-
1
-
-
0025183708
-
Basic local alignment search tool
-
Altschul, S.F., W. Gish, W. Miller, E.W. Myers, and D.J. Lipman. 1990. Basic local alignment search tool. J. Mol. Biol. 215: 403-410.
-
(1990)
J. Mol. Biol.
, vol.215
, pp. 403-410
-
-
Altschul, S.F.1
Gish, W.2
Miller, W.3
Myers, E.W.4
Lipman, D.J.5
-
2
-
-
13344280348
-
Identification of trinucleotide repeat-containing genes in human pancreatic islets
-
Aoki, M., L. Koranyi, A.C. Riggs, J. Wasson, K.C. Chiu, M. Vaxillaire, P. Froguel, S. Gough, L. Liu, H. Donis-Keller et al. 1996. Identification of trinucleotide repeat-containing genes in human pancreatic islets. Diabetes 45: 157-164.
-
(1996)
Diabetes
, vol.45
, pp. 157-164
-
-
Aoki, M.1
Koranyi, L.2
Riggs, A.C.3
Wasson, J.4
Chiu, K.C.5
Vaxillaire, M.6
Froguel, P.7
Gough, S.8
Liu, L.9
Donis-Keller, H.10
-
3
-
-
0026567370
-
Cloning of the essential myotonic dystrophy region and mapping of the putative defect
-
Aslanidis, C., G. Jansen, C. Amemiya, G. Shutler, M. Mahadevan, C. Tsilfidis, C. Chen, J. Alleman, N.G. Wormskamp, M. Vooijs et al. 1992. Cloning of the essential myotonic dystrophy region and mapping of the putative defect. Nature 355: 548-551.
-
(1992)
Nature
, vol.355
, pp. 548-551
-
-
Aslanidis, C.1
Jansen, G.2
Amemiya, C.3
Shutler, G.4
Mahadevan, M.5
Tsilfidis, C.6
Chen, C.7
Alleman, J.8
Wormskamp, N.G.9
Vooijs, M.10
-
4
-
-
0028215549
-
Evidence for anticipation in schizophrenia
-
Bassett, A.S. and W.G. Honer. 1994. Evidence for anticipation in schizophrenia. Am. J. Hum. Genet. 54: 864-870.
-
(1994)
Am. J. Hum. Genet.
, vol.54
, pp. 864-870
-
-
Bassett, A.S.1
Honer, W.G.2
-
5
-
-
0029031694
-
The gene for autosomal dominant cerebellar ataxia with pigmentary macular dystrophy maps to chromosome 3p12-p21.1
-
Benomar, A., L. Krols, G. Stevanin, G. Cancel, E. LeGuern, G. David, H. Ouhabi, J.J. Martin, A. Durr, A. Zaim et al. 1995. The gene for autosomal dominant cerebellar ataxia with pigmentary macular dystrophy maps to chromosome 3p12-p21.1. Nature Genet. 10: 84-88.
-
(1995)
Nature Genet.
, vol.10
, pp. 84-88
-
-
Benomar, A.1
Krols, L.2
Stevanin, G.3
Cancel, G.4
LeGuern, E.5
David, G.6
Ouhabi, H.7
Martin, J.J.8
Durr, A.9
Zaim, A.10
-
6
-
-
0026321407
-
Statistical methods for multipoint radiation hybrid mapping
-
Boehnke M., K. Lange, and D.R. Cox. 1991. Statistical methods for multipoint radiation hybrid mapping. Am. J. Hum. Genet. 49: 1174-1188.
-
(1991)
Am. J. Hum. Genet.
, vol.49
, pp. 1174-1188
-
-
Boehnke, M.1
Lange, K.2
Cox, D.R.3
-
7
-
-
0029825936
-
Expansion of 50 CAG/CTG repeats excluded in Schizophrenia by application of a highly efficient approach using repeat expansion detection and a PCR screening set
-
Bowen, T., C. Guy, G. Speight, L. Jones, A. Cardno, K. Murphy, P. McGuffin, M.J. Owen, and M.C. O'Donovan. 1996. Expansion of 50 CAG/CTG repeats excluded in Schizophrenia by application of a highly efficient approach using repeat expansion detection and a PCR screening set. Am. J. Hum. Genet. 59: 912-917.
-
(1996)
Am. J. Hum. Genet.
