Author

L. R. Cadena

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· 1 Evolutionary Biology· 1

Signature Assays, Organisms & Methods

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Research Focus:cell type annotation· 2 Approach:experimental assay· 2 Research Focus:cell signaling & trafficking· 1 Research Focus:chromatin & epigenetic regulation· 1 Research Focus:development & morphogenesis· 1

Frequent Co-Authors

H. Hashimi· 2 shared A. J. Roger· 1 shared A. T. Gardiner· 1 shared A. Zikova· 1 shared B. Panicucci· 1 shared C. H. Slamovits· 1 shared J. Lukes· 1 shared J. T. Beatty· 1 shared

Activity by Year

2021-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 31 mutual co-author links

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2 shared papersEvolutionary Biology

H. Hashimi

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2 papers

Recent·Most cited

The development of intracytoplasmic membranes in alphaproteobacteria involves the conserved mitochondrial crista-developing protein Mic60

S. A. Munoz-Gomez, L. R. Cadena, A. T. Gardiner, M. M. Leger, S. Sheikh, L. Connell, T. Bily, K. Kopejtka, J. T. Beatty, M. Koblizek, A. J. Roger, C. H. Slamovits, J. Lukes, H. Hashimi

This study shows that Mic60 homologs in alphaproteobacteria are involved in intracytoplasmic membrane development and contact site formation, supporting the hypothesis that mitochondrial cristae evolved from bacterial ICMs.

bioRxiv · Jun 14, 2022 · PreprintEvolutionary Biology

MICOS and F1FO-ATP synthase crosstalk is a fundamental property of mitochondrial cristae

L. R. Cadena, O. Gahura, B. Panicucci, A. Zikova, H. Hashimi

The paper shows that MICOS and F1FO-ATP synthase crosstalk, which shapes mitochondrial cristae, is conserved in Trypanosoma brucei despite 2 billion years of independent evolution.

bioRxiv · Apr 1, 2021 · PreprintCell Biology