-
1
-
-
0034192381
-
Microsatellite instability at selected tetranucleotide repeats is associated with p53 mutations in non-small cell lung cancer
-
Ahrendt SA, Decker PA, Doffek K, Wang B, Xu L, Demeure MJ, Jen J, Sidransky D: Microsatellite instability at selected tetranucleotide repeats is associated with p53 mutations in non-small cell lung cancer. Cancer Res 60:2488-2491 (2000).
-
(2000)
Cancer Res
, vol.60
, pp. 2488-2491
-
-
Ahrendt, S.A.1
Decker, P.A.2
Doffek, K.3
Wang, B.4
Xu, L.5
Demeure, M.J.6
Jen, J.7
Sidransky, D.8
-
2
-
-
0035863895
-
Role for CCG-trinucleotide repeats in the pathogenesis of chronic lymphocytic leukemia
-
Auer RL, Jones C, Mullenbach RA, Syndercombe-Court D, Milligan DW, Fegan CD, Cotter FE: Role for CCG-trinucleotide repeats in the pathogenesis of chronic lymphocytic leukemia. Blood 97:509-515 (2001).
-
(2001)
Blood
, vol.97
, pp. 509-515
-
-
Auer, R.L.1
Jones, C.2
Mullenbach, R.A.3
Syndercombe-Court, D.4
Milligan, D.W.5
Fegan, C.D.6
Cotter, F.E.7
-
3
-
-
0027982948
-
p53 binds single-stranded DNA ends and catalyzes DNA renaturation and strand transfer
-
USA
-
Bakalkin G, Yakovleva T, Selivanova G, Magnusson KP, Szekely L, Kiseleva E, Klein G, Terenius L, Wiman KG: p53 binds single-stranded DNA ends and catalyzes DNA renaturation and strand transfer. Proc natl Acad Sci, USA 91:413-417 (1994).
-
(1994)
Proc Natl Acad Sci
, vol.91
, pp. 413-417
-
-
Bakalkin, G.1
Yakovleva, T.2
Selivanova, G.3
Magnusson, K.P.4
Szekely, L.5
Kiseleva, E.6
Klein, G.7
Terenius, L.8
Wiman, K.G.9
-
4
-
-
0030930925
-
Increase of spontaneous intrachromosomal homologous recombination in mammalian cells expressing a mutant p53 protein
-
Bertrand P, Rouillard D, Boulet A, Levalois C, Soussi T, Lopez BS: Increase of spontaneous intrachromosomal homologous recombination in mammalian cells expressing a mutant p53 protein. Oncogene 14:1117-1122 (1997).
-
(1997)
Oncogene
, vol.14
, pp. 1117-1122
-
-
Bertrand, P.1
Rouillard, D.2
Boulet, A.3
Levalois, C.4
Soussi, T.5
Lopez, B.S.6
-
5
-
-
0030979178
-
Folate deficiency causes uracil misincorporation into human DNA and chromosome breakage: Implications for cancer and neuronal damage
-
USA
-
Blount BC, Mack MM, Wehr CM, MacGregor JT, Hiatt RA, Wang G, Wickramasinghe SN, Everson RB, Ames BN: Folate deficiency causes uracil misincorporation into human DNA and chromosome breakage: implications for cancer and neuronal damage. Proc natl Acad Sci, USA 94:3290-3295 (1997).
-
(1997)
Proc Natl Acad Sci
, vol.94
, pp. 3290-3295
-
-
Blount, B.C.1
Mack, M.M.2
Wehr, C.M.3
MacGregor, J.T.4
Hiatt, R.A.5
Wang, G.6
Wickramasinghe, S.N.7
Everson, R.B.8
Ames, B.N.9
-
6
-
-
0036287009
-
Minisatellites show rare and simple intra-allelic instability in the mouse germ line
-
Bois PR, Grant GR, Jeffreys AJ: Minisatellites show rare and simple intra-allelic instability in the mouse germ line. Genomics 80:2-4 (2002).
