-
1
-
-
0033041179
-
Association of an extended haplotype in the tau gene with progressive supranuclear palsy
-
M. Baker I. Litvan H. Houlden J. Adamson D. Dickson J. Perez-Tur J. Hardy T. Lynch E. Bigio M. Hutton Association of an extended haplotype in the tau gene with progressive supranuclear palsy Hum. Mol. Genet. 8 1999 711 715
-
(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
-
2
-
-
0039575094
-
Comparative biochemistry of tau in progressive supranuclear palsy, corticobasal degeneration, FTDP-17 and Pick’s disease
-
L. Buee A. Dalacourte Comparative biochemistry of tau in progressive supranuclear palsy, corticobasal degeneration, FTDP-17 and Pick’s disease Brain Pathol. 9 1999 681 693
-
(1999)
Brain Pathol.
, vol.9
, pp. 681-693
-
-
Buee, L.1
Dalacourte, A.2
-
3
-
-
0034210637
-
Translational pathophysiology: a novel molecular mechanism of human disease
-
M. Cazzola R.C. Skoda Translational pathophysiology: a novel molecular mechanism of human disease Blood 95 2000 3280 3288
-
(2000)
Blood
, vol.95
, pp. 3280-3288
-
-
Cazzola, M.1
Skoda, R.C.2
-
4
-
-
0032859650
-
Overexpression of four-repeat tau mRNA isoforms in progressive supranuclear palsy but not in Alzheimer’s disease
-
C.B. Chambers J.M. Lee J.C. Troncoso S. Reich N.A. Muma 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
-
5
-
-
0031044850
-
Genetic evidence for the involvement of τ in progressive supranuclear palsy
-
C.C. Conrad A. Andreadis J.Q. Trojanowski D.W. Dickson D. Kang X. Chen W. Wiederholt L. Hansen E. Masliah L.J. Thal R. Katzman Y. Xia T. Saitoh Genetic evidence for the involvement of τ in progressive supranuclear palsy Ann. Neurol. 41 1997 277 281
-
(1997)
Ann. Neurol.
, vol.41
, pp. 277-281
-
-
Conrad, C.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
-
6
-
-
0345627999
-
Differences in a dinucleotide repeat polymorphism in the tau gene between Caucasian and Japanese populations: implication for progressive supranuclear palsy
-
C. Conrad N. Amano A. Andreadis Y. Xia K. Namekataf F. Oyama K. Ikeda K. Wakabayashi T. Hitoshi L.J. Thal R. Katzman D.A. Schackelford M. Matsushita E. Masliah A. Sawa Differences in a dinucleotide repeat polymorphism in the tau gene between Caucasian and Japanese populations: implication for progressive supranuclear palsy Neurosci. Lett. 250 1998 135 137
-
(1998)
Neurosci. Lett.
, vol.250
, pp. 135-137
-
-
Conrad, C.1
Amano, N.2
Andreadis, A.3
Xia, Y.4
Namekataf, K.5
Oyama, F.6
Ikeda, K.7
Wakabayashi, K.8
Hitoshi, T.9
Thal, L.J.10
Katzman, R.11
Schackelford, D.A.12
Matsushita, M.13
Masliah, E.14
Sawa, A.15
-
7
-
-
0034625379
-
Determinants of 4-repeat tau expression
-
I. D’Souza G.D. Schellenberg Determinants of 4-repeat tau expression J. Biol. Chem. 275 2000 17700 17709
-
(2000)
J. Biol. Chem.
, vol.275
, pp. 17700-17709
-
-
D’Souza, I.1
Schellenberg, G.D.2
-
8
-
-
0033545946
-
Missense and silent tau gene mutations cause frontotemporal dementia with parkinsonism-chromosome 17 type, by affecting multiple alternative RNA splicing regulatory elements
-
I. D’Souza P. Poorkaj M. Hong D. Nochlin V.M-Y. Lee T. Bird G.D. Schellenberg 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-Y.5
Bird, T.6
Schellenberg, G.D.7
-
9
-
-
0034011659
-
Corticobasal degeneration shares a common genetic background with progressive supranuclear palsy
-
E. Di Maria M. Tabaton T. Vigo G. Abbruzzese E. Bellone C. Donati E. Frasson R. Marchase P. Montagna D.G. Munoz P.P. Pramstaller G. Zanuzzo F. Ajmar P. Mandich Corticobasal degeneration shares a common genetic background with progressive supranuclear palsy Ann. Neurol. 47 2000 374 377
-
(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
Marchase, R.8
Montagna, P.9
Munoz, D.G.10
Pramstaller, P.P.11
Zanuzzo, G.12
Ajmar, F.13
Mandich, P.14
-
10
-
-
85120190689
-
-
D.W. Dickson, W.K. Liu, H. Ksiezak-Reding, S.H. Yen, Neuropathological and molecular considerations, in: I. Litvan, C.G. Goetz, A.E. Lang (Eds.), Corticobasal degeneration, Adv. Neurol. 82, Lippincott, Williams and Wilkins, Philadelphia, 2000, pp. 9–27.
