| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| Bradley F Boeve, Mike Hutto. Refining frontotemporal dementia with parkinsonism linked to chromosome 17: introducing FTDP-17 (MAPT) and FTDP-17 (PGRN). Archives of neurology. vol 65. issue 4. 2008-05-21. PMID:18413467. |
refining frontotemporal dementia with parkinsonism linked to chromosome 17: introducing ftdp-17 (mapt) and ftdp-17 (pgrn). |
2008-05-21 |
2023-08-12 |
Not clear |
| Christian Wider, Zbigniew K Wszole. Etiology and pathophysiology of frontotemporal dementia, Parkinson disease and Alzheimer disease: lessons from genetic studies. Neuro-degenerative diseases. vol 5. issue 3-4. 2008-05-15. PMID:18322368. |
the tau gene (mapt) causes frontotemporal dementia with parkinsonism linked to chromosome 17. |
2008-05-15 |
2023-08-12 |
Not clear |
| Bernardino Ghetti, Salvatore Spina, Jill R Murrell, Edward D Huey, Pietro Pietrini, Brian Sweeney, Eric M Wassermann, Catherine Keohane, Martin R Farlow, Jordan Grafma. In vivo and postmortem clinicoanatomical correlations in frontotemporal dementia and parkinsonism linked to chromosome 17. Neuro-degenerative diseases. vol 5. issue 3-4. 2008-05-15. PMID:18322394. |
frontotemporal dementia and parkinsonism linked to chromosome 17 (ftdp-17) is associated with mutations in the microtubule-associated protein tau(mapt) gene or the progranulin(pgrn) gene. |
2008-05-15 |
2023-08-12 |
Not clear |
| Simon M Laws, Robert Perneczky, Alexander Drzezga, Janine Diehl-Schmid, Bernd Ibach, Josef Bäuml, Tamara Eisele, Hans Förstl, Alexander Kurz, Matthias Riemenschneide. Association of the tau haplotype H2 with age at onset and functional alterations of glucose utilization in frontotemporal dementia. The American journal of psychiatry. vol 164. issue 10. 2007-11-01. PMID:17898350. |
the aim of this study was to investigate the mapt haplotypes in relation to risk for, and functional alterations of glucose metabolism in, patients with frontotemporal dementia (ftd). |
2007-11-01 |
2023-08-12 |
Not clear |
| S Davion, N Johnson, S Weintraub, M-M Mesulam, A Engberg, M Mishra, M Baker, J Adamson, M Hutton, R Rademakers, E H Bigi. Clinicopathologic correlation in PGRN mutations. Neurology. vol 69. issue 11. 2007-10-11. PMID:17522386. |
frontotemporal dementia (ftd) has been linked to the microtubule associated protein tau (mapt) gene region of chromosome 17. |
2007-10-11 |
2023-08-12 |
Not clear |
| A Lladó, M Ezquerra, R Sánchez-Valle, L Rami, E Tolosa, J L Molinuev. A novel MAPT mutation (P301T) associated with familial frontotemporal dementia. European journal of neurology. vol 14. issue 8. 2007-09-12. PMID:17662000. |
a novel mapt mutation (p301t) associated with familial frontotemporal dementia. |
2007-09-12 |
2023-08-12 |
Not clear |
| Samir Kumar-Singh, Christine Van Broeckhove. Frontotemporal lobar degeneration: current concepts in the light of recent advances. Brain pathology (Zurich, Switzerland). vol 17. issue 1. 2007-06-26. PMID:17493044. |
mutations in mapt were found to cause frontotemporal dementia and parkinsonism linked to chromosome 17 (ftdp-17), a familial disorder with filamentous tau inclusions in nerve cells and glial cells. |
2007-06-26 |
2023-08-12 |
Not clear |
| Jerzy Slowinski, Jake Dominik, Ryan J Uitti, Zeshan Ahmed, Dennis D Dickson, Zbigniew K Wszole. Frontotemporal dementia and Parkinsonism linked to chromosome 17 with the N279K tau mutation. Neuropathology : official journal of the Japanese Society of Neuropathology. vol 27. issue 1. 2007-03-29. PMID:17319286. |
