-
1
-
-
0028227962
-
Role of abnormally phosphorylated tau in the breakdown of microtubules in Alzheimer-disease
-
Alonso AC, Zaidi T, Grundke-Iqbal I, Iqbal K: Role of abnormally phosphorylated tau in the breakdown of microtubules in Alzheimer-disease. Proc. Natl. Acad. Sci. U.S.A. 91:5562-5566, 1994.
-
(1994)
Proc. Natl. Acad. Sci. U.S.A.
, vol.91
, pp. 5562-5566
-
-
Alonso, A.C.1
Zaidi, T.2
Grundke-Iqbal, I.3
Iqbal, K.4
-
2
-
-
0344517353
-
Lithium protects cultured neurons against beta-amyloid-induced neurodegeneration
-
Alvarez G, Munoz-Montano JR, Satrustegui J, Avila J, Bogonez E, Diaz-Nido J: Lithium protects cultured neurons against beta-amyloid-induced neurodegeneration. FEBS Lett. 453:260-264, 1999.
-
(1999)
FEBS Lett.
, vol.453
, pp. 260-264
-
-
Alvarez, G.1
Munoz-Montano, J.R.2
Satrustegui, J.3
Avila, J.4
Bogonez, E.5
Diaz-Nido, J.6
-
3
-
-
0026740795
-
Neurofibrillary tangles but not senile plaques parallel duration and severity of Alzheimer's disease
-
Arriagada PV, Growdon JH, Hedley-Whyte ET, Hyman BT: Neurofibrillary tangles but not senile plaques parallel duration and severity of Alzheimer's disease. Neurology 42:631-639, 1992
-
(1992)
Neurology
, vol.42
, pp. 631-639
-
-
Arriagada, P.V.1
Growdon, J.H.2
Hedley-Whyte, E.T.3
Hyman, B.T.4
-
4
-
-
0036937699
-
Specific tau phosphorylation sites correlate with severity of neuronal cytopathology in Alzheimer's disease
-
Augustinack JC, Schneider A, Mandelkow EM Hyman BT: Specific tau phosphorylation sites correlate with severity of neuronal cytopathology in Alzheimer's disease. Acta Neuropathol. 103:26-35, 2002a.
-
(2002)
Acta Neuropathol.
, vol.103
, pp. 26-35
-
-
Augustinack, J.C.1
Schneider, A.2
Mandelkow, E.M.3
Hyman, B.T.4
-
5
-
-
0036275991
-
Colocalization and fluorescence resonance energy transfer between cdk5 and AT8 suggests a close association in preneurofibrillary tangles and neurofibrillary tangles
-
Augustinack JC, Sanders JL, Tsai LH, Hyman BT: Colocalization and fluorescence resonance energy transfer between cdk5 and AT8 suggests a close association in preneurofibrillary tangles and neurofibrillary tangles. J. Neuropathol. Exp. Neurol. 61:557-564, 2002b.
-
(2002)
J. Neuropathol. Exp. Neurol.
, vol.61
, pp. 557-564
-
-
Augustinack, J.C.1
Sanders, J.L.2
Tsai, L.H.3
Hyman, B.T.4
-
6
-
-
0033041179
-
Association of an extended haplotype in the tau gene with progressive supranuclear palsy
-
Baker M, Litvan I, Houlden H, Adamson J, Dickson D, Perez-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. 8:711-715, 1999.
-
(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
-
-
33746919083
-
Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17
-
Baker M, Mackenzie IR, Pickering-Brown SM, Gass J, Rademakers R, Lindholm C, Snowden J, Adamson J, Sadovnick AD, Rollinson S, Cannon A, Dwosh E et al.: Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17. Nature 442:916-919, 2006.
-
(2006)
Nature
, vol.442
, pp. 916-919
-
-
Baker, M.1
Mackenzie, I.R.2
Pickering-Brown, S.M.3
Gass, J.4
Rademakers, R.5
Lindholm, C.6
Snowden, J.7
Adamson, J.8
Sadovnick, A.D.9
Rollinson, S.10
Cannon, A.11
Dwosh, E.12
-
8
-
-
0034808141
-
Pathological glial tau accumulations in neurodegenerative disease: Review and case report
-
Berry RW, Quinn B, Johnson N, Cochran EJ, Ghoshal N, Binder LI: Pathological glial tau accumulations in neurodegenerative disease: review and case report. Neurochem. Int. 39:469-479, 2001.
-
(2001)
Neurochem. Int.
, vol.39
, pp. 469-479
-
-
Berry, R.W.1
Quinn, B.2
Johnson, N.3
Cochran, E.J.4
Ghoshal, N.5
Binder, L.I.6
-
9
-
-
0022365608
-
The distribution of tau in the mammalian central - Nervous system
-
Binder LI, Frankfurter A, Rebhun LI: The distribution of tau in the mammalian central - nervous system. J. Cell Biol. 101:1371-1378, 1985.
-
(1985)
J. Cell Biol.
, vol.101
, pp. 1371-1378
-
-
Binder, L.I.1
Frankfurter, A.2
Rebhun, L.I.3
-
10
-
-
10944241542
-
Tau alteration and neuronal degeneration in tauopathies: Mechanisms and models
-
Brandt R, Hundelt M, Shahani N: Tau alteration and neuronal degeneration in tauopathies: mechanisms and models. Biochim. Biophys. Acta 1739:331-354, 2005.
-
(2005)
Biochim. Biophys. Acta
, vol.1739
, pp. 331-354
-
-
Brandt, R.1
Hundelt, M.2
Shahani, N.3
-
11
-
-
27644460461
-
Hereditary Pick's disease with the G272V tau mutation shows predominant three-repeat tau pathology
-
Bronner IF, Ter Meulen BC, Azmani A, Severijnen LA, Willemsen R, Kamphorst W, Ravid R, Heutink P, van Swieten JC: Hereditary Pick's disease with the G272V tau mutation shows predominant three-repeat tau pathology. Brain 128:2645-2653, 2005.
-
(2005)
Brain
, vol.128
, pp. 2645-2653
-
-
Bronner, I.F.1
Ter Meulen, B.C.2
Azmani, A.3
Severijnen, L.A.4
Willemsen, R.5
Kamphorst, W.6
Ravid, R.7
Heutink, P.8
van Swieten, J.C.9
-
12
-
-
0033850407
-
Tau protein isoforms, phosphorylation and role in neurodegenerative disorders
-
Buee L, Bussiere T, Buee-Scherrer V, Delacourte A, Hof PR: Tau protein isoforms, phosphorylation and role in neurodegenerative disorders. Brain Res. Brain Res. Rev. 33:95-130, 2000.
