Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Janne J M van Schie"'
Autor:
Atiq Faramarz, Jesper A Balk, Janne J M van Schie, Anneke B Oostra, Cherien A Ghandour, Martin A Rooimans, Rob M F Wolthuis, Job de Lange
Publikováno v:
PLoS ONE, Vol 15, Iss 1, p e0220348 (2020)
In a process linked to DNA replication, duplicated chromosomes are entrapped in large, circular cohesin complexes and functional sister chromatid cohesion (SCC) is established by acetylation of the SMC3 cohesin subunit. Roberts Syndrome (RBS) and War
Externí odkaz:
https://doaj.org/article/70c181c7128843c4bada5b22ebd8f2ca
Autor:
Renaud L. M. Tissier, Janne J. M. van Schie, Rob M. F. Wolthuis, Job de Lange, Renée de Menezes
Publikováno v:
BMC Bioinformatics, Vol 24, Iss 1, Pp 1-21 (2023)
Abstract Background CRISPR screens provide large-scale assessment of cellular gene functions. Pooled libraries typically consist of several single guide RNAs (sgRNAs) per gene, for a large number of genes, which are transduced in such a way that ever
Externí odkaz:
https://doaj.org/article/aae7e52e22ba42efa7783aa38dc7a984
Autor:
Renaud L. M. Tissier, Janne J. M. van Schie, Rob M. F. Wolthuis, Job de Lange, Renée de Menezes
Background CRISPR screens provide large-scale assessment of cellular gene functions. Pooled libraries typically consist of several single guide RNAs (sgRNAs) per gene, for a large number of genes, which are transduced in such a way that every cell re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2fb380cf14c7038264e35821d7029a80
https://doi.org/10.1101/2022.03.31.486584
https://doi.org/10.1101/2022.03.31.486584
Autor:
Josephine C. Dorsman, Khashayar Roohollahi, Rob M. F. Wolthuis, Daphne E. C. Boer, Johannes C. Walter, Mats Ljungman, Román González-Prieto, Yuichiro Hara, Job de Lange, Tomoo Ogi, Alfred C.O. Vertegaal, Yuka Nakazawa, Yana van der Weegen, Ishwarya Venkata Narayanan, Tycho E. T. Mevissen, Klaas de Lint, Sylvie M. Noordermeer, Diana van den Heuvel, Marta San Martin Alonso, Martijn S. Luijsterburg, Annelotte P. Wondergem, Noud H. M. Klaassen, Janne J. M. van Schie
Publikováno v:
Nature Cell Biology, 23(6), 595-607. Nature Publishing Group
Nature Cell Biology
Nature Cell Biology, 23(6), 595-607. NATURE RESEARCH
van der Weegen, Y, de Lint, K, van den Heuvel, D, Nakazawa, Y, Mevissen, T E T, van Schie, J J M, San Martin Alonso, M, Boer, D E C, González-Prieto, R, Narayanan, I V, Klaassen, N H M, Wondergem, A P, Roohollahi, K, Dorsman, J C, Hara, Y, Vertegaal, A C O, de Lange, J, Walter, J C, Noordermeer, S M, Ljungman, M, Ogi, T, Wolthuis, R M F & Luijsterburg, M S 2021, ' ELOF1 is a transcription-coupled DNA repair factor that directs RNA polymerase II ubiquitylation ', Nature Cell Biology, vol. 23, no. 6, pp. 595-607 . https://doi.org/10.1038/s41556-021-00688-9
Nature cell biology, 23(6), 595-607. Nature Publishing Group
Nat Cell Biol
Nature Cell Biology
Nature Cell Biology, 23(6), 595-607. NATURE RESEARCH
van der Weegen, Y, de Lint, K, van den Heuvel, D, Nakazawa, Y, Mevissen, T E T, van Schie, J J M, San Martin Alonso, M, Boer, D E C, González-Prieto, R, Narayanan, I V, Klaassen, N H M, Wondergem, A P, Roohollahi, K, Dorsman, J C, Hara, Y, Vertegaal, A C O, de Lange, J, Walter, J C, Noordermeer, S M, Ljungman, M, Ogi, T, Wolthuis, R M F & Luijsterburg, M S 2021, ' ELOF1 is a transcription-coupled DNA repair factor that directs RNA polymerase II ubiquitylation ', Nature Cell Biology, vol. 23, no. 6, pp. 595-607 . https://doi.org/10.1038/s41556-021-00688-9
Nature cell biology, 23(6), 595-607. Nature Publishing Group
Nat Cell Biol
Two side-by-side papers report that the transcription elongation factor ELOF1 drives transcription-coupled repair and prevents replication stress.Cells employ transcription-coupled repair (TCR) to eliminate transcription-blocking DNA lesions. DNA dam
