Author

S. S. Apte

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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Research Focus:cell type annotation· 2 Approach:experimental assay· 2 Assay:proteomics· 2 Research Focus:differential expression· 1 Organism:human· 1 Organism:mouse· 1

Frequent Co-Authors

D. K. Tacdol· 1 shared D. Martin· 1 shared G. Deshpande· 1 shared G. S. Gojanovich· 1 shared J. R. Heckl· 1 shared J. R. Johansooz· 1 shared J. T. Kuwabara· 1 shared K. L. Robert· 1 shared

Activity by Year

2021-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 24 mutual co-author links

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1 shared paperCell Biology

D. K. Tacdol

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2 papers

Recent·Most cited

Degradomic identification of membrane type 1-matrix metalloproteinase (MT1-MMP/MMP14) as an ADAMTS9 and ADAMTS20 substrate

S. Nandadasa, D. Martin, G. Deshpande, K. L. Robert, M. S. Stack, Y. Itoh, S. S. APTE

This study identifies ADAMTS9 and ADAMTS20 as substrates of MT1-MMP using N-terminomics, showing their role in regulating MT1-MMP activity and cell-surface function.

Molecular & Cellular Proteomics · Jun 1, 2023Peer-reviewedBiochemistry

Consequences of PDGFRα+ fibroblast reduction in adult murine hearts

J. T. Kuwabara, S. Bhutada, V. Shettigar, G. S. Gojanovich, L. P. DeAngelo, J. R. Heckl, J. R. Johansooz, D. K. Tacdol, M. T. Ziolo, S. S. Apte, M. D. Tallquist

This study shows that reducing PDGFRα+ fibroblasts in adult mice improves cardiac function after injury without altering fibrillar collagen, suggesting potential therapeutic benefits.

bioRxiv · May 7, 2021Cell Biology