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Volumn 129, Issue 3, 2006, Pages

Neuropathology in the S305S tau gene mutation [1]

Author keywords

[No Author keywords available]

Indexed keywords

TAU PROTEIN;

EID: 33244486505     PISSN: 00068950     EISSN: None     Source Type: Journal    
DOI: 10.1093/brain/awh720     Document Type: Letter
Times cited : (15)

References (14)
  • 1
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    • Recent advances in the understanding of tau protein and movement disorders
    • Arvanitakis Z, Wszolek ZK. Recent advances in the understanding of tau protein and movement disorders. Curr Opin Neurol 2001; 14: 491-7.
    • (2001) Curr Opin Neurol , vol.14 , pp. 491-497
    • Arvanitakis, Z.1    Wszolek, Z.K.2
  • 2
    • 0037327535 scopus 로고    scopus 로고
    • Tau phosphorylation and kinase activation in familial tauopathy linked to deln296 mutation
    • Ferrer I, Pastor P, Rey MJ, Munoz E, Puig B, Pastor E, et al. Tau phosphorylation and kinase activation in familial tauopathy linked to deln296 mutation. Neuropathol Appl Neurobiol 2003; 29: 23-34.
    • (2003) Neuropathol Appl Neurobiol , vol.29 , pp. 23-34
    • Ferrer, I.1    Pastor, P.2    Rey, M.J.3    Munoz, E.4    Puig, B.5    Pastor, E.6
  • 4
    • 0034877085 scopus 로고    scopus 로고
    • Familial frontotemporal dementia and parkinsonism with a novel N296H mutation in exon 10 of the tau gene and widespread tau accumulation in the glial cells
    • Iseki E, Matsumura T, Marui W, Hino H, Odawara T, Sugiyama N, et al. Familial frontotemporal dementia and parkinsonism with a novel N296H mutation in exon 10 of the tau gene and widespread tau accumulation in the glial cells. Acta Neuropathol 2001; 102: 285-92.
    • (2001) Acta Neuropathol , vol.102 , pp. 285-292
    • Iseki, E.1    Matsumura, T.2    Marui, W.3    Hino, H.4    Odawara, T.5    Sugiyama, N.6
  • 5
    • 0038796582 scopus 로고    scopus 로고
    • Frontotemporal dementia and parkinsonism with P301S tau gene mutation in a Jewish family
    • Lossos A, Reches A, Gal A, Newman JP, Soffer D, Gomori JM, et al. Frontotemporal dementia and parkinsonism with P301S tau gene mutation in a Jewish family. J Neurol 2003; 250: 733-40.
    • (2003) J Neurol , vol.250 , pp. 733-740
    • Lossos, A.1    Reches, A.2    Gal, A.3    Newman, J.P.4    Soffer, D.5    Gomori, J.M.6
  • 6
    • 0035134195 scopus 로고    scopus 로고
    • Familial atypical progressive supranuclear palsy associated with homozygosity for the delN296 mutation in the tau gene
    • Pastor P, Pastor E, Carnero C, Vela R, Garcia T, Amer G, et al. Familial atypical progressive supranuclear palsy associated with homozygosity for the delN296 mutation in the tau gene. Ann Neurol 2001; 49: 263-67.
    • (2001) Ann Neurol , vol.49 , pp. 263-267
    • Pastor, P.1    Pastor, E.2    Carnero, C.3    Vela, R.4    Garcia, T.5    Amer, G.6
  • 7
    • 0036316037 scopus 로고    scopus 로고
    • Progressive supranuclear palsy: Clinical and genetic aspects
    • Pastor P, Tolosa E. Progressive supranuclear palsy: clinical and genetic aspects. Curr Opin Neurol 2002; 15: 429-37.
    • (2002) Curr Opin Neurol , vol.15 , pp. 429-437
    • Pastor, P.1    Tolosa, E.2
  • 10
    • 0034051721 scopus 로고    scopus 로고
    • Tau mutations in familial frontotemporal dementia
    • Spillantini MG, Goedert M. Tau mutations in familial frontotemporal dementia. [Editorial]. Brain 2000; 123: 857-9.
    • (2000) Brain , vol.123 , pp. 857-859
    • Spillantini, M.G.1    Goedert, M.2
  • 11
    • 0034093228 scopus 로고    scopus 로고
    • Progressive supranuclear palsy pathology caused by a novel silent mutation in exon 10 of the tau gene. Expansion of the disease phenotype caused by tau gene mutations
    • Stanford PM, Halliday GM, Brooks WS, Kwok JBJ, Storey CE, Creasey H, et al. Progressive supranuclear palsy pathology caused by a novel silent mutation in exon 10 of the tau gene. Expansion of the disease phenotype caused by tau gene mutations. Brain 2000; 123: 880-93.
    • (2000) Brain , vol.123 , pp. 880-893
    • Stanford, P.M.1    Halliday, G.M.2    Brooks, W.S.3    Kwok, J.B.J.4    Storey, C.E.5    Creasey, H.6
  • 12
    • 33244488121 scopus 로고    scopus 로고
    • Progressive supranuclear palsy, frontotemporal dementia with parkinsonism linked to chromosome 17 and familial tauopathies
    • Stanford PM, Halliday GM, Brooks WS, Kwok JBJ, Schofield PR. Progressive supranuclear palsy, frontotemporal dementia with parkinsonism linked to chromosome 17 and familial tauopathies [reply]. Brain 2001; 124: 1668-70.
    • (2001) Brain , vol.124 , pp. 1668-1670
    • Stanford, P.M.1    Halliday, G.M.2    Brooks, W.S.3    Kwok, J.B.J.4    Schofield, P.R.5
  • 13
    • 0242317909 scopus 로고    scopus 로고
    • Mutations in the tau gene that cause an increase in three repeat tau and frontotemporal dementia
    • Stanford PM, Shepherd CE, Halliday GM, Brooks WS, Schofield PW, Brodaty H, et al. Mutations in the tau gene that cause an increase in three repeat tau and frontotemporal dementia. Brain 2003; 126: 814-26.
    • (2003) Brain , vol.126 , pp. 814-826
    • Stanford, P.M.1    Shepherd, C.E.2    Halliday, G.M.3    Brooks, W.S.4    Schofield, P.W.5    Brodaty, H.6
  • 14
    • 0034907406 scopus 로고    scopus 로고
    • Progressive supranuclear palsy as a disease phenotype caused by S305S tau gene mutation
    • Wszolek ZK, Tsuboi Y, Uitti RJ, Reed L, Hutton ML, Dickson DW. Progressive supranuclear palsy as a disease phenotype caused by S305S tau gene mutation [letter]. Brain 2001; 124: 1666-8.
    • (2001) Brain , vol.124 , pp. 1666-1668
    • Wszolek, Z.K.1    Tsuboi, Y.2    Uitti, R.J.3    Reed, L.4    Hutton, M.L.5    Dickson, D.W.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.