-
(2000)
Brain Res. Brain Res. Rev.
, vol.33
, pp. 95-130
-
-
Buee, L.1
Bussiere, T.2
Buee-Scherrer, V.3
Delacourte, A.4
Hof, P.R.5
-
13
-
-
0037181485
-
Phosphorylation of microtubule-associated protein tau by stress-activated protein kinases in intact cells
-
Buee-Scherrer V, Goedert M: Phosphorylation of microtubule-associated protein tau by stress-activated protein kinases in intact cells. FEBS Lett. 515:151-154, 2002.
-
(2002)
FEBS Lett.
, vol.515
, pp. 151-154
-
-
Buee-Scherrer, V.1
Goedert, M.2
-
14
-
-
0036338203
-
Differential diagnosis of Alzheimer disease with cerebrospinal fluid levels of tau protein phosphorylated at threonine 231
-
Buerger K, Zinkowski R, Teipel SJ, Tapiola T, Arai H, Blennow K, Andreasen N, Hofmann-Kiefer K, DeBernardis J, Kerkman D, McCulloch C, Kohnken R et al.: Differential diagnosis of Alzheimer disease with cerebrospinal fluid levels of tau protein phosphorylated at threonine 231. Arch. Neurol. 59:1267-1272, 2002.
-
(2002)
Arch. Neurol.
, vol.59
, pp. 1267-1272
-
-
Buerger, K.1
Zinkowski, R.2
Teipel, S.J.3
Tapiola, T.4
Arai, H.5
Blennow, K.6
Andreasen, N.7
Hofmann-Kiefer, K.8
DeBernardis, J.9
Kerkman, D.10
McCulloch, C.11
Kohnken, R.12
-
15
-
-
0022967090
-
Microheterogeneity of microtubule-associated tau proteins is due to differences in phosphorylation
-
Butler M, Shelanski ML: Microheterogeneity of microtubule-associated tau proteins is due to differences in phosphorylation. J. Neurochem. 47:1517-1522, 1986.
-
(1986)
J. Neurochem.
, vol.47
, pp. 1517-1522
-
-
Butler, M.1
Shelanski, M.L.2
-
16
-
-
0031044850
-
Genetic evidence for the involvement of tau in progressive supranuclear palsy
-
Conrad C, Andreadis A, Trojanowski JQ, Dickson DW, Kang D, Chen XH, Wiederholt W, Hansen L, Masliah E, Thal LJ, Katzman R, Xia Y, et al.: Genetic evidence for the involvement of tau in progressive supranuclear palsy. Ann. Neurol. 41:277-281, 1997.
-
(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
-
17
-
-
33746910649
-
Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q2l
-
Cruts M, Gijselinck I, van der Zee J, Engelborghs S, Wils H, Pirici D, Rademakers R, Vandenberghe R, Dermaut B, Martin JJ, van Duijn C, Peeters K et al.: Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q2l. Nature 442:920-924, 2006.
-
(2006)
Nature
, vol.442
, pp. 920-924
-
-
Cruts, M.1
Gijselinck, I.2
van der Zee, J.3
Engelborghs, S.4
Wils, H.5
Pirici, D.6
Rademakers, R.7
Vandenberghe, R.8
Dermaut, B.9
Martin, J.J.10
van Duijn, C.11
Peeters, K.12
-
18
-
-
11144357241
-
A novel presenilin 1 mutation associated with Pick's disease but not beta-amyloid plaques
-
Dermaut B, Kumar-Singh S, Engelborghs S, Theuns J, Rademakers I, Sacrens J, Pickut BA, Peeters K, van den Broeck M, Vennekens K, Claes S, Cruts M et al.: A novel presenilin 1 mutation associated with Pick's disease but not beta-amyloid plaques. Ann. Neurol. 55:617-626, 2004.
-
(2004)
Ann. Neurol.
, vol.55
, pp. 617-626
-
-
Dermaut, B.1
Kumar-Singh, S.2
Engelborghs, S.3
Theuns, J.4
Rademakers, I.5
Sacrens, J.6
Pickut, B.A.7
Peeters, K.8
van den Broeck, M.9
Vennekens, K.10
Claes, S.11
Cruts, M.12
-
19
-
-
11144306360
-
Regulation of tau isoform expression and dementia
-
D'Souza I, Schellenberg GD: Regulation of tau isoform expression and dementia. Biochim. Biophys. Acta 1739:104-115, 2005.
-
(2005)
Biochim. Biophys. Acta
, vol.1739
, pp. 104-115
-
-
D'Souza, I.1
Schellenberg, G.D.2
-
20
-
-
0035659377
-
Phosphorylated mitogen-activated protein kinase (MAPK/ERK-P), protein kinase of 38 kDa (p38-P), stress-activated protein kinase (SAPK/JNK-P), and calcium/calmodulin-dependent kinase II (CaM kinase II) are differentially expressed in tau deposits in neurons and glial cells in tauopathies
-
Ferrer I, Blanco R, Carmona M, Puig B: Phosphorylated mitogen-activated protein kinase (MAPK/ERK-P), protein kinase of 38 kDa (p38-P), stress-activated protein kinase (SAPK/JNK-P), and calcium/ calmodulin-dependent kinase II (CaM kinase II) are differentially expressed in tau deposits in neurons and glial cells in tauopathies. J. Neural. Transm. 108:1397-1415, 2001.
-
(2001)
J. Neural. Transm.
, vol.108
, pp. 1397-1415
-
-
Ferrer, I.1
Blanco, R.2
Carmona, M.3
Puig, B.4
-
21
-
-
25844458239
-
Current advances on different kinases involved in tau phosphorylation, and implications in Alzheimer's disease and tauopathies
-
Ferrer I, Gomez-Isla T, Puig B, Freixes M, Ribe E, Dalfo E, Avila J: Current advances on different kinases involved in tau phosphorylation, and implications in Alzheimer's disease and tauopathies. Curr. Alzheimer Res. 2:3-18, 2005.
-
(2005)
Curr. Alzheimer Res.
