-
1
-
-
0030841343
-
Conformational disease
-
Carrell RW, Lomas DA. Conformational disease. Lancet 1997;350:134-38
-
(1997)
Lancet
, vol.350
, pp. 134-138
-
-
Carrell, R.W.1
Lomas, D.A.2
-
2
-
-
0031932169
-
Protein aggregation: Folding aggregates, inclusion bodies and amyloid
-
Fink AL. Protein aggregation: Folding aggregates, inclusion bodies and amyloid. Fold Des 1998;3:R9-23
-
(1998)
Fold Des
, vol.3
-
-
Fink, A.L.1
-
3
-
-
0034458454
-
The cerebral proteopathies: Neurodegenerative disorders of protein conformation and assembly
-
Walker LC, LeVine H. The cerebral proteopathies: Neurodegenerative disorders of protein conformation and assembly. Mol Neurobiol 2000;21:83-95
-
(2000)
Mol Neurobiol
, vol.21
, pp. 83-95
-
-
Walker, L.C.1
LeVine, H.2
-
4
-
-
0347357617
-
Protein folding and misfolding
-
Dobson CM. Protein folding and misfolding. Nature 2003;426:884-90
-
(2003)
Nature
, vol.426
, pp. 884-890
-
-
Dobson, C.M.1
-
5
-
-
0037264120
-
Unfolding the role of protein misfolding in neurodegenerative diseases
-
Soto C. Unfolding the role of protein misfolding in neurodegenerative diseases. Nat Rev Neurosci 2003;4:49-60
-
(2003)
Nat Rev Neurosci
, vol.4
, pp. 49-60
-
-
Soto, C.1
-
6
-
-
0036301160
-
Familial Conformational diseases and dementias
-
Crowther DC. Familial Conformational diseases and dementias. Hum Mutat 2002;20:1-14
-
(2002)
Hum Mutat
, vol.20
, pp. 1-14
-
-
Crowther, D.C.1
-
7
-
-
0036376917
-
Disordered proteins in dementia
-
Ingelsson M, Hyman BT. Disordered proteins in dementia. Ann Med 2002;34:259-71
-
(2002)
Ann Med
, vol.34
, pp. 259-271
-
-
Ingelsson, M.1
Hyman, B.T.2
-
8
-
-
0033653177
-
New familial forms of cerebral amyloid and dementia
-
Vidal R, Ghiso J, Frangione B. New familial forms of cerebral amyloid and dementia. Mol Psychiatry 2000;5:575-76
-
(2000)
Mol Psychiatry
, vol.5
, pp. 575-576
-
-
Vidal, R.1
Ghiso, J.2
Frangione, B.3
-
9
-
-
0034941118
-
Mutation in the gene encoding ferritin light polypeptide causes dominant adult-onset basal ganglia disease
-
Curtis AR, Fey C, Morris CM, et al. Mutation in the gene encoding ferritin light polypeptide causes dominant adult-onset basal ganglia disease. Nat Genet 2001;28:350-54
-
(2001)
Nat Genet
, vol.28
, pp. 350-354
-
-
Curtis, A.R.1
Fey, C.2
Morris, C.M.3
-
10
-
-
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, et al. 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;63:363-80
-
(2004)
J Neuropathol Exp Neurol
, vol.63
, pp. 363-380
-
-
Vidal, R.1
Ghetti, B.2
Takao, M.3
-
12
-
-
0001355224
-
A form of familial presenile dementia with spastic paralysis (including the pathological examination of a case)
-
Worster-Drought C, Greenfield JG, McMenemey WH. A form of familial presenile dementia with spastic paralysis (including the pathological examination of a case). Brain 1940;63:237-54
-
(1940)
Brain
, vol.63
, pp. 237-254
-
-
Worster-Drought, C.1
Greenfield, J.G.2
McMenemey, W.H.3
-
13
-
-
0002046853
-
A form of familial presenile dementia with spastic paralysis
-
Worster-Drought C, Greenfield JG, McMenemey WH. A form of familial presenile dementia with spastic paralysis. Brain 1944;67:38-43
-
(1944)
Brain
, vol.67
, pp. 38-43
-
-
Worster-Drought, C.1
Greenfield, J.G.2
McMenemey, W.H.3
-
14
-
-
0025316704
-
Familial cerebral amyloid angiopathy with nonneuritic amyloid plaque formation
-
Plant GT, Revesz T, Barnard RO, Harding AE, Gautier-Smith PC. Familial cerebral amyloid angiopathy with nonneuritic amyloid plaque formation. Brain 1990;113:721-47
-
(1990)
Brain
, vol.113
, pp. 721-747
-
-
Plant, G.T.1
Revesz, T.2
Barnard, R.O.3
Harding, A.E.4
Gautier-Smith, P.C.5
-
15
-
-
0034100159
-
Familial British dementia with amyloid angiopathy. Early clinical, neuropsychological and imaging findings
-
Mead S, James-Galton M, Revesz T, et al. Familial British dementia with amyloid angiopathy. Early clinical, neuropsychological and imaging findings. Brain 2000;123:975-91
-
(2000)
Brain
, vol.123
, pp. 975-991
-
-
Mead, S.1
James-Galton, M.2