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2732c1379e417cb3de9574f29cff90d4
https://doi.org/10.1038/s41556-021-00688-9
https://doi.org/10.1038/s41556-021-00688-9
Autor:
Bente Benedict, Hein te Riele, Anneke B. Oostra, Janne J. M. van Schie, Rob M. F. Wolthuis, Jesper A. Balk, Job de Lange
Publikováno v:
Developmental Cell, 52(6), 683-698.e7. Cell Press
Benedict, B, van Schie, J J M, Oostra, A B, Balk, J A, Wolthuis, R M F, Riele, H T & de Lange, J 2020, ' WAPL-Dependent Repair of Damaged DNA Replication Forks Underlies Oncogene-Induced Loss of Sister Chromatid Cohesion ', Developmental Cell, vol. 52, no. 6, pp. 683-698.e7 . https://doi.org/10.1016/j.devcel.2020.01.024
Developmental cell, 52(6), 683-698.e7. Cell Press
Benedict, B, van Schie, J J M, Oostra, A B, Balk, J A, Wolthuis, R M F, Riele, H T & de Lange, J 2020, ' WAPL-Dependent Repair of Damaged DNA Replication Forks Underlies Oncogene-Induced Loss of Sister Chromatid Cohesion ', Developmental Cell, vol. 52, no. 6, pp. 683-698.e7 . https://doi.org/10.1016/j.devcel.2020.01.024
Developmental cell, 52(6), 683-698.e7. Cell Press
Summary Premature loss of sister chromatid cohesion at metaphase is a diagnostic marker for different cohesinopathies. Here, we report that metaphase spreads of many cancer cell lines also show premature loss of sister chromatid cohesion. Cohesion lo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c192ac2928199eade74f6e1f8dd1387a
https://research.vumc.nl/en/publications/7e131367-b0d7-44c9-be9c-eaa2cefff403
https://research.vumc.nl/en/publications/7e131367-b0d7-44c9-be9c-eaa2cefff403
Autor:
Anneke B. Oostra, Jesper A. Balk, Cherien A. Ghandour, Rob M. F. Wolthuis, Job de Lange, Atiq Faramarz, Martin A. Rooimans, Janne J. M. van Schie
Publikováno v:
PLoS ONE, 15(1):e0220348. Public Library of Science
PLoS ONE, Vol 15, Iss 1, p e0220348 (2020)
Faramarz, A, Balk, J A, van Schie, J J M, Oostra, A B, Ghandour, C A, Rooimans, M A, Wolthuis, R M F & de Lange, J 2020, ' Non-redundant roles in sister chromatid cohesion of the DNA helicase DDX11 and the SMC3 acetyl transferases ESCO1 and ESCO2 ', PLoS ONE, vol. 15, no. 1, e0220348, pp. e0220348 . https://doi.org/10.1371/journal.pone.0220348
PLoS ONE
PLoS ONE, Vol 15, Iss 1, p e0220348 (2020)
Faramarz, A, Balk, J A, van Schie, J J M, Oostra, A B, Ghandour, C A, Rooimans, M A, Wolthuis, R M F & de Lange, J 2020, ' Non-redundant roles in sister chromatid cohesion of the DNA helicase DDX11 and the SMC3 acetyl transferases ESCO1 and ESCO2 ', PLoS ONE, vol. 15, no. 1, e0220348, pp. e0220348 . https://doi.org/10.1371/journal.pone.0220348
PLoS ONE
In a process linked to DNA replication, duplicated chromosomes are entrapped in large, circular cohesin complexes and functional sister chromatid cohesion (SCC) is established by acetylation of the SMC3 cohesin subunit. Roberts Syndrome (RBS) and War
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::64c2656aa59e74c81bcf9a92bdd88143
https://research.vumc.nl/en/publications/ecd743ae-f239-4fe2-a504-4286627096d4
https://research.vumc.nl/en/publications/ecd743ae-f239-4fe2-a504-4286627096d4
Autor:
Najim Ameziane, Francesca M. Pisani, Erika Cantelli, Joanna L Parish, Job de Lange, Atiq Faramarz, Marjon van Slegtenhorst, Ingeborg Barišić, Jesper A. Balk, Grant S. Stewart, Martin A. Rooimans, Janne J. M. van Schie, Rob M. F. Wolthuis, Katja Dumic, Hein te Riele, Karin E. M. Diderich, Cynthia de Almeida Estéves, Anneke B. Oostra, Mohammad Mahtab
Publikováno v:
Nature communications 11 (2020): 4287–4305. doi:10.1038/s41467-020-18066-8
info:cnr-pdr/source/autori:van Schie J.J.M.; Faramarz A.; Balk J.A.; Stewart G.S.; Cantelli E.; Oostra A.B.; Rooimans M.A.; Parish J.L.; de Almeida Esteves C.; Dumic K.; Barisic I.; Diderich K.E.M.; van Slegtenhorst M.A.; Mahtab M.; Pisani F.M.; te Riele H.; Ameziane N.; Wolthuis R.M.F.; de Lange J./titolo:Warsaw Breakage Syndrome associated DDX11 helicase resolves G-quadruplex structures to support sister chromatid cohesion/doi:10.1038%2Fs41467-020-18066-8/rivista:Nature communications/anno:2020/pagina_da:4287/pagina_a:4305/intervallo_pagine:4287–4305/volume:11
