-
1
-
-
0029163222
-
SCA1 transgenic mice: A model for neurodegeration caused by an expanded CAG trinucleotide repeat
-
Burright, E.N., Clark, H.B., Servadio, A., Matilla, T., Fedderson, R.M., Yunis, W.S., Duvick, L.A., Zoghbi, H.Y., and Orr, H.T. (1995). SCA1 transgenic mice: a model for neurodegeration caused by an expanded CAG trinucleotide repeat. Cell 82, 937-948.
-
(1995)
Cell
, vol.82
, pp. 937-948
-
-
Burright, E.N.1
Clark, H.B.2
Servadio, A.3
Matilla, T.4
Fedderson, R.M.5
Yunis, W.S.6
Duvick, L.A.7
Zoghbi, H.Y.8
Orr, H.T.9
-
2
-
-
0023750525
-
Morphometric demonstration of atrophic changes in the cerebral cortex, white matter and neostriatum in Huntington's disease
-
de la Monte, S.M., Vonsattel, J.-P., and Richardson, E.P. (1988). Morphometric demonstration of atrophic changes in the cerebral cortex, white matter and neostriatum in Huntington's disease. J. Neuropath. Exp. Neurol. 47, 516-525.
-
(1988)
J. Neuropath. Exp. Neurol.
, vol.47
, pp. 516-525
-
-
De La Monte, S.M.1
Vonsattel, J.-P.2
Richardson, E.P.3
-
3
-
-
0028989602
-
Huntingtin is a cytoplasmic protein associated with vesicles in human and rat brain neurons
-
DiFiglia, M., Sapp, E., Chase, K., Schwarz, C., Meloni, A., Young, C., Martin, E., Vonstattel, J.-P., Carraway, R., Reeves, S.A., Boyce, F.M., and Aronin, N. (1995). Huntingtin is a cytoplasmic protein associated with vesicles in human and rat brain neurons. Neuron 14, 1075-1081.
-
(1995)
Neuron
, vol.14
, pp. 1075-1081
-
-
DiFiglia, M.1
Sapp, E.2
Chase, K.3
Schwarz, C.4
Meloni, A.5
Young, C.6
Martin, E.7
Vonstattel, J.-P.8
Carraway, R.9
Reeves, S.A.10
Boyce, F.M.11
Aronin, N.12
-
4
-
-
9244225693
-
Spinocerebellar ataxia 3 and Machado-Joseph disease: Clinical, molecular and neuropathological features
-
Durr, A., Stevanin, G., Cancel, G., Duyckaerts, C., Abbas, N., Didierjean, O., Chneiweiss, H., Benomar, A., Lyon-Caen, O., Julien, J., et al. (1996). Spinocerebellar ataxia 3 and Machado-Joseph disease: clinical, molecular and neuropathological features. Ann. Neurol. 39, 490-499.
-
(1996)
Ann. Neurol.
, vol.39
, pp. 490-499
-
-
Durr, A.1
Stevanin, G.2
Cancel, G.3
Duyckaerts, C.4
Abbas, N.5
Didierjean, O.6
Chneiweiss, H.7
Benomar, A.8
Lyon-Caen, O.9
Julien, J.10
-
6
-
-
0028799793
-
Early loss of early neostriatal neurons in Huntington's disease
-
Hedreen, J.C., and Folstein, S.E. (1995). Early loss of early neostriatal neurons in Huntington's disease. J. Neuropath. Exp. Neurol. 54, 105-120.
-
(1995)
J. Neuropath. Exp. Neurol.
, vol.54
, pp. 105-120
-
-
Hedreen, J.C.1
Folstein, S.E.2
-
7
-
-
0027480960
-
A novel gene containing a trinucleotide repeat that is unstable on Huntington's disease chromosomes
-
Huntington's Disease Collaborative Research Group (1993). A novel gene containing a trinucleotide repeat that is unstable on Huntington's disease chromosomes. Cell 72, 971-983.
