T
Tomara J. Fleury
Researcher at Purdue University
Publications - 7
Citations - 621
Tomara J. Fleury is an academic researcher from Purdue University. The author has contributed to research in topics: Chromatin & Nucleosome. The author has an hindex of 4, co-authored 7 publications receiving 552 citations. Previous affiliations of Tomara J. Fleury include Agricultural Research Service.
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Journal ArticleDOI
Histone H1 Depletion in Mammals Alters Global Chromatin Structure but Causes Specific Changes in Gene Regulation
Yuhong Fan,Tatiana Nikitina,Jie Zhao,Tomara J. Fleury,Riddhi Bhattacharyya,Eric E. Bouhassira,Arnold Stein,Christopher L. Woodcock,Arthur I. Skoultchi +8 more
TL;DR: Results indicate that linker histones can participate in epigenetic regulation of gene expression by contributing to the maintenance or establishment of specific DNA methylation patterns.
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A giant NLR gene confers broad-spectrum resistance to Phytophthora sojae in soybean.
Weidong Wang,Liyang Chen,Kevin Fengler,Joy Bolar,Victor Llaca,Xutong Wang,Chancelor B. Clark,Tomara J. Fleury,Tomara J. Fleury,Jon Myrvold,David Oneal,Maria Magdalena van Dyk,Ashley Hudson,Jesse Munkvold,Andy Baumgarten,Jeff D. Thompson,Guohong Cai,Guohong Cai,Oswald Crasta,Rajat Aggarwal,Jianxin Ma +20 more
TL;DR: In this paper, a 27.7-kb nucleotide-binding site-leucine-rich repeat (NBS-LRR) gene was found to have broad spectrum resistance to P. sojae.
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Long-range oscillation in a periodic DNA sequence motif may influence nucleosome array formation
TL;DR: Evidence that computationally predictable information in the DNA sequence may affect nucleosome array formation in animal tissue is provided.
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Circle ligation of in vitro assembled chromatin indicates a highly flexible structure.
TL;DR: Evidence is provided that some condensed linker histone-containing chromatin structures are highly flexible in solutions containing 2 mM Mg2+, suggesting that the structure was a flexible one, rather than a rigid one having DNA ends that were fortuitously juxtaposed.
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Aspects of large-scale chromatin structures in mouse liver nuclei can be predicted from the DNA sequence
TL;DR: It is estimated experimentally that less than 20% of the chromatin in mouse liver nuclei has a nucleosome repeat length that is 15 bp, or more, shorter than the bulk repeat value, which may be useful for identifying distinctive chromatin structures computationally from the DNA sequence.