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Journal Abstract Search

455 related items for PubMed ID: 21696412

  • 21. The RNA-binding motif 45 (RBM45) protein accumulates in inclusion bodies in amyotrophic lateral sclerosis (ALS) and frontotemporal lobar degeneration with TDP-43 inclusions (FTLD-TDP) patients.
    Collins M, Riascos D, Kovalik T, An J, Krupa K, Krupa K, Hood BL, Conrads TP, Renton AE, Traynor BJ, Bowser R.
    Acta Neuropathol; 2012 Nov; 124(5):717-32. PubMed ID: 22993125
    [Abstract] [Full Text] [Related]

  • 22. Genetic and clinical features of progranulin-associated frontotemporal lobar degeneration.
    Chen-Plotkin AS, Martinez-Lage M, Sleiman PM, Hu W, Greene R, Wood EM, Bing S, Grossman M, Schellenberg GD, Hatanpaa KJ, Weiner MF, White CL, Brooks WS, Halliday GM, Kril JJ, Gearing M, Beach TG, Graff-Radford NR, Dickson DW, Rademakers R, Boeve BF, Pickering-Brown SM, Snowden J, van Swieten JC, Heutink P, Seelaar H, Murrell JR, Ghetti B, Spina S, Grafman J, Kaye JA, Woltjer RL, Mesulam M, Bigio E, Lladó A, Miller BL, Alzualde A, Moreno F, Rohrer JD, Mackenzie IR, Feldman HH, Hamilton RL, Cruts M, Engelborghs S, De Deyn PP, Van Broeckhoven C, Bird TD, Cairns NJ, Goate A, Frosch MP, Riederer PF, Bogdanovic N, Lee VM, Trojanowski JQ, Van Deerlin VM.
    Arch Neurol; 2011 Apr; 68(4):488-97. PubMed ID: 21482928
    [Abstract] [Full Text] [Related]

  • 23. TDP-43 variants of frontotemporal lobar degeneration.
    Bigio EH.
    J Mol Neurosci; 2011 Nov; 45(3):390-401. PubMed ID: 21607722
    [Abstract] [Full Text] [Related]

  • 24. Neuronal cytoplasmic inclusions in tau, TDP-43, and FUS molecular subtypes of frontotemporal lobar degeneration share similar spatial patterns.
    A Armstrong R.
    Folia Neuropathol; 2017 Nov; 55(3):185-192. PubMed ID: 28984110
    [Abstract] [Full Text] [Related]

  • 25. Comprehensive assessment of TDP-43 neuropathology data in the National Alzheimer's Coordinating Center database.
    Woodworth DC, Nguyen KM, Sordo L, Scambray KA, Head E, Kawas CH, Corrada MM, Nelson PT, Sajjadi SA.
    Acta Neuropathol; 2024 Jun 19; 147(1):103. PubMed ID: 38896163
    [Abstract] [Full Text] [Related]

  • 26. Asymmetric TDP-43 distribution in primary progressive aphasia with progranulin mutation.
    Gliebus G, Bigio EH, Gasho K, Mishra M, Caplan D, Mesulam MM, Geula C.
    Neurology; 2010 May 18; 74(20):1607-10. PubMed ID: 20479359
    [Abstract] [Full Text] [Related]

  • 27. FTLD-TDP With and Without GRN Mutations Cause Different Patterns of CA1 Pathology.
    Mao Q, Zheng X, Gefen T, Rogalski E, Spencer CL, Rademakers R, Fought AJ, Kohler M, Weintraub S, Xia H, Mesulam MM, Bigio EH.
    J Neuropathol Exp Neurol; 2019 Sep 01; 78(9):844-853. PubMed ID: 31361008
    [Abstract] [Full Text] [Related]

  • 28. Old age genetically confirmed frontotemporal lobar degeneration with TDP-43 has limbic predominant TDP-43 deposition.
    Buciuc M, Whitwell JL, Baker MC, Rademakers R, Dickson DW, Josephs KA.
    Neuropathol Appl Neurobiol; 2021 Dec 01; 47(7):1050-1059. PubMed ID: 33969528
    [Abstract] [Full Text] [Related]

  • 29. Lower motor neuron involvement in TAR DNA-binding protein of 43 kDa-related frontotemporal lobar degeneration and amyotrophic lateral sclerosis.
    Riku Y, Watanabe H, Yoshida M, Tatsumi S, Mimuro M, Iwasaki Y, Katsuno M, Iguchi Y, Masuda M, Senda J, Ishigaki S, Udagawa T, Sobue G.
    JAMA Neurol; 2014 Feb 01; 71(2):172-9. PubMed ID: 24378564
    [Abstract] [Full Text] [Related]

  • 30. No interaction between tau and TDP-43 pathologies in either frontotemporal lobar degeneration or motor neurone disease.
    Robinson AC, Thompson JC, Weedon L, Rollinson S, Pickering-Brown S, Snowden JS, Davidson YS, Mann DM.
    Neuropathol Appl Neurobiol; 2014 Dec 01; 40(7):844-54. PubMed ID: 24861427
    [Abstract] [Full Text] [Related]

