-
2
-
-
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 1993;72:971-983.
-
(1993)
Cell
, vol.72
, pp. 971-983
-
-
-
3
-
-
0027519511
-
Analysis of the huntingtin gene reveals a trinucleotide-length polymorphism in the region of the gene that contains two CCG-rich stretches and a correlation between decreased age of onset of Huntington's disease and CAG repeat number
-
Rubinsztein DC, Barton DE, Davison BCC, Ferguson-Smith MA: Analysis of the huntingtin gene reveals a trinucleotide-length polymorphism in the region of the gene that contains two CCG-rich stretches and a correlation between decreased age of onset of Huntington's disease and CAG repeat number. Hum Mol Genet 1993;2:1713-1715.
-
(1993)
Hum Mol Genet
, vol.2
, pp. 1713-1715
-
-
Rubinsztein, D.C.1
Barton, D.E.2
Davison, B.C.C.3
Ferguson-Smith, M.A.4
-
4
-
-
0028177342
-
A CCG repeat polymorphism adjacent to the CAG repeat in the Huntington disease gene: Implications for diagnostic accuracy and predictive testing
-
Andrew SE, Goldberg YP, Theilmann J, Zeisler J, Hayden MR: A CCG repeat polymorphism adjacent to the CAG repeat in the Huntington disease gene: Implications for diagnostic accuracy and predictive testing. Hum Mol Genet 1994;3:65-67.
-
(1994)
Hum Mol Genet
, vol.3
, pp. 65-67
-
-
Andrew, S.E.1
Goldberg, Y.P.2
Theilmann, J.3
Zeisler, J.4
Hayden, M.R.5
-
5
-
-
0027955775
-
A single allele from the polymorphic CCG-rich sequence immediately 3′ to the unstable CAG trinucleotide in the IT15 cDNA shows almost complete disequilibrium with Huntington's disease chromosomes in the Scottish population
-
Barron LH, Rae A, Holloway S, Brock DJ, Warner JP: A single allele from the polymorphic CCG-rich sequence immediately 3′ to the unstable CAG trinucleotide in the IT15 cDNA shows almost complete disequilibrium with Huntington's disease chromosomes in the Scottish population. Hum Mol Genet 1994;3:173-175.
-
(1994)
Hum Mol Genet
, vol.3
, pp. 173-175
-
-
Barron, L.H.1
Rae, A.2
Holloway, S.3
Brock, D.J.4
Warner, J.P.5
-
6
-
-
0028332346
-
Polymorphism analysis of the huntingtin gene in Italian families affected with Huntington disease
-
Novelletto A, Persichetti F, Sabbadini G, Mandich P, Bellone E, Ajmar F, Squitieri F, Campanella G, Bozza A, MacDonald ME, Gusella JF, Frontali M: Polymorphism analysis of the huntingtin gene in Italian families affected with Huntington disease. Hum Mol Genet 1994;3:1129-1132.
-
(1994)
Hum Mol Genet
, vol.3
, pp. 1129-1132
-
-
Novelletto, A.1
Persichetti, F.2
Sabbadini, G.3
Mandich, P.4
Bellone, E.5
Ajmar, F.6
Squitieri, F.7
Campanella, G.8
Bozza, A.9
MacDonald, M.E.10
Gusella, J.F.11
Frontali, M.12
-
7
-
-
0029027047
-
Analysis of triplet repeats in the huntingtin gene in Japanese families affected with Huntington's disease
-
Masuda N, Goto J, Murayama N, Watanabe M, Kondo I, Kanazawa I: Analysis of triplet repeats in the huntingtin gene in Japanese families affected with Huntington's disease. J Med Genet 1995;32:701-705.