Revesz, T.3
-
16
-
-
0032972176
-
Cytoskeletal pathology in familial cerebral amyloid angiopathy (British type) with non-neuritic amyloid plaque formation
-
Revesz T, Holton JL, Doshi B, Anderton BH, Scaravilli F, Plant GT. Cytoskeletal pathology in familial cerebral amyloid angiopathy (British type) with non-neuritic amyloid plaque formation. Acta Neuropathol (Berl) 1999;97:170-76
-
(1999)
Acta Neuropathol (Berl)
, vol.97
, pp. 170-176
-
-
Revesz, T.1
Holton, J.L.2
Doshi, B.3
Anderton, B.H.4
Scaravilli, F.5
Plant, G.T.6
-
17
-
-
0035137042
-
Regional distribution of amyloid-Bri deposition and its association with neurofibrillary degeneration in familial British dementia
-
Holton JL, Ghiso J, Lashley T, et al. Regional distribution of amyloid-Bri deposition and its association with neurofibrillary degeneration in familial British dementia. Am J Pathol 2001;158:515-26
-
(2001)
Am J Pathol
, vol.158
, pp. 515-526
-
-
Holton, J.L.1
Ghiso, J.2
Lashley, T.3
-
18
-
-
0031949628
-
A variant of Alzheimer's disease with spastic paraparesis and unusual plaques due to deletion of exon 9 of presenilin 1
-
Crook R, Verkkoniemi A, PerezTur J, et al. A variant of Alzheimer's disease with spastic paraparesis and unusual plaques due to deletion of exon 9 of presenilin 1. Nat Med 1998;4:452-55
-
(1998)
Nat Med
, vol.4
, pp. 452-455
-
-
Crook, R.1
Verkkoniemi, A.2
PerezTur, J.3
-
19
-
-
84990082204
-
Cataract, deafness, cerebellar ataxia, psychosis and dementia: A new syndrome
-
Strömgren E, Dalby A, Dalby MA, Ranheim B. Cataract, deafness, cerebellar ataxia, psychosis and dementia: A new syndrome. Acta Neurol Scand 1970;46(Suppl 43):261-62
-
(1970)
Acta Neurol Scand
, vol.46
, Issue.SUPPL. 43
, pp. 261-262
-
-
Strömgren, E.1
Dalby, A.2
Dalby, M.A.3
Ranheim, B.4
-
20
-
-
0000223592
-
Heredopathia ophthalmo-oto-encephalica
-
Vinken PJ, Bruyn GW, eds. Amsterdam: North-Holland Publishing Company
-
Strömgren E. Heredopathia ophthalmo-oto-encephalica. In: Vinken PJ, Bruyn GW, eds. Handbook of clinical neurology. Amsterdam: North-Holland Publishing Company, 1981;42:150-52
-
(1981)
Handbook of Clinical Neurology
, vol.42
, pp. 150-152
-
-
Strömgren, E.1
-
21
-
-
0002608996
-
Familial cerebral amyloid angiopathies
-
Esiri MM, Morris JH, eds. Cambridge: University Press
-
Plant GT, Esiri MM. Familial cerebral amyloid angiopathies. In: Esiri MM, Morris JH, eds. The neuropathology of dementia. Cambridge: University Press, 1977:260-76
-
(1977)
The Neuropathology of Dementia
, pp. 260-276
-
-
Plant, G.T.1
Esiri, M.M.2
-
22
-
-
0036194067
-
Familial Danish dementia: A novel form of cerebral amyloidosis associated with deposition of both amyloid-Dan and amyloid-beta
-
Holton JL, Lashley T, Ghiso J, et al. Familial Danish dementia: A novel form of cerebral amyloidosis associated with deposition of both amyloid-Dan and amyloid-beta. J Neuropathol Exp Neurol 2002;61:254-67
-
(2002)
J Neuropathol Exp Neurol
, vol.61
, pp. 254-267
-
-
Holton, J.L.1
Lashley, T.2
Ghiso, J.3
-
23
-
-
0033764338
-
Ocular changes in heredo-oto-ophthalmo-encephalopathy
-
Bek T. Ocular changes in heredo-oto-ophthalmo-encephalopathy. Br J Ophthalmol 2000;84:1298-302
-
(2000)
Br J Ophthalmol
, vol.84
, pp. 1298-1302
-
-
Bek, T.1
-
24
-
-
0034712749
-
A decamer duplication in the 3′ region of the BRI gene originates an amyloid peptide that is associated with dementia in a Danish kindred
-
Vidal R, Revesz T, Rostagno A, et al. A decamer duplication in the 3′ region of the BRI gene originates an amyloid peptide that is associated with dementia in a Danish kindred. Proc Natl Acad Sci USA 2000;97:4920-25
-
(2000)
Proc Natl Acad Sci USA
, vol.97
, pp. 4920-4925
-
-
Vidal, R.1
Revesz, T.2
Rostagno, A.3
-
25
-
-
0035140013
-
Codeposition of cystatin C with amyloid-beta protein in the brain of Alzheimer disease patients
-
Levy E, Sastre M, Kumar A, et al. Codeposition of cystatin C with amyloid-beta protein in the brain of Alzheimer disease patients. J Neuropathol Exp Neurol 2001;60:94-104