, vol.59
, pp. 912-917
-
-
Bowen, T.1
Guy, C.2
Speight, G.3
Jones, L.4
Cardno, A.5
Murphy, K.6
McGuffin, P.7
Owen, M.J.8
O'Donovan, M.C.9
-
8
-
-
0026566108
-
Molecular basis of myotonic dystrophy: Expansion of a trinucleotide (CTG) repeat at the 3′ end of a transcript encoding a protein kinase family member
-
Brook, J.D., M.E. McCurrach, H.G. Harley, A.J. Buckler, D. Church, H. Aburatani, K. Hunter, V.P. Stanton, J.P. Thirion, T. Hudson et al. 1992. Molecular basis of myotonic dystrophy: Expansion of a trinucleotide (CTG) repeat at the 3′ 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
Buckler, A.J.4
Church, D.5
Aburatani, H.6
Hunter, K.7
Stanton, V.P.8
Thirion, J.P.9
Hudson, T.10
-
9
-
-
0029119112
-
Familial non-specific dementia maps to chromosome 3
-
Brown, J., A. Ashworth, S. Gydesen, A. Sorensen, M. Rossor, J. Hardy, and J. Collinge. 1995. Familial non-specific dementia maps to chromosome 3. Hum. Mol. Genet. 4: 1625-1628.
-
(1995)
Hum. Mol. Genet.
, vol.4
, pp. 1625-1628
-
-
Brown, J.1
Ashworth, A.2
Gydesen, S.3
Sorensen, A.4
Rossor, M.5
Hardy, J.6
Collinge, J.7
-
10
-
-
13344270899
-
Friedrich's ataxia: Autosomal recessive disease caused by an intronic GAA triplet repeat expansion
-
Campuzano, V., L. Montermini, M.D. Molto, L. Pianese, M. Cossée, F. Cavalcanti, E. Monros, F. Rodius, F. Duclos, A. Monticelli et al. 1996. Friedrich's ataxia: Autosomal recessive disease caused by an intronic GAA triplet repeat expansion. Science 271: 1423-1427.
-
(1996)
Science
, vol.271
, pp. 1423-1427
-
-
Campuzano, V.1
Montermini, L.2
Molto, M.D.3
Pianese, L.4
Cossée, M.5
Cavalcanti, F.6
Monros, E.7
Rodius, F.8
Duclos, F.9
Monticelli, A.10
-
11
-
-
0027495515
-
Evidence for a mechanism predisposing to intergenerational CAG repeat instability in spinocerebellar ataxia type 1
-
Chung, M.Y., L.P.W. Ranum, L.A. Duvick, A. Servadio, H.Y. Zoghbi, and H.T. Orr. 1993. Evidence for a mechanism predisposing to intergenerational CAG repeat instability in spinocerebellar ataxia type 1. Nature Genet. 3: 254-258.
-
(1993)
Nature Genet.
, vol.3
, pp. 254-258
-
-
Chung, M.Y.1
Ranum, L.P.W.2
Duvick, L.A.3
Servadio, A.4
Zoghbi, H.Y.5
Orr, H.T.6
-
12
-
-
0025131820
-
Radiation hybrid mapping: A somatic cell genetic method for constructing high-resolution maps of mammalian chromosomes
-
Cox, D.R., M. Burmeister, E.R. Price, S. Kim, and R.M. Myers. 1990. Radiation hybrid mapping: A somatic cell genetic method for constructing high-resolution maps of mammalian chromosomes. Science 250: 245-250.
-
(1990)
Science
, vol.250
, pp. 245-250
-
-
Cox, D.R.1
Burmeister, M.2
Price, E.R.3
Kim, S.4
Myers, R.M.5
-
13
-
-
9244225693
-
Spinocerebellar ataxia 3 and Machado-Joseph disease: Clinical, molecular, and neuropathological features
-
Durr, A., G. Stevanin, G. Cancel, C. Duyckaerts, N. Abbas, O. Didierjean, H. Chneiweiss, A. Benomar, O. Lynn-Caen, J. Julien 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
Lynn-Caen, O.9
Julien, J.10
-
14
-
-
0027240431
-
Trinucleotide repeat length instability and age of onset in Huntington's disease
-
Duyao, M., C. Ambrose, R. Myers, A. Novelletto, F. Persichetti, M. Frontali, S. Folstein, C. Ross, M. Franz, M. Abbott et al. 1993. Trinucleotide repeat length instability and age of onset in Huntington's disease. Nat. Genet. 4: 387-392.
-
(1993)
Nat. Genet.
, vol.4
, pp. 387-392
-
-
Duyao, M.1
Ambrose, C.2
Myers, R.3
Novelletto, A.4
Persichetti, F.5
Frontali, M.6
Folstein, S.7
Ross, C.8
Franz, M.9
Abbott, M.10
-
15
-
-
0028885609
-
Anticipation in unipolar affective disorder
-
Engstrom, C., A.S. Thornlund, A.L. Johansson, M. Langstrom, J. Chotai, R. Adolfsson, and P.O. Nylander. 1995. Anticipation in unipolar affective disorder. J. Affect. Disord. 35: 31-40.
