-
1
-
-
0033041179
-
Association of an extended haplotype in the tau gene with Progressive Supranuclear Palsy
-
Baker M., et al. 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
-
2
-
-
0345580607
-
Transgenic expression of the shortest human tau affects its compartimentalization and its phosphorylation as in the pretangle stage of Alzheimer's disease
-
Brion J.P., et al. Transgenic expression of the shortest human tau affects its compartimentalization and its phosphorylation as in the pretangle stage of Alzheimer's disease. Am. J. Pathol. 154:1999;255-270.
-
(1999)
Am. J. Pathol.
, vol.154
, pp. 255-270
-
-
Brion, J.P.1
-
3
-
-
0031044850
-
Genetic evidence of the involvement of τ in Progressive Supranuclear Palsy
-
Conrad C., et al. Genetic evidence of the involvement of τ in Progressive Supranuclear Palsy. Ann. Neurol. 41:1997;277-281.
-
(1997)
Ann. Neurol.
, vol.41
, pp. 277-281
-
-
Conrad, C.1
-
4
-
-
0033042978
-
Mutations in tau reduce its microtubule-binding properties in intact living cells
-
Dayanandan R., et al. Mutations in tau reduce its microtubule-binding properties in intact living cells. FEBS Lett. 446:1999;228-232.
-
(1999)
FEBS Lett.
, vol.446
, pp. 228-232
-
-
Dayanandan, R.1
-
5
-
-
0030831959
-
Neurodegenerative diseases with cytoskeletal pathology: A biochemical classification
-
Dickson D. Neurodegenerative diseases with cytoskeletal pathology: a biochemical classification. Ann. Neurol. 42:1997;541-543.
-
(1997)
Ann. Neurol.
, vol.42
, pp. 541-543
-
-
Dickson, D.1
-
6
-
-
0033545946
-
Missense and silent tau gene mutations cause frontotemporal dementia with parkisonism-chromosome 17 type, by affecting multiple alternative RNA splicing regulatory elements
-
D'Souza I., et al. Missense and silent tau gene mutations cause frontotemporal dementia with parkisonism-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
-
7
-
-
0030977392
-
Frontotemporal dementia and parkinsonism linked to chromosome 17: A consensus conference
-
Review
-
Foster N.L., et al. Frontotemporal dementia and parkinsonism linked to chromosome 17: a consensus conference. Ann. Neurol. 41:1997;706-715. Review.
-
(1997)
Ann. Neurol
, vol.41
, pp. 706-715
-
-
Foster, N.L.1
-
8
-
-
0032428153
-
A nucleated assembly mechanism of Alzheimer paired helical filaments
-
Friedhoff P., et al. A nucleated assembly mechanism of Alzheimer paired helical filaments. Proc. Natl Acad. Sci. USA. 95:1998;15712-15717.
-
(1998)
Proc. Natl Acad. Sci. USA
, vol.95
, pp. 15712-15717
-
-
Friedhoff, P.1
-
9
-
-
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., et al. 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
-
10
-
-
0032919462
-
Effects of frontotemporal dementia FTDP-17 mutations on heparin-induced assembly of tau filaments
-
Goedert M., et al. Effects of frontotemporal dementia FTDP-17 mutations on heparin-induced assembly of tau filaments. FEBS Lett. 450:1999;306-311.
-
(1999)
FEBS Lett.
, vol.450
, pp. 306-311
-
-
Goedert, M.1
-
11
-
-
0028965635
-
Somatodendritic localisation and hyperphosphorylation of tau protein in transgenic mice expressing the longest human brain tau isoform
-
Götz J., et al. Somatodendritic localisation and hyperphosphorylation of tau protein in transgenic mice expressing the longest human brain tau isoform. EMBO J. 14:1995;1304-1313.
-
(1995)
EMBO J.
, vol.14
, pp. 1304-1313
-
-
Götz, J.1
-
12
-
-
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
-
Grover A., et al. 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
-
13
-
-
0032150877
-
Genetic dissection of Alzheimer's and related dementias: Amyloid and its relationship to Tau
-
Hardy J., et al. Genetic dissection of Alzheimer's and related dementias: amyloid and its relationship to Tau. Nature Neurosci. 1:1998;355-358.
-
(1998)
Nature Neurosci.
, vol.1
, pp. 355-358
-
-
Hardy, J.1
-
14
-
-
0032561415
-
Tau proteins with FTDP-17 mutations have a reduced ability to promote microtubule assembly
-
Hasegawa M., et al. 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
-
15
-
-
0032484089
-
Mutation-specific functional impairments in distinct tau isoforms of hereditary FTDP-17
-
Hong H., et al. Mutation-specific functional impairments in distinct tau isoforms of hereditary FTDP-17. Science. 282:1998;1914-1917.
-
(1998)
Science
, vol.282
, pp. 1914-1917
-
-
Hong, H.1
-
16
-
-
0032543684
-
Association of missense and 5(-splice mutations in tau with the inherited dementia FTDP-17
-
Hutton M., et al. Association of missense and 5(-splice mutations in tau with the inherited dementia FTDP-17. Nature. 393:1998;702-705.
-
(1998)
Nature
, vol.393
, pp. 702-705
-
-
Hutton, M.1
-
17
-
-
0032875760
-
Missense and splicing mutations in tau associated with FTDP-17: Multiple pathogenic mechanisms
-
Hutton M. Missense and splicing mutations in tau associated with FTDP-17: multiple pathogenic mechanisms. Neurosci. News. 2:1999;73-82.
