-
1
-
-
0028846524
-
Anomalous rapid electrophoretic mobility of DNA containing triplet repeats associated with human disease genes
-
Chastain, P. D., II, Eichler, E. E., Kang, S., Nelson, D. L., Levene, S. D. & Sinden, R. R. (1995). Anomalous rapid electrophoretic mobility of DNA containing triplet repeats associated with human disease genes. Biochemistry, 34, 16125-16131.
-
(1995)
Biochemistry
, vol.34
, pp. 16125-16131
-
-
Chastain P.D. II1
Eichler, E.E.2
Kang, S.3
Nelson, D.L.4
Levene, S.D.5
Sinden, R.R.6
-
2
-
-
0011818677
-
On the origin and nature of achromatic lesions
-
Chaudhuri, J. P. (1972). On the origin and nature of achromatic lesions. Chromosome Today, 3, 147-151.
-
(1972)
Chromosome Today
, vol.3
, pp. 147-151
-
-
Chaudhuri, J.P.1
-
3
-
-
0019888109
-
High sequence specificity of micrococcal nuclease
-
Dingwall, C., Lomonossoff, G. P. & Laskey, R. A. (1981). High sequence specificity of micrococcal nuclease. Nucl. Acids Res. 9, 2659-2673.
-
(1981)
Nucl. Acids Res.
, vol.9
, pp. 2659-2673
-
-
Dingwall, C.1
Lomonossoff, G.P.2
Laskey, R.A.3
-
4
-
-
0028168645
-
Length of uninterrupted CCG repeats determines instability in the FMR-1 gene
-
Eichler, E. E., Holden, J. J. A., Popovich, B. W., Reiss, A. L., Snow, K., Thibodeau, S. N., Richards, C. S., Ward, P. A. & Nelson, D. L. (1994). Length of uninterrupted CCG repeats determines instability in the FMR-1 gene. Nature Genet. 8, 88-94.
-
(1994)
Nature Genet.
, vol.8
, pp. 88-94
-
-
Eichler, E.E.1
Holden, J.J.A.2
Popovich, B.W.3
Reiss, A.L.4
Snow, K.5
Thibodeau, S.N.6
Richards, C.S.7
Ward, P.A.8
Nelson, D.L.9
-
5
-
-
0028886722
-
Population survey of the human FMR1 CGG repeats structure suggests biased polarity for the loss of AGG interruptions
-
Eichler, E. E., Hammond, H. A., MacPherson, J. N., Ward, P. A. & Nelson, D. L. (1995). Population survey of the human FMR1 CGG repeats structure suggests biased polarity for the loss of AGG interruptions. Hum. Mol. Genet. 4, 2199-2208.
-
(1995)
Hum. Mol. Genet.
, vol.4
, pp. 2199-2208
-
-
Eichler, E.E.1
Hammond, H.A.2
MacPherson, J.N.3
Ward, P.A.4
Nelson, D.L.5
-
6
-
-
0026598119
-
An unstable triplet repeat in a gene related to myotonic dystrophy
-
Fu, Y.-H., Pizzuti, A., Fenwick, R. G., Jr, King, J., Rajnarayan, S., Dunne, P. W., Dubel, J., Nasser, G. A., Ashizawa, T., De Jong, P., Wieringa, B., Korneluk, R., Perryman, M. B., Epstein, H. F. & Caskey, C. T. (1992). An unstable triplet repeat in a gene related to myotonic dystrophy. Science, 255, 1256-1258.
-
(1992)
Science
, vol.255
, pp. 1256-1258
-
-
Fu, Y.-H.1
Pizzuti, A.2
Fenwick, R.G.3
King J., Jr.4
Rajnarayan, S.5
Dunne, P.W.6
Dubel, J.7
Nasser, G.A.8
Ashizawa, T.9
De Jong, P.10
Wieringa, B.11
Korneluk, R.12
Perryman, M.B.13
Epstein, H.F.14
Caskey, C.T.15
-
7
-
-
0017869441
-
Electron microscope visualization of chromatin and other DNA-protein complexes
-
Griffith, J. D. & Christiansen, G. (1978). Electron microscope visualization of chromatin and other DNA-protein complexes. Annu. Rev. Biophys. Bioeng. 7, 19-35.