, vol.2
, pp. 3-18
-
-
Ferrer, I.1
Gomez-Isla, T.2
Puig, B.3
Freixes, M.4
Ribe, E.5
Dalfo, E.6
Avila, J.7
-
22
-
-
0141884373
-
Alteration in calcium channel properties is responsible for the neurotoxic action of a familial frontotemporal dementia tau mutation
-
Furukawa K, Wang Y, Yao PJ, Fu WM, Mattson MP, Itoyama Y, Onodera H, D'Souza I, Poorkaj PH, Bird TD, Schellenberg GD: Alteration in calcium channel properties is responsible for the neurotoxic action of a familial frontotemporal dementia tau mutation. J. Neurochem. 87:427-436, 2003.
-
(2003)
J. Neurochem.
, vol.87
, pp. 427-436
-
-
Furukawa, K.1
Wang, Y.2
Yao, P.J.3
Fu, W.M.4
Mattson, M.P.5
Itoyama, Y.6
Onodera, H.7
D'Souza, I.8
Poorkaj, P.H.9
Bird, T.D.10
Schellenberg, G.D.11
-
23
-
-
29144473245
-
Familial frontotemporal dementia associated with the novel MAPT mutation T427M
-
Giaccone G, Rossi G, Farina L, Marcon G, Di Fede G, Catania M, Morbin M, Sacco L, Bugiani O, Tagliavini F: Familial frontotemporal dementia associated with the novel MAPT mutation T427M. J. Neurol. 252:1543-1545, 2005.
-
(2005)
J. Neurol.
, vol.252
, pp. 1543-1545
-
-
Giaccone, G.1
Rossi, G.2
Farina, L.3
Marcon, G.4
Di Fede, G.5
Catania, M.6
Morbin, M.7
Sacco, L.8
Bugiani, O.9
Tagliavini, F.10
-
24
-
-
11144258263
-
Mutations causing neurodegenerative tauopathies
-
Goedert M, Jakes R: Mutations causing neurodegenerative tauopathies. Biochim. Biophys. Acta 1739:240-250, 2005.
-
(2005)
Biochim. Biophys. Acta
, vol.1739
, pp. 240-250
-
-
Goedert, M.1
Jakes, R.2
-
25
-
-
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
-
Goedert M, Spillantini MG, Potier MC, Ulrich J, Crowther RA: 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. 8:393-399, 1989.
-
(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
-
26
-
-
0028064431
-
Dephosphorylation of Alzheimer's disease abnormally phosphorylated tau by protein phosphatase-2A
-
Gong CX, Grundke-Iqbal I, Iqbal K: Dephosphorylation of Alzheimer's disease abnormally phosphorylated tau by protein phosphatase-2A. Neuroscience 61:765-772, 1994a.
-
(1994)
Neuroscience
, vol.61
, pp. 765-772
-
-
Gong, C.X.1
Grundke-Iqbal, I.2
Iqbal, K.3
-
27
-
-
0028350740
-
Dephosphorylation of microtubule-associated protein tau by protein phosphatase-1 and -2C and its implication in Alzheimer disease
-
Gong CX, Grundke-Iqbal I, Damuni Z, Iqbal K: Dephosphorylation of microtubule-associated protein tau by protein phosphatase-1 and -2C and its implication in Alzheimer disease. FEBS Lett. 341:94-98, 1994b.
-
(1994)
FEBS Lett.
, vol.341
, pp. 94-98
-
-
Gong, C.X.1
Grundke-Iqbal, I.2
Damuni, Z.3
Iqbal, K.4
-
28
-
-
18544390506
-
Post-translational modifications of tau protein in Alzheimer's disease
-
Gong CX, Liu F, Grundke-Iqbal I, Iqbal K: Post-translational modifications of tau protein in Alzheimer's disease. J. Neural. Transm. 112:813-838, 2005.
-
(2005)
J. Neural. Transm.
, vol.112
, pp. 813-838
-
-
Gong, C.X.1
Liu, F.2
Grundke-Iqbal, I.3
Iqbal, K.4
-
29
-
-
0035943436
-
Formation of neurofibrillary tangles in P3011 tau transgenic mice induced by Abeta 42 fibrils
-
Gotz J, Chen F, van Dorpe J, Nitsch RM: Formation of neurofibrillary tangles in P3011 tau transgenic mice induced by Abeta 42 fibrils. Science 293:1491-1495, 2001
-
(2001)
Science
, vol.293
, pp. 1491-1495
-
-
Gotz, J.1
Chen, F.2
van Dorpe, J.3
Nitsch, R.M.4
-
30
-
-
33749596351
-
Alzheimer's disease and frontotemporal dementia: Prospects of a tailored therapy?
-
Gotz J, Ittner LM, Schonrock N: Alzheimer's disease and frontotemporal dementia: prospects of a tailored therapy? Med. J. Aust. 185:381-384, 2006
-
(2006)
Med. J. Aust.
, vol.185
, pp. 381-384
-
-
Gotz, J.1
Ittner, L.M.2
Schonrock, N.3
-
31
-
-
0037134098
-
Effects on splicing and protein function of three mutations in codon N296 of tau in vitro
-
Grover A, DeTure M, Yen SH, Hutton M: Effects on splicing and protein function of three mutations in codon N296 of tau in vitro. Neurosci Lett. 323:33-36, 2002.
-
(2002)
Neurosci Lett.
, vol.323
, pp. 33-36
-
-
Grover, A.1
DeTure, M.2
Yen, S.H.3
Hutton, M.4
-
32
-
-
0033615580
-
The presenilins in Alzheimer's disease-proteolysis holds the key
-
Haass C, De Strooper B: The presenilins in Alzheimer's disease-proteolysis holds the key. Science 286:916-919, 1999
-
(1999)
Science
, vol.286
, pp. 916-919
-
-
Haass, C.1
De Strooper, B.2
-
33
-
-
19944428327
-
Pick bodies in a family with presenilin-1 Alzheimer's disease
-
Halliday GM, Song YJ, Lepar G, Brooks WS, Kwok JB, Kersaitis C, Gregory G, Shepherd CE, Rahimi F, Schofield PR, Kril JJ: Pick bodies in a family with presenilin-1 Alzheimer's disease. Ann. Neurol. 57:139-143, 2005.
-
(2005)
Ann. Neurol.
, vol.57
, pp. 139-143
-
-
Halliday, G.M.1
Song, Y.J.2
Lepar, G.3
Brooks, W.S.4
Kwok, J.B.5
Kersaitis, C.6
Gregory, G.7
Shepherd, C.E.8
Rahimi, F.9
Schofield, P.R.10
Kril, J.J.11
-
34
-
-
0037135111
-
Medicine - The amyloid hypothesis of Alzheimer's disease: Progress and problems on the road to therapeutics
-
Hardy J, Selkoe DJ: Medicine - The amyloid hypothesis of Alzheimer's disease: progress and problems on the road to therapeutics. Science 297:353-356, 2002
-
(2002)
Science
, vol.297
, pp. 353-356
-
-
Hardy, J.1
Selkoe, D.J.2
-
35
-
-
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. 51:525-530, 2002.
