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Instability of a 550-base pair DNA segment and abnormal methylation in fragile X syndrome.
Science. 1991 May 24;252(5009):1097-102
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In vitro rescue of an integrated hybrid adeno-associated virus/simian virus 40 genome.
J Mol Biol. 1991 Apr 20;218(4):791-804
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Mapping of DNA instability at the fragile X to a trinucleotide repeat sequence p(CCG)n.
Science. 1991 Jun 21;252(5013):1711-4
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A shuttle vector for analysis of illegitimate recombination in mammalian cells: effects of DNA topoisomerase inhibitors on deletion frequency.
Gene. 1991 May 30;101(2):285-9
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Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy.
Nature. 1991 Jul 4;352(6330):77-9
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Molecular mechanisms of deletion formation in Escherichia coli plasmids. I. Deletion formation mediated by long direct repeats.
Mol Gen Genet. 1991 Aug;228(1-2):153-9
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A new type of insertion mutation in monkey cells: insertion accompanied by long target site duplication.
Mol Gen Genet. 1991 Oct;229(3):325-33
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Variation of the CGG repeat at the fragile X site results in genetic instability: resolution of the Sherman paradox.
Cell. 1991 Dec 20;67(6):1047-58
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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. 1992 Feb 21;68(4):799-808
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Two alternative pathways of double-strand break repair that are kinetically separable and independently modulated.
Mol Cell Biol. 1992 Mar;12(3):1292-303
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Myotonic dystrophy mutation: an unstable CTG repeat in the 3' untranslated region of the gene.
Science. 1992 Mar 6;255(5049):1253-5
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An unstable triplet repeat in a gene related to myotonic muscular dystrophy.
Science. 1992 Mar 6;255(5049):1256-8
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Cloning and sequencing of Escherichia coli mutR shows its identity to topB, encoding topoisomerase III.
J Bacteriol. 1992 Aug;174(15):5168-70
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Recombination between similar but not identical DNA sequences during yeast transformation occurs within short stretches of identity.
Cell. 1992 Aug 21;70(4):659-70
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Identification of an Alu retrotransposition event in close proximity to a strong candidate gene for Huntington's disease.
Nature. 1993 Mar 25;362(6418):370-3
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Clues to the pathogenesis of familial colorectal cancer.
Science. 1993 May 7;260(5109):812-6
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Ubiquitous somatic mutations in simple repeated sequences reveal a new mechanism for colonic carcinogenesis.
Nature. 1993 Jun 10;363(6429):558-61
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The human mutator gene homolog MSH2 and its association with hereditary nonpolyposis colon cancer.
Cell. 1993 Dec 3;75(5):1027-38
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Hypermutability and mismatch repair deficiency in RER+ tumor cells.
Cell. 1993 Dec 17;75(6):1227-36
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Selective extraction of polyoma DNA from infected mouse cell cultures.
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Unequal meiotic recombination within tandem arrays of yeast ribosomal DNA genes.
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SV40 DNA transfection of cells in suspension: analysis of efficiency of transcription and translation of T-antigen.
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On the formation of spontaneous deletions: the importance of short sequence homologies in the generation of large deletions.
Cell. 1982 Jun;29(2):319-28
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Model for homologous recombination during transfer of DNA into mouse L cells: role for DNA ends in the recombination process.
Mol Cell Biol. 1984 Jun;4(6):1020-34
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Replication and recombination in adenovirus-infected cells are temporally and functionally related.
J Virol. 1984 Sep;51(3):571-7
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Recombination in adenovirus: analysis of crossover sites in intertypic overlap recombinants.
Virology. 1984 Nov;139(1):43-52
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The minimum amount of homology required for homologous recombination in mammalian cells.
Mol Cell Biol. 1984 Nov;4(11):2253-8
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In vitro replication of duplex circular DNA containing the simian virus 40 DNA origin site.
Proc Natl Acad Sci U S A. 1985 Sep;82(17):5710-4
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Homologous recombination in Escherichia coli: dependence on substrate length and homology.
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Heteroduplex deoxyribonucleic acid base mismatch repair in bacteria.
Microbiol Rev. 1986 Jun;50(2):133-65
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Homology requirement for efficient gene conversion between duplicated chromosomal sequences in mammalian cells.
Genetics. 1987 Jan;115(1):161-7
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Differential effects of base-pair mismatch on intrachromosomal versus extrachromosomal recombination in mouse cells.
Proc Natl Acad Sci U S A. 1987 Aug;84(15):5340-4
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Meiotic recombination between repeated transposable elements in Saccharomyces cerevisiae.
Mol Cell Biol. 1988 Jul;8(7):2942-54
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Mitotic recombination in the rDNA of S. cerevisiae is suppressed by the combined action of DNA topoisomerases I and II.
Cell. 1988 Nov 4;55(3):413-25
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A new role for a yeast transcriptional silencer gene, SIR2, in regulation of recombination in ribosomal DNA.
Cell. 1989 Mar 10;56(5):771-6
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A subthreshold level of DNA topoisomerases leads to the excision of yeast rDNA as extrachromosomal rings.
Cell. 1989 Jun 16;57(6):975-85
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A hyper-recombination mutation in S. cerevisiae identifies a novel eukaryotic topoisomerase.
Cell. 1989 Jul 28;58(2):409-19
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Genetic and physical analysis of double-strand break repair and recombination in Saccharomyces cerevisiae.
Genetics. 1989 Jul;122(3):519-34
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Double-strand breaks stimulate alternative mechanisms of recombination repair.
J Mol Biol. 1989 Jun 5;207(3):527-41
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Effect of base pair mismatches on recombination via the RecBCD pathway.
Mol Gen Genet. 1989 Aug;218(2):358-60
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The barrier to recombination between Escherichia coli and Salmonella typhimurium is disrupted in mismatch-repair mutants.
Nature. 1989 Nov 23;342(6248):396-401
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Intermolecular recombination between DNAs introduced into mouse L cells is mediated by a nonconservative pathway that leads to crossover products.
Mol Cell Biol. 1990 Jan;10(1):103-12
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Hypervariable minisatellite DNA is a hotspot for homologous recombination in human cells.
Cell. 1990 Jan 12;60(1):95-103
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The Z-DNA motif d(TG)30 promotes reception of information during gene conversion events while stimulating homologous recombination in human cells in culture.
Mol Cell Biol. 1990 Feb;10(2):785-93
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A defect in mismatch repair in Saccharomyces cerevisiae stimulates ectopic recombination between homeologous genes by an excision repair dependent process.
Genetics. 1990 Nov;126(3):535-47
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A unique pathway of double-strand break repair operates in tandemly repeated genes.
Mol Cell Biol. 1991 Mar;11(3):1222-31
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Characterization of recombination intermediates from DNA injected into Xenopus laevis oocytes: evidence for a nonconservative mechanism of homologous recombination.
Mol Cell Biol. 1991 Jun;11(6):3278-87
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