-
1
-
-
0022395922
-
Neuropathological classification of Huntington's disease
-
Vonsattel, J.P. et al. Neuropathological classification of Huntington's disease. J. Neuropathol. Exp. Neurol. 44, 559-577 (1985).
-
(1985)
J. Neuropathol. Exp. Neurol.
, vol.44
, pp. 559-577
-
-
Vonsattel, J.P.1
-
2
-
-
0004293147
-
-
Johns Hopkins University Press, Baltimore
-
Folstein, S.E. Huntington's Disease (Johns Hopkins University Press, Baltimore, 1990).
-
(1990)
Huntington's Disease
-
-
Folstein, S.E.1
-
3
-
-
0025885733
-
Neuronal loss in layers V and VI of cerebral cortex in Huntington's disease
-
Hedreen, J.C., Peyser, C.E., Folstein, S.E. & Ross, C.A. Neuronal loss in layers V and VI of cerebral cortex in Huntington's disease. Neurosci. Lett. 133, 257-261 (1991).
-
(1991)
Neurosci. Lett.
, vol.133
, pp. 257-261
-
-
Hedreen, J.C.1
Peyser, C.E.2
Folstein, S.E.3
Ross, C.A.4
-
4
-
-
0027276977
-
Neuronal loss in the hippocampus in Huntington's disease: A comparison with HIV infection
-
Spargo, E., Everall, I.P. & Lantos, P.L. Neuronal loss in the hippocampus in Huntington's disease: a comparison with HIV infection. J. Neurol. Neurosurg. Psychiatry 56, 487-491 (1993).
-
(1993)
J. Neurol. Neurosurg. Psychiatry
, vol.56
, pp. 487-491
-
-
Spargo, E.1
Everall, I.P.2
Lantos, P.L.3
-
5
-
-
0027480960
-
A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes
-
The Huntington's Disease Collaborative Research Group. A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes. Cell 72, 971-983 (1993).
-
(1993)
Cell
, vol.72
, pp. 971-983
-
-
-
6
-
-
0027176364
-
The relationship between trinucleotide (CAG) repeat length and clinical features of Huntington's disease
-
Andrew, S.E. et al. The relationship between trinucleotide (CAG) repeat length and clinical features of Huntington's disease. Nature Genet. 4, 398-403 (1993).
-
(1993)
Nature Genet.
, vol.4
, pp. 398-403
-
-
Andrew, S.E.1
-
7
-
-
0027240431
-
Trinucleotide repeat length instability and age of onset in Huntington's disease
-
Duyao, M. et al. Trinucleotide repeat length instability and age of onset in Huntington's disease. Nature Genet. 4, 387-392 (1993).
-
(1993)
Nature Genet.
, vol.4
, pp. 387-392
-
-
Duyao, M.1
-
8
-
-
0027377151
-
Correlation between the onset age of Huntington's disease and length of the trinucleotide repeat in IT-15
-
Stine, O.C. et al. Correlation between the onset age of Huntington's disease and length of the trinucleotide repeat in IT-15. Hum. Mol. Genet. 2, 1547-1549 (1993).
-
(1993)
Hum. Mol. Genet.
, vol.2
, pp. 1547-1549
-
-
Stine, O.C.1
-
9
-
-
0027484673
-
Huntington's disease gene (IT15) is widely expressed in human and rat tissues
-
Li, S.H. et al. Huntington's disease gene (IT15) is widely expressed in human and rat tissues. Neuron 11, 985-993 (1993).
-
(1993)
Neuron
, vol.11
, pp. 985-993
-
-
Li, S.H.1
-
10
-
-
0027432418
-
Widespread expression of the human and rat Huntington's disease gene in brain and nonneural tissues
-
Strong, T.V. et al. Widespread expression of the human and rat Huntington's disease gene in brain and nonneural tissues. Nature Genet. 5, 259-265 (1993).
-
(1993)
Nature Genet.
, vol.5
, pp. 259-265
-
-
Strong, T.V.1
-
11
-
-
0029034511
-
Widespread expression of Huntington's disease gene (IT15) protein product
-
Sharp, A.H. et al. Widespread expression of Huntington's disease gene (IT15) protein product. Neuron 14, 1065-1074 (1995).