-
(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
-
36
-
-
0033918014
-
Loss of thalamic intralaminar nuclei in progressive supranuclear palsy and Parkinson's disease: Clinical and therapeutic implications
-
Henderson JM, Carpenter K, Cartwright H, Halliday GM: Loss of thalamic intralaminar nuclei in progressive supranuclear palsy and Parkinson's disease: clinical and therapeutic implications. Brain 123:1410-1421, 2000.
-
(2000)
Brain
, vol.123
, pp. 1410-1421
-
-
Henderson, J.M.1
Carpenter, K.2
Cartwright, H.3
Halliday, G.M.4
-
37
-
-
0036685608
-
Transgenic mouse model of tauopathies with glial pathology and nervous system degeneration
-
Higuchi M, Ishihara T, Zhang B, Hong M, Andreadis A, Trojanowski JQ, Lee VMY: Transgenic mouse model of tauopathies with glial pathology and nervous system degeneration. Neuron 35:433-446, 2002.
-
(2002)
Neuron
, vol.35
, pp. 433-446
-
-
Higuchi, M.1
Ishihara, T.2
Zhang, B.3
Hong, M.4
Andreadis, A.5
Trojanowski, J.Q.6
Lee, V.M.Y.7
-
38
-
-
0142062488
-
The L266V tau mutation is associated with frontotemporal dementia and Pick-like 3R and 4R tauopathy
-
Hogg M, Grujic ZM, Baker M, Demirci S, Guillozet AL, Sweet AP, Herzog LL, Weintraub S, Mesulam MM, LaPointe NE, Gamblin TC, Berry RW et al.: The L266V tau mutation is associated with frontotemporal dementia and Pick-like 3R and 4R tauopathy. Acta Neuropathol. 106:323-336, 2003.
-
(2003)
Acta Neuropathol.
, vol.106
, pp. 323-336
-
-
Hogg, M.1
Grujic, Z.M.2
Baker, M.3
Demirci, S.4
Guillozet, A.L.5
Sweet, A.P.6
Herzog, L.L.7
Weintraub, S.8
Mesulam, M.M.9
LaPointe, N.E.10
Gamblin, T.C.11
Berry, R.W.12
-
39
-
-
0035954364
-
Corticobasal degeneration and progressive supranuclear palsy share common tau haplotype
-
Houlden H, Baker M, Morris HR, MacDonald N, Pickering-Brown S, Adamson J, Lees AJ, Rossor MN, Quinn NP, Kertesz A, Khan MN, Hardy J et al.: Corticobasal degeneration and progressive supranuclear palsy share common tau haplotype. Neurology 56: 1702-1706, 2001.
-
(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
-
40
-
-
0032543684
-
Association of missense and 5′-splice-site mutations in tau with the inherited dementia FTDP-17
-
Hutton M, Lendon CL, Rizzu P, Baker M, Froelich S, Houlden H, Pickering-Brown S, Chakraverty S, Isaacs A, Grover A, Hackett J, Adamson J et al.: Association of missense and 5′-splice-site mutations in tau with the inherited dementia FTDP-17. Nature.393:702-705, 1998.
-
(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
-
41
-
-
0035183407
-
A long story starting with a short paper: Early history of Pick's disease
-
Karenberg A: A long story starting with a short paper: Early history of Pick's disease. Fortschr. Neurol. Psychiatr. 69:545-550, 2001.
-
(2001)
Fortschr. Neurol. Psychiatr.
, vol.69
, pp. 545-550
-
-
Karenberg, A.1
-
42
-
-
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 MP, Baker M, Yu X, Duff K, Hardy J et al.: Neurofibrillary tangles, amyotrophy and progressive motor disturbance in mice expressing mutant (P301L) tau protein. Nat. Genet. 25:402-405, 2000.
-
(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
-
43
-
-
17944382037
-
Enhanced neurofibrillary degeneration in transgeni mice expressing mutant tau and APP
-
Lewis J, Dickson DW, Lin WL, Chisholm L, Corral A, Jones G, Yen SH, Sahara N, Skipper L, Yager D, Eckman C, Hardy J et al.: Enhanced neurofibrillary degeneration in transgeni mice expressing mutant tau and APP. Science 293:1487-1491, 2001.
-
(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
-
44
-
-
0021338217
-
Phosphorylation affects the ability of tau-protein to promote microtubule assembly
-
Lindwall G, Cole RD: Phosphorylation affects the ability of tau-protein to promote microtubule assembly. J. Biol. Chem. 259:5301-5305, 1984.
-
(1984)
J. Biol. Chem.
, vol.259
, pp. 5301-5305
-
-
Lindwall, G.1
Cole, R.D.2
-
45
-
-
0033674152
-
Frontotemporal dementia with novel tau pathology and a Glu342Val tau mutation
-
Lippa CF, Zhukareva V, Kawarai T, Uryu K, Shafiq M, Nee LE, Grafman J, Liang Y, St George-Hyslop PH, Trojanowski JQ, Lee VMY: Frontotemporal dementia with novel tau pathology and a Glu342Val tau mutation. Ann. Neurol. 48:850-858, 2000.
-
(2000)
Ann. Neurol.
, vol.48
, pp. 850-858
-
-
Lippa, C.F.1
Zhukareva, V.2
Kawarai, T.3
Uryu, K.4
Shafiq, M.5
Nee, L.E.6
Grafman, J.7
Liang, Y.8
St George-Hyslop, P.H.9
Trojanowski, J.Q.10
Lee, V.M.Y.11
-
46
-
-
0032405638
-
Clinical and genetic aspects of progressive supranuclear palsy
-
Litvan I, Hutton M: Clinical and genetic aspects of progressive supranuclear palsy. J. Geriatr. Psychiatry Neurol. 11: 107-114, 1998.
-
(1998)
J. Geriatr. Psychiatry Neurol.
, vol.11
, pp. 107-114
-
-
Litvan, I.1
Hutton, M.2
-
47
-
-
0035232501
-
Tau proteins with frontotemporal dementia-17 mutations have both altered expression levels and phosphorylation profiles in differentiated neuroblastoma cells
-
Mack TG, Dayanandan R, Van Slegtenhorst M, Whone A, Hutton M, Lovestone S, Anderton BH: Tau proteins with frontotemporal dementia-17 mutations have both altered expression levels and phosphorylation profiles in differentiated neuroblastoma cells. Neuroscience 108:701-712, 2001.