-
(1995)
J. Affect. Disord.
, vol.35
, pp. 31-40
-
-
Engstrom, C.1
Thornlund, A.S.2
Johansson, A.L.3
Langstrom, M.4
Chotai, J.5
Adolfsson, R.6
Nylander, P.O.7
-
16
-
-
0026598119
-
An unstable triplet repeat in a gene related to myotonic muscular dystrophy
-
Fu, Y.H., A. Pizzuti, R.G. Fenwock, J. King, S. Raynarayan, P.W. Dunne, J. Dubel, G.A. Nasser, T. Ashizawa, P. de Jong et al. 1992. An unstable triplet repeat in a gene related to myotonic muscular dystrophy. Science 255: 1256-1258.
-
(1992)
Science
, vol.255
, pp. 1256-1258
-
-
Fu, Y.H.1
Pizzuti, A.2
Fenwock, R.G.3
King, J.4
Raynarayan, S.5
Dunne, P.W.6
Dubel, J.7
Nasser, G.A.8
Ashizawa, T.9
De Jong, P.10
-
17
-
-
0029912537
-
n dynamic mutations
-
n dynamic mutations. Genomics 32: 75-85.
-
(1996)
Genomics
, vol.32
, pp. 75-85
-
-
Gastier, J.M.1
Brody, T.2
Pulido, J.C.3
Businga, T.4
Sunden, S.5
Hu, X.6
Maitra, S.7
Buetow, K.H.8
Murray, J.C.9
Sheffield, V.C.10
-
18
-
-
9044240048
-
A radiation hybrid map of the human genome
-
Gyapay, G., K. Schmitt, C. Fizames, H. Jones, N. Vega-Czarny, D. Spillett, D. Muselet, J.D. Prud'Homme, C. Dib, C. Auffray et al. 1996. A radiation hybrid map of the human genome. Hum. Mol. Genet. 5: 339-346.
-
(1996)
Hum. Mol. Genet.
, vol.5
, pp. 339-346
-
-
Gyapay, G.1
Schmitt, K.2
Fizames, C.3
Jones, H.4
Vega-Czarny, N.5
Spillett, D.6
Muselet, D.7
Prud'Homme, J.D.8
Dib, C.9
Auffray, C.10
-
19
-
-
0023685544
-
A survey on intron and exon lengths
-
Hawkins, J.D. 1988. A survey on intron and exon lengths. Nucleic Acids Res. 16: 9893-9908.
-
(1988)
Nucleic Acids Res.
, vol.16
, pp. 9893-9908
-
-
Hawkins, J.D.1
-
20
-
-
0030155253
-
Regional assignment of human ESTs by whole-genome radiation hybrid mapping
-
Hayes, P.D., K. Schmitt, H.B. Jones, G. Gyapay, J. Weissenbach, and P.N. Goodfellow. 1996. Regional assignment of human ESTs by whole-genome radiation hybrid mapping. Mamm. Genome 7: 446-450.
-
(1996)
Mamm. Genome
, vol.7
, pp. 446-450
-
-
Hayes, P.D.1
Schmitt, K.2
Jones, H.B.3
Gyapay, G.4
Weissenbach, J.5
Goodfellow, P.N.6
-
21
-
-
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. 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
-
-
-
22
-
-
0030294345
-
Cloning of the gene for spinocerebellar ataxia 2 reveals a locus with high sensitivity to expanded CAG/glutamine repeats
-
Imbert, G., F. Saudou, G. Yvert, D. Devis, Y. Trottier, J.-M. Garnier, C. Weber, J.L. Mandel, G. Cancel, N. Abbas et al. 1996. Cloning of the gene for spinocerebellar ataxia 2 reveals a locus with high sensitivity to expanded CAG/glutamine repeats. Nature Genet. 14: 285-291.
-
(1996)
Nature Genet.
, vol.14
, pp. 285-291
-
-
Imbert, G.1
Saudou, F.2
Yvert, G.3
Devis, D.4
Trottier, Y.5
Garnier, J.-M.6
Weber, C.7
Mandel, J.L.8
Cancel, G.9
Abbas, N.10
-
23
-
-
0028827297
-
Characterization of four novel CAG repeat-containing cDNAs
-
Jiang, J.-X., R.H. Lekanne Deprez, E.C. Zwarthoff, and P.J. Riegman. 1995. Characterization of four novel CAG repeat-containing cDNAs. Genomics 30: 91-93.
