| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| Michael A DeTure, Luca Di Noto, Daniel L Puric. In vitro assembly of Alzheimer-like filaments. How a small cluster of charged residues in Tau and MAP2 controls filament morphology. The Journal of biological chemistry. vol 277. issue 38. 2002-10-24. PMID:12023276. |
moreover, tau appears to be the exclusive building block of the neuropathic filaments observed in alzheimer's disease and certain frontotemporal dementias (ftds). |
2002-10-24 |
2023-08-12 |
Not clear |
| Tomonori Kobayashi, Hideo Mori, Yasuyuki Okuma, Dennis W Dickson, Natalie Cookson, Yoshio Tsuboi, Yumiko Motoi, Ryota Tanaka, Nobuo Miyashita, Midori Anno, Hirotaro Narabayashi, Yoshikuni Mizun. Contrasting genotypes of the tau gene in two phenotypically distinct patients with P301L mutation of frontotemporal dementia and parkinsonism linked to chromosome 17. Journal of neurology. vol 249. issue 6. 2002-09-20. PMID:12111297. |
contrasting genotypes of the tau gene in two phenotypically distinct patients with p301l mutation of frontotemporal dementia and parkinsonism linked to chromosome 17. |
2002-09-20 |
2023-08-12 |
Not clear |
| Tomonori Kobayashi, Hideo Mori, Yasuyuki Okuma, Dennis W Dickson, Natalie Cookson, Yoshio Tsuboi, Yumiko Motoi, Ryota Tanaka, Nobuo Miyashita, Midori Anno, Hirotaro Narabayashi, Yoshikuni Mizun. Contrasting genotypes of the tau gene in two phenotypically distinct patients with P301L mutation of frontotemporal dementia and parkinsonism linked to chromosome 17. Journal of neurology. vol 249. issue 6. 2002-09-20. PMID:12111297. |
association between clinical characteristics and types of the tau gene mutation has been observed in frontotemporal dementia and parkinsonism linked to chromosome 17 (ftdp-17). |
2002-09-20 |
2023-08-12 |
Not clear |
| Pau Pastor, Mario Ezquerra, Eduardo Tolosa, Esteban Muñoz, María José Martí, Francesc Valldeoriola, José Luís Molinuevo, Matilde Calopa, Rafael Oliv. Further extension of the H1 haplotype associated with progressive supranuclear palsy. Movement disorders : official journal of the Movement Disorder Society. vol 17. issue 3. 2002-09-16. PMID:12112206. |
furthermore, we analyzed some markers located in the common region of linkage (d17s800-d17s791), associated with some cases of familial frontotemporal dementia (ftdp-17), and the snps rs1816 and rs937 close to the tau gene, to determine their possible association with sporadic psp. |
2002-09-16 |
2023-08-12 |
Not clear |
| Sonia M Rosso, John C van Swiete. New developments in frontotemporal dementia and parkinsonism linked to chromosome 17. Current opinion in neurology. vol 15. issue 4. 2002-09-13. PMID:12151838. |
the identification of tau mutations in frontotemporal dementia and parkinsonism linked to chromosome 17 (ftdp-17) has revealed invaluable information regarding the role of the tau protein in neurodegenerative disease. |
2002-09-13 |
2023-08-12 |
Not clear |
| Ian D'Souza, Gerard D Schellenber. tau Exon 10 expression involves a bipartite intron 10 regulatory sequence and weak 5' and 3' splice sites. The Journal of biological chemistry. vol 277. issue 29. 2002-09-06. PMID:12000767. |
tau mutations that deregulate alternative exon 10 (e10) splicing cause frontotemporal dementia with parkinsonism chromosome 17-type by several mechanisms. |
2002-09-06 |
2023-08-12 |
Not clear |
