Author

Kirsten M. Adams

University of North Carolina at Chapel HillORCID 0000-0002-5997-3099Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

Click to filter author papers

Signature Assays, Organisms & Methods

Click to filter · or open tag

Research Focus:cell type annotation· 1 Assay:ChIP-seq· 1 Research Focus:differential expression· 1 Organism:Drosophila· 1 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1

Frequent Co-Authors

A. Gregory MateraiD· 1 shared Benjamin D. McMichaeliD· 1 shared Daniel J. McKayiD· 1 shared Harmony R. SalzleriD· 1 shared Jeremy M. SimoniD· 1 shared John C. BrowniD· 1 shared Mary P Leatham-JenseniD· 1 shared Michael P. MeersiD· 1 shared

Activity by Year

2023-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

1 shared paperGenomics

A. Gregory MateraORCID

Mutual co-authors in cluster

Author profile →

1 paper

Recent·Most cited

Distinct roles for canonical and variant histone H3 lysine 36 in Polycomb silencing

Harmony R. Salzler, Vasudha Vandadi, Benjamin D. McMichael, John C. Brown, Sally A. Boerma, Mary P Leatham-Jensen, Kirsten M. Adams, Michael P. Meers, Jeremy M. Simon, Robert J. Duronio, Daniel J. McKay, A. Gregory Matera

The paper shows that H3.2 and H3.3 K36 residues have distinct roles in maintaining Polycomb silencing of Hox genes through different mechanisms, enabling development.

Science Advances · Mar 1, 2023Peer-reviewedGenomics