-
1
-
-
0031950826
-
Frontal lobe volume in patients with Huntington's disease
-
Aylward EH, Anderson NB, Bylsma FW, Wagster MV, Barta PE, Sherr M, Feeney J, Davis A, Rosenblatt A, Pearlson GD, Ross CA (1998) Frontal lobe volume in patients with Huntington's disease. Neurology 50:252-258.
-
(1998)
Neurology
, vol.50
, pp. 252-258
-
-
Aylward, E.H.1
Anderson, N.B.2
Bylsma, F.W.3
Wagster, M.V.4
Barta, P.E.5
Sherr, M.6
Feeney, J.7
Davis, A.8
Rosenblatt, A.9
Pearlson, G.D.10
Ross, C.A.11
-
2
-
-
0031918640
-
Intranuclear neuronal inclusions in Huntington's disease and dentatorubral and pallidoluysian atrophy: Correlation between the density of inclusions and IT15 CAG triplet repeat length
-
Becher MW, Kotzuk JA, Sharp AH, Davies SW, Bates GP, Price DL, Ross CA (1998) Intranuclear neuronal inclusions in Huntington's disease and dentatorubral and pallidoluysian atrophy: correlation between the density of inclusions and IT15 CAG triplet repeat length. Neurobiol Dis 4:387-397.
-
(1998)
Neurobiol Dis
, vol.4
, pp. 387-397
-
-
Becher, M.W.1
Kotzuk, J.A.2
Sharp, A.H.3
Davies, S.W.4
Bates, G.P.5
Price, D.L.6
Ross, C.A.7
-
3
-
-
7144253143
-
Truncated N-terminal fragments of huntingtin with expanded glutamine repeats form nuclear and cytoplasmic aggregates in cell culture
-
Cooper J, Schilling G, Peters M, Herring W, Sharp A, Kaminsky Z, Masone J, Khan F, Delanoy M, Borchelt D, Dawson V, Dawson T, Ross C (1998) Truncated N-terminal fragments of huntingtin with expanded glutamine repeats form nuclear and cytoplasmic aggregates in cell culture. Hum Mol Genet 7:783-790.
-
(1998)
Hum Mol Genet
, vol.7
, pp. 783-790
-
-
Cooper, J.1
Schilling, G.2
Peters, M.3
Herring, W.4
Sharp, A.5
Kaminsky, Z.6
Masone, J.7
Khan, F.8
Delanoy, M.9
Borchelt, D.10
Dawson, V.11
Dawson, T.12
Ross, C.13
-
4
-
-
0025239753
-
Degeneration of pyramidal projection neurons in Huntington's disease cortex
-
Cudkowicz M, Kowall NW (1990) Degeneration of pyramidal projection neurons in Huntington's disease cortex. Ann Neurol 27:200-204.
-
(1990)
Ann Neurol
, vol.27
, pp. 200-204
-
-
Cudkowicz, M.1
Kowall, N.W.2
-
5
-
-
0031838352
-
Chaperone suppression of aggregation and altered subcellular proteasome localization imply protein misfolding in SCA1
-
Cummings CJ, Mancini MA, Antalffy B, DeFranco DB, Orr HT, Zoghbi HY (1998) Chaperone suppression of aggregation and altered subcellular proteasome localization imply protein misfolding in SCA1. Nat Genet 19:148-154.
-
(1998)
Nat Genet
, vol.19
, pp. 148-154
-
-
Cummings, C.J.1
Mancini, M.A.2
Antalffy, B.3
DeFranco, D.B.4
Orr, H.T.5
Zoghbi, H.Y.6
-
6
-
-
18544410106
-
Formation of neuronal intranuclear inclusions underlies the neurological dysfunction in mice transgenic for the HD mutation
-
Davies SW, Turmaine M, Cozens BA, DiFiglia M, Sharp AH, Ross CA, Scherzinger E, Wanker EE, Mangiarini L, Bates GP (1997) Formation of neuronal intranuclear inclusions underlies the neurological dysfunction in mice transgenic for the HD mutation. Cell 90:537-548.