-
(2001)
J Neuropathol Exp Neurol
, vol.60
, pp. 94-104
-
-
Levy, E.1
Sastre, M.2
Kumar, A.3
-
26
-
-
0033600228
-
A stop-codon mutation in the BRI gene associated with familial British dementia
-
Vidal R, Frangione B, Rostagno A, et al. A stop-codon mutation in the BRI gene associated with familial British dementia. Nature 1999;399:776-81
-
(1999)
Nature
, vol.399
, pp. 776-781
-
-
Vidal, R.1
Frangione, B.2
Rostagno, A.3
-
27
-
-
0029742884
-
Isolation of markers for chondro-osteogenic differentiation using cDNA library subtraction. Molecular cloning and characterization of a gene belonging to a novel multigene family of integral membrane proteins
-
Deleersnijder W, Hong G, Cortvrindt R, et al. Isolation of markers for chondro-osteogenic differentiation using cDNA library subtraction. Molecular cloning and characterization of a gene belonging to a novel multigene family of integral membrane proteins. J Biol Chem 1996;271:19475-82
-
(1996)
J Biol Chem
, vol.271
, pp. 19475-19482
-
-
Deleersnijder, W.1
Hong, G.2
Cortvrindt, R.3
-
28
-
-
0033584235
-
ITM2A is induced during thymocyte selection and T cell activation and causes downregulation of CD8 when overexpressed in CD4(+)CD8(+) double positive thymocytes
-
Kirchner J, Bevan MJ. ITM2A is induced during thymocyte selection and T cell activation and causes downregulation of CD8 when overexpressed in CD4(+)CD8(+) double positive thymocytes. J Exp Med 1999;190:217-28
-
(1999)
J Exp Med
, vol.190
, pp. 217-228
-
-
Kirchner, J.1
Bevan, M.J.2
-
29
-
-
0033352083
-
Furin mediates enhanced production of fibrillogenic ABri peptides in familial British dementia
-
Kim SH, Wang R, Gordon DJ, et al. Furin mediates enhanced production of fibrillogenic ABri peptides in familial British dementia. Nat Neurosci 1999;2:984-88
-
(1999)
Nat Neurosci
, vol.2
, pp. 984-988
-
-
Kim, S.H.1
Wang, R.2
Gordon, D.J.3
-
30
-
-
0035925577
-
3, a member of the BRI gene family
-
3, a member of the BRI gene family. Gene 2001;266:95-102
-
(2001)
Gene
, vol.266
, pp. 95-102
-
-
Vidal, R.1
Calero, M.2
Revesz, T.3
Plant, G.4
Ghiso, J.5
Frangione, B.6
-
31
-
-
0032776145
-
Genomic organization and chromosomal localization of the Itm2a gene
-
Pittois K, Wauters J, Bossuyt P, Deleersnijder W, Merregaert J. Genomic organization and chromosomal localization of the Itm2a gene. Mamm Genome 1999;10:54-56
-
(1999)
Mamm Genome
, vol.10
, pp. 54-56
-
-
Pittois, K.1
Wauters, J.2
Bossuyt, P.3
Deleersnijder, W.4
Merregaert, J.5
-
32
-
-
0032517098
-
cDNA sequence analysis, chromosomal assignment and expression pattern of the gene coding for integral membrane protein 2B
-
Pittois K, Deleersnijder W, Merregaert J. cDNA sequence analysis, chromosomal assignment and expression pattern of the gene coding for integral membrane protein 2B. Gene 1998;217:141-49
-
(1998)
Gene
, vol.217
, pp. 141-149
-
-
Pittois, K.1
Deleersnijder, W.2
Merregaert, J.3
-
33
-
-
0034097948
-
Collagenase-3 (MMP-13) and integral membrane protein 2a (Itm2a) are marker genes of chondrogenic/osteoblastic cells in bone formation: Sequential temporal, and spatial expression of Itm2a, alkaline phosphatase, MMP-13, and osteocalcin in the mouse
-
Tuckermann JP, Pittois K, Partridge NC, Merregaert J, Angel P. Collagenase-3 (MMP-13) and integral membrane protein 2a (Itm2a) are marker genes of chondrogenic/osteoblastic cells in bone formation: Sequential temporal, and spatial expression of Itm2a, alkaline phosphatase, MMP-13, and osteocalcin in the mouse. J Bone Miner Res 2000;15:1257-65
-
(2000)
J Bone Miner Res
, vol.15
, pp. 1257-1265
-
-
Tuckermann, J.P.1
Pittois, K.2
Partridge, N.C.3
Merregaert, J.4
Angel, P.5
-
34
-
-
13144302844
-
Identification of genes expressed in human CD34(+) hematopoietic stem/progenitor cells by expressed sequence tags and efficient full-length cDNA cloning
-
Mao M, Fu G, Wu JS, et al. Identification of genes expressed in human CD34(+) hematopoietic stem/progenitor cells by expressed sequence tags and efficient full-length cDNA cloning. Proc Natl Acad Sci USA 1998;95:8175-80