-
(1978)
Annu. Rev. Biophys. Bioeng.
, vol.7
, pp. 19-35
-
-
Griffith, J.D.1
Christiansen, G.2
-
8
-
-
0028133504
-
Precursor arrays for triplet repeat expansion at the fragile X locus
-
Hirst, M. C. Grewal, P. K. & Davies, K. E. (1994). Precursor arrays for triplet repeat expansion at the fragile X locus. Hum. Mol. Genet. 3, 1553-1560.
-
(1994)
Hum. Mol. Genet.
, vol.3
, pp. 1553-1560
-
-
Hirst, M.C.1
Grewal, P.K.2
Davies, K.E.3
-
9
-
-
0027377155
-
High resolution methylation analysis of the FMR-1 gene trinucleotide repeat region in fragile X syndrome
-
Hornstra, I. K., Nelson, D. L., Warren, S. T. & Yang, T. P. (1993). High resolution methylation analysis of the FMR-1 gene trinucleotide repeat region in fragile X syndrome. Hum. Mol. Genet. 2, 1659-1665.
-
(1993)
Hum. Mol. Genet.
, vol.2
, pp. 1659-1665
-
-
Hornstra, I.K.1
Nelson, D.L.2
Warren, S.T.3
Yang, T.P.4
-
10
-
-
0019888118
-
Sequence specific cleavage of DNA by micrococcal nuclease
-
Horz, W. & Altenburger, W. (1981). Sequence specific cleavage of DNA by micrococcal nuclease. Nucl. Acids Res. 9, 2643-2658.
-
(1981)
Nucl. Acids Res.
, vol.9
, pp. 2643-2658
-
-
Horz, W.1
Altenburger, W.2
-
11
-
-
0024297584
-
The terminus of SV40 replication and transcription contains a sharp sequence-directed curve
-
Hsieh, C.-H. & Griffith, J. D. (1988). The terminus of SV40 replication and transcription contains a sharp sequence-directed curve. Cell, 52, 535-544.
-
(1988)
Cell
, vol.52
, pp. 535-544
-
-
Hsieh, C.-H.1
Griffith, J.D.2
-
12
-
-
0028896099
-
Association of a chromosome deletion syndrome with a fragile site within the proto-oncogene CBL2
-
Jones, C., Penny, L., Mattina, T., Yu, S., Baker, E., Voullaire, L., Langdon, W. Y., Sutherland G. R., Richards, R. I. & Tunnacliffe, A. (1995). Association of a chromosome deletion syndrome with a fragile site within the proto-oncogene CBL2. Nature, 376, 145-149.
-
(1995)
Nature
, vol.376
, pp. 145-149
-
-
Jones, C.1
Penny, L.2
Mattina, T.3
Yu, S.4
Baker, E.5
Voullaire, L.6
Langdon, W.Y.7
Sutherland G, R.8
Richards, R.I.9
Tunnacliffe, A.10
-
13
-
-
0027203684
-
Tinucleotide repeat amplification and hypermethylation of a CpG island in FraXE mental retardation
-
Knight, S., Flannery, A. V., Hirst, M. C., Campbell, L., Christodoulou, Z., Phelps, S. R., Pointon, J., Middleton-Price, H. R., Barnicoat, A., Pembrey, M. E., Holland, J., Oostra, B. A., Bobrow, M. & Davies, K. E. (1993). Tinucleotide 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
Holland, J.11
Oostra, B.A.12
Bobrow, M.13
Davies, K.E.14
-
14
-
-
0025800165
-
Mapping of DNA instability at the fragile X to a trinucleotide repeat sequence
-
Kremer, E. J., Pritchard, M., Lynch, M., Yu, S., Holman, K., Baker, E., Warren, S. T., Schlessinger, D., Sutherland, G. R. & Richards, R. I. (1991). Mapping of DNA instability at the fragile X to a trinucleotide repeat sequence. Science, 252, 1711-1718.