-
(2001)
Neuroscience
, vol.108
, pp. 701-712
-
-
Mack, T.G.1
Dayanandan, R.2
Van Slegtenhorst, M.3
Whone, A.4
Hutton, M.5
Lovestone, S.6
Anderton, B.H.7
-
48
-
-
0034531541
-
Pathological tau phenotypes. The weight of mutations, polymorphisms, and differential neuronal vulnerabilities
-
Mailliot C, Bussiere T, Hamdane M, Sergeant N, Caillet ML, Delacourte A, Buee L: Pathological tau phenotypes. The weight of mutations, polymorphisms, and differential neuronal vulnerabilities. Ann. N. Y. Acad Sci. 920:107-114, 2000.
-
(2000)
Ann. N. Y. Acad Sci.
, vol.920
, pp. 107-114
-
-
Mailliot, C.1
Bussiere, T.2
Hamdane, M.3
Sergeant, N.4
Caillet, M.L.5
Delacourte, A.6
Buee, L.7
-
49
-
-
0031855023
-
The case described by Alois Alzheimer in 1911. Historical and conceptual perspectives based on the clinical record and neurohistological sections
-
Moller HJ, Graeber MB: The case described by Alois Alzheimer in 1911. Historical and conceptual perspectives based on the clinical record and neurohistological sections. Eur. Arch. Psychiatry Clin. Neurosci. 248:111-122, 1998.
-
(1998)
Eur. Arch. Psychiatry Clin. Neurosci.
, vol.248
, pp. 111-122
-
-
Moller, H.J.1
Graeber, M.B.2
-
50
-
-
10944256376
-
Frontotemporal dementia and frontotemporal degeneration - How to define?
-
(In Japanese)
-
Mori H: Frontotemporal dementia and frontotemporal degeneration - how to define? (In Japanese). Rinsho Shinkeigaka 44:872-874, 2004.
-
(2004)
Rinsho Shinkeigaka
, vol.44
, pp. 872-874
-
-
Mori, H.1
-
51
-
-
0036238673
-
Pathological, clinical and genetic heterogeneity in progressive supranuclear palsy
-
Morris HR, Gibb G, Katzenschlager R, Wood NW, Hanger DP, Strand C, Lashley T, Daniel SE, Lees AJ, Anderton BH, Revesz T: Pathological, clinical and genetic heterogeneity in progressive supranuclear palsy. Brain 125:969-975, 2002.
-
(2002)
Brain
, vol.125
, pp. 969-975
-
-
Morris, H.R.1
Gibb, G.2
Katzenschlager, R.3
Wood, N.W.4
Hanger, D.P.5
Strand, C.6
Lashley, T.7
Daniel, S.E.8
Lees, A.J.9
Anderton, B.H.10
Revesz, T.11
-
52
-
-
0038353463
-
Tau exon 10 + 16 mutation FTDP-17 presenting clinically as sporadic young onset PSP
-
Morris HR, Osaki Y, Holton J, Lees AJ, Wood NW, Revesz T, Quinn N: Tau exon 10 + 16 mutation FTDP-17 presenting clinically as sporadic young onset PSP. Neurology 61:102-104, 2003.
-
(2003)
Neurology
, vol.61
, pp. 102-104
-
-
Morris, H.R.1
Osaki, Y.2
Holton, J.3
Lees, A.J.4
Wood, N.W.5
Revesz, T.6
Quinn, N.7
-
53
-
-
0032763203
-
Tau gene mutation G389R causes a tauopathy with abundant pick body-like inclusions and axonal deposits
-
Murrell JR, Spillantini MG, Zolo P, Guazzelli M, Smith MJ, Hasegawa M, Redi F, Crowther RA, Pietrini P, Ghetti B, Goedert M: Tau gene mutation G389R causes a tauopathy with abundant pick body-like inclusions and axonal deposits. J. Neuropathol. Exp. Neurol. 58: 1207-1226, 1999.
-
(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
-
54
-
-
0034790437
-
Pick's disease associated with the novel Tau gene mutation K369I
-
Neumann M, Schulz-Schaeffer W, Crowther RA, Smith MJ, Spillantini MG, Goedert M, Kretzschmar HA: Pick's disease associated with the novel Tau gene mutation K369I. Ann. Neurol. 50:503-513, 2001.
-
(2001)
Ann. Neurol.
, vol.50
, pp. 503-513
-
-
Neumann, M.1
Schulz-Schaeffer, W.2
Crowther, R.A.3
Smith, M.J.4
Spillantini, M.G.5
Goedert, M.6
Kretzschmar, H.A.7
-
55
-
-
0242290057
-
An English kindred with a novel recessive tauopathy and respiratory failure
-
Nicholl DJ, Greenstone MA, Clarke CE, Rizzu P, Crooks D, Crowe A, Trojanowski JQ, Lee VMY, Heutink P: An English kindred with a novel recessive tauopathy and respiratory failure. Ann. Neurol. 54:682-686, 2003.
-
(2003)
Ann. Neurol.
, vol.54
, pp. 682-686
-
-
Nicholl, D.J.1
Greenstone, M.A.2
Clarke, C.E.3
Rizzu, P.4
Crooks, D.5
Crowe, A.6
Trojanowski, J.Q.7
Lee, V.M.Y.8
Heutink, P.9
-
56
-
-
0344845132
-
Amyloid deposition precedes tangle formation in a triple transgenic model of Alzheimer's disease
-
Oddo S, Caccamo A, Kitazawa M, Tseng BP, LaFerla FM: Amyloid deposition precedes tangle formation in a triple transgenic model of Alzheimer's disease. Neurobiol. Aging 24:1063-1070, 2003.
-
(2003)
Neurobiol. Aging
, vol.24
, pp. 1063-1070
-
-
Oddo, S.1
Caccamo, A.2
Kitazawa, M.3
Tseng, B.P.4
LaFerla, F.M.5
-
57
-
-
4043167747
-
Abeta immunotherapy leads to clearance of early, but not late, hyperphosphorylated tau aggregates via the proteasome
-
Oddo S, Billings L, Kesslak JP, Cribbs DH, LaFerla FM: Abeta immunotherapy leads to clearance of early, but not late, hyperphosphorylated tau aggregates via the proteasome. Neuron 43:321-332, 2004.