-
(2002)
Genomics
, vol.80
, pp. 2-4
-
-
Bois, P.R.1
Grant, G.R.2
Jeffreys, A.J.3
-
7
-
-
0035423079
-
98 repeat in the Fmr1 promoter
-
98 repeat in the Fmr1 promoter. Hum molec Genet 10:1693-1699 (2001).
-
(2001)
Hum Molec Genet
, vol.10
, pp. 1693-1699
-
-
Bontekoe, C.J.M.1
Bakker, C.E.2
Nieuwenhuizen, I.M.3
Van Der Linde, H.4
Lans, H.5
De Lange, D.6
Hirst, M.C.7
Oostra, B.A.8
-
8
-
-
0035201633
-
The intrinsically unstable life of DNA triplet repeats associated with human hereditary disorders
-
Bowater RP, Wells RD: The intrinsically unstable life of DNA triplet repeats associated with human hereditary disorders. Prog Nucl Acid Res Mol Biol 66:159-202 (2001).
-
(2001)
Prog Nucl Acid Res Mol Biol
, vol.66
, pp. 159-202
-
-
Bowater, R.P.1
Wells, R.D.2
-
9
-
-
0036161562
-
Roles of the Werner syndrome protein in pathways required for maintenance of genome stability
-
Brosh RM Jr, Bohr VA: Roles of the Werner syndrome protein in pathways required for maintenance of genome stability. Exp Gerontol 37:491-506 (2002).
-
(2002)
Exp Gerontol
, vol.37
, pp. 491-506
-
-
Brosh Jr., R.M.1
Bohr, V.A.2
-
10
-
-
0035887046
-
Werner syndrome protein interacts with human flap endonuclease 1 and stimulates its cleavage activity
-
Brosh RM Jr, von Kobbe C, Sommers JA, Karmakar P, Opresko PL, Piotrowski J, Dianova I, Dianov GL, Bohr VA: Werner syndrome protein interacts with human flap endonuclease 1 and stimulates its cleavage activity. EMBO J 20:5791-5801 (2001).
-
(2001)
EMBO J
, vol.20
, pp. 5791-5801
-
-
Brosh Jr., R.M.1
Von Kobbe, C.2
Sommers, J.A.3
Karmakar, P.4
Opresko, P.L.5
Piotrowski, J.6
Dianova, I.7
Dianov, G.L.8
Bohr, V.A.9
-
11
-
-
0032741610
-
Saccharomyces cerevisiae pol30 (proliferating cell nuclear antigen) mutations impair replication fidelity and mismatch repair
-
Chen C, Merrill BJ, Lau PJ, Holm C, Kolodner RD: Saccharomyces cerevisiae pol30 (proliferating cell nuclear antigen) mutations impair replication fidelity and mismatch repair. Mol Cell Biol 19:7801-7815 (1999).
-
(1999)
Mol Cell Biol
, vol.19
, pp. 7801-7815
-
-
Chen, C.1
Merrill, B.J.2
Lau, P.J.3
Holm, C.4
Kolodner, R.D.5
-
12
-
-
0030904279
-
Expression of fragile sites triggers intrachromosomal mammalian gene amplification and sets boundaries to early amplicons
-
Coquelle A, Pipiras E, Toledo F, Buttin G, Debatisse M: Expression of fragile sites triggers intrachromosomal mammalian gene amplification and sets boundaries to early amplicons. Cell 89:215-225 (1997).
-
(1997)
Cell
, vol.89
, pp. 215-225
-
-
Coquelle, A.1
Pipiras, E.2
Toledo, F.3
Buttin, G.4
Debatisse, M.5
-
13
-
-
0028873249
-
Hotspot for deletions in the CGG repeat region of FMR1 in fragile X patients
-
de Graaff E, Rouillard P, Willems PJ, Smits AP, Rousseau F, Oostra BA: Hotspot for deletions in the CGG repeat region of FMR1 in fragile X patients. Hum molec Genet 4:45-49 (1995).