| Makoto Higuchi, Takeshi Ishihara, Bin Zhang, Ming Hong, Athena Andreadis, John Trojanowski, Virginia M-Y Le. Transgenic mouse model of tauopathies with glial pathology and nervous system degeneration. Neuron. vol 35. issue 3. 2002-09-04. PMID:12165467. |
frontotemporal dementias (ftds), including corticobasal degeneration (cbd) and progressive supranuclear palsy (psp), are neurodegenerative tauopathies characterized by widespread cns neuronal and glial tau pathologies, but there are no tau transgenic (tg) mice that model neurodegeneration with glia tau lesions. |
2002-09-04 |
2023-08-12 |
mouse |
| Ana Cuadrado, Luis F García-Fernández, Takao Imai, Hideyuki Okano, Alberto Muño. Regulation of tau RNA maturation by thyroid hormone is mediated by the neural RNA-binding protein musashi-1. Molecular and cellular neurosciences. vol 20. issue 2. 2002-08-29. PMID:12093154. |
additionally, mutations affecting tau pre-mrna alternative splicing of exon 10 are associated with frontotemporal dementia and parkinsonism linked to chromosome 17. |
2002-08-29 |
2023-08-12 |
rat |
| Luc Buée, Malika Hamdane, Patrice Delobel, Anne-Véronique Sambo, Séverine Bégard, Antoine Ghestem, Nicolas Sergeant, André Delacourt. [Tau story: from frontotemporal dementia to other tauopathies]. Journal de la Societe de biologie. vol 196. issue 1. 2002-08-23. PMID:12134624. |
[tau story: from frontotemporal dementia to other tauopathies]. |
2002-08-23 |
2023-08-12 |
human |
| A Michotte, S Goldman, P Tugendhaft, D Zegers de Bey. Frontotemporal dementia: a clinical-pathological study. Acta neurologica Belgica. vol 101. issue 4. 2002-08-12. PMID:11851030. |
we discuss the nosology of the frontotemporal dementias, the diagnostic value of pet scan, the recent genetical developments which strongly support the pathogenic role of tau and we emphasize the importance of immunohistochemical examination for a definite neuropathological diagnosis. |
2002-08-12 |
2023-08-12 |
Not clear |
| Lysia S Forno, J William Langston, Maie K Herrick, Jon D Wilson, Shigeo Murayam. Ubiquitin-positive neuronal and tau 2-positive glial inclusions in frontotemporal dementia of motor neuron type. Acta neuropathologica. vol 103. issue 6. 2002-08-07. PMID:12012092. |
ubiquitin-positive neuronal and tau 2-positive glial inclusions in frontotemporal dementia of motor neuron type. |
2002-08-07 |
2023-08-12 |
Not clear |
| Anna Kowalska, Keikichi Takahashi, Wojciech Kozubski, Takeshi Tabir. Microtubule associated protein (tau) gene variability in patients with frontotemporal dementia. Folia neuropathologica. vol 40. issue 1. 2002-08-06. PMID:12121033. |
microtubule associated protein (tau) gene variability in patients with frontotemporal dementia. |
2002-08-06 |
2023-08-12 |
Not clear |
| Anna Kowalska, Keikichi Takahashi, Wojciech Kozubski, Takeshi Tabir. Microtubule associated protein (tau) gene variability in patients with frontotemporal dementia. Folia neuropathologica. vol 40. issue 1. 2002-08-06. PMID:12121033. |
recently, mutations in the microtubule-associated protein (tau) gene have been found in families with frontotemporal dementia and parkinsonism linked to chromosome 17 (ftdp-17). |
2002-08-06 |
2023-08-12 |
Not clear |
| George R Jackson, Martina Wiedau-Pazos, Tzu-Kang Sang, Naveed Wagle, Carlos A Brown, Sasan Massachi, Daniel H Geschwin. Human wild-type tau interacts with wingless pathway components and produces neurofibrillary pathology in Drosophila. Neuron. vol 34. issue 4. 2002-07-16. PMID:12062036. |
