-
1
-
-
0028878844
-
Stability of an expanded trinucleotide repeat in the androgen receptor gene in transgenic mice
-
Bingham, P. M., M. O. Scott, S. Wang, M. J. McPhaul, E. M. Wilson, J. Y. Garbern, D. E. Merry, and K. H. Fischbeck. 1995. Stability of an expanded trinucleotide repeat in the androgen receptor gene in transgenic mice. Nat. Genet. 9:191-196.
-
(1995)
Nat. Genet.
, vol.9
, pp. 191-196
-
-
Bingham, P.M.1
Scott, M.O.2
Wang, S.3
McPhaul, M.J.4
Wilson, E.M.5
Garbern, J.Y.6
Merry, D.E.7
Fischbeck, K.H.8
-
3
-
-
0025219753
-
Mismatch repair-induced meiotic recombination requires the pms1 gene product
-
Borts, R. H., W. Y. Leung, W. Kramer, B. Kramer, M. Williamson, S. Fogel, and J. E. Haber. 1990. Mismatch repair-induced meiotic recombination requires the pms1 gene product. Genetics 124:573-584.
-
(1990)
Genetics
, vol.124
, pp. 573-584
-
-
Borts, R.H.1
Leung, W.Y.2
Kramer, W.3
Kramer, B.4
Williamson, M.5
Fogel, S.6
Haber, J.E.7
-
4
-
-
0031000629
-
A yeast replicative helicase, Dna2 helicase, interacts with yeast FEN-1 nuclease in carrying out its function
-
Budd, M. E., and J. L. Campbell. 1997. A yeast replicative helicase, Dna2 helicase, interacts with yeast FEN-1 nuclease in carrying out its function. Mol. Cell. Biol. 17:2136-2142.
-
(1997)
Mol. Cell. Biol.
, vol.17
, pp. 2136-2142
-
-
Budd, M.E.1
Campbell, J.L.2
-
5
-
-
0026751517
-
Analysis of full fragile X mutations in fetal tissues and monozygotic twins indicate that abnormal methylation and somatic heterogeneity are established early in development
-
Devys, D., V. Biancalana, F. Rousseau, J. Boue, J. L. Mandel, and I. Oberle. 1992. Analysis of full fragile X mutations in fetal tissues and monozygotic twins indicate that abnormal methylation and somatic heterogeneity are established early in development. Am. J. Med. Genet. 43:208-216.
-
(1992)
Am. J. Med. Genet.
, vol.43
, pp. 208-216
-
-
Devys, D.1
Biancalana, V.2
Rousseau, F.3
Boue, J.4
Mandel, J.L.5
Oberle, I.6
-
6
-
-
0030601348
-
Tosca: A Drosophila gene encoding a nuclease specifically expressed in the female germline
-
Digilio, F. A., A. Pannuti, J. C. Lucchesi, M. Furia, and L. C. Polito. 1996. Tosca: a Drosophila gene encoding a nuclease specifically expressed in the female germline. Dev. Biol. 178:90-100.
-
(1996)
Dev. Biol.
, vol.178
, pp. 90-100
-
-
Digilio, F.A.1
Pannuti, A.2
Lucchesi, J.C.3
Furia, M.4
Polito, L.C.5
-
7
-
-
0028168645
-
Length of uninterrupted CGG repeats determines instability in the FMR1 gene
-
Eichler, E., J. Holden, B. Popovich, A. Reiss, K. Snow, S. Thibodeau, C. Richards, P. Ward, and D. Nelson. 1994. Length of uninterrupted CGG repeats determines instability in the FMR1 gene. Nat. Genet. 8:88-94.
-
(1994)
Nat. Genet.
, vol.8
, pp. 88-94
-
-
Eichler, E.1
Holden, J.2
Popovich, B.3
Reiss, A.4
Snow, K.5
Thibodeau, S.6
Richards, C.7
Ward, P.8
Nelson, D.9
-
8
-
-
0031961248
-
The yeast HSM3 gene acts in one of the mismatch repair pathways
-
Fedorova, I. V., L. M. Gracheva, S. V. Kovaltzova, T. A. Evstuhina, S. Y. Alekseev, and V. G. Korolev. 1998. The yeast HSM3 gene acts in one of the mismatch repair pathways. Genetics 148:963-973.
-
(1998)
Genetics
, vol.148
, pp. 963-973
-
-
Fedorova, I.V.1
Gracheva, L.M.2
Kovaltzova, S.V.3
Evstuhina, T.A.4
Alekseev, S.Y.5
Korolev, V.G.6
-
9
-
-
0028969636
-
The fragile X premutation in carriers and its effect on mutation size in offspring
-
Fisch, G. S., K. Snow, S. N. Thibodeau, M. Chalifaux, J. J. Holden, D. L. Nelson, P. N. Howard-Peebles, and A. Maddalena. 1995. The fragile X premutation in carriers and its effect on mutation size in offspring. Am. J. Hum. Genet. 56:1147-1155.