-
(1993)
Cell
, vol.72
, pp. 971-983
-
-
-
8
-
-
0030058208
-
Expanded polyglutamine in the Machado-Joseph disease protein induces cell death in vitro and in vivo
-
Ikeda, H., Yamaguchi, M., Sugai, S., Aze, Y., Narumiya, S., and Kakizuka, A. (1996). Expanded polyglutamine in the Machado-Joseph disease protein induces cell death in vitro and in vivo. Nature Genet. 13, 196-202.
-
(1996)
Nature Genet.
, vol.13
, pp. 196-202
-
-
Ikeda, H.1
Yamaguchi, M.2
Sugai, S.3
Aze, Y.4
Narumiya, S.5
Kakizuka, A.6
-
9
-
-
0028904293
-
Evidence from antibody studies that the CAG repeat in the Huntington disease gene is expressed in the protein
-
Jou, Y.-S., and Myers, R.M. (1995). 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)
Hum. Mol. Genet.
, vol.4
, pp. 465-469
-
-
Jou, Y.-S.1
Myers, R.M.2
-
10
-
-
0028143527
-
CAG expansions in a novel gene for Machado-Joseph disease at chromosome 14q32.1
-
Kawaguchi, Y., Okamoto, T., Taniwaki, M., Aizawa, M., Inoue, M., Katayama, S., Kawakami, H., Nakamura, S., Nishimura, M., Akiguchi, I., Kimura, J., Narumiya, S., and Kakizuka, A. (1994). CAG expansions in a novel gene for Machado-Joseph disease at chromosome 14q32.1. Nature Genet. 8, 221-228.
-
(1994)
Nature Genet.
, vol.8
, pp. 221-228
-
-
Kawaguchi, Y.1
Okamoto, T.2
Taniwaki, M.3
Aizawa, M.4
Inoue, M.5
Katayama, S.6
Kawakami, H.7
Nakamura, S.8
Nishimura, M.9
Akiguchi, I.10
Kimura, J.11
Narumiya, S.12
Kakizuka, A.13
-
11
-
-
0014310582
-
Progressive proximal spinal and bulbar atrophy of late onset. A sex linked recessive trait
-
Kennedy, W.R., Alter, M., and Sung, J.H. (1968). Progressive proximal spinal and bulbar atrophy of late onset. A sex linked recessive trait. Neurology 18, 671-680.
-
(1968)
Neurology
, vol.18
, pp. 671-680
-
-
Kennedy, W.R.1
Alter, M.2
Sung, J.H.3
-
12
-
-
0028216760
-
Unstable expansion of CAG repeat in hereditary dentatorubral-pallidoluysian atrophy (DRPLA)
-
Koide, R., Ikeuchi, T., Onodera, O., Tanaka, H., Igarashi, S., Endo, K., Takahashi, H., Kondo, R., Ishikawa, A., Hayashi, T., et al. (1994). Unstable expansion of CAG repeat in hereditary dentatorubral-pallidoluysian atrophy (DRPLA). Nature Genet. 6, 9-13.
-
(1994)
Nature Genet.
, vol.6
, pp. 9-13
-
-
Koide, R.1
Ikeuchi, T.2
Onodera, O.3
Tanaka, H.4
Igarashi, S.5
Endo, K.6
Takahashi, H.7
Kondo, R.8
Ishikawa, A.9
Hayashi, T.10
-
13
-
-
0025800526
-
Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy
-
La Spada, A.R., Wilson, E.M., Lubahn, D.B., Harding, A.E., and Fischbeck, K.H. (1991). Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy. Nature 352, 77-79.
-
(1991)
Nature
, vol.352
, pp. 77-79
-
-
La Spada, A.R.1
Wilson, E.M.2
Lubahn, D.B.3
Harding, A.E.4
Fischbeck, K.H.5
-
14
-
-
1642379955
-
A survey of canine distemper
-
Lauder, I.M., Martin, W.B., Gordon, E.D., Lawson, D.D., Campbell, R.S.F., and Watrach, A.M. (1954). A survey of canine distemper. Veterinary Record 66, 607-611.
