Author

A. Poti

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· 2 Cell Biology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 3 Research Focus:cell type annotation· 2 Organism:human· 2 Research Focus:chromatin & epigenetic regulation· 1 Assay:DNA methylation· 1 Research Focus:drug response / drug discovery· 1 Research Focus:host-pathogen & immune response· 1 Approach:microscopy & imaging analysis· 1

Frequent Co-Authors

D. Szuts· 2 shared A. Bekesi· 1 shared A. Ciliberto· 1 shared A. Remenyi· 1 shared B. G. Vertessy· 1 shared B. Gyorffy· 1 shared C. Gemma· 1 shared E. Chiroli· 1 shared

Activity by Year

2019-2020 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 24 mutual co-author links

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2 shared papersCell Biology

D. Szuts

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Epistasis, aneuploidy, and gain-of-function mutations underlie the evolution ofresistance to induced microtubule depolymerization

M. Pavani, P. Bonaiuti, E. Chiroli, F. Gross, F. Natali, F. Macaluso, A. Poti, S. Pasqualato, S. Pompei, M. Cosentino Lagomarsino, G. Rancati, D. Szuts, A. Ciliberto

The paper evolves yeast populations with impaired microtubule polymerization and identifies mutations and chromosome duplications that confer resistance to microtubule depolymerizing drugs.

bioRxiv · Oct 7, 2020 · PreprintCell Biology

Genome-wide alterations of uracil distribution patterns in human DNA upon chemotherapeutic treatments

H. L. Palinkas, A. Bekesi, G. Rona, L. Pongor, G. Tihanyi, E. Holub, A. Poti, C. Gemma, S. Ali, M. J. Morten, E. Rothenberg, M. Pagano, D. Szuts, B. Gyorffy, B. G. Vertessy

The paper investigates genome-wide uracil distribution changes in human cells after chemotherapy, finding drug-induced shifts toward active genomic regions.

bioRxiv · Mar 4, 2020Biochemistry

High throughput competitive fluorescence polarization assay reveals functionalredundancy in the S100 protein family

M. Simon, G. Gogl, P. Ecsedi, G. M. Kovacs, A. Poti, A. Remenyi, J. Kardos, L. Nyitray

The paper uses a high-throughput fluorescence polarization assay to analyze the functional redundancy and interaction patterns of the human S100 protein family.

bioRxiv · Jul 29, 2019Biochemistry