-
1
-
-
0033593027
-
Apolipoprotein E is essential for amyloid deposition in the APP (V717F) transgenic mouse model of Alzheimer's disease
-
Bales K. R., Verina T., Cummins D. J., et al. (1999) Apolipoprotein E is essential for amyloid deposition in the APP (V717F) transgenic mouse model of Alzheimer's disease. Proc. Natl. Acad. Sci. USA 96, 15,233-15,238.
-
(1999)
Proc. Natl. Acad. Sci. USA
, vol.96
, pp. 15233-15238
-
-
Bales, K.R.1
Verina, T.2
Cummins, D.J.3
-
2
-
-
0026566108
-
Molecular basis of myotonic dystrophy: Expansion of a trinucleotide (CTG) repeat at the 3-prime end of a transcript encoding a protein kinase family member
-
Brook J. D., McCurrach M. E., Harley, H. G., et al. (1992). Molecular basis of myotonic dystrophy: expansion of a trinucleotide (CTG) repeat at the 3-prime end of a transcript encoding a protein kinase family member. Cell 68, 799-808.
-
(1992)
Cell
, vol.68
, pp. 799-808
-
-
Brook, J.D.1
McCurrach, M.E.2
Harley, H.G.3
-
3
-
-
0030863352
-
Niemann-Pick C1 disease gene: Homology to mediators of cholesterol homeostasis
-
Carstea E. D., Morris J. A., Coleman, K. G., et al. (1997) Niemann-Pick C1 disease gene: homology to mediators of cholesterol homeostasis. Science 277, 228-231.
-
(1997)
Science
, vol.277
, pp. 228-231
-
-
Carstea, E.D.1
Morris, J.A.2
Coleman, K.G.3
-
4
-
-
0028985574
-
Alzheimer-type neuropathology in transgenic mice overexpressing V717F Beta-amyloid precursor protein
-
Games D., Adams D., Alessandrini R., et al. (1995). Alzheimer-type neuropathology in transgenic mice overexpressing V717F Beta-amyloid precursor protein. Nature 373, 523-527.
-
(1995)
Nature
, vol.373
, pp. 523-527
-
-
Games, D.1
Adams, D.2
Alessandrini, R.3
-
5
-
-
0026088977
-
Segregation of a missense mutation in the amyloid precursor protein gene with familial Alzheimer's disease
-
Goate A. M., Chartier-Harlin M. C., Mullan M. C., et al. (1991) Segregation of a missense mutation in the amyloid precursor protein gene with familial Alzheimer's disease. Nature 349, 704-706.
-
(1991)
Nature
, vol.349
, pp. 704-706
-
-
Goate, A.M.1
Chartier-Harlin, M.C.2
Mullan, M.C.3
-
6
-
-
0029907548
-
Assembly of microtubule-associated protein tau into Alzheimer-like filaments induced by sulphated glycosaminoglycans
-
Goedert M., Jakes R., Spillantini M. G., Hasegawa M., Smith M. J., and Crowther R. A. (1996) Assembly of microtubule-associated protein tau into Alzheimer-like filaments induced by sulphated glycosaminoglycans. Nature 383, 550-553.
-
(1996)
Nature
, vol.383
, pp. 550-553
-
-
Goedert, M.1
Jakes, R.2
Spillantini, M.G.3
Hasegawa, M.4
Smith, M.J.5
Crowther, R.A.6
-
7
-
-
0031052381
-
Amyloid, the presenilins and Alzheimer's disease
-
Hardy J. (1997) Amyloid, the presenilins and Alzheimer's disease. Trends Neurosci. 20, 154-159.
-
(1997)
Trends Neurosci.
, vol.20
, pp. 154-159
-
-
Hardy, J.1
-
8
-
-
0032774457
-
Pathways to primary neurodegenerative disease
-
Hardy, J. (1999) Pathways to primary neurodegenerative disease. Mayo Clinic Proc. 74, 835-837.
-
(1999)
Mayo Clinic Proc.
, vol.74
, pp. 835-837
-
-
Hardy, J.1
-
9
-
-
0026849947
-
Mutant prion proteins in Gerstmann-Straussler-Scheinker disease with neurofibrillary tangles
-
Hsiao K., Dlouhy S. R., Farlow M. R., et al. (1992) Mutant prion proteins in Gerstmann-Straussler-Scheinker disease with neurofibrillary tangles. Nat. Genet. 1, 68-71.
-
(1992)
Nat. Genet.
, vol.1
, pp. 68-71
-
-
Hsiao, K.1
Dlouhy, S.R.2
Farlow, M.R.3
-
10
-
-
0028364691
-
Lewy bodies in the brain of two members of a family with the 717 (Val to Ile) mutation of the amyloid precursor protein gene
-
Lantos P. L., Ovenstone I. M., Johnson J., Clelland C. A., Roques P., and Rossor M. N. (1994) Lewy bodies in the brain of two members of a family with the 717 (Val to Ile) mutation of the amyloid precursor protein gene. Neurosci. Lett. 172, 77-79.