-
(1997)
Cell
, vol.90
, pp. 537-548
-
-
Davies, S.W.1
Turmaine, M.2
Cozens, B.A.3
DiFiglia, M.4
Sharp, A.H.5
Ross, C.A.6
Scherzinger, E.7
Wanker, E.E.8
Mangiarini, L.9
Bates, G.P.10
-
7
-
-
0032501740
-
Are neuronal intranuclear inclusions the common neuropathology of triplet-repeat disorders with polyglutamine-repeat expansions?
-
Davies SW, Beardsall K, Turmaine M, DiFiglia M, Aronin N, Bates GP (1998) Are neuronal intranuclear inclusions the common neuropathology of triplet-repeat disorders with polyglutamine-repeat expansions? Lancet 351:131-133.
-
(1998)
Lancet
, vol.351
, pp. 131-133
-
-
Davies, S.W.1
Beardsall, K.2
Turmaine, M.3
DiFiglia, M.4
Aronin, N.5
Bates, G.P.6
-
8
-
-
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, Vonsattel JP, Carraway R, Reeves SA, Boyce FM, 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
Vonsattel, J.P.8
Carraway, R.9
Reeves, S.A.10
Boyce, F.M.11
Aronin, N.12
-
9
-
-
0030752709
-
Aggregation of huntingtin in neuronal intranuclear inclusions and dystrophic neurites in brain
-
DiFiglia M, Sapp E, Chase KO, Davies SW, Bates GP, Vonsattel JP, Aronin N (1997) Aggregation of huntingtin in neuronal intranuclear inclusions and dystrophic neurites in brain. Science 277:1990-1993.
-
(1997)
Science
, vol.277
, pp. 1990-1993
-
-
DiFiglia, M.1
Sapp, E.2
Chase, K.O.3
Davies, S.W.4
Bates, G.P.5
Vonsattel, J.P.6
Aronin, N.7
-
10
-
-
0026320986
-
Proliferative and degenerative changes in striatal spiny neurons in Huntington's disease: A combined study using the section-Golgi method and calbindin D28k immunocytochemistry
-
Ferrante RJ, Kowall NW, Richardson Jr EP (1991) Proliferative and degenerative changes in striatal spiny neurons in Huntington's disease: a combined study using the section-Golgi method and calbindin D28k immunocytochemistry. J Neurosci 11:3877-3887.
-
(1991)
J Neurosci
, vol.11
, pp. 3877-3887
-
-
Ferrante, R.J.1
Kowall, N.W.2
Richardson E.P., Jr.3
-
11
-
-
0030950980
-
Heterogeneous topographic and cellular distribution of huntingtin expression in the normal human neostriatum
-
Ferrante R, Gutekunst C-A, Persichetti F, McNeil S, Kowall N, Gusella J, MacDonald M, Beal M, Hersch S (1997) Heterogeneous topographic and cellular distribution of huntingtin expression in the normal human neostriatum. J Neurosci 17:3052-3063.
-
(1997)
J Neurosci
, vol.17
, pp. 3052-3063
-
-
Ferrante, R.1
Gutekunst, C.-A.2
Persichetti, F.3
McNeil, S.4
Kowall, N.5
Gusella, J.6
MacDonald, M.7
Beal, M.8
Hersch, S.9
-
12
-
-
15144351709
-
Differential distribution of the normal and mutated forms of huntingtin in the human brain
-
Gourfinkel-An I, Cancel G, Trottier Y, Devys D, Tora L, Lutz Y, Imbert G, Saudou F, Stevanin G, Agid Y, Brice A, Mandel JL, Hirsch EC (1997) Differential distribution of the normal and mutated forms of huntingtin in the human brain. Ann Neurol 42:712-719.