-
(1998)
Proc Natl Acad Sci USA
, vol.95
, pp. 8175-8180
-
-
Mao, M.1
Fu, G.2
Wu, J.S.3
-
35
-
-
0036143022
-
Identification of underexpressed genes in early- and late-stage primary ovarian tumors by suppression subtraction hybridization
-
Shridhar V, Sen A, Chien J, et al. Identification of underexpressed genes in early- and late-stage primary ovarian tumors by suppression subtraction hybridization. Cancer Res 2002;62:262-70
-
(2002)
Cancer Res
, vol.62
, pp. 262-270
-
-
Shridhar, V.1
Sen, A.2
Chien, J.3
-
36
-
-
0037468158
-
Expression of mBRI2 in mice
-
Pickford F, Onstead L, Camacho-Prihar C, Hardy J, McGowan E. Expression of mBRI2 in mice. Neurosci Lett 2003;338:95-98
-
(2003)
Neurosci Lett
, vol.338
, pp. 95-98
-
-
Pickford, F.1
Onstead, L.2
Camacho-Prihar, C.3
Hardy, J.4
McGowan, E.5
-
38
-
-
0347093672
-
Expression of BRI, the normal precursor of the amyloid protein of familial British dementia, in human brain
-
Akiyama H, Kondo H, Arai T, et al. Expression of BRI, the normal precursor of the amyloid protein of familial British dementia, in human brain. Acta Neuropathol (Berl) 2004;107:53-58
-
(2004)
Acta Neuropathol (Berl)
, vol.107
, pp. 53-58
-
-
Akiyama, H.1
Kondo, H.2
Arai, T.3
-
39
-
-
1442265701
-
Axonal transport of British and Danish amyloid peptides via secretory vesicles
-
Choi SI, Vidal R, Frangione B, Levy E. Axonal transport of British and Danish amyloid peptides via secretory vesicles. FASEB J 2004;18:373-75
-
(2004)
FASEB J
, vol.18
, pp. 373-375
-
-
Choi, S.I.1
Vidal, R.2
Frangione, B.3
Levy, E.4
-
40
-
-
0042329653
-
Extensive analysis of the 13ql4 region in human prostate tumors: DNA analysis and quantitative expression of genes lying in the interval of deletion
-
Latil A, Chene L, Mangin P, Fournier G, Berthon P, Cussenot O. Extensive analysis of the 13ql4 region in human prostate tumors: DNA analysis and quantitative expression of genes lying in the interval of deletion. Prostate 2003;57:39-50
-
(2003)
Prostate
, vol.57
, pp. 39-50
-
-
Latil, A.1
Chene, L.2
Mangin, P.3
Fournier, G.4
Berthon, P.5
Cussenot, O.6
-
41
-
-
85047695204
-
Proapoptotic activity of ITM2B(s), a BH3-only protein induced upon IL-2-deprivation which interacts with Bcl-2
-
Fleischer A, Ayllon V, Dumoutier L, Renauld JC, Rebollo A. Proapoptotic activity of ITM2B(s), a BH3-only protein induced upon IL-2-deprivation which interacts with Bcl-2. Oncogene 2002;21:3181-89
-
(2002)
Oncogene
, vol.21
, pp. 3181-3189
-
-
Fleischer, A.1
Ayllon, V.2
Dumoutier, L.3
Renauld, J.C.4
Rebollo, A.5
-
42
-
-
1642491746
-
Induction of p53-independent apoptosis by the BH3-only protein ITM2Bs
-
Fleischer A, Rebollo A. Induction of p53-independent apoptosis by the BH3-only protein ITM2Bs. FEES Lett 2004;557:283-87
-
(2004)
FEES Lett
, vol.557
, pp. 283-287
-
-
Fleischer, A.1
Rebollo, A.2
-
43
-
-
0036838526
-
Subtractive hybridization reveals the expression of immunoglobulin-like transcript 7, Eph-B1, granzyme B, and 3 novel transcripts in human plasmacytoid dendritic cells
-
Rissoan MC, Duhen T, Bridon JM, et al. Subtractive hybridization reveals the expression of immunoglobulin-like transcript 7, Eph-B1, granzyme B, and 3 novel transcripts in human plasmacytoid dendritic cells. Blood 2002;100:3295-303
-
(2002)
Blood
, vol.100
, pp. 3295-3303
-
-
Rissoan, M.C.1
Duhen, T.2
Bridon, J.M.3
-
44
-
-
0036629254
-
BRICHOS: A conserved domain in proteins associated with dementia, respiratory distress and cancer
-
Sanchez-Pulido L, Devos D, Valencia A. BRICHOS: A conserved domain in proteins associated with dementia, respiratory distress and cancer. Trends Biochem Sci 2002;27:329-32
-
(2002)
Trends Biochem Sci
, vol.27
, pp. 329-332
-
-
Sanchez-Pulido, L.1
Devos, D.2
Valencia, A.3
-
45
-
-
0037127261
-
Proteolytic processing of familial British dementia-associated BRI variants: Evidence for enhanced intracellular accumulation of amyloidogenic peptides
-
