-
4
-
-
0031614136
-
Computational applications of DNA structural scales
-
In Proceedings of the 1998 Conference on Intelligent Systems for Molecular Biology (ISMB98) The AAI Press, Menlo Park, CA
-
(1998)
, pp. 35-42
-
-
Baldi, P.1
Chauvin, Y.2
Pedersen, A.G.3
Brunak, S.4
-
13
-
-
13344270899
-
Friedreich's ataxia: Autosomal recessive disease caused by an intronic GAA triplet repeat expansion
-
(1996)
Science
, vol.271
, pp. 1423-1427
-
-
Campuzano, V.1
Montermini, L.2
Molto, M.D.3
Pianese, L.4
Cossee, M.5
Cavalcanti, F.6
Montos, E.7
Rodius, F.8
Duclos, F.9
Monticelli, A.10
Zara, F.11
Canizares, J.12
Koutnikova, H.13
Bidichandani, S.I.14
Gellera, C.15
Brice, A.16
Trouillaas17
Frutos, R.D.18
Palau, F.19
Patel, P.I.20
Donato, S.D.21
Mandel, J.L.22
Cocozza, S.23
Koenig, M.24
Pandolfo, M.25
more..
-
15
-
-
0029008288
-
Hairpins are formed by the single DNA strands of the fragile X triplet repeats: Structure and biological implications
-
(1995)
Proc. Natl. Acad. Sci. USA
, vol.52
, pp. 5199-5203
-
-
Chen, X.1
Mariappan, S.V.S.2
Catasti, P.3
Ratliff, R.4
Moyzis, R.K.5
Ali, L.6
Smith, S.S.7
Bradbury, E.M.8
Gupta, G.9
-
16
-
-
0027744223
-
FSHD associated DNA rearrangements are due to deletions of integral copies of a 3.3 kb tandemly repeated unit
-
(1993)
Hum. Mol. Genet.
, vol.2
, pp. 2037-2042
-
-
van Deutekom, J.T.1
Wijmenga, C.2
van Tienhoven, E.A.E.3
Gruter, A.M.4
Hewitt, J.E.5
Padberg, G.W.6
van Ommen, G.J.B.7
Hofker, M.H.8
Frants, R.R.9
-
20
-
-
0002465261
-
The FRAXA fragile site and fragile X syndrome
-
Rubinsztein, D.C. and Hayden, M.R. (eds), Analysis of Triplet Repeat Disorders BIOS, Oxford
-
(1998)
, pp. 13-50
-
-
Eichler, E.E.1
Nelson, D.L.2
-
21
-
-
0002649291
-
-
An Introduction to Probability Theory and its Applications. 2nd edn, Wiley, New York.
-
(1971)
, vol.2
-
-
Feller, W.1
-
22
-
-
0001215523
-
Exact method for numerically analyzing a model of local denaturation in superhelically stressed DNA
-
(1999)
Phys. Rev. E
, vol.59
, pp. 3408-3426
-
-
Fye, R.M.1
Benham, C.J.2
-
32
-
-
0032059864
-
FRA10B structure reveals common elements in repeat expansion and chromosomal fragile site genesis
-
(1998)
Mol. Cell
, vol.1
, pp. 773-781
-
-
Hewett, D.R.1
Handt, O.2
Hobson, L.3
Mangelsdorf, M.4
Eyre, H.J.5
Baker, E.6
Sutherland, G.R.7
Schuffenhauer, S.8
Mao, J.I.9
Richards, R.I.10
-
33
-
-
0028040601
-
Analysis of the tandem repeat locus D4Z4 associated with facioscapulohumeral muscular dystrophy
-
(1994)
Hum. Mol. Genet.
, vol.3
, pp. 1287-1295
-
-
Hewitt, J.E.1
Lyle, R.2
Clark, L.N.3
Valleley, E.M.4
Wright, T.J.5
Wijmenga, C.6
van Deutekom, J.C.7
Francis, F.8
Sharpe, P.T.9
Hofker, M.H.10
-
35
-
-
0029026719
-
Poly (dA:dT), a ubiquitous promoter element that stimulates transcription via its intrinsic DNA structure
-
(1995)
EMBO J.