-
(1997)
Ann Neurol
, vol.42
, pp. 712-719
-
-
Gourfinkel-An, I.1
Cancel, G.2
Trottier, Y.3
Devys, D.4
Tora, L.5
Lutz, Y.6
Imbert, G.7
Saudou, F.8
Stevanin, G.9
Agid, Y.10
Brice, A.11
Mandel, J.L.12
Hirsch, E.C.13
-
13
-
-
0021982117
-
Evidence for degenerative and regenerative changes in neostriatal spiny neurons in Huntington's disease
-
Graveland GA, Williams RS, DiFiglia M (1985) Evidence for degenerative and regenerative changes in neostriatal spiny neurons in Huntington's disease. Science 227:770-773.
-
(1985)
Science
, vol.227
, pp. 770-773
-
-
Graveland, G.A.1
Williams, R.S.2
DiFiglia, M.3
-
14
-
-
85009332113
-
Unified Huntington's disease rating scale: Reliability and consistency
-
Huntington Study Group
-
Group HS (1996) Unified Huntington's disease rating scale: reliability and consistency. Huntington Study Group. Mov Disord 11:136-142.
-
(1996)
Mov Disord
, vol.11
, pp. 136-142
-
-
Group, H.S.1
-
15
-
-
0029152808
-
Identification and localization of huntingtin in brain and human lymphoblastoid cell lines with anti-fusion protein antibodies
-
Gutekunst CA, Levey AI, Heilman CJ, Whaley WL, Yi H, Nash NR, Rees HD, Madden JJ, Hersch SM (1995) Identification and localization of huntingtin in brain and human lymphoblastoid cell lines with anti-fusion protein antibodies. Proc Natl Acad Sci USA 92:8710-8714.
-
(1995)
Proc Natl Acad Sci USA
, vol.92
, pp. 8710-8714
-
-
Gutekunst, C.A.1
Levey, A.I.2
Heilman, C.J.3
Whaley, W.L.4
Yi, H.5
Nash, N.R.6
Rees, H.D.7
Madden, J.J.8
Hersch, S.M.9
-
16
-
-
0032190391
-
The cellular and subcellular localization of huntingtin-associated protein 1 (HAP1): Comparison with huntingtin in rat and human
-
Gutekunst C-A, Li S-H, Ferrante R, Li X-J, Hersch S (1998) The cellular and subcellular localization of huntingtin-associated protein 1 (HAP1): comparison with huntingtin in rat and human. J Neurosci 18:7674-7686.
-
(1998)
J Neurosci
, vol.18
, pp. 7674-7686
-
-
Gutekunst, C.-A.1
Li, S.-H.2
Ferrante, R.3
Li, X.-J.4
Hersch, S.5
-
17
-
-
0032101287
-
The influence of huntingtin protein size on nuclear localization and cellular toxicity
-
Hackam A, Singaraja R, Wellington C, Metzler M, McCutcheon K, Zhang T, Kalchman M, Hayden M (1998) The influence of huntingtin protein size on nuclear localization and cellular toxicity. J Cell Biol 141:1097-1105.
-
(1998)
J Cell Biol
, vol.141
, pp. 1097-1105
-
-
Hackam, A.1
Singaraja, R.2
Wellington, C.3
Metzler, M.4
McCutcheon, K.5
Zhang, T.6
Kalchman, M.7
Hayden, M.8
-
19
-
-
0025885733
-
Neuronal loss in layers V and VI of cerebral cortex in Huntington's disease
-
Hedreen JC, Peyser CE, Folstein SE, Ross CA (1991) Neuronal loss in layers V and VI of cerebral cortex in Huntington's disease. Neurosci Lett 133:257-261.
-
(1991)
Neurosci Lett
, vol.133
, pp. 257-261
-
-
Hedreen, J.C.1
Peyser, C.E.2
Folstein, S.E.3
Ross, C.A.4
-
20
-
-
0002436484
-
Neuropathology and pathophysiology of Huntington's disease, movement disorders
-
Watts RL, Koller WC, eds. New York: McGraw-Hill
-
Hersch S, Ferrante R (1997) Neuropathology and pathophysiology of Huntington's disease, movement disorders. Neurologic principles and practice (Watts RL, Koller WC, eds). pp 503-526. New York: McGraw-Hill.
