Author

K. E. Ankenbauer

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

Signature Assays, Organisms & Methods

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Organism:human· 2 Assay:bulk RNA-seq· 1 Research Focus:cell signaling & trafficking· 1 Research Focus:cell type annotation· 1 Research Focus:differential expression· 1 Approach:experimental assay· 1 Assay:proteomics· 1 Approach:statistical model· 1

Frequent Co-Authors

A. Judd· 1 shared A. Kruse· 1 shared A. L. Mattheyses· 1 shared A. Maitra· 1 shared B. Jarvis· 1 shared B. Kumar· 1 shared C. Copeland· 1 shared F. Revetta· 1 shared

Activity by Year

2023-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 36 mutual co-author links

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1 shared paperCancer Biology

A. Judd

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Author profile →

2 papers

Recent·Most cited

Mutant GNAS drives a pyloric metaplasia with tumor suppressive glycans in intraductal papillary mucinous neoplasia

V. Q.-H. Trinh, K. E. Ankenbauer, S. M. Torbit, J. Liu, M. Batardiere, B. Kumar, H. C. Maurer, F. Revetta, Z. Chen, A. Kruse, A. Judd, C. Copeland, J. Wong, O. Ben-Levy, B. Jarvis, , K. E. DelGiorno

This study identifies GNASR201C as a driver of pyloric metaplasia in IPMN, characterized by tumor-suppressive glycans that inhibit cancer progression.

bioRxiv · Feb 25, 2024 · PreprintCancer Biology

Sialylation of EGFR by ST6GAL1 induces receptor activation and modulates trafficking dynamics

K. E. Ankenbauer, T. C. Rao, A. L. Mattheyses, S. L. Bellis

This study shows that ST6GAL1-mediated 2,6 sialylation of EGFR enhances receptor activation, dimerization, and recycling while inhibiting lysosomal degradation.

bioRxiv · Jun 3, 2023Cell Biology