, vol.14
, pp. 2570-2579
-
-
Iyer, V.1
Struhl, K.2
-
36
-
-
0030664543
-
Spontaneous and induced minisatellite instability in the human genome
-
(1997)
Clin. Sci.
, vol.93
, pp. 383-390
-
-
Jeffreys, A.J.1
-
41
-
-
0032406199
-
CCG repeats in cDNAs from human brain
-
(1998)
Hum. Genet.
, vol.103
, pp. 666-673
-
-
Kleiderlein, J.J.1
Nisson, P.E.2
Jessee, J.3
Li, W.4
Becker, K.G.5
Derby, M.L.6
Ross, C.A.7
Margolis, R.L.8
-
42
-
-
0000256612
-
Friedreich's ataxia
-
Rubinsztein, D.C. Hayden, M.R. (eds), Analysis of Triplet Repeat Disorders BIOS, Oxford
-
(1998)
, pp. 219-238
-
-
Koenig, M.1
-
44
-
-
0030964106
-
Dodecamer repeat expansion in cystatin B gene in progressive myoclonus epilepsy
-
(1997)
Nature
, vol.386
, pp. 847-851
-
-
Lalioti, M.D.1
Scott, H.S.2
Buresi, C.3
Rossier, C.4
Bottani, A.5
Morris, M.A.6
Malafosse, A.7
Antonarakis, S.E.8
-
45
-
-
17344372332
-
A PCR amplification method reveals instability of the dodecamer repeat in progressive myoclonus epilepsy (EPM1) and no correlation between the size of the repeat and age at onset
-
(1998)
Am. J. Hum. Genet.
, vol.62
, pp. 842-847
-
-
Lalioti, M.D.1
Scott, H.S.2
Genton, P.3
Grid, D.4
Ouazzani, R.5
M'Rabet, A.6
Ibrahim, S.7
Gouider, R.8
Dravet, C.9
Chkili, T.10
Bottani, A.11
Buresi, C.12
Malafosse, A.13
Antonarakis, S.E.14
-
46
-
-
0002467287
-
Spinocerebellar ataxia type 6 (SCA6)
-
Rubinsztein, D.C. and Hayden, M.R. (eds), Analysis of Triplet Repeat Disorders BIOS, Oxford
-
(1998)
, pp. 145-154
-
-
Lee, C.C.1
-
59
-
-
0002649633
-
Polyglutamine tract vs. protein context in SCA1 pathogenesis
-
Rubinsztein, D.C. and Hayden, M.R. (eds), Analysis of Triplet Repeat Disorders BIOS, Oxford
-
(1998)
, pp. 105-118
-
-
Orr, H.T.1
Zoghbi, H.Y.2
-
60
-
-
0027164698
-
Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1
-
(1993)
Nature Genet.
, vol.4
, pp. 221-226
-
-
Orr, H.T.1
Chung, M.2
Banfi S. T.J.K., Jr.3
Servadio, A.4
Beaudet, A.L.5
McCall, A.E.6
Duvick, L.A.7
Ranum, L.P.W.8
Zoghbi, H.Y.9
-
62
-
-
0002466486
-
Spinocerebellar ataxia type 3/machado-joseph disease
-
Rubinsztein, D.C. and Hayden, M.R. (eds), Analysis of Triplet Repeat Disorders BIOS, Oxford
-
(1998)
, pp. 129-144
-
-
Paulson, H.L.1
-
63
-
-
0030850412
-
Intranuclear inclusions of expanded polyglutamine protein in spinocerebellar ataxia type 3
-
(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
-
64
-
-
0030986934
-
SWI2/SNF2 and related proteins: ATP-driven motors that disrupt protein-DNA interactions?