we present a case of frontotemporal dementia and parkinsonism linked to chromosome 17 (ftdp-17) harboring the n279k mutation in the mapt gene from the family known as pallido-ponto-nigral degeneration (ppnd). |
2007-03-29 |
2023-08-12 |
Not clear |
| Stuart M Pickering-Brown, Matt Baker, Jenny Gass, Bradley F Boeve, Clement T Loy, William S Brooks, Ian R A Mackenzie, Ralph N Martins, John B J Kwok, Glenda M Halliday, Jillian Kril, Peter R Schofield, David M A Mann, Mike Hutto. Mutations in progranulin explain atypical phenotypes with variants in MAPT. Brain : a journal of neurology. vol 129. issue Pt 11. 2006-12-11. PMID:17071927. |
mutations in presenilin-1 (psen1) cause autosomal dominant alzheimer's disease and mutations in mapt cause the familial tauopathy frontotemporal dementia linked to chromosome 17 (ftdp-17). |
2006-12-11 |
2023-08-12 |
Not clear |
| Alan M Pittman, Hon-Chung Fung, Rohan de Silv. Untangling the tau gene association with neurodegenerative disorders. Human molecular genetics. vol 15 Spec No 2. 2006-11-20. PMID:16987883. |
mutations in the tau gene, mapt, cause familial frontotemporal dementia with parkinsonism linked to chromosome 17 (ftdp-17), and common variation in mapt is strongly associated with the risk of psp, corticobasal degeneration and, to a lesser extent, ad and parkinson's disease (pd), implicating the involvement of tau in common neurodegenerative pathway(s). |
2006-11-20 |
2023-08-12 |
Not clear |
| Edward D Huey, Jordan Grafman, Eric M Wassermann, Pietro Pietrini, Michael C Tierney, Bernardino Ghetti, Salvatore Spina, Matt Baker, Mike Hutton, Joshua W Elder, Stephen L Berger, Kyle A Heflin, John Hardy, Parastoo Momen. Characteristics of frontotemporal dementia patients with a Progranulin mutation. Annals of neurology. vol 60. issue 3. 2006-11-14. PMID:16983677. |
mutations in the progranulin gene (pgrn) recently have been discovered to be associated with frontotemporal dementia (ftd) linked to 17q21 without identified mapt mutations. |
2006-11-14 |
2023-08-12 |
Not clear |
| Ilse Gijselinck, Veerle Bogaerts, Rosa Rademakers, Julie van der Zee, Christine Van Broeckhoven, Marc Crut. Visualization of MAPT inversion on stretched chromosomes of tau-negative frontotemporal dementia patients. Human mutation. vol 27. issue 10. 2006-10-02. PMID:16906510. |
visualization of mapt inversion on stretched chromosomes of tau-negative frontotemporal dementia patients. |
2006-10-02 |
2023-08-12 |
Not clear |
| Marc Cruts, Ilse Gijselinck, Julie van der Zee, Sebastiaan Engelborghs, Hans Wils, Daniel Pirici, Rosa Rademakers, Rik Vandenberghe, Bart Dermaut, Jean-Jacques Martin, Cornelia van Duijn, Karin Peeters, Raf Sciot, Patrick Santens, Tim De Pooter, Maria Mattheijssens, Marleen Van den Broeck, Ivy Cuijt, Krist'l Vennekens, Peter P De Deyn, Samir Kumar-Singh, Christine Van Broeckhove. Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21. Nature. vol 442. issue 7105. 2006-09-22. PMID:16862115. |
frontotemporal dementia (ftd) with ubiquitin-immunoreactive neuronal inclusions (both cytoplasmic and nuclear) of unknown nature has been linked to a chromosome 17q21 region (ftdu-17) containing mapt (microtubule-associated protein tau). |
2006-09-22 |
2023-08-12 |
Not clear |
