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Volumn 1812, Issue 4, 2011, Pages 544-548

Iron loading-induced aggregation and reduction of iron incorporation in heteropolymeric ferritin containing a mutant light chain that causes neurodegeneration

Author keywords

Ferritin; Hereditary ferritinopathy; Iron; Neurodegeneration; Pore

Indexed keywords

APOFERRITIN; FERRITIN; HETEROPOLYMERIC FERRITIN; IRON; PHENYLALANINE; POLYMER; UNCLASSIFIED DRUG;

EID: 79951671438     PISSN: 09254439     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bbadis.2010.10.010     Document Type: Article
Times cited : (25)

References (18)
  • 10
    • 42049109697 scopus 로고    scopus 로고
    • Neuroferritinopathy in a Japanese family with a duplication in the ferritin light chain gene
    • Ohta E., Nagasaka T., Shindo K., Toma S., Nagasaka K., Ohta K., Shiozawa Z. Neuroferritinopathy in a Japanese family with a duplication in the ferritin light chain gene. Neurology 2008, 70:1493-1494.
    • (2008) Neurology , vol.70 , pp. 1493-1494
    • Ohta, E.1    Nagasaka, T.2    Shindo, K.3    Toma, S.4    Nagasaka, K.5    Ohta, K.6    Shiozawa, Z.7
  • 11
    • 67651103065 scopus 로고    scopus 로고
    • A novel ferritin light chain gene mutation in a Japanese family with neuroferritinopathy: description of clinical features and implications for genotype-phenotype correlations
    • Kubota A., Hida A., Ichikawa Y., Momose Y., Goto J., Igeta Y., Hashida H., Yoshida K., Ikeda S., Kanazawa I., Tsuji S. A novel ferritin light chain gene mutation in a Japanese family with neuroferritinopathy: description of clinical features and implications for genotype-phenotype correlations. Mov. Disord. 2009, 24:441-445.
    • (2009) Mov. Disord. , vol.24 , pp. 441-445
    • Kubota, A.1    Hida, A.2    Ichikawa, Y.3    Momose, Y.4    Goto, J.5    Igeta, Y.6    Hashida, H.7    Yoshida, K.8    Ikeda, S.9    Kanazawa, I.10    Tsuji, S.11
  • 12
    • 67649414590 scopus 로고    scopus 로고
    • Clinical features and natural history of neuroferritinopathy caused by the 458dupA FTL mutation
    • Devos D., Jissendi Tchofo P., Vuillaume I., Destée A., Batey S., Burn J., Chinnery P.F. Clinical features and natural history of neuroferritinopathy caused by the 458dupA FTL mutation. Brain 2008, 132(Pt 6):e109.
    • (2008) Brain , vol.132 , Issue.PART 6
    • Devos, D.1    Jissendi Tchofo, P.2    Vuillaume, I.3    Destée, A.4    Batey, S.5    Burn, J.6    Chinnery, P.F.7
  • 13
    • 3843069669 scopus 로고    scopus 로고
    • Neurodegeneration caused by proteins with an aberrant carboxyl-terminus
    • Vidal R., Delisle M.B., Ghetti B. Neurodegeneration caused by proteins with an aberrant carboxyl-terminus. J. Neuropathol. Exp. Neurol. 2004, 63:787-800.
    • (2004) J. Neuropathol. Exp. Neurol. , vol.63 , pp. 787-800
    • Vidal, R.1    Delisle, M.B.2    Ghetti, B.3
  • 14
    • 57649133953 scopus 로고    scopus 로고
    • Iron-mediated aggregation and a localized structural change characterize ferritin from a mutant light chain polypeptide that causes neurodegeneration
    • Baraibar M.A., Barbeito A.G., Muhoberac B.B., Vidal R. Iron-mediated aggregation and a localized structural change characterize ferritin from a mutant light chain polypeptide that causes neurodegeneration. J. Biol. Chem. 2008, 283:31679-31689.
    • (2008) J. Biol. Chem. , vol.283 , pp. 31679-31689
    • Baraibar, M.A.1    Barbeito, A.G.2    Muhoberac, B.B.3    Vidal, R.4
  • 15
    • 76249107256 scopus 로고    scopus 로고
    • Unraveling of the E helices and disruption of 4-fold pores are associated with iron mishandling in a mutant ferritin causing neurodegeneration
    • Baraibar M.A., Muhoberac B.B., Garringer H.J., Hurley T.D., Vidal R. Unraveling of the E helices and disruption of 4-fold pores are associated with iron mishandling in a mutant ferritin causing neurodegeneration. J. Biol. Chem. 2010, 285:1950-1956.
    • (2010) J. Biol. Chem. , vol.285 , pp. 1950-1956
    • Baraibar, M.A.1    Muhoberac, B.B.2    Garringer, H.J.3    Hurley, T.D.4    Vidal, R.5
  • 18
    • 77953713610 scopus 로고    scopus 로고
    • Accumulation of oxidative DNA damage in brain mitochondria in mouse model of hereditary ferritinopathy
    • Deng X., Vidal R., Englander E.W. Accumulation of oxidative DNA damage in brain mitochondria in mouse model of hereditary ferritinopathy. Neurosci. Lett. 2010, 479:44-48.
    • (2010) Neurosci. Lett. , vol.479 , pp. 44-48
    • Deng, X.1    Vidal, R.2    Englander, E.W.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.