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Vassilis Roukos

Showing results (31-40 of 40) with videos related to

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Science Advances|October 22, 2021
RNA polymerase II is required for spatial chromatin reorganization following exit from mitosisShu Zhang, Nadine Übelmesser, Natasa Josipovic, et al.
Nucleic Acids Research|November 9, 2022
PARP1 proximity proteomics reveals interaction partners at stressed replication forksThorsten Mosler, H Irem Baymaz, Justus F Gräf, et al.
Nucleic Acids Research|September 26, 2025
Coordinated control of genome-nuclear lamina interactions by topoisomerase 2B and lamin B receptorTom van Schaik, Mikhail Magnitov, Marcel de Haas, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 11, 2018
PARP-1 protects against colorectal tumor induction, but promotes inflammation-driven colorectal tumor progressionBastian Dörsam, Nina Seiwert, Sebastian Foersch, et al.
Molecular Cell|November 1, 2024
Type II topoisomerases shape multi-scale 3D chromatin folding in regions of positive supercoilsGabriel M C Longo, Sergi Sayols, Maria E Stefanova, et al.
The Journal of Pathology|October 10, 2022
Cdt1 overexpression drives colorectal carcinogenesis through origin overlicensing and DNA damageMichalis Petropoulos, Spyridon Champeris Tsaniras, Sofia Nikou, et al.
Molecular Cell|June 17, 2019
Spatial Chromosome Folding and Active Transcription Drive DNA Fragility and Formation of Oncogenic MLL TranslocationsHenrike Johanna Gothe, Britta Annika Maria Bouwman, Eduardo Gade Gusmao, et al.
Molecular Cell|May 1, 2018
HMGB2 Loss upon Senescence Entry Disrupts Genomic Organization and Induces CTCF Clustering across Cell TypesAnne Zirkel, Milos Nikolic, Konstantinos Sofiadis, et al.
Nature Communications|April 24, 2024
High clonal diversity and spatial genetic admixture in early prostate cancer and surrounding normal tissueNing Zhang, Luuk Harbers, Michele Simonetti, et al.
The Journal of Clinical Investigation|January 13, 2022
RECON syndrome is a genome instability disorder caused by mutations in the DNA helicase RECQL1Bassam Abu-Libdeh, Satpal S Jhujh, Srijita Dhar, et al.
Pageof 4

Showing results (31-40 of 40) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 40 results.
Science Advances|October 22, 2021
RNA polymerase II is required for spatial chromatin reorganization following exit from mitosisShu Zhang, Nadine Übelmesser, Natasa Josipovic, et al.
Nucleic Acids Research|November 9, 2022
PARP1 proximity proteomics reveals interaction partners at stressed replication forksThorsten Mosler, H Irem Baymaz, Justus F Gräf, et al.
Nucleic Acids Research|September 26, 2025
Coordinated control of genome-nuclear lamina interactions by topoisomerase 2B and lamin B receptorTom van Schaik, Mikhail Magnitov, Marcel de Haas, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 11, 2018
PARP-1 protects against colorectal tumor induction, but promotes inflammation-driven colorectal tumor progressionBastian Dörsam, Nina Seiwert, Sebastian Foersch, et al.
Molecular Cell|November 1, 2024
Type II topoisomerases shape multi-scale 3D chromatin folding in regions of positive supercoilsGabriel M C Longo, Sergi Sayols, Maria E Stefanova, et al.
The Journal of Pathology|October 10, 2022
Cdt1 overexpression drives colorectal carcinogenesis through origin overlicensing and DNA damageMichalis Petropoulos, Spyridon Champeris Tsaniras, Sofia Nikou, et al.
Molecular Cell|June 17, 2019
Spatial Chromosome Folding and Active Transcription Drive DNA Fragility and Formation of Oncogenic MLL TranslocationsHenrike Johanna Gothe, Britta Annika Maria Bouwman, Eduardo Gade Gusmao, et al.
Molecular Cell|May 1, 2018
HMGB2 Loss upon Senescence Entry Disrupts Genomic Organization and Induces CTCF Clustering across Cell TypesAnne Zirkel, Milos Nikolic, Konstantinos Sofiadis, et al.
Nature Communications|April 24, 2024
High clonal diversity and spatial genetic admixture in early prostate cancer and surrounding normal tissueNing Zhang, Luuk Harbers, Michele Simonetti, et al.
The Journal of Clinical Investigation|January 13, 2022
RECON syndrome is a genome instability disorder caused by mutations in the DNA helicase RECQL1Bassam Abu-Libdeh, Satpal S Jhujh, Srijita Dhar, et al.
Pageof 4