Author

J. Boskovic

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 Biophysics· 1 Cell Biology· 1

Signature Assays, Organisms & Methods

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Research Focus:cell signaling & trafficking· 3 Research Focus:cell type annotation· 2 Research Focus:chromatin & epigenetic regulation· 2 Assay:cryo-EM· 2 Approach:experimental assay· 2 Organism:Arabidopsis· 1 Research Focus:development & morphogenesis· 1 Approach:genetic perturbation / CRISPR· 1

Frequent Co-Authors

A. Lopez-Perrote· 2 shared O. Llorca· 2 shared A. Behrens· 1 shared A. Cwersch· 1 shared A. Gonzalez-Corpas· 1 shared A. Palacios-Abella· 1 shared A. Pierani· 1 shared C. F. Rodriguez· 1 shared

Activity by Year

2020-2024 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 18 mutual co-author links

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2 shared papersBiochemistry

A. Lopez-Perrote

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

The structure of the R2T complex reveals a different architecture of the related HSP90 co-chaperones R2T and R2TP

A. Palacios-Abella, A. Lopez-Perrote, J. Boskovic, S. Fonseca, C. Urbez, V. Rubio, O. Llorca, D. Alabadi

The paper determines the cryoEM structure of the Arabidopsis R2T complex, revealing its dodecameric organization and distinct architecture compared to the human R2TP complex.

bioRxiv · Mar 27, 2024 · PreprintBiochemistry

Regulation of RUVBL1-RUVBL2 AAA-ATPases by the nonsense-mediated mRNA decay factor DHX34, as evidenced by Cryo-EM

O. Llorca, A. Lopez-Perrote, N. Hug, A. Gonzalez-Corpas, C. F. Rodriguez, M. Serna, C. Garcia-Martin, J. Boskovic, R. Fernandez-Leiro, J. F. Caceres

The paper shows DHX34 interacts with RUVBL1-RUVBL2 and alters its conformation to reduce ATP hydrolysis, linking it to NMD activation.

bioRxiv · Sep 28, 2020Biophysics

Lack of adaptation to centriolar defects leads to p53-independent microcephaly in the absence of Cep135

J. Gonzalez-Martinez, A. Cwersch, D. Martinez-Alonso, L. R. Lopez, J. Almagro, D. Megias, J. Boskovic, J. Gilabert, O. Grana Castro, A. Pierani, A. Behrens, S. Ortega, M. Malumbres

This study shows that Cep135 loss causes microcephaly in mice through p53-independent mechanisms due to neural progenitor adaptation failure to centriole defects.

bioRxiv · May 7, 2020 · PreprintCell Biology