-
(1995)
Neuron
, vol.14
, pp. 1065-1074
-
-
Sharp, A.H.1
-
12
-
-
16044373842
-
Exon 1 of the HD gene with an expanded CAG repeat is sufficient to cause a progressive neurological phenotype in transgenic mice
-
Mangiarini, L. et al. Exon 1 of the HD gene with an expanded CAG repeat is sufficient to cause a progressive neurological phenotype in transgenic mice. Cell 87, 493-506 (1996).
-
(1996)
Cell
, vol.87
, pp. 493-506
-
-
Mangiarini, L.1
-
13
-
-
0031469707
-
Ectopically expressed CAG repeats cause intranuclear inclusions and a progressive late onset neurological phenotype in the mouse
-
Ordway, J.M. et al. Ectopically expressed CAG repeats cause intranuclear inclusions and a progressive late onset neurological phenotype in the mouse. Cell 91, 753-764 (1997).
-
(1997)
Cell
, vol.91
, pp. 753-764
-
-
Ordway, J.M.1
-
14
-
-
0029947276
-
Partial characterisation of murine huntingtin and apparent variations in the subcellular localisation of huntingtin in human, mouse and rat brain
-
Wood, J.D., MacMillan, J.C., Harper, P.S., Lowenstein, P.R. & Jones, A.L. Partial characterisation of murine huntingtin and apparent variations in the subcellular localisation of huntingtin in human, mouse and rat brain. Hum. Mol. Genet. 5, 481-487 (1996).
-
(1996)
Hum. Mol. Genet.
, vol.5
, pp. 481-487
-
-
Wood, J.D.1
MacMillan, J.C.2
Harper, P.S.3
Lowenstein, P.R.4
Jones, A.L.5
-
15
-
-
0030613177
-
Huntingtin is required for neurogenesis and is not impaired by the Huntington's disease CAG expansion
-
White, J.K. et al. Huntingtin is required for neurogenesis and is not impaired by the Huntington's disease CAG expansion. Nature Genet. 17, 404-410 (1997).
-
(1997)
Nature Genet.
, vol.17
, pp. 404-410
-
-
White, J.K.1
-
17
-
-
0029040355
-
In situ evidence for DNA fragmentation in Huntington's disease striatum and Alzheimer's disease temporal lobes
-
Dragunow, M. et al. In situ evidence for DNA fragmentation in Huntington's disease striatum and Alzheimer's disease temporal lobes. Neuroreport 6, 1053-1057 (1995).
-
(1995)
Neuroreport
, vol.6
, pp. 1053-1057
-
-
Dragunow, M.1
-
18
-
-
0029072690
-
Evidence for apoptotic cell death in Huntington disease and excitotoxic animal models
-
Portera-Cailliau, C., Hedreen, J.C, Price, D.L. & Koliatsos, K.E. Evidence for apoptotic cell death in Huntington disease and excitotoxic animal models. J. Neurosci. 15, 3775-3787 (1995).
-
(1995)
J. Neurosci.
, vol.15
, pp. 3775-3787
-
-
Portera-Cailliau, C.1
Hedreen, J.C.2
Price, D.L.3
Koliatsos, K.E.4
-
19
-
-
0029086807
-
DNA end labeling (TUNEL) in Huntington's disease and other neuropathological conditions
-
Thomas, L.B. et al. DNA end labeling (TUNEL) in Huntington's disease and other neuropathological conditions. Exp. Neurol. 133, 265-272 (1995).
-
(1995)
Exp. Neurol.
, vol.133
, pp. 265-272
-
-
Thomas, L.B.1
-
20
-
-
18544410106
-
Formation of neuronal intranuclear inclusions underlies the neurological dysfunction in mice transgenic for the HD mutation
-
Davies, S.W. et al. Formation of neuronal intranuclear inclusions underlies the neurological dysfunction in mice transgenic for the HD mutation. Cell 90, 537-548 (1997).
-
(1997)
Cell
, vol.90
, pp. 537-548
-
-
Davies, S.W.1
-
21
-
-
0030752709
-
Aggregation of huntingtin in neuronal intranuclear inclusions and dystrophic neurites in brain
-
DiFiglia, M. et al. Aggregation of huntingtin in neuronal intranuclear inclusions and dystrophic neurites in brain. Science 277, 1990-1993 (1997).
