-
1
-
-
12944268979
-
Hyperphosphorylated tau and neurofilament and cytoskeletal disruptions in mice overexpressing human p25, an activator of cdk5
-
(2000)
Proc. Natl. Acad. Sci. USA
, vol.97
, pp. 2910-2915
-
-
Ahlijanian, M.K.1
Barrezueta, N.X.2
Williams, R.D.3
Jakowski, A.4
Kowsz, K.P.5
McCarthy, S.6
Coskran, T.7
Carlo, A.8
Seymour, P.A.9
Burkhardt, J.E.10
Nelson, R.B.11
McNeish, J.D.12
-
4
-
-
0034624917
-
Two brothers with frontotemporal dementia and parkinsonism with an N279K mutation of the tau gene
-
(2000)
Neurology
, vol.54
, pp. 1787-1795
-
-
Arima, K.1
Kowalska, A.2
Hasegawa, M.3
Mukoyama, M.4
Watanabe, R.5
Kawai, M.6
Takahashi, K.7
Iwatsubo, T.8
Tabira, T.9
Sunohara, N.10
-
6
-
-
0033041179
-
Association of an extended haplotype in the tau gene with progressive supranuclear palsy
-
(1999)
Hum. Mol. Genet.
, vol.8
, pp. 711-715
-
-
Baker, M.1
Litvan, I.2
Houlden, H.3
Adamson, J.4
Dickson, D.5
Perez-Tur, J.6
Hardy, J.7
Lynch, T.8
Bigio, E.9
Hutton, M.10
-
7
-
-
0023630392
-
Phosphorylation of tau proteins to a state like that in Alzheimer's brain is catalyzed by a calcium/calmodulin-dependent kinase and modulated by phospholipids
-
(1987)
J. Biol. Chem.
, vol.262
, pp. 17577-17583
-
-
Baudier, J.1
Cole, R.D.2
-
9
-
-
0031681409
-
Direct genetic evidence for involvement of tau in progressive supranuclear palsy. European study group on atypical parkinsonism consortium
-
(1998)
Neurology
, vol.51
, pp. 982-985
-
-
Bennett, P.1
Bonifati, V.2
Bonuccelli, U.3
Colosimo, C.4
De Mari, M.5
Fabbrini, G.6
Marconi, R.7
Meco, G.8
Nicholl, D.J.9
Stocchi, F.10
Vanacore, N.11
Vieregge, P.12
Williams, A.C.13
-
12
-
-
0031007546
-
Regulated phosphorylation and dephosphorylation of tau protein: Effects on microtubule interaction, intracellular trafficking and neurodegeneration
-
(1997)
Biochem. J.
, vol.323
, pp. 577-591
-
-
Billingsley, M.L.1
Kincaid, R.L.2
-
14
-
-
0032897924
-
A clinical pathological comparison of three families with frontotemporal dementia and identical mutations in the tau gene (P301L)
-
(1999)
Brain
, vol.122
, pp. 741-756
-
-
Bird, T.D.1
Nochlin, D.2
Poorkaj, P.3
Cherrier, M.4
Kaye, J.5
Payami, H.6
Peskind, E.7
Lampe, T.H.8
Nemens, E.9
Boyer, P.J.10
Schellenberg, G.D.11
-
15
-
-
0030983011
-
Chromosome 17 and hereditary dementia: Linkage studies in three non-Alzheimer families and kindreds with late-onset FAD
-
(1997)
Neurology
, vol.48
, pp. 949-954
-
-
Bird, T.D.1
Wijsman, E.M.2
Nochlin, D.3
Leehey, M.4
Sumi, S.M.5
Payami, H.6
Poorkaj, P.7
Nemens, E.8
Rafkind, M.9
Schellenberg, G.D.10
-
16
-
-
0032887313
-
The tau gene in progressive supranuclear palsy: Exclusion of mutations in coding exons and exon 10 splice sites, and identification of a new intronic variant of the disease-associated H1 haplotype in Italian cases
-
(1999)
Neurosci. Lett.
, vol.274
, pp. 61-65
-
-
Bonifati, V.1
Joosse, M.2
Nicholl, D.J.3
Vanacore, N.4
Bennett, P.5
Rizzu, P.6
Fabbrini, G.7
Marconi, R.8
Colosimo, C.9
Locuratolo, N.10
Stocchi, F.11
Bonuccelli, U.12
De Mari, M.13
Wenning, G.14
Vieregge, P.15
Oostra, B.16
Meco, G.17
Heutink, P.18
-
18
-
-
0345580607
-
Transgenic expression of the shortest human tau affects its compartmentalization and its phosphorylation as in the pretangle stage of Alzheimer's disease
-
(1999)
Am. J. Pathol.