-
(1995)
Hum Molec Genet
, vol.4
, pp. 45-49
-
-
De Graaff, E.1
Rouillard, P.2
Willems, P.J.3
Smits, A.P.4
Rousseau, F.5
Oostra, B.A.6
-
14
-
-
0029900477
-
The fragile X phenotype in a mosaic male with a deletion showing expression of the FMR1 protein in 28% of the cells
-
de Graaff E, de Vries BB, Willemsen R, van Hemel JO, Mohkamsing S, Oostra BA, van den Ouweland AM: The fragile X phenotype in a mosaic male with a deletion showing expression of the FMR1 protein in 28% of the cells. Am J med Genet 64:302-308 (1996).
-
(1996)
Am J Med Genet
, vol.64
, pp. 302-308
-
-
De Graaff, E.1
De Vries, B.B.2
Willemsen, R.3
Van Hemel, J.O.4
Mohkamsing, S.5
Oostra, B.A.6
Van Den Ouweland, A.M.7
-
15
-
-
0028978183
-
Mice lacking p21CIP1/WAF1 undergo normal development, but are defective in G1 checkpoint control
-
Deng C, Zhang P, Harper JW, Elledge SJ, Leder P: Mice lacking p21CIP1/WAF1 undergo normal development, but are defective in G1 checkpoint control. Cell 82:675-684 (1995).
-
(1995)
Cell
, vol.82
, pp. 675-684
-
-
Deng, C.1
Zhang, P.2
Harper, J.W.3
Elledge, S.J.4
Leder, P.5
-
16
-
-
0026561121
-
Mice deficient for p53 are developmentally normal but susceptible to spontaneous tumours
-
Donehower LA, Harvey M, Slagle BL, McArthur MJ, Montgomery CA Jr, Butel JS, Bradley A: Mice deficient for p53 are developmentally normal but susceptible to spontaneous tumours. Nature 356:215-221 (1992).
-
(1992)
Nature
, vol.356
, pp. 215-221
-
-
Donehower, L.A.1
Harvey, M.2
Slagle, B.L.3
McArthur, M.J.4
Montgomery Jr., C.A.5
Butel, J.S.6
Bradley, A.7
-
17
-
-
0032488872
-
Expansion and length-dependent fragility of CTG repeats in yeast
-
Freudenreich CH, Kantrow SM, Zakian VA: Expansion and length-dependent fragility of CTG repeats in yeast. Science 279:853-856 (1998).
-
(1998)
Science
, vol.279
, pp. 853-856
-
-
Freudenreich, C.H.1
Kantrow, S.M.2
Zakian, V.A.3
-
18
-
-
0034025077
-
Homologous and non-homologous recombination resulting in deletion: Effects of p53 status, microhomology, and repetitive DNA length and orientation
-
Gebow D, Miselis N, Liber HL: Homologous and non-homologous recombination resulting in deletion: effects of p53 status, microhomology, and repetitive DNA length and orientation. Mol cell Biol 20:4028-4035 (2000).
-
(2000)
Mol Cell Biol
, vol.20
, pp. 4028-4035
-
-
Gebow, D.1
Miselis, N.2
Liber, H.L.3
-
19
-
-
0023789150
-
Chromosome breakage and recombination at fragile sites
-
Glover TW, Stein CK: Chromosome breakage and recombination at fragile sites. Am J hum Genet 43:265-273 (1988).
-
(1988)
Am J Hum Genet
, vol.43
, pp. 265-273
-
-
Glover, T.W.1
Stein, C.K.2
-
21
-
-
0031038809
-
Moderate intergenerational and somatic instability of a 55-CTG repeat in transgenic mice
-
Gourdon G, Radvanyi F, Lia AS, Duros C, Blanche M, Abitbol M, Junien C, Hofmann-Radvanyi H: Moderate intergenerational and somatic instability of a 55-CTG repeat in transgenic mice [see comments] Nature Genet 15:190-192 (1997).
-
(1997)
Nature 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
-
22
-
-
0030894828
-
A variable domain of delayed replication in FRAXA fragile X chromosomes: X inactivation-like spread of late replication
-
USA
-
Hansen RS, Canfield TK, Fjeld AD, Mumm S, Laird CD, Gartler SM: A variable domain of delayed replication in FRAXA fragile X chromosomes: X inactivation-like spread of late replication. Proc natl Acad Sci, USA 94:4587-4592 (1997).