Nature Communications, 11(1):4287. Nature Publishing Group
Nature Communications
Nature communications, 11(1):4287. Nature Publishing Group
Nature Communications, 11(1):4287. Nature Publishing Group UK
Nature Communications, Vol 11, Iss 1, Pp 1-18 (2020)
van Schie, J J M, Faramarz, A, Balk, J A, Stewart, G S, Cantelli, E, Oostra, A B, Rooimans, M A, Parish, J L, de Almeida Estéves, C, Dumic, K, Barisic, I, Diderich, K E M, van Slegtenhorst, M A, Mahtab, M, Pisani, F M, Te Riele, H, Ameziane, N, Wolthuis, R M F & de Lange, J 2020, ' Warsaw Breakage Syndrome associated DDX11 helicase resolves G-quadruplex structures to support sister chromatid cohesion ', Nature Communications, vol. 11, no. 1, 4287, pp. 4287 . https://doi.org/10.1038/s41467-020-18066-8
info:cnr-pdr/source/autori:van Schie J.J.M.; Faramarz A.; Balk J.A.; Stewart G.S.; Cantelli E.; Oostra A.B.; Rooimans M.A.; Parish J.L.; de Almeida Esteves C.; Dumic K.; Barisic I.; Diderich K.E.M.; van Slegtenhorst M.A.; Mahtab M.; Pisani F.M.; te Riele H.; Ameziane N.; Wolthuis R.M.F.; de Lange J./titolo:Warsaw Breakage Syndrome associated DDX11 helicase resolves G-quadruplex structures to support sister chromatid cohesion/doi:10.1038%2Fs41467-020-18066-8/rivista:Nature communications/anno:2020/pagina_da:4287/pagina_a:4305/intervallo_pagine:4287–4305/volume:11
Nature Communications, 11(1):4287. Nature Publishing Group
Nature Communications
Nature communications, 11(1):4287. Nature Publishing Group
Nature Communications, 11(1):4287. Nature Publishing Group UK
Nature Communications, Vol 11, Iss 1, Pp 1-18 (2020)
van Schie, J J M, Faramarz, A, Balk, J A, Stewart, G S, Cantelli, E, Oostra, A B, Rooimans, M A, Parish, J L, de Almeida Estéves, C, Dumic, K, Barisic, I, Diderich, K E M, van Slegtenhorst, M A, Mahtab, M, Pisani, F M, Te Riele, H, Ameziane, N, Wolthuis, R M F & de Lange, J 2020, ' Warsaw Breakage Syndrome associated DDX11 helicase resolves G-quadruplex structures to support sister chromatid cohesion ', Nature Communications, vol. 11, no. 1, 4287, pp. 4287 . https://doi.org/10.1038/s41467-020-18066-8
Warsaw Breakage Syndrome (WABS) is a rare disorder related to cohesinopathies and Fanconi anemia, caused by bi-allelic mutations in DDX11. Here, we report multiple compound heterozygous WABS cases, each displaying destabilized DDX11 protein and resid
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0d2904393f00b9ed4fde7c1c05a3cda8
Autor:
Janne J. M. van Schie, Atiq Faramarz, Jesper A. Balk, Grant S. Stewart, Erika Cantelli, Anneke B. Oostra, Martin A. Rooimans, Joanna L. Parish, Cynthia de Almeida Estéves, Katja Dumic, Ingeborg Barisic, Karin E. M. Diderich, Marjon A. van Slegtenhorst, Mohammad Mahtab, Francesca M. Pisani, Hein te Riele, Najim Ameziane, Rob M. F. Wolthuis, Job de Lange
Publikováno v:
Nature Communications, Vol 11, Iss 1, Pp 1-18 (2020)
WABS patient derived cells display loss of sister chromatid cohesion. Here the authors by analyzing WABS patient derived cells, reveal a role of the DDX11 helicase in resolving G-Quadruplex structures to support sister chromatid cohesion.
Externí odkaz:
https://doaj.org/article/d1dd653aad8b4232927aa9fceeb46e31
Autor:
Janne J. M. van Schie, Job de Lange
Publikováno v:
Cells, Vol 10, Iss 12, p 3455 (2021)
The cohesin complex facilitates faithful chromosome segregation by pairing the sister chromatids after DNA replication until mitosis. In addition, cohesin contributes to proficient and error-free DNA replication. Replisome progression and establishme
Externí odkaz:
https://doaj.org/article/b3b6356a77934e049bd27f97c21c9994