Kim SH, Creemers JW, Chu S, Thinakaran G, Sisodia SS. Proteolytic processing of familial British dementia-associated BRI variants: Evidence for enhanced intracellular accumulation of amyloidogenic peptides. J Biol Chem 2002;277:1872-77
-
(2002)
J Biol Chem
, vol.277
, pp. 1872-1877
-
-
Kim, S.H.1
Creemers, J.W.2
Chu, S.3
Thinakaran, G.4
Sisodia, S.S.5
-
46
-
-
0030725756
-
Furin: A mammalian subtilisin/Kex2p-like endoprotease involved in processing of a wide variety of precursor proteins
-
Nakayama K. Furin: A mammalian subtilisin/Kex2p-like endoprotease involved in processing of a wide variety of precursor proteins. Biochem J 1997;327:625-35
-
(1997)
Biochem J
, vol.327
, pp. 625-635
-
-
Nakayama, K.1
-
47
-
-
0033597852
-
Proteolytic processing in the secretory pathway
-
Zhou A, Webb G, Zhu X, Steiner DF. Proteolytic processing in the secretory pathway. J Biol Chem 1999;274:20745-48
-
(1999)
J Biol Chem
, vol.274
, pp. 20745-20748
-
-
Zhou, A.1
Webb, G.2
Zhu, X.3
Steiner, D.F.4
-
48
-
-
0035958631
-
Expression of BRI-amyloid beta peptide fusion proteins: A novel method for specific high-level expression of amyloid beta peptides
-
Lewis PA, Piper S, Baker M, et al. Expression of BRI-amyloid beta peptide fusion proteins: A novel method for specific high-level expression of amyloid beta peptides. Biochim Biophys Acta 2001;1537:58-62
-
(2001)
Biochim Biophys Acta
, vol.1537
, pp. 58-62
-
-
Lewis, P.A.1
Piper, S.2
Baker, M.3
-
49
-
-
0035941310
-
Systemic amyloid deposits in familial British dementia
-
Ghiso JA, Holton J, Miravalle L, et al. Systemic amyloid deposits in familial British dementia. J Biol Chem 2001;276:43909-14
-
(2001)
J Biol Chem
, vol.276
, pp. 43909-43914
-
-
Ghiso, J.A.1
Holton, J.2
Miravalle, L.3
-
51
-
-
0030582387
-
Amino-and carboxyl-terminal heterogeneity of beta-amyloid peptides deposited in human brain
-
Saido TC, Yamao-Harigaya W, Iwatsubo T, Kawashima S. Amino-and carboxyl-terminal heterogeneity of beta-amyloid peptides deposited in human brain. Neurosci Lett 1996;215:173-76
-
(1996)
Neurosci Lett
, vol.215
, pp. 173-176
-
-
Saido, T.C.1
Yamao-Harigaya, W.2
Iwatsubo, T.3
Kawashima, S.4
-
52
-
-
0029849644
-
Full-length amyloid-beta (1-42(43)) and amino-terminally modified and truncated amyloid-beta 42(43) deposit in diffuse plaques
-
Iwatsubo T, Saido TC, Mann DM, Lee VM, Trojanowski JQ. Full-length amyloid-beta (1-42(43)) and amino-terminally modified and truncated amyloid-beta 42(43) deposit in diffuse plaques. Am J Pathol 1996;149:1823-30
-
(1996)
Am J Pathol
, vol.149
, pp. 1823-1830
-
-
Iwatsubo, T.1
Saido, T.C.2
Mann, D.M.3
Lee, V.M.4
Trojanowski, J.Q.5
-
53
-
-
0031985080
-
N-terminal heterogeneity of parenchymal and cerebrovascular Abeta deposits
-
Tekirian TL, Saido TC, Markesbery WR, et al. N-terminal heterogeneity of parenchymal and cerebrovascular Abeta deposits. J Neuropathol Exp Neurol 1998;57:76-94
-
(1998)
J Neuropathol Exp Neurol
, vol.57
, pp. 76-94
-
-
Tekirian, T.L.1
Saido, T.C.2
Markesbery, W.R.3
-
54
-
-
0033578402
-
The A beta 3-pyroglutamyl and 11-pyroglutamyl peptides found in senile plaque have greater beta-sheet forming and aggregation propensities in vitro than full-length A beta
-
He W, Barrow CJ. The A beta 3-pyroglutamyl and 11-pyroglutamyl peptides found in senile plaque have greater beta-sheet forming and aggregation propensities in vitro than full-length A beta. Biochemistry 1999;38:10871-77
-
(1999)
Biochemistry
, vol.38
, pp. 10871-10877
-
-
He, W.1
Barrow, C.J.2
-
55
-
-
3843099086
-
Co-existence of amyloid ADan and amyloid-β in familial Danish dementia
-
Tomidokoro Y, Fleire S, Rostagno A, et al. Co-existence of amyloid ADan and amyloid-β in familial Danish dementia. Neurobiol Aging 2002;23:S455
-
(2002)
Neurobiol Aging
, vol.23
-
-
Tomidokoro, Y.1
Fleire, S.2
Rostagno, A.3
-
56
-
-
0035957220
-
Effect of the disulfide bridge and the C-terminal extension on the oligomerization of the amyloid peptide ABri implicated in familial British dementia
-
