| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| H R Morris, J C Janssen, O Bandmann, S E Daniel, M N Rossor, A J Lees, N W Woo. The tau gene A0 polymorphism in progressive supranuclear palsy and related neurodegenerative diseases. Journal of neurology, neurosurgery, and psychiatry. vol 66. issue 5. 1999-05-25. PMID:10209184. |
other diseases which may involve tau deposition include frontotemporal dementia and corticobasal degeneration. |
1999-05-25 |
2023-08-12 |
human |
| H R Morris, J C Janssen, O Bandmann, S E Daniel, M N Rossor, A J Lees, N W Woo. The tau gene A0 polymorphism in progressive supranuclear palsy and related neurodegenerative diseases. Journal of neurology, neurosurgery, and psychiatry. vol 66. issue 5. 1999-05-25. PMID:10209184. |
this polymorphism has been studied in a series of subjects with progressive supranuclear palsy, corticobasal degeneration, frontotemporal dementia, idiopathic parkinson's disease, and normal controls to (1) confirm this association in a large series and (2) to investigate a possible role for this association in other disorders which involve tau deposition. |
1999-05-25 |
2023-08-12 |
human |
| S S Mirra, J R Murrell, M Gearing, M G Spillantini, M Goedert, R A Crowther, A I Levey, R Jones, J Green, J M Shoffner, B H Wainer, M L Schmidt, J Q Trojanowski, B Ghett. Tau pathology in a family with dementia and a P301L mutation in tau. Journal of neuropathology and experimental neurology. vol 58. issue 4. 1999-05-06. PMID:10218629. |
familial forms of frontotemporal dementia and parkinsonism linked to chromosome 17 (ftdp-17) have recently been associated with coding region and intronic mutations in the tau gene. |
1999-05-06 |
2023-08-12 |
Not clear |
| T D Bird, D Nochlin, P Poorkaj, M Cherrier, J Kaye, H Payami, E Peskind, T H Lampe, E Nemens, P J Boyer, G D Schellenber. A clinical pathological comparison of three families with frontotemporal dementia and identical mutations in the tau gene (P301L) Brain : a journal of neurology. vol 122 ( Pt 4). 1999-05-06. PMID:10219785. |
a clinical pathological comparison of three families with frontotemporal dementia and identical mutations in the tau gene (p301l) we investigated three separate families (designated d, f and g) with frontotemporal dementia that have the same molecular mutation in exon 10 of the tau gene (p301l). |
1999-05-06 |
2023-08-12 |
Not clear |
| P Nacharaju, J Lewis, C Easson, S Yen, J Hackett, M Hutton, S H Ye. Accelerated filament formation from tau protein with specific FTDP-17 missense mutations. FEBS letters. vol 447. issue 2-3. 1999-05-05. PMID:10214944. |
the identification of missense and splicing mutations in tau associated with the inherited frontotemporal dementia and parkinsonism linked to chromosome 17 demonstrated that tau dysfunction can cause neurodegeneration. |
1999-05-05 |
2023-08-12 |
Not clear |
| P Nacharaju, J Lewis, C Easson, S Yen, J Hackett, M Hutton, S H Ye. Accelerated filament formation from tau protein with specific FTDP-17 missense mutations. FEBS letters. vol 447. issue 2-3. 1999-05-05. PMID:10214944. |
here, we present evidence that frontotemporal dementia and parkinsonism linked to chromosome 17 missense mutations, p301l, v337m and r406w, cause an accelerated aggregation of tau into filaments. |
1999-05-05 |
2023-08-12 |
Not clear |
| M Goedert, M G Spillantini, R A Crowther, S G Chen, P Parchi, M Tabaton, D J Lanska, W R Markesbery, K C Wilhelmsen, D W Dickson, R B Petersen, P Gambett. Tau gene mutation in familial progressive subcortical gliosis. Nature medicine. vol 5. issue 4. 1999-04-29. PMID:10202939. |
familial forms of frontotemporal dementias are associated with mutations in the tau gene. |
1999-04-29 |
2023-08-12 |
Not clear |
| J Hardy, K Duff, K G Hardy, J Perez-Tur, M Hutto. Genetic dissection of Alzheimer's disease and related dementias: amyloid and its relationship to tau. Nature neuroscience. vol 1. issue 5. 1999-04-28. PMID:10196523. |
tau is produced either indirectly, by a beta 42, or directly, in some forms of frontotemporal dementia by mutations in tau itself. |
1999-04-28 |
2023-08-12 |
Not clear |
| P Rizzu, J C Van Swieten, M Joosse, M Hasegawa, M Stevens, A Tibben, M F Niermeijer, M Hillebrand, R Ravid, B A Oostra, M Goedert, C M van Duijn, P Heutin. High prevalence of mutations in the microtubule-associated protein tau in a population study of frontotemporal dementia in the Netherlands. American journal of human genetics. vol 64. issue 2. 1999-04-13. PMID:9973279. |
high prevalence of mutations in the microtubule-associated protein tau in a population study of frontotemporal dementia in the netherlands. |
1999-04-13 |
2023-08-12 |
Not clear |