-
(1997)
Proc Natl Acad Sci
, vol.94
, pp. 4587-4592
-
-
Hansen, R.S.1
Canfield, T.K.2
Fjeld, A.D.3
Mumm, S.4
Laird, C.D.5
Gartler, S.M.6
-
23
-
-
0034117095
-
Replication delay along FRA7H, a common fragile site on human chromosome 7, leads to chromosomal instability
-
Hellman A, Rahat A, Scherer SW, Darvasi A, Tsui LC, Kerem B: Replication delay along FRA7H, a common fragile site on human chromosome 7, leads to chromosomal instability. Mol cell Biol 20:4420-4427 (2000).
-
(2000)
Mol Cell Biol
, vol.20
, pp. 4420-4427
-
-
Hellman, A.1
Rahat, A.2
Scherer, S.W.3
Darvasi, A.4
Tsui, L.C.5
Kerem, B.6
-
24
-
-
0025914050
-
Sister chromatid exchanges are preferentially induced at expressed and nonexpressed common fragile sites
-
Hirsch B: Sister chromatid exchanges are preferentially induced at expressed and nonexpressed common fragile sites. Hum Genet 87:302-306 (1991).
-
(1991)
Hum Genet
, vol.87
, pp. 302-306
-
-
Hirsch, B.1
-
25
-
-
0033895728
-
The impact of lagging strand replication mutations on the stability of CAG repeat tracts in yeast
-
Ireland MJ, Reinke SS, Livingston DM: The impact of lagging strand replication mutations on the stability of CAG repeat tracts in yeast. Genetics 155:1657-1665 (2000).
-
(2000)
Genetics
, vol.155
, pp. 1657-1665
-
-
Ireland, M.J.1
Reinke, S.S.2
Livingston, D.M.3
-
26
-
-
0034695575
-
DNA polymerase III proofreading mutants enhance the expansion and deletion of triplet repeat sequences in Escherichia coli
-
Iyer RR, Pluciennik A, Rosche WA, Sinden RR, Wells RD: DNA polymerase III proofreading mutants enhance the expansion and deletion of triplet repeat sequences in Escherichia coli. J biol Chem 275:2174-2184 (2000).
-
(2000)
J Biol Chem
, vol.275
, pp. 2174-2184
-
-
Iyer, R.R.1
Pluciennik, A.2
Rosche, W.A.3
Sinden, R.R.4
Wells, R.D.5
-
27
-
-
0033551777
-
Genetic instabilities in (CTG.CAG) repeats occur by recombination
-
Jakupciak JP, Wells RD: Genetic instabilities in (CTG.CAG) repeats occur by recombination. J biol Chem 274:23468-23479 (1999).
-
(1999)
J Biol Chem
, vol.274
, pp. 23468-23479
-
-
Jakupciak, J.P.1
Wells, R.D.2
-
28
-
-
0028788635
-
n triplet repeats from human hereditary diseases
-
USA
-
n triplet repeats from human hereditary diseases. Proc natl Acad Sci, USA 92:11019-11023 (1995).
-
(1995)
Proc Natl Acad Sci
, vol.92
, pp. 11019-11023
-
-
Jaworski, A.1
Rosche, W.A.2
Gellibolian, R.3
Kang, S.4
Shimizu, M.5
Bowater, R.P.6
Sinden, R.R.7
Wells, R.D.8
-
29
-
-
0342424768
-
Colocalisation of CCG repeats and chromosome deletion breakpoints in Jacobsen syndrome: Evidence for a common mechanism of chromosome breakage
-
Jones C, Mullenbach R, Grossfeld P, Auer R, Favier R, Chien K, James M, Tunnacliffe A, Cotter F: Colocalisation of CCG repeats and chromosome deletion breakpoints in Jacobsen syndrome: evidence for a common mechanism of chromosome breakage. Hum molec Genet 9:1201-1208 (2000).
