Author

A. M. Webb

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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Biochemistry· 1 Cell Biology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Research Focus:cell signaling & trafficking· 1 Research Focus:development & morphogenesis· 1 Research Focus:protein folding & dynamics· 1 Assay:protein sequence· 1 Assay:proteomics· 1 Organism:zebrafish· 1

Frequent Co-Authors

C. R. Francis· 1 shared E. J. Kushner· 1 shared H. Kincross· 1 shared J. J. Ottesen· 1 shared J. M. Webb· 1 shared K. M. Lundy· 1 shared M. G. Poirier· 1 shared N. L. Burge· 1 shared

Activity by Year

2019-2020 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 21 mutual co-author links

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1 shared paperCell Biology

C. R. Francis

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

EHBP1 and EHD2 regulate Dll4 caveolin-mediated endocytosis during blood vessel development

A. M. Webb, C. R. Francis, J. M. Webb, H. Kincross, K. M. Lundy, R. Judson, S. M. Meadows, E. J. Kushner

This study identifies EHBP1 and EHD2 as regulators of Dll4 endocytosis in endothelial cells, showing their role in caveolin-mediated processes during blood vessel development.

bioRxiv · May 19, 2020 · PreprintCell Biology

Convergent Hybrid Phase Ligation Strategy for Efficient Total Synthesis of Large Proteins Demonstrated for 212-residue Linker Histone H1.2

Z. Z. Hong, R. R. Yu, X. Zhang, A. M. Webb, N. L. Burge, M. G. Poirier, J. J. Ottesen

The paper develops a convergent hybrid phase ligation strategy for synthesizing large proteins, demonstrating its effectiveness with the 212-residue histone H1.2.

bioRxiv · Jun 6, 2019Biochemistry