-
(1991)
Science
, vol.252
, pp. 1711-1718
-
-
Kremer, E.J.1
Pritchard, M.2
Lynch, M.3
Yu, S.4
Holman, K.5
Baker, E.6
Warren, S.T.7
Schlessinger, D.8
Sutherland, G.R.9
Richards, R.I.10
-
15
-
-
0028360849
-
Cryptic and polar variation of the fragile X repeat could result in predisposing normal alleles
-
Kunst, C. & Warren, S. (1994). Cryptic and polar variation of the Fragile X repeat could result in predisposing normal alleles. Cell, 77, 853-861.
-
(1994)
Cell
, vol.77
, pp. 853-861
-
-
Kunst, C.1
Warren, S.2
-
16
-
-
0026603841
-
Myotonic dystrophy mutation: An unstable CTG repeat in the 3′ untranslated region of the gene
-
Mahadevan, M., Tsilfidis, C., Sabourin, L., Shutler, G., Amemiya, C., Jasen, G., Neville, C., Narang, M., Barcelo, J., O'Hoy, K., Leblond, S., Earle-MacDonald, J., De Jong, P. J., Wieringa, B. & Korneluk, R. G. (1992). Myotonic dystrophy mutation: an unstable CTG repeat in the 3′ untranslated region of the gene. Science, 255, 1253-1255.
-
(1992)
Science
, vol.255
, pp. 1253-1255
-
-
Mahadevan, M.1
Tsilfidis, C.2
Sabourin, L.3
Shutler, G.4
Amemiya, C.5
Jasen, G.6
Neville, C.7
Narang, M.8
Barcelo, J.9
O'Hoy, K.10
Leblond, S.11
Earle-MacDonald, J.12
De Jong, P.J.13
Wieringa, B.14
Korneluk, R.G.15
-
17
-
-
0025179659
-
The human ETS-2 gene promoter: Molecular dissection and nuclease hypersensitivity
-
Mavrothalassitis, G. J., Watson, D. K. & Papas, T. S. (1990). The human ETS-2 gene promoter: molecular dissection and nuclease hypersensitivity. Oncogene, 5, 1337-1342.
-
(1990)
Oncogene
, vol.5
, pp. 1337-1342
-
-
Mavrothalassitis, G.J.1
Watson, D.K.2
Papas, T.S.3
-
18
-
-
0027981933
-
Implication of FRA16A structure for the mechanism of chromosomal fragile site genesis
-
Nancarrow, J. K., Kremer, E., Holman, K., Eyre, H., Doggett, N. A., Paslier, D. L., Callen, D. F., Sutherland, G. R. & Richards, R. I. (1994). Implication of FRA16A structure for the mechanism of chromosomal fragile site genesis. Science, 264, 1938-1941.
-
(1994)
Science
, vol.264
, pp. 1938-1941
-
-
Nancarrow, J.K.1
Kremer, E.2
Holman, K.3
Eyre, H.4
Doggett, N.A.5
Paslier, D.L.6
Callen, D.F.7
Sutherland, G.R.8
Richards, R.I.9
-
20
-
-
0029242153
-
The fragile X syndromes
-
Nelson, D. L. (1995). The fragile X syndromes. Seminars Cell Biol. 6, 5-11.
-
(1995)
Seminars Cell Biol.
, vol.6
, pp. 5-11
-
-
Nelson, D.L.1
-
21
-
-
0028099702
-
Isolation of a GCC repeat showing expansion in FRAXAF, a fragile site distal to FRAXA and FRAXE
-
Parrish, J. E., Oostra, B. A., Verkerk, A. J. M. H., Richards, C. S., Reynolds, J., Spikes, A. S., Shaffer, L. G. & Nelson, D. L. (1994). Isolation of a GCC repeat showing expansion in FRAXAF, a fragile site distal to FRAXA and FRAXE. Nature Genet. 8, 229-235.