-
(1997)
Science
, vol.277
, pp. 1990-1993
-
-
DiFiglia, M.1
-
22
-
-
0030850412
-
Intranuclear inclusions of expanded polyglutamine protein in spinocerebellar ataxia type 3
-
Paulson, H.L. et al. Intranuclear inclusions of expanded polyglutamine protein in spinocerebellar ataxia type 3. Neuron 19, 333-344 (1997).
-
(1997)
Neuron
, vol.19
, pp. 333-344
-
-
Paulson, H.L.1
-
23
-
-
0030666001
-
Ataxin-1 with an expanded glutamine tract alters nuclear matrix-associated structures
-
Skinner, P.J. et al. Ataxin-1 with an expanded glutamine tract alters nuclear matrix-associated structures. Nature 389, 971-974 (1997).
-
(1997)
Nature
, vol.389
, pp. 971-974
-
-
Skinner, P.J.1
-
24
-
-
0030999657
-
3-Nitropropionic acid animal model and Huntington's disease
-
Borlongan, C.V., Koutouzis, T.K. & Sanberg, P.R. 3-Nitropropionic acid animal model and Huntington's disease. Neurosci. Biobehav. Rev. 21, 289-293 (1997).
-
(1997)
Neurosci. Biobehav. Rev.
, vol.21
, pp. 289-293
-
-
Borlongan, C.V.1
Koutouzis, T.K.2
Sanberg, P.R.3
-
25
-
-
0030935035
-
The likelihood of being affected with Huntington disease by a particular age, for a specific CAG size
-
Brinkman, R.R., Mezei, M.M., Theilmann, J., Almqvist, E. & Hayden, M.R. The likelihood of being affected with Huntington disease by a particular age, for a specific CAG size. Am. J. Hum. Genet. 60, 1202-1210 (1997).
-
(1997)
Am. J. Hum. Genet.
, vol.60
, pp. 1202-1210
-
-
Brinkman, R.R.1
Mezei, M.M.2
Theilmann, J.3
Almqvist, E.4
Hayden, M.R.5
-
26
-
-
0031127812
-
Huntingtin immunoreactivity in the rat neostriatum: Differential accumulation in projection and interneurons
-
Kosinski, C.M. et al. Huntingtin immunoreactivity in the rat neostriatum: differential accumulation in projection and interneurons. Exp. Neurol. 144, 239-247 (1997).
-
(1997)
Exp. Neurol.
, vol.144
, pp. 239-247
-
-
Kosinski, C.M.1
-
27
-
-
0030985156
-
The complex pathology of trinucleotide repeats
-
Reddy, P.S. & Housman, D.E. The complex pathology of trinucleotide repeats. Curr. Opin. Cell Biol. 9, 364-372 (1997).
-
(1997)
Curr. Opin. Cell Biol.
, vol.9
, pp. 364-372
-
-
Reddy, P.S.1
Housman, D.E.2
-
28
-
-
0030716768
-
The cerebellar leucine-rich acidic nuclear protein interacts with ataxin-1
-
Matilla, A. et al. The cerebellar leucine-rich acidic nuclear protein interacts with ataxin-1. Nature 389, 974-978 (1997).
-
(1997)
Nature
, vol.389
, pp. 974-978
-
-
Matilla, A.1
-
29
-
-
0028904293
-
Evidence from antibody studies that the CAG repeat in the Huntington disease gene is expressed in the protein
-
Jou, Y.S. & Myers, R.M. Evidence from antibody studies that the CAG repeat in the Huntington disease gene is expressed in the protein. Hum. Mol. Genet. 4, 465-469 (1995).
-
(1995)
Hum. Mol. Genet.
, vol.4
, pp. 465-469
-
-
Jou, Y.S.1
Myers, R.M.2
-
30
-
-
0000790724
-
SH3 domain-dependent association of huntingtin with epidermal growth factor receptor signaling complexes
-
Liu, Y.F., Deth, R.C. & Devys, D.E. SH3 domain-dependent association of huntingtin with epidermal growth factor receptor signaling complexes. J. Biol. Chem. 272, 8121-8124 (1997).
-
(1997)
J. Biol. Chem.
, vol.272
, pp. 8121-8124
-
-
Liu, Y.F.1
Deth, R.C.2
Devys, D.E.3
|