-
-
-
-
11
-
-
85120188167
-
-
D.W. Dickson, Neuropathologic differentiation of progressive supranuclear palsy and corticobasal degeneration, J. Neurol. 246(Suppl. 2) (1999) II/6–II/15.
-
-
-
-
13
-
-
0030049067
-
Neuropathologic overlap of progressive supranuclear palsy, Pick’s disease and corticobasal degeneration
-
M.B. Feany L.A. Mattiace D.W. Dickson Neuropathologic overlap of progressive supranuclear palsy, Pick’s disease and corticobasal degeneration J. Neuropathol. Exp. Neurol. 55 1996 53 67
-
(1996)
J. Neuropathol. Exp. Neurol.
, vol.55
, pp. 53-67
-
-
Feany, M.B.1
Mattiace, L.A.2
Dickson, D.W.3
-
15
-
-
0002792366
-
Cloning and sequencing of the cDNA encoding a core protein of the paired helical filament of Alzheimer disease; identification as the microtubule-associated protein tau
-
M. Goedert C.M. Wischik R.A. Crowther J.E. Walker A. Klug Cloning and sequencing of the cDNA encoding a core protein of the paired helical filament of Alzheimer disease; identification as the microtubule-associated protein tau Proc. Natl. Acad. Sci. USA 85 1988 4051 4055
-
(1988)
Proc. Natl. Acad. Sci. USA
, vol.85
, pp. 4051-4055
-
-
Goedert, M.1
Wischik, C.M.2
Crowther, R.A.3
Walker, J.E.4
Klug, A.5
-
16
-
-
0024387161
-
Cloning and sequencing of the cDNA encoding an isoform of microtubule-associated protein tau containing four tandem repeats: differential expression of tau protein mRNAs in human brain
-
M. Goedert M.G. Spillantini M.C. Potier J. Ulrich R.A. Crowther Cloning and sequencing of the cDNA encoding an isoform of microtubule-associated protein tau containing four tandem repeats: differential expression of tau protein mRNAs in human brain EMBO J. 8 1989 393 399
-
(1989)
EMBO J.
, vol.8
, pp. 393-399
-
-
Goedert, M.1
Spillantini, M.G.2
Potier, M.C.3
Ulrich, J.4
Crowther, R.A.5
-
17
-
-
0024745894
-
Multiple isoforms of human microtubule-associated protein tau: sequences and localization in neurofibrillary tangles of Alzheimer’s disease
-
M. Goedert M.G. Spillantini R. Jakes D. Rutherford R.A. Crowther 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
-
18
-
-
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
-
A. Grover H.M. Houlden M. Baker J. Adamson J. Lewis G. Prihar S. Pickering-Brown K. Duff M. Hutton 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 J. Biol. Chem. 274 1999 15134 15143
-
(1999)
J. Biol. Chem.
, vol.274
, pp. 15134-15143
-
-
Grover, A.1
Houlden, H.M.2
Baker, M.3
Adamson, J.4
Lewis, J.5
Prihar, G.6
Pickering-Brown, S.7
Duff, K.8
Hutton, M.9
-
19
-
-
0033060662
-
FTDP-17 mutations N279K and S305N in tau produce increased splicing of exon 10
-
M. Hasegawa M.J. Smith M. Iijima T. Tabira M. Goedert 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
-
20
-
-
0028092015
-
Preliminary NINDS neuropathologic criteria for Steel-Richardson-Olszewski syndrome (progressive supranuclear palsy)
-
J.J. Hauw S.E. Daniel D.W. Dickson D.S. Horoupian K. Jellinger P.L. Lantos A. McKee M. Tabaton I. Litven Preliminary NINDS neuropathologic criteria for Steel-Richardson-Olszewski syndrome (progressive supranuclear palsy) Neurology 44 1994 2015 2019
-
(1994)
Neurology
, vol.44
, pp. 2015-2019
-
-
Hauw, J.J.1
Daniel, S.E.2
Dickson, D.W.3
Horoupian, D.S.4
Jellinger, K.5
Lantos, P.L.6
McKee, A.7
Tabaton, M.8
Litven, I.9
-
23
-
-
0032543684
-
Association of missense and 5′-splice-site mutations in tau with the inherited dementia FTDP-17
-
M. Hutton C.L. Lendon P. Rizzu M. Baker S. Froelich H. Houlden S. Pickering-Brown S. Chakraverthy A. Isaacs A. Grover J. Hackett J. Adamson A. Lincoln D. Dickson P. Davis R.C. Petersen M. Stevens E. de Graaff E. Wauters J. van Baren M. Hillebrand M. Joosse J.M. Kwon P. Nowothny L.K. Che J. Norton J.C. Morris L.A. Reed J. Trojanowski H. Basun L. Lannfelt M. Neystat S. Fahn F. Dark T. Tannenberg P.R. Dodd N. Hayward J.B.L. Kwok P.R. Schofield A. Andreadis J. Snowden D. Craufurd D. Neary F. Owen B.A. Oostra J. Hardy A. Goate J. van Swieten D. Mann T. Lynch P. Heutink 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
Froelich, S.5
Houlden, H.6
Pickering-Brown, S.7
Chakraverthy, S.8
Isaacs, A.9
Grover, A.10
Hackett, J.11
Adamson, J.12
Lincoln, A.13
Dickson, D.14
Davis, 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
Nowothny, P.24
Che, L.K.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.L.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..