-
(1995)
Genomics
, vol.30
, pp. 91-93
-
-
Jiang, J.-X.1
Lekanne Deprez, R.H.2
Zwarthoff, E.C.3
Riegman, P.J.4
-
24
-
-
0028557941
-
Physical linkage of the fragile site FRA11B and a Jacobsen syndrome chromosome deletion break point in 11q23.3
-
Jones, C., P. Slijepcevic, S. Marsh, E. Baker, W.Y. Langdow, R.I. Richards, and A. Tunnacliffe. 1994. Physical linkage of the fragile site FRA11B and a Jacobsen syndrome chromosome deletion break point in 11q23.3. Hum. Mol. Genet. 3. 2123-2130.
-
(1994)
Hum. Mol. Genet.
, vol.3
, pp. 2123-2130
-
-
Jones, C.1
Slijepcevic, P.2
Marsh, S.3
Baker, E.4
Langdow, W.Y.5
Richards, R.I.6
Tunnacliffe, A.7
-
25
-
-
0028143527
-
CAG expansions in a novel gene for Macado-Joseph disease at chromosome 14q32.1
-
Kawagushi, Y., T. Okamoto, M. Taniwaki, M. Aizawa, M. Inoue, S. Katayama, H. Kawakami, S. Nakamura, M. Nishimura, I. Akiguchi et al. 1994. CAG expansions in a novel gene for Macado-Joseph disease at chromosome 14q32.1. Nature Genet. 8: 221-228.
-
(1994)
Nature Genet.
, vol.8
, pp. 221-228
-
-
Kawagushi, 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
-
26
-
-
0027203684
-
Trinucleotide repeat amplification and hypermethylation of a CpG island in FRAXE mental retardation
-
Knight, S., A.V. Flannery, M.C. Hirst, L. Campbell, Z. Christodoulou, S.R. Phelps, J. Pointon, H.R. Middleton-Price, A. Barnicoat, M.E. Pembrey et al. 1993. Trinucleotide repeat amplification and hypermethylation of a CpG island in FRAXE mental retardation. Cell 74: 127-134.
-
(1993)
Cell
, vol.74
, pp. 127-134
-
-
Knight, S.1
Flannery, A.V.2
Hirst, M.C.3
Campbell, L.4
Christodoulou, Z.5
Phelps, S.R.6
Pointon, J.7
Middleton-Price, H.R.8
Barnicoat, A.9
Pembrey, M.E.10
-
27
-
-
0028216760
-
Unstable expansion of CAG repeat in hereditary dentatorubral-pallidoluysian atrophy (DRPLA)
-
Koide, R., T. Ikeuchi, O. Onodera, H. Tanaka, S. Igarashi, K. Endo, H. Takahashi, R. Kondo, A. Ishikawa, T. Hayashi et al. 1994. Unstable expansion of CAG repeat in hereditary dentatorubral-pallidoluysian atrophy (DRPLA). Nature Genet. 1: 9-13.
-
(1994)
Nature Genet.
, vol.1
, 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
-
28
-
-
0025938638
-
Isolation of a human DNA sequence which spans the fragile X
-
Kremer, E.J., S. Yu, M. Pritchard, R. Nagaraja, D. Heitz, M. Lynch, E. Baker, V.J. Hyland, R.D. Little, M. Wada et al. 1991. Isolation of a human DNA sequence which spans the fragile X. Am. J. Hum. Genet. 49: 656-661.
-
(1991)
Am. J. Hum. Genet.
, vol.49
, pp. 656-661
-
-
Kremer, E.J.1
Yu, S.2
Pritchard, M.3
Nagaraja, R.4
Heitz, D.5
Lynch, M.6
Baker, E.7
Hyland, V.J.8
Little, R.D.9
Wada, M.10
-
29
-
-
0025800526
-
Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy
-
La Spada, A.R., E.M. Wilson, D.B. Lubahn, A.E. Harding, and K.H. Fishbeck. 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
Fishbeck, K.H.5
-
30
-
-
0028080406
-
Trinucleotide repeat expansion in neurological disease
-
La Spada, A.R., H.L. Paulson, and K.H. Fishbeck. 1994. Trinucleotide repeat expansion in neurological disease. Ann. Neurol. 36: 814-822.
-
(1994)
Ann. Neurol.
, vol.36
, pp. 814-822
-
-
La Spada, A.R.1
Paulson, H.L.2
Fishbeck, K.H.3
-
31
-
-
0027297703
-
Novel triplet repeat containing genes in human brain: Cloning, expression, and length polymorphisms
-
Li, S.H., M.G. McInnis, R.L. Margolis, S.E. Antonarakis, and C.A. Ross. 1993. Novel triplet repeat containing genes in human brain: Cloning, expression, and length polymorphisms. Genomics 16: 572-579.
