T
Thomas D. Petes
Researcher at Duke University
Publications - 197
Citations - 17517
Thomas D. Petes is an academic researcher from Duke University. The author has contributed to research in topics: Saccharomyces cerevisiae & Homologous recombination. The author has an hindex of 74, co-authored 194 publications receiving 16935 citations. Previous affiliations of Thomas D. Petes include Saint Petersburg State University & University of North Carolina at Chapel Hill.
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Relationships among DNA sequences of the 1.3 kb EcoRI family of mouse DNA
TL;DR: Although certain regions of the repeat were highly conserved between classes, there was more intraspecific sequence divergence among the sequenced regions than has been observed for the short interspersedAlu family of repeated sequences sin mammals.
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High-Resolution Mapping of Homologous Recombination Events in rad3 Hyper-Recombination Mutants in Yeast.
Sabrina L. Andersen,Aimee Zhang,Margaret Dominska,María Moriel-Carretero,Emilia Herrera-Moyano,Andrés Aguilera,Thomas D. Petes +6 more
TL;DR: It is suggested that a sub-set of spontaneous events in wild-type cells may be initiated by incomplete NER reactions, and that DSCBs, which cannot be repaired by sister-chromatid recombination, are a major source of mitotic recombination between homologous chromosomes.
Recombination between genes located on nonhomologous chromosomes
TL;DR: By genetic and physical analysis, it is shown that Leu+ or Ura+ revertants can arise by a variety of different genetic interactions, and reciprocal recombination between repeated genes, resulting in reciprocally translocated chromosomes.
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The Transient Inactivation of the Master Cell Cycle Phosphatase Cdc14 Causes Genomic Instability in Diploid Cells of Saccharomyces cerevisiae
TL;DR: This work shows that a brief and reversible inactivation of the key phosphatase Cdc14 in the model organism Saccharomyces cerevisiae is enough to result in diploid cells with multiple gross chromosomal rearrangements and changes in ploidy, and observes that such transient loss yields a characteristic fingerprint.