El-Agnaf OM, Sheridan JM, Sidera C, et al. Effect of the disulfide bridge and the C-terminal extension on the oligomerization of the amyloid peptide ABri implicated in familial British dementia. Biochemistry 2001;40:3449-57
-
(2001)
Biochemistry
, vol.40
, pp. 3449-3457
-
-
El-Agnaf, O.M.1
Sheridan, J.M.2
Sidera, C.3
-
57
-
-
0035967889
-
Non-fibrillar oligomeric species of the amyloid ABri peptide, implicated in familial British dementia, are more potent at inducing apoptotic cell death than protofibrils or mature fibrils
-
El-Agnaf OM, Nagala S, Patel BP, Austen BM. Non-fibrillar oligomeric species of the amyloid ABri peptide, implicated in familial British dementia, are more potent at inducing apoptotic cell death than protofibrils or mature fibrils. J Mol Biol 2001;310:157-68
-
(2001)
J Mol Biol
, vol.310
, pp. 157-168
-
-
El-Agnaf, O.M.1
Nagala, S.2
Patel, B.P.3
Austen, B.M.4
-
58
-
-
0034971080
-
Predicted fold for the ABri amyloid subunit: A model for amyloidogenesis in familial British dementia
-
Mahadevan D, Chattopadhyay T, Palmer RA, O'Brien R, Saldanha JW. Predicted fold for the ABri amyloid subunit: A model for amyloidogenesis in familial British dementia. Protein Pept Letters 2001;8:171-78
-
(2001)
Protein Pept Letters
, vol.8
, pp. 171-178
-
-
Mahadevan, D.1
Chattopadhyay, T.2
Palmer, R.A.3
O'Brien, R.4
Saldanha, J.W.5
-
59
-
-
0142247606
-
pH-dependent amyloid and protofibril formation by the ABri peptide of familial British dementia
-
Srinivasan R, Jones EM, Liu K, Ghiso J, Marchant RE, Zagorski MG. pH-dependent amyloid and protofibril formation by the ABri peptide of familial British dementia. J Mol Biol 2003;333:1003-23
-
(2003)
J Mol Biol
, vol.333
, pp. 1003-1023
-
-
Srinivasan, R.1
Jones, E.M.2
Liu, K.3
Ghiso, J.4
Marchant, R.E.5
Zagorski, M.G.6
-
60
-
-
0347087364
-
Oligomerization and neurotoxicity of the amyloid ADan peptide implicated in familial Danish dementia
-
Gibson G, Gunasekera N, Lee M, et al. Oligomerization and neurotoxicity of the amyloid ADan peptide implicated in familial Danish dementia. J Neurochem 2004;88:281-90
-
(2004)
J Neurochem
, vol.88
, pp. 281-290
-
-
Gibson, G.1
Gunasekera, N.2
Lee, M.3
-
61
-
-
0033520461
-
Amyloid beta-protein fibrillogenesis. Structure and biological activity of protofibrillar intermediates
-
Walsh DM, Hartley DM, Kusumoto Y, et al. Amyloid beta-protein fibrillogenesis. Structure and biological activity of protofibrillar intermediates. J Biol Chem 1999;274:25945-52
-
(1999)
J Biol Chem
, vol.274
, pp. 25945-25952
-
-
Walsh, D.M.1
Hartley, D.M.2
Kusumoto, Y.3
-
62
-
-
0347298759
-
Complement activation in chromosome 13 dementias. Similarities with Alzheimer's disease
-
Rostagno A, Revesz T, Lashley T, et al. Complement activation in chromosome 13 dementias. Similarities with Alzheimer's disease. J Biol Chem 2002;277:49782-90
-
(2002)
J Biol Chem
, vol.277
, pp. 49782-49790
-
-
Rostagno, A.1
Revesz, T.2
Lashley, T.3
-
63
-
-
0043280850
-
Neuroferritinopathy in a French family with late onset dominant dystonia
-
Chinnery PF, Curtis AR, Fey C, et al. Neuroferritinopathy in a French family with late onset dominant dystonia. J Med Genet 2003;40:69
-
(2003)
J Med Genet
, vol.40
, pp. 69
-
-
Chinnery, P.F.1
Curtis, A.R.2
Fey, C.3
-
65
-
-
1842562623
-
A neurodegenerative disease with intranuclear deposits: Clinical and neuropathologic studies
-
Delisle MB, Uro-Coste E, Rascol O, et al. A neurodegenerative disease with intranuclear deposits: Clinical and neuropathologic studies. J Neuropathol Exp Neurol 2001;60:514
-
(2001)
J Neuropathol Exp Neurol
, vol.60
, pp. 514
-
-
Delisle, M.B.1
Uro-Coste, E.2
Rascol, O.3
-
66
-
-
1842457990
-
A neurodegenerative disease with intranuclear protein deposits: Electron microscopic and biochemical studies
-
Vidal R, Benson MD, Liepnieks JM, et al. A neurodegenerative disease with intranuclear protein deposits: Electron microscopic and biochemical studies. J Neuropathol Exp Neurol 2001;60:515
-
(2001)
J Neuropathol Exp Neurol
, vol.60
