-
1
-
-
0034624917
-
Two brothers with frontotemporal dementia and parkinsonism with an N279K mutation of the tau gene
-
Arima K., Kowalska A., Hasegawa M., Mukoyama M., Watanabe R., Kawai M., Takahashi K., Iwatsubo T., Tabira T., Sunohara N. Two brothers with frontotemporal dementia and parkinsonism with an N279K mutation of the tau gene. Neurology. 54:2000;1787-1795.
-
(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
-
2
-
-
0032859650
-
Overexpression of four-repeat tau mRNA isoforms in progressive supranuclear palsy but not in Alzheimer's disease
-
Chambers C.B., Lee J.M., Troncoso J.C., Reich S., Muma N.A. Overexpression of four-repeat tau mRNA isoforms in progressive supranuclear palsy but not in Alzheimer's disease. Ann. Neurol. 46:1999;325-332.
-
(1999)
Ann. Neurol.
, vol.46
, pp. 325-332
-
-
Chambers, C.B.1
Lee, J.M.2
Troncoso, J.C.3
Reich, S.4
Muma, N.A.5
-
3
-
-
0033545946
-
Missense and silent tau gene mutations cause frontotemporal dementia with parkinsonism-chromosome 17 type by affecting multiple alternative RNA splicing regulatory elements
-
D'Souza I., Poorkaj P., Hong M., Nochlin D., Lee V.M., Bird T.D., Schellenberg G.D. Missense and silent tau gene mutations cause frontotemporal dementia with parkinsonism-chromosome 17 type by affecting multiple alternative RNA splicing regulatory elements. Proc. Natl. Acad. Sci. USA. 96:1999;5598-5603.
-
(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
-
4
-
-
0035370261
-
The significance of tau and alpha-synuclein inclusions in neurodegenerative diseases
-
Goedert M. The significance of tau and alpha-synuclein inclusions in neurodegenerative diseases. Curr. Opin. Genet. Dev. 11:2001;343-351.
-
(2001)
Curr. Opin. Genet. Dev.
, vol.11
, pp. 343-351
-
-
Goedert, M.1
-
5
-
-
0026595846
-
Tau proteins of Alzheimer paired helical filaments: Abnormal phosphorylation of all six brain isoforms
-
Goedert M., Spillantini M.G., Cairns N.J., Crowther R.A. Tau proteins of Alzheimer paired helical filaments: abnormal phosphorylation of all six brain isoforms. Neuron. 8:1992;159-168.
-
(1992)
Neuron
, vol.8
, pp. 159-168
-
-
Goedert, M.1
Spillantini, M.G.2
Cairns, N.J.3
Crowther, R.A.4
-
6
-
-
0024745894
-
Multiple isoforms of human microtubule-associated protein tau: Sequences and localization in neurofibrillary tangles of Alzheimer's disease
-
Goedert M., Spillantini M.G., Jakes R., Rutherford D., Crowther R.A. Multiple isoforms of human microtubule-associated protein tau: sequences and localization in neurofibrillary tangles of Alzheimer's disease. Neuron. 3:1989;519-526.
-
(1989)
Neuron
, vol.3
, pp. 519-526
-
-
Goedert, M.1
Spillantini, M.G.2
Jakes, R.3
Rutherford, D.4
Crowther, R.A.5
-
7
-
-
0029879046
-
Characterization of mAb AP422, a novel phosphorylation-dependent monoclonal antibody against tau protein
-
Hasegawa M., Jakes R., Crowther R.A., Lee V.M., Ihara Y., Goedert M. Characterization of mAb AP422, a novel phosphorylation-dependent monoclonal antibody against tau protein. FEBS Lett. 384:1996;25-30.
-
(1996)
FEBS Lett.
, vol.384
, pp. 25-30
-
-
Hasegawa, M.1
Jakes, R.2
Crowther, R.A.3
Lee, V.M.4
Ihara, Y.5
Goedert, M.6
-
8
-
-
0032561415
-
Tau proteins with FTDP-17 mutations have a reduced ability to promote microtubule assembly
-
Hasegawa M., Smith M.J., Goedert M. Tau proteins with FTDP-17 mutations have a reduced ability to promote microtubule assembly. FEBS Lett. 437:1998;207-210.
-
(1998)
FEBS Lett.
, vol.437
, pp. 207-210
-
-
Hasegawa, M.1
Smith, M.J.2
Goedert, M.3
-
9
-
-
0033060662
-
FTDP-17 mutations N279K and S305N in tau produce increased splicing of exon 10
-
Hasegawa M., Smith M.J., Iijima M., Tabira T., Goedert M. FTDP-17 mutations N279K and S305N in tau produce increased splicing of exon 10. FEBS Lett. 443:1999;93-96.
-
(1999)
FEBS Lett.
, vol.443
, pp. 93-96
-
-
Hasegawa, M.1
Smith, M.J.2
Iijima, M.3
Tabira, T.4
Goedert, M.5
-
10
-
-
0036198120
-
Late-onset frontotemporal dementia with a novel exon 1 (Arg5His) tau gene mutation
-
Hayashi S., Toyoshima Y., Hasegawa M., Umeda Y., Wakabayashi K., Tokiguchi S., Iwatsubo T., Takahashi H. Late-onset frontotemporal dementia with a novel exon 1 (Arg5His) tau gene mutation. Ann. Neurol. 51:2002;525-530.
-
(2002)
Ann. Neurol.
