Author

Janet L. Thornton

University of Kansas Medical Center

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Systems Biology· 2 Molecular Biology· 1

Signature Assays, Organisms & Methods

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Organism:human· 3 Approach:experimental assay· 2 Research Focus:protein structure prediction· 2 Approach:statistical model· 2 Research Focus:cell type annotation· 1 Research Focus:cell-cell communication· 1 Assay:protein sequence· 1 Assay:protein structure· 1

Frequent Co-Authors

Cassandra G. KempfiD· 3 shared Laurence A. FlorensiD· 3 shared Michael P. WashburniD· 3 shared Rosalyn C. ZimmermanniD· 2 shared Sayem MiahiD· 2 shared Alexis Murray· 1 shared Allen J. GiesiD· 1 shared Charles A.S. BanksiD· 1 shared

Activity by Year

2020-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 36 mutual co-author links

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3 shared papersSystems Biology

Cassandra G. KempfORCID

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Author profile →

3 papers

Recent·Most cited

Multicomplex Integrative Structural Modeling of a Human Histone Deacetylase Interactome

Jules Nde, Kartik Majila, Rosalyn C. Zimmermann, Cassandra G. Kempf, Ying Zhang, Joseph Cesare, Janet L. Thornton, Jerry L. Workman, Laurence A. Florens, Shruthi Viswanath, Michael P. Washburn

The paper builds structural models of HDAC1/2-containing chromatin remodeling complexes using XL-MS and integrative modeling, revealing how the CTD IDR of HDAC1 folds into alpha helices.

Molecular & Cellular Proteomics · Sep 2, 2026Peer-reviewedSystems Biology

Beyond the Sin3/HDAC Complex: FAM60A emerges as a regulator of RNA Splicing

M. Nazmul Huda, Rosalyn C. Zimmermann, Preeti Nagar, Jahangir Alam, Md. Rafikul Islam, Gerald Dayebgadoh, Mojnu Miah, Cassandra G. Kempf, Janet L. Thornton, Ying Zhang, Zhihui Wen, Gaye Hatem, Allen J. Gies, Stephanie D. Byrum, Mohammad Alinoor Rahman, , Sayem Miah

This study identifies FAM60A as a regulator of RNA splicing, showing it interacts with HDAC1 and spliceosome components, expanding its known role beyond the Sin3/HDAC complex.

bioRxiv · Jan 16, 2024 · PreprintMolecular Biology

Differential complex formation via paralogs in the human Sin3 protein interaction network.

Mark K. Adams, Charles A.S. Banks, Janet L. Thornton, Cassandra G. Kempf, Ying Zhang, Sayem Miah, Yan Hao, Mihaela E. Sardiu, Maxime Killer, Gaye L. Hattem, Alexis Murray, Maria L. Katt, Laurence A. Florens, Michael P. Washburn

The paper investigates how paralog switching affects Sin3 complex interaction networks in humans, revealing shared and distinct interactions between SIN3A and SIN3B.

Molecular & Cellular Proteomics · May 28, 2020Peer-reviewedSystems Biology