-
(1995)
J Med Genet
, vol.32
, pp. 701-705
-
-
Masuda, N.1
Goto, J.2
Murayama, N.3
Watanabe, M.4
Kondo, I.5
Kanazawa, I.6
-
8
-
-
0033812250
-
Analysis of CAG and CCG repeats in Huntington gene among HD patients and normal populations of India
-
Pramanik S, Basu P, Gangopadhaya PK, Sinha KK, Jha DK, Sinha S, Das SK, Maity BK, Mukherjee SC, Roychoudhuri S, Majumder PP, Bhattacharyya NP: Analysis of CAG and CCG repeats in Huntington gene among HD patients and normal populations of India. Eur J Hum Genet 2000;8:678-682.
-
(2000)
Eur J Hum Genet
, vol.8
, pp. 678-682
-
-
Pramanik, S.1
Basu, P.2
Gangopadhaya, P.K.3
Sinha, K.K.4
Jha, D.K.5
Sinha, S.6
Das, S.K.7
Maity, B.K.8
Mukherjee, S.C.9
Roychoudhuri, S.10
Majumder, P.P.11
Bhattacharyya, N.P.12
-
9
-
-
0030937818
-
Genotypes at the GluR6 kainate receptor locus are associated with variation in the age of onset of Huntington disease
-
Rubinsztein DC, Leggo J, Chiano M, Dodge A, Norbury G, Rosser E, Craufurd D: Genotypes at the GluR6 kainate receptor locus are associated with variation in the age of onset of Huntington disease. Proc Natl Acad Sci USA 1997;94:3872-3876.
-
(1997)
Proc Natl Acad Sci USA
, vol.94
, pp. 3872-3876
-
-
Rubinsztein, D.C.1
Leggo, J.2
Chiano, M.3
Dodge, A.4
Norbury, G.5
Rosser, E.6
Craufurd, D.7
-
10
-
-
0028999064
-
Hereditary late-onset chorea without significant dementia. Genetic evidence for substantial phenotypic variant in HD
-
Britton JW, Uitti RJ, Ahlskog JE, Robinson RG, Kremer B, Hayden MR: Hereditary late-onset chorea without significant dementia. Genetic evidence for substantial phenotypic variant in HD. Neurology 1995;45:443-447.
-
(1995)
Neurology
, vol.45
, pp. 443-447
-
-
Britton, J.W.1
Uitti, R.J.2
Ahlskog, J.E.3
Robinson, R.G.4
Kremer, B.5
Hayden, M.R.6
-
11
-
-
0031785792
-
Levodopa responsive parkinsonism in an adult with Huntington's disease
-
Racette BA, Perlmutter JS: Levodopa responsive parkinsonism in an adult with Huntington's disease. J Neurol Neurosurg Psychiatry 1998;65:577-579.
-
(1998)
J Neurol Neurosurg Psychiatry
, vol.65
, pp. 577-579
-
-
Racette, B.A.1
Perlmutter, J.S.2
-
12
-
-
0034057350
-
Late onset levodopa responsive Huntington's disease with minimal chorea masquerading as Parkinson plus syndrome
-
Reuter I, Hu MT, Andrews TC, Brooks DJ, Clough C, Chaudhuri KR: Late onset levodopa responsive Huntington's disease with minimal chorea masquerading as Parkinson plus syndrome. J Neurol Neurosurg Psychiatry 2000;68:238-241.
-
(2000)
J Neurol Neurosurg Psychiatry
, vol.68
, pp. 238-241
-
-
Reuter, I.1
Hu, M.T.2
Andrews, T.C.3
Brooks, D.J.4
Clough, C.5
Chaudhuri, K.R.6
-
13
-
-
0026802299
-
Huntington's disease in Chinese: A hypothesis of its origin
-
Leung CM, Chan YW, Chang CM, Yu YL, Chen CN: Huntington's disease in Chinese: a hypothesis of its origin. J Neurol Neurosurg Psychiatry 1992;55:681-684.