, vol.154
, pp. 255-270
-
-
Brion, J.P.1
Tremp, G.2
Octave, J.N.3
-
19
-
-
0029870639
-
Hyperphosphorylated tau proteins differentiate corticobasal degeneration and Pick's disease
-
(1996)
Acta Neuropathol. (Berl)
, vol.91
, pp. 351-359
-
-
Buée-Scherrer, V.1
Hof, P.R.2
Buée, L.3
Leveugle, B.4
Vermersch, P.5
Perl, D.P.6
Olanow, C.W.7
Delacourte, A.8
-
21
-
-
0033059975
-
Frontotemporal dementia and corticobasal degeneration in a family with a P301S mutation in tau
-
(1999)
J. Neuropathol. Exp. Neurol.
, vol.58
, pp. 667-677
-
-
Bugiani, O.1
Murrell, J.R.2
Giaccone, G.3
Hasegawa, M.4
Ghigo, G.5
Tabaton, M.6
Morbin, M.7
Primavera, A.8
Carella, F.9
Solaro, C.10
Grisoli, M.11
Savoiardo, M.12
Spillantini, M.G.13
Tagliavini, F.14
Goedert, M.15
Ghetti, B.16
-
25
-
-
0032573083
-
Pathogenic implications of mutations in the tau gene in pallido-ponto-nigral degeneration and related neurodegenerative disorders linked to chromosome 17
-
(1998)
Proc. Natl. Acad. Sci. USA
, vol.95
, pp. 13103-13107
-
-
Clark, L.N.1
Poorkaj, P.2
Wszolek, Z.3
Geschwind, D.H.4
Nasreddine, Z.S.5
Miller, B.6
Li, D.7
Payami, H.8
Awert, F.9
Markopoulou, K.10
Andreadis, A.11
D'Souza, I.12
Lee, V.M.-Y.13
Reed, L.14
Trojanowski, J.Q.15
Zhukareva, V.16
Bird, T.17
Schellenberg, G.18
Wilhelmsen, K.C.19
-
27
-
-
0031044850
-
Genetic evidence for the involvement of tau in progressive supranuclear palsy
-
(1997)
Ann. Neurol.
, vol.41
, pp. 277-281
-
-
Conrad, C.1
Andreadis, A.2
Trojanowski, J.Q.3
Dickson, D.W.4
Kang, D.5
Chen, X.6
Wiederholt, W.7
Hansen, L.8
Masliah, E.9
Thal, L.J.10
Katzman, R.11
Xia, Y.12
Saitoh, T.13
-
29
-
-
0027194791
-
Gene dose of apolipoprotein E type 4 allele and the risk of Alzheimer's disease in late onset families
-
(1993)
Science
, vol.261
, pp. 921-923
-
-
Corder, E.H.1
Saunders, A.M.2
Strittmatter, W.J.3
Schmechel, D.E.4
Gaskell, P.C.5
Small, G.W.6
Roses, A.D.7
Haines, J.L.8
Pericak-Vance, M.A.9
-
33
-
-
0033545946
-
Missense and silent tau gene mutations cause frontotemporal dementia with parkinsonism-chromosome 17 type, by affecting multiple alternative RNA splicing regulatory elements
-
(1999)
Proc. Natl. Acad. Sci. USA
, vol.96
, pp. 5598-5603
-
-
D'Souza, I.1
Poorkaj, P.2
Hong, M.3
Nochlin, D.4
Lee, V.M.5
Bird, T.D.6
Schellenberg, G.D.7
-
34
-
-
0034625379
-
Determinants of 4 repeat tau expression: Coordination between enhancing and inhibitory splicing sequences for exon 10 inclusion
-
(2000)
J. Biol. Chem.
, vol.275
, pp. 17700-17709
-
-
D'Souza, I.1
Schellenberg, D.2
-
35
-
-
0033042978
-
Mutations in tau reduce its microtubule binding properties in intact cells and affect its phosphorylation
-
(1999)
FEBS Lett.
, vol.446
, pp. 228-232
-
-
Dayanandan, R.1
Van Slegtenhorst, M.2
Mack, T.G.3
Ko, L.4
Yen, S.H.5
Leroy, K.6
Brion, J.P.7
Anderton, B.H.8
Hutton, M.9
Lovestone, S.10
-
36
-
-
0029670872
-
Specific pathological tau protein variants characterize Pick's disease
-
(1996)
J. Neuropathol. Exp. Neurol.
, vol.55
, pp. 159-168
-
-
Delacourte, A.1
Robitaille, Y.2
Sergeant, N.3
Buée, L.4
Hof, P.R.5
Wattez, A.6
Laroche-Cholette, A.7
Mathieu, J.8
Chagnon, P.9
Gauvreau, D.10
-
37
-
-
0033002879
-
A mutation at codon 279 (N279K) in exon 10 of the tau gene causes a tauopathy with dementia and supranuclear palsy
-
(1999)
Acta Neuropathol. (Berl)
, vol.98
, pp. 62-77
-
-
Delisle, M.B.1
Murrell, J.R.2
Richardson, R.3
Trofatter, J.A.4
Rascol, O.5
Soulages, X.6
Mohr, M.7
Calvas, P.8
Ghetti, B.9
-
38
-
-
0033982344
-
Missense tau mutations identified in FTDP-17 have a small effect on tau-microtubule interactions
-
(2000)
Brain Res.