-
(1995)
Am. J. Hum. Genet.
, vol.56
, pp. 1147-1155
-
-
Fisch, G.S.1
Snow, K.2
Thibodeau, S.N.3
Chalifaux, M.4
Holden, J.J.5
Nelson, D.L.6
Howard-Peebles, P.N.7
Maddalena, A.8
-
10
-
-
0032488872
-
Expansion and length dependent fragility of CTG repeats in yeast
-
Freudenreich, C. H., S. M. Kantrow, and V. A. Zakian. 1998. Expansion and length dependent fragility of CTG repeats in yeast. Science 279:853-856.
-
(1998)
Science
, vol.279
, pp. 853-856
-
-
Freudenreich, C.H.1
Kantrow, S.M.2
Zakian, V.A.3
-
11
-
-
0029975070
-
Stability of microsatellites and minisatellites in Bloom syndrome, a human syndrome of genetic instability
-
Foucault, F., J. Buard, F. Praz, C. Jaulin, D. Stoppa-Lyonnet, G. Vergnaud, and M. Amor-Gueret. 1996. Stability of microsatellites and minisatellites in Bloom syndrome, a human syndrome of genetic instability. Mutat. Res. 362:227-236.
-
(1996)
Mutat. Res.
, vol.362
, pp. 227-236
-
-
Foucault, F.1
Buard, J.2
Praz, F.3
Jaulin, C.4
Stoppa-Lyonnet, D.5
Vergnaud, G.6
Amor-Gueret, M.7
-
12
-
-
84967842681
-
Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox
-
Fu, Y., D. Kuhl, A. Pizzuti, M. Piereti, J. Sutcliffe, S. Richards, A. Verkerk, J. Holden, R. Fenwick, S. Warren, B. Oostra, D. Nelson, and C. Caskey. 1991. Variation of the CGG repeat at the fragile X site results in genetic instability: resolution of the Sherman paradox. Cell 61:1-20.
-
(1991)
Cell
, vol.61
, pp. 1-20
-
-
Fu, Y.1
Kuhl, D.2
Pizzuti, A.3
Piereti, M.4
Sutcliffe, J.5
Richards, S.6
Verkerk, A.7
Holden, J.8
Fenwick, R.9
Warren, S.10
Oostra, B.11
Nelson, D.12
Caskey, C.13
-
13
-
-
0029053371
-
Trinucleotide repeats that expand in human disease from hairpin structures in vitro
-
Gacy, A. M., G. Goellner, N. Juranic, S. Macura, and C. T. McMurray. 1995. Trinucleotide repeats that expand in human disease from hairpin structures in vitro. Cell 81:533-540.
-
(1995)
Cell
, vol.81
, pp. 533-540
-
-
Gacy, A.M.1
Goellner, G.2
Juranic, N.3
Macura, S.4
McMurray, C.T.5
-
14
-
-
0028954118
-
Studies on the transformation of intact yeast cells by the LiAc/SS-DNA/PEG procedure
-
Gietz, R. D., R. H. Schiestl, A. R. Willems, and R. A. Woods. 1995. Studies on the transformation of intact yeast cells by the LiAc/SS-DNA/PEG procedure. Yeast 11:355-360.
-
(1995)
Yeast
, vol.11
, pp. 355-360
-
-
Gietz, R.D.1
Schiestl, R.H.2
Willems, A.R.3
Woods, R.A.4
-
15
-
-
0029744342
-
Nucleosome assembly on methylated CGG triplet repeats in the fragile X mental retardation gene 1 promoter
-
Godde, J. S., S. U. Kass, M. C. Hirst, and A. P. Wolffe. 1996. Nucleosome assembly on methylated CGG triplet repeats in the fragile X mental retardation gene 1 promoter. J. Biol. Chem. 271:24325-24328.
-
(1996)
J. Biol. Chem.
, vol.271
, pp. 24325-24328
-
-
Godde, J.S.1
Kass, S.U.2
Hirst, M.C.3
Wolffe, A.P.4
-
16
-
-
17544367055
-
Nucleosome assembly on CTG triplet repeats
-
Godde, J. S., and A. P. Wolffe. 1996. Nucleosome assembly on CTG triplet repeats. J. Biol. Chem. 271:15222-15229.
-
(1996)
J. Biol. Chem.
, vol.271
, pp. 15222-15229
-
-
Godde, J.S.1
Wolffe, A.P.2
-
17
-
-
9044229711
-
Absence of disease phenotype and intergenerational stability of the CAG repeat in transgenic mice expressing the human Huntington disease transcript
-
Goldberg, Y. P., M. A. Kalchman, M. Metzler, J. Nasir, J. Zeisler, R. Graham, H. B. Koide, J. O'Kusky, A. H. Sharp, C. A. Ross, F. Jirik, and M. R. Hayden. 1996. Absence of disease phenotype and intergenerational stability of the CAG repeat in transgenic mice expressing the human Huntington disease transcript. Hum. Mol. Genet. 5:177-185.
