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Volumn 65, Issue 6, 2008, Pages 700-704

Molecular pathogenesis of frontotemporal lobar degeneration: Basic science seminar in neurology

Author keywords

[No Author keywords available]

Indexed keywords

NUCLEOTIDE;

EID: 45149122248     PISSN: 00039942     EISSN: 15383687     Source Type: Journal    
DOI: 10.1001/archneur.65.6.700     Document Type: Review
Times cited : (1)

References (16)
  • 1
  • 2
    • 0000244405 scopus 로고
    • Uber die Beziehungen der senilen Hirnatrophie zur Aphasie.
    • Pick A. Uber die Beziehungen der senilen Hirnatrophie zur Aphasie. Prag Med Wochenschr. 1892;17:165-167.
    • (1892) Prag Med Wochenschr , vol.17 , pp. 165-167
    • Pick, A.1
  • 3
    • 0032543684 scopus 로고    scopus 로고
    • Association of missense and 5′-splice-site mutations in tau with the inherited dementia FTDP-17
    • Hutton M, Lendon CL, Rizzu P, et al. Association of missense and 5′-splice-site mutations in tau with the inherited dementia FTDP-17. Nature. 1998;393(6686):702-705.
    • (1998) Nature , vol.393 , Issue.6686 , pp. 702-705
    • Hutton, M.1    Lendon, C.L.2    Rizzu, P.3
  • 4
    • 33846055457 scopus 로고    scopus 로고
    • Progranulin mutations in ubiquitin-positive frontotemporal dementia linked to chromosome 17q21
    • Cruts M, Kumar-Singh S, Van Broeckhoven C. Progranulin mutations in ubiquitin-positive frontotemporal dementia linked to chromosome 17q21. Curr Alzheimer Res. 2006;3(5):485-491.
    • (2006) Curr Alzheimer Res , vol.3 , Issue.5 , pp. 485-491
    • Cruts, M.1    Kumar-Singh, S.2    Van Broeckhoven, C.3
  • 5
    • 25144503548 scopus 로고    scopus 로고
    • Densecore plaques in Tg2576 and PSAPP mouse models of Alzheimer's disease are centered on vessel walls
    • Kumar-Singh S, Pirici D, McGowan E, et al. Densecore plaques in Tg2576 and PSAPP mouse models of Alzheimer's disease are centered on vessel walls. Am J Pathol. 2005;167(2):527-543.
    • (2005) Am J Pathol , vol.167 , Issue.2 , pp. 527-543
    • Kumar-Singh, S.1    Pirici, D.2    McGowan, E.3
  • 6
    • 26444608642 scopus 로고    scopus 로고
    • Genomic architecture of human 17q21 linked to frontotemporal dementia uncovers a highly homologous family of low-copy repeats in the tau region
    • Cruts M, Rademakers R, Gijselinck I, et al. Genomic architecture of human 17q21 linked to frontotemporal dementia uncovers a highly homologous family of low-copy repeats in the tau region. Hum Mol Genet. 2005;14(13):1753-1763.
    • (2005) Hum Mol Genet , vol.14 , Issue.13 , pp. 1753-1763
    • Cruts, M.1    Rademakers, R.2    Gijselinck, I.3
  • 7
    • 33749012575 scopus 로고    scopus 로고
    • Visualization of MAPT inversion on stretched chromosomes of tau-negative frontotemporal dementia patients [letter]
    • Gijselinck I, Bogaerts V, Rademakers R, van der Zee J, Van Broeckhoven C, Cruts M. Visualization of MAPT inversion on stretched chromosomes of tau-negative frontotemporal dementia patients [letter]. Hum Mutat. 2006;27(10):1057-1059.
    • (2006) Hum Mutat , vol.27 , Issue.10 , pp. 1057-1059
    • Gijselinck, I.1    Bogaerts, V.2    Rademakers, R.3    van der Zee, J.4    Van Broeckhoven, C.5    Cruts, M.6
  • 8
    • 33746910649 scopus 로고    scopus 로고
    • Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21
    • Cruts M, Gijselinck I, van der Zee J, et al. Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21. Nature. 2006;442(7105):920-924.
    • (2006) Nature , vol.442 , Issue.7105 , pp. 920-924
    • Cruts, M.1    Gijselinck, I.2    van der Zee, J.3