, vol.853
, pp. 5-14
-
-
DeTure, M.1
Ko, L.W.2
Yen, S.3
Nacharaju, P.4
Easson, C.5
Lewis, J.6
Van Slegtenhorst, M.7
Hutton, M.8
Yen, S.H.9
-
39
-
-
0034011659
-
Corticobasal degeneration shares a common genetic background with progressive supranuclear palsy
-
(2000)
Ann. Neurol.
, vol.47
, pp. 374-377
-
-
Di Maria, E.1
Tabaton, M.2
Vigo, T.3
Abbruzzese, G.4
Bellone, E.5
Donati, C.6
Frasson, E.7
Marchese, R.8
Montagna, P.9
Munoz, D.G.10
Pramstaller, P.P.11
Zanusso, G.12
Ajmar, F.13
Mandich, P.14
-
41
-
-
0032833626
-
Neuropathologic differentiation of progressive supranuclear palsy and corticobasal degeneration
-
(1999)
J. Neurol.
, vol.246
, Issue.SUPPL. 2
-
-
Dickson, D.W.1
-
44
-
-
0034016093
-
Characterization of pathology in transgenic mice over-expressing human genomic and cDNA tau transgenes
-
(2000)
Neurobiol. Dis.
, vol.7
, pp. 87-98
-
-
Duff, K.1
Knight, H.2
Refolo, L.M.3
Sanders, S.4
Yu, X.5
Picciano, M.6
Malester, B.7
Hutton, M.8
Adamson, J.9
Goedert, M.10
Burki, K.11
Davies, P.12
-
45
-
-
7344220963
-
Segregation of a missense mutation in the microtubule-associated protein tau gene with familial frontotemporal dementia and parkinsonism
-
(1998)
Hum. Mol. Genet.
, vol.7
, pp. 1825-1829
-
-
Dumanchin, C.1
Camuzat, A.2
Campion, D.3
Verpillat, P.4
Hannequin, D.5
Dubois, B.6
Saugier-Veber, P.7
Martin C., Jr.8
Penet, C.9
Charbonnier, F.10
Agid, Y.11
Frebourg, T.12
Brice, A.13
-
52
-
-
0034677185
-
Pro-apoptotic effects of tau mutations in chromosome 17 frontotemporal dementia and parkinsonism
-
(2000)
Neuroreport
, vol.11
, pp. 57-60
-
-
Furukawa, K.1
D'Souza, I.2
Crudder, C.H.3
Onodera, H.4
Itoyama, Y.5
Poorkaj, P.6
Bird, T.D.7
Schellenberg, G.D.8
-
53
-
-
0028985574
-
Alzheimer-type neuropathology in transgenic mice overexpressing V717F beta-amyloid precursor protein
-
(1995)
Nature
, vol.373
, pp. 523-527
-
-
Games, D.1
Adams, D.2
Alessandrini, R.3
Barbour, R.4
Berthelette, P.5
Blackwell, C.6
Carr, T.7
Clemens, J.8
Donaldson, T.9
Gillespie, F.10
-
58
-
-
0025600995
-
Expression of separate isoforms of human tau protein: Correlation with the tau pattern in brain and effects on tubulin polymerization
-
(1990)
EMBO J.
, vol.9
, pp. 4225-4230
-
-
Goedert, M.1
Jakes, R.2
-
61
-
-
0032950744
-
Tau gene mutation in familial progressive subcortical gliosis
-
(1999)
Nat. Med.
, vol.5
, pp. 454-457
-
-
Goedert, M.1
Spillantini, M.G.2
Crowther, R.A.3
Chen, S.G.4
Parchi, P.5
Tabaton, M.6
Lanska, D.J.7
Markesbery, W.R.8
Wilhelmsen, K.C.9
Dickson, D.W.10
Petersen, R.B.11
Gambetti, P.12
-
62
-
-
0029031214
-
Molecular dissection of the paired helical filament
-
(1995)
Neurobiol. Aging
, vol.16
, pp. 325-334
-
-
Goedert, M.1
Spillantini, M.G.2
Jakes, R.3
Crowther, R.A.4
Vanmechelen, E.5
Probst, A.6
Gotz, J.7
Burki, K.8
Cohen, P.9
-
67
-
-
0028175215
-
Identification of a novel microtubule binding and assembly domain in the developmentally regulated inter-repeat region of tau
-
(1994)
J. Cell Biol.
, vol.124
, pp. 769-782
-
-
Goode, B.L.1
Feinstein, S.C.2
-
71
-
-
0033591225
-
5′ splice site mutations in tau associated with the inherited dementia FTDP-17 affect a stem-loop structure that regulates alternative splicing of exon 10
-
(1999)