-
(1996)
Hum. Mol. Genet.
, vol.5
, pp. 177-185
-
-
Goldberg, Y.P.1
Kalchman, M.A.2
Metzler, M.3
Nasir, J.4
Zeisler, J.5
Graham, R.6
Koide, H.B.7
O'Kusky, J.8
Sharp, A.H.9
Ross, C.A.10
Jirik, F.11
Hayden, M.R.12
-
19
-
-
0031038809
-
Moderate integenerational and somatic instability of a 55-CTG repeat in transgenic mice
-
Gourdon, G., F. Radvanyi, A. S. Lia, C. Duros. M. Blanche, M. Abitbol, C. Junien, and H. Hofmann-Radvanyi. 1997. Moderate integenerational and somatic instability of a 55-CTG repeat in transgenic mice. Nat. Genet. 15:190-192.
-
(1997)
Nat. Genet.
, vol.15
, pp. 190-192
-
-
Gourdon, G.1
Radvanyi, F.2
Lia, A.S.3
Duros, C.4
Blanche, M.5
Abitbol, M.6
Junien, C.7
Hofmann-Radvanyi, H.8
-
20
-
-
0027051362
-
Bloom's syndrome. XVIII. Hypermutability at a tandem repeat locus
-
Groden, J., and J. German. 1992. Bloom's syndrome. XVIII. Hypermutability at a tandem repeat locus. Hum. Genet. 90:360-367.
-
(1992)
Hum. Genet.
, vol.90
, pp. 360-367
-
-
Groden, J.1
German, A.J.2
-
21
-
-
0026951222
-
Methylation analysis of CGG sites in the CpG island of the human FMR1 gene
-
Hansen, R. S., S. M. Gartler, C. R. Scott, S. H. Chen, and C. D. Laird. 1992. Methylation analysis of CGG sites in the CpG island of the human FMR1 gene. Hum. Mol. Genet. 1:571-578.
-
(1992)
Hum. Mol. Genet.
, vol.1
, pp. 571-578
-
-
Hansen, R.S.1
Gartler, S.M.2
Scott, C.R.3
Chen, S.H.4
Laird, C.D.5
-
22
-
-
0026462708
-
Inheritance of the fragile X syndrome: Size of the fragile X premutation is a major determinant of the transition to full mutation
-
Heitz, D., D. Devys, G. Imbert, C. Kretz, and J. L. Mandel. 1992. Inheritance of the fragile X syndrome: size of the fragile X premutation is a major determinant of the transition to full mutation. J. Med. Genet. 29:794-801.
-
(1992)
J. Med. Genet.
, vol.29
, pp. 794-801
-
-
Heitz, D.1
Devys, D.2
Imbert, G.3
Kretz, C.4
Mandel, J.L.5
-
23
-
-
0026769505
-
Instability of simple sequence DNA in Saccharomyces cerevisiae
-
Henderson, S. T., and T. D. Petes. 1992. Instability of simple sequence DNA in Saccharomyces cerevisiae. Mol. Cell. Biol. 12:2749-2757.
-
(1992)
Mol. Cell. Biol.
, vol.12
, pp. 2749-2757
-
-
Henderson, S.T.1
Petes, T.D.2
-
24
-
-
0028917961
-
Sequence of human FEN-1, a structure specific endonuclease, and chromosomal localisation of the gene (FEN1) in mouse and human
-
Hiraoka, L., J. J. Harrington, D. S. Gerhard, M. R. Lieber, and C.-L. Hseih. 1995. Sequence of human FEN-1, a structure specific endonuclease, and chromosomal localisation of the gene (FEN1) in mouse and human. Genomics 25:220-225.
-
(1995)
Genomics
, vol.25
, pp. 220-225
-
-
Hiraoka, L.1
Harrington, J.J.2
Gerhard, D.S.3
Lieber, M.R.4
Hseih, C.-L.5
-
25
-
-
0028133504
-
Precursor arrays for triplet repeat expansion at the fragile X locus
-
Hirst, M., P. Grewal, and K. Davies. 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.1
Grewal, P.2
Davies, K.3
-
26
-
-
0032524466
-
Cloned human FMR1 trinucleotide repeats exhibit a length- And orientation-dependent instability suggestive of in vivo lagging strand secondary structure
-
Hirst, M. C., and P. J. White. 1998. Cloned human FMR1 trinucleotide repeats exhibit a length- and orientation-dependent instability suggestive of in vivo lagging strand secondary structure. Nucleic Acids Res. 26:2353-2358.
-
(1998)
Nucleic Acids Res.
, vol.26
, pp. 2353-2358
-
-
Hirst, M.C.1
White, P.J.2
-
28
-
-
0029982353
-
In vitro expansion of GGC:GCC repeats: Identification of the preferred strand of expansion
-
Ji, J., N. J. Clegg, K. R. Petersen, A. L. Jackson, C. D. Laird, and L. A. Loeb. 1996. In vitro expansion of GGC:GCC repeats: identification of the preferred strand of expansion. Nucleic Acids Res. 24:2835-2840.