  • 9
    • 33746919083 scopus 로고    scopus 로고
    • Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17
    • Baker M, Mackenzie IR, Pickering-Brown SM, et al. Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17. Nature. 2006;442(7105):916-919.
    • (2006) Nature , vol.442 , Issue.7105 , pp. 916-919
    • Baker, M.1    Mackenzie, I.R.2    Pickering-Brown, S.M.3
  • 10
    • 38149123302 scopus 로고    scopus 로고
    • Progranulin locus deletion in frontotemporal dementia
    • Gijselinck I, van der Zee J, Engelborghs S, et al. Progranulin locus deletion in frontotemporal dementia. Hum Mutat. 2008;29(1):53-58.
    • (2008) Hum Mutat , vol.29 , Issue.1 , pp. 53-58
    • Gijselinck, I.1    van der Zee, J.2    Engelborghs, S.3
  • 11
    • 34247868937 scopus 로고    scopus 로고
    • Mutations other than null mutations producing a pathogenic loss of progranulin in frontotemporal dementia
    • van der Zee J, Le Ber I, Maurer-Stroh S, et al. Mutations other than null mutations producing a pathogenic loss of progranulin in frontotemporal dementia. Hum Mutat. 2007;28(4):416.
    • (2007) Hum Mutat , vol.28 , Issue.4 , pp. 416
    • van der Zee, J.1    Le Ber, I.2    Maurer-Stroh, S.3
  • 12
    • 38349173569 scopus 로고    scopus 로고
    • Missense mutations in the progranulin gene linked to frontotemporal lobar degeneration with ubiquitin-immunoreactive inclusions reduce progranulin production and secretion
    • Shankaran SS, Capell A, Hruscha AT, et al. Missense mutations in the progranulin gene linked to frontotemporal lobar degeneration with ubiquitin-immunoreactive inclusions reduce progranulin production and secretion. J Biol Chem. 2008;283(3):1744-1753.
    • (2008) J Biol Chem , vol.283 , Issue.3 , pp. 1744-1753
    • Shankaran, S.S.1    Capell, A.2    Hruscha, A.T.3
  • 13
    • 35348872039 scopus 로고    scopus 로고
    • Alzheimer and Parkinson diagnoses in progranulin null mutation carriers in an extended founder family
    • Brouwers N, Nuytemans K, van der Zee J, et al. Alzheimer and Parkinson diagnoses in progranulin null mutation carriers in an extended founder family. Arch Neurol. 2007;64(10):1436-1446.
    • (2007) Arch Neurol , vol.64 , Issue.10 , pp. 1436-1446
    • Brouwers, N.1    Nuytemans, K.2    van der Zee, J.3
  • 14
    • 34447102219 scopus 로고    scopus 로고
    • Frontotemporal lobar degeneration recent progress in antemortem diagnosis
    • Bian H, Grossman M. Frontotemporal lobar degeneration recent progress in antemortem diagnosis. Acta Neuropathol. 2007;114(1):23-29.
    • (2007) Acta Neuropathol , vol.114 , Issue.1 , pp. 23-29
    • Bian, H.1    Grossman, M.2
  • 15
    • 42049120518 scopus 로고    scopus 로고
    • Sleegers K, Brouwers N, Maurer-Stroh S, et al. Progranulin genetic variability contributes to amyotrophic lateral sclerosis [published online ahead of print January 9, 2008]. Neurology. 2008. doi:10.1212/01.wnl. 0000289191.54852.75.
    • Sleegers K, Brouwers N, Maurer-Stroh S, et al. Progranulin genetic variability contributes to amyotrophic lateral sclerosis [published online ahead of print January 9, 2008]. Neurology. 2008. doi:10.1212/01.wnl. 0000289191.54852.75.
  • 16
    • 33749632259 scopus 로고    scopus 로고
    • Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis
    • Neumann M, Sampathu DM, Kwong LK, et al. Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis. Science. 2006;314(5796):130-133.
    • (2006) Science , vol.314 , Issue.5796 , pp. 130-133
    • Neumann, M.1    Sampathu, D.M.2    Kwong, L.K.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.