J. Biol. Chem.
, vol.274
, pp. 15134-15143
-
-
Grover, A.1
Houlden, H.2
Baker, M.3
Adamson, J.4
Lewis, J.5
Prihar, G.6
Pickering-Brown, S.7
Duff, K.8
Hutton, M.9
-
75
-
-
0028301455
-
Altered microtubule organization in small-calibre axons of mice lacking tau protein
-
(1994)
Nature
, vol.369
, pp. 488-491
-
-
Harada, A.1
Oguchi, K.2
Okabe, S.3
Kuno, J.4
Terada, S.5
Ohshima, T.6
Sato-Yoshitake, R.7
Takei, Y.8
Noda, T.9
Hirokawa, N.10
-
79
-
-
0028092015
-
Preliminary NINDS neuropathologic criteria for Steele-Richardson-Olszewski syndrome (progressive supranuclear palsy)
-
(1994)
Neurology
, vol.44
, pp. 2015-2019
-
-
Hauw, J.J.1
Daniel, S.E.2
Dickson, D.3
Horoupian, D.S.4
Jellinger, K.5
Lantos, P.L.6
McKee, A.7
Tabaton, M.8
Litvan, I.9
-
80
-
-
0031045491
-
Hereditary frontotemporal dementia is linked to chromosome 17q21-q22: A genetic and clinicopathological study of three Dutch families
-
(1997)
Ann. Neurol.
, vol.41
, pp. 150-159
-
-
Heutink, P.1
Stevens, M.2
Rizzu, P.3
Bakker, E.4
Kros, J.M.5
Tibben, A.6
Niermeijer, M.F.7
Van Duijn, C.M.8
Oostra, B.A.9
Van Swieten, J.C.10
-
83
-
-
0345281583
-
The tau gene A0 allele and progressive supranuclear palsy
-
(1999)
Neurology
, vol.53
, pp. 1219-1225
-
-
Hoenicka, J.1
Perez, M.2
Perez-Tur, J.3
Barabash, A.4
Godoy, M.5
Vidal, L.6
Astarloa, R.7
Avila, J.8
Nygaard, T.9
De Yebenes, J.G.10
-
85
-
-
0030748390
-
Insulin and insulin-like growth factor-1 regulate tau phosphorylation in cultured human neurons
-
(1997)
J. Biol. Chem.
, vol.272
, pp. 19547-19553
-
-
Hong, M.1
Lee, V.M.-Y.2
-
87
-
-
0032484089
-
Mutation-specific functional impairments in distinct tau isoforms of hereditary FTDP-17
-
(1998)
Science
, vol.282
, pp. 1914-1917
-
-
Hong, M.1
Zhukareva, V.2
Vogelsberg-Ragaglia, V.3
Wszolek, Z.4
Reed, L.5
Miller, B.I.6
Geschwind, D.H.7
Bird, T.D.8
McKeel D., Jr.9
Goate, A.10
Morris, J.C.11
Wilhelmsen, K.C.12
Schellenberg, G.D.13
Trojanowski, J.Q.14
Lee, V.M.-Y.15
-
88
-
-
0029742199
-
Correlative memory deficits, Abeta elevation, and amyloid plaques in transgenic mice
-
(1996)
Science
, vol.274
, pp. 99-102
-
-
Hsiao, K.1
Chapman, P.2
Nilsen, S.3
Eckman, C.4
Harigaya, Y.5
Younkin, S.6
Yang, F.7
Cole, G.8
-
89
-
-
0032815068
-
Neuropathological features of frontotemporal dementia and parkinsonism linked to chromosome 17q21-22 (FTDP-17): Duke Family 1684
-
(1999)
J. Neuropathol. Exp. Neurol.
, vol.58
, pp. 859-866
-
-
Hulette, C.M.1
Pericak-Vance, M.A.2
Roses, A.D.3
Schmechel, D.E.4
Yamaoka, L.H.5
Gaskell, P.C.6
Welsh-Bohmer, K.A.7
Crowther, R.A.8
Spillantini, M.G.9
-
90
-
-
0032543684
-
Association of missense and 5′-splice-site mutations in tau with the inherited dementia FTDP-17
-
(1998)
Nature
, vol.393
, pp. 702-705
-
-
Hutton, M.1
Lendon, C.L.2
Rizzu, P.3
Baker, M.4
Froelich, S.5
Houlden, H.6
Pickering-Brown, S.7
Chakraverty, S.8
Isaacs, A.9
Grover, A.10
Hackett, J.11
Adamson, J.12
Lincoln, S.13
Dickson, D.14
Davies, P.15
Petersen, R.C.16
Stevens, M.17
De Graaff, E.18
Wauters, E.19
Van Baren, J.20
Hillebrand, M.21
Joosse, M.22
Kwon, J.M.23
Nowotny, P.24
Heutink, P.25
more..
