Author

L. M. Glendenning

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

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Signature Assays, Organisms & Methods

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Approach:experimental assay· 4 Assay:proteomics· 4 Organism:mouse· 3 Research Focus:cell type annotation· 2 Research Focus:cell signaling & trafficking· 1 Research Focus:host-pathogen & immune response· 1 Organism:human· 1

Frequent Co-Authors

B. A. Cobb· 4 shared J. Y. Zhou· 3 shared E. N. Kukan· 2 shared K. M. Reynero· 2 shared R. D. Cummings· 2 shared C. Gao· 1 shared D. M. Oswald· 1 shared M. D. Long· 1 shared

Activity by Year

2022-2023 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 28 mutual co-author links

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4 shared papersImmunology

B. A. Cobb

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4 papers

Recent·Most cited

IgG sialylation occurs via the FcRn-mediated recycling pathway in endothelial cells

L. M. Glendenning, K. M. Reynero, E. N. Kukan, M. D. Long, B. A. Cobb

The paper shows that endothelial cells regulate IgG sialylation through the FcRn-mediated recycling pathway, impacting inflammatory responses.

bioRxiv · Jun 30, 2023 · PreprintImmunology

Platelet-Localized ST6Gal1 Does Not Impact IgG Sialylation

L. M. Glendenning, J. Y. Zhou, E. N. Kukan, C. Gao, R. D. Cummings, S. Joshi, S. W. Whiteheart, B. A. Cobb

This study investigates whether platelet-localized ST6Gal1 affects IgG sialylation and finds no significant impact.

bioRxiv · Jun 15, 2023Immunology

Plasma ST6Gal1 is Dispensable for IgG Sialylation

D. M. Oswald, S. D. Lehoux, J. Y. Zhou, L. M. Glendenning, R. D. Cummings, B. A. Cobb

The paper shows that plasma ST6Gal1 is not required for IgG 2,6-sialylation, as IgG sialylation remains normal in mice lacking ST6Gal1 in hepatocytes or B cells.

bioRxiv · Feb 1, 2022Immunology

Divergent Golgi Trafficking Limits B cell-Mediated IgG Sialylation

L. M. Glendenning, J. Y. Zhou, K. M. Reynero, B. A. Cobb

This study shows that IgG sialylation and fucosylation diverge from B cell surface glycoprotein modification, with IgG avoiding sialylation and favoring fucosylation due to distinct trafficking patterns.

bioRxiv · Jan 25, 2022Immunology