Author

E. Calvani

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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Microbiology· 2 Biochemistry· 1 Cancer Biology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 3 Research Focus:cell type annotation· 2 Research Focus:host-pathogen & immune response· 2 Organism:human· 2 Assay:proteomics· 2 Assay:bulk RNA-seq· 1 Research Focus:chromatin & epigenetic regulation· 1 Research Focus:metabolism & bioenergetics· 1

Frequent Co-Authors

A. P. Snijders· 2 shared A. Ramaprasad· 2 shared J. I. MacRae· 2 shared P.-C. Burda· 2 shared A. Andrusaite· 1 shared A. Ghanate· 1 shared A. McKee· 1 shared A. Rossi· 1 shared

Activity by Year

2019-2023 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 16 mutual co-author links

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2 shared papersMicrobiology

A. P. Snijders

Mutual co-authors in cluster

Author profile →

4 papers

Recent·Most cited

A malaria parasite phospholipase facilitates efficient asexual blood stage egress

A. Ramaprasad, P.-C. Burda, K. Koussis, J. A. Thomas, E. Pietsch, E. Calvani, S. A. Howell, J. I. MacRae, A. P. Snijders, T. W. Gilberger, M. J. Blackman

This study identifies LCAT as a key enzyme required for efficient egress of malaria parasites from red blood cells during the asexual blood stage.

bioRxiv · Mar 13, 2023Microbiology

A choline-releasing glycerophosphodiesterase essential for phosphatidylcholine biosynthesis and blood stage development in the malaria parasite

A. Ramaprasad, P.-C. Burda, E. Calvani, A. Sait, S. A. Palma-Duran, C. Withers-Martinez, F. Hackett, J. I. MacRae, L. Collinson, T. Gilberger, M. Blackman

This study identifies PfGDPD as a choline-releasing glycerophosphodiesterase essential for phosphatidylcholine biosynthesis and blood stage development in Plasmodium falciparum.

bioRxiv · Jun 14, 2022Microbiology

m6A reader Pho92 is recruited co-transcriptionally and couples translation efficacy to mRNA decay to promote meiotic fitness in yeast

R. A. Varier, T. Sideri, C. Capitanchik, Z. Manova, E. Calvani, A. Rossi, R. Edupuganti, I. Ensinck, V. W. C. Chan, H. Patel, J. Kirkpatrick, P. Faull, A. P. Snijders, M. Vermeulen, M. Ralser, , F. van Werven

bioRxiv · Jan 20, 2022Biochemistry

Perturbation of the gut microbiota by antibiotics results in accelerated breast tumour growth and metabolic dysregulation

B. Kirkup, A. McKee, K. Makin, J. Paveley, S. Caim, C. Alcon-Giner, C. Leclaire, M. Dalby, G. Le Gall, A. Andrusaite, P. Kreuzaler, P. Driscoll, J. MacRae, E. Calvani, A. Ghanate, , S. D. Robinson

This study shows that antibiotics disrupt the gut microbiota, leading to faster breast tumour growth and metabolic changes in mice.

bioRxiv · Feb 19, 2019 · PreprintCancer Biology