-
1
-
-
0033041179
-
Association of an extended haplotype in the tau gene with progressive supranuclear palsy
-
Baker M., Litvan I., Houlden H., Adamson J., Dickson D., Pérez-Tur J., Hardy J., Lynch T., Bigio E., Hutton M. Association of an extended haplotype in the tau gene with progressive supranuclear palsy. Hum. Mol. Genet. 4:1999;711-715
-
(1999)
Hum. Mol. Genet.
, vol.4
, pp. 711-715
-
-
Baker, M.1
Litvan, I.2
Houlden, H.3
Adamson, J.4
Dickson, D.5
Pérez-Tur, J.6
Hardy, J.7
Lynch, T.8
Bigio, E.9
Hutton, M.10
-
2
-
-
0031044850
-
Genetic evidence for the involvement of tau in progressive supranuclear palsy
-
Conrad C., Andreadis A., Trojanowski J.Q., Dickson D.W., Kang D., Chen X., Wiederholt W., Hansen L., Masliah E., Thal L.J., Katzman R., Xia Y., Saitoh T. Genetic evidence for the involvement of tau in progressive supranuclear palsy. Ann. Neurol. 41:1997;277-281
-
(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
-
3
-
-
18444402765
-
A large Calabrian family segregating frontal temporal dementia
-
Curcio S.A., Kawarai T., Paterson A.D., Maletta R.G., Pucci G., Perri M.D., Palermo S., Foncin J.F., Hyslop P.H., Bruni A.C. A large Calabrian family segregating frontal temporal dementia. J. Neurol. 249:2002;911-922
-
(2002)
J. Neurol.
, vol.249
, pp. 911-922
-
-
Curcio, S.A.1
Kawarai, T.2
Paterson, A.D.3
Maletta, R.G.4
Pucci, G.5
Perri, M.D.6
Palermo, S.7
Foncin, J.F.8
Hyslop, P.H.9
Bruni, A.C.10
-
4
-
-
0035880458
-
α-Synuclein gene haplotypes are associated with Parkinson's disease
-
Farrer M., Maraganore D.M., Lockhart P., Singleton A., Lesnick T.G., de Andrade M., West A., de Silva R., Hardy J., Hernandez D. α-Synuclein gene haplotypes are associated with Parkinson's disease. Hum. Mol. Genet. 10:2001;1847-1851
-
(2001)
Hum. Mol. Genet.
, vol.10
, pp. 1847-1851
-
-
Farrer, M.1
Maraganore, D.M.2
Lockhart, P.3
Singleton, A.4
Lesnick, T.G.5
De Andrade, M.6
West, A.7
De Silva, R.8
Hardy, J.9
Hernandez, D.10
-
5
-
-
0042821633
-
Extended investigation of tau and mutation screening of other candidate genes on chromosome 17q21 in a Swedish FTDP-17 family
-
Froelich Fabre S., Axelman P., Almkvist A., Basun H., Lannfelt L. Extended investigation of tau and mutation screening of other candidate genes on chromosome 17q21 in a Swedish FTDP-17 family. Am. J. Med. Genet. 121B:2000;112-118
-
(2000)
Am. J. Med. Genet.
, vol.121
, pp. 112-118
-
-
Froelich Fabre, S.1
Axelman, P.2
Almkvist, A.3
Basun, H.4
Lannfelt, L.5
-
6
-
-
0035961293
-
From genetics to pathology: Tau and alpha-synuclein assemblies in neurodegenerative diseases
-
Goedert M., Spillantini M.G., Serpell L.C., Berriman J., Smith M.J., Jakes R., Crowther R.A. From genetics to pathology: tau and alpha-synuclein assemblies in neurodegenerative diseases. Philos. Trans. R. Soc. Lond. B Biol. Sci. 356:2001;213-227
-
(2001)
Philos. Trans. R. Soc. Lond. B Biol. Sci.
, vol.356
, pp. 213-227
-
-
Goedert, M.1
Spillantini, M.G.2
Serpell, L.C.3
Berriman, J.4
Smith, M.J.5
Jakes, R.6
Crowther, R.A.7
-
7
-
-
0027967997
-
Lewy bodies in Alzheimer's disease in which the primary lesion is a mutation in the amyloid precursor protein
-
Hardy J. Lewy bodies in Alzheimer's disease in which the primary lesion is a mutation in the amyloid precursor protein. Neurosci. Lett. 180:1994;290-292
-
(1994)
Neurosci. Lett.