-
91
-
-
0033602013
-
A distinct familial presenile dementia with a novel missense mutation in the tau gene
-
(1999)
Neuroreport
, vol.10
, pp. 497-501
-
-
Iijima, M.1
Tabira, T.2
Poorkaj, P.3
Schellenberg, G.D.4
Trojanowski, J.Q.5
Lee, V.M.-Y.6
Schmidt, M.L.7
Takahashi, K.8
Nabika, T.9
Matsumoto, T.10
Yamashita, Y.11
Yoshioka, S.12
Ishino, H.13
-
97
-
-
37049048544
-
Paired helical filaments in electron microscopy of Alzheimer's disease
-
(1963)
Nature
, vol.197
, pp. 192-194
-
-
Kidd, M.1
-
98
-
-
0027426029
-
A cdc2-related kinase PSSALRE/cdk5 is homologous with the 30 kDa subunit of tau protein kinase II, a proline-directed protein kinase associated with microtubule
-
(1993)
FEBS Lett.
, vol.335
, pp. 171-175
-
-
Kobayashi, S.1
Ishiguro, K.2
Omori, A.3
Takamatsu, M.4
Arioka, M.5
Imahori, K.6
Uchida, T.7
-
99
-
-
0032886469
-
Tau-positive glial inclusions in progressive supranuclear palsy, corticobasal degeneration and Pick's disease
-
(1999)
Brain Pathol.
, vol.9
, pp. 663-679
-
-
Komori, T.1
-
102
-
-
0028091523
-
Ultrastructure and biochemical composition of paired helical filaments in corticobasal degeneration
-
(1994)
Am. J. Pathol.
, vol.145
, pp. 1496-1508
-
-
Ksiezak-Reding, H.1
Morgan, K.2
Mattiace, L.A.3
Davies, P.4
Liu, W.K.5
Yen, S.H.6
Weidenheim, K.7
Dickson, D.W.8
-
106
-
-
0031799683
-
Hereditary dysphasic disinhibition dementia: A frontotemporal dementia linked to 17q21-22
-
(1998)
Neurology
, vol.50
, pp. 1546-1555
-
-
Lendon, C.L.1
Lynch, T.2
Norton, J.3
McKeel, D.W.4
Busfield, F.5
Craddock, N.6
Chakraverty, S.7
Gopalakrishnan, G.8
Shears, S.D.9
Grimmett, W.10
Wilhelmsen, K.C.11
Hansen, L.12
Morris, J.C.13
Goate, A.M.14
-
107
-
-
0034426011
-
Neurofibrillary tangles, amyotrophy and progressive motor disturbance in mice expressing mutant (P301L) tau protein
-
(2000)
Nat. Genet.
, vol.25
, pp. 402-405
-
-
Lewis, J.1
McGowan, E.2
Rockwood, J.3
Melrose, H.4
Nacharaju, P.5
Van Slegtenhorst, M.6
Gwinn-Hardy, K.7
Paul, M.M.8
Baker, M.9
Yu, X.10
Duff, K.11
Hardy, J.12
Corral, A.13
Lin, W.L.14
Yen, S.H.15
Dickson, D.W.16
Davies, P.17
Hutton, M.18
-
109
-
-
0031887227
-
Cognitive, neuroimaging, and pathological studies in a patient with Pick's disease
-
(1998)
Ann. Neurol.
, vol.43
, pp. 259-265
-
-
Lieberman, A.P.1
Trojanowski, J.Q.2
Lee, V.M.-Y.3
Balin, B.J.4
Ding, X.S.5
Greenberg, J.6
Morrison, D.7
Reivich, M.8
Grossman, M.9
-
111
-
-
8944226575
-
Clinical research criteria for the diagnosis of progressive supranuclear palsy (Steele-Richardson-Olszewski syndrome): Report of the NINDS-SPSP international workshop
-
(1996)
Neurology
, vol.47
, pp. 1-9
-
-
Litvan, I.1
Agid, Y.2
Calne, D.3
Campbell, G.4
Dubois, B.5
Duvoisin, R.C.6
Goetz, C.G.7
Golbe, L.I.8
Grafman, J.9
Growdon, J.H.10
Hallett, M.11
Jankovic, J.12
Quinn, N.P.13
Tolosa, E.14
Zee, D.S.15
-
112
-
-
13344269690
-
Validity and reliability of the preliminary NINDS neuropathologic criteria for progressive supranuclear palsy and related disorders
-
(1996)
J. Neuropathol. Exp. Neurol.
, vol.55
, pp. 97-105
-
-
Litvan, I.1
Hauw, J.J.2
Bartko, J.J.3
Lantos, P.L.4
Daniel, S.E.5
Horoupian, D.S.6
McKee, A.7
Dickson, D.8
Bancher, C.9
Tabaton, M.10
Jellinger, K.11
Anderson, D.W.12
-
119
-
-
0031924815
-
Dementia of frontal type and dementias with subcortical gliosis
-
(1998)
Brain Pathol.
