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Journal Abstract Search

488 related items for PubMed ID: 12883828

  • 1. The L266V tau mutation is associated with frontotemporal dementia and Pick-like 3R and 4R tauopathy.
    Hogg M, Grujic ZM, Baker M, Demirci S, Guillozet AL, Sweet AP, Herzog LL, Weintraub S, Mesulam MM, LaPointe NE, Gamblin TC, Berry RW, Binder LI, de Silva R, Lees A, Espinoza M, Davies P, Grover A, Sahara N, Ishizawa T, Dickson D, Yen SH, Hutton M, Bigio EH.
    Acta Neuropathol; 2003 Oct; 106(4):323-36. PubMed ID: 12883828
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  • 2. Hereditary Pick's disease with the G272V tau mutation shows predominant three-repeat tau pathology.
    Bronner IF, ter Meulen BC, Azmani A, Severijnen LA, Willemsen R, Kamphorst W, Ravid R, Heutink P, van Swieten JC.
    Brain; 2005 Nov; 128(Pt 11):2645-53. PubMed ID: 16014652
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  • 3. The DeltaK280 mutation in MAP tau favors exon 10 skipping in vivo.
    van Swieten JC, Bronner IF, Azmani A, Severijnen LA, Kamphorst W, Ravid R, Rizzu P, Willemsen R, Heutink P.
    J Neuropathol Exp Neurol; 2007 Jan; 66(1):17-25. PubMed ID: 17204933
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  • 4. Increase in the relative expression of tau with four microtubule binding repeat regions in frontotemporal lobar degeneration and progressive supranuclear palsy brains.
    Ingelsson M, Ramasamy K, Russ C, Freeman SH, Orne J, Raju S, Matsui T, Growdon JH, Frosch MP, Ghetti B, Brown RH, Irizarry MC, Hyman BT.
    Acta Neuropathol; 2007 Nov; 114(5):471-9. PubMed ID: 17721707
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  • 7. Quantitative analysis of tau isoform transcripts in sporadic tauopathies.
    Connell JW, Rodriguez-Martin T, Gibb GM, Kahn NM, Grierson AJ, Hanger DP, Revesz T, Lantos PL, Anderton BH, Gallo JM.
    Brain Res Mol Brain Res; 2005 Jun 13; 137(1-2):104-9. PubMed ID: 15950767
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  • 8. A novel L266V mutation of the tau gene causes frontotemporal dementia with a unique tau pathology.
    Kobayashi T, Ota S, Tanaka K, Ito Y, Hasegawa M, Umeda Y, Motoi Y, Takanashi M, Yasuhara M, Anno M, Mizuno Y, Mori H.
    Ann Neurol; 2003 Jan 13; 53(1):133-7. PubMed ID: 12509859
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  • 11. Frontotemporal dementia with novel tau pathology and a Glu342Val tau mutation.
    Lippa CF, Zhukareva V, Kawarai T, Uryu K, Shafiq M, Nee LE, Grafman J, Liang Y, St George-Hyslop PH, Trojanowski JQ, Lee VM.
    Ann Neurol; 2000 Dec 13; 48(6):850-8. PubMed ID: 11117541
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  • 13. A new family with frontotemporal dementia with intronic 10+3 splice site mutation in the tau gene: neuropathology and molecular effects.
    Neumann M, Mittelbronn M, Simon P, Vanmassenhove B, de Silva R, Lees A, Klapp J, Meyermann R, Kretzschmar HA.
    Neuropathol Appl Neurobiol; 2005 Aug 13; 31(4):362-73. PubMed ID: 16008820
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  • 14. Cellular tau pathology and immunohistochemical study of tau isoforms in sporadic tauopathies.
    Yoshida M.
    Neuropathology; 2006 Oct 13; 26(5):457-70. PubMed ID: 17080726
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  • 16. A peculiar constellation of tau pathology defines a subset of dementia in the elderly.
    Kovacs GG, Molnár K, László L, Ströbel T, Botond G, Hönigschnabl S, Reiner-Concin A, Palkovits M, Fischer P, Budka H.
    Acta Neuropathol; 2011 Aug 13; 122(2):205-22. PubMed ID: 21437732
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  • 18. Neurodegenerative disorder FTDP-17-related tau intron 10 +16C → T mutation increases tau exon 10 splicing and causes tauopathy in transgenic mice.
    Umeda T, Yamashita T, Kimura T, Ohnishi K, Takuma H, Ozeki T, Takashima A, Tomiyama T, Mori H.
    Am J Pathol; 2013 Jul 13; 183(1):211-25. PubMed ID: 23680655
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