-
(1996)
Nucleic Acids Res.
, vol.24
, pp. 2835-2840
-
-
Ji, J.1
Clegg, N.J.2
Petersen, K.R.3
Jackson, A.L.4
Laird, C.D.5
Loeb, L.A.6
-
29
-
-
0029039868
-
Requirement of the yeast RTH1 5′ = 3′ exonuclease for the stability of simple repetitive DNA
-
Johnson, R. E., G. K. Kovvali, L. Prakash, and S. Prakash. 1995. Requirement of the yeast RTH1 5′ = 3′ exonuclease for the stability of simple repetitive DNA. Science 269:238-240.
-
(1995)
Science
, vol.269
, pp. 238-240
-
-
Johnson, R.E.1
Kovvali, G.K.2
Prakash, L.3
Prakash, S.4
-
30
-
-
0028807448
-
Pausing of DNA synthesis in vitro at specific loci in CTG and CGG triplet repeats from human hereditary disease genes
-
Kang, S., K. Ohshima, M. Shimizu, S. Amirhaeri, and R. D. Wells. 1995. Pausing of DNA synthesis in vitro at specific loci in CTG and CGG triplet repeats from human hereditary disease genes. J. Biol. Chem. 270:27014-27021.
-
(1995)
J. Biol. Chem.
, vol.270
, pp. 27014-27021
-
-
Kang, S.1
Ohshima, K.2
Shimizu, M.3
Amirhaeri, S.4
Wells, R.D.5
-
31
-
-
0029784320
-
Biochemistry and genetics of eukaryotic mismatch repair
-
Kolodner, R. 1996. Biochemistry and genetics of eukaryotic mismatch repair. Genes Dev. 10:1433-1442.
-
(1996)
Genes Dev.
, vol.10
, pp. 1433-1442
-
-
Kolodner, R.1
-
32
-
-
0030957997
-
Second pathway for completion of human DNA base-excision-repair: Reconstitution with purified proteins and requirement for DNase IV (FEN1)
-
Klungland, A., and T. Lindahl. 1997. Second pathway for completion of human DNA base-excision-repair: reconstitution with purified proteins and requirement for DNase IV (FEN1). EMBO J. 16:3341-3348.
-
(1997)
EMBO J.
, vol.16
, pp. 3341-3348
-
-
Klungland, A.1
Lindahl, T.2
-
33
-
-
0031953438
-
Destabilisation of yeast micro- And mini-satellite DNa sequences by mutations affecting a nuclease involved in Okazaki fragment processing (rad27) and DNa polymerase δ (pol3-t)
-
Kokoska, R. J., L. Stefanovic, H. P. Tran, M. A. Resnick, D. A. Gordenin, and T. D. Petes. 1998. Destabilisation of yeast micro- and mini-satellite DNA sequences by mutations affecting a nuclease involved in Okazaki fragment processing (rad27) and DNA polymerase δ (pol3-t). Mol. Cell. Biol. 18:2779-2788.
-
(1998)
Mol. Cell. Biol.
, vol.18
, pp. 2779-2788
-
-
Kokoska, R.J.1
Stefanovic, L.2
Tran, H.P.3
Resnick, M.A.4
Gordenin, D.A.5
Petes, T.D.6
-
34
-
-
0031471659
-
Mutator specificity and disease: Looking over the FENce
-
Kunkel, T. A., M. A. Resnick, and D. A. Gordenin. 1997. Mutator specificity and disease: looking over the FENce. Cell 88:155-158.
-
(1997)
Cell
, vol.88
, pp. 155-158
-
-
Kunkel, T.A.1
Resnick, M.A.2
Gordenin, D.A.3
-
35
-
-
0028360849
-
Cryptic and polar variation of the fragile X repeat could result in predisposing normal alleles
-
Kunst, C., and S. Warren. 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
-
37
-
-
0031104841
-
The FEN-1 family of structure specific nucleases in eukaryotic DNA replication, recombination and repair
-
Lieber, M. R. 1997. The FEN-1 family of structure specific nucleases in eukaryotic DNA replication, recombination and repair. Bioessays 19:233-240.
-
(1997)
Bioessays
, vol.19
, pp. 233-240
-
-
Lieber, M.R.1
-
38
-
-
0031045874
-
Characterization of the full fragile X syndrome mutation in fetal gametes
-
Malter, H. E., J. C. Iber, R. Willemsen, E. de Graaff, J. C. Tarleton, J. Leisti, S. T. Warren, and B. A. Oostra. 1997. Characterization of the full fragile X syndrome mutation in fetal gametes. Nat. Genet. 15:165-169.
-
(1997)
Nat. Genet.