-
(1954)
Veterinary Record
, vol.66
, pp. 607-611
-
-
Lauder, I.M.1
Martin, W.B.2
Gordon, E.D.3
Lawson, D.D.4
Campbell, R.S.F.5
Watrach, A.M.6
-
15
-
-
0028803757
-
A huntingtin-associated protein enriched in brain with implications for pathology
-
Li, X.-J., Li, S.-H., Sharp, A.H., Nucifora, F.C., Schilling, G., Lanahan, A., Worley, P., Snyder, S.H., and Ross, C.A. (1995). A huntingtin-associated protein enriched in brain with implications for pathology. Nature 378, 398-402.
-
(1995)
Nature
, vol.378
, pp. 398-402
-
-
Li, X.-J.1
Li, S.-H.2
Sharp, A.H.3
Nucifora, F.C.4
Schilling, G.5
Lanahan, A.6
Worley, P.7
Snyder, S.H.8
Ross, C.A.9
-
17
-
-
0021863554
-
Detection of deletions spanning the duchenne muscular dystrophy locus using a tightly linked DNA probe
-
Monaco, A.P., Bertelson, C.J., Middlesworth, W., Colletti, C.-A., Aldridge, J., Fischbeck, K.H., Bartlett, R., Pericak-Vance, M.A., Roses, A.D., and Kunkel, L.M. (1985). Detection of deletions spanning the Duchenne muscular dystrophy locus using a tightly linked DNA probe. Nature 316, 842-845.
-
(1985)
Nature
, vol.316
, pp. 842-845
-
-
Monaco, A.P.1
Bertelson, C.J.2
Middlesworth, W.3
Colletti, C.-A.4
Aldridge, J.5
Fischbeck, K.H.6
Bartlett, R.7
Pericak-Vance, M.A.8
Roses, A.D.9
Kunkel, L.M.10
-
18
-
-
0023865274
-
Clinical and neuropathological assessment of severity in Huntington's disease
-
Myers, R.H., Vonsattel, J.P., Stevens, T.J., Cupples, L.A., Richardson, E.P., Martin, J.B., and Bird, E.D. (1988). Clinical and neuropathological assessment of severity in Huntington's disease. Neurology 38, 341-347.
-
(1988)
Neurology
, vol.38
, pp. 341-347
-
-
Myers, R.H.1
Vonsattel, J.P.2
Stevens, T.J.3
Cupples, L.A.4
Richardson, E.P.5
Martin, J.B.6
Bird, E.D.7
-
19
-
-
0025993794
-
Decreased neuronal and increased oligodendroglial densities in Huntington's disease caudate nucleus
-
Myers, R.H., Vonsattel, J.P., Paskevich, P.A., Kiely, D.K., Stevens, T.J., Cupples, L.A., Richardson, E.P., and Bird, E.D. (1991). Decreased neuronal and increased oligodendroglial densities in Huntington's disease caudate nucleus. J. Neuropath. Exp. Neurol. 50, 729-742.
-
(1991)
J. Neuropath. Exp. Neurol.
, vol.50
, pp. 729-742
-
-
Myers, R.H.1
Vonsattel, J.P.2
Paskevich, P.A.3
Kiely, D.K.4
Stevens, T.J.5
Cupples, L.A.6
Richardson, E.P.7
Bird, E.D.8
-
20
-
-
0027164698
-
Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1
-
Orr, H.T., Chung, M., Banfi, S., Kwiatkowski, T.J., Jr., Servadio, A., Beaudet, A.L., McCall, A.E., Duvick, L.A., Ranum, L.P.W., and Zoghbi, H.Y. (1993). Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1. Nature Genet. 4, 221-226.
-
(1993)
Nature Genet.