, vol.8
, pp. 325-338
-
-
Mann, D.M.1
-
121
-
-
0025331812
-
Spinal cord neurofibrillary tangles of Guamanian amyotrophic lateral sclerosis and parkinsonism-dementia complex: An immunohistochemical study
-
(1990)
Neurology
, vol.40
, pp. 975-979
-
-
Matsumoto, S.1
Hirano, A.2
Goto, S.3
-
126
-
-
0032920233
-
Tau pathology in a family with dementia and a P301L mutation in tau
-
(1999)
J. Neuropathol. Exp. Neurol.
, vol.58
, pp. 335-345
-
-
Mirra, S.S.1
Murrell, J.R.2
Gearing, M.3
Spillantini, M.G.4
Goedert, M.5
Crowther, R.A.6
Levey, A.I.7
Jones, R.8
Green, J.9
Shoffner, J.M.10
Wainer, B.H.11
Schmidt, M.L.12
Trojanowski, J.Q.13
Ghetti, B.14
-
128
-
-
0029010035
-
Hyperphosphorylation of tau in PHF
-
(1995)
Neurobiol. Aging
, vol.16
, pp. 365-371
-
-
Morishima-Kawashima, M.1
Hasegawa, M.2
Takio, K.3
Suzuki, M.4
Yoshida, H.5
Watanabe, A.6
Titani, K.7
Ihara, Y.8
-
130
-
-
0032965787
-
Mutation in the tau exon 10 splice site region in familial frontotemporal dementia
-
(1999)
Ann. Neurol.
, vol.45
, pp. 270-271
-
-
Morris, H.R.1
Perez-Tur, J.2
Janssen, J.C.3
Brown, J.4
Lees, A.J.5
Wood, N.W.6
Hardy, J.7
Hutton, M.8
Rossor, M.N.9
-
131
-
-
0030812529
-
Familial multiple-system tauopathy with presenile dementia is localized to chromosome 17
-
(1997)
Am. J. Hum. Genet.
, vol.61
, pp. 1131-1138
-
-
Murrell, J.R.1
Koller, D.2
Foroud, T.3
Goedert, M.4
Spillantini, M.G.5
Edenberg, H.J.6
Farlow, M.R.7
Ghetti, B.8
-
132
-
-
0032763203
-
Tau gene mutation G389R causes a tauopathy with abundant pick body-like inclusions and axonal deposits
-
(1999)
J. Neuropathol. Exp. Neurol.
, vol.58
, pp. 1207-1226
-
-
Murrell, J.R.1
Spillantini, M.G.2
Zolo, P.3
Guazzelli, M.4
Smith, M.J.5
Hasegawa, M.6
Redi, F.7
Crowther, R.A.8
Pietrini, P.9
Ghetti, B.10
Goedert, M.11
-
134
-
-
0032976201
-
From genotype to phenotype: A clinical pathological, and biochemical investigation of frontotemporal dementia and parkinsonism (FTDP-17) caused by the P301L tau mutation
-
(1999)
Ann. Neurol.
, vol.45
, pp. 704-715
-
-
Nasreddine, Z.S.1
Loginov, M.2
Clark, L.N.3
Lamarche, J.4
Miller, B.L.5
Lamontagne, A.6
Zhukareva, V.7
Lee, V.M.-Y.8
Wilhelmsen, K.C.9
Geschwind, D.H.10
-
135
-
-
0031672540
-
Frontotemporal lobar degeneration: A consensus on clinical diagnostic criteria
-
(1998)
Neurology
, vol.51
, pp. 1546-1554
-
-
Neary, D.1
Snowden, J.S.2
Gustafson, L.3
Passant, U.4
Stuss, D.5
Black, S.6
Freedman, M.7
Kertesz, A.8
Robert, P.H.9
Albert, M.10
Boone, K.11
Miller, B.L.12
Cummings, J.13
Benson, D.F.14
-
140
-
-
14444284106
-
Tau is a candidate gene for chromosome 17 frontotemporal dementia
-
(1998)
Ann. Neurol.
, vol.43
, pp. 815-825
-
-
Poorkaj, P.1
Bird, T.D.2
Wijsman, E.3
Nemens, E.4
Garruto, R.M.5
Anderson, L.6
Andreadis, A.7
Wiederholt, W.C.8
Raskind, M.9
Schellenberg, G.D.10
-
141
-
-
0342803685
-
Axonopathy and amyotrophy in mice transgenic for human four-repeat tau protein
-
(2000)
Acta Neuropathol. (Berl)
, vol.99
, pp. 469-481
-
-
Probst, A.1
Gotz, J.2
Wiederhold, K.H.3
Tolnay, M.4
Mistl, C.5
Jaton, A.L.6
Hong, M.7
Ishihara, T.8
Lee, V.M.-Y.9
Trojanowski, J.Q.10
Jakes, R.11
Crowther, R.A.12
Spillantini, M.G.13
Burki, K.14
Goedert, M.15
-
145
-
-
0030826625
-
Autosomal dominant dementia with widespread neurofibrillary tangles
-
(1997)
Ann. Neurol.