-
(1994)
Neurosci. Lett.
, vol.172
, pp. 77-79
-
-
Lantos, P.L.1
Ovenstone, I.M.2
Johnson, J.3
Clelland, C.A.4
Roques, P.5
Rossor, M.N.6
-
11
-
-
0034657414
-
Capacitative calcium entry deficits and elevated luminal calcium content in mutant presenilin-1 knockin mice
-
Leissring M. A., Akbari Y., Fanger, C. M., Cahalan M. D., Mattson M. P., and LaFerla F. M. (2000) Capacitative calcium entry deficits and elevated luminal calcium content in mutant presenilin-1 knockin mice. J. Cell Biol. 149, 793-798.
-
(2000)
J. Cell Biol.
, vol.149
, pp. 793-798
-
-
Leissring, M.A.1
Akbari, Y.2
Fanger, C.M.3
Cahalan, M.D.4
Mattson, M.P.5
LaFerla, F.M.6
-
12
-
-
0029087026
-
Candidate gene for the chromosome 1 familial Alzheimer's disease locus
-
Levy-Lahad E., Wasco W., Poorkaj P., et al. (1995) Candidate gene for the chromosome 1 familial Alzheimer's disease locus. Science 269, 973-977.
-
(1995)
Science
, vol.269
, pp. 973-977
-
-
Levy-Lahad, E.1
Wasco, W.2
Poorkaj, P.3
-
13
-
-
18344417178
-
Lewy bodies contain altered alpha-synuclein in brains of many familial Alzheimer's disease patients with mutations in presenilin and amyloid precursor protein genes
-
Lippa C. F., Fujiwara H., Mann D. M., et al. (1998) Lewy bodies contain altered alpha-synuclein in brains of many familial Alzheimer's disease patients with mutations in presenilin and amyloid precursor protein genes. Am. J. Pathol. 153, 1365-1370.
-
(1998)
Am. J. Pathol.
, vol.153
, pp. 1365-1370
-
-
Lippa, C.F.1
Fujiwara, H.2
Mann, D.M.3
-
14
-
-
0031721141
-
Pathologic and biochemical studies of juvenile parkinsonism linked to chromosome 6q
-
Mori H., Kondo T., Yokochi M., et al., (1998) Pathologic and biochemical studies of juvenile parkinsonism linked to chromosome 6q. Neurology, 51, 890-892.
-
(1998)
Neurology
, vol.51
, pp. 890-892
-
-
Mori, H.1
Kondo, T.2
Yokochi, M.3
-
15
-
-
0034704197
-
Susceptibility locus for Alzheimer's disease on chromosome 10
-
Myers A., Holmans P., Marshall H., et al., (2000) Susceptibility locus for Alzheimer's disease on chromosome 10. Science 290, 2304-2305.
-
(2000)
Science
, vol.290
, pp. 2304-2305
-
-
Myers, A.1
Holmans, P.2
Marshall, H.3
-
16
-
-
0029004341
-
Cloning of a gene bearing missense mutations in early-onset familial Alzheimer's disease
-
Sherrington R., Rogaev E. I., Liang Y., et al. (1995) Cloning of a gene bearing missense mutations in early-onset familial Alzheimer's disease. Nature 375, 754-760.
-
(1995)
Nature
, vol.375
, pp. 754-760
-
-
Sherrington, R.1
Rogaev, E.I.2
Liang, Y.3
-
17
-
-
0033600228
-
A stop-codon mutation in the BRI gene associated with familial British dementia
-
Vidal R., Frangione B., Rostagno A., Mead S., Revesz T., Plant G., and Ghiso J. (1994) A stop-codon mutation in the BRI gene associated with familial British dementia. Nature 399, 776-781.
-
(1994)
Nature
, vol.399
, pp. 776-781
-
-
Vidal, R.1
Frangione, B.2
Rostagno, A.3
Mead, S.4
Revesz, T.5
Plant, G.6
Ghiso, J.7
-
18
-
-
0033538502
-
Genetic variability at the amyloid-beta precursor protein locus may contribute to the risk of late-onset Alzheimer's disease
-
Wavrant-De Vrieze F., Crook R., Holmans P., et al. (1999). Genetic variability at the amyloid-beta precursor protein locus may contribute to the risk of late-onset Alzheimer's disease. Neurosci. Lett. 269, 67-70.
-
(1999)
Neurosci. Lett.
, vol.269
, pp. 67-70
-
-
Wavrant-De Vrieze, F.1
Crook, R.2
Holmans, P.3
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