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Journal Abstract Search

282 related items for PubMed ID: 15651320

  • 21. Variable phenotypic expression and extensive tau pathology in two families with the novel tau mutation L315R.
    van Herpen E, Rosso SM, Serverijnen LA, Yoshida H, Breedveld G, van de Graaf R, Kamphorst W, Ravid R, Willemsen R, Dooijes D, Majoor-Krakauer D, Kros JM, Crowther RA, Goedert M, Heutink P, van Swieten JC.
    Ann Neurol; 2003 Nov; 54(5):573-81. PubMed ID: 14595646
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  • 22. Alpha1-antichymotrypsin, an inflammatory protein overexpressed in Alzheimer's disease brain, induces tau phosphorylation in neurons.
    Padmanabhan J, Levy M, Dickson DW, Potter H.
    Brain; 2006 Nov; 129(Pt 11):3020-34. PubMed ID: 16987932
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  • 23. Abnormal tau-containing filaments in neurodegenerative diseases.
    Crowther RA, Goedert M.
    J Struct Biol; 2000 Jun; 130(2-3):271-9. PubMed ID: 10940231
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  • 24. 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; 48(6):850-8. PubMed ID: 11117541
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  • 27. 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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  • 29. Longitudinal characterization of two siblings with frontotemporal dementia and parkinsonism linked to chromosome 17 associated with the S305N tau mutation.
    Boeve BF, Tremont-Lukats IW, Waclawik AJ, Murrell JR, Hermann B, Jack CR, Shiung MM, Smith GE, Nair AR, Lindor N, Koppikar V, Ghetti B.
    Brain; 2005 Apr; 128(Pt 4):752-72. PubMed ID: 15615814
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  • 30. 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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  • 31. Histopathological changes underlying frontotemporal lobar degeneration with clinicopathological correlation.
    Shi J, Shaw CL, Du Plessis D, Richardson AM, Bailey KL, Julien C, Stopford C, Thompson J, Varma A, Craufurd D, Tian J, Pickering-Brown S, Neary D, Snowden JS, Mann DM.
    Acta Neuropathol; 2005 Nov; 110(5):501-12. PubMed ID: 16222525
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  • 34. Regulation of tau isoform expression and dementia.
    D'Souza I, Schellenberg GD.
    Biochim Biophys Acta; 2005 Jan 03; 1739(2-3):104-15. PubMed ID: 15615630
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  • 35. A novel mutation (K317M) in the MAPT gene causes FTDP and motor neuron disease.
    Zarranz JJ, Ferrer I, Lezcano E, Forcadas MI, Eizaguirre B, Atarés B, Puig B, Gómez-Esteban JC, Fernández-Maiztegui C, Rouco I, Pérez-Concha T, Fernández M, Rodríguez O, Rodríguez-Martínez AB, de Pancorbo MM, Pastor P, Pérez-Tur J.
    Neurology; 2005 May 10; 64(9):1578-85. PubMed ID: 15883319
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  • 37. [A 54-year-old man with familial parkinsonism, gaze palsy, and dementia].
    Shimura H, Mori H, Komatsuzaki Y, Nakamura K, Takanashi M, Hattori N, Mizuno Y.
    No To Shinkei; 2005 Dec 10; 57(12):1104-12. PubMed ID: 16375198
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  • 38. [Molecular analysis of tau deposited in the FTDP-17 brain].
    Morishima-Kawashima M.
    Rinsho Shinkeigaku; 2001 Dec 10; 41(12):1107-10. PubMed ID: 12235810
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  • 39. Progressive supranuclear palsy and corticobasal degeneration: lumping versus splitting.
    Scaravilli T, Tolosa E, Ferrer I.
    Mov Disord; 2005 Aug 10; 20 Suppl 12():S21-8. PubMed ID: 16092076
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  • 40. 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 10; 53(1):133-7. PubMed ID: 12509859
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