Author

D. Ascencio

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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Evolutionary Biology· 2

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Organism:yeast· 2 Research Focus:cell signaling & trafficking· 1 Research Focus:cell type annotation· 1 Research Focus:chromatin & epigenetic regulation· 1 Research Focus:development & morphogenesis· 1 Assay:protein sequence· 1 Assay:protein structure· 1

Frequent Co-Authors

A. K. Dube· 2 shared C. R. Landry· 2 shared I. Gagnon-Arsenault· 2 shared A. Cisneros· 1 shared A. DeLuna· 1 shared A. Marchant· 1 shared C. Eberlein· 1 shared D. Evans-Yamamoto· 1 shared

Activity by Year

2019-2020 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 35 mutual co-author links

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2 shared papersEvolutionary Biology

A. K. Dube

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2 papers

Recent·Most cited

Expression attenuation as a mechanism of robustness to gene duplication in protein complexes

D. Ascencio, G. Diss, I. Gagnon-Arsenault, A. K. Dube, A. DeLuna, C. R. Landry

The paper investigates the fitness effects of gene duplication in budding yeast, finding that most protein complex subunits have minimal fitness impact, while large complexes are protected by reduced protein abundance.

bioRxiv · Jul 9, 2020 · PreprintEvolutionary Biology

The role of structural pleiotropy and regulatory evolution in the retention of heteromers of paralogs

A. Marchant, A. Cisneros, A. K. Dube, I. Gagnon-Arsenault, D. Ascencio, H. Jain, S. Aube, C. Eberlein, D. Evans-Yamamoto, N. Yachie, C. R. Landry

The paper investigates how structural pleiotropy and regulatory evolution influence the retention of heteromers formed by paralogs in budding yeast.

bioRxiv · Jul 16, 2019Evolutionary Biology