-
3
-
-
0039575094
-
Comparative biochemistry of tau in progressive supranuclear palsy, corticobasal degeneration, FTDP-17 and Pick's disease
-
(1999)
Brain Pathol.
, vol.9
, pp. 681-693
-
-
Buee, L.1
Delacourte, A.2
-
4
-
-
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
-
5
-
-
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
-
6
-
-
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.H.6
Wiederholt, W.7
Hansen, L.8
Masliah, E.9
Thal, L.J.10
Katzman, R.11
Xia, Y.12
Saitoh, T.13
-
10
-
-
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.A.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
-
12
-
-
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.-Y.5
Bird, T.D.6
Schellenberg, G.D.7
-
13
-
-
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.8
Penet, C.9
Charbonnier, F.10
Agid, Y.11
Frebourg, T.12
Brice, A.13
-
15
-
-
0026088977
-
Segregation of a missense mutation in the amyloid precursor protein gene with familial Alzheimer's disease
-
(1991)
Nature
, vol.349
, pp. 704-706
-
-
Goate, A.1
-
20
-
-
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
-
28
-
-
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.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
-
29
-
-
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
-
30
-
-
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
-
31
-
-
37049048544
-
Paired helical filaments in electron microscopy of Alzheimer's disease
-
(1963)
Nature
, vol.197
, pp. 192-193
-
-
Kidd, M.1
-
32
-
-
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
-
33
-
-
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
-
35
-
-
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
-
37
-
-
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
-
39
-
-
0027398169
-
Molecular characterization of the minimal protease resistant tau unit of the Alzheimer's disease paired helical filament
-
(1993)
EMBO J.
, vol.12
, pp. 365-370
-
-
Novak, M.1
Kabat, J.2
Wischik, C.M.3
-
40
-
-
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
-
42
-
-
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
-
44
-
-
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
-
53
-
-
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 Koning, I.6
Kamphorst, W.7
Ravid, R.8
Spillantini, M.G.9
Niermeijer, M.F.10
Heutink, P.11
-
54
-
-
0033529304
-
Structure of tau exon 10 splicing regulatory element RNA and destabilisation 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
-
59
-
-
0034074542
-
A novel mutation at position +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, G.D.15
Tanaka, C.16
|