-
(1997)
Neurologic Principles and Practice
, pp. 503-526
-
-
Hersch, S.1
Ferrante, R.2
-
21
-
-
7144229376
-
Spinocerebellar ataxia type 7 (SCA7): A neurodegenerative disorder with neuronal intranuclear inclusions
-
Holmberg M, Duyckaerts C, Durr A, Cancel G, Gourfinkel-An I, Damier P, Faucheux B, Trottier Y, Hirsch EC, Agid Y, Brice A (1998) Spinocerebellar ataxia type 7 (SCA7): a neurodegenerative disorder with neuronal intranuclear inclusions. Hum Mol Genet 7:913-918.
-
(1998)
Hum Mol Genet
, vol.7
, pp. 913-918
-
-
Holmberg, M.1
Duyckaerts, C.2
Durr, A.3
Cancel, G.4
Gourfinkel-An, I.5
Damier, P.6
Faucheux, B.7
Trottier, Y.8
Hirsch, E.C.9
Agid, Y.10
Brice, A.11
-
22
-
-
0027480960
-
A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes
-
Huntington's Disease Collaborative Research Group (1993) A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes. Cell 72:971-983.
-
(1993)
Cell
, vol.72
, pp. 971-983
-
-
-
23
-
-
0029856046
-
Peptides containing glutamine repeats as substrates for transglutaminase-catalyzed cross-linking: Relevance to diseases of the nervous system
-
Kahlem P, Terre C, Green H, Djian P (1996) Peptides containing glutamine repeats as substrates for transglutaminase-catalyzed cross-linking: relevance to diseases of the nervous system. Proc Natl Acad Sci USA 93:14580-14585.
-
(1996)
Proc Natl Acad Sci USA
, vol.93
, pp. 14580-14585
-
-
Kahlem, P.1
Terre, C.2
Green, H.3
Djian, P.4
-
24
-
-
0030986659
-
HIP1, a human homologue of S. cerevisiae Sla2p: Interacts with membrane-associated huntingtin in the brain
-
Kalchman MA, Koide HB, McCutcheon K, Graham RK, Nichol K, Nishiyama K, Kazemi-Esfarjani P, Lynn FC, Wellington C, Metzler M, Goldberg YP, Kanazawa I, Gietz RD, Hayden MR (1997) HIP1, a human homologue of S. cerevisiae Sla2p: interacts with membrane-associated huntingtin in the brain. Nat Genet 16:44-53.
-
(1997)
Nat Genet
, vol.16
, pp. 44-53
-
-
Kalchman, M.A.1
Koide, H.B.2
McCutcheon, K.3
Graham, R.K.4
Nichol, K.5
Nishiyama, K.6
Kazemi-Esfarjani, P.7
Lynn, F.C.8
Wellington, C.9
Metzler, M.10
Goldberg, Y.P.11
Kanazawa, I.12
Gietz, R.D.13
Hayden, M.R.14
-
25
-
-
0032475941
-
Ataxin-1 nuclear localization and aggregation: Role in polyglutamine-induced disease in SCA1 transgenic mice
-
Klement I, Skinner P, Kaytor M, Yi H, Hersch S, Clark H, Zoghbi H, Orr H (1998) Ataxin-1 nuclear localization and aggregation: role in polyglutamine-induced disease in SCA1 transgenic mice. Cell 95:41-53.
-
(1998)
Cell
, vol.95
, pp. 41-53
-
-
Klement, I.1
Skinner, P.2
Kaytor, M.3
Yi, H.4
Hersch, S.5
Clark, H.6
Zoghbi, H.7
Orr, H.8
-
26
-
-
0343436542
-
Cellular distribution of huntingtin aggregation in spared and vulnerable neurons in Huntington's disease
-
Kuemmerle S, Klein A, Gutekunst C-A, Li X-J, Li S-H, Hersch S, Ferrante R (1998) Cellular distribution of huntingtin aggregation in spared and vulnerable neurons in Huntington's disease. Soc Neurosci Abstr 24:973.