-
(1992)
J Neurol Neurosurg Psychiatry
, vol.55
, pp. 681-684
-
-
Leung, C.M.1
Chan, Y.W.2
Chang, C.M.3
Yu, Y.L.4
Chen, C.N.5
-
14
-
-
0028564730
-
DNA haplotype analysis of Huntington disease reveals clues to the origins and mechanisms of CAG expansion and reasons for geographic variations of prevalence
-
Squitieri F, Andrew SE, Goldberg YP, Kremer B, Spence N, Zeisler J, Nichol K, Theilmann J, Greenberg J, Goto J, Kanazawa I, Vesa J, Peltonen L, Almqvist E, Anvret M, Telenius H, Lin B, Napolitano G, Morgan K, Hayden MR: DNA haplotype analysis of Huntington disease reveals clues to the origins and mechanisms of CAG expansion and reasons for geographic variations of prevalence. Hum Mol Genet 1994;3:2103-2114.
-
(1994)
Hum Mol Genet
, vol.3
, pp. 2103-2114
-
-
Squitieri, F.1
Andrew, S.E.2
Goldberg, Y.P.3
Kremer, B.4
Spence, N.5
Zeisler, J.6
Nichol, K.7
Theilmann, J.8
Greenberg, J.9
Goto, J.10
Kanazawa, I.11
Vesa, J.12
Peltonen, L.13
Almqvist, E.14
Anvret, M.15
Telenius, H.16
Lin, B.17
Napolitano, G.18
Morgan, K.19
Hayden, M.R.20
more..
-
15
-
-
4644361166
-
Molecular analysis of the Huntington's disease with expanded CAG trinucleotide repeat in Chinese
-
Zeng YT, Mao YH, Chen MJ, Ren ZR, Zhou G, Sheng M, Wang XY, Xu ZD, Yie WH, Zhao XZ, He X, Huang SZ: Molecular analysis of the Huntington's disease with expanded CAG trinucleotide repeat in Chinese. J Genet Mol Biol 1996;7:1-6.
-
(1996)
J Genet Mol Biol
, vol.7
, pp. 1-6
-
-
Zeng, Y.T.1
Mao, Y.H.2
Chen, M.J.3
Ren, Z.R.4
Zhou, G.5
Sheng, M.6
Wang, X.Y.7
Xu, Z.D.8
Yie, W.H.9
Zhao, X.Z.10
He, X.11
Huang, S.Z.12
-
16
-
-
0038042172
-
Modulation of age at onset in Huntington's disease and spinocerebellar ataxia type 2 patients originated from eastern India
-
Chattopadhyay B, Ghosh S, Gangopadhyay PK, Das SK, Roy T, Sinha KK, Jha DK, Mukherjee SC, Chakraborty A, Singhal BS, Bhattacharya AK, Bhattacharyya NP: Modulation of age at onset in Huntington's disease and spinocerebellar ataxia type 2 patients originated from eastern India. Neurosci Lett 2003;345:93-96.
-
(2003)
Neurosci Lett
, vol.345
, pp. 93-96
-
-
Chattopadhyay, B.1
Ghosh, S.2
Gangopadhyay, P.K.3
Das, S.K.4
Roy, T.5
Sinha, K.K.6
Jha, D.K.7
Mukherjee, S.C.8
Chakraborty, A.9
Singhal, B.S.10
Bhattacharya, A.K.11
Bhattacharyya, N.P.12
-
17
-
-
0031747231
-
Genetic polymorphisms adjacent to the CAG repeat influence clinical features at onset in Huntington's disease
-
Vuillaume I, Vermersch P, Destee A, Petit H, Sablonnière B: Genetic polymorphisms adjacent to the CAG repeat influence clinical features at onset in Huntington's disease. J Neurol Neurosurg Psychiatry 1998;64:758-762.
-
(1998)
J Neurol Neurosurg Psychiatry
, vol.64
, pp. 758-762
-
-
Vuillaume, I.1
Vermersch, P.2
Destee, A.3
Petit, H.4
Sablonnière, B.5
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