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Journal Abstract Search

301 related items for PubMed ID: 33486486

  • 21. Premature termination codon readthrough upregulates progranulin expression and improves lysosomal function in preclinical models of GRN deficiency.
    Frew J, Baradaran-Heravi A, Balgi AD, Wu X, Yan TD, Arns S, Shidmoossavee FS, Tan J, Jaquith JB, Jansen-West KR, Lynn FC, Gao FB, Petrucelli L, Feldman HH, Mackenzie IR, Roberge M, Nygaard HB.
    Mol Neurodegener; 2020 Mar 16; 15(1):21. PubMed ID: 32178712
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  • 23. Frontotemporal lobar degeneration: epidemiology, pathology, diagnosis and management.
    Seltman RE, Matthews BR.
    CNS Drugs; 2012 Oct 01; 26(10):841-70. PubMed ID: 22950490
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  • 25. Brain progranulin expression in GRN-associated frontotemporal lobar degeneration.
    Chen-Plotkin AS, Xiao J, Geser F, Martinez-Lage M, Grossman M, Unger T, Wood EM, Van Deerlin VM, Trojanowski JQ, Lee VM.
    Acta Neuropathol; 2010 Jan 01; 119(1):111-22. PubMed ID: 19649643
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  • 26. Serum C-Peptide, Visfatin, Resistin, and Ghrelin are Altered in Sporadic and GRN-Associated Frontotemporal Lobar Degeneration.
    Zanardini R, Benussi L, Fostinelli S, Saraceno C, Ciani M, Borroni B, Padovani A, Binetti G, Ghidoni R.
    J Alzheimers Dis; 2018 Jan 01; 61(3):1053-1060. PubMed ID: 29226876
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  • 29. Novel progranulin mutations with reduced serum-progranulin levels in frontotemporal lobar degeneration.
    Chiang HH, Forsell C, Lilius L, Öijerstedt L, Thordardottir S, Shanmugarajan K, Westerlund M, Nennesmo I, Thonberg H, Graff C.
    Eur J Hum Genet; 2013 Nov 01; 21(11):1260-5. PubMed ID: 23463024
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  • 31. 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 01; 53():195.e11-195.e17. PubMed ID: 28268100
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  • 33. Modelling the cascade of biomarker changes in GRN-related frontotemporal dementia.
    Panman JL, Venkatraghavan V, van der Ende EL, Steketee RME, Jiskoot LC, Poos JM, Dopper EGP, Meeter LHH, Donker Kaat L, Rombouts SARB, Vernooij MW, Kievit AJA, Premi E, Cosseddu M, Bonomi E, Olives J, Rohrer JD, Sánchez-Valle R, Borroni B, Bron EE, Van Swieten JC, Papma JM, Klein S, GENFI consortium investigators.
    J Neurol Neurosurg Psychiatry; 2021 May 01; 92(5):494-501. PubMed ID: 33452053
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  • 34. [Frontotemporal dementia: clinical features, genetics, pathogenesis and treatment].
    Rosenmann H, Meiner Z.
    Harefuah; 2013 Nov 01; 152(11):661-6, 687. PubMed ID: 24416825
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  • 35. A Novel Loss-of-Function GRN Mutation p.(Tyr229*): Clinical and Neuropathological Features.
    Kuuluvainen L, Pöyhönen M, Pasanen P, Siitonen M, Rummukainen J, Tienari PJ, Paetau A, Myllykangas L.
    J Alzheimers Dis; 2017 Nov 01; 55(3):1167-1174. PubMed ID: 27767988
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  • 37. Genetic variants in progranulin upstream open reading frames increase downstream protein expression.
    Frydas A, Cacace R, van der Zee J, Van Broeckhoven C, Wauters E.
    Neurobiol Aging; 2022 Feb 01; 110():113-121. PubMed ID: 34620513
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  • 40. Frontotemporal lobar degeneration: Pathogenesis, pathology and pathways to phenotype.
    Mann DMA, Snowden JS.
    Brain Pathol; 2017 Nov 01; 27(6):723-736. PubMed ID: 28100023
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