Author

Katherine M. McKenney

University of MinnesotaORCID 0000-0002-7423-266XUnclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Organism:human· 3 Assay:bulk RNA-seq· 2 Research Focus:differential expression· 2 Approach:experimental assay· 2 Approach:statistical model· 1

Frequent Co-Authors

Aaron C. GoldstrohmiD· 3 shared Elise B. DunsheeiD· 3 shared Robert P. ConnacheriD· 2 shared Carmen Hernandez-PereziD· 1 shared Eugene ValkoviD· 1 shared John M. PumiD· 1 shared Justin BrumbaughiD· 1 shared Khadija RebbaniiD· 1 shared

Activity by Year

2024-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 33 mutual co-author links

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3 shared papersMolecular Biology

Aaron C. GoldstrohmORCID

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3 papers

Recent·Most cited

BiochemistrybioRxivPreprintOct 2, 2026

Global Regulatory Functions of the Human CCR4-NOT Complex in mRNA Deadenylation and Decay

Katherine M. McKenney, Mika Nevo, Robert P. Connacher…·Aaron C. Goldstrohm

The paper identifies the regulatory roles of the CCR4-NOT complex in mRNA deadenylation and decay by analyzing transcriptome-wide effects of subunit depletion.

DOI 10.64898/2026.09.30.755734

humanbulk RNA-seq

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Molecular BiologybioRxivPreprintOct 2, 2025

Cytoplasmic poly-adenosine binding proteins modulate susceptibility of mRNAs to RNA-binding protein-directed decay

Katherine M. McKenney, Carmen Hernandez-Perez, Elise B. Dunshee…·Aaron C. Goldstrohm

This study shows that PABPCs modulate PUM1/2-mediated mRNA decay by protecting poly(A) tails, with PABPC levels determining mRNA susceptibility to degradation.

DOI 10.1101/2025.10.02.680050

humanexperimental assay

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Molecular BiologyRNAPeer-reviewedJan 24, 2024

Chemi-Northern: a versatile chemiluminescent northern blot method for analysis and quantitation of RNA molecules.

Katherine M. McKenney, Robert P. Connacher, Elise B. Dunshee, Aaron C. Goldstrohm

The paper introduces Chemi-Northern, a chemiluminescent northern blot method for RNA detection and quantitation, showing it is sensitive, fast, and suitable for analyzing natural and engineered RNAs.

10 citations

humanbulk RNA-seq

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