Author

E. R. Porrello

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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Cell Biology· 2 Physiology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 3 Research Focus:cell type annotation· 2 Organism:human· 2 Organism:mouse· 2 Assay:bulk RNA-seq· 1 Research Focus:cell signaling & trafficking· 1 Research Focus:differential expression· 1 Research Focus:drug response / drug discovery· 1

Frequent Co-Authors

B. L. Parker· 2 shared D. A. Elliott· 2 shared H. K. Voges· 2 shared J. Molendijk· 2 shared K. Karavendzas· 2 shared R. J. Mills· 2 shared A. Suhrbier· 1 shared B. Griffen· 1 shared

Activity by Year

2020-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 37 mutual co-author links

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2 shared papersPhysiology

B. L. Parker

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Affinity purification-mass spectrometry and single fiber physiology/proteomics reveals mechanistic insights of C18ORF25

Y.-K. Ng, R. Blazev, J. McNamara, M. Dutt, J. Molendijk, E. R. Porrello, D. Elliott, B. L. Parker

The paper identifies C18ORF25 interactors and characterizes its role in skeletal muscle physiology using mass spectrometry and single fiber proteomics.

bioRxiv · Oct 30, 2023Physiology

Alpha kinase 3 signaling at the M-band maintains sarcomere integrity and proteostasis in striated muscle.

J. W. McNamara, B. L. Parker, H. K. Voges, N. R. R. Mehdiabadi, F. Bolk, D. D. Chung, N. Charitakis, J. Molendijk, S. Lal, M. Ramialison, K. Karavendzas, H. L. Pointer, P. Syrris, L. R. Lopes, E. M. Perry, , D. A. Elliott

This study identifies ALPK3's role in maintaining sarcomere integrity and proteostasis in striated muscle by localizing to the M-band and interacting with SQSTM1.

bioRxiv · Sep 1, 2022Cell Biology

Bromodomain and Extraterminal Inhibition Blocks Inflammation-Induced Cardiac Dysfunction and SARS-CoV-2 Infection (Pre-Clinical)

R. J. Mills, S. J. Humphrey, P. R. Fortuna, M. Lor, S. R. Foster, G. A. Quaife-Ryan, R. L. Johnston, T. Dumenil, C. Bishop, R. Ruraraju, D. J. Rawle, T. Le, W. Zhao, L. Lee, C. Mackenzie-Kludas, , E

The paper identifies BET inhibitors as potential cardio-protective drugs that block inflammation-induced cardiac dysfunction and SARS-CoV-2 infection in pre-clinical models.

bioRxiv · Aug 23, 2020 · PreprintCell Biology