-
(1998)
Soc Neurosci Abstr
, vol.24
, pp. 973
-
-
Kuemmerle, S.1
Klein, A.2
Gutekunst, C.-A.3
Li, X.-J.4
Li, S.-H.5
Hersch, S.6
Ferrante, R.7
-
27
-
-
0031945025
-
Aggregation of N-terminus of huntingtin is dependent on the length of its glutamine repeat
-
Li S-H, Li X-J (1998) Aggregation of N-terminus of huntingtin is dependent on the length of its glutamine repeat. Hum Mol Genet 7:777-782.
-
(1998)
Hum Mol Genet
, vol.7
, pp. 777-782
-
-
Li, S.-H.1
Li, X.-J.2
-
28
-
-
0032519646
-
Interaction of huntingtin associated protein with dynactin p150Glued
-
Li S-H, Gutekunst C, Hersch S, Li X-J (1998) Interaction of huntingtin associated protein with dynactin p150Glued. J Neurosci 18:1261-1269.
-
(1998)
J Neurosci
, vol.18
, pp. 1261-1269
-
-
Li, S.-H.1
Gutekunst, C.2
Hersch, S.3
Li, X.-J.4
-
29
-
-
0028803757
-
A huntingtin-associated protein enriched in brain with implications for pathology
-
Li XJ, Li SH, Sharp AH, Nucifora Jr FC, Schilling G, Lanahan A, Worley P, Snyder SH, Ross CA (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., Jr.4
Schilling, G.5
Lanahan, A.6
Worley, P.7
Snyder, S.H.8
Ross, C.A.9
-
30
-
-
16044373842
-
Exon 1 of the HD gene with an expanded CAG repeat is sufficient to cause a progressive neurological phenotypc in transgenic mice
-
Mangiarini L, Sathasivam K, Seller M, Cozens B, Harper A, Hetherington C, Lawton M, Trottier Y, Lehrach H, Davies SW, Bates GP (1996) Exon 1 of the HD gene with an expanded CAG repeat is sufficient to cause a progressive neurological phenotypc in transgenic mice. Cell 87:493-506.
-
(1996)
Cell
, vol.87
, pp. 493-506
-
-
Mangiarini, L.1
Sathasivam, K.2
Seller, M.3
Cozens, B.4
Harper, A.5
Hetherington, C.6
Lawton, M.7
Trottier, Y.8
Lehrach, H.9
Davies, S.W.10
Bates, G.P.11
-
31
-
-
17344363559
-
Length of huntingtin and its polyglutamine tract influences localization and frequency of intracellular aggregates
-
Martindale D, Hackam A, Wieczorek A, Ellerby L, Wellington C, McCutcheon K, Singaraja R, Kazemi-Esfarjani P, Devon R, Kim SU, Bredesen DE, Tufaro F, Hayden MR (1998) Length of huntingtin and its polyglutamine tract influences localization and frequency of intracellular aggregates. Nat Genet 18:150-154.
-
(1998)
Nat Genet
, vol.18
, pp. 150-154
-
-
Martindale, D.1
Hackam, A.2
Wieczorek, A.3
Ellerby, L.4
Wellington, C.5
McCutcheon, K.6
Singaraja, R.7
Kazemi-Esfarjani, P.8
Devon, R.9
Kim, S.U.10
Bredesen, D.E.11
Tufaro, F.12
Hayden, M.R.13
-
32
-
-
0023865274
-
Clinical and neuropathologic assessment of severity in Huntington's disease
-
Myers RH, Vonsattel JP, Stevens TJ, Cupples LA, Richardson EP, Martin JB, Bird ED (1988) Clinical and neuropathologic 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
-
33
-
-
0031469707
-
Ectopically expressed CAG repeats cause intranuclear inclusions and a progressive late onset neurological phenotype in the mouse
-
Ordway JM, Tallaksen-Greene S, Gutekunst CA, Bernstein EM, Cearley JA, Wiener H W, Dure LS, Lindsey R, Hersch SM, Jope RS, Albin RL, Detloff PJ (1997) Ectopically expressed CAG repeats cause intranuclear inclusions and a progressive late onset neurological phenotype in the mouse. Cell 91:753-763.