, vol.15
, pp. 165-169
-
-
Malter, H.E.1
Iber, J.C.2
Willemsen, R.3
De Graaff, E.4
Tarleton, J.C.5
Leisti, J.6
Warren, S.T.7
Oostra, B.A.8
-
39
-
-
0031056685
-
Instability of highly expanded CAG repeats in mice transgenic for the Huntington's disease mutation
-
Mangiarini, L., K. Sathasivam, A. Mahal, R. Mott, M. Seller, and G. P. Bates. 1997. Instability of highly expanded CAG repeats in mice transgenic for the Huntington's disease mutation. Nat. Genet. 15:197-200.
-
(1997)
Nat. Genet.
, vol.15
, pp. 197-200
-
-
Mangiarini, L.1
Sathasivam, K.2
Mahal, A.3
Mott, R.4
Seller, M.5
Bates, G.P.6
-
40
-
-
0029958255
-
Orientation dependence of trinucleotide CAG repeat instability in Saccharomyces cerevisiae
-
Maurer, D. J., B. L. O'Callaghan, and D. M. Livingston. 1996. Orientation dependence of trinucleotide CAG repeat instability in Saccharomyces cerevisiae. Mol. Cell. Biol. 16:6617-6622.
-
(1996)
Mol. Cell. Biol.
, vol.16
, pp. 6617-6622
-
-
Maurer, D.J.1
O'Callaghan, B.L.2
Livingston, D.M.3
-
41
-
-
0028857157
-
Mechanisms of DNA expansion
-
McMurray, C. T. 1995. Mechanisms of DNA expansion. Chromosoma 104: 2-13.
-
(1995)
Chromosoma
, vol.104
, pp. 2-13
-
-
McMurray, C.T.1
-
42
-
-
0030991670
-
Characterisation of a novel DNA damage inducible gene of Saccharomyces cerevisiae, DIN7, which is a structural homolog of the RAD2 and RAD27 DNA repair genes
-
Mieczkowski, P. A., M. U. Fikus, and Z. Ciesla. 1997. Characterisation of a novel DNA damage inducible gene of Saccharomyces cerevisiae, DIN7, which is a structural homolog of the RAD2 and RAD27 DNA repair genes. Mol. Gen. Genet. 253:655-665.
-
(1997)
Mol. Gen. Genet.
, vol.253
, pp. 655-665
-
-
Mieczkowski, P.A.1
Fikus, M.U.2
Ciesla, Z.3
-
43
-
-
0030737538
-
Trinucleotide repeats associated with human disease
-
Mitas, M. 1997. Trinucleotide repeats associated with human disease. Nucleic Acids Res. 25:2245-2253.
-
(1997)
Nucleic Acids Res.
, vol.25
, pp. 2245-2253
-
-
Mitas, M.1
-
44
-
-
0031054076
-
Hypermutable myotonic dystrophy CTG repeats in transgenic mice
-
Monckton, D. G., M. I. Coolbaugh, K. T. Ashizawa, M. J. Siciliano, and C. T. Caskey. 1997. Hypermutable myotonic dystrophy CTG repeats in transgenic mice. Nat. Genet. 15:193-196.
-
(1997)
Nat. Genet.
, vol.15
, pp. 193-196
-
-
Monckton, D.G.1
Coolbaugh, M.I.2
Ashizawa, K.T.3
Siciliano, M.J.4
Caskey, C.T.5
-
45
-
-
0030833799
-
Transition from premutation to full mutation in fragile X syndrome is likely to be prezygotic
-
Moutou, C., M. C. Vincent, V. Biancalana, and J. L. Mandel. 1997. Transition from premutation to full mutation in fragile X syndrome is likely to be prezygotic. Hum. Mol. Genet. 6:971-979.
-
(1997)
Hum. Mol. Genet.
, vol.6
, pp. 971-979
-
-
Moutou, C.1
Vincent, M.C.2
Biancalana, V.3
Mandel, J.L.4
-
46
-
-
85038154464
-
-
Personal communication
-
44a. Newton, C. Personal communication.
-
-
-
Newton, C.1
-
47
-
-
0026339303
-
Instability of a 550bp DNA fragment and abnormal methylation in fragile X syndrome
-
Oberlé, I., F. Rousseau, D. Heitz, C. Kretz, D. Devys, A. Hanauer, J. Boue, M. Bertheas, and J. Mandel. 1991. Instability of a 550bp DNA fragment and abnormal methylation in fragile X syndrome. Science 252:1097-1102.
-
(1991)
Science
, vol.252
, pp. 1097-1102
-
-
Oberlé, I.1
Rousseau, F.2
Heitz, D.3
Kretz, C.4
Devys, D.5
Hanauer, A.6
Boue, J.7
Bertheas, M.8
Mandel, J.9
-
48
-
-
0030752987
-
Human MSH2 binds to trinucleotide repeat DNA structures associated with neurodegenerative disease
-
Pearson, C. E., A. Ewel, S. Acharya, R. A. Fishel, and R. R. Sinden. 1997. Human MSH2 binds to trinucleotide repeat DNA structures associated with neurodegenerative disease. Hum. Mol. Genet. 6:1117-1123.