, vol.42
, pp. 564-572
-
-
Reed, L.A.1
Grabowski, T.J.2
Schmidt, M.L.3
Morris, J.C.4
Goate, A.5
Solodkin, A.6
Van Hoesen, G.W.7
Schelper, R.L.8
Talbot, C.J.9
Wragg, M.A.10
Trojanowski, J.Q.11
-
146
-
-
0031780496
-
The neuropathology of a chromosome 17-linked autosomal dominant parkinsonism and dementia ("pallido-ponto-nigral degeneration")
-
(1998)
J. Neuropathol. Exp. Neurol.
, vol.57
, pp. 588-601
-
-
Reed, L.A.1
Schmidt, M.L.2
Wszolek, Z.K.3
Balin, B.J.4
Soontornniyomkij, V.5
Lee, V.M.-Y.6
Trojanowski, J.Q.7
Schelper, R.L.8
-
149
-
-
0033070197
-
High prevalence of mutations in the microtubule-associated protein tau in a population study of frontotemporal dementia in the Netherlands
-
(1999)
Am. J. Hum. Genet.
, vol.64
, pp. 414-421
-
-
Rizzu, P.1
Van Swieten, J.C.2
Joosse, M.3
Hasegawa, M.4
Stevens, M.5
Tibben, A.6
Niermeijer, M.F.7
Hillebrand, M.8
Ravid, R.9
Oostra, B.A.10
Goedert, M.11
Van Duijn, C.M.12
Heutink, P.13
-
150
-
-
0034193290
-
Missense point mutations of tau to segregate with FTDP-17 exhibit site-specific effects on microtubule structure in COS cells: A novel action of R406W mutation
-
(2000)
J. Neurosci. Res.
, vol.60
, pp. 380-387
-
-
Sahara, N.1
Tomiyama, T.2
Mori, H.3
-
151
-
-
0029971280
-
Neurofibrillary tangles in progressive supranuclear palsy contain the same tau epitopes identified in Alzheimer's disease PHFtau
-
(1996)
J. Neuropathol. Exp. Neurol.
, vol.55
, pp. 534-539
-
-
Schmidt, M.L.1
Huang, R.2
Martin, J.A.3
Henley, J.4
Mawal-Dewan, M.5
Hurtig, H.I.6
Lee, V.M.-Y.7
Trojanowski, J.Q.8
-
152
-
-
0034701238
-
The origins of Alzheimer disease: A is for amyloid
-
(2000)
JAMA
, vol.283
, pp. 1615-1617
-
-
Selkoe, D.J.1
-
157
-
-
0028978701
-
Detection of phosphorylated Ser262 in fetal tau, adult tau, and paired helical filament tau
-
(1995)
J. Biol. Chem.
, vol.270
, pp. 18917-18922
-
-
Seubert, P.1
Mawal-Dewan, M.2
Barbour, R.3
Jakes, R.4
Goedert, M.5
Johnson, G.V.6
Litersky, J.M.7
Schenk, D.8
Lieberburg, I.9
Trojanowski, J.Q.10
Lee, V.M.-Y.11
-
160
-
-
0029944376
-
The neuropathology of chromosome 17-linked dementia
-
(1996)
Ann. Neurol.
, vol.39
, pp. 734-743
-
-
Sima, A.A.1
Defendini, R.2
Keohane, C.3
D'Amato, C.4
Foster, N.L.5
Parchi, P.6
Gambetti, P.7
Lynch, T.8
Wilhelmsen, K.C.9
-
165
-
-
0033520355
-
Molecular interactions among protein phosphatase 2A, tau, and microtubules. Implications for the regulation of tau phosphorylation and the development of tauopathies
-
(1999)
J. Biol. Chem.
, vol.274
, pp. 25490-25498
-
-
Sontag, E.1
Nunbhakdi-Craig, V.2
Lee, G.3
Brandt, R.4
Kamibayashi, C.5
Kuret, J.6
White III, C.L.7
Mumby, M.C.8
Bloom, G.S.9
-
166
-
-
0032724611
-
FTDP-17: An early-onset phenotype with parkinsonism and epileptic seizures caused by a novel mutation
-
(1999)
Ann. Neurol.
, vol.46
, pp. 708-715
-
-
Sperfeld, A.D.1
Collatz, M.B.2
Baier, H.3
Palmbach, M.4
Storch, A.5
Schwarz, J.6
Tatsch, K.7
Reske, S.8
Joosse, M.9
Heutink, P.10
Ludolph, A.C.11
-
170
-
-
0032786370
-
Prominent axonopathy in the brain and spinal cord of transgenic mice overexpressing four-repeat human tau protein
-
(1999)
Am. J. Pathol.
