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Journal Abstract Search

361 related items for PubMed ID: 22817715

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2. Regulation of alternative splicing of tau exon 10.
    Qian W, Liu F.
    Neurosci Bull; 2014 Apr; 30(2):367-77. PubMed ID: 24627328
    [Abstract] [Full Text] [Related]

  • 3. Tau Isoforms: Gaining Insight into MAPT Alternative Splicing.
    Corsi A, Bombieri C, Valenti MT, Romanelli MG.
    Int J Mol Sci; 2022 Dec 06; 23(23):. PubMed ID: 36499709
    [Abstract] [Full Text] [Related]

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  • 5. Tau Interacting Proteins: Gaining Insight into the Roles of Tau in Health and Disease.
    Stancu IC, Ferraiolo M, Terwel D, Dewachter I.
    Adv Exp Med Biol; 2019 Dec 06; 1184():145-166. PubMed ID: 32096036
    [Abstract] [Full Text] [Related]

  • 6. Dysregulated coordination of MAPT exon 2 and exon 10 splicing underlies different tau pathologies in PSP and AD.
    Bowles KR, Pugh DA, Oja LM, Jadow BM, Farrell K, Whitney K, Sharma A, Cherry JD, Raj T, Pereira AC, Crary JF, Goate AM.
    Acta Neuropathol; 2022 Feb 06; 143(2):225-243. PubMed ID: 34874463
    [Abstract] [Full Text] [Related]

  • 7. 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 10; 485(2):130-8. PubMed ID: 21723381
    [Abstract] [Full Text] [Related]

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  • 9. What's in a Gene? The Outstanding Diversity of MAPT.
    Ruiz-Gabarre D, Carnero-Espejo A, Ávila J, García-Escudero V.
    Cells; 2022 Mar 01; 11(5):. PubMed ID: 35269461
    [Abstract] [Full Text] [Related]

  • 10. Tau protein in familial and sporadic diseases.
    Yancopoulou D, Spillantini MG.
    Neuromolecular Med; 2003 Mar 01; 4(1-2):37-48. PubMed ID: 14528051
    [Abstract] [Full Text] [Related]

  • 11. MAPT mutations, tauopathy, and mechanisms of neurodegeneration.
    Strang KH, Golde TE, Giasson BI.
    Lab Invest; 2019 Jul 01; 99(7):912-928. PubMed ID: 30742061
    [Abstract] [Full Text] [Related]

  • 12. Retiring the term FTDP-17 as MAPT mutations are genetic forms of sporadic frontotemporal tauopathies.
    Forrest SL, Kril JJ, Stevens CH, Kwok JB, Hallupp M, Kim WS, Huang Y, McGinley CV, Werka H, Kiernan MC, Götz J, Spillantini MG, Hodges JR, Ittner LM, Halliday GM.
    Brain; 2018 Feb 01; 141(2):521-534. PubMed ID: 29253099
    [Abstract] [Full Text] [Related]

  • 13. [The genetics of dementias. Part 1: Molecular basis of frontotemporal dementia and parkinsonism linked to chromosome 17 (FTDP-17)].
    Kowalska A.
    Postepy Hig Med Dosw (Online); 2009 Jun 15; 63():278-86. PubMed ID: 19535823
    [Abstract] [Full Text] [Related]

  • 14. Transactive response DNA-binding protein 43 (TDP-43) regulates alternative splicing of tau exon 10: Implications for the pathogenesis of tauopathies.
    Gu J, Chen F, Iqbal K, Gong CX, Wang X, Liu F.
    J Biol Chem; 2017 Jun 23; 292(25):10600-10612. PubMed ID: 28487370
    [Abstract] [Full Text] [Related]

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  • 16. A new non-aggregative splicing isoform of human Tau is decreased in Alzheimer's disease.
    García-Escudero V, Ruiz-Gabarre D, Gargini R, Pérez M, García E, Cuadros R, Hernández IH, Cabrera JR, García-Escudero R, Lucas JJ, Hernández F, Ávila J.
    Acta Neuropathol; 2021 Jul 23; 142(1):159-177. PubMed ID: 33934221
    [Abstract] [Full Text] [Related]

  • 17. The human MAPT locus generates circular RNAs.
    Welden JR, van Doorn J, Nelson PT, Stamm S.
    Biochim Biophys Acta Mol Basis Dis; 2018 Sep 23; 1864(9 Pt B):2753-2760. PubMed ID: 29729314
    [Abstract] [Full Text] [Related]

  • 18. Clinicopathologic heterogeneity in frontotemporal dementia and parkinsonism linked to chromosome 17 (FTDP-17) due to microtubule-associated protein tau (MAPT) p.P301L mutation, including a patient with globular glial tauopathy.
    Tacik P, Sanchez-Contreras M, DeTure M, Murray ME, Rademakers R, Ross OA, Wszolek ZK, Parisi JE, Knopman DS, Petersen RC, Dickson DW.
    Neuropathol Appl Neurobiol; 2017 Apr 23; 43(3):200-214. PubMed ID: 27859539
    [Abstract] [Full Text] [Related]

  • 19. Abeta(1-42) induces abnormal alternative splicing of tau exons 2/3 in NGF-induced PC12 cells.
    Lagunes T, Herrera-Rivero M, Hernández-Aguilar ME, Aranda-Abreu GE.
    An Acad Bras Cienc; 2014 Dec 23; 86(4):1927-34. PubMed ID: 25590729
    [Abstract] [Full Text] [Related]

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