pathologic alterations in the microtubule-associated protein tau have been implicated in a number of neurodegenerative disorders, including alzheimer's disease (ad), progressive supranuclear palsy (psp), and frontotemporal dementia (ftd). |
2002-07-16 |
2023-08-12 |
human |
| Patrice Verpillat, Agnès Camuzat, Didier Hannequin, Catherine Thomas-Anterion, Michèle Puel, Serge Belliard, Bruno Dubois, Mira Didic, Bernard-François Michel, Lucette Lacomblez, Olivier Moreaud, François Sellal, Véronique Golfier, Dominique Campion, Françoise Clerget-Darpoux, Alexis Bric. Association between the extended tau haplotype and frontotemporal dementia. Archives of neurology. vol 59. issue 6. 2002-07-01. PMID:12056929. |
association between the extended tau haplotype and frontotemporal dementia. |
2002-07-01 |
2023-08-12 |
human |
| Patrice Verpillat, Agnès Camuzat, Didier Hannequin, Catherine Thomas-Anterion, Michèle Puel, Serge Belliard, Bruno Dubois, Mira Didic, Bernard-François Michel, Lucette Lacomblez, Olivier Moreaud, François Sellal, Véronique Golfier, Dominique Campion, Françoise Clerget-Darpoux, Alexis Bric. Association between the extended tau haplotype and frontotemporal dementia. Archives of neurology. vol 59. issue 6. 2002-07-01. PMID:12056929. |
recent studies have shown an association between an extended tau haplotype (h1) that covers the entire human tau gene and progressive supranuclear palsy or, more inconsistently, other neurodegenerative disorders, such as corticobasal degeneration, parkinson disease, alzheimer disease, and frontotemporal dementia (ftd). |
2002-07-01 |
2023-08-12 |
human |
| S M Pickering-Brown, A M T Richardson, J S Snowden, A M McDonagh, A Burns, W Braude, M Baker, W-K Liu, S-H Yen, J Hardy, M Hutton, Y Davies, D Allsop, D Craufurd, D Neary, D M A Man. Inherited frontotemporal dementia in nine British families associated with intronic mutations in the tau gene. Brain : a journal of neurology. vol 125. issue Pt 4. 2002-05-10. PMID:11912108. |
inherited frontotemporal dementia in nine british families associated with intronic mutations in the tau gene. |
2002-05-10 |
2023-08-12 |
Not clear |
| J C Janssen, E K Warrington, H R Morris, P Lantos, J Brown, T Revesz, N Wood, M N Khan, L Cipolotti, N C Fox, M N Rosso. Clinical features of frontotemporal dementia due to the intronic tau 10(+16) mutation. Neurology. vol 58. issue 8. 2002-05-07. PMID:11971081. |
clinical features of frontotemporal dementia due to the intronic tau 10(+16) mutation. |
2002-05-07 |
2023-08-12 |
Not clear |
| J C Janssen, E K Warrington, H R Morris, P Lantos, J Brown, T Revesz, N Wood, M N Khan, L Cipolotti, N C Fox, M N Rosso. Clinical features of frontotemporal dementia due to the intronic tau 10(+16) mutation. Neurology. vol 58. issue 8. 2002-05-07. PMID:11971081. |
to describe the clinical features of nine british families with neuropathologically verified frontotemporal dementia (ftd) due to the intronic tau exon 10(+16) mutation. |
2002-05-07 |
2023-08-12 |
Not clear |
| P L Lantos, N J Cairns, M N Khan, A King, T Revesz, J C Janssen, H Morris, M N Rosso. Neuropathologic variation in frontotemporal dementia due to the intronic tau 10(+16) mutation. Neurology. vol 58. issue 8. 2002-05-07. PMID:11971082. |
neuropathologic variation in frontotemporal dementia due to the intronic tau 10(+16) mutation. |
2002-05-07 |
2023-08-12 |
Not clear |