-
(2000)
Hum Molec Genet
, vol.9
, pp. 1201-1208
-
-
Jones, C.1
Mullenbach, R.2
Grossfeld, P.3
Auer, R.4
Favier, R.5
Chien, K.6
James, M.7
Tunnacliffe, A.8
Cotter, F.9
-
31
-
-
0034641887
-
Dramatic mutation instability in HD mouse striatum: Does polyglutamine load contribute to cell-specific vulnerability in Huntington's disease?
-
Kennedy L, Shelbourne PF: Dramatic mutation instability in HD mouse striatum: does polyglutamine load contribute to cell-specific vulnerability in Huntington's disease? Hum molec Genet 9:2539-2544 (2000).
-
(2000)
Hum Molec Genet
, vol.9
, pp. 2539-2544
-
-
Kennedy, L.1
Shelbourne, P.F.2
-
32
-
-
0030768181
-
DNA-conformation is an important determinant of sequence-specific DNA binding by tumor suppressor p53
-
Kim E, Albrechtsen N, Deppert W: DNA-conformation is an important determinant of sequence-specific DNA binding by tumor suppressor p53. Oncogene 15:857-869 (1997).
-
(1997)
Oncogene
, vol.15
, pp. 857-869
-
-
Kim, E.1
Albrechtsen, N.2
Deppert, W.3
-
33
-
-
0032964872
-
A mutation of the yeast gene encoding PCNA destabilizes both microsatellite and minisatellite DNA sequences
-
Kokoska RJ, Stefanovic L, Buermeyer AB, Liskay RM, Petes TD: A mutation of the yeast gene encoding PCNA destabilizes both microsatellite and minisatellite DNA sequences. Genetics 151:511-519 (1999).
-
(1999)
Genetics
, vol.151
, pp. 511-519
-
-
Kokoska, R.J.1
Stefanovic, L.2
Buermeyer, A.B.3
Liskay, R.M.4
Petes, T.D.5
-
34
-
-
0031953438
-
Destabilization of yeast micro- and minisatellite DNA sequences by mutations affecting a nuclease involved in Okazaki fragment processing (rad27) and DNA polymerase delta (pol3-t)
-
Kokoska RJ, Stefanovic L, Tran HT, Resnick MA, Gordenin DA, Petes TD: Destabilization of yeast micro- and minisatellite DNA sequences by mutations affecting a nuclease involved in Okazaki fragment processing (rad27) and DNA polymerase delta (pol3-t). Mol cell Biol 18:2779-2788 (1998).
-
(1998)
Mol Cell Biol
, vol.18
, pp. 2779-2788
-
-
Kokoska, R.J.1
Stefanovic, L.2
Tran, H.T.3
Resnick, M.A.4
Gordenin, D.A.5
Petes, T.D.6
-
35
-
-
0035065524
-
Trinucleotide expansion in haploid germ cells by gap repair
-
Kovtun IV, McMurray CT: Trinucleotide expansion in haploid germ cells by gap repair. Nature Genet 27:407-411 (2001).
-
(2001)
Nature Genet
, vol.27
, pp. 407-411
-
-
Kovtun, I.V.1
McMurray, C.T.2
-
36
-
-
0029930837
-
Stability of triplet repeats of myotonic dystrophy and fragile X loci in human mutator mismatch repair cell lines
-
Kramer PR, Pearson CE, Sinden RR: Stability of triplet repeats of myotonic dystrophy and fragile X loci in human mutator mismatch repair cell lines. Hum Genet 98:151-157 (1996).
-
(1996)
Hum Genet
, vol.98
, pp. 151-157
-
-
Kramer, P.R.1
Pearson, C.E.2
Sinden, R.R.3
-
37
-
-
7144256250
-
Androgen receptor YAC transgenic mice carrying CAG 45 alleles show trinucleotide repeat instability
-
La Spada AR, Peterson KR, Meadows SA, McClain ME, Jeng G, Chmelar RS, Haugen HA, Chen K, Singer MJ, Moore D, et al: Androgen receptor YAC transgenic mice carrying CAG 45 alleles show trinucleotide repeat instability. Hum molec Genet 7:959-967 (1998).
