Author

K. McLaughlin

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

Biology Disciplines

Click to filter author papers

Biochemistry· 2 Bioengineering· 1 Cancer Biology· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

Approach:experimental assay· 4 Research Focus:cell type annotation· 2 Organism:mouse· 2 Research Focus:cancer & tumor microenvironment· 1 Research Focus:cell signaling & trafficking· 1 Assay:ChIP-seq· 1 Research Focus:chromatin & epigenetic regulation· 1 Research Focus:development & morphogenesis· 1

Frequent Co-Authors

A. Dest· 1 shared A. E. Ryan· 1 shared A. Enrriques· 1 shared A. J. McIntyre· 1 shared A. Lees· 1 shared A. Pereyra· 1 shared C. Coletti· 1 shared C. Gao· 1 shared

Activity by Year

2019-2023 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 10 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 paperBiochemistry

A. Dest

Mutual co-authors in cluster

Author profile →

4 papers

Recent·Most cited

Pan-tissue mitochondrial phenotyping reveals lower OXPHOS expression and function across tumor types

I. Boykov, M. Montgomery, J. Hagen, R. Aruleba, K. McLaughlin, H. Coalson, M. Nelson, A. Pereyra, J. Ellis, T. Zeczycki, N. Vohra, S.-F. Tan, M. Cabot, K. Fisher-Wellman

The paper evaluates mitochondrial OXPHOS expression and function across murine tumors and normal tissues, finding lower OXPHOS levels in tumors compared to normal and high OXPHOS organs.

bioRxiv · Jun 4, 2023 · PreprintBiochemistry

Structure-Property-Processing Correlations of Graphene Bioscaffolds for Proliferation and Differentiation of C2C12 Cells

L. Karriem, J. Eixenberger, S. Frahs, D. Convertino, T. Webb, T. Pandhi, K. McLaughlin, A. Enrriques, P. Davis, H. Subbaraman, C. Coletti, J. Oxford, D. Estrada

This study examines how different graphene bioscaffold production methods affect C2C12 cell morphology, gene expression, and differentiation.

bioRxiv · Apr 25, 2023 · PreprintBioengineering

Structural insights into the recognition of mono- and di-acetylated histones by the ATAD2B bromodomain

J. T. Lloyd, K. McLaughlin, M. Y. Lubula, J. C. Gay, A. Dest, C. Gao, M. Phillips, M. Tonelli, G. Cornilescu, M. R. Marunde, C. M. Evans, S. P. Boyson, S. Carlson, M.-C. Keogh, J. L. Markley, , K. C. Glass

This study investigates the ligand specificity of the ATAD2B bromodomain, showing it binds mono- and di-acetylated histones and identifies structural features critical for this recognition.

bioRxiv · May 12, 2020 · PreprintBiochemistry

FLIP(L) determines p53 induced life or death

A. Lees, A. J. McIntyre, F. Falcone, N. T. Crawford, C. McCann, G. P. Quinn, J. Z. Roberts, T. Sessler, P. F. Gallagher, K. McAllister, K. McLaughlin, W. L. Allen, C. Holohan, L. J. Egan, A. E. Ryan, , S. S. McDade

This study identifies FLIP(L) as a p53 target that determines cell fate by promoting cell cycle arrest and inhibiting apoptosis.

bioRxiv · Nov 28, 2019 · PreprintCancer Biology