-
(1997)
Hum. Mol. Genet.
, vol.6
, pp. 1117-1123
-
-
Pearson, C.E.1
Ewel, A.2
Acharya, S.3
Fishel, R.A.4
Sinden, R.R.5
-
49
-
-
0025833298
-
Absence of expression of the FMR1 gene in fragile X patients
-
Pierreti, M., F. Zhang, Y. Fu, S. Warren, B. Oostra, C. Caskey, and D. Nelson. 1991. Absence of expression of the FMR1 gene in fragile X patients. Cell 66:817-822.
-
(1991)
Cell
, vol.66
, pp. 817-822
-
-
Pierreti, M.1
Zhang, F.2
Fu, Y.3
Warren, S.4
Oostra, B.5
Caskey, C.6
Nelson, D.7
-
50
-
-
0028890919
-
Characterization of a mutant strain of Saccharomyces cerevisiae with a deletion of the RAD27 gene, a structural homolog of the RAD2 nucleotide excision repair gene
-
Reagan, M. S., C. Pittenger, W. Siede, and E. C. Friedberg. 1995. Characterization of a mutant strain of Saccharomyces cerevisiae with a deletion of the RAD27 gene, a structural homolog of the RAD2 nucleotide excision repair gene. J. Bacteriol. 177:364-371.
-
(1995)
J. Bacteriol.
, vol.177
, pp. 364-371
-
-
Reagan, M.S.1
Pittenger, C.2
Siede, W.3
Friedberg, E.C.4
-
51
-
-
0027288903
-
The full mutation in the FMR-1 gene of male fragile X patients is absent in their sperm
-
Reyniers, E., L. Vits, K. De Boulle, B. Van Roy, D. Van Velzen, E. de Graaff, A. J. Verkerk, H. Z. Jorens, J. K. Darby, B. Oostra, et al. 1993. The full mutation in the FMR-1 gene of male fragile X patients is absent in their sperm. Nat. Genet. 4:143-146.
-
(1993)
Nat. Genet.
, vol.4
, pp. 143-146
-
-
Reyniers, E.1
Vits, L.2
De Boulle, K.3
Van Roy, B.4
Van Velzen, D.5
De Graaff, E.6
Verkerk, A.J.7
Jorens, H.Z.8
Darby, J.K.9
Oostra, B.10
-
52
-
-
0028242797
-
Simple repeat DNA is not replicated simply
-
Richards, R. I., and G. S. Sutherland. 1994. Simple repeat DNA is not replicated simply. Nat. Genet. 6:114-116.
-
(1994)
Nat. Genet.
, vol.6
, pp. 114-116
-
-
Richards, R.I.1
Sutherland, G.S.2
-
53
-
-
0030664357
-
Dynamic mutations: Possible mechanisms and significance in human disease
-
Richards, R. I., and G. S. Sutherland, 1997. Dynamic mutations: possible mechanisms and significance in human disease. Trends Biochem. Sci. 22: 432-435.
-
(1997)
Trends Biochem. Sci.
, vol.22
, pp. 432-435
-
-
Richards, R.I.1
Sutherland, G.S.2
-
54
-
-
0030725454
-
Trinucleotide repeats affect DNA replication in vivo
-
Samadashwily, G. M., R. Raca, and S. M. Mirkin. 1997. Trinucleotide repeats affect DNA replication in vivo. Nat. Genet. 17:298-304.
-
(1997)
Nat. Genet.
, vol.17
, pp. 298-304
-
-
Samadashwily, G.M.1
Raca, R.2
Mirkin, S.M.3
-
55
-
-
0031057683
-
Destabilisation of CAG trinucleotide repeat tracts by mismatch repair mutations in yeast
-
Schweitzer, J. K., and D. M. Livingston. 1997. Destabilisation of CAG trinucleotide repeat tracts by mismatch repair mutations in yeast. Hum. Mol. Genet. 6:349-355.
-
(1997)
Hum. Mol. Genet.
, vol.6
, pp. 349-355
-
-
Schweitzer, J.K.1
Livingston, D.M.2
-
56
-
-
0031965224
-
Expansions of CAG repeat tracts are frequent in a yeast mutant defective in Okazaki fragment maturation
-
Schweitzer, J. K., and D. M. Livingston. 1998. Expansions of CAG repeat tracts are frequent in a yeast mutant defective in Okazaki fragment maturation. Hum. Mol. Genet. 7:69-74.
-
(1998)
Hum. Mol. Genet.