-
(1998)
Hum Molec Genet
, vol.7
, pp. 959-967
-
-
La Spada, A.R.1
Peterson, K.R.2
Meadows, S.A.3
McClain, M.E.4
Jeng, G.5
Chmelar, R.S.6
Haugen, H.A.7
Chen, K.8
Singer, M.J.9
Moore, D.10
-
39
-
-
0032104278
-
Long uninterrupted CGG repeats within the first exon of the human FMR1 gene are not intrinsically unstable in transgenic mice
-
Lavedan C, Grabczyk E, Usdin K, Nussbaum RL: Long uninterrupted CGG repeats within the first exon of the human FMR1 gene are not intrinsically unstable in transgenic mice. Genomics 50:229-240 (1998).
-
(1998)
Genomics
, vol.50
, pp. 229-240
-
-
Lavedan, C.1
Grabczyk, E.2
Usdin, K.3
Nussbaum, R.L.4
-
40
-
-
0031924605
-
Replication of a common fragile site, FRA3B, occurs late in S phase and is delayed further upon induction: Implications for the mechanism of fragile site induction
-
Le Beau MM, Rassool FV, Neilly ME, Espinosa R 3(rd), Glover TW, Smith DI, McKeithan TW: Replication of a common fragile site, FRA3B, occurs late in S phase and is delayed further upon induction: implications for the mechanism of fragile site induction. Hum molec Genet 7:755-761 (1998).
-
(1998)
Hum Molec Genet
, vol.7
, pp. 755-761
-
-
Le Beau, M.M.1
Rassool, F.V.2
Neilly, M.E.3
Espinosa III, R.4
Glover, T.W.5
Smith, D.I.6
McKeithan, T.W.7
-
41
-
-
0032573157
-
A deletion within the murine Werner syndrome helicase induces sensitivity to inhibitors of topoisomerase and loss of cellular proliferative capacity
-
USA
-
Lebel M, Leder P: A deletion within the murine Werner syndrome helicase induces sensitivity to inhibitors of topoisomerase and loss of cellular proliferative capacity. Proc natl Acad Sci, USA 95:13097-13102 (1998).
-
(1998)
Proc Natl Acad Sci
, vol.95
, pp. 13097-13102
-
-
Lebel, M.1
Leder, P.2
-
42
-
-
0030985675
-
Human p53 binds Holliday junctions strongly and facilitates their cleavage
-
Lee S, Cavallo L, Griffith J: Human p53 binds Holliday junctions strongly and facilitates their cleavage. J biol Chem 272:7532-7539 (1997).
-
(1997)
J Biol Chem
, vol.272
, pp. 7532-7539
-
-
Lee, S.1
Cavallo, L.2
Griffith, J.3
-
43
-
-
0027332996
-
Differential induction of transcriptionally active p53 following UV or ionizing radiation: Defects in chromosome instability syndromes?
-
Lu X, Lane DP: Differential induction of transcriptionally active p53 following UV or ionizing radiation: defects in chromosome instability syndromes? Cell 75:765-778 (1993).
-
(1993)
Cell
, vol.75
, pp. 765-778
-
-
Lu, X.1
Lane, D.P.2
-
44
-
-
0030915139
-
Inactivation of p53 results in high rates of homologous recombination
-
Mekeel KL, Tang W, Kachnic LA, Luo CM, DeFrank JS, Powell SN: Inactivation of p53 results in high rates of homologous recombination Oncogene 14:1847-1857 (1997).
-
(1997)
Oncogene
, vol.14
, pp. 1847-1857
-
-
Mekeel, K.L.1
Tang, W.2
Kachnic, L.A.3
Luo, C.M.4
DeFrank, J.S.5
Powell, S.N.6
-
45
-
-
0030012165
-
Mosaicism for the fragile X syndrome full mutation and deletions within the CGG repeat of the FMR1 gene
-
Mila M, Castellvi-Bel S, Sanchez A, Lazaro C, Villa M, Estivill X: Mosaicism for the fragile X syndrome full mutation and deletions within the CGG repeat of the FMR1 gene. J Med Genet 33:338-340 (1996).