, vol.51
, pp. 525-530
-
-
Hayashi, S.1
Toyoshima, Y.2
Hasegawa, M.3
Umeda, Y.4
Wakabayashi, K.5
Tokiguchi, S.6
Iwatsubo, T.7
Takahashi, H.8
-
11
-
-
0032543684
-
Association of missense and 5′-splice-site mutations in tau with the inherited dementia FTDP-17
-
Hutton M., Lendon C.L., Rizzu P., Baker M., et al. Association of missense and 5′-splice-site mutations in tau with the inherited dementia FTDP-17. Nature. 393:1998;702-705.
-
(1998)
Nature
, vol.393
, pp. 702-705
-
-
Hutton, M.1
Lendon, C.L.2
Rizzu, P.3
Baker, M.4
-
12
-
-
0036771837
-
An R5L tau mutation in a subject with a progressive supranuclear palsy phenotype
-
Poorkaj P., Muma N.A., Zhukareva V., Cochran E.J., Shannon K.M., Hurtig H., Koller W.C., Bird T.D., Trojanowski J.Q., Lee V.M., Schellenberg G.D. An R5L tau mutation in a subject with a progressive supranuclear palsy phenotype. Ann. Neurol. 52:2002;511-516.
-
(2002)
Ann. Neurol.
, vol.52
, pp. 511-516
-
-
Poorkaj, P.1
Muma, N.A.2
Zhukareva, V.3
Cochran, E.J.4
Shannon, K.M.5
Hurtig, H.6
Koller, W.C.7
Bird, T.D.8
Trojanowski, J.Q.9
Lee, V.M.10
Schellenberg, G.D.11
-
13
-
-
0032560487
-
Mutation in the tau gene in familial multiple system tauopathy with presenile dementia
-
Spillantini M.G., Murrell J.R., Goedert M., Farlow M.R., Klug A., Ghetti B. Mutation in the tau gene in familial multiple system tauopathy with presenile dementia. Proc. Natl. Acad. Sci. USA. 95:1998;7737-7741.
-
(1998)
Proc. Natl. Acad. Sci. USA
, vol.95
, pp. 7737-7741
-
-
Spillantini, M.G.1
Murrell, J.R.2
Goedert, M.3
Farlow, M.R.4
Klug, A.5
Ghetti, B.6
-
14
-
-
0037103844
-
Expression patterns of tau mRNA isoforms correlate with susceptible lesions in progressive supranuclear palsy and corticobasal degeneration
-
Takanashi M., Mori H., Arima K., Mizuno Y., Hattori N. Expression patterns of tau mRNA isoforms correlate with susceptible lesions in progressive supranuclear palsy and corticobasal degeneration. Brain Res. Mol. Brain Res. 104:2002;210-219.
-
(2002)
Brain Res. Mol. Brain Res.
, vol.104
, pp. 210-219
-
-
Takanashi, M.1
Mori, H.2
Arima, K.3
Mizuno, Y.4
Hattori, N.5
-
15
-
-
0842265475
-
The neuropathology of frontotemporal lobar degeneration with respect to the cytological and biochemical characteristics of tau protein
-
Taniguchi S., MacDonagh A.M., Pickering-Brown S.M., Umeda Y., Iwatsubo T., Hasegawa M., Mann D.M. The neuropathology of frontotemporal lobar degeneration with respect to the cytological and biochemical characteristics of tau protein. Neuropathol. Appl. Neurobiol. 30:2004;1-18.
-
(2004)
Neuropathol. Appl. Neurobiol.
, vol.30
, pp. 1-18
-
-
Taniguchi, S.1
MacDonagh, A.M.2
Pickering-Brown, S.M.3
Umeda, Y.4
Iwatsubo, T.5
Hasegawa, M.6
Mann, D.M.7
-
16
-
-
0034074542
-
A novel mutation at position +12 in the intron following exon 10 of the tau gene in familial frontotemporal dementia (FTD-Kumamoto)
-
Yasuda M., Takamatsu J., D'Souza I., Crowther R.A., Kawamata T., Hasegawa M., Hasegawa H., Spillantini M.G., Tanimukai S., Poorhaj P., Varami L., Varami G., Iwatsubo T., Goedert M., Schellenberg D.G., Tanaka C. A novel mutation at position +12 in the intron following exon 10 of the tau gene in familial frontotemporal dementia (FTD-Kumamoto). Ann. Neurol. 47:2000;422-429.
-
(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
Poorhaj, P.10
Varami, L.11
Varami, G.12
Iwatsubo, T.13
Goedert, M.14
Schellenberg, D.G.15
Tanaka, C.16
-
17
-
-
0035138764
-
Loss of brain tau defines novel sporadic and familial tauopathies with frontotemporal dementia
-
Zhukareva V., Vogelsberg-Ragaglia V., Van Deerlin V.M., Bruce J., Shuck T., Grossman M., Clark C.M., Arnold S.E., Masliah E., Galasko D., Trojanowski J.Q., Lee V.M. Loss of brain tau defines novel sporadic and familial tauopathies with frontotemporal dementia. Ann. Neurol. 49:2001;165-175.
-
(2001)
Ann. Neurol.
, vol.49
, pp. 165-175
-
-
Zhukareva, V.1
Vogelsberg-Ragaglia, V.2
Van Deerlin, V.M.3
Bruce, J.4
Shuck, T.5
Grossman, M.6
Clark, C.M.7
Arnold, S.E.8
Masliah, E.9
Galasko, D.10
Trojanowski, J.Q.11
Lee, V.M.12
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