-
1
-
-
8344265251
-
Iron, brain ageing and neurodegenerative disorders
-
Zecca L., Youdim M.B., Riederer P., Connor J.R., Crichton R.R. Iron, brain ageing and neurodegenerative disorders. Nat. Rev. Neurosci. 2004, 5:863-873.
-
(2004)
Nat. Rev. Neurosci.
, vol.5
, pp. 863-873
-
-
Zecca, L.1
Youdim, M.B.2
Riederer, P.3
Connor, J.R.4
Crichton, R.R.5
-
3
-
-
0030069026
-
Thermal stability of horse spleen apoferritin and human recombinant H apoferritin
-
Stefanini S., Cavallo S., Wang C.-Q., Tataseo P., Vecchini P., Giartosio A., Chiancone E. Thermal stability of horse spleen apoferritin and human recombinant H apoferritin. Arch. Biochem. Biophys. 1996, 325:58-64.
-
(1996)
Arch. Biochem. Biophys.
, vol.325
, pp. 58-64
-
-
Stefanini, S.1
Cavallo, S.2
Wang, C.-Q.3
Tataseo, P.4
Vecchini, P.5
Giartosio, A.6
Chiancone, E.7
-
4
-
-
0026716421
-
Evidence that a salt bridge in the light chain contributes to the physical stability difference between heavy and light human ferritins
-
Santambrogio P., Levi S., Arosio P., Palagi L., Vecchio G., Lawson D.M., Yewdall S.J., Artymiuk P.J., Harrison P.M., Jappelli R., Cesareni G. Evidence that a salt bridge in the light chain contributes to the physical stability difference between heavy and light human ferritins. J. Biol. Chem. 1992, 267:14077-14083.
-
(1992)
J. Biol. Chem.
, vol.267
, pp. 14077-14083
-
-
Santambrogio, P.1
Levi, S.2
Arosio, P.3
Palagi, L.4
Vecchio, G.5
Lawson, D.M.6
Yewdall, S.J.7
Artymiuk, P.J.8
Harrison, P.M.9
Jappelli, R.10
Cesareni, G.11
-
5
-
-
0028276960
-
The role of the L-chain in ferritin iron incorporation. Studies of homo and heteropolymers
-
Levi S., Santambrogio P., Cozzi A., Rovida E., Corsi B., Tamborini E., Spada S., Albertini A., Arosio P. The role of the L-chain in ferritin iron incorporation. Studies of homo and heteropolymers. J. Mol. Biol. 1994, 238:649-654.
-
(1994)
J. Mol. Biol.
, vol.238
, pp. 649-654
-
-
Levi, S.1
Santambrogio, P.2
Cozzi, A.3
Rovida, E.4
Corsi, B.5
Tamborini, E.6
Spada, S.7
Albertini, A.8
Arosio, P.9
-
6
-
-
0031547971
-
Comparison of the three-dimensional structures of recombinant human H and horse L ferritins at high resolution
-
Hempstead P.D., Yewdall S.J., Fernie A.R., Lawson D.M., Artymiuk P.J., Rice D.W., Ford G.C., Harrison P.M. Comparison of the three-dimensional structures of recombinant human H and horse L ferritins at high resolution. J. Mol. Biol. 1997, 268:424-448.
-
(1997)
J. Mol. Biol.
, vol.268
, pp. 424-448
-
-
Hempstead, P.D.1
Yewdall, S.J.2
Fernie, A.R.3
Lawson, D.M.4
Artymiuk, P.J.5
Rice, D.W.6
Ford, G.C.7
Harrison, P.M.8
-
7
-
-
0034941118
-
Mutation in the gene encoding ferritin light polypeptide causes dominant adult-onset basal ganglia disease
-
Curtis A.R., Fey C., Morris C.M., Bindoff L.A., Ince P.G., Chinnery P.F., Coulthard A., Jackson M.J., Jackson A.P., McHale D.P., Hay D., Barker W.A., Markham A.F., Bates D., Curtis A., Burn J. Mutation in the gene encoding ferritin light polypeptide causes dominant adult-onset basal ganglia disease. Nat. Genet. 2001, 28:350-354.