-
(1996)
J Med Genet
, vol.33
, pp. 338-340
-
-
Mila, M.1
Castellvi-Bel, S.2
Sanchez, A.3
Lazaro, C.4
Villa, M.5
Estivill, X.6
-
46
-
-
18244408334
-
Frataxin knockin mouse
-
Miranda CJ, Santos MM, Ohshima K, Smith J, Li L, Bunting M, Cossee M, Koenig M, Sequeiros J, Kaplan J, et al: Frataxin knockin mouse. FEBS Lett 512:291-297 (2002).
-
(2002)
FEBS Lett
, vol.512
, pp. 291-297
-
-
Miranda, C.J.1
Santos, M.M.2
Ohshima, K.3
Smith, J.4
Li, L.5
Bunting, M.6
Cossee, M.7
Koenig, M.8
Sequeiros, J.9
Kaplan, J.10
-
47
-
-
0031054076
-
Hypermutable myotonic dystrophy CTG repeats in transgenic mice
-
Monckton DG, Coolbaugh MI, Ashizawa KT, Siciliano MJ, Caskey CT: Hypermutable myotonic dystrophy CTG repeats in transgenic mice. Nature Genet 15:193-196 (1997).
-
(1997)
Nature 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
-
48
-
-
0001386998
-
Expansion of DNA repeats in Escherichia coli: Effects of recombination and replication functions
-
Morag AS, Saveson CJ, Lovett ST: Expansion of DNA repeats in Escherichia coli: effects of recombination and replication functions. J molec Biol 289: 21-27 (1999).
-
(1999)
J Molec Biol
, vol.289
, pp. 21-27
-
-
Morag, A.S.1
Saveson, C.J.2
Lovett, S.T.3
-
49
-
-
0030604728
-
p53 Protein exhibits 3′to-5′ exonuclease activity
-
Mummenbrauer T, Janus F, Muller B, Wiesmuller L, Deppert W, Grosse F: p53 Protein exhibits 3′to-5′ exonuclease activity. Cell 85: 1089-1099 (1996).
-
(1996)
Cell
, vol.85
, pp. 1089-1099
-
-
Mummenbrauer, T.1
Janus, F.2
Muller, B.3
Wiesmuller, L.4
Deppert, W.5
Grosse, F.6
-
50
-
-
0028242797
-
Simple repeat DNA is not replicated simply
-
Richards RI, Sutherland GR: Simple repeat DNA is not replicated simply. Nature Genet 6:114-116 (1994).
-
(1994)
Nature Genet
, vol.6
, pp. 114-116
-
-
Richards, R.I.1
Sutherland, G.R.2
-
51
-
-
0032779262
-
The effect of DNA replication mutations on CAG tract stability in yeast
-
Schweitzer JK, Livingston DM: The effect of DNA replication mutations on CAG tract stability in yeast. Genetics 152:953-963 (1999).
-
(1999)
Genetics
, vol.152
, pp. 953-963
-
-
Schweitzer, J.K.1
Livingston, D.M.2
-
52
-
-
0033369989
-
Inhibition of FEN-1 processing by DNA secondary structure at trinucleotide repeats
-
Spiro C, Pelletier R, Rolfsmeier ML, Dixon MJ, Lahue RS, Gupta G, Park MS, Chen X, Mariappan SV, McMurray CT: Inhibition of FEN-1 processing by DNA secondary structure at trinucleotide repeats. Mol Cell 4:1079-1085 (1999).
-
(1999)
Mol Cell
, vol.4
, pp. 1079-1085
-
-
Spiro, C.1
Pelletier, R.2
Rolfsmeier, M.L.3
Dixon, M.J.4
Lahue, R.S.5
Gupta, G.6
Park, M.S.7
Chen, X.8
Mariappan, S.V.9
McMurray, C.T.10
-
53
-
-
0029969418
-
p53 is linked directly to homologous recombination processes via RAD51/RecA protein interaction
-
Sturzbecher HW, Donzelmann B, Henning W, Knippschild U, Buchhop S: p53 is linked directly to homologous recombination processes via RAD51/RecA protein interaction. EMBO J 15:1992-2002 (1996).