-
(1993)
Genomics
, vol.16
, pp. 572-579
-
-
Li, S.H.1
McInnis, M.G.2
Margolis, R.L.3
Antonarakis, S.E.4
Ross, C.A.5
-
32
-
-
0026744212
-
Localization of adenylyl and guanylyl cyclase in rat brain by in site hybridization: Comparison with calmodulin mRNA distribution
-
Matsuoka, I., G. Giuili, M. Poyard, D. Stengel, J. Parma, G. Guellaen, and J. Hanoune. 1992. Localization of adenylyl and guanylyl cyclase in rat brain by in site hybridization: Comparison with calmodulin mRNA distribution. J. Neurosci. 12: 3350-3360.
-
(1992)
J. Neurosci.
, vol.12
, pp. 3350-3360
-
-
Matsuoka, I.1
Giuili, G.2
Poyard, M.3
Stengel, D.4
Parma, J.5
Guellaen, G.6
Hanoune, J.7
-
33
-
-
0027491810
-
Anticipation in bipolar affective disorder
-
McInnis M.G., F.J. McMahon, G.A. Chase, S.G. Simpson, C.A. Ross, and J.R. DePaulo. 1993. Anticipation in bipolar affective disorder. Am. J. Hum. Genet. 83: 385-390.
-
(1993)
Am. J. Hum. Genet.
, vol.83
, pp. 385-390
-
-
McInnis, M.G.1
McMahon, F.J.2
Chase, G.A.3
Simpson, S.G.4
Ross, C.A.5
DePaulo, J.R.6
-
34
-
-
0028784037
-
CAG repeat expansions and schizophrenia: Association with disease in female and with early age-at-onset
-
Morris, A.G., E. Gaitonde, P.J. McKenna, J.D. Mollon, and D.M. Hunt. 1995. CAG repeat expansions and schizophrenia: Association with disease in female and with early age-at-onset. Hum. Mol. Genet. 4: 1957-1961.
-
(1995)
Hum. Mol. Genet.
, vol.4
, pp. 1957-1961
-
-
Morris, A.G.1
Gaitonde, E.2
McKenna, P.J.3
Mollon, J.D.4
Hunt, D.M.5
-
35
-
-
0029871929
-
Altered growth and branching patterns in Synpolydactyly caused by mutations in HOXD13
-
Muragaki, Y., S. Mundlos, J. Upton, and B.R. Olsen. 1996. Altered growth and branching patterns in Synpolydactyly caused by mutations in HOXD13. Science 272: 548-551.
-
(1996)
Science
, vol.272
, pp. 548-551
-
-
Muragaki, Y.1
Mundlos, S.2
Upton, J.3
Olsen, B.R.4
-
36
-
-
0028335386
-
Dentatorubral pallidoluysian atrophy expansion of an unstable CAG trinucleotide on chromosome 12p
-
Nagafuchi, S., H. Yanagisawa, K. Sato, T. Shirayama, F., Ohsaki, M. Bundo, T. Takeda, K. Tadokoro, I. Kondo, N. Murayama et al. 1994. Dentatorubral pallidoluysian atrophy expansion of an unstable CAG trinucleotide on chromosome 12p. Nature Genet. 1: 14-18.
-
(1994)
Nature Genet.
, vol.1
, pp. 14-18
-
-
Nagafuchi, S.1
Yanagisawa, H.2
Sato, K.3
Shirayama, T.4
Ohsaki, F.5
Bundo, M.6
Takeda, T.7
Tadokoro, K.8
Kondo, I.9
Murayama, N.10
-
37
-
-
0027981933
-
Implications of FRA16A structure for the mechanism of chromosomal fragile sites genesis
-
Nancarrow, J.K., E. Kremer, K. Holman, H. Eyre, N.A. Dogett, D. Paslier, D.F. Callen. G.R. Sutherland, and R.I. Richards. 1994. Implications of FRA16A structure for the mechanism of chromosomal fragile sites genesis. Science 264: 1938-1944.
-
(1994)
Science
, vol.264
, pp. 1938-1944
-
-
Nancarrow, J.K.1
Kremer, E.2
Holman, K.3
Eyre, H.4
Dogett, N.A.5
Paslier, D.6
Callen, D.F.7
Sutherland, G.R.8
Richards, R.I.9
-
38
-
-
8944262197
-
Survey of CAG/CTG repeats in human cDNAs representing new genes: Candidates for inherited neurological disorders
-
Néri, C., V. Albaneèse, A.-S. Lèbre, S. Holbert, C. Saada, L. Bougueleret, S. Meier-Ewert, I. LeGall, P. Millasseau, H. Bui et al. 1996. Survey of CAG/CTG repeats in human cDNAs representing new genes: Candidates for inherited neurological disorders. Hum. Mol. Genet. 5: 1001-1009.
