Author

M. Veliova

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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Biochemistry· 1 Bioengineering· 1 Physiology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 3 Organism:mouse· 3 Research Focus:metabolism & bioenergetics· 2 Assay:ATAC-seq· 1 Assay:bulk RNA-seq· 1 Research Focus:cancer & tumor microenvironment· 1 Research Focus:cell signaling & trafficking· 1 Research Focus:cell type annotation· 1

Frequent Co-Authors

A. E. Jones· 2 shared A. Petcherski· 2 shared M. F. Oliveira· 2 shared M. Liesa· 2 shared O. S. Shirihai· 2 shared A. Brownstein· 1 shared A. Colby· 1 shared A. Martin· 1 shared

Activity by Year

2018-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 27 mutual co-author links

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2 shared papersBiochemistry

A. E. Jones

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

ENDO-LYSOSOME-TARGETED NANOPARTICLE DELIVERY OF ANTIVIRAL THERAPY FOR CORONAVIRUS INFECTIONS

A. Petcherski, B. Tingley, A. Martin, S. Adams, A. Brownstein, R. Steinberg, B. Shabane, C. Osto, J. Ngo, G. Garcia, M. Veliova, V. Arumugaswami, A. Colby, O. Shirihai, M. Grinstaff

This study develops lysosome-targeted nanoparticles loaded with mefloquine to inhibit coronavirus infection, showing effectiveness against SARS-CoV-2 and its variants in cell models.

bioRxiv · May 8, 2023 · PreprintBioengineering

Blocking mitochondrial pyruvate import causes energy wasting via futile lipid cycling in brown fat

M. Veliova, C. Mendes Ferreira, I. Y. Benador, A. E. Jones, B. R. Desousa, K. Mahdaviani, R. Acin-Perez, A. Petcherski, A. S. Divakaruni, M. Prentki, B. E. Corkey, M. Liesa, M. F. Oliveira, O. S. Shirihai

The paper shows that blocking mitochondrial pyruvate import increases ATP synthesis via futile lipid cycling in brown adipocytes, enhancing energy expenditure without adrenergic stimulation.

bioRxiv · Nov 15, 2019 · PreprintBiochemistry

NCLX prevents cell death during adrenergic activation of the brown adipose tissue

E. A. Assali, A. E. Jones, M. Veliova, M. Taha, N. Miller, M. Shum, M. F. Oliveira, G. Las, M. Liesa, I. Sekler, O. S. Shirihai

This study identifies NCLX as a critical mitochondrial Na+/Ca2+ exchanger that prevents cell death during adrenergic activation of brown adipose tissue by mitigating Ca2+ overload.

bioRxiv · Nov 6, 2018Physiology