, pp. 515
-
-
Vidal, R.1
Benson, M.D.2
Liepnieks, J.M.3
-
67
-
-
0030608152
-
The ferritins: Molecular properties, iron storage function and cellular regulation
-
Harrison PM, Arosio P. The ferritins: Molecular properties, iron storage function and cellular regulation. Biochim Biophys Acta 1996;1275:161-203
-
(1996)
Biochim Biophys Acta
, vol.1275
, pp. 161-203
-
-
Harrison, P.M.1
Arosio, P.2
-
70
-
-
0029758487
-
Molecular control of vertebrate iron metabolism: mRNA-based regulatory circuits operated by iron, nitric oxide, and oxidative stress
-
Hentze MW, Kuhn LC. Molecular control of vertebrate iron metabolism: mRNA-based regulatory circuits operated by iron, nitric oxide, and oxidative stress. Proc Natl Acad Sci USA 1996;93:8175-82
-
(1996)
Proc Natl Acad Sci USA
, vol.93
, pp. 8175-8182
-
-
Hentze, M.W.1
Kuhn, L.C.2
-
71
-
-
0030624029
-
Regulation of iron metabolism in eukaryotes
-
Rouault T, Klausner R. Regulation of iron metabolism in eukaryotes. Curr Top Cell Regul 1997;35:1-19
-
(1997)
Curr Top Cell Regul
, vol.35
, pp. 1-19
-
-
Rouault, T.1
Klausner, R.2
-
72
-
-
0029930904
-
Ironsulfur clusters as biosensors of oxidants and iron
-
Rouault TA, Klausner RD. Ironsulfur clusters as biosensors of oxidants and iron. Trends Biochem Sci 1996;21:174-77
-
(1996)
Trends Biochem Sci
, vol.21
, pp. 174-177
-
-
Rouault, T.A.1
Klausner, R.D.2
-
73
-
-
0029815291
-
Superoxide and hydrogen peroxide-dependent inhibition of iron regulatory protein activity: A protective stratagem against oxidative injury
-
Cairo G, Castrusini E, Minotti G, Bernelli-Zazzera A. Superoxide and hydrogen peroxide-dependent inhibition of iron regulatory protein activity: A protective stratagem against oxidative injury. FASEB J 1996;10:1326-35
-
(1996)
FASEB J
, vol.10
, pp. 1326-1335
-
-
Cairo, G.1
Castrusini, E.2
Minotti, G.3
Bernelli-Zazzera, A.4
-
74
-
-
0035397392
-
Ferritin and the response to oxidative stress
-
Orino K, Lehman L, Tsuji Y, et al. Ferritin and the response to oxidative stress. Biochem J 2001;357:241-47
-
(2001)
Biochem J
, vol.357
, pp. 241-247
-
-
Orino, K.1
Lehman, L.2
Tsuji, Y.3
-
75
-
-
0034210637
-
Translational pathophysiology: A novel molecular mechanism of human disease
-
Cazzola M, Skoda RC. Translational pathophysiology: A novel molecular mechanism of human disease. Blood 2000;95:3280-88
-
(2000)
Blood
, vol.95
, pp. 3280-3288
-
-
Cazzola, M.1
Skoda, R.C.2
-
77
-
-
0034964604
-
A mutation in the iron-responsive element of H ferritin mRNA, causing autosomal dominant iron overload
-
Kato J, Fujikawa K, Kanda M, et al. A mutation in the iron-responsive element of H ferritin mRNA, causing autosomal dominant iron overload. Am J Hum Genet 2001;69:191-97
-
(2001)
Am J Hum Genet
, vol.69
, pp. 191-197
-
-
Kato, J.1
Fujikawa, K.2
Kanda, M.3
-
78
-
-
0035138456
-
Targeted deletion of the gene encoding iron regulatory protein-2 causes misregulation of iron metabolism and neurodegenerative disease in mice
-
LaVaute T, Smith S, Cooperman S, et al. Targeted deletion of the gene encoding iron regulatory protein-2 causes misregulation of iron metabolism and neurodegenerative disease in mice. Nat Genet 2001;27:209-14
-
(2001)
Nat Genet
, vol.27
, pp. 209-214
-
-
LaVaute, T.1
Smith, S.2
Cooperman, S.3
-
79
-
-
0041952925
-
Neuroferritinopathy: A window on the role of iron in neurodegeneration
-
Crompton DE, Chinnery PF, Fey C, et al. Neuroferritinopathy: A window on the role of iron in neurodegeneration. Blood Cells Mol Dis 2002;29:522-31
-
(2002)
Blood Cells Mol Dis
, vol.29
, pp. 522-531
-
-
Crompton, D.E.1
Chinnery, P.F.2
Fey, C.3
-
80
-
-
0037254460
-
Structural description of the active sites of mouse L-chain ferritin at 1.2 A resolution
-
Granier T, Langlois d'Estaintot B, et al. Structural description of the active sites of mouse L-chain ferritin at 1.2 A resolution. J Biol Inorg Chem 2003;8:105-11
-
(2003)
J Biol Inorg Chem
, vol.8
, pp. 105-111
-
-
Granier, T.1
Langlois D'Estaintot, B.2
-
81
-
-
0026700576
-