-
(1997)
Cell
, vol.91
, pp. 753-763
-
-
Ordway, J.M.1
Tallaksen-Greene, S.2
Gutekunst, C.A.3
Bernstein, E.M.4
Cearley, J.A.5
Wiener, H.W.6
Dure, L.S.7
Lindsey, R.8
Hersch, S.M.9
Jope, R.S.10
Albin, R.L.11
Detloff, P.J.12
-
34
-
-
0030850412
-
Intranuclear inclusions of expanded polyglutamine protein in spinocerebellar ataxia type 3
-
Paulson HL, Perez MK, Trottier Y, Trojanowski JQ, Subramony SH, Das SS, Vig P, Mandel JL, Fischbeck KH, Pittman RN (1997) Intranuclear inclusions of expanded polyglutamine protein in spinocerebellar ataxia type 3. Neuron 19:333-344.
-
(1997)
Neuron
, vol.19
, pp. 333-344
-
-
Paulson, H.L.1
Perez, M.K.2
Trottier, Y.3
Trojanowski, J.Q.4
Subramony, S.H.5
Das, S.S.6
Vig, P.7
Mandel, J.L.8
Fischbeck, K.H.9
Pittman, R.N.10
-
35
-
-
0028283985
-
Glutamine repeats as polar zippers: Their possible role in inherited neurodegenerative diseases
-
Perutz MF, Johnson T, Suzuki M, Finch JT (1994) Glutamine repeats as polar zippers: their possible role in inherited neurodegenerative diseases. Proc Natl Acad Sci USA 91:5355-5358.
-
(1994)
Proc Natl Acad Sci USA
, vol.91
, pp. 5355-5358
-
-
Perutz, M.F.1
Johnson, T.2
Suzuki, M.3
Finch, J.T.4
-
36
-
-
0032498817
-
Neuronal and glial somal size in the prefrontal cortex: A postmortem morphometric study of schizophrenia and Huntington disease
-
Rajkowska G, Selemon LD, Goldman-Rakic PS (1998) Neuronal and glial somal size in the prefrontal cortex: a postmortem morphometric study of schizophrenia and Huntington disease. Arch Gen Psychiatry 55:215-224.
-
(1998)
Arch Gen Psychiatry
, vol.55
, pp. 215-224
-
-
Rajkowska, G.1
Selemon, L.D.2
Goldman-Rakic, P.S.3
-
37
-
-
0031446233
-
Intranuclear neuronal inclusions: A common pathogenic mechanism for glutamine-repeat neurodegenerative diseases?
-
Ross CA (1997) Intranuclear neuronal inclusions: a common pathogenic mechanism for glutamine-repeat neurodegenerative diseases? Neuron 19:1147-1150.
-
(1997)
Neuron
, vol.19
, pp. 1147-1150
-
-
Ross, C.A.1
-
38
-
-
0032475931
-
Huntingtin acts in the nucleus to induce apoptosis but death does not correlate with the formation of intranuclear inclusions
-
Saudou F, Finkbeiner S, Devys D, Greenberg M (1998) Huntingtin acts in the nucleus to induce apoptosis but death does not correlate with the formation of intranuclear inclusions. Cell 95:55-66.
-
(1998)
Cell
, vol.95
, pp. 55-66
-
-
Saudou, F.1
Finkbeiner, S.2
Devys, D.3
Greenberg, M.4
-
39
-
-
18544400323
-
Huntingtin-encoded polyglutamine expansions form amyloid-like protein aggregates in vitro and in vivo
-
Scherzinger E, Lurz R, Turmaine M, Mangiarini L, Hollenbach B, Hasenbank R, Bates GP, Davies SW, Lehrach H, Wanker EE (1997) Huntingtin-encoded polyglutamine expansions form amyloid-like protein aggregates in vitro and in vivo. Cell 90:549-558.