  • 31. Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions.
    Van Deerlin VM, Sleiman PM, Martinez-Lage M, Chen-Plotkin A, Wang LS, Graff-Radford NR, Dickson DW, Rademakers R, Boeve BF, Grossman M, Arnold SE, Mann DM, Pickering-Brown SM, Seelaar H, Heutink P, van Swieten JC, Murrell JR, Ghetti B, Spina S, Grafman J, Hodges J, Spillantini MG, Gilman S, Lieberman AP, Kaye JA, Woltjer RL, Bigio EH, Mesulam M, Al-Sarraj S, Troakes C, Rosenberg RN, White CL, Ferrer I, Lladó A, Neumann M, Kretzschmar HA, Hulette CM, Welsh-Bohmer KA, Miller BL, Alzualde A, Lopez de Munain A, McKee AC, Gearing M, Levey AI, Lah JJ, Hardy J, Rohrer JD, Lashley T, Mackenzie IR, Feldman HH, Hamilton RL, Dekosky ST, van der Zee J, Kumar-Singh S, Van Broeckhoven C, Mayeux R, Vonsattel JP, Troncoso JC, Kril JJ, Kwok JB, Halliday GM, Bird TD, Ince PG, Shaw PJ, Cairns NJ, Morris JC, McLean CA, DeCarli C, Ellis WG, Freeman SH, Frosch MP, Growdon JH, Perl DP, Sano M, Bennett DA, Schneider JA, Beach TG, Reiman EM, Woodruff BK, Cummings J, Vinters HV, Miller CA, Chui HC, Alafuzoff I, Hartikainen P, Seilhean D, Galasko D, Masliah E, Cotman CW, Tuñón MT, Martínez MC, Munoz DG, Carroll SL, Marson D, Riederer PF, Bogdanovic N, Schellenberg GD, Hakonarson H, Trojanowski JQ, Lee VM.
    Nat Genet; 2010 Mar 01; 42(3):234-9. PubMed ID: 20154673
    [Abstract] [Full Text] [Related]

  • 32. Senile plaque-associated transactive response DNA-binding protein 43 in Alzheimer's disease: A case report spanning 16 years of memory loss.
    Carlos AF, Koga S, Graff-Radford NR, Baker MC, Rademakers R, Ross OA, Dickson DW, Josephs KA.
    Neuropathology; 2024 Apr 01; 44(2):115-125. PubMed ID: 37525358
    [Abstract] [Full Text] [Related]

  • 33. C-terminal and full length TDP-43 specie differ according to FTLD-TDP lesion type but not genetic mutation.
    Josephs KA, Zhang YJ, Baker M, Rademakers R, Petrucelli L, Dickson DW.
    Acta Neuropathol Commun; 2019 Jul 02; 7(1):100. PubMed ID: 31266542
    [Abstract] [Full Text] [Related]

  • 34. Microglia in frontotemporal lobar degeneration with progranulin or C9ORF72 mutations.
    Sakae N, Roemer SF, Bieniek KF, Murray ME, Baker MC, Kasanuki K, Graff-Radford NR, Petrucelli L, Van Blitterswijk M, Rademakers R, Dickson DW.
    Ann Clin Transl Neurol; 2019 Sep 02; 6(9):1782-1796. PubMed ID: 31448566
    [Abstract] [Full Text] [Related]

  • 35. Altered microRNA expression in frontotemporal lobar degeneration with TDP-43 pathology caused by progranulin mutations.
    Kocerha J, Kouri N, Baker M, Finch N, DeJesus-Hernandez M, Gonzalez J, Chidamparam K, Josephs KA, Boeve BF, Graff-Radford NR, Crook J, Dickson DW, Rademakers R.
    BMC Genomics; 2011 Oct 27; 12():527. PubMed ID: 22032330
    [Abstract] [Full Text] [Related]

  • 36. Frontotemporal lobar degeneration: Pathogenesis, pathology and pathways to phenotype.
    Mann DMA, Snowden JS.
    Brain Pathol; 2017 Nov 27; 27(6):723-736. PubMed ID: 28100023
    [Abstract] [Full Text] [Related]

  • 37. Hippocampal sclerosis in Lewy body disease is a TDP-43 proteinopathy similar to FTLD-TDP Type A.
    Aoki N, Murray ME, Ogaki K, Fujioka S, Rutherford NJ, Rademakers R, Ross OA, Dickson DW.
    Acta Neuropathol; 2015 Jan 27; 129(1):53-64. PubMed ID: 25367383
    [Abstract] [Full Text] [Related]

  • 38. Human genetics as a tool to identify progranulin regulators.
    Nicholson AM, Finch NA, Rademakers R.
    J Mol Neurosci; 2011 Nov 27; 45(3):532-7. PubMed ID: 21626010
    [Abstract] [Full Text] [Related]

  • 39. Reappraisal of TDP-43 pathology in FTLD-U subtypes.
    Mackenzie IR, Neumann M.
    Acta Neuropathol; 2017 Jul 27; 134(1):79-96. PubMed ID: 28466142
    [Abstract] [Full Text] [Related]

  • 40. Sporadic corticobasal syndrome due to FTLD-TDP.
    Tartaglia MC, Sidhu M, Laluz V, Racine C, Rabinovici GD, Creighton K, Karydas A, Rademakers R, Huang EJ, Miller BL, DeArmond SJ, Seeley WW.
    Acta Neuropathol; 2010 Mar 27; 119(3):365-74. PubMed ID: 19876635
    [Abstract] [Full Text] [Related]

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