, vol.155
, pp. 2153-2165
-
-
Spittaels, K.1
Van den, H.C.2
Van Dorpe, J.3
Bruynseels, K.4
Vandezande, K.5
Laenen, I.6
Geerts, H.7
Mercken, M.8
Sciot, R.9
Van Lommel, A.10
Loos, R.11
Van Leuven, F.12
-
171
-
-
0034093228
-
Progressive supranuclear palsy pathology caused by a novel silent mutation in exon 10 of the tau gene: Expansion of the disease phenotype caused by tau gene mutations
-
(2000)
Brain
, vol.123
, pp. 880-893
-
-
Stanford, P.M.1
Halliday, G.M.2
Brooks, W.S.3
Kwok, J.B.4
Storey, C.E.5
Creasey, H.6
Morris, J.G.7
Fulham, M.J.8
Schofield, P.R.9
-
173
-
-
0011444914
-
Two amyloid precursor protein transgenic mouse models with Alzheimer disease-like pathology
-
(1997)
Proc. Natl. Acad. Sci. USA
, vol.94
, pp. 13287-13292
-
-
Sturchler-Pierrat, C.1
Abramowski, D.2
Duke, M.3
Wiederhold, K.H.4
Mistl, C.5
Rothacher, S.6
Ledermann, B.7
Burki, K.8
Frey, P.9
Paganetti, P.A.10
Waridel, C.11
Calhoun, M.E.12
Jucker, M.13
Probst, A.14
Staufenbiel, M.15
Sommer, B.16
-
181
-
-
0032880430
-
Phenotypic variation in hereditary frontotemporal dementia with tau mutations
-
(1999)
Ann. Neurol.
, vol.46
, pp. 617-626
-
-
Van Swieten, J.C.1
Stevens, M.2
Rosso, S.M.3
Rizzu, P.4
Joosse, M.5
De, K.6
Kamphorst, I.7
Ravid, W.8
Spillantini, R.9
Niermeijer, M.G.10
Heutink, P.11
-
182
-
-
0033529304
-
Structure of tau exon 10 splicing regulatory element RNA and destabilization by mutations of frontotemporal dementia and parkinsonism linked to chromosome 17
-
(1999)
Proc. Natl. Acad. Sci. USA
, vol.96
, pp. 8229-8234
-
-
Varani, L.1
Hasegawa, M.2
Spillantini, M.G.3
Smith, M.J.4
Murrell, J.R.5
Ghetti, B.6
Klug, A.7
Goedert, M.8
Varani, G.9
-
184
-
-
0027370141
-
In vivo phosphorylation sites in fetal and adult rat tau
-
(1993)
J. Biol. Chem.
, vol.268
, pp. 25712-25717
-
-
Watanabe, A.1
Hasegawa, M.2
Suzuki, M.3
Takio, K.4
Morishima-Kawashima, M.5
Titani, K.6
Arai, T.7
Kosik, K.S.8
Ihara, Y.9
-
186
-
-
9044220964
-
Localization of the gene for rapidly progressive autosomal dominant parkinsonism and dementia with pallido-ponto-nigral degeneration to chromosome 17q21
-
(1996)
Hum. Mol. Genet.
, vol.5
, pp. 151-154
-
-
Wijker, M.1
Wszolek, Z.K.2
Wolters, E.C.3
Rooimans, M.A.4
Pals, G.5
Pfeiffer, R.F.6
Lynch, T.7
Rodnitzky, R.L.8
Wilhelmsen, K.C.9
Arwert, F.10
-
188
-
-
0003986552
-
Isolation of a fragment of tau derived from the core of the paired helical filament of Alzheimer disease
-
(1988)
Proc. Natl. Acad. Sci. USA
, vol.85
, pp. 4506-4510
-
-
Wischik, C.M.1
Novak, M.2
Thogersen, H.C.3
Edwards, P.C.4
Runswick, M.J.5
Jakes, R.6
Walker, J.E.7
Milstein, C.8
Roth, M.9
Klug, A.10
-
190
-
-
0033546987
-
A mutation in the microtubule-associated protein tau in pallido-nigro-luysian degeneration
-
(1999)
Neurology
, vol.53
, pp. 864-868
-
-
Yasuda, M.1
Kawamata, T.2
Komure, O.3
Kuno, S.4
D'Souza, I.5
Poorkaj, P.6
Kawai, J.7
Tanimukai, S.8
Yamamoto, Y.9
Hasegawa, H.10
Sasahara, M.11
Hazama, F.12
Schellenberg, G.D.13
Tanaka, C.14
-
191
-
-
0034074542
-
A novel mutation at posititon +12 in the intron following exon 10 of the tau gene in familial frontotemporal dementia (FTD-Kumamoto)
-
(2000)
Ann. Neurol.
, vol.47
, pp. 422-429
-
-
Yasuda, M.1
Takamatsu, J.2
D'Souza, I.3
Crowther, R.A.4
Kawamata, T.5
Hasegawa, M.6
Hasegawa, H.7
Spillantini, M.G.8
Tanimukai, S.9
Poorkaj, P.10
Varani, L.11
Varani, G.12
Iwatsubo, T.13
Goedert, M.14
Schellenberg, D.G.15
Tanaka, C.16
-
192
-
-
0027237861
-
Tau in paired helical filaments is functionally distinct from fetal tau: Assembly incompetence of paired helical filament-tau
-
(1993)
J. Neurochem.
, vol.61
, pp. 1183-1186
-
-
Yoshida, H.1
Ihara, Y.2
|