-
(1997)
Cell
, vol.90
, pp. 549-558
-
-
Scherzinger, E.1
Lurz, R.2
Turmaine, M.3
Mangiarini, L.4
Hollenbach, B.5
Hasenbank, R.6
Bates, G.P.7
Davies, S.W.8
Lehrach, H.9
Wanker, E.E.10
-
40
-
-
0029034511
-
Widespread expression of Huntington's disease gene (IT15) protein product
-
Sharp A, Locv S, Schilling G, Li S-H, Li X-J, Bao J, Wagster M, Kotzuk J, Steiner J, Lo A, Hedreen J, Sisodia S, Snyder S, Dawson T, Ryugo D, Ross C (1995) Widespread expression of Huntington's disease gene (IT15) protein product. Neuron 14:1065-1074.
-
(1995)
Neuron
, vol.14
, pp. 1065-1074
-
-
Sharp, A.1
Locv, S.2
Schilling, G.3
Li, S.-H.4
Li, X.-J.5
Bao, J.6
Wagster, M.7
Kotzuk, J.8
Steiner, J.9
Lo, A.10
Hedreen, J.11
Sisodia, S.12
Snyder, S.13
Dawson, T.14
Ryugo, D.15
Ross, C.16
-
41
-
-
0030666001
-
Ataxin-1 with an expanded glutamine tract alters nuclear matrix-associated structures
-
Skinner PJ, Koshy BT, Cummings CJ, Klement IA, Helin K, Servadio A, Zoghbi HY, Orr HT (1997) Ataxin-1 with an expanded glutamine tract alters nuclear matrix-associated structures. Nature 389:971-974.
-
(1997)
Nature
, vol.389
, pp. 971-974
-
-
Skinner, P.J.1
Koshy, B.T.2
Cummings, C.J.3
Klement, I.A.4
Helin, K.5
Servadio, A.6
Zoghbi, H.Y.7
Orr, H.T.8
-
42
-
-
0027377217
-
Evidence for neuronal degeneration and dendritic plasticity in cortical pyramidal neurons of Huntington's disease: A quantitative Golgi study
-
Sotrel A, Williams RS, Kaufmann WE, Myers RH (1993) Evidence for neuronal degeneration and dendritic plasticity in cortical pyramidal neurons of Huntington's disease: a quantitative Golgi study. Neurology 43:2088-2096.
-
(1993)
Neurology
, vol.43
, pp. 2088-2096
-
-
Sotrel, A.1
Williams, R.S.2
Kaufmann, W.E.3
Myers, R.H.4
-
43
-
-
0029055601
-
Cellular localization of the Huntington's disease protein and discrimination of the normal and mutated form
-
Trottier Y, Devys D, Imbert G, Saudou F, An I, Lutz Y, Weber C, Agid Y, Hirsch EC, Mandel JL (1995) Cellular localization of the Huntington's disease protein and discrimination of the normal and mutated form. Nat Genet 10:104-110.
-
(1995)
Nat Genet
, vol.10
, pp. 104-110
-
-
Trottier, Y.1
Devys, D.2
Imbert, G.3
Saudou, F.4
An, I.5
Lutz, Y.6
Weber, C.7
Agid, Y.8
Hirsch, E.C.9
Mandel, J.L.10
-
44
-
-
0022395922
-
Neuropathological classification of Huntington's disease
-
Vonsattel JP, Myers RH, Stevens TJ, Ferrante RJ, Bird ED, Richardson EP, Jr (1985) Neuropathological classification of Huntington's disease. J Neuropathol Exp Neurol 44:559-577.
-
(1985)
J Neuropathol 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., Jr.6
-
45
-
-
0031056478
-
HIP-I: A huntingtin interacting protein isolated by the yeast two-hybrid system
-
Wanker EE, Rovira C, Scherzinger E, Hasenbank R, Walter S, Tait D, Colicelli J, Lehrach H (1997) HIP-I: a huntingtin interacting protein isolated by the yeast two-hybrid system. Hum Mol Genet 6:487-495.
-
(1997)
Hum Mol Genet
, vol.6
, pp. 487-495
-
-
Wanker, E.E.1
Rovira, C.2
Scherzinger, E.3
Hasenbank, R.4
Walter, S.5
Tait, D.6
Colicelli, J.7
Lehrach, H.8
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