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Liu, D. MAPT Gene. Encyclopedia. Available online: https://encyclopedia.pub/entry/4470 (accessed on 27 September 2026).
Liu D. MAPT Gene. Encyclopedia. Available at: https://encyclopedia.pub/entry/4470. Accessed September 27, 2026.
Liu, Dean. "MAPT Gene" Encyclopedia, https://encyclopedia.pub/entry/4470 (accessed September 27, 2026).
Liu, D. (2020, December 23). MAPT Gene. In Encyclopedia. https://encyclopedia.pub/entry/4470
Liu, Dean. "MAPT Gene." Encyclopedia. Web. 23 December, 2020.
MAPT Gene
Edit

Microtubule associated protein tau

genes

References

  1. 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. 1999 Apr;8(4):711-5.
  2. Conrad C, Andreadis A, Trojanowski JQ, Dickson DW, Kang D, Chen X, Wiederholt W, Hansen L, Masliah E, Thal LJ, Katzman R, Xia Y, Saitoh T. Genetic evidence forthe involvement of tau in progressive supranuclear palsy. Ann Neurol. 1997Feb;41(2):277-81.
  3. Goedert M. Tau protein and neurodegeneration. Semin Cell Dev Biol. 2004Feb;15(1):45-9. Review.
  4. 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, Lincoln S, Dickson D,Davies P, Petersen RC, Stevens M, de Graaff E, Wauters E, van Baren J, HillebrandM, Joosse M, Kwon JM, Nowotny P, Che LK, Norton J, Morris JC, Reed LA,Trojanowski J, Basun H, Lannfelt L, Neystat M, Fahn S, Dark F, Tannenberg T, DoddPR, Hayward N, Kwok JB, Schofield PR, Andreadis A, Snowden J, Craufurd D, NearyD, Owen F, Oostra BA, Hardy J, Goate A, van Swieten J, Mann D, Lynch T, HeutinkP. Association of missense and 5'-splice-site mutations in tau with the inheriteddementia FTDP-17. Nature. 1998 Jun 18;393(6686):702-5.
  5. Lee VM, Goedert M, Trojanowski JQ. Neurodegenerative tauopathies. Annu RevNeurosci. 2001;24:1121-59. Review.
  6. Ludolph AC, Kassubek J, Landwehrmeyer BG, Mandelkow E, Mandelkow EM, Burn DJ, Caparros-Lefebvre D, Frey KA, de Yebenes JG, Gasser T, Heutink P, Höglinger G,Jamrozik Z, Jellinger KA, Kazantsev A, Kretzschmar H, Lang AE, Litvan I, LucasJJ, McGeer PL, Melquist S, Oertel W, Otto M, Paviour D, Reum T, Saint-Raymond A, Steele JC, Tolnay M, Tumani H, van Swieten JC, Vanier MT, Vonsattel JP, Wagner S,Wszolek ZK; Reisensburg Working Group for Tauopathies With Parkinsonism.Tauopathies with parkinsonism: clinical spectrum, neuropathologic basis,biological markers, and treatment options. Eur J Neurol. 2009 Mar;16(3):297-309. doi: 10.1111/j.1468-1331.2008.02513.x. Review.
  7. Nicholl DJ, Greenstone MA, Clarke CE, Rizzu P, Crooks D, Crowe A, Trojanowski JQ, Lee VM, Heutink P. An English kindred with a novel recessive tauopathy andrespiratory failure. Ann Neurol. 2003 Nov;54(5):682-6.
  8. Pastor P, Ezquerra M, Tolosa E, Muñoz E, Martí MJ, Valldeoriola F, MolinuevoJL, Calopa M, Oliva R. Further extension of the H1 haplotype associated withprogressive supranuclear palsy. Mov Disord. 2002 May;17(3):550-6.
  9. Rademakers R, Melquist S, Cruts M, Theuns J, Del-Favero J, Poorkaj P, Baker M,Sleegers K, Crook R, De Pooter T, Bel Kacem S, Adamson J, Van den Bossche D, Van den Broeck M, Gass J, Corsmit E, De Rijk P, Thomas N, Engelborghs S, Heckman M,Litvan I, Crook J, De Deyn PP, Dickson D, Schellenberg GD, Van Broeckhoven C,Hutton ML. High-density SNP haplotyping suggests altered regulation of tau geneexpression in progressive supranuclear palsy. Hum Mol Genet. 2005 Nov1;14(21):3281-92.
  10. Spillantini MG, Van Swieten JC, Goedert M. Tau gene mutations infrontotemporal dementia and parkinsonism linked to chromosome 17 (FTDP-17).Neurogenetics. 2000 Mar;2(4):193-205. Review.
  11. van Swieten J, Spillantini MG. Hereditary frontotemporal dementia caused byTau gene mutations. Brain Pathol. 2007 Jan;17(1):63-73. Review.
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