA Spillantini, MG
Citation: C. Rizzini et al., Tau gene mutation K257T causes a tauopathy similar to Pick's disease, J NE EXP NE, 59(11), 2000, pp. 990-1001
Tau mutations in familial frontotemporal dementia
Authors: Spillantini, MG Goedert, M
Citation: Mg. Spillantini et M. Goedert, Tau mutations in familial frontotemporal dementia, BRAIN, 123, 2000, pp. 857-859
Axonopathy and amyotrophy in mice transgenic for human four-repeat tau protein
Authors: Probst, A Gotz, J Wiederhold, KH Tolnay, M Mistl, C Jaton, AL Hong, M Ishihara, T Lee, VMY Trojanowski, JQ Jakes, R Crowther, RA Spillantini, MG Burki, K Goedert, M
Citation: A. Probst et al., Axonopathy and amyotrophy in mice transgenic for human four-repeat tau protein, ACT NEUROP, 99(5), 2000, pp. 469-481
Parkinson's disease, dementia with Lewy bodies and multiple system atrophyare alpha-synucleinopathies
Authors: Spillantini, MG
Citation: Mg. Spillantini, Parkinson's disease, dementia with Lewy bodies and multiple system atrophyare alpha-synucleinopathies, PARKINS R D, 5(4), 1999, pp. 157-162
Tau gene mutation in familial progressive subcortical gliosis
Authors: Goedert, M Spillantini, MG Crowther, RA Chen, SG Parchi, P Tabaton, M Lanska, DJ Markesbery, WR Wilhelmsen, KC Dickson, DW Petersen, RB Gambetti, P
Citation: M. Goedert et al., Tau gene mutation in familial progressive subcortical gliosis, NAT MED, 5(4), 1999, pp. 454-457
Phenotypic variation in hereditary frontotemporal dementia with tau mutations
Authors: van Swieten, JC Stevens, M Rosso, SM Rizzu, P Joosse, M de Koning, I Kamphorst, W Ravid, R Spillantini, MG Niermeijer, MF Heutink, P
Citation: Jc. Van Swieten et al., Phenotypic variation in hereditary frontotemporal dementia with tau mutations, ANN NEUROL, 46(4), 1999, pp. 617-626
Mutations in the Tau gene cause frontotemporal dementia
Authors: Ghetti, B Murrell, J Spillantini, MG
Citation: B. Ghetti et al., Mutations in the Tau gene cause frontotemporal dementia, BRAIN RES B, 50(5-6), 1999, pp. 471-472
Dehydroepiandrosterone antagonizes the neurotoxic effects of corticosterone and translocation of stress-activated protein kinase 3 in hippocampal primary cultures
Authors: Kimonides, VG Spillantini, MG Sofroniew, MV Fawcett, JW Herbert, J
Citation: Vg. Kimonides et al., Dehydroepiandrosterone antagonizes the neurotoxic effects of corticosterone and translocation of stress-activated protein kinase 3 in hippocampal primary cultures, NEUROSCIENC, 89(2), 1999, pp. 429-436
Structure of tau exon 10 splicing regulatory element RNA and destabilization by mutations of frontotemporal dementia and parkinsonism linked to chromosome 17
Authors: Varani, L Hasegawa, M Spillantini, MG Smith, MJ Murrell, JR Ghetti, B Klug, A Goedert, M Varani, G
Citation: L. Varani et al., Structure of tau exon 10 splicing regulatory element RNA and destabilization by mutations of frontotemporal dementia and parkinsonism linked to chromosome 17, P NAS US, 96(14), 1999, pp. 8229-8234
Neuropathological features of frontotemporal dementia and parkinsonism linked to chromosome 17q21-22 (FTDP-17): Duke family 1684
Authors: Hulette, CM Pericak-Vance, MA Roses, AD Schmechel, DE Yamaoka, LH Gaskell, PC Welsh-Bohmer, KA Crowther, RA Spillantini, MG
Citation: Cm. Hulette et al., Neuropathological features of frontotemporal dementia and parkinsonism linked to chromosome 17q21-22 (FTDP-17): Duke family 1684, J NE EXP NE, 58(8), 1999, pp. 859-866
Frontotemporal dementia and corticobasal degeneration in a family with a P301S mutation in tau
Authors: Bugiani, O Murrell, JR Giaccone, G Hasegawa, M Ghigo, G Tabaton, M Morbin, M Primavera, A Carella, F Solaro, C Grisoli, M Savoiardo, M Spillantini, MG Tagliavini, F Goedert, M Ghetti, B
Citation: O. Bugiani et al., Frontotemporal dementia and corticobasal degeneration in a family with a P301S mutation in tau, J NE EXP NE, 58(6), 1999, pp. 667-677
Tau pathology in a family with dementia and a P301L mutation in tau
Authors: Mirra, SS Murrell, JR Gearing, M Spillantini, MG Goedert, M Crowther, A Levey, AI Jones, R Green, J Shoffner, JM Wainer, BH Schmidt, ML Trojanowski, JQ Ghetti, B
Citation: Ss. Mirra et al., Tau pathology in a family with dementia and a P301L mutation in tau, J NE EXP NE, 58(4), 1999, pp. 335-345
Tau gene mutation G389R causes a tauopathy with abundant pick body-like inclusions and axonal deposits
Authors: Murrell, JR Spillantini, MG Zolo, P Guazzelli, M Smith, MJ Hasegawa, M Redi, F Crowther, RA Pietrini, P Ghetti, B Goedert, M
Citation: Jr. Murrell et al., Tau gene mutation G389R causes a tauopathy with abundant pick body-like inclusions and axonal deposits, J NE EXP NE, 58(12), 1999, pp. 1207-1226
Stress-activated protein kinase-3 interacts with the PDZ domain of alpha 1-syntrophin - A mechanism for specific substrate recognition
Authors: Hasegawa, M Cuenda, A Spillantini, MG Thomas, GM Buee-Scherrer, V Cohen, P Goedert, M
Citation: M. Hasegawa et al., Stress-activated protein kinase-3 interacts with the PDZ domain of alpha 1-syntrophin - A mechanism for specific substrate recognition, J BIOL CHEM, 274(18), 1999, pp. 12626-12631
Risultati: 1-25 | 26-28