BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

272 related articles for article (PubMed ID: 10393977)

  • 21. Mutation in the tau gene in familial multiple system tauopathy with presenile dementia.
    Spillantini MG; Murrell JR; Goedert M; Farlow MR; Klug A; Ghetti B
    Proc Natl Acad Sci U S A; 1998 Jun; 95(13):7737-41. PubMed ID: 9636220
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Accelerated filament formation from tau protein with specific FTDP-17 missense mutations.
    Nacharaju P; Lewis J; Easson C; Yen S; Hackett J; Hutton M; Yen SH
    FEBS Lett; 1999 Mar; 447(2-3):195-9. PubMed ID: 10214944
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Tau exon 10, whose missplicing causes frontotemporal dementia, is regulated by an intricate interplay of cis elements and trans factors.
    Wang J; Gao QS; Wang Y; Lafyatis R; Stamm S; Andreadis A
    J Neurochem; 2004 Mar; 88(5):1078-90. PubMed ID: 15009664
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Tau gene mutations and neurodegeneration.
    Goedert M; Spillantini MG
    Biochem Soc Symp; 2001; (67):59-71. PubMed ID: 11447840
    [TBL] [Abstract][Full Text] [Related]  

  • 25. 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; 183(1):211-25. PubMed ID: 23680655
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Identification of ligands for the Tau exon 10 splicing regulatory element RNA by using dynamic combinatorial chemistry.
    López-Senín P; Gómez-Pinto I; Grandas A; Marchán V
    Chemistry; 2011 Feb; 17(6):1946-53. PubMed ID: 21274946
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Familial frontotemporal dementia and parkinsonism with a novel N296H mutation in exon 10 of the tau gene and a widespread tau accumulation in the glial cells.
    Iseki E; Matsumura T; Marui W; Hino H; Odawara T; Sugiyama N; Suzuki K; Sawada H; Arai T; Kosaka K
    Acta Neuropathol; 2001 Sep; 102(3):285-92. PubMed ID: 11585254
    [TBL] [Abstract][Full Text] [Related]  

  • 28. The tau gene in progressive supranuclear palsy: exclusion of mutations in coding exons and exon 10 splice sites, and identification of a new intronic variant of the disease-associated H1 haplotype in Italian cases.
    Bonifati V; Joosse M; Nicholl DJ; Vanacore N; Bennett P; Rizzu P; Fabbrini G; Marconi R; Colosimo C; Locuratolo N; Stocchi F; Bonuccelli U; De Mari M; Wenning G; Vieregge P; Oostra B; Meco G; Heutink P
    Neurosci Lett; 1999 Oct; 274(1):61-5. PubMed ID: 10530520
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Search for a mutation in the tau gene in a Swiss family with frontotemporal dementia.
    Savioz A; Kövari E; Anastasiu R; Rossier C; Saini K; Bouras C; Leuba G
    Exp Neurol; 2000 Jan; 161(1):330-5. PubMed ID: 10683298
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Tau gene mutations in frontotemporal dementia and parkinsonism linked to chromosome 17 (FTDP-17). Their relevance for understanding the neurogenerative process.
    Goedert M; Ghetti B; Spillantini MG
    Ann N Y Acad Sci; 2000; 920():74-83. PubMed ID: 11193179
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Pro-apoptotic effects of tau mutations in chromosome 17 frontotemporal dementia and parkinsonism.
    Furukawa K; D'Souza I; Crudder CH; Onodera H; Itoyama Y; Poorkaj P; Bird TD; Schellenberg GD
    Neuroreport; 2000 Jan; 11(1):57-60. PubMed ID: 10683829
    [TBL] [Abstract][Full Text] [Related]  

  • 32. An SRp75/hnRNPG complex interacting with hnRNPE2 regulates the 5' splice site of tau exon 10, whose misregulation causes frontotemporal dementia.
    Wang Y; Wang J; Gao L; Stamm S; Andreadis A
    Gene; 2011 Oct; 485(2):130-8. PubMed ID: 21723381
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Tau proteins with FTDP-17 mutations have a reduced ability to promote microtubule assembly.
    Hasegawa M; Smith MJ; Goedert M
    FEBS Lett; 1998 Oct; 437(3):207-10. PubMed ID: 9824291
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Tau mutations in familial frontotemporal dementia.
    Spillantini MG; Goedert M
    Brain; 2000 May; 123 ( Pt 5)():857-9. PubMed ID: 10775532
    [No Abstract]   [Full Text] [Related]  

  • 35. Heterogeneous nuclear ribonucleoprotein E3 modestly activates splicing of tau exon 10 via its proximal downstream intron, a hotspot for frontotemporal dementia mutations.
    Wang Y; Gao L; Tse SW; Andreadis A
    Gene; 2010 Feb; 451(1-2):23-31. PubMed ID: 19914360
    [TBL] [Abstract][Full Text] [Related]  

  • 36. [Clinical symptoms and speech disturbance in frontotemporal dementia and parkinsonism linked to chromosome 17 with tau mutation].
    Wada C; Toyoshima I
    No To Shinkei; 2002 Mar; 54(3):221-33. PubMed ID: 11968813
    [No Abstract]   [Full Text] [Related]  

  • 37. Determination of the gene structure of human GFAP and absence of coding region mutations associated with frontotemporal dementia with parkinsonism linked to chromosome 17.
    Isaacs A; Baker M; Wavrant-De Vrièze F; Hutton M
    Genomics; 1998 Jul; 51(1):152-4. PubMed ID: 9693047
    [No Abstract]   [Full Text] [Related]  

  • 38. Stabilization of the tau exon 10 stem loop alters pre-mRNA splicing.
    Donahue CP; Muratore C; Wu JY; Kosik KS; Wolfe MS
    J Biol Chem; 2006 Aug; 281(33):23302-6. PubMed ID: 16782711
    [TBL] [Abstract][Full Text] [Related]  

  • 39. SR protein 9G8 modulates splicing of tau exon 10 via its proximal downstream intron, a clustering region for frontotemporal dementia mutations.
    Gao L; Wang J; Wang Y; Andreadis A
    Mol Cell Neurosci; 2007 Jan; 34(1):48-58. PubMed ID: 17137791
    [TBL] [Abstract][Full Text] [Related]  

  • 40. A mutation at codon 279 (N279K) in exon 10 of the Tau gene causes a tauopathy with dementia and supranuclear palsy.
    Delisle MB; Murrell JR; Richardson R; Trofatter JA; Rascol O; Soulages X; Mohr M; Calvas P; Ghetti B
    Acta Neuropathol; 1999 Jul; 98(1):62-77. PubMed ID: 10412802
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 14.