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Volumn 74, Issue 5, 2010, Pages 354-356

FUS: A new actor on the frontotemporal lobar degeneration stage

Author keywords

[No Author keywords available]

Indexed keywords

COPPER ZINC SUPEROXIDE DISMUTASE; TAR DNA BINDING PROTEIN;

EID: 76349123573     PISSN: 00283878     EISSN: 1526632X     Source Type: Journal    
DOI: 10.1212/WNL.0b013e3181ce5dd6     Document Type: Editorial
Times cited : (14)

References (10)
  • 1
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    • TDP-43 A315T mutation in familial motor neuron disease
    • Gitcho MA, Baloh RH, Chakraverty S, et al. TDP-43 A315T mutation in familial motor neuron disease. Ann Neurol 2008;63:535-538.
    • (2008) Ann Neurol , vol.63 , pp. 535-538
    • Gitcho, M.A.1    Baloh, R.H.2    Chakraverty, S.3
  • 2
    • 41149180753 scopus 로고    scopus 로고
    • TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis
    • Sreedharan J, Blair IP, Tripathi VB, et al. TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis. Science 2008;319:1668-1672.
    • (2008) Science , vol.319 , pp. 1668-1672
    • Sreedharan, J.1    Blair, I.P.2    Tripathi, V.B.3
  • 3
    • 65649112431 scopus 로고    scopus 로고
    • TARDBP mutations in motoneuron disease with frontotemporal lobar degeneration
    • Benajiba L, Le Ber I, Camuzat A, et al. TARDBP mutations in motoneuron disease with frontotemporal lobar degeneration. Ann Neurol 2009;65:470-473.
    • (2009) Ann Neurol , vol.65 , pp. 470-473
    • Benajiba, L.1    Le Ber, I.2    Camuzat, A.3
  • 4
    • 70449528427 scopus 로고    scopus 로고
    • TARDBP 3'-UTR variant in autopsy-confirmed frontotemporal lobar degeneration with TDP-43 proteinopathy
    • Gitcho MA, Bigio EH, Mishra M, et al. TARDBP 3'-UTR variant in autopsy-confirmed frontotemporal lobar degeneration with TDP-43 proteinopathy. Acta Neuro-pathol 2009;118:633-645.
    • (2009) Acta Neuro-pathol , vol.118 , pp. 633-645
    • Gitcho, M.A.1    Bigio, E.H.2    Mishra, M.3
  • 5
    • 61349162349 scopus 로고    scopus 로고
    • Mutations in FUS, an RNA processing protein, cause familial amyotrophic lateral sclerosis type 6
    • Vance C, Rogelj B, Hortobagyi T, et al. Mutations in FUS, an RNA processing protein, cause familial amyotrophic lateral sclerosis type 6. Science 2009;323:1208-1211.
    • (2009) Science , vol.323 , pp. 1208-1211
    • Vance, C.1    Rogelj, B.2    Hortobagyi, T.3
  • 6
    • 61349156118 scopus 로고    scopus 로고
    • Mutations in the FUS/TLS gene on chromosome 16 cause fa-milial amyotrophic lateral sclerosis
    • Kwiatkowski TJ Jr, Bosco DA, Leclerc AL, et al. Mutations in the FUS/TLS gene on chromosome 16 cause fa-milial amyotrophic lateral sclerosis. Science 2009;323: 1205-1208.
    • (2009) Science , vol.323 , pp. 1205-1208
    • Kwiatkowski Jr., T.J.1    Bosco, D.A.2    Leclerc, A.L.3
  • 8
    • 34249946466 scopus 로고    scopus 로고
    • Pathological TDP-43 distinguishes sporadic amyotrophic lateral sclerosis from amyotrophic lateral sclerosis with SOD1 mutations
    • Mackenzie IR, Bigio EH, Ince PG, et al. Pathological TDP-43 distinguishes sporadic amyotrophic lateral sclerosis from amyotrophic lateral sclerosis with SOD1 mutations. Ann Neurol 2007;61:427-434.
    • (2007) Ann Neurol , vol.61 , pp. 427-434
    • MacKenzie, I.R.1    Bigio, E.H.2    Ince, P.G.3
  • 9
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    • Genetic contribution of FUS to frontotemporal lobar degeneration
    • Van Langenhove T, van der Zee J, Sleegers K, et al. Genetic contribution of FUS to frontotemporal lobar degeneration. Neurology 2010;74:366-371.
    • (2010) Neurology , vol.74 , pp. 366-371
    • Van Langenhove, T.1    Van Der Zee, J.2    Sleegers, K.3
  • 10
    • 70350156915 scopus 로고    scopus 로고
    • Analysis of FUS gene mutation in familial amyotrophic lateral sclerosis within an Italian cohort
    • Ticozzi N, Silani V, Leclerc AL, et al. Analysis of FUS gene mutation in familial amyotrophic lateral sclerosis within an Italian cohort. Neurology 2009;73:1180-1185.
    • (2009) Neurology , vol.73 , pp. 1180-1185
    • Ticozzi, N.1    Silani, V.2    Leclerc, A.L.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.