Author

P. Risteski

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· 4

Signature Assays, Organisms & Methods

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Approach:experimental assay· 4 Research Focus:cell signaling & trafficking· 3 Organism:human· 3 Assay:imaging· 2 Research Focus:chromatin & epigenetic regulation· 1

Frequent Co-Authors

I. M. Tolic· 4 shared M. Jagric· 3 shared J. Martincic· 2 shared A. Bosilj· 1 shared A. Milas· 1 shared D. Bozan· 1 shared E. Tintor· 1 shared I. Ponjavic· 1 shared

Activity by Year

2019-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 21 mutual co-author links

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4 shared papersCell Biology

I. M. Tolic

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4 papers

Recent·Most cited

Microtubule poleward flux as a target for modifying chromosome segregation errors

P. Risteski, J. Martincic, E. Tintor, M. Jagric, I. M. Tolic

This study shows that reducing microtubule poleward flux can rescue chromosome segregation errors in cancer cells by slowing kinetochore microtubule growth and improving alignment.

bioRxiv · Mar 11, 2024Cell Biology

Coordinated poleward flux of sister kinetochore fibers drives chromosome alignment

P. Risteski, D. Bozan, M. Jagric, A. Bosilj, N. Pavin, I. M. Tolic

The paper introduces a flux-driven model for chromosome alignment, showing that length-dependent kinetochore fiber flux, regulated by Kif18A, Kif4A, and NuMA, promotes proper chromosome positioning.

Cell Reports · Aug 1, 2022Peer-reviewedCell Biology

Optogenetic control of PRC1 reveals that bridging fibers promote chromosome alignment by overlap length-dependent forces

M. Jagric, P. Risteski, J. Martincic, A. Milas, I. M. Tolic

This study uses optogenetic removal of PRC1 to show that bridging fibers promote chromosome alignment through overlap length-dependent forces.

bioRxiv · Jul 14, 2020Cell Biology

Chromosome segregation is driven by joint microtubule sliding action of kinesins KIF4A and EG5

K. Vukusic, R. Buđa, I. Ponjavic, P. Risteski, I. M. Tolic

The paper identifies KIF4A and EG5 as essential for spindle elongation through microtubule sliding in human cells, showing two independent sliding modules drive this process.

bioRxiv · Dec 20, 2019Cell Biology