Author

N. T. Woods

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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Cancer Biology· 1 Cell Biology· 1 Immunology· 1 Microbiology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 4 Research Focus:cell signaling & trafficking· 2 Research Focus:cell type annotation· 2 Organism:human· 2 Organism:mouse· 2 Assay:proteomics· 2 Assay:bulk RNA-seq· 1 Research Focus:cancer & tumor microenvironment· 1

Frequent Co-Authors

A. DiFeo· 1 shared A. Lawrence· 1 shared A. R. Black· 1 shared C. M. O'Connor· 1 shared D. Lagundzin· 1 shared E. A. Rucks· 1 shared G. Narla· 1 shared H. C. H. Law· 1 shared

Activity by Year

2019-2022 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 14 mutual co-author links

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Curved chords = mutual co-authorship

1 shared paperCancer Biology

A. DiFeo

Mutual co-authors in cluster

Author profile →

4 papers

Recent·Most cited

Small Molecule Activators of B56-PP2A Restore 4E-BP Expression and Function to Suppress Cap-dependent Translation in Cancer Cells

M. A. Lum, K. A. Jonas-Breckenridge, A. R. Black, N. T. Woods, C. M. O'Connor, R. A. Avelar, A. DiFeo, G. Narla, J. D. Black

bioRxiv · May 24, 2022Cancer Biology

Functional Requirements for a Samd14-Capping Protein Complex in Stress Erythropoiesis

S. Ray, L. Chee, Y. Zhou, M. A. Schaefer, M. J. Naldrett, S. Alvarez, N. T. Woods, K. Hewitt

This study identifies a Samd14-CP complex interaction that promotes stress erythropoiesis by enhancing SCF/c-Kit signaling in erythroid precursors.

bioRxiv · Dec 31, 2021Cell Biology

E3 Ligase UBR5 HECT domain mutations in lymphoma control maturation of B cells via alternative splicing

S. A. Swenson, T. J. Gilbreath, H. Vahle, R. W. Hynes-Smith, H. C. H. Law, N. T. Woods, M. R. Green, S. M. Buckley

This study shows that UBR5 HECT domain mutations in lymphoma disrupt B cell maturation by altering alternative splicing, suggesting a role in mantle cell lymphoma initiation.

bioRxiv · Aug 12, 2019 · PreprintImmunology

Proximity Labeling to Map Host-Pathogen Interactions at the Membrane of a Bacteria Containing Vacuole in Chlamydia trachomatis Infected Human Cells

M. G. Olson, R. E. Widner, L. M. Jorgenson, A. Lawrence, D. Lagundzin, N. T. Woods, S. P. Ouellette, E. A. Rucks

The paper uses APEX2 proximity labeling to identify Inc-Inc and Inc-host interactions at the chlamydial inclusion membrane in C. trachomatis infected human cells, revealing LRRF1 as a host protein interacting with multiple Incs.

bioRxiv · Apr 23, 2019Microbiology