-
(2004)
Neuron
, vol.43
, pp. 321-332
-
-
Oddo, S.1
Billings, L.2
Kesslak, J.P.3
Cribbs, D.H.4
LaFerla, F.M.5
-
58
-
-
0023505501
-
Phosphorylation determines 2 distinct species of Tau in the central-nervous-system
-
Papasozomenos SC, Binder LI: Phosphorylation determines 2 distinct species of Tau in the central-nervous-system. Cell Motil, Cytoskeleton 8:210-226, 1987.
-
(1987)
Cell Motil, Cytoskeleton
, vol.8
, pp. 210-226
-
-
Papasozomenos, S.C.1
Binder, L.I.2
-
59
-
-
0027421625
-
Brain proline-directed protein kinase phosphorylates tau on sites that are abnormally phosphorylated in tau associated with Alzheimer's paired helical filaments
-
Paudel HK, Lew J, Ali Z, Wang JH: Brain proline-directed protein kinase phosphorylates tau on sites that are abnormally phosphorylated in tau associated with Alzheimer's paired helical filaments. J. Biol. Chem. 268:23512-23518, 1993.
-
(1993)
J. Biol. Chem.
, vol.268
, pp. 23512-23518
-
-
Paudel, H.K.1
Lew, J.2
Ali, Z.3
Wang, J.H.4
-
60
-
-
0035087703
-
Localization of active forms of C-jun kinase (JNK) and p38 kinase in Alzheimer's disease brains at different stages of neurofibrillary degeneration
-
Pei JJ, Braak E, Braak H, Grundke-Iqbal I., Iqbal K, Winblad B, Cowburn RF: Localization of active forms of C-jun kinase (JNK) and p38 kinase in Alzheimer's disease brains at different stages of neurofibrillary degeneration. J. Alzheimers Dis. 3:41-48, 2001.
-
(2001)
J. Alzheimers Dis.
, vol.3
, pp. 41-48
-
-
Pei, J.J.1
Braak, E.2
Braak, H.3
Grundke-Iqbal, I.4
Iqbal, K.5
Winblad, B.6
Cowburn, R.F.7
-
61
-
-
0033669232
-
Pick's disease is associated with mutations in the tau gene
-
Pickering-Brown S, Baker M, Yen SH, Liu WK, Hasegawa M, Cairns N, Lantos PL, Rossor M, lwatsubo T, Davies Y, Allsop D, Furlong R et al.: Pick's disease is associated with mutations in the tau gene. Ann. Neurol. 48:859-867, 2000.
-
(2000)
Ann. Neurol.
, vol.48
, pp. 859-867
-
-
Pickering-Brown, S.1
Baker, M.2
Yen, S.H.3
Liu, W.K.4
Hasegawa, M.5
Cairns, N.6
Lantos, P.L.7
Rossor, M.8
Iwatsubo, T.9
Davies, Y.10
Allsop, D.11
Furlong, R.12
-
62
-
-
2942590743
-
Frontotemporal dementia with Pick-type histology associated with Q336R mutation in the tau gene
-
Pickering-Brown SM, Baker M, Nonaka T, Ikeda K, Sharma S, Mackenzie J, Simpson SA, Moore JW, Snowden JS, de Silva R, Revesz T, Hasegawa M et al.: Frontotemporal dementia with Pick-type histology associated with Q336R mutation in the tau gene. Brain 127:1415-1426, 2004
-
(2004)
Brain
, vol.127
, pp. 1415-1426
-
-
Pickering-Brown, S.M.1
Baker, M.2
Nonaka, T.3
Ikeda, K.4
Sharma, S.5
Mackenzie, J.6
Simpson, S.A.7
Moore, J.W.8
Snowden, J.S.9
de Silva, R.10
Revesz, T.11
Hasegawa, M.12
-
63
-
-
14444284106
-
Tau is a candidate gene for chromosome 17 frontotemporal dementia
-
Poorkaj P, Bird TD, Wijsman E, Nemens E, Garruto RM, Anderson L, Andreadis A, Wiederholt WC, Raskind M, Schellenberg GD: Tau is a candidate gene for chromosome 17 frontotemporal dementia. Ann. Neurol. 43:815-825, 1998.
-
(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
-
64
-
-
0036771837
-
An (R)5(L) tau mutation in a subject with a progressive supranuclear palsy phenotype
-
Poorkaj P, Muma NA, Zhukareva V, Cochran EJ, Shannon KM, Hurtig H, Koller WC, Bird TD, Trojanowski JQ, Lee VMY, Schellenberg GD: An (R)5(L) tau mutation in a subject with a progressive supranuclear palsy phenotype. Ann. Neurol. 52:511-516, 2002.
-
(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.Y.10
Schellenberg, G.D.11
-
65
-
-
0029850476
-
Pick's disease: Hyperphosphorylated tau protein segregates to the somatoaxonal compartment
-
Probst A, Tolnay M, Langui D, Goedert M, Spillantini MG: Pick's disease: hyperphosphorylated tau protein segregates to the somatoaxonal compartment. Acta Neuropathol. 92:588-596, 1996.
-
(1996)
Acta Neuropathol.
, vol.92
, pp. 588-596
-
-
Probst, A.1
Tolnay, M.2
Langui, D.3
Goedert, M.4
Spillantini, M.G.5
-
66
-
-
1342326136
-
Active stress kinase p38 enhances and perpetuates abnormal tau phosphorylation and deposition in Pick's disease
-
Puig B, Vinals F, Ferrer I: Active stress kinase p38 enhances and perpetuates abnormal tau phosphorylation and deposition in Pick's disease. Acta Neuropathol. 107:185-189, 2004.
-
(2004)
Acta Neuropathol.
, vol.107
, pp. 185-189
-
-
Puig, B.1
Vinals, F.2
Ferrer, I.3
-
67
-
-
0034067992
-
Phosphorylation sites on tau identified by nanoelectrospray mass spectrometry: Differences in vitro between the mitogen-activated protein kinases ERK2, c-Jun N-terminal kinase and P38, and glycogen synthase kinase-3beta
-
Reynolds CH, Betts JC, Blackstock WP, Nebreda AR, Anderton BH: Phosphorylation sites on tau identified by nanoelectrospray mass spectrometry: differences in vitro between the mitogen-activated protein kinases ERK2, c-Jun N-terminal kinase and P38, and glycogen synthase kinase-3beta. J. Neurochem. 74:1587-1595, 2000.
