These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

289 related articles for article (PubMed ID: 18832465)

  • 1. Parkinsonism and impaired axonal transport in a mouse model of frontotemporal dementia.
    Ittner LM; Fath T; Ke YD; Bi M; van Eersel J; Li KM; Gunning P; Götz J
    Proc Natl Acad Sci U S A; 2008 Oct; 105(41):15997-6002. PubMed ID: 18832465
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Two brothers with frontotemporal dementia and parkinsonism with an N279K mutation of the tau gene.
    Arima K; Kowalska A; Hasegawa M; Mukoyama M; Watanabe R; Kawai M; Takahashi K; Iwatsubo T; Tabira T; Sunohara N
    Neurology; 2000 May; 54(9):1787-95. PubMed ID: 10802785
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Parkinsonian syndrome in familial frontotemporal dementia.
    Siuda J; Fujioka S; Wszolek ZK
    Parkinsonism Relat Disord; 2014 Sep; 20(9):957-64. PubMed ID: 24998994
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Parkinsonism and distinct dementia patterns in a family with the MAPT R406W mutation.
    Carney RM; Kohli MA; Kunkle BW; Naj AC; Gilbert JR; Züchner S; Pericak-Vance MA
    Alzheimers Dement; 2014 May; 10(3):360-5. PubMed ID: 23727082
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [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; 63():278-86. PubMed ID: 19535823
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The impact of near-infrared light on dopaminergic cell survival in a transgenic mouse model of parkinsonism.
    Purushothuman S; Nandasena C; Johnstone DM; Stone J; Mitrofanis J
    Brain Res; 2013 Oct; 1535():61-70. PubMed ID: 23998985
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Interaction between a MAPT variant causing frontotemporal dementia and mutant APP affects axonal transport.
    Adalbert R; Milde S; Durrant C; Ando K; Stygelbout V; Yilmaz Z; Gould S; Brion JP; Coleman MP
    Neurobiol Aging; 2018 Aug; 68():68-75. PubMed ID: 29729423
    [TBL] [Abstract][Full Text] [Related]  

  • 8. In vivo axonal transport deficits in a mouse model of fronto-temporal dementia.
    Majid T; Ali YO; Venkitaramani DV; Jang MK; Lu HC; Pautler RG
    Neuroimage Clin; 2014; 4():711-7. PubMed ID: 24936422
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Blocking Site-Specific Cleavage of Human Tau Delays Progression of Disease-Related Phenotypes in Genetically Matched Tau-Transgenic Mice Modeling Frontotemporal Dementia.
    Steuer EL; Kemper LJ; Hlynialuk CJW; Leinonen-Wright K; Montonye ML; Lapcinski IP; Forster CL; Ashe KH; Liu P
    J Neurosci; 2022 Jun; 42(23):4737-4754. PubMed ID: 35508385
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Clioquinol rescues Parkinsonism and dementia phenotypes of the tau knockout mouse.
    Lei P; Ayton S; Appukuttan AT; Volitakis I; Adlard PA; Finkelstein DI; Bush AI
    Neurobiol Dis; 2015 Sep; 81():168-75. PubMed ID: 25796563
    [TBL] [Abstract][Full Text] [Related]  

  • 11. The behavioural phenotype of 14-month-old female TAU58/2 transgenic mice.
    Kreilaus F; Masanetz R; Watt G; Przybyla M; Ittner A; Ittner L; Karl T
    Behav Brain Res; 2021 Jan; 397():112943. PubMed ID: 33017638
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The tau N279K exon 10 splicing mutation recapitulates frontotemporal dementia and parkinsonism linked to chromosome 17 tauopathy in a mouse model.
    Dawson HN; Cantillana V; Chen L; Vitek MP
    J Neurosci; 2007 Aug; 27(34):9155-68. PubMed ID: 17715352
    [TBL] [Abstract][Full Text] [Related]  

  • 13. K369I Tau Mice Demonstrate a Shift Towards Striatal Neuron Burst Firing and Goal-directed Behaviour.
    Mo M; Jönsson ME; Mathews MA; Johnstone D; Ke YD; Ittner LM; Balleine BW; Furlong TM; Camp AJ
    Neuroscience; 2020 Nov; 449():46-62. PubMed ID: 32949670
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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; 64(9):1578-85. PubMed ID: 15883319
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Intrafamilial variable phenotype including corticobasal syndrome in a family with p.P301L mutation in the MAPT gene: first report in South America.
    Gatto EM; Allegri RF; Da Prat G; Chrem Mendez P; Hanna DS; Dorschner MO; Surace EI; Zabetian CP; Mata IF
    Neurobiol Aging; 2017 May; 53():195.e11-195.e17. PubMed ID: 28268100
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Familial frontotemporal dementia with ubiquitin-positive, tau-negative inclusions.
    Kertesz A; Kawarai T; Rogaeva E; St George-Hyslop P; Poorkaj P; Bird TD; Munoz DG
    Neurology; 2000 Feb; 54(4):818-27. PubMed ID: 10690970
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Familial frontotemporal dementia and parkinsonism with a novel mutation at an intron 10+11-splice site in the tau gene.
    Miyamoto K; Kowalska A; Hasegawa M; Tabira T; Takahashi K; Araki W; Akiguchi I; Ikemoto A
    Ann Neurol; 2001 Jul; 50(1):117-20. PubMed ID: 11456301
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Disinhibition-like behavior in a P301S mutant tau transgenic mouse model of frontotemporal dementia.
    Przybyla M; Stevens CH; van der Hoven J; Harasta A; Bi M; Ittner A; van Hummel A; Hodges JR; Piguet O; Karl T; Kassiou M; Housley GD; Ke YD; Ittner LM; van Eersel J
    Neurosci Lett; 2016 Sep; 631():24-29. PubMed ID: 27521751
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Tauopathies--a new class of neurodegenerative diseases].
    Ludolph AC; Sperfeld A; Collatz BM; Storch A
    Nervenarzt; 2001 Feb; 72(2):78-85. PubMed ID: 11256158
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Distinct genetic forms of frontotemporal dementia.
    Seelaar H; Kamphorst W; Rosso SM; Azmani A; Masdjedi R; de Koning I; Maat-Kievit JA; Anar B; Donker Kaat L; Breedveld GJ; Dooijes D; Rozemuller JM; Bronner IF; Rizzu P; van Swieten JC
    Neurology; 2008 Oct; 71(16):1220-6. PubMed ID: 18703462
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 15.