-
(1999)
Neurosci. News
, vol.2
, pp. 73-82
-
-
Hutton, M.1
-
18
-
-
0033230886
-
Age-dependent emergence and progression of a tauopathy in transgenic mice overexpressing the shortest human tau isoform
-
Ishihara T., et al. Age-dependent emergence and progression of a tauopathy in transgenic mice overexpressing the shortest human tau isoform. Neuron. 24:1999;751-762.
-
(1999)
Neuron
, vol.24
, pp. 751-762
-
-
Ishihara, T.1
-
19
-
-
0024641959
-
Developmentally regulated expression of specific tau sequences
-
Kosik K. Developmentally regulated expression of specific tau sequences. Neuron. 2:1989;1389-1397.
-
(1989)
Neuron
, vol.2
, pp. 1389-1397
-
-
Kosik, K.1
-
20
-
-
0024675418
-
The microtubule binding domain of Tau protein
-
Lee G., et al. The microtubule binding domain of Tau protein. Neuron. 2:1989;1615-1624.
-
(1989)
Neuron
, vol.2
, pp. 1615-1624
-
-
Lee, G.1
-
21
-
-
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. 11:1998;107-114.
-
(1998)
J. Geriatr. Psychiatry Neurol.
, vol.11
, pp. 107-114
-
-
Litvan, I.1
Hutton, M.2
-
22
-
-
0028853922
-
Functional implications for the microtubule -associated protein Tau: Localisation in oligodendrocytes
-
LoPresti P., et al. Functional implications for the microtubule -associated protein Tau: localisation in oligodendrocytes. Proc. Natl Acad. Sci. USA. 92:1995;10369-10373.
-
(1995)
Proc. Natl Acad. Sci. USA
, vol.92
, pp. 10369-10373
-
-
Lopresti, P.1
-
23
-
-
0033011181
-
Accelerated filament formation from tau protein with specific FTDP-17 missense mutations
-
Nacharaju P., et al. Accelerated filament formation from tau protein with specific FTDP-17 missense mutations. FEBS Lett. 447:1999;195-199.
-
(1999)
FEBS Lett.
, vol.447
, pp. 195-199
-
-
Nacharaju, P.1
-
24
-
-
14444284106
-
Tau is a candidate gene for chromosome 17 frontotemporal dementia
-
Poorkaj P., et al. 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
-
25
-
-
0342803685
-
Axonopathy and amyotrophy in mice transgenic for human four-repeat tau protein
-
Probst A., et al. Axonopathy and amyotrophy in mice transgenic for human four-repeat tau protein. Acta Neuropathol (Berl). 99:2000;469-481.
-
(2000)
Acta Neuropathol (Berl)
, vol.99
, pp. 469-481
-
-
Probst, A.1
-
26
-
-
0033070197
-
High prevalence of mutations in the microtubule-associated protein tau in a population study of frontotemporal dementia in the Netherlands
-
Rizzu P., et al. High prevalence of mutations in the microtubule-associated protein tau in a population study of frontotemporal dementia in the Netherlands. Am. J. Hum. Genet. 64:1999;414-421.
-
(1999)
Am. J. Hum. Genet.
, vol.64
, pp. 414-421
-
-
Rizzu, P.1
-
27
-
-
0031949084
-
Frontotemporal Dementia and Parkinsonism Linked to Chromosome 17: A new group of Tauopathies
-
Spillantini M.G., et al. Frontotemporal Dementia and Parkinsonism Linked to Chromosome 17: a new group of Tauopathies. Brain Pathol. 8:1998a;387-402.
-
(1998)
Brain Pathol.
, vol.8
, pp. 387-402
-
-
Spillantini, M.G.1
-
28
-
-
0032560487
-
Mutation in the tau gene in familial multiple system tauopathy with presenile dementia
-
Spillantini M.G., et al. Mutation in the tau gene in familial multiple system tauopathy with presenile dementia. Proc. Natl Acad. Sci. USA. 95:1998b;7737-7741.
-
(1998)
Proc. Natl Acad. Sci. USA
, vol.95
, pp. 7737-7741
-
-
Spillantini, M.G.1
-
29
-
-
0032786370
-
Prominent axonopathy in the brain and spinal cord of transgenic mice overexpressing four-repeat human tau protein
-
Spittaels K., et al. Prominent axonopathy in the brain and spinal cord of transgenic mice overexpressing four-repeat human tau protein. Am. J. Pathol. 155:1999;2153-2165.
-
(1999)
Am. J. Pathol.
, vol.155
, pp. 2153-2165
-
-
Spittaels, K.1
-
30
-
-
0033529304
-
Structure of tau exon 10 splicing regulatory element RNA and destabilisation by mutation of Frontotemporal Dementia and Parkinsonism linked to Chromosome 17
-
Varini, et al. Structure of tau exon 10 splicing regulatory element RNA and destabilisation by mutation 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
-
-
Varini1
-
31
-
-
0032704956
-
FTDP-17 tau mutations decrease the susceptibility of tau to calpain digestion
-
Yen S., et al. FTDP-17 tau mutations decrease the susceptibility of tau to calpain digestion. FEBS Lett. 461:1999;91-95.
-
(1999)
FEBS Lett.
, vol.461
, pp. 91-95
-
-
Yen, S.1
|