-
(2000)
J. Neurochem.
, vol.74
, pp. 1587-1595
-
-
Reynolds, C.H.1
Betts, J.C.2
Blackstock, W.P.3
Nebreda, A.R.4
Anderton, B.H.5
-
68
-
-
33747878233
-
Very long term studies of the seeding of beta-amyloidosis in primates
-
Ridley RM, Baker HF, Windle CP, Cummings RM: Very long term studies of the seeding of beta-amyloidosis in primates. J. Neural. Transm. 113:1243-1251, 2006.
-
(2006)
J. Neural. Transm.
, vol.113
, pp. 1243-1251
-
-
Ridley, R.M.1
Baker, H.F.2
Windle, C.P.3
Cummings, R.M.4
-
69
-
-
0033763736
-
Tau gene mutation K257T causes a tauopathy similar to Pick's disease
-
Rizzini C, Goedert M, Hodges JR, Smith MJ, Jakes R, Hills R, Xuereb JH, Crowther RA, Spillantini MG: Tau gene mutation K257T causes a tauopathy similar to Pick's disease. J. Neuropathol. Exp. Neurol. 59:990-1001, 2000.
-
(2000)
J. Neuropathol. Exp. Neurol.
, vol.59
, pp. 990-1001
-
-
Rizzini, C.1
Goedert, M.2
Hodges, J.R.3
Smith, M.J.4
Jakes, R.5
Hills, R.6
Xuereb, J.H.7
Crowther, R.A.8
Spillantini, M.G.9
-
70
-
-
25144460507
-
A new mutation of the tau gene, G303V, in early-onset familial progressive supranuclear palsy
-
Ros R, Thobois S, Streichenberger N, Kopp N, Sanchez MP, Perez M, Hoenicha J, Avila J, Honnorat J, de Yebenes JG: A new mutation of the tau gene, G303V, in early-onset familial progressive supranuclear palsy. Arch. Neurol. 62:1444-1450, 2005a.
-
(2005)
Arch. Neurol.
, vol.62
, pp. 1444-1450
-
-
Ros, R.1
Thobois, S.2
Streichenberger, N.3
Kopp, N.4
Sanchez, M.P.5
Perez, M.6
Hoenicha, J.7
Avila, J.8
Honnorat, J.9
de Yebenes, J.G.10
-
71
-
-
20944444262
-
Genetic linkage of autosomal dominant progressive supranuclear palsy to 1q31.1
-
Ros R, Gomez Garre P, Hirano M, Tai YF, Ampuero I, Vidal L, Rojo A, Fontan A, Vazquez A, Fanjul S, Hernandez J, Cantarero S et al.: Genetic linkage of autosomal dominant progressive supranuclear palsy to 1q31.1. Ann. Neurol. 57:634-641, 2005b.
-
(2005)
Ann. Neurol.
, vol.57
, pp. 634-641
-
-
Ros, R.1
Gomez Garre, P.2
Hirano, M.3
Tai, Y.F.4
Ampuero, I.5
Vidal, L.6
Rojo, A.7
Fontan, A.8
Vazquez, A.9
Fanjul, S.10
Hernandez, J.11
Cantarero, S.12
-
72
-
-
0036199419
-
A novel tau mutation, S320F, causes a tauopathy with inclusions similar to those in Pick's disease
-
Rosso SM, van Herpen E, Deelen W, Kamphorst W, Severijnen LA, Willemsen R, Ravid R, Niermeijer MF, Dooijes D, Smith MJ, Goedert M, Heutink P et al.: A novel tau mutation, S320F, causes a tauopathy with inclusions similar to those in Pick's disease. Ann. Neurol. 51:373-376, 2002.
-
(2002)
Ann. Neurol.
, vol.51
, pp. 373-376
-
-
Rosso, S.M.1
van Herpen, E.2
Deelen, W.3
Kamphorst, W.4
Severijnen, L.A.5
Willemsen, R.6
Ravid, R.7
Niermeijer, M.F.8
Dooijes, D.9
Smith, M.J.10
Goedert, M.11
Heutink, P.12
-
73
-
-
22344438508
-
Tau suppression in a neurodegenerative mouse model improves memory function
-
Santacruz K, Lewis J, Spires T, Paulson J, Kotilinek L, Ingelsson M, Guimaraes A, DeTure M, Ramsden M, McGowan E, Forster C, Yue M et al.: Tau suppression in a neurodegenerative mouse model improves memory function. Science 309:476-481, 2005
-
(2005)
Science
, vol.309
, pp. 476-481
-
-
Santacruz, K.1
Lewis, J.2
Spires, T.3
Paulson, J.4
Kotilinek, L.5
Ingelsson, M.6
Guimaraes, A.7
DeTure, M.8
Ramsden, M.9
McGowan, E.10
Forster, C.11
Yue, M.12
-
74
-
-
0034622242
-
Casein kinase 1 delta is associated with pathological accumulation of tau in several neurodegenerative diseases
-
Schwab C, DeMaggio AJ, Ghoshal N, Binder LI, Kuret J, McGeer PL: Casein kinase 1 delta is associated with pathological accumulation of tau in several neurodegenerative diseases. Neurobiol. Aging 21:503-510, 2000.
-
(2000)
Neurobiol. Aging
, vol.21
, pp. 503-510
-
-
Schwab, C.1
DeMaggio, A.J.2
Ghoshal, N.3
Binder, L.I.4
Kuret, J.5
McGeer, P.L.6
-
76
-
-
1642456618
-
Positional effects of presenilin-1 mutations on tau phosphorylation in cortical plaques
-
Shepherd CE, Gregory GC, Vickers JC, Brooks WS, Kwok JBJ, Schofield PR, Kril JJ, Halliday GM: Positional effects of presenilin-1 mutations on tau phosphorylation in cortical plaques. Neurobiol. Dis. 15:115-119, 2004.
-
(2004)
Neurobiol. Dis.
, vol.15
, pp. 115-119
-
-
Shepherd, C.E.1
Gregory, G.C.2
Vickers, J.C.3
Brooks, W.S.4
Kwok, J.B.J.5
Schofield, P.R.6
Kril, J.J.7
Halliday, G.M.8
-
77
-
-
0003374626
-
Tau protein pathology in neurodegenerative diseases
-
Spillantini MG, Goedert M: Tau protein pathology in neurodegenerative diseases. Trends Neurosci. 21:428-433, 1998.
-
(1998)
Trends Neurosci.
, vol.21
, pp. 428-433
-
-
Spillantini, M.G.1
Goedert, M.2
-
78
-
-
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
-
Stanford PM, Halliday GM, Brooks WS, Kwok JBJ, Storey CE, Creasey H, Morris JGL, Fulham MJ, Schofield PR: 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 123:880-893, 2000.