-
(1996)
Hum. Mol. Genet.
, vol.5
, pp. 1001-1009
-
-
Néri, C.1
Albaneèse, V.2
Lèbre, A.-S.3
Holbert, S.4
Saada, C.5
Bougueleret, L.6
Meier-Ewert, S.7
LeGall, I.8
Millasseau, P.9
Bui, H.10
-
39
-
-
0029355769
-
Expanded CAG repeats in schizophrenia and bipolar disorder
-
O'Donovan, M.C., C. Gui, N. Craddock, K.C. Murphy, A.G. Cardno, L.A. Jones, M.J. Owen, and P. McGuffin. 1995. Expanded CAG repeats in schizophrenia and bipolar disorder. Nature Genet. 10: 380-381.
-
(1995)
Nature Genet.
, vol.10
, pp. 380-381
-
-
O'Donovan, M.C.1
Gui, C.2
Craddock, N.3
Murphy, K.C.4
Cardno, A.G.5
Jones, L.A.6
Owen, M.J.7
McGuffin, P.8
-
40
-
-
0030043058
-
CTG triplet repeats from human hereditary diseas are dominant genetic expamion products in Escherichla coli
-
Ohshima, K., S. Kang, and R.D. Wells. 1996. CTG triplet repeats from human hereditary diseas are dominant genetic expamion products in Escherichla coli. J. Biol. Chem. 271: 1853-1856.
-
(1996)
J. Biol. Chem.
, vol.271
, pp. 1853-1856
-
-
Ohshima, K.1
Kang, S.2
Wells, R.D.3
-
41
-
-
0027164698
-
Expansion of an unstable trinucleotide (CAG) repeat in spinocerebellar ataxia type 1
-
Orr, H.T., M. Chung, S. Banfi, T.J. Kwiatkowski, A. Serviado, A.L. Beaudet, A.E. McCall, L.A. Duvick, L.P. Ranum, and H.Y. Zoghbi. 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.4
Serviado, A.5
Beaudet, A.L.6
McCall, A.E.7
Duvick, L.A.8
Ranum, L.P.9
Zoghbi, H.Y.10
-
42
-
-
0028914399
-
Characterization of a large population of mRNAs from human testis
-
Pawlak, A., C. Tussaint, I. Levy, F. Bulle, M. Poyard, R. Barouki, and G. Guellaen. 1995. Characterization of a large population of mRNAs from human testis. Genomics 26: 151-158.
-
(1995)
Genomics
, vol.26
, pp. 151-158
-
-
Pawlak, A.1
Tussaint, C.2
Levy, I.3
Bulle, F.4
Poyard, M.5
Barouki, R.6
Guellaen, G.7
-
43
-
-
0028099702
-
Isolation of a GCC repeat showing expansion in FRAXF, a fragile site distal to FRAXA and FRAXE
-
Reynolds, I.S. Spikes, L.G. Shaffer, and D.L. Nelson. 1994. Isolation of a GCC repeat showing expansion in FRAXF, a fragile site distal to FRAXA and FRAXE. Nature Genet. 8: 229-235.
-
(1994)
Nature Genet.
, vol.8
, pp. 229-235
-
-
Reynolds1
Spikes, I.S.2
Shaffer, L.G.3
Nelson, D.L.4
-
44
-
-
0025079483
-
Expression of neurotransmitter synthesizing enzyme glutamic acid decarboxylase in male germ cells
-
Persson, H., M. Pelto-Huikko, and M. Metsis. 1990. Expression of neurotransmitter synthesizing enzyme glutamic acid decarboxylase in male germ cells. Mol. Cell. Biol. 10: 4701-4711.
-
(1990)
Mol. Cell. Biol.
, vol.10
, pp. 4701-4711
-
-
Persson, H.1
Pelto-Huikko, M.2
Metsis, M.3
-
45
-
-
0028283985
-
Glutamine repeats as polar zippers: Their possible role in inherited neurodegenerative diseases
-
Perutz, M.F., T. Johnson, M. Suzuki, and J.T. Finch. 1994. Glutamine repeats as polar zippers: Their possible role in inherited neurodegenerative diseases. Proc. Natl. Acad. Sci., 91: 5355-5358.
-
(1994)
Proc. Natl. Acad. Sci.