-
(1997)
Cell
, vol.88
, pp. 737-740
-
-
Pazin, M.J.1
Kadonaga, J.T.2
-
65
-
-
0000486352
-
Slipped strand DNA, dynamic mutations and human disease
-
Wells, R.D. and Warren, S.T. (eds), Genetic Instabilities and Hereditary Neurological Diseases Academic Press, New York
-
(1998)
, pp. 585-621
-
-
Pearson, C.E.1
Sinden, R.R.2
-
71
-
-
4243211725
-
Spinocerebellar ataxia type 2
-
Rubinsztein D.C. Hayden M.R. (eds), Analysis of Triplet Repeat Disorders BIOS, Oxford
-
(1998)
, pp. 119-128
-
-
Pulst, S.-M.1
-
72
-
-
0010750292
-
Some examples of normal approximations by Stein's method
-
Aldous, D. and Pemantle, R. (eds), Random Discrete Structures Springer, New York
-
(1996)
, pp. 25-44
-
-
Rinott, Y.1
Dembo, A.2
-
73
-
-
0029089172
-
When more is less: Pathogenesis of glutamine repeat neurodegenerative diseases
-
(1995)
Neuron
, vol.15
, pp. 493-496
-
-
Ross, C.A.1
-
74
-
-
0000810812
-
Trinucleotide repeat mutation processes
-
Rubinsztein, D.C. and Hayden, M.R. (eds), Analysis of Triplet Repeat Disorders BIOS, Oxford
-
(1998)
, pp. 257-268
-
-
Rubinsztein, D.C.1
Amos, B.2
-
75
-
-
0002554971
-
-
Introduction. In Rubinsztein, D.C. and Hayden, M.R. (eds), Analysis of Triplet Repeat Disorders BIOS, Oxford
-
(1998)
, pp. 1-12
-
-
Rubinsztein, D.C.1
Hayden, M.R.2
-
79
-
-
0002634196
-
-
DNA Structure and Function. Academic Press, San Diego, CA.
-
(1994)
-
-
Sinden, R.R.1
-
82
-
-
0002562498
-
Spinocerebellar ataxia type 7 (SCA7)
-
Rubinsztein, D.C. and Hayden, M.R. (eds), Analysis of Triplet Repeat Disorders BIOS, Oxford
-
(1998)
, pp. 155-168
-
-
Stevanin, G.1
Daviid, G.2
Abbas, N.3
Durr, A.4
Holmberg, M.5
Duyckaerts, C.6
Giunti, P.7
Cancel, G.8
Ruberg, M.9
Mandel, J.-L.10
Brice, A.11
-
84
-
-
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)
Cell
, vol.72
, pp. 971-983
-
-
-
87
-
-
0028932050
-
Expanded CTG triplet blocks from the myotonic dystrophy gene create the strongest known natural nucleosome positioning elements
-
(1995)
Genomics
, vol.25
, pp. 570-573
-
-
Wang, Y.-H.1
Griffith, J.D.2
-
91
-
-
0028303398
-
The DNA rearrangement associated with facioscapulohumeral muscular dystrophy involves a heterochromatin-associated repetitive element: Implications for a role of chromatin structure in the pathogenesis of the disease
-
(1994)
Chromosome Res.
, vol.2
, pp. 225-234
-
-
Winokur, S.T.1
Bengtsson, U.2
Feddersen, J.3
Mathews, K.D.4
Weiffenbach, B.5
Bailey, H.6
Markovich, R.P.7
Murray, J.C.8
Wasmuth, J.J.9
Altherr, M.R.10
Schutte, B.C.11
-
92
-
-
0002001025
-
DNA structure: Implications for chromatin structure and function
-
Elgin, S.C.R. (ed.), Chromatin Structure and Gene Expression IRL Press, Oxford
-
(1995)
, pp. 27-48
-
-
Wolffe, A.P.1
Drew, H.R.2
-
94
-
-
0030297549
-
A specialized nucleosome modulates transcription factor access to a C.glabrata metal responsive promoter
-
(1996)
Cell
, vol.87
, pp. 459-470
-
-
Zhu, Z.1
Thiele, D.J.2
|