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John J. Wyrick

Researcher at Washington State University

Publications -  78
Citations -  9227

John J. Wyrick is an academic researcher from Washington State University. The author has contributed to research in topics: DNA repair & Nucleosome. The author has an hindex of 29, co-authored 69 publications receiving 8660 citations. Previous affiliations of John J. Wyrick include Massachusetts Institute of Technology.

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Transcriptional Regulatory Networks in Saccharomyces cerevisiae

TL;DR: This work determines how most of the transcriptional regulators encoded in the eukaryote Saccharomyces cerevisiae associate with genes across the genome in living cells, and identifies network motifs, the simplest units of network architecture, and demonstrates that an automated process can use motifs to assemble a transcriptional regulatory network structure.
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Genome-wide location and function of dna binding proteins

TL;DR: In this paper, a method for identifying a set of genes where cell cycle regulator binding correlates with gene expression and identifying genomic targets of cell cycle transcription activators in living cells is also encompassed.
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Serial Regulation of Transcriptional Regulators in the Yeast Cell Cycle

TL;DR: Genome-wide location analysis was used to determine how the yeast cell cycle gene expression program is regulated by each of the nine known cell cycle transcriptional activators, and revealed how the nine transcriptional regulators coordinately regulate global gene expression and diverse stage-specific functions to produce a continuous cycle of cellular events.
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Genome-wide distribution of ORC and MCM proteins in S. cerevisiae: high-resolution mapping of replication origins

TL;DR: These findings identify the global set of yeast replication origins and open avenues of investigation into the role(s) ORC and MCM proteins play in chromosomal architecture and dynamics.
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Chromosomal landscape of nucleosome-dependent gene expression and silencing in yeast

TL;DR: The results indicate that histones make Sir-independent contributions to telomeric silencing, and that the role of histones located elsewhere in chromosomes is gene specific rather than generally repressive.