-
(2000)
Brain
, vol.123
, pp. 880-893
-
-
Stanford, P.M.1
Halliday, G.M.2
Brooks, W.S.3
Kwok, J.B.J.4
Storey, C.E.5
Creasey, H.6
Morris, J.G.L.7
Fulham, M.J.8
Schofield, P.R.9
-
79
-
-
75549116708
-
Progressive supranuclear palsy. A heterogeneous degeneration involving the brain stem, basal ganglia and cerebellum with vertical gaze and pseudobulbar palsy, nuchal dystonia and dementia
-
Steele JC, Richardson JC, Olszewski J: Progressive supranuclear palsy. A heterogeneous degeneration involving the brain stem, basal ganglia and cerebellum with vertical gaze and pseudobulbar palsy, nuchal dystonia and dementia. Arch. Neurol. 10:333-359, 1964.
-
(1964)
Arch. Neurol.
, vol.10
, pp. 333-359
-
-
Steele, J.C.1
Richardson, J.C.2
Olszewski, J.3
-
80
-
-
0036138044
-
Neurodegeneration with tau accumulation in a transgenic mouse expressing V337M human tau
-
Tanemura K, Murayama M, Akagi T, Hashikawa T, Tominaga T, Ichikawa M, Yamaguchi H, Takashima A: Neurodegeneration with tau accumulation in a transgenic mouse expressing V337M human tau. J. Neurosci. 22:133-141, 2002.
-
(2002)
J. Neurosci.
, vol.22
, pp. 133-141
-
-
Tanemura, K.1
Murayama, M.2
Akagi, T.3
Hashikawa, T.4
Tominaga, T.5
Ichikawa, M.6
Yamaguchi, H.7
Takashima, A.8
-
81
-
-
0035896451
-
Tau-tubulin kinase phosphorylates tau at Ser-208 and Ser-210, sites found in paired helical filament-tau
-
Tomizawa K, Omori A, Ohtake A, Sato K, Takahashi M: Tau-tubulin kinase phosphorylates tau at Ser-208 and Ser-210, sites found in paired helical filament-tau. FEBS Lett. 492:221-227, 2001.
-
(2001)
FEBS Lett.
, vol.492
, pp. 221-227
-
-
Tomizawa, K.1
Omori, A.2
Ohtake, A.3
Sato, K.4
Takahashi, M.5
-
83
-
-
0008538685
-
A protein factor essential for microtubule assembly
-
Weingarten MD, Lockwood AH, Hwo SY, Kirschner MW: A protein factor essential for microtubule assembly. Proc. Natl. Acad. Sci. U.S.A. 72:1858-1862, 1975.
-
(1975)
Proc. Natl. Acad. Sci. U.S.A.
, vol.72
, pp. 1858-1862
-
-
Weingarten, M.D.1
Lockwood, A.H.2
Hwo, S.Y.3
Kirschner, M.W.4
-
84
-
-
17044433857
-
Apolipoprotein E genotype regulates amyloid-beta cytotoxicity
-
Wilhelmus MM, Otte-Holler I, Davis J, Van Nostrand WE, de Waal RMW, Verbeek MM: Apolipoprotein E genotype regulates amyloid-beta cytotoxicity. J. Neurosci. 25:3621-3627, 2005.
-
(2005)
J. Neurosci.
, vol.25
, pp. 3621-3627
-
-
Wilhelmus, M.M.1
Otte-Holler, I.2
Davis, J.3
Van Nostrand, W.E.4
de Waal, R.M.W.5
Verbeek, M.M.6
-
85
-
-
0032885930
-
Fibrillogenesis of tau: Insights from tau missense mutations in FTDP-17
-
Yen SH, Hutton M, DeTure M, Ko LW, Nacharaju P: Fibrillogenesis of tau: insights from tau missense mutations in FTDP-17. Brain Pathol. 9:695-705, 1999.
-
(1999)
Brain Pathol.
, vol.9
, pp. 695-705
-
-
Yen, S.H.1
Hutton, M.2
DeTure, M.3
Ko, L.W.4
Nacharaju, P.5
-
86
-
-
0036488210
-
Functional effects of tau gene mutations Delta N296 and N296H
-
Yoshida H, Crowther RA, Goedert M: Functional effects of tau gene mutations Delta N296 and N296H. J. Neurochem. 80:548-551, 2002.
-
(2002)
J. Neurochem.
, vol.80
, pp. 548-551
-
-
Yoshida, H.1
Crowther, R.A.2
Goedert, M.3
-
87
-
-
20944443640
-
A novel mutation (K317M) in the MAPT gene causes FTDP and motor neuron disease
-
Zarranz JJ, Ferrer I, Lezcano E, Forcadas MI, Eizaguirre B, Atares B, Puig B, Gomez-Esteban JC, Fernandez-Maiztegui C, Rouco I, Perez-Concha T, Fernandez M et al.: A novel mutation (K317M) in the MAPT gene causes FTDP and motor neuron disease. Neurology 64:1578-1585, 2005.
-
(2005)
Neurology
, vol.64
, pp. 1578-1585
-
-
Zarranz, J.J.1
Ferrer, I.2
Lezcano, E.3
Forcadas, M.I.4
Eizaguirre, B.5
Atares, B.6
Puig, B.7
Gomez-Esteban, J.C.8
Fernandez-Maiztegui, C.9
Rouco, I.10
Perez-Concha, T.11
Fernandez, M.12
-
88
-
-
0036264527
-
Sporadic Pick's disease: A tauopathy characterized by a spectrum of pathological tau isoforms in gray and white matter
-
Zhukareva V, Mann D, Pickering-Brown S, Uryu K, Shuck T, Shah K, Grossman M, Miller BL, Hulette CM, Feinstein SC, Trojanowski JQ, Lee VMY: Sporadic Pick's disease: a tauopathy characterized by a spectrum of pathological tau isoforms in gray and white matter. Ann. Neurol. 51:730-739, 2002.
-
(2002)
Ann. Neurol.
, vol.51
, pp. 730-739
-
-
Zhukareva, V.1
Mann, D.2
Pickering-Brown, S.3
Uryu, K.4
Shuck, T.5
Shah, K.6
Grossman, M.7
Miller, B.L.8
Hulette, C.M.9
Feinstein, S.C.10
Trojanowski, J.Q.11
Lee, V.M.Y.12
|