-
(1996)
EMBO J
, vol.15
, pp. 1992-2002
-
-
Sturzbecher, H.W.1
Donzelmann, B.2
Henning, W.3
Knippschild, U.4
Buchhop, S.5
-
54
-
-
0028874391
-
CGG repeats associated with DNA instability and chromosome fragility form structures that block DNA synthesis in vitro
-
Usdin K, Woodford KJ: CGG repeats associated with DNA instability and chromosome fragility form structures that block DNA synthesis in vitro. Nucl Acids Res 23:4202-4209 (1995).
-
(1995)
Nucl Acids Res
, vol.23
, pp. 4202-4209
-
-
Usdin, K.1
Woodford, K.J.2
-
55
-
-
0028989236
-
p53 modulation of TFIIH-associated nucleotide excision repair activity
-
Wang XW, Yeh H, Schaeffer L, Roy R, Moncollin V, Egly JM, Wang Z, Freidberg EC, Evans MK, Taffe BG, et al: p53 modulation of TFIIH-associated nucleotide excision repair activity. Nature Genet 10:188-195 (1995).
-
(1995)
Nature Genet
, vol.10
, pp. 188-195
-
-
Wang, X.W.1
Yeh, H.2
Schaeffer, L.3
Roy, R.4
Moncollin, V.5
Egly, J.M.6
Wang, Z.7
Freidberg, E.C.8
Evans, M.K.9
Taffe, B.G.10
-
56
-
-
0032938295
-
Length-dependent gametic CAG repeat instability in the Huntington's disease knock-in mouse
-
Wheeler VC, Auerbach W, White JK, Srinidhi J, Auerbach A, Ryan A, Duyao MP, Vrbanac V, Weaver M, Gusella JF, et al: Length-dependent gametic CAG repeat instability in the Huntington's disease knock-in mouse. Hum molec Genet 8:115-122 (1999).
-
(1999)
Hum Molec Genet
, vol.8
, pp. 115-122
-
-
Wheeler, V.C.1
Auerbach, W.2
White, J.K.3
Srinidhi, J.4
Auerbach, A.5
Ryan, A.6
Duyao, M.P.7
Vrbanac, V.8
Weaver, M.9
Gusella, J.F.10
-
57
-
-
0032771002
-
Stability of the human fragile X (CGG)(n) triplet repeat array in Saccharomyces cerevisiae deficient in aspects of DNA metabolism
-
White PJ, Borts RH, Hirst MC: Stability of the human fragile X (CGG)(n) triplet repeat array in Saccharomyces cerevisiae deficient in aspects of DNA metabolism. Mol cell Biol 19:5675-5684 (1999).
-
(1999)
Mol Cell Biol
, vol.19
, pp. 5675-5684
-
-
White, P.J.1
Borts, R.H.2
Hirst, M.C.3
-
58
-
-
0030068266
-
In vivo assay of p53 function in homologous recombination between simian virus 40 chromosomes
-
Wiesmuller L, Cammenga J, Deppert WW: In vivo assay of p53 function in homologous recombination between simian virus 40 chromosomes. J Virol 70: 737-744 (1996).
-
(1996)
J Virol
, vol.70
, pp. 737-744
-
-
Wiesmuller, L.1
Cammenga, J.2
Deppert, W.W.3
-
59
-
-
0026801977
-
Wild-type p53 restores cell cycle control and inhibits gene amplification in cells with mutant p53 alleles
-
Yin Y, Tainsky MA, Bischoff FZ, Strong LC, Wahl GM: Wild-type p53 restores cell cycle control and inhibits gene amplification in cells with mutant p53 alleles. Cell 70:937-948 (1992).
-
(1992)
Cell
, vol.70
, pp. 937-948
-
-
Yin, Y.1
Tainsky, M.A.2
Bischoff, F.Z.3
Strong, L.C.4
Wahl, G.M.5
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