, vol.180
, pp. 290-292
-
-
Hardy, J.1
-
8
-
-
0035954364
-
Corticobasal degeneration and progressive supranuclear palsy share a common tau haplotype
-
Houlden H., Baker M., Morris H.R., MacDonald N., Pickering-Brown S., Adamson J., Lees A.J., Rossor M.N., Quinn N.P., Kertesz A., Khan M.N., Hardy J., Lantos P.L., St George-Hyslop P., Munoz D.G., Mann D., Lang A.E., Bergeron C., Bigio E.H., Litvan I., Bhatia K.P., Dickson D., Wood N.W., Hutton M. Corticobasal degeneration and progressive supranuclear palsy share a common tau haplotype. Neurology. 56:2001;1702-1706
-
(2001)
Neurology
, vol.56
, pp. 1702-1706
-
-
Houlden, H.1
Baker, M.2
Morris, H.R.3
MacDonald, N.4
Pickering-Brown, S.5
Adamson, J.6
Lees, A.J.7
Rossor, M.N.8
Quinn, N.P.9
Kertesz, A.10
Khan, M.N.11
Hardy, J.12
Lantos, P.L.13
St George-Hyslop, P.14
Munoz, D.G.15
Mann, D.16
Lang, A.E.17
Bergeron, C.18
Bigio, E.H.19
Litvan, I.20
Bhatia, K.P.21
Dickson, D.22
Wood, N.W.23
Hutton, M.24
more..
-
9
-
-
0032543684
-
Coding and splice donor site mutations in tau cause autosomal dominant dementia (FTDP-17)
-
Hutton M., Lendon C.L., Rizzu P., Baker M., Froelich S., Houlden H., Pickering-Brown S., Chakraverty S., Isaacs A., Grover A., Hackett J., Adamson J., Lincoln S., Dickson D., Davies P., Petersen R.C., Stevens M., de Graaff E., Wauters E., van Baren J., Hillebrand M., Joosse M., Kwon J.M., Nowotny P., Che L., Norton J., Morris J.C., Reed L.A., Trojanowski J., Basun H., Lannfelt L., Neystat M., Fahn S., Dark F., Tannenberg T., Dodd P.R., Hayward N., Kwok J.B.J., Schofield P.R., Andreadis A., Snowden J., Craufurd D., Neary D., Owen F., Oostra B.A., Hardy J., Goate A., Van Swieten J., Mann D., Lynch T., Heutink P. Coding and splice donor site mutations in tau cause autosomal dominant 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
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
Che, L.25
Norton, J.26
Morris, J.C.27
Reed, L.A.28
Trojanowski, J.29
Basun, H.30
Lannfelt, L.31
Neystat, M.32
Fahn, S.33
Dark, F.34
Tannenberg, T.35
Dodd, P.R.36
Hayward, N.37
Kwok, J.B.J.38
Schofield, P.R.39
Andreadis, A.40
Snowden, J.41
Craufurd, D.42
Neary, D.43
Owen, F.44
Oostra, B.A.45
Hardy, J.46
Goate, A.47
Van Swieten, J.48
Mann, D.49
Lynch, T.50
Heutink, P.51
more..
-
10
-
-
0342950666
-
Increased susceptibility to sporadic Parkinson's disease by a certain combined alpha-synuclein/apolipoprotein e genotype
-
Kruger R., Vieira-Saecker A.M., Kuhn W., Berg D., Muller T., Kuhnl N., Fuchs G.A., Storch A., Hungs M., Woitalla D., Przuntek H., Epplen J.T., Schols L., Riess O. Increased susceptibility to sporadic Parkinson's disease by a certain combined alpha-synuclein/apolipoprotein E genotype. Ann. Neurol. 45:1999;611-617
-
(1999)
Ann. Neurol.
, vol.45
, pp. 611-617
-
-
Kruger, R.1
Vieira-Saecker, A.M.2
Kuhn, W.3
Berg, D.4
Muller, T.5
Kuhnl, N.6
Fuchs, G.A.7
Storch, A.8
Hungs, M.9
Woitalla, D.10
Przuntek, H.11
Epplen, J.T.12
Schols, L.13
Riess, O.14
-
11
-
-
17944382037
-
Enhanced neurofibrillary degeneration in transgenic mice expressing mutant tau and APP
-
Lewis J., Dickson D.W., Lin W.L., Chisholm L., Corral A., Jones G., Yen S.H., Sahara N., Skipper L., Yager D., Eckman C., Hardy J., Hutton M., McGowan E. Enhanced neurofibrillary degeneration in transgenic mice expressing mutant tau and APP. Science. 293:2001;1487-1491
-
(2001)
Science
, vol.293
, pp. 1487-1491
-
-
Lewis, J.1
Dickson, D.W.2
Lin, W.L.3
Chisholm, L.4
Corral, A.5
Jones, G.6
Yen, S.H.7
Sahara, N.8
Skipper, L.9
Yager, D.10
Eckman, C.11
Hardy, J.12
Hutton, M.13
McGowan, E.14
-
12
-
-
0034426011
-
Neurofibrillary tangles, amyotrophy and progressive motor disturbance in mice expressing mutant (P301L) tau protein
-