-
(1994)
Nature Genet.
, vol.8
, pp. 229-235
-
-
Parrish, J.E.1
Oostra, B.A.2
Verkerk, A.J.M.H.3
Richards, C.S.4
Reynolds, J.5
Spikes, A.S.6
Shaffer, L.G.7
Nelson, D.L.8
-
22
-
-
0028197078
-
Frequency and stability of the fragile X syndrome
-
Reiss, A. L., Kazazian, H. H., Jr, Krebs, C. M., McAughan, A., Boehm, C. D., Abrams, M. T. & Nelson, D. L. (1994). Frequency and stability of the fragile X syndrome. Hum. Mol. Genet. 3, 393-398.
-
(1994)
Hum. Mol. Genet.
, vol.3
, pp. 393-398
-
-
Reiss, A.L.1
Kazazian H.H., Jr.2
Krebs, C.M.3
McAughan, A.4
Boehm, C.D.5
Abrams, M.T.6
Nelson, D.L.7
-
23
-
-
0018372296
-
Nucleosome cores reconstituted from poly (dA-dT) and the octamer of histones
-
Rhodes, D. (1979). Nucleosome cores reconstituted from poly (dA-dT) and the octamer of histones. Nucl. Acids Res. 6, 1805-1816.
-
(1979)
Nucl. Acids Res.
, vol.6
, pp. 1805-1816
-
-
Rhodes, D.1
-
24
-
-
0018460380
-
Chromatin and core particles formed from the inner histones and synthetic polydeoxyribonucleotides of defined sequence
-
Simpson, R. T. & Kanzler, P. (1979). Chromatin and core particles formed from the inner histones and synthetic polydeoxyribonucleotides of defined sequence. Nucl. Acids Res. 6, 1387-1415.
-
(1979)
Nucl. Acids Res.
, vol.6
, pp. 1387-1415
-
-
Simpson, R.T.1
Kanzler, P.2
-
25
-
-
0022637302
-
Chromatin structure of the human dihydrofolate reductase gene promoter
-
Shimada, T., Inokuchi, K. & Nienhuis, A. W. (1986). Chromatin structure of the human dihydrofolate reductase gene promoter. J. Biol. Chem. 261, 1445-145.
-
(1986)
J. Biol. Chem.
, vol.261
, pp. 1445-2145
-
-
Shimada, T.1
Inokuchi, K.2
Nienhuis, A.W.3
-
26
-
-
0029983269
-
Cloning, characterization, and properties of plasmids containing CGG triplet repeats from the FMR-1 gene
-
Shimizu, M., Gellibolian, R. Oostra, B. A. & Wells, R. D. (1996). Cloning, characterization, and properties of plasmids containing CGG triplet repeats from the FMR-1 gene. J. Mol. Biol. 258, 614-626.
-
(1996)
J. Mol. Biol.
, vol.258
, pp. 614-626
-
-
Shimizu, M.1
Gellibolian, R.2
Oostra, B.A.3
Wells, R.D.4
-
27
-
-
0028074287
-
Sequence analysis of the fragile X trinucleotide repeat: Implications for the origin of the fragile X mutation
-
Snow, K., Tester, D. J., Kruckeberg, K. E. Schaid, D. J. & Thibodeau, S. N. (1994). Sequence analysis of the fragile X trinucleotide repeat: implications for the origin of the fragile X mutation. Hum. Mol. Genet. 3, 1543-1551.
-
(1994)
Hum. Mol. Genet.
, vol.3
, pp. 1543-1551
-
-
Snow, K.1
Tester, D.J.2
Kruckeberg, K.E.3
Schaid, D.J.4
Thibodeau, S.N.5
-
28
-
-
44949275580
-
Chromosomal fragile sites
-
Sutherland, G. R. (1991). Chromosomal fragile sites. GATA, 8, 161-166.