| A-M Shiarli, R Jennings, J Shi, K Bailey, Y Davidson, J Tian, E H Bigio, B Ghetti, J R Murrell, M B Delisle, S Mirra, B Crain, P Zolo, K Arima, E Iseki, S Murayama, H Kretzschmar, M Neumann, C Lippa, G Halliday, J Mackenzie, N Khan, R Ravid, D Dickson, Z Wszolek, T Iwatsubo, S M Pickering-Brown, D M A Man. Comparison of extent of tau pathology in patients with frontotemporal dementia with Parkinsonism linked to chromosome 17 (FTDP-17), frontotemporal lobar degeneration with Pick bodies and early onset Alzheimer's disease. Neuropathology and applied neurobiology. vol 32. issue 4. 2006-09-19. PMID:16866983. |
in order to gain insight into the pathogenesis of frontotemporal lobar degeneration (ftld), the mean tau load in frontal cortex was compared in 34 patients with frontotemporal dementia linked to chromosome 17 (ftdp-17) with 12 different mutations in the tau gene (mapt), 11 patients with sporadic ftld with pick bodies and 25 patients with early onset alzheimer's disease (eoad). |
2006-09-19 |
2023-08-12 |
Not clear |
| Roberta Ghidoni, Simona Signorini, Laura Barbiero, Elena Sina, Paola Cominelli, Aldo Villa, Luisa Benussi, Giuliano Binett. The H2 MAPT haplotype is associated with familial frontotemporal dementia. Neurobiology of disease. vol 22. issue 2. 2006-07-25. PMID:16410051. |
the h2 mapt haplotype is associated with familial frontotemporal dementia. |
2006-07-25 |
2023-08-12 |
Not clear |
| Roberta Ghidoni, Simona Signorini, Laura Barbiero, Elena Sina, Paola Cominelli, Aldo Villa, Luisa Benussi, Giuliano Binett. The H2 MAPT haplotype is associated with familial frontotemporal dementia. Neurobiology of disease. vol 22. issue 2. 2006-07-25. PMID:16410051. |
there is now considerable evidence that the gene encoding for tau protein (mapt) is implicated in frontotemporal dementia (ftd). |
2006-07-25 |
2023-08-12 |
Not clear |
| Roneil Malkani, Ian D'Souza, Katrina Gwinn-Hardy, Gerard D Schellenberg, John Hardy, Parastoo Momen. A MAPT mutation in a regulatory element upstream of exon 10 causes frontotemporal dementia. Neurobiology of disease. vol 22. issue 2. 2006-07-25. PMID:16503405. |
a mapt mutation in a regulatory element upstream of exon 10 causes frontotemporal dementia. |
2006-07-25 |
2023-08-12 |
Not clear |
| Roneil Malkani, Ian D'Souza, Katrina Gwinn-Hardy, Gerard D Schellenberg, John Hardy, Parastoo Momen. A MAPT mutation in a regulatory element upstream of exon 10 causes frontotemporal dementia. Neurobiology of disease. vol 22. issue 2. 2006-07-25. PMID:16503405. |
we report here the genetic analysis of a newly ascertained kindred in which frontotemporal dementia occurs in an apparent autosomal dominant fashion, and in which a novel mapt gene mutation co-segregates with disease. |
2006-07-25 |
2023-08-12 |
Not clear |
| Giorgio Giaccone, Giacomina Rossi, Laura Farina, Gabriella Marcon, Giuseppe Di Fede, Marcella Catania, Michela Morbin, Leonardo Sacco, Orso Bugiani, Fabrizio Tagliavin. Familial frontotemporal dementia associated with the novel MAPT mutation T427M. Journal of neurology. vol 252. issue 12. 2006-06-28. PMID:15940384. |
familial frontotemporal dementia associated with the novel mapt mutation t427m. |
2006-06-28 |
2023-08-12 |
Not clear |
| Zbigniew K Wszołek, Jerzy Słowiński, Maciej Golan, Dennis W Dickso. Frontotemporal dementia and parkinsonism linked to chromosome 17. Folia neuropathologica. vol 43. issue 4. 2006-04-21. PMID:16416390. |
frontotemporal dementia and parkinsonism linked to chromosome 17 (ftdp-17) is an autosomal dominant neurodegenerative disorder caused by mutations in the mapt gene which encodes the microtubule-associated protein tau. |
2006-04-21 |
2023-08-12 |
Not clear |