Lewis J., McGowan E., Rockwood J., Melrose H., Nacharaju P., Van Slegtenhorst M., Gwinn-Hardy K., Murphy M.P., Baker M., Yu X., Duff K., Hardy J., Corrall A., Lin W.L., Yen S.H., Dickson D.W., Davies D.W., Hutton M. Neurofibrillary tangles, amyotrophy and progressive motor disturbance in mice expressing mutant (P301L) tau protein. Nat. Genet. 25:2000;402-405
-
(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
Murphy, M.P.8
Baker, M.9
Yu, X.10
Duff, K.11
Hardy, J.12
Corrall, A.13
Lin, W.L.14
Yen, S.H.15
Dickson, D.W.16
Davies, D.W.17
Hutton, M.18
-
13
-
-
0034681471
-
Dopaminergic loss and inclusion body formation in alpha-synuclein mice: Implications for neurodegenerative disorders
-
Masliah E., Rockenstein E., Veinbergs I., Mallory M., Hashimoto M., Takeda A., Sagara Y., Sisk A., Mucke L. Dopaminergic loss and inclusion body formation in alpha-synuclein mice: implications for neurodegenerative disorders. Science. 287:2000;1265-1269
-
(2000)
Science
, vol.287
, pp. 1265-1269
-
-
Masliah, E.1
Rockenstein, E.2
Veinbergs, I.3
Mallory, M.4
Hashimoto, M.5
Takeda, A.6
Sagara, Y.7
Sisk, A.8
Mucke, L.9
-
14
-
-
0035834076
-
Beta-amyloid peptides enhance alpha-synuclein accumulation and neuronal deficits in a transgenic mouse model linking Alzheimer's disease and Parkinson's disease
-
Masliah E., Rockenstein E., Veinbergs I., Sagara Y., Mallory M., Hashimoto M., Mucke L. Beta-amyloid peptides enhance alpha-synuclein accumulation and neuronal deficits in a transgenic mouse model linking Alzheimer's disease and Parkinson's disease. Proc. Natl. Acad. Sci. USA. 98:2001;12245-12250
-
(2001)
Proc. Natl. Acad. Sci. USA
, vol.98
, pp. 12245-12250
-
-
Masliah, E.1
Rockenstein, E.2
Veinbergs, I.3
Sagara, Y.4
Mallory, M.5
Hashimoto, M.6
Mucke, L.7
-
15
-
-
0030744876
-
Mutation in the alpha-synuclein gene identified in families with Parkinson's disease
-
Polymeropoulos M.H., Lavedan C., Leroy E., Ide S.E., Dehejia A., Dutra A., Pike B., Root H., Rubenstein J., Boyer R., Stenroos E.S., Chandrasekharappa S., Athanassiadou A., Papapetropoulos T., Johnson W.G., Lazzarini A.M., Duvoisin R.C., Di Iorio G., Golbe L.I., Nussbaum R.L. Mutation in the alpha-synuclein gene identified in families with Parkinson's disease. Science. 276:1997;2045-2047
-
(1997)
Science
, vol.276
, pp. 2045-2047
-
-
Polymeropoulos, M.H.1
Lavedan, C.2
Leroy, E.3
Ide, S.E.4
Dehejia, A.5
Dutra, A.6
Pike, B.7
Root, H.8
Rubenstein, J.9
Boyer, R.10
Stenroos, E.S.11
Chandrasekharappa, S.12
Athanassiadou, A.13
Papapetropoulos, T.14
Johnson, W.G.15
Lazzarini, A.M.16
Duvoisin, R.C.17
Di Iorio, G.18
Golbe, L.I.19
Nussbaum, R.L.20
more..
-
16
-
-
14444284106
-
Tau is a candidate gene for chromosome 17 frontotemporal dementia
-
Poorkaj P., Bird T.D., Wijsman E., Nemens E., Garruto R.M., Anderson L., Andreadis A., Wiederholt W.C., Raskind M., Schellenberg G.D. Tau is a candidate gene for chromosome 17 frontotemporal dementia. Ann. Neurol. 43:1998;815-825
-
(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
-
17
-
-
0242300619
-
α-Synuclein locus triplication causes Parkinson's disease
-
Singleton A., Farrer M., Johnson J., Singleton A., Hague S., Kachergus J., Hulihan M., Peuralinna T., Dutra A., Nussbaum R., Lincoln S., Crawley A., Hanson M., Maraganore D., Adler C., Cookson M.R., Muenter M., Baptista M., Miller D., Blancato J., Hardy J., Gwinn-Hardy K. α-Synuclein locus triplication causes Parkinson's disease. Science. 302:2003;841
-
(2003)
Science
, vol.302
, pp. 841
-
-
Singleton, A.1
Farrer, M.2
Johnson, J.3
Singleton, A.4
Hague, S.5
Kachergus, J.6
Hulihan, M.7
Peuralinna, T.8
Dutra, A.9
Nussbaum, R.10
Lincoln, S.11
Crawley, A.12
Hanson, M.13
Maraganore, D.14
Adler, C.15
Cookson, M.R.16
Muenter, M.17
Baptista, M.18
Miller, D.19
Blancato, J.20
Hardy, J.21
Gwinn-Hardy, K.22
more..
|