, vol.4
, pp. 221-226
-
-
Orr, H.T.1
Chung, M.2
Banfi, S.3
Kwiatkowski T.J., Jr.4
Servadio, A.5
Beaudet, A.L.6
McCall, A.E.7
Duvick, L.A.8
Ranum, L.P.W.9
Zoghbi, H.Y.10
-
21
-
-
0019796509
-
Body weight and dietary factors on Huntington's disease patients compared with matched controls
-
Sanberg, P.R., Fibiger, H.C., and Mark, R.F. (1981). Body weight and dietary factors on Huntington's disease patients compared with matched controls. Med. J. Aust. 1, 407-409.
-
(1981)
Med. J. Aust.
, vol.1
, pp. 407-409
-
-
Sanberg, P.R.1
Fibiger, H.C.2
Mark, R.F.3
-
22
-
-
0029014180
-
Expression analysis of the ataxin-1 protein in tissues from normal and spinocerebelar ataxia type 1 individuals
-
Servadio, A., Koshy, B., Armstrong, D., Antalffy, B., Orr, H.T., and Zoghbi, H.Y. (1995). Expression analysis of the ataxin-1 protein in tissues from normal and spinocerebelar ataxia type 1 individuals. Nature Genet. 10, 94-98.
-
(1995)
Nature Genet.
, vol.10
, pp. 94-98
-
-
Servadio, A.1
Koshy, B.2
Armstrong, D.3
Antalffy, B.4
Orr, H.T.5
Zoghbi, H.Y.6
-
23
-
-
0003546652
-
-
Cambridge, Massachusetts: Harvard University Press
-
Sidman, R.L., Angevine, J.B.J., and Taber-Pierce, E. (1971). Atlas of the Mouse Brain and Spinal Cord (Cambridge, Massachusetts: Harvard University Press).
-
(1971)
Atlas of the Mouse Brain and Spinal Cord
-
-
Sidman, R.L.1
Angevine, J.B.J.2
Taber-Pierce, E.3
-
24
-
-
0027432418
-
Widespread expression of the human and rat Huntington's disease gene in brain and nonneuronal tissues
-
Strong, T.V., Tagle, D.A., Valdes, J.M., Elmer, L.W., Boehm, K., Swaroop, M., Kaatz, K.W., Collins, F.S., and Albin, R.L. (1993). Widespread expression of the human and rat Huntington's disease gene in brain and nonneuronal tissues. Nature Genet. 5, 259-263.
-
(1993)
Nature Genet.
, vol.5
, pp. 259-263
-
-
Strong, T.V.1
Tagle, D.A.2
Valdes, J.M.3
Elmer, L.W.4
Boehm, K.5
Swaroop, M.6
Kaatz, K.W.7
Collins, F.S.8
Albin, R.L.9
-
25
-
-
0023680089
-
Hereditary dentatorubral-pallidoluysian atrophy: Clinical and pathological variants in a family
-
Takahashi, H., Ohama, E., Naito, H., Takeda, S., Nakashima, S., Makifuchi, T., and Ikuta, F. (1988). Hereditary dentatorubral-pallidoluysian atrophy: clinical and pathological variants in a family. Neurology 38, 1065-1070.
-
(1988)
Neurology
, vol.38
, pp. 1065-1070
-
-
Takahashi, H.1
Ohama, E.2
Naito, H.3
Takeda, S.4
Nakashima, S.5
Makifuchi, T.6
Ikuta, F.7
-
26
-
-
0027381482
-
Molecular analysis of juvenile Huntington disease: The major influence on (CAG)n repeat length is the sex of the affected parent
-
Telenius, H., Kremer, H.P.H., Theilmann, J., Andrew, S.E., Almquist, E., Anvret, M., Greenberg, C., Greenberg, J., Lucotte, G., Squitieri, F., Starr, E., Goldberg, Y.P., and Hayden, M.R. (1993). Molecular analysis of juvenile Huntington disease: the major influence on (CAG)n repeat length is the sex of the affected parent. Hum. Mol. Genet. 2, 1535-1540.
-
(1993)
Hum. Mol. Genet.