-
24
-
-
0024675418
-
The microtubule binding domain of tau protein
-
G. Lee R.L. Neve K.S. Kosik The microtubule binding domain of tau protein Neuron 2 1989 1615 1624
-
(1989)
Neuron
, vol.2
, pp. 1615-1624
-
-
Lee, G.1
Neve, R.L.2
Kosik, K.S.3
-
25
-
-
0033009603
-
Neurofibrillary degeneration in progressive supranuclear palsy and corticobasal degeneration: tau pathologies with exclusively ‘exon 10’ isoforms
-
N. Sergeant A. Wattez A. Delacourte Neurofibrillary degeneration in progressive supranuclear palsy and corticobasal degeneration: tau pathologies with exclusively ‘exon 10’ isoforms J. Neurochem. 72 1999 1243 1249
-
(1999)
J. Neurochem.
, vol.72
, pp. 1243-1249
-
-
Sergeant, N.1
Wattez, A.2
Delacourte, A.3
-
27
-
-
0033663879
-
A novel tau mutation (N296N) in familial dementia with swollen achromatic neurons and corticobasal inclusion bodies
-
M.G. Spillantini H. Yoshida C. Rizzini P.L. Lantos N. Khan M.N. Rosser M. Goedert J. Brown A novel tau mutation (N296N) in familial dementia with swollen achromatic neurons and corticobasal inclusion bodies Ann. Neurol. 48 2000 939 943
-
(2000)
Ann. Neurol.
, vol.48
, pp. 939-943
-
-
Spillantini, M.G.1
Yoshida, H.2
Rizzini, C.3
Lantos, P.L.4
Khan, N.5
Rosser, M.N.6
Goedert, M.7
Brown, J.8
-
28
-
-
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
-
P.M. Stanford G.M. Halliday W.S. Brooks J.B.L. Kwok C.E. Storey H. Creasey J.G. Morris M.J. Fulham P.R. Schofield 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 Brain 123 2000 880 893
-
(2000)
Brain
, vol.123
, pp. 880-893
-
-
Stanford, P.M.1
Halliday, G.M.2
Brooks, W.S.3
Kwok, J.B.L.4
Storey, C.E.5
Creasey, H.6
Morris, J.G.7
Fulham, M.J.8
Schofield, P.R.9
-
29
-
-
0033529304
-
Structure of tau exon 10 splicing regulatory element RNA and destabilization by mutations of frontotemporal dementia and parkinsonism linked to chromosome 17
-
L. Varani M. Hasegawa M.G. Spillantini M.J. Smith J.R. Murrell B. Ghetti A. Klug M. Goedert G. Varani Structure of tau exon 10 splicing regulatory element RNA and destabilization by mutations of frontotemporal dementia and parkinsonism linked to chromosome 17 Proc. Natl. Acad. Sci. USA 96 1999 8229 8234
-
(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
-
30
-
-
0035138764
-
Loss of brain tau defines novel sporadic and familial tauopathies with frontotemporal dementia
-
V. Zhukareva V. Vogelsberg-Ragaglia V. Deerlin J. Bruce T. Shuck M. Grossman C.M. Clark S.E. Arnold E. Masliah D. Galasko J.Q. Trolanowski V.M.-Y. Lee 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
Deerlin, V.3
Bruce, J.4
Shuck, T.5
Grossman, M.6
Clark, C.M.7
Arnold, S.E.8
Masliah, E.9
Galasko, D.10
Trolanowski, J.Q.11
Lee, V.M.-Y.12
|