Loop mutations can cause a substantial conformational change in the carboxy terminus of the ferritin protein
-
Jappelli R, Luzzago A, Tataseo P, Pernice I, Cesareni G. Loop mutations can cause a substantial conformational change in the carboxy terminus of the ferritin protein. J Mol Biol 1992;227:532-43
-
(1992)
J Mol Biol
, vol.227
, pp. 532-543
-
-
Jappelli, R.1
Luzzago, A.2
Tataseo, P.3
Pernice, I.4
Cesareni, G.5
-
82
-
-
0032544542
-
Cooperativity of mutational effects within a six amino acid residues substitution that induces a major conformational change in human H ferritin
-
Jappelli R, Cesareni G. Cooperativity of mutational effects within a six amino acid residues substitution that induces a major conformational change in human H ferritin. Biochem Biophys Res Commun 1998;250:342-46
-
(1998)
Biochem Biophys Res Commun
, vol.250
, pp. 342-346
-
-
Jappelli, R.1
Cesareni, G.2
-
83
-
-
0031743986
-
Intranuclear iron deposition in hepatocytes and renal tubular cells in mice treated with ferric nitrilotriacetate
-
Kondo A, Deguchi J, Okada S. Intranuclear iron deposition in hepatocytes and renal tubular cells in mice treated with ferric nitrilotriacetate. Virchows Arch 1998;433:543-48
-
(1998)
Virchows Arch
, vol.433
, pp. 543-548
-
-
Kondo, A.1
Deguchi, J.2
Okada, S.3
-
84
-
-
0025668709
-
Characterization and accumulation of ferritin in hepatocyte nuclei of mice with iron overload
-
Smith AG, Carthew P, Francis JE, Edwards RE, Dinsdale D. Characterization and accumulation of ferritin in hepatocyte nuclei of mice with iron overload. Hepatology 1990;12:1399-405
-
(1990)
Hepatology
, vol.12
, pp. 1399-1405
-
-
Smith, A.G.1
Carthew, P.2
Francis, J.E.3
Edwards, R.E.4
Dinsdale, D.5
-
85
-
-
0030992780
-
Ferritin is a developmentally regulated nuclear protein of avian corneal epithelial cells
-
Cai CX, Birk DE, Linsenmayer TF. Ferritin is a developmentally regulated nuclear protein of avian corneal epithelial cells. J Biol Chem 1997;272:12831-39
-
(1997)
J Biol Chem
, vol.272
, pp. 12831-12839
-
-
Cai, C.X.1
Birk, D.E.2
Linsenmayer, T.F.3
-
86
-
-
0037092516
-
Regulation, mechanisms and proposed function of ferritin translocation to cell nuclei
-
Thompson KJ, Fried MG, Ye Z, Boyer P, Connor JR. Regulation, mechanisms and proposed function of ferritin translocation to cell nuclei. J Cell Sci 2002;115:2165-77
-
(2002)
J Cell Sci
, vol.115
, pp. 2165-2177
-
-
Thompson, K.J.1
Fried, M.G.2
Ye, Z.3
Boyer, P.4
Connor, J.R.5
-
87
-
-
0034935874
-
Nuclear translocation of ferritin in corneal epithelial cells
-
Cai CX, Linsenmayer TF. Nuclear translocation of ferritin in corneal epithelial cells. J Cell Sci 2001;114:2327-34
-
(2001)
J Cell Sci
, vol.114
, pp. 2327-2334
-
-
Cai, C.X.1
Linsenmayer, T.F.2
-
88
-
-
0031446233
-
Intranuclear neuronal inclusions: A common pathogenic mechanism for glutamine-repeat neurodegenerative diseases?
-
Ross CA. Intranuclear neuronal inclusions: A common pathogenic mechanism for glutamine-repeat neurodegenerative diseases? Neuron 1997;19:1147-50
-
(1997)
Neuron
, vol.19
, pp. 1147-1150
-
-
Ross, C.A.1
-
89
-
-
0028893380
-
Familial cerebral amyloid angiopathy (British type) with nonneuritic amyloid plaque formation may be due to a novel amyloid protein
-
Ghiso J, Plant GT, Revesz T, Wisniewski T, Frangione B. Familial cerebral amyloid angiopathy (British type) with nonneuritic amyloid plaque formation may be due to a novel amyloid protein. J Neurol Sci 1995;129:74-75
-
(1995)
J Neurol Sci
, vol.129
, pp. 74-75
-
-
Ghiso, J.1
Plant, G.T.2
Revesz, T.3
Wisniewski, T.4
Frangione, B.5
-
90
-
-
0035065275
-
The Worster-Drought syndrome and other syndromes of dementia with spastic paraparesis: The paradox of molecular pathology
-
Masters CL, Beyreuther K. The Worster-Drought syndrome and other syndromes of dementia with spastic paraparesis: The paradox of molecular pathology. J Neuropathol Exp Neurol 2001;60:317-19
-
(2001)
J Neuropathol Exp Neurol
, vol.60
, pp. 317-319
-
-
Masters, C.L.1
Beyreuther, K.2
|