Author

B. Panicucci

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 Microbiology· 1

Signature Assays, Organisms & Methods

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

Frequent Co-Authors

A. Zikova· 2 shared C. Hierro-Yap· 1 shared E. Pineda· 1 shared F. Bringaud· 1 shared G. Taleva· 1 shared H. Hashimi· 1 shared L. R. Cadena· 1 shared M. Biran· 1 shared

Activity by Year

2021-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 31 mutual co-author links

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2 shared papersMicrobiology

A. Zikova

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

Trypanosoma brucei bloodstream form mitochondrion is capable of ATP production by substrate phoshorylation

G. Taleva, M. Husova, B. Panicucci, C. Hierro-Yap, E. Pineda, M. Biran, M. Moos, P. Simek, F. Bringaud, A. Zikova

This study shows that Trypanosoma brucei mitochondria can produce ATP via substrate phosphorylation, which is crucial under nutrient-limited conditions.

bioRxiv · May 26, 2023 · PreprintMicrobiology

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