, vol.91
, pp. 5355-5358
-
-
Perutz, M.F.1
Johnson, T.2
Suzuki, M.3
Finch, J.T.4
-
46
-
-
0029820490
-
Search for unstable DNA in Schizophrenia families with evidence for genetic anticipation
-
Petronis, A., A.S. Bassett, W.G. Honer, J.B. Vincent, Y. Tatuch, T. Sasaki, D.J. Ying, T.A. Klempar, and J.L. Kennedy. 1996. Search for unstable DNA in Schizophrenia families with evidence for genetic anticipation. Am. J. Hum. Genet. 59: 905-911.
-
(1996)
Am. J. Hum. Genet.
, vol.59
, pp. 905-911
-
-
Petronis, A.1
Bassett, A.S.2
Honer, W.G.3
Vincent, J.B.4
Tatuch, Y.5
Sasaki, T.6
Ying, D.J.7
Klempar, T.A.8
Kennedy, J.L.9
-
47
-
-
0030292488
-
Moderate expansion of a normally biallelic trinucleotide repeat in spinocerebellar ataxia type 2
-
Pulst, S.-M., A. Nechiporuk, T. Nechiporuk, S. Gispert, X-N. Chen, I. Lopes-Cendes, S. Pearlman, S. Starkman, G. Orozco-Diaz, A. Lunkes et al. 1996. Moderate expansion of a normally biallelic trinucleotide repeat in spinocerebellar ataxia type 2. Nature Genet. 14: 269-276.
-
(1996)
Nature Genet.
, vol.14
, pp. 269-276
-
-
Pulst, S.-M.1
Nechiporuk, A.2
Nechiporuk, T.3
Gispert, S.4
Chen, X.-N.5
Lopes-Cendes, I.6
Pearlman, S.7
Starkman, S.8
Orozco-Diaz, G.9
Lunkes, A.10
-
48
-
-
84970050019
-
Human genes containing polymorphic trinucleotide repeats
-
Riggins, G.J., L.K. Lokey, J.L. Chastain, H.A. Leiner, S.L. Sherman, K.D. Wilkinson, and S.T. Warren. 1992. Human genes containing polymorphic trinucleotide repeats. Nature Genet. 2: 186-191.
-
(1992)
Nature Genet.
, vol.2
, pp. 186-191
-
-
Riggins, G.J.1
Lokey, L.K.2
Chastain, J.L.3
Leiner, H.A.4
Sherman, S.L.5
Wilkinson, K.D.6
Warren, S.T.7
-
49
-
-
0027300219
-
Genes with triplet repeats: Candidate mediators of neuropsychiatric disorders
-
Ross, C.A., M.G. McInnis, R.L. Margolis, and S.H. Li. 1993. Genes with triplet repeats: Candidate mediators of neuropsychiatric disorders. Trends Neurosci. 16: 254-260.
-
(1993)
Trends Neurosci.
, vol.16
, pp. 254-260
-
-
Ross, C.A.1
McInnis, M.G.2
Margolis, R.L.3
Li, S.H.4
-
50
-
-
0024438993
-
A computer program for choosing optimal oligonucleotides for filter hybridization, sequencing and in vitro amplification of DNA
-
Rychlik, W. and R.E. Rhoads 1989. A computer program for choosing optimal oligonucleotides for filter hybridization, sequencing and in vitro amplification of DNA. Nucleic Acids Res. 17: 8543-8551.
-
(1989)
Nucleic Acids Res.
, vol.17
, pp. 8543-8551
-
-
Rychlik, W.1
Rhoads, R.E.2
-
51
-
-
0030292368
-
Identification of the spinocerebellar ataxia type 2 gene using a direct identification of repeat expansion and cloning technique, DIRECT
-
Sanpei, K., H. Takano, S. Igarashi, T. Sato, M. Oyake, H. Sasaki, A. Wakisaka, K. Tashiro, Y. Ishida, T. Ikeuchi et al. 1996. Identification of the spinocerebellar ataxia type 2 gene using a direct identification of repeat expansion and cloning technique, DIRECT. Nature Genet. 14: 277-284.
-
(1996)
Nature Genet.
, vol.14
, pp. 277-284
-
-
Sanpei, K.1
Takano, H.2
Igarashi, S.3
Sato, T.4
Oyake, M.5
Sasaki, H.6
Wakisaka, A.7
Tashiro, K.8
Ishida, Y.9
Ikeuchi, T.10
-
52
-
-
13344277348
-
Psychosis and genes with trinucleotide repeat polymorphism
-
Sasaki, T., E. Billett, A. Petronis, D. Ying, T. Parsons, F.M. Macciardi, H.Y. Meltzer, J. Lieberman, R.T. Joffe, C.A. Ross et al. 1996. Psychosis and genes with trinucleotide repeat polymorphism. Hum. Genet. 97: 244-246.