, vol.2
, pp. 1535-1540
-
-
Telenius, H.1
Kremer, H.P.H.2
Theilmann, J.3
Andrew, S.E.4
Almquist, E.5
Anvret, M.6
Greenberg, C.7
Greenberg, J.8
Lucotte, G.9
Squitieri, F.10
Starr, E.11
Goldberg, Y.P.12
Hayden, M.R.13
-
27
-
-
0029055601
-
Cellular localisation of the Huntington's disease protein and discrimination of the normal and mutated forms
-
Trottier, Y., Devys, D., Imbert, G., Sandou, F., An, I., Lutz, Y., Weber, C., Agid, Y., Hirsch, E.C., and Mandel, J.-L. (1995a). Cellular localisation of the Huntington's disease protein and discrimination of the normal and mutated forms. Nature Genet. 10, 104-110.
-
(1995)
Nature Genet.
, vol.10
, pp. 104-110
-
-
Trottier, Y.1
Devys, D.2
Imbert, G.3
Sandou, F.4
An, I.5
Lutz, Y.6
Weber, C.7
Agid, Y.8
Hirsch, E.C.9
Mandel, J.-L.10
-
28
-
-
0028972448
-
Polyglutamine expansion as a pathological epitope in Huntington's disease and four dominant cerebellar ataxias
-
Trottier, Y., Lutz, Y., Stevanin, G., Imbert, G., Devys, D., Cancel, G., Sandou, F., Weber, C., David, G., Tora, L., et al. (1995b). Polyglutamine expansion as a pathological epitope in Huntington's disease and four dominant cerebellar ataxias. Nature 378, 403-406.
-
(1995)
Nature
, vol.378
, pp. 403-406
-
-
Trottier, Y.1
Lutz, Y.2
Stevanin, G.3
Imbert, G.4
Devys, D.5
Cancel, G.6
Sandou, F.7
Weber, C.8
David, G.9
Tora, L.10
-
29
-
-
0022395922
-
Neuropathological classification of Huntington's disease
-
Vonsattel, J.-P., Myers, R.H., Stevens, T.J., Ferrante, R.J., Bird, E.D., and Richardson, E.P. (1985). Neuropathological classification of Huntington's disease. J. Neuropath. Exp. Neurol. 44, 559-577.
-
(1985)
J. Neuropath. Exp. Neurol.
, vol.44
, pp. 559-577
-
-
Vonsattel, J.-P.1
Myers, R.H.2
Stevens, T.J.3
Ferrante, R.J.4
Bird, E.D.5
Richardson, E.P.6
-
30
-
-
0022006358
-
Vesicourethral function in Huntington's chorea
-
Wheeler, J.S., Sax, D.S., Krane, R.J., and Siroky, M.B. (1985). Vesicourethral function in Huntington's chorea. Brit. J. Urol. 57, 63-66.
-
(1985)
Brit. J. Urol.
, vol.57
, pp. 63-66
-
-
Wheeler, J.S.1
Sax, D.S.2
Krane, R.J.3
Siroky, M.B.4
-
31
-
-
0029015557
-
Abnormal gene product identified in hereditary dentatorubral-pallidoluysian atrophy (DRPLA) brain
-
Yazawa, I., Nukina, N., Hashida, H., Goto, J., Yamada, M., and Kanazawa, I. (1995). Abnormal gene product identified in hereditary dentatorubral-pallidoluysian atrophy (DRPLA) brain. Nature Genet. 10, 99-103.
-
(1995)
Nature Genet.
, vol.10
, pp. 99-103
-
-
Yazawa, I.1
Nukina, N.2
Hashida, H.3
Goto, J.4
Yamada, M.5
Kanazawa, I.6
-
32
-
-
0011915513
-
-
S.H. Appel, ed. (St. Louis, MO: Mosby-Year Book)
-
Zoghbi, H.Y. (1993). In Current Neurology, S.H. Appel, ed. (St. Louis, MO: Mosby-Year Book), pp. 87-110.
-
(1993)
Current Neurology
, pp. 87-110
-
-
Zoghbi, H.Y.1
|