-
(1991)
GATA
, vol.8
, pp. 161-166
-
-
Sutherland, G.R.1
-
29
-
-
0028997643
-
Simple tandem DNA repeats and human genetic disease
-
Sutherland, G. R. & Richards, R. I. (1995). Simple tandem DNA repeats and human genetic disease. Proc. Natl Acad. Sci. USA, 92, 3636-3641.
-
(1995)
Proc. Natl Acad. Sci. USA
, vol.92
, pp. 3636-3641
-
-
Sutherland, G.R.1
Richards, R.I.2
-
30
-
-
0025905795
-
Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome
-
Verkerk, A. J. M. H., Pieretti, M., Sutcliffe, J. S., Fu, Y.-H., Kuhl, D. P. A., Pizzuti, A., Reiner, O., Richards, S., Victoria, M. F., Zhang, F., Eussen, B. E., van Ommen, G.-J. B., Blonden, L. A. J., Riggins, G. J., Chastain, J. L., Kunst, C. B., Galaard, H., Caskey, C. T., Nelson, D. L., Oostra, B. A. & Warren, S. T. (1991). Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome. Cell, 65, 905-914.
-
(1991)
Cell
, vol.65
, pp. 905-914
-
-
Verkerk, A.J.M.H.1
Pieretti, M.2
Sutcliffe, J.S.3
Fu, Y.-H.4
Kuhl, D.P.A.5
Pizzuti, A.6
Reiner, O.7
Richards, S.8
Victoria, M.F.9
Zhang, F.10
Eussen, B.E.11
Van Ommen, G.-J.B.12
Blonden, L.A.J.13
Riggins, G.J.14
Chastain, J.L.15
Kunst, C.B.16
Galaard, H.17
Caskey, C.T.18
Nelson, D.L.19
Oostra, B.A.20
Warren, S.T.21
more..
-
31
-
-
0028932050
-
Expanded CTG triplet blocks from the myotonic dystrophy gene create the strongest known natural nucleosome positioning elements
-
Wang, Y.-H. & Griffith, J. D. (1995). Expanded CTG triplet blocks from the myotonic dystrophy gene create the strongest known natural nucleosome positioning elements. Genomics, 25, 570-573.
-
(1995)
Genomics
, vol.25
, pp. 570-573
-
-
Wang, Y.-H.1
Griffith, J.D.2
-
32
-
-
0029664913
-
The [(G/C)3NN]n motif: A common DNA repeat that excludes nucleosomes
-
Wang, Y.-H. & Griffith, J. D. (1996a). The [(G/C)3NN]n motif: a common DNA repeat that excludes nucleosomes. Proc. Natl Acad. Sci. USA. 93, 8863-8867.
-
(1996)
Proc. Natl Acad. Sci. USA.
, vol.93
, pp. 8863-8867
-
-
Wang, Y.-H.1
Griffith, J.D.2
-
33
-
-
0029790784
-
Methylation of expanded CCG triplet repeat DNA from fragile X syndrome patients enhances nucleosome exclusion
-
In the press
-
Wang, Y.-H. & Griffith, J. D. (1996b). Methylation of expanded CCG triplet repeat DNA from fragile X syndrome patients enhances nucleosome exclusion. J. Biol. Chem. In the press.
-
(1996)
J. Biol. Chem.
-
-
Wang, Y.-H.1
Griffith, J.D.2
-
34
-
-
0027941198
-
Preferential nucleosome assembly at DNA triplet repeats from the myotonic dystrophy gene
-
Wang, Y.-H., Amirhaeri, S., Kang, S., Wells, R. D. & Griffith, J. D. (1994). Preferential nucleosome assembly at DNA triplet repeats from the myotonic dystrophy gene. Science, 265, 669-671.
-
(1994)
Science
, vol.265
, pp. 669-671
-
-
Wang, Y.-H.1
Amirhaeri, S.2
Kang, S.3
Wells, R.D.4
Griffith, J.D.5
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