-
(2001)
Nat. Genet.
, vol.28
, pp. 350-354
-
-
Curtis, A.R.1
Fey, C.2
Morris, C.M.3
Bindoff, L.A.4
Ince, P.G.5
Chinnery, P.F.6
Coulthard, A.7
Jackson, M.J.8
Jackson, A.P.9
McHale, D.P.10
Hay, D.11
Barker, W.A.12
Markham, A.F.13
Bates, D.14
Curtis, A.15
Burn, J.16
-
8
-
-
12144288949
-
Intracellular ferritin accumulation in neural and extraneural tissue characterizes a neurodegenerative disease associated with a mutation in the ferritin light polypeptide gene
-
Vidal R., Ghetti B., Takao M., Brefel-Courbon C., Uro-Coste E., Glazier B.S., Siani V., Benson M.D., Calvas P., Miravalle L., Rascol O., Delisle M.B. Intracellular ferritin accumulation in neural and extraneural tissue characterizes a neurodegenerative disease associated with a mutation in the ferritin light polypeptide gene. J. Neuropathol. Exp. Neurol. 2004, 63:363-380.
-
(2004)
J. Neuropathol. Exp. Neurol.
, vol.63
, pp. 363-380
-
-
Vidal, R.1
Ghetti, B.2
Takao, M.3
Brefel-Courbon, C.4
Uro-Coste, E.5
Glazier, B.S.6
Siani, V.7
Benson, M.D.8
Calvas, P.9
Miravalle, L.10
Rascol, O.11
Delisle, M.B.12
-
9
-
-
16844363930
-
Hereditary ferritinopathy: a novel mutation, its cellular pathology, and pathogenetic insights
-
Mancuso M., Davidzon G., Kurlan R.M., Tawil R., Bonilla E., Di Mauro S., Powers J.M. Hereditary ferritinopathy: a novel mutation, its cellular pathology, and pathogenetic insights. J. Neuropathol. Exp. Neurol. 2005, 64:280-294.
-
(2005)
J. Neuropathol. Exp. Neurol.
, vol.64
, pp. 280-294
-
-
Mancuso, M.1
Davidzon, G.2
Kurlan, R.M.3
Tawil, R.4
Bonilla, E.5
Di Mauro, S.6
Powers, J.M.7
-
10
-
-
42049109697
-
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
-
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
-
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
-
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
-
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
-
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
-
16
-
-
38149140232
-
Expression of a mutant form of the ferritin light chain gene induces neurodegeneration and iron overload in transgenic mice
-
Vidal R., Miravalle L., Gao X., Barbeito A.G., Baraibar M.A., Hekmatyar S.K., Widel M., Bansal N., Delisle M.B., Ghetti B. Expression of a mutant form of the ferritin light chain gene induces neurodegeneration and iron overload in transgenic mice. J. Neurosci. 2008, 28:60-67.
-
(2008)
J. Neurosci.
, vol.28
, pp. 60-67
-
-
Vidal, R.1
Miravalle, L.2
Gao, X.3
Barbeito, A.G.4
Baraibar, M.A.5
Hekmatyar, S.K.6
Widel, M.7
Bansal, N.8
Delisle, M.B.9
Ghetti, B.10
-
17
-
-
65649154118
-
Abnormal iron metabolism and oxidative stress in mice expressing a mutant form of the ferritin light polypeptide gene
-
Barbeito A.G., Garringer H.J., Baraibar M.A., Gao X., Arredondo M., Núñez M.T., Smith M.A., Ghetti B., Vidal R. Abnormal iron metabolism and oxidative stress in mice expressing a mutant form of the ferritin light polypeptide gene. J. Neurochem. 2009, 109:1067-1078.
-
(2009)
J. Neurochem.
, vol.109
, pp. 1067-1078
-
-
Barbeito, A.G.1
Garringer, H.J.2
Baraibar, M.A.3
Gao, X.4
Arredondo, M.5
Núñez, M.T.6
Smith, M.A.7
Ghetti, B.8
Vidal, R.9
-
18
-
-
77953713610
-
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
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