, vol.7
, pp. 69-74
-
-
Schweitzer, J.K.1
Livingston, D.M.2
-
57
-
-
0029983269
-
Cloning, characterisation and properties of CGG triplet repeats from the FMR-1 gene
-
Shimizu, M., R. Gellibolian, B. A. Oostra, and R. D. Wells. 1996. Cloning, characterisation and properties of 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
-
58
-
-
0028074287
-
Sequence analysis of the fragile X trinucleotide repeat: Implications for the origin of the fragile X mutation
-
Snow, K., D. Tester, K. Kruckeberg, D. Schaid, and S. Thibodeau. 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.2
Kruckeberg, K.3
Schaid, D.4
Thibodeau, S.5
-
59
-
-
0028947298
-
Conditional lethality of null mutations in RTH1 that encodes the yeast counterpart of a mammalian 5′- to 3′-exonuclease required for lagging strand DNA synthesis in reconstituted systems
-
Sommers, C. H., E. J. Miller, B. Dujon, S. Prakash, and L. Prakash. 1995. Conditional lethality of null mutations in RTH1 that encodes the yeast counterpart of a mammalian 5′- to 3′-exonuclease required for lagging strand DNA synthesis in reconstituted systems. J. Biol. Chem. 270:4193-4196.
-
(1995)
J. Biol. Chem.
, vol.270
, pp. 4193-4196
-
-
Sommers, C.H.1
Miller, E.J.2
Dujon, B.3
Prakash, S.4
Prakash, L.5
-
60
-
-
0027306173
-
Destabilisation of tracts of simple repetitive DNA in yeast by mutations affecting DNA mismatch repair
-
Strand, M., T. A. Prolla, R. M. Liskay, and T. D. Petes. 1993. Destabilisation of tracts of simple repetitive DNA in yeast by mutations affecting DNA mismatch repair. Nature 365:274-276.
-
(1993)
Nature
, vol.365
, pp. 274-276
-
-
Strand, M.1
Prolla, T.A.2
Liskay, R.M.3
Petes, T.D.4
-
61
-
-
0026922707
-
DNA methylation represses FMR-1 transcription in fragile X syndrome
-
Sutcliffe, J. S., D. L. Nelson, F. Zhang, M. Pieretti, C. T. Caskey, D. Saxe, and S. T. Warren. 1992. DNA methylation represses FMR-1 transcription in fragile X syndrome. Hum. Mol. Genet. 1:397-400.
-
(1992)
Hum. Mol. Genet.
, vol.1
, pp. 397-400
-
-
Sutcliffe, J.S.1
Nelson, D.L.2
Zhang, F.3
Pieretti, M.4
Caskey, C.T.5
Saxe, D.6
Warren, S.T.7
-
62
-
-
0031442653
-
A novel mutation avoidance mechanism dependent upon S. cerevisiae RAD27 is distinct from DNA mismatch repair
-
Tishkoff, D. X., N. Filosi, G. M. Gaida, and R. D. Kolodner. 1997. A novel mutation avoidance mechanism dependent upon S. cerevisiae RAD27 is distinct from DNA mismatch repair. Cell 88:253-263.
-
(1997)
Cell
, vol.88
, pp. 253-263
-
-
Tishkoff, D.X.1
Filosi, N.2
Gaida, G.M.3
Kolodner, R.D.4
-
63
-
-
0030806219
-
Identification and characterisation of Saccharomyces cerevisiae EXO1, a gene encoding an exonuclease that interacts with MSH2
-
Tishkoff, D. X., A. L. Boerger, P. Betrand, N. Filosi, G. M. Gaida, M. F. Kane, and R. D. Kolodner. 1997. Identification and characterisation of Saccharomyces cerevisiae EXO1, a gene encoding an exonuclease that interacts with MSH2. Proc. Natl. Acad. Sci. USA 94:7487-7492.
-
(1997)
Proc. Natl. Acad. Sci. USA
, vol.94
, pp. 7487-7492
-
-
Tishkoff, D.X.1
Boerger, A.L.2
Betrand, P.3
Filosi, N.4
Gaida, G.M.5
Kane, M.F.6
Kolodner, R.D.7
-
64
-
-
0028874391
-
CGG repeats associated with DNA instability and chromosome fragility form structures that block DNA synthesis in vitro
-
Usdin, K., and K. J. Woodford. 1995. CGG repeats associated with DNA instability and chromosome fragility form structures that block DNA synthesis in vitro. Nucleic Acids Res. 23:4202-4209.
-
(1995)
Nucleic Acids Res.
, vol.23
, pp. 4202-4209
-
-
Usdin, K.1
Woodford, K.J.2
-
65
-
-
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., M. Pieretti, J. Sutcliffe, Y. Fu, D. Kuhl, A. Pizzuti, O. Reiner, S. Richards, M. Victoria, F. Zhang, B. Eussen, G. van Ommen, L. Blonden, G. Riggins, J. Chastain, C. Kunst, H. Galjaad, C. Caskey, D. Nelson, B. Oostra, and S. Warren. 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.1
Pieretti, M.2
Sutcliffe, J.3
Fu, Y.4
Kuhl, D.5
Pizzuti, A.6
Reiner, O.7
Richards, S.8
Victoria, M.9
Zhang, F.10
Eussen, B.11
Van Ommen, G.12
Blonden, L.13
Riggins, G.14
Chastain, J.15
Kunst, C.16
Galjaad, H.17
Caskey, C.18
Nelson, D.19
Oostra, B.20
Warren, S.21
more..