| P Rizzu, J C Van Swieten, M Joosse, M Hasegawa, M Stevens, A Tibben, M F Niermeijer, M Hillebrand, R Ravid, B A Oostra, M Goedert, C M van Duijn, P Heutin. High prevalence of mutations in the microtubule-associated protein tau in a population study of frontotemporal dementia in the Netherlands. American journal of human genetics. vol 64. issue 2. 1999-04-13. PMID:9973279. |
mutations in microtubule-associated protein tau recently have been identified in familial cases of frontotemporal dementia (ftd). |
1999-04-13 |
2023-08-12 |
Not clear |
| H R Morris, J Perez-Tur, J C Janssen, J Brown, A J Lees, N W Wood, J Hardy, M Hutton, M N Rosso. Mutation in the tau exon 10 splice site region in familial frontotemporal dementia. Annals of neurology. vol 45. issue 2. 1999-03-29. PMID:9989634. |
mutation in the tau exon 10 splice site region in familial frontotemporal dementia. |
1999-03-29 |
2023-08-12 |
Not clear |
| I Litvan, M Hutto. Clinical and genetic aspects of progressive supranuclear palsy. Journal of geriatric psychiatry and neurology. vol 11. issue 2. 1999-03-18. PMID:9877531. |
in addition, the recent identification of mutations in the tau gene associated with a similar neurodegenerative condition (frontotemporal dementia and parkinsonism linked to chromosome 17) has further strengthened the argument that tau dysfunction is somehow involved in the pathogenesis of psp. |
1999-03-18 |
2023-08-12 |
Not clear |
| N Sergeant, A Wattez, A Delacourt. Neurofibrillary degeneration in progressive supranuclear palsy and corticobasal degeneration: tau pathologies with exclusively "exon 10" isoforms. Journal of neurochemistry. vol 72. issue 3. 1999-03-18. PMID:10037497. |
the recently described mutations of the tau gene responsible for familial frontotemporal dementias also support this hypothesis. |
1999-03-18 |
2023-08-12 |
Not clear |
| M Hasegawa, M J Smith, M Iijima, T Tabira, M Goeder. FTDP-17 mutations N279K and S305N in tau produce increased splicing of exon 10. FEBS letters. vol 443. issue 2. 1999-03-02. PMID:9989582. |
missense mutations and intronic mutations in the tau gene cause frontotemporal dementia and parkinsonism linked to chromosome 17 (ftdp-17). |
1999-03-02 |
2023-08-12 |
Not clear |
| M Goedert, M G Spillantini, S W Davie. Filamentous nerve cell inclusions in neurodegenerative diseases. Current opinion in neurobiology. vol 8. issue 5. 1999-01-07. PMID:9811617. |
over the past year, mutations in the genes for tau and alpha-synuclein have been identified as the genetic causes of some familial forms of frontotemporal dementia and parkinson's disease, respectively. |
1999-01-07 |
2023-08-12 |
Not clear |
| M Goedert, R A Crowther, M G Spillantin. Tau mutations cause frontotemporal dementias. Neuron. vol 21. issue 5. 1999-01-04. PMID:9856453. |
tau mutations cause frontotemporal dementias. |
1999-01-04 |
2023-08-12 |
Not clear |
| M Hong, V Zhukareva, V Vogelsberg-Ragaglia, Z Wszolek, L Reed, B I Miller, D H Geschwind, T D Bird, D McKeel, A Goate, J C Morris, K C Wilhelmsen, G D Schellenberg, J Q Trojanowski, V M Le. Mutation-specific functional impairments in distinct tau isoforms of hereditary FTDP-17. Science (New York, N.Y.). vol 282. issue 5395. 1998-12-28. PMID:9836646. |
tau proteins aggregate as cytoplasmic inclusions in a number of neurodegenerative diseases, including alzheimer's disease and hereditary frontotemporal dementia and parkinsonism linked to chromosome 17 (ftdp-17). |
1998-12-28 |
2023-08-12 |
Not clear |
| M G Spillantini, M Goeder. Tau protein pathology in neurodegenerative diseases. Trends in neurosciences. vol 21. issue 10. 1998-12-18. PMID:9786340. |
filamentous tau pathology is also central to a number of other dementing disorders, such as pick's disease, progressive supranuclear palsy, corticobasal degeneration and familial frontotemporal dementia and parkinsonism linked to chromosome 17 (ftdp-17). |
1998-12-18 |
2023-08-12 |
Not clear |
| M Hasegawa, M J Smith, M Goeder. Tau proteins with FTDP-17 mutations have a reduced ability to promote microtubule assembly. FEBS letters. vol 437. issue 3. 1998-12-10. PMID:9824291. |
recently exonic and intronic mutations in the gene for microtubule-associated protein tau have been discovered in cases of familial frontotemporal dementia and parkinsonism linked to chromosome 17 (ftdp-17). |
1998-12-10 |
2023-08-12 |
Not clear |
| C Dumanchin, A Camuzat, D Campion, P Verpillat, D Hannequin, B Dubois, P Saugier-Veber, C Martin, C Penet, F Charbonnier, Y Agid, T Frebourg, A Bric. Segregation of a missense mutation in the microtubule-associated protein tau gene with familial frontotemporal dementia and parkinsonism. Human molecular genetics. vol 7. issue 11. 1998-12-01. PMID:9736786. |
segregation of a missense mutation in the microtubule-associated protein tau gene with familial frontotemporal dementia and parkinsonism. |
1998-12-01 |
2023-08-12 |
human |