-
(1996)
Hum. Genet.
, vol.97
, pp. 244-246
-
-
Sasaki, T.1
Billett, E.2
Petronis, A.3
Ying, D.4
Parsons, T.5
Macciardi, F.M.6
Meltzer, H.Y.7
Lieberman, J.8
Joffe, R.T.9
Ross, C.A.10
-
53
-
-
10244230901
-
A gene map of the human genome
-
Schuler, G.D., M.S. Boguski, E.A. Stewart, L.D. Stein, G. Gayapay, K. Rice, R.E. White, P. Rodriguez-Tome, A. Aggarwal, E. Bajork et al. 1996. A gene map of the human genome. Science 274: 540-546.
-
(1996)
Science
, vol.274
, pp. 540-546
-
-
Schuler, G.D.1
Boguski, M.S.2
Stewart, E.A.3
Stein, L.D.4
Gayapay, G.5
Rice, K.6
White, R.E.7
Rodriguez-Tome, P.8
Aggarwal, A.9
Bajork, E.10
-
54
-
-
0028986597
-
n changes in Huntington disease
-
n changes in Huntington disease. Hum. Mol. Genet. 4: 189-195.
-
(1995)
Hum. Mol. Genet.
, vol.4
, pp. 189-195
-
-
Telenius, H.1
Almqvist, E.2
Kremer, B.3
Spence, N.4
Squitieri, F.5
Nichol, K.6
Grandell, U.7
Starr, E.8
Benjamin, C.9
Castaldo, I.10
-
55
-
-
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. 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
-
-
-
56
-
-
0025905795
-
Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X synchrome
-
Verkerk, A.J.M.H., M. Pierretti, J.S. Sutcliffe, Y.H. Fu, D.P. Kuhl, and A. Pizzuti. 1991. Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X synchrome. Cell 65: 905-914.
-
(1991)
Cell
, vol.65
, pp. 905-914
-
-
Verkerk, A.J.M.H.1
Pierretti, M.2
Sutcliffe, J.S.3
Fu, Y.H.4
Kuhl, D.P.5
Pizzuti, A.6
-
57
-
-
0026265963
-
List of cloned mouse genes with unique expression patterns during spermatogenesis
-
Wolgemuth, D. and F. Watrin. 1991. List of cloned mouse genes with unique expression patterns during spermatogenesis. Mamm. Genome 1: 283-288.
-
(1991)
Mamm. Genome
, vol.1
, pp. 283-288
-
-
Wolgemuth, D.1
Watrin, F.2
-
58
-
-
0026347628
-
Fragile X genotype characterized by an unstable region of DNA
-
Yu, S., M. Pritchard, E. Kremer, M. Lynch, J. Nancarrow, E. Baker, K. Holman, J.C. Mulley, S.T. Warren, D. Schlessinger et al. 1991. Fragile X genotype characterized by an unstable region of DNA. Science 252: 1179-1181.
-
(1991)
Science
, vol.252
, pp. 1179-1181
-
-
Yu, S.1
Pritchard, M.2
Kremer, E.3
Lynch, M.4
Nancarrow, J.5
Baker, E.6
Holman, K.7
Mulley, J.C.8
Warren, S.T.9
Schlessinger, D.10
-
59
-
-
0028925739
-
CAG repeat length variation in sperm from a patient with Kennedy's disease
-
Zhang, L., K.H. Fischbeck, and N. Arnheim. 1995. CAG repeat length variation in sperm from a patient with Kennedy's disease. Hum. Mol. Genet. 4: 303-305.
-
(1995)
Hum. Mol. Genet.
, vol.4
, pp. 303-305
-
-
Zhang, L.1
Fischbeck, K.H.2
Arnheim, N.3
-
60
-
-
0031012399
-
Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the alpha 1A-voltage-dependent calcium channel
-
Zhuchenko, O., J. Bailey, P. Bonnen, T. Ashizawa, D.W. Stockton, C. Amos, W.B. Dobyns, S.H. Subramony, H.Y. Zoghbi, and C.C. Lee. 1997. Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the alpha 1A-voltage-dependent calcium channel. Nature Genet. 15: 62-69.
-
(1997)
Nature Genet.
, vol.15
, pp. 62-69
-
-
Zhuchenko, O.1
Bailey, J.2
Bonnen, P.3
Ashizawa, T.4
Stockton, D.W.5
Amos, C.6
Dobyns, W.B.7
Subramony, S.H.8
Zoghbi, H.Y.9
Lee, C.C.10
|