-
66
-
-
0028676232
-
New heterologous modules for classical or PCR-based gene disruptions in Saccharomyces cerevisiae
-
Wach, A., A. Brachat, R. Pohlmann, and P. Phillippsen. 1994. New heterologous modules for classical or PCR-based gene disruptions in Saccharomyces cerevisiae. Yeast 10:1793-1808.
-
(1994)
Yeast
, vol.10
, pp. 1793-1808
-
-
Wach, A.1
Brachat, A.2
Pohlmann, R.3
Phillippsen, P.4
-
67
-
-
0028932050
-
Expanded CTG triplet blocks from the myotonic dystrophy gene create the strongest known natural nucleosome positioning elements
-
Wang, Y. H., and J. Griffith. 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.2
-
68
-
-
0029657781
-
SGS1, a homologue of the Bloom's and Werner's syndrome genes, is required for maintenance of genome stability in Saccharomyces cerevisiae
-
Watt, P. M., I. D. Hickson, R. H. Borts, and E. J. Louis. 1996. SGS1, a homologue of the Bloom's and Werner's syndrome genes, is required for maintenance of genome stability in Saccharomyces cerevisiae. Genetics 144: 935-945.
-
(1996)
Genetics
, vol.144
, pp. 935-945
-
-
Watt, P.M.1
Hickson, I.D.2
Borts, R.H.3
Louis, E.J.4
-
69
-
-
0032529299
-
Hex1: A new human Rad2 nuclease family member with homology to yeast exonuclease 1
-
Wilson, D. M., J. P. Carney, M. A. Coleman, A. W. Adamson, M. Christensen, and J. E. Lamerdin. 1998. Hex1: a new human Rad2 nuclease family member with homology to yeast exonuclease 1. Nucleic Acids Res. 26:3762-3768.
-
(1998)
Nucleic Acids Res.
, vol.26
, pp. 3762-3768
-
-
Wilson, D.M.1
Carney, J.P.2
Coleman, M.A.3
Adamson, A.W.4
Christensen, M.5
Lamerdin, J.E.6
-
70
-
-
0026572250
-
Genotype variation in fragile X fetal tissues
-
Wohrle, D., M. Hirst, K. Davies, and P. Steinbach. 1992. Genotype variation in fragile X fetal tissues. Hum. Genet. 89:114-116.
-
(1992)
Hum. Genet.
, vol.89
, pp. 114-116
-
-
Wohrle, D.1
Hirst, M.2
Davies, K.3
Steinbach, P.4
-
71
-
-
0027310525
-
Mitotic stability of fragile X mutations in differentiated cells indicates early post-conceptional trinucleotide repeat expansion
-
Wohrle, D., I. Hennig, W. Vogel, and P. Steinbach. 1993. Mitotic stability of fragile X mutations in differentiated cells indicates early post-conceptional trinucleotide repeat expansion. Nat. Genet. 4:140-142.
-
(1993)
Nat. Genet.
, vol.4
, pp. 140-142
-
-
Wohrle, D.1
Hennig, I.2
Vogel, W.3
Steinbach, P.4
-
72
-
-
0031971691
-
Unusual mutations in high functioning fragile X males: Apparent instability of expanded un-methylated CGG repeats
-
Wohrle, D. A., U. A. Salat, D. A. Glaser, J. A. Mucke, M. A. Meiselstosiek, D. A. Schindler, W. A. Vogel, and P. Steinbach. 1998. Unusual mutations in high functioning fragile X males: apparent instability of expanded un-methylated CGG repeats. J. Med. Genet. 35:103-111.
-
(1998)
J. Med. Genet.
, vol.35
, pp. 103-111
-
-
Wohrle, D.A.1
Salat, U.A.2
Glaser, D.A.3
Mucke, J.A.4
Meiselstosiek, M.A.5
Schindler, D.A.6
Vogel, W.A.7
Steinbach, P.8
-
73
-
-
0026347628
-
Fragile X genotype characterised by an unstable region of DNA
-
Yu, S., M. Pritchard, E. Kremer, M. Lynch, J. Nancarrow, E. Baker, K. Holman, J. Mulley, S. Warren, D. Schlessinger, G. Sutherland, and R. Richards. 1991. Fragile X genotype characterised 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.8
Warren, S.9
Schlessinger, D.10
Sutherland, G.11
Richards, R.12
-
74
-
-
0029017085
-
Fragile X gene instability: Anchoring AGGs and linked microsatellites
-
Zhong, N., W. Yang, C. Dobkin, and W. Brown. 1995. Fragile X gene instability: anchoring AGGs and linked microsatellites. Am. J. Hum. Genet. 57:351-361.
-
(1995)
Am. J. Hum. Genet.
, vol.57
, pp. 351-361
-
-
Zhong, N.1
Yang, W.2
Dobkin, C.3
Brown, W.4
|